U.S. patent application number 14/793954 was filed with the patent office on 2016-01-14 for devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose, and/or throat.
The applicant listed for this patent is Acclarent, Inc.. Invention is credited to John Y. Chang, William M. Facteau, Eric Goldfarb, Joshua Makower, John H. Morriss.
Application Number | 20160008017 14/793954 |
Document ID | / |
Family ID | 40877012 |
Filed Date | 2016-01-14 |
United States Patent
Application |
20160008017 |
Kind Code |
A1 |
Makower; Joshua ; et
al. |
January 14, 2016 |
DEVICES, SYSTEMS AND METHODS FOR DIAGNOSING AND TREATING SINUSITIS
AND OTHER DISORDERS OF THE EARS, NOSE, AND/OR THROAT
Abstract
Various diagnostic procedures and devices are used to perform
imaging studies, mucus flow studies, air/gas flow studies, anatomic
dimension studies, endoscopic studies and transillumination
studies. Devices and methods for visually confirming the
positioning of a distal end portion of an illuminating device
placed within a patient include inserting a distal end portion of
an illuminating device internally into a patient, emitting light
from the distal end portion of the illuminating device, observing
transillumination resulting from the light emitted from the distal
end portion of the illuminating device that occurs on an external
surface of the patient, and correlating the location of the
observed transillumination on the external surface of the patient
with an internal location of the patient that underlies the
location of observed transillumination, to confirm positioning of
the distal end portion of the illuminating device.
Inventors: |
Makower; Joshua; (Los Altos,
CA) ; Chang; John Y.; (Los Altos, CA) ;
Goldfarb; Eric; (Belmont, CA) ; Morriss; John H.;
(Emerald Hills, CA) ; Facteau; William M.;
(Atherton, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Acclarent, Inc. |
Menlo Park |
CA |
US |
|
|
Family ID: |
40877012 |
Appl. No.: |
14/793954 |
Filed: |
July 8, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12355492 |
Jan 16, 2009 |
9101384 |
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14793954 |
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10829917 |
Apr 21, 2004 |
7654997 |
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12355492 |
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11522497 |
Sep 15, 2006 |
7559925 |
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10829917 |
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Current U.S.
Class: |
600/424 |
Current CPC
Class: |
A61B 1/0661 20130101;
A61B 17/12136 20130101; A61B 17/12104 20130101; A61B 17/320783
20130101; A61B 17/12186 20130101; A61B 2017/22061 20130101; A61B
90/39 20160201; A61M 25/0082 20130101; A61B 17/12172 20130101; A61B
17/3478 20130101; A61B 90/36 20160201; A61B 17/320725 20130101;
A61B 17/12045 20130101; A61M 25/0068 20130101; A61M 25/10 20130101;
A61M 2025/0037 20130101; A61B 8/12 20130101; A61M 25/0074 20130101;
A61B 17/12022 20130101; A61B 5/107 20130101; A61M 2025/109
20130101; A61B 8/445 20130101; A61B 5/411 20130101; A61M 2025/004
20130101; A61B 17/1219 20130101; A61B 17/32075 20130101; A61B
2090/3945 20160201; A61M 25/003 20130101; A61M 2025/0087 20130101;
A61B 17/24 20130101; A61B 2217/005 20130101; A61M 2025/1052
20130101; A61B 17/1214 20130101; A61B 17/320758 20130101; A61M
2025/0096 20130101; A61M 25/007 20130101 |
International
Class: |
A61B 17/24 20060101
A61B017/24; A61B 1/06 20060101 A61B001/06; A61M 25/00 20060101
A61M025/00; A61B 19/00 20060101 A61B019/00; A61B 17/12 20060101
A61B017/12 |
Claims
1. A method of confirming the location of an elongate member
configured for placement within a patient's sinus cavity
comprising: introducing the elongate member through a nasal
passageway to place a distal tip of the elongate member in a test
position, the elongate member configured to emit illuminating light
via the distal end of the elongate member; and viewing the location
of the light through the patient's skin to confirm the positioning
of the elongate member.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS
[0001] This application is a continuation-in-part of U.S. patent
application Ser. No. 10/829,917 filed on Apr. 21, 2004, and is also
a continuation-in-part of U.S. patent application Ser. No.
11/522,497 filed on Sep. 15, 2006; the entireties of which are
herein incorporated by reference.
FIELD OF THE INVENTION
[0002] The present invention relates generally to medical devices
and methods and more particularly to minimally invasive, catheter
based devices, systems and methods for treating sinusitis and other
ear, nose & throat disorders, and which reduce the need to
provide fluoroscopic or other radiographic visualization.
BACKGROUND OF THE INVENTION
[0003] The human nose is responsible for warming, humidifying and
filtering inspired air and for conserving heat and moisture from
expired air. The nose is also an important cosmetic feature of the
face. The nose is formed mainly of cartilage, bone, mucous
membranes and skin. The right and left nostrils lead into right and
left nasal cavities on either side of the intranasal septum. The
right and left nasal cavities extend back to the soft palate, where
they merge to form the posterior choanae. The posterior choanae
opens into the nasopharynx. The roof of the nose is formed, in
part, by a bone known as the cribriform plate. The cribriform plate
contains numerous tiny perforations through which sensory nerve
fibers extend to the olfactory bulbs. The sensation of smell occurs
when inhaled odors contact a small area of mucosa in the superior
region of the nose, stimulating the nerve fibers that lead to the
olfactory bulbs.
[0004] The paranasal sinuses are cavities formed within the bones
of the face. The paranasal sinuses include frontal sinuses, ethmoid
sinuses, sphenoidal sinuses and maxillary sinuses. The paranasal
sinuses are lined with mucous-producing epithelial tissue.
Normally, mucous produced by the linings of the paranasal sinuses
slowly drains out of each sinus through an opening known as an
ostium, and into the nasopharynx. Disorders that interfere with
drainage of mucous (e.g., occlusion of the sinus ostia) can result
in a reduced ability of the paranasal sinuses to function normally.
This results in mucosal congestion within the paranasal sinuses.
Such mucosal congestion of the sinuses can cause damage to the
epithelium that lines the sinus with subsequent decreased oxygen
tension and microbial growth (e.g., a sinus infection).
[0005] The nasal turbinates are three (or sometimes four) bony
processes that extend inwardly from the lateral walls of the nose
and are covered with mucosal tissue. These turbinates serve to
increase the interior surface area of the nose and to impart warmth
and moisture to air that is inhaled through the nose. The mucosal
tissue that covers the turbinates is capable of becoming engorged
with blood and swelling or becoming substantially devoid of blood
and shrinking, in response to changes in physiologic or
environmental conditions. The curved edge of each turbinate defines
a passageway known as a meatus. For example, the inferior meatus is
a passageway that passes beneath the inferior turbinate. Ducts,
known as the nasolacrimal ducts, drain tears from the eyes into the
nose through openings located within the inferior meatus. The
middle meatus is a passageway that extends inferior to the middle
turbinate. The middle meatus contains the semilunar hiatus, with
openings or ostia leading into the maxillary, frontal, and anterior
ethmoid sinuses. The superior meatus is located between the
superior and medial turbinates.
[0006] Nasal Polyps:
[0007] Nasal polyps are benign masses that grow from the lining of
the nose or paranasal sinuses. Nasal polyps often result from
chronic allergic rhinitis or other chronic inflammation of the
nasal mucosa. Nasal polyps are also common in children who suffer
from cystic fibrosis. In cases where nasal polyps develop to a
point where they obstruct normal drainage from the paranasal
sinuses, they can cause sinusitis.
[0008] Sinusitis:
[0009] The term "sinusitis" refers generally to any inflammation or
infection of the paranasal sinuses. Sinusitis can be caused by
bacteria, viruses, fungi (molds), allergies or combinations
thereof. It has been estimated that chronic sinusitis (e.g.,
lasting more than 3 months or so) results in 18 million to 22
million physician office visits per year in the United States.
[0010] Patients who suffer from sinusitis typically experience at
least some of the following symptoms: [0011] headaches or facial
pain [0012] nasal congestion or post-nasal drainage [0013]
difficulty breathing through one or both nostrils [0014] bad breath
[0015] pain in the upper teeth
[0016] Proposed Mechanism of Sinus Pain & Diagnosis
[0017] The sinuses consist of a series of cavities connected by
passageways, ultimately opening into the nasal cavity. As described
previously, these passageways and cavities are formed by bone, but
covered in mucosa. If the mucosa of one of these passageways
becomes inflamed for any reason, the cavities which drain through
that passageway can become blocked. This trapping of mucous can be
periodic (resulting in episodes of pain) or chronic. Chronically
blocked passageways are targets of infection. Ultimately, it is the
dimensions of the bony passageways and thickness of the overlying
mucosa and its chronicity that dictate the duration and severity of
sinus symptoms. Thus, the primary target for sinus therapy is the
passageway, with the primary goal to regain drainage. Often CT will
not reveal these dimensional issues, especially when the patient is
not currently experiencing severe symptoms. Therefore there exists
a need to dynamically evaluate the sinus passageways under normal
conditions, in response to challenging stimuli. As suggested
herein, if it would be possible to assess sinus disease and its
dynamic component, one might better target therapy for sinusitis
and possibly be able to treat patients in a more focused and
minimally invasive manner. Such focus on the passageway and the use
of flexible instrumentation suggests an entirely new approach to
sinus intervention: one utilizing flexible catheters and guidance
tools, with passageway and cavity modifying devices capable of
being delivered with minimal damage to the surrounding tissues.
[0018] Deviated Septum:
[0019] The intranasal septum is a cartilaginous anatomical
structure that divides one side of the nose from the other.
Normally, the septum is relatively straight. A deviated septum is a
condition where the cartilage that forms the septum is abnormally
curved or bent. A deviated nasal septum may develop as the nose
grows or, in some cases, may result from trauma to the nose. A
deviated septum can interfere with proper breathing or may obstruct
normal drainage of nasal discharge, especially in patient's whose
nasal turbinates are swollen or enlarged due to allergy, overuse of
decongestant medications, etc., Such interference with drainage of
the sinuses can predispose the patient to sinus infections.
[0020] A deviated nasal septum that interferes with proper function
of the nose can be surgically corrected by a procedure known as
septoplasty. In a typical septoplasty procedure, an endoscope is
inserted into the nose and the surgeon makes an incision inside the
nose, lifts up the lining of the septum, and removes and
straightens the underlying bone and cartilage that is abnormally
deviated. Such surgical septoplasty procedures can effectively
straighten a deviated septum but, because the nasal cartilage has
some memory, the septum may tend to resume its original deviated
shape.
[0021] Reduction/Removal of Nasal Turbinates
[0022] Various surgical techniques, including endoscopic surgery,
have been used for reduction and/or removal of the inferior
turbinate in patient's whose inferior turbinate is chronically
enlarged such that it is obstructing normal breathing and/or normal
drainage from the paranasal sinuses. Typically, chronic enlargement
of the inferior turbinates is the result of allergies or chronic
inflammation. Enlargement of the inferior turbinate can be
especially problematic in patient's who also suffer from a deviated
septum that crowds or impinges upon the soft tissue of the
turbinate. Thus, a septoplasty to straighten the deviated septum is
sometimes performed concurrently with a reduction of the inferior
turbinates.
[0023] Sinus Tumors
[0024] Most polyps are benign, but one form of a nasal polyp, known
as an inverting papilloma, can develop into a malignancy. Unlike
most benign polyps, which typically occur on both sides of the
nose, an inverting papilloma is usually found on just one side.
Thus, in cases where a unilateral polyp is observed, it is usually
biopsied to determine if it is malignant. If an inverting papilloma
is detected before it becomes malignant and is removed completely,
it will typically not recur. However, using the technology that has
heretofore been available, it has sometimes been difficult to
determine if the papilloma has been entirely removed unless and
until regrowth of the polyp is observed on long term post-surgical
follow-up.
[0025] Various benign sinus tumors have also been known to occur,
but are relatively rare. The most common form of malignant sinus
tumor is squamous cell carcinoma. Even with surgery and radiation
treatment, squamous cell carcinoma of the paranasal sinus is
associated with a relatively poor prognosis. Other types of
malignant tumors that invade the paranasal sinuses include
adenocarcinoma and, more rarely, lymphoma and even more rarely,
melanoma.
[0026] Facial Fractures
[0027] The most common cause of fractures of the facial bones is
auto accidents, but facial fractures are also frequently caused by
sports injuries, industrial accidents, falls, assaults and gunshot
wounds. Some facial fractures involve bones that are accessible
from inside the nasal cavities or paranasal sinuses. Notably, the
nose is the most commonly injured facial structure due to its
prominent position on the face. Thus, fractures of the nasal bone
(with or without resultant deviated septum) are not uncommon. Other
facial fractures such as fractures of the orbital floor and/or the
ethmoid or frontal sinuses are also accessible from inside the nose
or sinuses. A common type of orbital floor fracture is a "blowout"
fracture that typically results from blunt trauma to the eye where
the force is transmitted downwardly causing the relatively thin
bone that forms the floor of the orbit to fracture downwardly. This
can cause the periorbital tissues to herniate into the maxillary
sinus and sometimes can also create a "trap door" of bone that
extends downwardly into the maxillary sinus.
[0028] Endoscopic Sinus Surgery and Other Current Procedures
[0029] Functional Endoscopic Sinus Surgery
[0030] The most common corrective surgery for chronic sinusitis is
functional endoscopic sinus surgery (FESS). In FESS, an endoscope
is inserted into the nose and, under visualization through the
endoscope, the surgeon may remove diseased or hypertrophic tissue
or bone and may enlarge the ostia of the sinuses to restore normal
drainage of the sinuses. FESS procedures can be effective in the
treatment of sinusitis and for the removal of tumors, polyps and
other aberrant growths from the nose. Other endoscopic intranasal
procedures have been used to remove pituitary tumors, to treat
Graves disease (i.e., a complication of hyperthyroidism which
results in protrusion of the eyes) and surgical repair of rare
conditions wherein cerebrospinal fluid leaks into the nose (i.e.,
cerebrospinal fluid rhinorrhea).
[0031] Surgery to reduce the size of the inferior turbinates can be
accomplished with endoscopic visualization (with magnification
where desired) and is typically performed with the patient under
general anesthesia. An incision is typically made in the mucosa
that lines the turbinate to expose the underlying bone. Some
quantity of the underlying bone may then be removed. If selective
removal of some of the mucosa or soft tissue is also desired, such
soft tissue can be debulked or removed through by traditional
surgical cutting or by the use of other tissue ablation or
debulking apparatus such as microdebriders or lasers. Less
frequently, chronically enlarged inferior turbinates have been
treated by cryotherapy. It is typically desirable to remove only as
much tissue as necessary to restore normal breathing and drainage,
as removal of too much tissue from the turbinates can impair the
ability of the turbinates to perform their physiological functions
of warming and humidifying inspired air and conserving warmth and
moisture from expired air. Complications associated with inferior
turbinate surgery include bleeding, crusting, dryness, and
scarring.
[0032] In some patients, the middle turbinate is enlarged due to
the presence of an invading air cell (concha bullosa), or the
middle turbinate may be malformed (paradoxically bent). Severe
ethmoid sinusitis or nasal polyps can also result in enlargement or
malformation of the middle turbinates. Since a substantial amount
of drainage from the sinuses passes through the middle meatus
(i.e., the passage that runs alongside middle turbinate) any
enlargement or malformation of the middle turbinate can contribute
to sinus problems and require surgical correction. Thus, in some
FESS procedures carried out to treat sinusitis, the middle meatus
is cleared (e.g., the polyps or hypertorophic tissue are removed)
thereby improving sinus drainage. However, the middle turbinate can
include some of the olfactory nerve endings that contribute to the
patient's sense of smell. For this reason, any reduction of the
middle turbinate is typically performed in a very conservative
manner with care being taken to preserve as much tissue as
possible. In patients who suffer from concha bullosa, this may
involve removing the bone on one side of an invading air sac. In
the cases where the middle turbinate is malformed, just the
offending portion(s) of the turbinate may be removed.
[0033] Extended Endoscopic Frontal Sinus Surgery
[0034] Because of its narrow anatomical configuration, inflammation
of the frontal sinuses can be particularly persistent, even after
surgery and/or medical therapy has resolved the inflammation in the
other paranasal sinuses. In cases of persistent inflammation of the
frontal sinuses, a surgery known as a trans-septal frontal
sinusotomy, or modified Lothrop procedure, is sometimes performed.
In this procedure, the surgeon removes a portion of the nasal
septum and the bony partition between the sinuses to form one large
common drainage channel for draining the frontal sinuses into the
nose. This complicated procedure, as well as some other ear, nose
and throat surgical procedures, can carry a risk of penetrating the
cranial vault and causing leakage of cerebrospinal fluid (CSF).
Also, some sinus surgeries as well as other ear, nose and throat
procedures are performed close to the optic nerves, the eyes, and
the brain and can cause damage to those structures. To minimize the
potential for such untoward complications or damage, image-guided
surgery systems have been used to perform some complex head and
neck procedures. In image guided surgery, integrated anatomical
information is supplied through CT-scan images or other anatomical
mapping data taken before the operation. Data from a preoperative
CT scan or other anatomical mapping procedure is downloaded into a
computer and special sensors known as localizers are attached to
the surgical instruments. Thus, using the computer, the surgeon can
ascertain, in three dimensions, the precise position of each
localizer-equipped surgical instrument at any given point in time.
This information, coupled with the visual observations made through
the standard endoscope, can help the surgeon to carefully position
the surgical instruments to avoid creating CSF leaks and to avoid
causing damage to nerves or other critical structures.
[0035] Shortcomings of FESS
[0036] Although FESS continues to be the gold standard therapy for
severe sinuses, it has several shortfalls. Often patients complain
of the post-operative pain and bleeding associated with the
procedure, and a significant subset of patients remain symptomatic
even after multiple surgeries. Since FESS is considered an option
only for the most severe cases (those showing abnormalities under
CT scan), a large population of patients exist that can neither
tolerate the prescribed medications nor be considered candidates
for surgery. Further, because the methodologies to assess sinus
disease are primarily static measurements (CT, MRI), patients whose
symptoms are episodic are often simply offered drug therapy when in
fact underlying mechanical factors may play a significant role. To
date, there is no mechanical therapy offered for these patients,
and even though they may fail pharmaceutical therapies, no other
course of action is indicated. This leaves a large population of
patients in need of relief, unwilling or afraid to take steroids,
but not sick enough to qualify for surgery.
[0037] One of the reasons why FESS and sinus surgery is so bloody
and painful relates to the fact that straight instrumentation with
rigid shafts are used. Due to the fact that the sinuses are so
close to the brain and other important structures, physicians have
developed techniques using straight tools and image guidance to
reduce the likelihood of penetrating into unwanted areas. In an
effort to target deep areas of the anatomy, this reliance on
straight instrumentation has resulted in the need to resect and
remove or otherwise manipulate any anatomical structures that may
lie in the path of the instruments, regardless of whether those
anatomical structures are part of the pathology. With the advances
in catheter based technology and imaging developed for the
cardiovascular system, there exists a significant opportunity to
reduce the morbidity of sinus interventional through the use of
flexible instrumentation and guidance.
[0038] If flexible tools could be developed such that sinus
intervention may be able to be carried out with even less bleeding
and post-operative pain, these procedures may be applicable to a
larger group of patients. Further, as described here, flexible
instrumentation may allow the application of new diagnostic and
therapeutic modalities that have never before been possible.
[0039] Laser or Radiofrequency Turbinate Reduction Soft Tissue
Only)
[0040] In cases where it is not necessary to revise the bone that
underlies the turbinate, the surgeon may elect to perform a laser
or radiofrequency procedure designed to create a coagulative lesion
in (or on) the turbinate, which in turn causes the soft tissue of
the turbinate to shrink. Also, in some cases, a plasma generator
wand may be used create high energy plasma adjacent to the
turbinate to cause a reduction in the size of the turbinate.
[0041] One example of a radio frequency procedure that may be used
to shrink enlarged inferior turbinates is radiofrequency volumetric
tissue reduction (RFVTR) using the Somnoplasty.RTM. system (Somnus
Medical Technologies, Sunnyvale, Calif.). The Somnoplasty.RTM.
system includes a radio frequency generator attached to a probe.
The probe is inserted through the mucosa into the underlying soft
tissue of the turbinate, usually under direct visualization.
Radiofrequency energy is then delivered to heat the submucosal
tissue around the probe, thereby creating a submucosal coagulative
lesion while allowing the mucosa to remain in tact. As the
coagulative lesion heals, the submucosal tissue shrinks thereby
reducing the overall size of the turbinate. Radiofrequency
volumetric tissue reduction (RFVTR) can be performed as an office
procedure with local anesthesia.
[0042] Many of the above-described procedures and techniques may be
adaptable to minimally invasive approaches and/or the use of
flexible instrumentation. There exists a need in the art for the
development of such minimally invasive procedures and techniques as
well as instrumentation (e.g., flexible instruments or catheters)
useable to perform such procedures and techniques.
[0043] The skull contains a series of cavities known as paranasal
sinuses that are connected by passageways. The paranasal sinuses
are lined with mucous-producing mucosal tissue and ultimately open
into the nasal cavity. Normally, mucous produced by the mucosal
tissue slowly drains out of each sinus through an opening known as
an ostium. If the mucosal tissue of one of these passageways
becomes inflamed for any reason, the cavities which drain through
that passageway can become blocked. This blockage can be periodic
(resulting in episodes of pain) or chronic. This interference with
drainage of mucous (e.g., occlusion of a sinus ostium) can result
in mucosal congestion within the paranasal sinuses. Chronic mucosal
congestion of the sinuses can cause damage to the epithelium that
lines the sinus with subsequent decreased oxygen tension and
microbial growth (e.g., a sinus infection).
[0044] The term "sinusitis" refers generally to any inflammation or
infection of the paranasal sinuses caused by bacteria, viruses,
fungi (molds), allergies or combinations thereof. It has been
estimated that chronic sinusitis (e.g., lasting more than 3 months
or so) results in 18 million to 22 million physician office visits
per year in the United States. Patients who suffer from sinusitis
typically experience at least some of the following symptoms:
headaches or facial pain; nasal congestion or post-nasal drainage;
difficulty breathing through one or both nostrils; bad breath;
and/or pain in the upper teeth.
[0045] One of the ways to treat sinusitis is by restoring the lost
mucous flow. The initial therapy is typically drug therapy using
anti-inflammatory agents to reduce the inflammation and antibiotics
to treat the infection. A large number of patients do not respond
to drug therapy. Currently, the gold standard for patients with
chronic sinusitis that do not respond to drug therapy is a
corrective surgery called Functional Endoscopic Sinus Surgery
(FESS).
[0046] As indicated above, FESS does have several shortcomings. For
example, FESS can cause significant post-operative pain. Also, some
FESS procedures are associated with significant postoperative
bleeding and, as a result, nasal packing is frequently placed in
the patient's nose for some period of time following the surgery.
Such nasal packing can be uncomfortable and can interfere with
normal breathing, eating, drinking etc. Also, some patients remain
symptomatic even after multiple FESS surgeries. Additionally, some
FESS procedures are associated with risks of iatrogenic orbital,
intracranial and sinonasal injury. Many otolaryngologists consider
FESS an option only for patients who suffer from severe sinus
disease (e.g., those showing significant abnormalities under CT
scan). Thus, patients with less severe disease may not be
considered candidates for FESS
[0047] In work done in connection with the present invention, new
devices, systems and techniques are being developed for the
treatment of sinusitis and other disorders of the ear, nose, throat
and paranasal sinuses. For example, various catheters, guidewires
and other devices useable to perform minimally invasive, minimally
traumatic ear, nose and throat surgery have been described in U.S.
patent application Ser. No. 10/829,917 entitled "Devices, Systems
and Methods for Diagnosing and Treating Sinusitis and Other
Disorders of the Ears, Nose and/or Throat," Ser. No. 10/912,578
entitled "Implantable Device and Methods for Delivering Drugs and
Other Substances to Treat Sinusitis and Other Disorders," Ser. No.
10/944,270 entitled "Apparatus and Methods for Dilating and
Modifying Ostia of Paranasal Sinuses and Other Intranasal or
Paranasal Structures" Ser. No. 11/037,548 entitled "Devices,
Systems and Methods For Treating Disorders of the Ear, Nose and
Throat", and Ser. No. 11/116,118 entitled "Methods and Devices For
Performing Procedures Within the Ear, Nose, Throat and Paranasal
Sinuses". Each of these applications is hereby incorporated herein,
in its entirety, by reference thereto. Many of these new devices,
systems and techniques are useable in conjunction with endoscopic,
radiographic and/or electronic assistance to facilitate precise
positioning and movement of catheters, guidewires and other devices
within the ear, nose, throat and paranasal sinuses and to avoid
undesirable trauma or damage to critical anatomical structures such
as the eyes, facial nerves and brain.
[0048] For example, in one new procedure (referred to in this
patent application as a "Flexible Transnasal Sinus Intervention" or
FTSI), a dilatation catheter (e.g., a balloon catheter or other
type of dilator) is advanced through the nose to a position within
the ostium of a paranasal sinus or other location, without
requiring removal or surgical alteration of other intranasal
anatomical structures. The dilatation catheter is then used to
dilate the ostium or other anatomical structures to facilitate
natural drainage from the sinus cavity. In some cases, a tubular
guide may be initially inserted through the nose and advanced to a
position near the sinus ostium and a guidewire may then be advanced
through the tubular guide and into the affected paranasal sinus.
The dilatation catheter may then be advanced over the guidewire and
through the tubular guide to a position where its dilator (e.g.,
balloon) is positioned within the sinus ostium. The dilator (e.g.,
balloon) is then expanded causing the ostium to dilate. In some
cases, such dilatation of the ostium may fracture, move or remodel
bony structures that surround or are adjacent to the ostium.
Optionally, in some procedures, irrigation solution and/or
therapeutic agents may be infused through a lumen of the dilatation
catheter and/or other working devices (e.g., guidewires, catheters,
cannula, tubes, dilators, balloons, substance injectors, needles,
penetrators, cutters, debriders, microdebriders, hemostatic
devices, cautery devices, cryosurgical devices, heaters, coolers,
scopes, endoscopes, light guides, phototherapy devices, drills,
rasps, saws, etc.) may be advanced through the tubular guide and/or
over the guidewire to deliver other therapy to the sinus or
adjacent tissues during the same procedure in which the FTSI is
carried out. It is to be understood that, in FTSI procedures,
structures and passageways other than sinus ostia may be dilated
using the tools described above, tissue may be resected or ablated,
bone may be restructured, drugs or drug delivery systems may be
deployed, etc., as described in the documents incorporated herein
by reference. Thus, for the purposes of this application the term
FTSI will be generally used to refer broadly to all of those
procedures, not just dilation of sinus ostia.
[0049] In FTSI procedures that include positioning of a guidewire
into a paranasal sinus, the placement of the guidewire is typically
confirmed by visualizing the procedure under fluoroscopy or other
x-ray visualization technique, for example. Appropriate positioning
of the tubular guide at the position near the sinus ostium may also
be confirmed via fluoroscopy. In order to reduce the radiation
exposure to the patient undergoing the procedure, and particularly
to the surgeon and other personnel that carry out many of these
types of procedures, there is a need for methods and devices that
eliminate or reduce the need to use fluoroscopic visualization
during such procedures.
SUMMARY OF THE INVENTION
[0050] In general, the present invention provides methods, devices
and systems for diagnosing and/or treating sinusitis or other
conditions of the ear, nose or throat.
[0051] In accordance with the present invention, there are provided
methods wherein one or more flexible catheters or other flexible
elongate devices as described herein are inserted in to the nose,
nasopharynx, paranasal sinus, middle ear or associated anatomical
passageways to perform an interventional or surgical procedure.
Examples of procedures that may be performed using these flexible
catheters or other flexible elongate devices include but are not
limited to: delivering contrast medium; delivering a
therapeutically effective amount of a therapeutic substance;
implanting a stent, tissue remodeling device, substance delivery
implant or other therapeutic apparatus; cutting, ablating,
debulking, cauterizing, heating, freezing, lasing, dilating or
otherwise modifying tissue such as nasal polyps, aberrant or
enlarged tissue, abnormal tissue, etc.; grafting or implanting
cells or tissue; reducing, setting, screwing, applying adhesive to,
affixing, decompressing or otherwise treating a fracture;
delivering a gene or gene therapy preparation; cutting, ablating,
debulking, cauterizing, heating, freezing, lasing, forming an
osteotomy or trephination in or otherwise modifying bony or
cartilaginous tissue within paranasal sinus or elsewhere within the
nose; remodeling or changing the shape, size or configuration of a
sinus ostium or other anatomical structure that affects drainage
from one or more paranasal sinuses; removing puss or aberrant
matter from the paranasal sinus or elsewhere within the nose;
scraping or otherwise removing cells that line the interior of a
paranasal sinus; removing all or a portion of a tumor; removing a
polyp; delivering histamine, an allergen or another substance that
causes secretion of mucous by tissues within a paranasal sinus to
permit assessment of drainage from the sinus; implanting a cochlear
implant or indwelling hearing aid or amplification device, etc.
[0052] Further in accordance with the invention, there are provided
methods for diagnosing and assessing sinus conditions, including
methods for delivering contrast media into cavities, assessing
mucosal flow, assessing passageway resistance and cilliary
function, exposing certain regions to antigen challenge, etc.
[0053] Still further in accordance with the invention, there are
provided novel devices for performing some or all of the procedures
described herein.
[0054] A method for visually confirming the positioning of a distal
end portion of a device placed within a patient is provided to
include: inserting a distal end portion of an illuminating device
internally into a patient, emitting light from the distal end
portion of the illuminating device; observing transillumination
resulting from the light emitted from the distal end portion of the
illuminating device that occurs on an external surface of the
patient; and correlating the location of the observed
transillumination on the external surface of the patient with an
internal location of the patient that underlies the location of
observed transillumination, to confirm positioning of the distal
end portion of the illuminating device.
[0055] In at least one embodiment, the observation is performed by
direct line of sight human observation, without the need for
fluoroscopy. In at least one embodiment, the observation is
performed by direct line of sight human observation, without the
need for any visualization equipment. In at least one embodiment,
the illuminating device comprises a guidewire. In at least one
embodiment, the illuminating device comprises an ostium seeker
device. In at least one embodiment, the illuminating device
comprises a sinus suction instrument. In at least one embodiment,
the illuminating device comprises an integrated wire dilatation
catheter, wherein an integrated illuminating guidewire extends
distally of a distal end of a dilatation catheter. In at least one
embodiment, the distal end portion of the illuminating guidewire is
inserted into a sinus passageway of the patient. In at least one
embodiment, the distal end portion of the illuminating guidewire is
inserted through an ostium opening to a sinus of the patient, and
the distal end portion is advanced into the sinus. In at least one
embodiment, the distal end portion of the illuminating guidewire is
initially inserted through a nostril of the patient and then
advanced into a sinus. In at least one embodiment, a scope is
inserted through the nostril of the patient, wherein the guidewire
is inserted adjacent the scope, and visualization of the
advancement of the distal end portion of the guide wire is
performed via the scope as the distal end portion is advanced
toward an ostium of the sinus. In at least one embodiment,
transillumination is observed when a light emitting portion of the
distal end portion is located in the sinus of the patient.
[0056] If observation of transillumination and correlation reveals
that the distal end portion of the illumination device has been
misrouted to a location other than a target location, distal end
portion of the device can be retracted and re-routed to the target
location, which can be confirmed by observing transillumination and
correlating.
[0057] In observing transillumination, the motion of the
transillumination spot resulting from the light emitted from the
distal end portion of the illuminating device can be observed and
tracked or followed visually, as the distal end portion is moved
relative to the patient, and this can be one way of confirming that
the transillumination spot in motion correlates to a position of
the distal end portion. This technique can be particularly useful
when there are additional sources of transillumination, such as a
light from a scope, for example.
[0058] Further, transillumination resulting from the light emitted
from the distal end portion of the device can be distinguished from
transillumination resulting from light emitted from a scope by
identifying a transillumination spot that is at least one of
brighter, smaller or more well-defined than other transillumination
effects observed. Alternatively, the transillumination resulting
from the light emitted from the distal end portion of the device
can be distinguished from transillumination resulting from light
emitted from a scope by turning off or down the light source to the
scope.
[0059] In at least one embodiment, a sinus guide is inserted within
the patient prior to inserting the device, and the distal end
portion of the illuminating device is inserted through the sinus
guide. In at least one embodiment, the illuminating device is
preloaded in the guide, and the guide and preloaded illuminating
device are inserted together into the patient. Advancement of the
illuminating device relative to the guide can then be performed to
extend a distal end portion of the illuminating device distally of
a distal end of the guide.
[0060] A scope may be inserted within the patient, wherein the
sinus guide is inserted adjacent the scope, and advancement of the
sinus guide can be visualized via the scope.
[0061] In at least one embodiment, visualization of the advancement
of the sinus guide is through use of the scope, up to a limit of
adequate illumination by the scope. After that, the light emitted
by the distal end portion of the illuminating device, having been
advanced distally of a distal end of the sinus guide, extends the
limit of adequate illumination of the scope, thereby extending a
length of the adequate illumination of the scope. In at least one
embodiment, the sinus guide can be further distally advanced under
visualization by the scope as facilitated by the extended length of
the adequate illumination. In at least one embodiment,
visualization of the advancement of the illuminating device
distally of the sinus guide can be performed via the scope, as
facilitated by the light emitted from the distal end portion of the
device. In at least one embodiment, the scope is inserted into a
nostril of the patient, and the sinus guide is inserted adjacent
the scope. In at least one embodiment, the scope and sinus guide
are advanced into a sinus passageway of the patient. In at least
one embodiment, the sinus guide is further advanced toward an
ostium of a sinus, and the advancement of the sinus guide is
visually observed via the scope. In at least one embodiment, the
scope is inserted into a nostril of the patient, and the sinus
guide is inserted adjacent the scope. The advancement of the sinus
guide into a sinus passageway is visualized via the scope until a
distal end of the sinus guide has reached a distal limit of
illumination emitted by the scope. In at least one embodiment,
further advancement of the sinus guide toward an ostium of a sinus
is visualized via the scope as facilitated by the extended length
of adequate illumination provided by the illumination device. In at
least one embodiment, the scope is inserted into a nostril of the
patient, and the sinus guide is inserted adjacent the scope. The
advancement of the sinus guide to place a distal end of the sinus
guide adjacent an approach to an ostium of a sinus is visualized
via the scope. In at least one embodiment, the distal end portion
of the illuminating device is advanced further distally of a distal
end of the sinus guide and distal of the limit of illumination of
the scope to emit illumination, thereby extending a length of a
space that is visualizable by the scope. In at least one
embodiment, the distal end portion of the device is further
advanced into and through the ostium, and visualization of the
advancement of the distal end portion into the ostium is performed
via the scope. In at least one embodiment the device comprises an
illuminating guidewire, a working device is advanced over the
guidewire to position a working end of the working device at a
target location, and a surgical procedure is performed with the
working device at the target location. The working device is
removed from the patient after performing the surgical procedure.
Optionally, an implant can be left at the target location.
[0062] A method of performing a minimally invasive surgical
procedure is provided, including the steps of: inserting a distal
end portion of an illuminating guidewire internally into a patient;
emitting light from the distal end portion of the illuminating
guidewire, wherein a proximal end portion is connected to a power
source to enable the distal end portion to emit light; observing
transillumination resulting from the light emitted from the distal
end portion of the illuminating guidewire that occurs on an
external surface of the patient; correlating the location of the
observed transillumination on the external surface of the patient
with an internal location of the patient that underlies the
location of observed transillumination, to confirm positioning of
the distal end portion of the illuminating guidewire; disconnecting
the proximal end portion of the illuminating guidewire from the
power source; advancing a working device over the guidewire so that
a proximal end of the guidewire extends proximally from the working
device; reconnecting the proximal end portion of the illuminating
guidewire to the power source so that the distal end portion of the
guidewire again emits light; positioning a working end of the
working device at a target location; and performing a surgical
procedure with the working device at the target location.
[0063] After performing the surgical procedure, the proximal end
portion of the illuminating guidewire is disconnected from the
power source; and the working device is removed from the patient
and from the guidewire. Optionally, an implant can be left at the
target location.
[0064] In at least one embodiment, a second working device is
advanced over the guidewire after removing the first working device
therefrom, so that a proximal end of the guidewire extends
proximally from the second working device. Then the proximal end
portion of the illuminating guidewire is reconnected to the power
source so that the distal end portion of the guidewire again emits
light. In at least one embodiment, the illuminating guidewire
includes at least one illumination fiber extending from a proximal
end of the guidewire to the distal end portion, and the power
source is a light source. In at least one embodiment, the
illuminating guidewire includes at least one laser fiber extending
from a proximal end of the guidewire to the distal end portion, and
the power source is a laser light source. In at least one
embodiment, the illuminating guidewire includes a light emitting
diode at the distal end portion and electrical wires extending
through the guidewire, electrically connecting the light emitting
diode to the power source, and wherein the power source is an
electrical power source.
[0065] A method for diagnosing and/or treating sinusitis or another
disorder affecting a nose, a sinus or other anatomical structure of
the ear, nose or throat in a human or animal patient is provided,
including the steps of: advancing an introducing device through the
nose and to a position where the distal end of the introducing
device is near an opening of a sinus; advancing a distal end
portion of an illuminating device that emits light from the distal
end portion thereof through the introducing device while a proximal
end of the illuminating device is connected to a power source; and
monitoring a position of the distal end portion of the illuminating
device distally of the distal end of the introducing device, by
observing transillumination on an external surface of the patient
that results from the light emitted by the distal end portion. The
light emitted can be a desired wavelength in the visible spectrum
and/or infrared spectrum.
[0066] In at least one embodiment, the distal end portion of the
illuminating device is advanced through the opening of the sinus;
and placement of the distal end portion of the illuminating device
in the sinus is confirmed by observing the transillumination
resulting from the light emitted from the distal end portion of the
illuminating device that occurs on the external surface of the
patient, and correlating the location of the observed
transillumination on the external surface of the patient with an
internal location of the patient that underlies the location of
observed transillumination. In at least one embodiment, the
external surface on which the transillumination is observed is on
the face of the patient. In at least one embodiment, the external
surface on which the transillumination is observed is on the palate
of the patient. In at least one embodiment the illuminating device
comprises an illuminating guidewire, and a working device is
provided that is positionable in an operative location and useable
to perform a diagnostic or therapeutic procedure there. The
proximal end of the illuminating guidewire is disconnected from the
power source, while maintaining the distal end portion of the
illuminating guidewire in its current position, and the working
device is advanced over the guidewire so that a proximal end of the
guidewire extends proximally from the working device. The proximal
end of the illuminating guidewire is then reconnected to the power
source so that the distal end portion of the guidewire again emits
light. The working device is further advanced to position a working
end of the working device at the operative location, and a
diagnostic or therapeutic procedure is performed with the working
device at the operative location. In at least one embodiment, the
operative location is the opening to the Sinus.
[0067] An illuminating guidewire device is provided, including: a
flexible distal end portion; a relatively less flexible proximal
end portion; at least one light emitting element in the distal end
portion; and at least one structure extending from a proximal end
of the device through the proximal end portion and at least part of
the distal end portion to connect the at least one light emitting
element with a power source located proximally of the device.
[0068] In at least one embodiment, the at least one light emitting
element comprises a distal end of at least one illumination fiber,
and the at least one structure comprises the at least one
illumination fiber running proximally of the distal end of the
fiber to the proximal end of the device. In at least one
embodiment, the power source is a light source. In at least one
embodiment, the at least one light emitting element of the
illuminating guidewire comprises a distal end of at least one laser
fiber, and the at least one structure comprises the at least one
laser fiber running proximally from the distal end of the fiber to
the proximal end of said device. In at least one embodiment, the
power source is a laser light source. In at least one embodiment,
the at least one light emitting element comprises a light emitting
diode, and the at least one structure comprises at least one
electrical wire electrically connected to the light emitting diode
and extending proximally of the light emitting diode to the
proximal end of the device. In at least one embodiment, the power
source is an electrical power source. In at least one embodiment,
the distal end portion of the guidewire has an outside diameter
configured and dimensioned to pass through an ostium of a sinus. In
at least one embodiment, the distal end portion of the guidewire
has an outside diameter less than about 0.038 inches. In at least
one embodiment, the distal end portion of the guidewire has an
outside diameter of about 0.035''.+-.0.005''. In at least one
embodiment, the illuminating guidewire has a maximum outside
diameter of less than about 0.038 inches. In at least one
embodiment, the illuminating guidewire has a maximum outside
diameter of less than about 0.035 inches. In at least one
embodiment, the illuminating guidewire has a maximum outside
diameter of about 0.035''.+-.0.005''. In at least one embodiment,
the distal end portion of the device comprises a flexible coil. In
at least one embodiment, the distal end portion further comprises a
core support extending internally of the coil. In at least one
embodiment, the core support is fixed to the coil. In at least one
embodiment, a core support extending within the distal and proximal
end portions of the device. In at least one embodiment, the core
support extends within substantially the full length of the distal
and proximal end portions. In at least one embodiment, the distal
end portion of the device includes a bend, such that a proximal
part of the distal end portion is substantially aligned with a
longitudinal axis of the device, and a distal part of the distal
end portion is angled with respect to the longitudinal axis. In at
least one embodiment, the distal end of at least one illumination
fiber is configured to emit light from a distal tip of the distal
end portion of the device. The distal tip can be designed to either
focus or distribute the light to achieve maximum transillumination.
The distal tip can include a lens, prism or diffracting element. In
at least one embodiment, the distal end of at least one
illumination fiber is positioned proximally of a distal tip of the
distal end portion of the device. In at least one embodiment, a
flexible distal portion of the distal end portion extends distally
of the distal end of the at least one illumination fiber. In at
least one embodiment, the distal end of at least one laser fiber is
configured to emit light from a distal tip of the distal end
portion of the device. In at least one embodiment, the distal end
of at least one laser fiber is positioned proximally of a distal
tip of the distal end portion of the device. In at least one
embodiment, a flexible distal portion of the distal end portion
extends distally of the distal end of at least one illumination
fiber. In at least one embodiment, a light emitting diode is
mounted at a distal tip of the distal end portion of the device. In
at least one embodiment, a light emitting diode is positioned
proximally of a distal tip of the distal end portion of the device.
In at least one embodiment, a flexible distal portion of the distal
end portion extends distally of the light emitting diode. In at
least one embodiment, an electrical power source is removably,
electrically connected to at least one structure to provide
electrical power to at least one light emitting element. In at
least one embodiment, at least one light conducting tube delivers
light from a proximal end portion of the device to a distal and of
the tube, where it is emitted. In at least one embodiment, each
light conducting tube is sealed in a proximal end of the device. In
at least one embodiment, each light emitting element is sealed at a
distal tip of the device. In at least one embodiment, a quick
release connector is mounted over at least part of the proximal end
portion of the guidewire. The quick release connector is adapted to
be connected to a power source and to quickly connect to and
release from the proximal end portion of the guidewire. In at least
one embodiment, the quick release connector is optically coupled
with a light source. In at least one embodiment, the proximal end
portion of the quick release connector is adapted to connect with a
light source. In at least one embodiment, the proximal end portion
of the quick release connector comprises an ACMI light post. In at
least one embodiment, the connector is rotatable with respect to a
light channel extending from a light source, when the connector is
connected to the light channel. In at least one embodiment, the
light cable comprises a fluid filled light cable. In at least one
embodiment, a distal end portion of the connector comprises an
opening configured to slidably receive the proximal end portion of
the guidewire device; and a quick release locking mechanism is
configured to fix the proximal end portion received in the
connector. In at least one embodiment, the quick release locking
mechanism is movable between an unlocked configuration in which the
proximal end portion can be slid from the connector to disconnect
therefrom, and a locked configuration that maintains the proximal
end portion in connection with the connector. In at least one
embodiment, the quick release locking mechanism is biased toward
the locked configuration. In at least one embodiment, a radiopaque
marker is provided on the distal end portion of the guidewire. In
at least one embodiment, an electromagnetic coil is provided at the
distal end portion of the guidewire. Alternatively, a magnet,
radiofrequency emitter or ultrasound crystal can be provided at the
distal end portion of the guidewire.
[0069] An illuminating device is provided, including a distal end
portion having an outside diameter configured and dimensioned to
pass through an ostium of a sinus, at least one light emitting
element in the distal end portion, and at least one structure
extending from a proximal end of the device through the proximal
end portion and at least part of the distal end portion to connect
the at least one light emitting element with a power source.
[0070] In at least one embodiment, the illuminating device
comprises an illuminating guidewire. In at least one embodiment,
the illuminating device comprises an ostium seeker device, and the
distal end portion is rigid or malleable. In at least one
embodiment, the illuminating device comprises an ostium seeker
device, and the distal end portion comprises a ball tip at a distal
end thereof. In at least one embodiment, the illuminating device
comprises a sinus suction instrument, and the distal end portion
further comprises a suction lumen configured and adapted to apply
suction therethrough. In at least one embodiment, the illuminating
device comprises an integrated wire dilatation catheter, wherein an
integrated illuminating guidewire extends distally of a distal end
of a dilatation catheter of the device.
[0071] An illuminating guidewire device is provided including: a
guidewire including an elongated main body having a flexible distal
end portion and a relatively less flexible proximal end portion; at
least one light conducting channel extending the length of the
elongated body, and configured and dimensioned to deliver light
from a proximal end of the guidewire to a distal end of the
guidewire and to emit light from the distal end of the
guidewire.
[0072] In at least one embodiment, the at least one light
conducting channel comprises at least one illumination fiber. In at
least one embodiment, the at least one light conducting channel
comprises at least two illumination fibers. In at least one
embodiment, the illumination fibers are formed of plastic. In at
least one embodiment, the at least one illumination fiber is formed
of glass. In at least one embodiment, the at least one light
conducting channel comprises at least one laser fiber. In at least
one embodiment, a quick release connector is mounted over at least
part of the proximal end portion of the elongated body, and is
adapted to be connected to a light channel extending from a light
source; and to quickly connect to and release from the proximal end
portion of the elongated body. In at least one embodiment, the
quick release connector is optically coupled with the light source.
In at least one embodiment, a proximal end portion of the connector
comprises a tapering light channel configured to adapt a relatively
larger inside diameter of the light channel to a relatively smaller
diameter of the proximal end of the elongated body. In at least one
embodiment, a proximal end portion of the quick release connector
is adapted to connect with a light source. In at least one
embodiment, the proximal end portion of the quick release connector
includes an ACMI light post. In at least one embodiment, the
connector is rotatable with respect to the light channel extending
from the light source, when the connector is connected to the light
channel. In at least one embodiment, the distal end portion of the
connector comprises an opening configured to slidably receive the
proximal end portion of the elongated body, and a quick release
locking mechanism is configured to fix the proximal end portion
received in the connector. In at least one embodiment, the quick
release locking mechanism, in a locked configuration, maintains a
proximal end of the elongated body in alignment with a distal end
of the tapering light channel of the connector. In at least one
embodiment, the quick release locking mechanism is movable between
an unlocked configuration in which the proximal end portion can be
slid from the connector to disconnect therefrom, and a locked
configuration that maintains the proximal end portion in connection
with the connector. In at least one embodiment, a core support
extends at least within the distal end portion of the elongated
body of the guidewire. In at least one embodiment, the core support
further extends within the proximal end portion.
[0073] An illuminating guide wire device is provided, including: a
guidewire having an elongated main body with a flexible distal end
portion and a relatively less flexible proximal end portion; a
light emitting diode mounted in the distal end portion and
configured to emit light from a distal tip of the distal end
portion; and at least one electrical wire extending the length of
the elongated body, being electrically connected to the light
emitting diode, and extending proximally of a proximal end of the
elongated body.
[0074] In at least one embodiment, the illuminating guidewire
device includes at least two such electrical wires. In at least one
embodiment, a core support extends at least within the distal end
portion of the elongated body. In at least one embodiment, the core
support further extends within the proximal end portion. In at
least one embodiment, a radiopaque marker is provided on the distal
end portion. In at least one embodiment, an electromagnetic coil is
provided on the distal end portion.
[0075] An illuminating guidewire device is provided, including: a
guidewire having a flexible distal end portion, a relatively less
flexible proximal end portion, and a transparent portion
interconnecting the distal and proximal end portions; a least one
light emitting element mounted in the guidewire and configured to
emit light through the transparent portion; and at least one
structure extending from a proximal end of the device through the
proximal end portion and connecting with the at least one light
emitting element.
[0076] In at least one embodiment, the transparent portion
comprises a clear tube. In at least one embodiment, the clear tube
includes cut out windows therein. In at least one embodiment, the
transparent portion comprises a plurality of struts interconnecting
the proximal and distal end portions of the guidewire. In at least
one embodiment, a deflector is mounted distally of the at least one
light emitting element in the transparent portion. In at least one
embodiment, a quick release connector is mounted over at least part
of the proximal end portion, and is adapted to be connected to a
light channel extending from a light source, and to quickly connect
to and release from the proximal end portion of the guidewire. In
at least one embodiment, a core support extends at least within the
distal end portion. In at least one embodiment, the core support
further extends within the proximal end portion.
[0077] A quick release connector for use with an illuminating
guidewire is provided to include: a main body having a proximal end
portion and a distal end portion; a channel in the distal end
portion and opening to a distal end of the main body, wherein the
channel is configured and dimensioned to slidably receive a
proximal end portion of the illuminating guidewire; and a quick
release locking mechanism configured to assume a locked position
and an unlocked position, wherein when in the locked position, the
quick release locking mechanism fixes the proximal end portion of
the illuminating guide wire in the channel.
[0078] In at least one embodiment, the quick release locking
mechanism is biased to the locked position. In at least one
embodiment, upon inserting the proximal end portion of the
illuminating guidewire into the channel, the proximal end portion
contacts portions of the quick release locking mechanism, driving
the portions apart to allow the proximal end portion to be slid
into the channel. In at least one embodiment, the quick release
locking mechanism comprises a locking arm that extends into the
channel and a portion that extends out of the housing, wherein the
portion extending out of the housing is manually retractable to
move the locking arm from the locked position to the unlocked
position. In at least one embodiment, the quick release locking
mechanism includes at least two locking arms provided
circumferentially about the distal end portion of the main body of
the connector. In at least one embodiment, the quick release
locking mechanism comprises a pin vise. In at least one embodiment,
the proximal end portion of the connector is adapted to be
connected to a light channel extending from a light source. In at
least one embodiment, the proximal end portion of the main body is
optically coupled with a light source. In at least one embodiment,
the proximal end portion of the main body includes a tapering light
channel configured to adapt a relatively larger inside diameter of
a light channel to a relatively smaller diameter of the proximal
end of the illuminating guidewire. In at least one embodiment, the
proximal end portion of the main body comprises an ACMI light post.
In at least one embodiment, the quick release connector is
rotatable with respect to a light channel extending from a light
source, when the connector is connected to the light channel.
[0079] These and other advantages and features of the invention
will become apparent to those persons skilled in the art upon
reading the details of the devices, methods and systems as more
fully described below. Further aspects, details and embodiments of
the present invention will be understood by those of skill in the
art upon reading the following detailed description of the
invention and the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0080] FIG. 1A (Prior Art) is a frontal view of a human head
showing the locations of the paranasal sinuses.
[0081] FIG. 1B (Prior Art) is a side view of a human head showing
the locations of the paranasal sinuses.
[0082] FIG. 2A is a partial sectional view of head of a human
patient showing the right nasal cavity, the right side of the
nasopharynx and the associated paranasal sinuses, with an
anterior/posterior occluder & access device of the present
invention inserted therein.
[0083] FIG. 2B is a partial sectional view of head of a human
patient showing the left nasal cavity, the left side of the
nasopharynx and the associated paranasal sinuses, with an anterior
occluder & access device of the present invention inserted
therein.
[0084] FIG. 2C is a cross-sectional view through line C-C of FIG.
2A.
[0085] FIG. 2D is a cross-sectional view through line D-D of FIG.
2B.
[0086] FIG. 2E is a perspective view of a posterior
occluder/suction/access device of the present invention that is
insertable through the oral cavity.
[0087] FIG. 2F is a cross-sectional view through Line 2F-2F of FIG.
2E.
[0088] FIG. 2G is a partial sectional view of head of a human
patient showing the right nasal cavity, the right side of the
nasopharynx and the associated paranasal sinuses, with an anterior
occluder & access device of the present invention inserted in
the right nasal cavity and a posterior occluder/suction/access
device of FIG. 2E inserted through the oral cavity.
[0089] FIG. 2H is a partial sectional view of head of a human
patient showing the left nasal cavity, the left side of the
nasopharynx and the associated paranasal sinuses, with an anterior
occluder & access device of the present invention inserted in
the left nasal cavity and the same posterior
occluder/suction/access device that appears in FIG. 2G extending
through the oral cavity.
[0090] FIG. 2I is a perspective view of a posterior
occluder/suction device of the present invention that is insertable
transnasally.
[0091] FIG. 2J is a cross-sectional view through Line 2J-2J of FIG.
2I.
[0092] FIG. 2K is a partial sectional view of head of a human
patient showing the right nasal cavity, the right side of the
nasopharynx and the associated paranasal sinuses, with the
posterior occluder/suction device shown in FIG. 2I inserted through
the right nasal cavity.
[0093] FIG. 2L is a partial sectional view of head of a human
patient showing the left nasal cavity, the left side of the
nasopharynx and the associated paranasal sinuses and showing the
posterior occluder portion of the device of FIG. 2K residing in and
occluding the nasopharynx at a location posterior to the septum and
superior to the glottis.
[0094] FIG. 2M is a partial sectional view of head of a human
patient showing the right nasal cavity, the right side of the
nasopharynx and the associated paranasal sinuses, with an extended
posterior occluder/suction device inserted through the right nasal
cavity.
[0095] FIG. 2N is a partial sectional view of head of a human
patient showing the left nasal cavity, the left side of the
nasopharynx and the associated paranasal sinuses and showing the
posterior occluder and distal tubular extension portions of the
device of FIG. 2M residing in the nasopharynx posterior to the
septum and superior to the glottis.
[0096] FIG. 2O is a partial sectional view of head of a human
patient showing the right nasal cavity, the right side of the
nasopharynx and the associated paranasal sinuses, with a posterior
occluder/slidable suction device inserted through the right nasal
cavity.
[0097] FIG. 2P is a partial sectional view of head of a human
patient showing the left nasal cavity, the left side of the
nasopharynx and the associated paranasal sinuses and showing the
posterior occluder and distal portion of the slidable suction
cannula of the device of FIG. 2O residing in the nasopharynx
posterior to the septum and superior to the glottis.
[0098] FIG. 2Q is a partial sectional view of head of a human
patient showing the right nasal cavity, the right side of the
nasopharynx and the associated paranasal sinuses, with another
posterior occluder/tapered suction device inserted through the
right nasal cavity.
[0099] FIG. 2R is a partial sectional view of head of a human
patient showing the left nasal cavity, the left side of the
nasopharynx and the associated paranasal sinuses and showing the
posterior occluder and distal portion of the tapered suction
cannula of the device of FIG. 2Q residing in the nasopharynx
posterior to the septum and superior to the glottis.
[0100] FIG. 3A is a partial perspective view of one embodiment of
an occluder/suction device of the present invention positioned
within an anatomical passageway.
[0101] FIG. 3B is a partial perspective view of another embodiment
of an occluder/suction device of the present invention positioned
within an anatomical passageway.
[0102] FIG. 3C is a partial perspective view of another embodiment
of an occluder/suction device of the present invention positioned
within an anatomical passageway.
[0103] FIG. 3C.sup.1 is a cross-sectional view through line
3C.sup.1-3C.sup.1 of FIG. 3C.
[0104] FIG. 3D is a partial perspective view of yet another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0105] FIGS. 3E.sup.1, 3E.sup.11 and 3E.sup.111 are partial
perspective views of still another embodiment of an
occluder/suction device of the present invention showing various
steps in a process by which the occluder/suction device is
positioned within an anatomical passageway.
[0106] FIG. 3F is a partial perspective view of still another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0107] FIGS. 3F.sup.1, 3F.sup.11 and 3F.sup.111 show alternative
constructions of the distal portion of the suction cannula of the
occluder/suction device shown in FIG. 3F.
[0108] FIG. 3G is a partial perspective view of still another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0109] FIG. 3H is a partial perspective view of still another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0110] FIG. 3I is a partial perspective view of still another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0111] FIG. 3J is a partial perspective view of still another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0112] FIG. 3K is a partial perspective view of still another
embodiment of an occluder/suction device of the present invention
positioned within an anatomical passageway.
[0113] FIGS. 3L.sup.1 and 3L.sup.11 show partial longitudinal
sectional views of another occluder/suction device of the present
invention.
[0114] FIGS. 3M.sup.1 and 3M.sup.11 show partial perspective views
of another occluder/suction device of the present invention
positioned within an anatomical passageway.
[0115] FIG. 4 is a longitudinal sectional view of the oropharynx
and anterior neck of a human patient having a nasopharyngeal
occluder/endotracheal tube device of the present invention inserted
through the right nasal cavity and into the trachea.
[0116] FIG. 5A is a partial perspective view of a side cutting or
ablation device being used in accordance with the present
invention.
[0117] FIG. 5B is a partial perspective view of a device having
laterally deployable needles, electrodes or other treatment
delivering projections, being used in accordance with the present
invention.
[0118] FIG. 5C is a partial perspective view of a drill (e.g., a
tissue drill, bone drill, or trephine device) being used in
accordance with the present invention.
[0119] FIG. 5D is a partial perspective view of a catheter having a
laterally deployed needle or tube for delivering a substance or
apparatus to a target location and an optional on-board imaging or
guidance apparatus, being used in accordance with the present
invention.
[0120] FIG. 5E is a partial perspective view of a balloon catheter
being used in accordance with the present invention.
[0121] FIG. 5F is a partial perspective view of a balloon catheter
having blades or electrodes thereon, being used in accordance with
the present invention.
[0122] FIG. 5G.sup.1 is a partial perspective view of a balloon
catheter having a stent positioned thereon being inserted into an
occluded region within the nose, nasopharynx or paranasal sinus in
accordance with the present invention.
[0123] FIG. 5G.sup.11 shows the balloon catheter and stent of FIG.
3G.sup.1, with the balloon inflated and the stent expanded so as to
open or dilate the occluded region within the nose, nasopharynx or
paranasal sinus.
[0124] FIG. 5G.sup.111 shows the balloon catheter and stent of FIG.
3G.sup.1 with the stent implanted, the balloon deflated and the
catheter being withdrawn and removed.
[0125] FIG. 5H is a partial perspective view of a tissue shrinking
electrode device being used in accordance with the present
invention.
[0126] FIG. 5I is a partial perspective view of a cryogenic or
plasma state treatment device being used in accordance with the
present invention.
[0127] FIG. 5J is a partial perspective view of an expandable
tissue expanding device positioned within a passageway in the nose,
nasopharynx or paranasal sinus in accordance with the present
invention.
[0128] FIG. 5K is a partial sectional view of one embodiment of a
forward cutting/suction catheter of the present invention.
[0129] FIG. 5K.sup.1 shows the device of FIG. 5K being used to
remove a nasal polyp or other obstructive mass from an anatomical
passage within the nose or paranasal sinus.
[0130] FIG. 5L is a partial sectional view of a forward
cutting/suction catheter/endoscope device of the present
invention.
[0131] FIG. 5M is a partial sectional view of a side
cutting/suction catheter device of the present invention.
[0132] FIG. 5N is a partial sectional view of a side
cutting/suction catheter device of the present invention having an
optional guidewire lumen and optional endoscopic component(s).
[0133] FIG. 5O is a partial perspective view of the distal end of a
guide catheter/endoscope of the present invention.
[0134] FIG. 5P is a partial perspective view of a balloon
catheter/pressure expandable intranasal stent/endoscope device of
the present invention.
[0135] FIG. 5Q is a partial perspective view of a delivery
catheter/self expanding intranasal stent/endoscope device of the
present invention.
[0136] FIG. 5Q.sup.1 is a cross-sectional view through line
5Q.sup.1-5Q.sup.1 of FIG. 5Q.
[0137] FIG. 5R.sup.1 shows an example of an optional modified shape
of the balloon and stent of FIG. 5P.
[0138] FIG. 5R.sup.11 shows another example of an optional modified
shape of the balloon and stent of FIG. 5P.
[0139] FIG. 5S is a partial perspective view of a snare catheter of
the present invention with optional endoscopic component(s).
[0140] FIG. 5T is a partial perspective view of a forceps device of
the present invention having optional endoscopic component(s).
[0141] FIG. 5U is a partial perspective view of a system of the
present invention, comprising a guide catheter, endoscope and
guidewire.
[0142] FIG. 5U.sup.1 is a cross-sectional view through line
5T.sup.1-5T.sup.1 of FIG. 5T.
[0143] FIG. 5V is a partial perspective view of a microdebrider
catheter of the present invention.
[0144] FIG. 5W is a partial perspective view of a bone remodeling
device of the present invention.
[0145] FIGS. 5W.sup.1 and 5W.sup.11 show steps in a method for
using the bone remodeling device of FIG. 5W.
[0146] FIGS. 5X.sup.1-5X.sup.1111 are partial perspective views of
alternative designs for bone remodeling devices of the present
invention.
[0147] FIGS. 5Y-5Y.sup.11111 are perspective views of examples of
substance delivering implant devices useable in the present
invention.
[0148] FIG. 6A is a perspective view of one embodiment of a
sphenoid sinus guide catheter of the present invention.
[0149] FIG. 6B is a perspective view of a frontal sinus guide
catheter of the present invention.
[0150] FIG. 6C is a perspective view of one embodiment of a
maxillary sinus guide catheter of the present invention.
[0151] FIG. 6D is a perspective view of one embodiment of an
ethmoid sinus guide catheter of the present invention.
[0152] FIG. 6E is a perspective view of one embodiment of a
plugging guide catheter of the present invention useable for
temporarily plugging the opening into a nasolacrimal duct or
Eustachian tube.
[0153] FIG. 7A is a sectional view of a paranasal sinus with a
catheter introducing an expandable electrode cage into the sinus in
accordance with the present invention.
[0154] FIG. 7B is a sectional view of a paranasal sinus that is
filled with a diagnostic or therapeutic substance and wherein a
plug tipped catheter is being used to plug the ostium of the sinus
to retain the substance within the sinus, in accordance with the
present invention.
[0155] FIG. 7C is a sectional view of a paranasal sinus with a
catheter introducing a diagnostic or therapeutic substance into
contact with the tissue lining the sinus, in accordance with the
present invention.
[0156] FIG. 7D is a sectional view of a paranasal sinus with a
catheter having emitters and/or sensors for 3-dimensional mapping
or navigation, in accordance with the present invention.
[0157] FIG. 7E is a sectional view of a paranasal sinus with a
catheter delivering a coil apparatus into the sinus to embolize the
sinus and/or to deliver a diagnostic or therapeutic substance into
the sinus in accordance with the present invention.
[0158] FIG. 7F is a sectional view of a paranasal sinus with a
guide catheter, guidewire and over-the-wire flexible endoscope
inserted into the sinus, in accordance with the present
invention.
[0159] FIG. 7G shows the guide catheter and endoscope of FIG. 5F
with a working device (e.g., a biopsy instrument) inserted through
a working channel of the endoscope to perform a procedure within
the sinus under endoscopic visualization, in accordance with the
present invention.
[0160] FIGS. 8A-8E show steps in a sinus treatment procedure
conducted in accordance with the present invention.
[0161] FIGS. 9A-9C show steps in a cochlear implant procedure
conducted in accordance with the present invention.
[0162] FIG. 10 is an illustration of a patient being treated by a
system for catheter-based minimally invasive sinus surgery.
[0163] FIGS. 11A through 11D are illustrations of partial sagittal
sectional views through a human head showing various steps of a
method of gaining access to a paranasal sinus using a sinus
guide.
[0164] FIG. 12 illustrates a scope introduced on the side of the
sinus guide.
[0165] FIG. 13 shows an illuminating guidewire according to one
embodiment of the present invention.
[0166] FIG. 14 shows a distal end portion of a guidewire having a
bent shape.
[0167] FIG. 15 is a cross-sectional illustration of a distal end
portion of a guidewire device showing a core support fixed to the
coil.
[0168] FIG. 16 shows a cross-sectional view of a guidewire device
that includes a fiber optic bundle of light fibers.
[0169] FIG. 17 shows an illuminating guidewire according to another
embodiment of the present invention.
[0170] FIG. 18 is a cross-sectional illustration of a distal end
portion of the guidewire shown in FIG. 8.
[0171] FIG. 19 shows an illuminating guidewire according to another
embodiment of the present invention.
[0172] FIG. 20 illustrates an alternative transparent portion that
may be included in a device shown in FIG. 19.
[0173] FIG. 21 illustrates another alternative transparent portion
that may be included in a device shown in FIG. 19.
[0174] FIG. 22A illustrates an illuminating guidewire device
including a quick release connector that is optically coupled to a
light source.
[0175] FIG. 22B is a view of the arrangement of FIG. 22A in which
the quick release locking mechanism is in the locked position.
[0176] FIG. 23A illustrates an alternative quick release
connector.
[0177] FIG. 23B illustrates the connector of FIG. 23A mounted over
a proximal end portion of an illuminating guidewire.
[0178] FIG. 24 illustrates another alternative quick release
connector.
[0179] FIG. 25 illustrates another alternative quick release
connector.
[0180] FIGS. 26A-26E are illustrations of partial coronal sectional
views through a human head showing various steps of a method for
treating an ostium that opens to a frontal sinus.
[0181] FIG. 27 illustrates a situation, like that described with
regard to FIG. 12, where a scope has been inserted as far as
possible without causing significant trauma to the patient.
Additionally, FIG. 27 shows an illuminating guidewire having been
extended distally of the limit of illumination of the scope, to
effectively extend the illumination distance viewable by the
scope.
[0182] FIG. 28 illustrates non-limiting examples of where one or
more filters may be placed in an illuminating guidewire device.
[0183] FIG. 29A schematically illustrates a connector having a
rotating shutter rotatably mounted therein.
[0184] FIG. 29B is an illustration of a plan view of the shutter of
FIG. 29A.
[0185] FIG. 30 shows a frontal ostium seeker instrument that can be
used to access a sinus ostium.
[0186] FIG. 31 shows a suction sinus instrument that is configured
to evacuate blood and/or other fluids from a target surgical site,
such as the frontal sinus.
[0187] FIG. 32 shows an integrated wire dilatation catheter 1.201
that includes an elongate, flexible catheter shaft having a balloon
mounted thereon.
DETAILED DESCRIPTION OF THE INVENTION
[0188] The following detailed description and the accompanying
drawings are intended to describe some, but not necessarily all,
examples or embodiments of the invention only and does not limit
the scope of the invention in any way.
[0189] Before the present devices and methods are described, it is
to be understood that this invention is not limited to particular
embodiments described, as such may, of course, vary. It is also to
be understood that the terminology used herein is for the purpose
of describing particular embodiments only, and is not intended to
be limiting, since the scope of the present invention will be
limited only by the appended claims.
[0190] Where a range of values is provided, it is understood that
each intervening value, to the tenth of the unit of the lower limit
unless the context clearly dictates otherwise, between the upper
and lower limits of that range is also specifically disclosed. Each
smaller range between any stated value or intervening value in a
stated range and any other stated or intervening value in that
stated range is encompassed within the invention. The upper and
lower limits of these smaller ranges may independently be included
or excluded in the range, and each range where either, neither or
both limits are included in the smaller ranges is also encompassed
within the invention, subject to any specifically excluded limit in
the stated range. Where the stated range includes one or both of
the limits, ranges excluding either or both of those included
limits are also included in the invention.
[0191] Unless defined otherwise, all technical and scientific terms
used herein have the same meaning as commonly understood by one of
ordinary skill in the art to which this invention belongs. Although
any methods and materials similar or equivalent to those described
herein can be used in the practice or testing of the present
invention, the preferred methods and materials are now described.
All publications mentioned herein are incorporated herein by
reference to disclose and describe the methods and/or materials in
connection with which the publications are cited.
[0192] It must be noted that as used herein and in the appended
claims, the singular forms "a", "an", and "the" include plural
referents unless the context clearly dictates otherwise. Thus, for
example, reference to "a tube" includes a plurality of such tubes
and reference to "the shaft" includes reference to one or more
shafts and equivalents thereof known to those skilled in the art,
and so forth.
[0193] The publications discussed herein are provided solely for
their disclosure prior to the filing date of the present
application. Nothing herein is to be construed as an admission that
the present invention is not entitled to antedate such publication
by virtue of prior invention. Further, the dates of publication
provided may be different from the actual publication dates which
may need to be independently confirmed.
[0194] A number of the drawings in this patent application show
anatomical structures of the ear, nose and throat. In general,
these anatomical structures are labeled with the following
reference letters:
TABLE-US-00001 Nasal Cavity NC Nasopharynx NP Superior Turbinate ST
Middle Turbinate MT Inferior Turbinate IT Frontal Sinus FS Ethmoid
Sinus ES Sphenoid Sinus SS Sphenoid Sinus Ostium SSO Maxillary
Sinus MS
[0195] The human nose has right and left nostrils or nares which
lead into separate right and left nasal cavities. The right and
left nasal cavities are separated by the intranasal septum, which
is formed substantially of cartilage and bone. Posterior to the
intranasal septum, the nasal cavities converge into a single
nasopharyngeal cavity. The right and left Eustachian tubes (i.e.,
auditory tubes) extend from the middle ear on each side of the head
to openings located on the lateral aspects of the nasopharynx. The
nasopharynx extends inferiorly over the uvula and into the pharynx.
As shown in FIGS. 1A and 1B, paranasal sinuses are formed in the
facial bones on either side of the face. The paranasal sinuses
open, through individual openings or ostia, into the nasal
cavities. The paranasal sinuses include frontal sinuses FS, ethmoid
sinuses ES, sphenoidal sinuses SS and maxillary sinuses MS.
[0196] The present invention provides a comprehensive system of
devices and associated methods for diagnosing and treating
disorders of the ears, nose and throat in a less invasive fashion
than current day approaches. Specifically, examples of which are
described below, the invention provides devices that wholly or
partially effect a fluid-tight seal of the operative field (e.g.,
the nasopharynx and/or one or more of the sinus cavities or
regional ducts). This fluid-tight sealing of the operative field
allows the cavities, ducts and passageways to be imaged using
fluid/gas based agents in combination with various imaging
modalities without the risk of aspiration or uncontrolled leakage
of fluid from the operative field. Further, this fluid-tight
sealing of the operative field permits the retention and collection
of any blood or flushing fluids released during the procedure.
Another aspect of the invention is a set of methods and devices
useable to assess the static and dynamic nature of the paranasal
sinuses and to provide for the guidance of specific therapies to
particular sinuses or particular target regions (e.g., stenotic
sinus ostia, infected tissues within sinuses, tumors, other target
structures). Another aspect of the invention is the use of devices
and methods which are designed for minimally invasive entry into
the sinus passageways or regional ducts under image and/or
endoscopic guidance to provide local therapy such as dilation,
ablation, resection, injection, implantation, etc., to the region
of concern. These devices and methods may be disposable or
temporary in their application, or they may be implantable with
on-going functionality (such as implantable drug delivery systems,
cochlear implants, etc.). In a number of embodiments, the present
invention utilizes flexible catheters and various working devices
that are mounted on or delivered through elongate flexible members
or catheters, to diagnose and treat a wide range of ear, nose and
throat disorders, including nasal polyps, sinusitis, enlarged
turbinates, deviated septum, tumors, infections, deformities, etc.,
The following pages describe a number of specific devices and
methods that are useable in accordance with this invention. It is
to be understood that any component, element, limitation, attribute
or step described in relation to any particular device or method
described herebelow, may be incorporated in or used with any other
device or method of the present invention unless to do so would
render the resultant device or method unusable for its intended
purpose.
[0197] A. Occluders and Access Port Devices
[0198] Many of the procedures of the present invention require the
insertion and positioning of one or more flexible catheters or
other flexible elongate working devices (examples of which are
shown in FIGS. 5A-5Y.sup.11111 and described herebelow) within the
nose, nasopharynx, middle ear or paranasal sinuses. To facilitate
the insertion and proper positioning of such catheters and/or other
elongate working devices and to prevent undesirable drainage of
blood or debris from the operative site, the present invention
includes a number of different occluder and/or access port devices,
examples of which are shown in FIGS. 2A-2R, that are inserted
through the nose and/or oral cavity and function to a) prevent
unwanted drainage or escape of fluid (e.g., gas or liquid) and b)
facilitate the insertion and positioning of guides and working
devices, examples of such working devices being shown in FIGS.
5A-5Y.sup.11111 and 6A-6E.
[0199] FIGS. 2A-2B show partial sectional views of opposite sides
of the head of a human patient having an anterior/posterior
occluder & access device 10 inserted through the right nasal
cavity and anterior occluder & access device 12 positioned in
the anterior region of the left nasal cavity. Specifically, FIG. 2A
shows the nasal cavity, the right side of the nasopharynx and the
associated paranasal sinuses, with an anterior/posterior occluder
& access device 10 of the present invention inserted therein.
The anterior/posterior occluder & access device 10 comprises an
anterior occluder 14 which occludes the right nasal cavity on the
right side of the nasal septum, a posterior occluder 18 that
occludes the posterior choanae, nasopharynx or pharynx posterior to
the nasal septum (but typically superior to the glottis) and a tube
16 that extends between the anterior occluder 14 and posterior
occluder 18. Devices for posterior occlusion and anterior occlusion
may be used alone or in combination. They may be coaxially deployed
or alternatively they may be deployed in a singular fashion, one in
each orifice. It should be noted that any combination of these
sealing modalities may be employed to achieve one or more of the
stated objectives. A cross-section through the tube 16 is shown in
FIG. 2C. Other cross-sectional configurations could also be
possible, including those that comprise more lumens to permit the
passage of multiple devices or fluids (e.g., liquid or gases). In
some embodiments, it may be desirable for the device 10 (or any of
the other occluder/access devices described herein) to have
separate lumens for infusion and aspiration, thereby allowing for
concurrent infusion of an irrigation fluid or other fluid and
suctioning of the irrigation fluid or other fluid from the
operative field. Such continuous turnover of fluid within a sealed
operative field may be useful for clearing blood or debris from the
operative field to facilitate unobstructed viewing of the
anatomical structures using an endoscope or for various other
reasons. A port body 28 as attached to the proximal end of the tube
16. A device insertion aperture 30 extends through the port body 28
into working lumen 50 of tube 16. One or more outlet openings 22,
24 are at location(s) in the tube such that a device (e.g., a
catheter, fluid injector or other elongate device examples of which
are shown in FIGS. A-5Y.sup.1111 and described herebelow) or
fluid(s) may be inserted into the device insertion opening 30,
advanced through the working lumen 50 and out of a selected one of
the outlet openings 22, 24 to a position within the nose,
nasopharynx or paranasal sinus. In the particular embodiment shown
in FIG. 2A the anterior and posterior 10 occluders 14, 18 comprise
balloons, but various other types of occluders could be used in
place of balloons, examples of which are shown in FIGS. 3A-3K and
described herebelow. Balloon inflation/deflation lumens 52, 56
extends from proximal Luer connectors 32, 36, through the tube 16
and to the anterior occluder 14 and posterior occluder 18,
respectively. Thus, a syringe or other fluid 15 expelling and/or
withdrawing device may be connected to connector 32 and used to
selectively inflate and/or deflate the anterior occluder 14.
Another syringe or other fluid expelling and/or withdrawing device
may be connected to connector 36 and used to selectively inflate
and/or deflate the posterior occluder 18. As may be appreciated
from the showing of FIG. 26, the posterior occluder (when fully
inflated) may be sized and shaped to occlude the entire posterior
choanae, nasopharynx or pharynx posterior to the nasal septum (but
typically superior to the glottis), thereby preventing blood or
other fluid or debris from draining into the patient's pharynx from
either the right or left nasal cavity. When fully inflated, the
anterior occluder 14 of the device 10 occludes only the right nasal
cavity and serves to prevent blood, other fluid or debris from
draining around the tube 16 and out of the right nostril during the
operative procedure. A one-way valve, such as a flapper valve,
duckbill valve, hemostatic valve or other one way valve of the type
well known in the art of biomedical device design, may be
positioned within the port body 28 to permit a catheter or other
elongate device (examples of which are shown in FIGS. 5A-5T and
described herebelow) to be advanced in the distal direction though
insertion port 30, through the port body 28 and through the working
lumen 50 but to prevent blood, other fluid or debris from draining
through the working lumen 50 out of the device insertion port 30.
In this manner, the device 10 forms a substantially fluid tight
anterior seal in the anterior aspect of the right nasal cavity and
a substantially fluid tight posterior seal in the posterior
choanae, nasopharynx or pharynx posterior to the nasal septum (but
typically superior to the glottis). Since a substantially fluid
tight seal is formed, one or more valves (not shown) may be
provided to relieve positive or negative pressure created between
the anterior or posterior occluders 14, 18 as a result of the
injection of matter (e.g., contrast medium, irrigation solution,
medicament, etc.) into the operative field and/or suctioning or
removal of matter (e.g., blood, other fluid or debris) from the
operative field. Additionally, a suction lumen 54 may extend from
suction Luer connector 34, through suction lumen 54 and to suction
openings 26 may be formed in the tube 16. A suction pump may be
connected to the suction connector 34 to aspirate blood, other
fluid and/or debris out of the right nasal operative region defined
between anterior occluder 14 and posterior occluder 18. It should
be appreciated that, while the occlusion/access devices shown in
the drawings and described herein are designed to isolate a
relatively large operative field (e.g., one or both nasal cavities,
sinus, nasal cavities-nasopharynx, etc.), once a specific problem
has been diagnosed and/or once a specific target region has been
identified, the occluders 14, 18 may be repositioned and/or other
occluder devices may be inserted to isolate and form a fluid tight
seal of just a portion of the original operative field (e.g., just
one sinus, one nasal cavity, one Eustachian tube, etc.) thereby
allowing the procedure to go forward with only the necessary
region(s) of the nose, nasopharynx, paranasal sinuses or other
structures sealed off and/or instrumented, to minimize trauma and
improve patient comfort.
[0200] It should be appreciated that in any embodiment of an
anterior/posterior occluder & access device, such as the device
10 shown in FIGS. 2A and 2B, the distance between the anterior
occluder 14 and posterior occluder 18 may be adjustable so as to
accommodate variations in anatomy and/or specific target regions or
isolated operative fields of interest. The anterior and posterior
occluders 14, 18 may be separate devices where the anterior
occluder may slide or pass through one lumen of the posterior
occluder, which may contain several lumens (e.g., inflation,
working channel, irrigation, etc.), and may or may not be
integrated with the posterior occluder. The posterior occluder may
also contain several lumens (e.g., inflation, working channel,
irrigation, etc.). Additionally, all lumens for both the anterior
and posterior occluders may contain valves so as to prevent leakage
or flow of gas, fluid, blood, etc.
[0201] It is to be further appreciated that in embodiments that
have anterior and posterior outlet openings 22, 24 (as shown in the
example of FIGS. 2A-2B) tools, instrumentation and fluids may be
delivered via either of the posterior or anterior access ports 22,
24. In some cases, access via a posterior outlet 24 is desirable to
gain a better perspective on the target anatomical lumen or lumen
(i.e., openings to the ethmoid cells).
[0202] As shown in FIGS. 2B and 2D, in some procedures wherein the
anterior/posterior occluder & access device 10 is inserted
through one nasal cavity, it may be desirable to position a
separate anterior occluder & access device 12 within the
opposite nasal cavity to prevent drainage of blood, other fluid or
debris from the other nostril and to facilitate insertion of
catheters or other elongate devices (examples of which are shown in
FIGS. 5A-5T and described herebelow) into the left nasal cavity and
the paranasal sinuses or other anatomical, structures accessible
from the other nasal cavity. As shown, in FIG. 2B, the anterior
occluder & access device 12 may comprise a tube 41 having an
anterior occluder 40 and a port body 42 attached thereto. A device
insertion aperture 44 extends through the port body 42 and through
a working lumen 58 of tube 41 to an outlet aperture in the distal
end of tube 41. A one-way valve (such as the valve described
hereabove in connection with the anterior/posterior occluder &
access device 10) may optionally be provided within port body 42 to
prevent draining of blood, other fluid or debris out of insertion
aperture 44. In the particular embodiment shown in FIGS. 2B and 2D,
the anterior occluder 40 is a balloon, but such occluder 40 may be
of various other constructions, examples of which are shown in
FIGS. 3A-3M.sup.11 and described herebelow. To facilitate inflation
and deflation of this balloon type anterior occluder 40, a balloon
inflation/deflation lumen 60 extends from Luer connector 48,
through tube 41 to the balloon-type anterior occluder 40. A syringe
or other fluid expelling and/or withdrawing device may be connected
to connector 48 and used to selectively inflate and/or deflate the
anterior occluder 40. Optionally, a side tube and Luer connector 46
may be connected to the working lumen 58 of tube 41 to allow blood,
other fluid and debris to be suctioned from the left nasal cavity
through the working lumen 58 of tube 41. In some embodiments,
dedicated suction and/or irrigation lumen(s) with separate suction
and/or irrigation ports may be formed in tube 41 in a manner
similar to that described hereabove with respect to the
anterior/posterior occluder & access device 10.
[0203] FIGS. 2E-2H show an alternative system for occlusion and
access, wherein anterior occluder & access device(s) 12 is/are
positioned in one or both nostrils or nasal cavities and an orally
insertable posterior occluder device 300 is inserted through the
patient's oral cavity and positioned so as to occlude the posterior
choanae, nasopharynx or pharynx posterior to the nasal septum (but
typically superior to the glottis). The embodiment of the orally
insertable posterior occluder device 300 shown in FIGS. 2E-2G
comprises a curved tube 302 having an occluder 304 positioned at or
near the distal end thereof. The device 300 is configured such that
it may be inserted through the patient's oral cavity to a position
where the occluder 304 is located within, and disposed, so as to
substantially occlude the posterior choanae, nasopharynx or pharynx
posterior to the nasal septum (but typically superior to the
glottis). The posterior occluder 304 may also be positioned next to
the Eustachian tube to block the Eustachian tube, thereby
preventing fluid from tracking into the Eustachian tube during the
procedure (if access to the Eustachian tube or middle ear or inner
ear is not desired). Further, it may be necessary to place specific
targeted balloons or occluders in ducts or channels which are not
intended to be intervened upon (lacrimal ducts, Eustachian tubes,
etc.). In such cases, these extra ductal occluders serve to prevent
aberrant fluid/gas loss and/or to maintain the integrity of the
lumen, while other nearby structures are being modified. In the
particular example shown in FIGS. 2E-2G, the occluder 304 comprises
a balloon. However, such occluder 304 may be constructed in various
alternative ways, examples of which are shown in FIGS. 3A-3K and
described herebelow. As may be appreciated from the cross-sectional
showing of FIG. 2F, in this example, a balloon inflation/deflation
lumen 318 may extend from Luer connector 314, through tube 302 to
the balloon-type occluder 304. A syringe or other
inflation/deflation apparatus may be attached to the Luer connector
314 and used to inflate and deflate the balloon 304. A stopcock or
other valve (not shown) may also be provided on balloon inflation
tube 318 to maintain inflation of the balloon when desired. In
routine use, the occluder 304 is initially deflated and the device
300 is inserted through the oral cavity and advanced to its desired
position with the deflated occluder positioned within the posterior
choanae, nasopharynx or pharynx posterior to the nasal septum (but
typically superior to the glottis). Thereafter, the occluder 304
may be expanded (e.g., inflated) such that it occludes or blocks
the posterior choanae, nasopharynx or pharynx posterior to the
nasal septum (but typically superior to the glottis), thereby
substantially preventing blood, other fluid or debris from draining
into the patient's esophagus or trachea during the procedure. In
some cases, as shown in FIGS. 2E-2H, the tube 302 may have one or
more lumen(s) 310 that extend(s) through the occluder 304 and
open(s) through an opening 310 distal to the balloon. Working
devices, such as catheters or other elongate devices examples of
which are shown in FIGS. 5A-5Y''''' and described herebelow may be
advanced through such a lumen 310 and into the patient's
nasopharynx, nasal cavities, paranasal sinuses, middle ears, etc.,
Alternatively, suction may be applied to such a lumen 310 to
suction blood, other fluid or debris from the area superior to the
occluder 304. In some cases, the lumen 310 shown may be divided
into a working lumen and a suction lumen. The suction lumen may
terminate in separate suction port(s) (not shown) at the distal end
of the tube and a connector (not shown) at the proximal end, such
that suction may be applied through a lumen that is separate from
the lumen through which the working device(s) is/are passed. A port
body 306 may be positioned on the proximal end of the tube 302. A
device insertion port 308 may extend through the port body 306 into
a lumen 310 of the tube 302. A one-way valve, such as a flapper
valve, duckbill valve, hemostatic valve or other one-way valve of
the type well known in the art of biomedical device design, may be
positioned within the port body 306 to permit a catheter or other
elongate device to be advanced in the distal direction though
insertion port 308, through the port body 306 and through a lumen
310 but to prevent blood, other fluid or debris from draining
through the lumen 310 and out of the device insertion port 308. In
some cases, the orally insertable posterior occluder device 300 may
be used without any anterior occluder device(s) positioned in the
nostril(s) or nasal cavity(ies). In other cases, it will be
desirable to use this orally insertable posterior occluder device
300 in combination with one or two anterior occluder & access
devices 12 as shown in the example of FIGS. 2G and 2H. The use of
these devices 300, 12 in combination serves to establish a
substantially fluid tight operative field between the posterior
occluder 304 and the anterior occluder(s) 40 while allowing various
catheters and other operative instruments to be inserted into the
operative field through optional access ports 44 and/or 308.
[0204] FIGS. 2I-2L show a transnasally insertable posterior
occluder device 301 that does not include any anterior occluder.
This device 301 comprises a curved tube 303 having an occluder 305
positioned at or near the distal end of the tube 303. As shown in
FIGS. 2K-2L, this device 301 is inserted through either the right
or left nasal cavity and advanced to a position where the occluder
305 substantially occludes the posterior choanae, nasopharynx or
pharynx posterior to the nasal septum (but typically superior to
the glottis). In the particular example shown, this occluder 305
comprises a balloon. However, such occluder 305 may be constructed
in various alternative ways, examples of which are shown in FIGS.
3A-3K and described herebelow. As may be appreciated from the
cross-sectional showing of FIG. 2J, in this example a balloon
inflation/deflation lumen 317 may extend from Luer connector 311,
through tube 303 to the balloon-type occluder 305. A syringe or
other inflation/deflation apparatus may be attached to the Luer
connector 311 and used to inflate and deflate the balloon-type
occluder 305. A stopcock or other valve (not shown) may also be
provided on balloon inflation lumen 317 to maintain inflation of
the balloon when desired. In routine use, the occluder 305 is
initially deflated and the device 301 is inserted through the right
or left nasal cavity and advanced to its desired position where the
deflated occluder 305 is positioned within the posterior choanae,
nasopharynx or pharynx posterior to the nasal septum (but typically
superior to the glottis). Thereafter, the occluder 305 may be
expanded (e.g., inflated) such that it occludes or blocks the
posterior choanae, nasopharynx or pharynx posterior to the nasal
septum (but typically superior to the glottis), thereby
substantially preventing blood, other fluid or debris from draining
into the patient's esophagus or trachea during the procedure.
Optionally, distal suction ports 309 and/or proximal suction ports
307 may open into lumen 315 of the tube 303 and such lumen 315 may
be attached to a suction connector 313. In this manner, suction may
be applied to remove blood, other fluid or debris from the
nasopharynx superior to the occluder 305 and/or from the nasal
cavity through which the device 3301 is inserted. As may be
appreciated from the showings of FIGS. 2K and 2L, in this example,
the transnasal posterior occluder device 301 is inserted through
the right nasal cavity. A working device WD such as a catheter or
other elongate operative apparatus (examples of which are shown in
FIGS. 5A-5Y.sup.11111 and described herebelow) may be advanced into
the right nasal cavity adjacent to the tube 303 or through the left
nasal cavity which remains open, as no anterior occlusion is
provided by this transnasal posterior occluder device 301. This
arrangement may be particularly suitable for procedures where the
physician desires to directly visualize, through the nostril(s),
the anatomical structures within the nose, such as the inferior,
middle or superior turbinates IT, MT, ST, as shown in FIGS.
2K-2L.
[0205] FIGS. 2M-2N show a modified version of the transnasal
posterior occluder 301 a which includes all of the elements
described above with respect to the transnasal posterior occluder
device 301 shown in FIGS. 2I-2L, as well as a distal extension 303a
of the tube 303 that extends distal to the occluder 305 and an
additional proximal connector 319. A separate lumen (not shown)
extends from connector 319 through tube 303 and through distal tube
extension 303a, which terminates in a distal end opening 321.
Suction may thus be applied to connector 319 to suction matter
through distal opening 321, through the distal tube extension 303a
and through tube 303. This distal tube extension 303a and
additional lumen may be optionally added to any other the other
posterior occluder devices described herein in cases where doing so
would not render the device unsuitable for its intended
application.
[0206] FIGS. 2O-2P show an alternative posterior occluder system
400 that comprises an intranasal catheter 402 that is inserted into
a nasal cavity and an occluder catheter 404 that is inserted
through the intranasal catheter 402, as shown. A posterior occluder
406 is located at or near the distal end of the occluder catheter
404. In the particular embodiment shown in FIGS. 2O-2P, the
occluder 406 is sized and configured to occlude the posterior
choanae, nasopharynx or pharynx posterior to the nasal septum (but
typically superior to the glottis). In the particular example
shown, this occluder 406 comprises a balloon. However, such
occluder 406 may be constructed in various alternative ways,
examples of which are shown in FIGS. 3A-3K and described herebelow.
In this example a balloon inflation/deflation lumen may extend from
Luer connector 408, through occluder catheter 404 and to the
balloon-type proximal occluder 406. A syringe or other
inflation/deflation apparatus may be attached to the Luer connector
408 and used to inflate and deflate the balloon-type posterior
occluder 406. A stopcock or other valve (not shown) may also be
provided on the balloon inflation/deflation lumen to maintain
inflation of the balloon-type posterior occluder 406, when desired.
Optionally, distal tubular extension 412 may extend distally of the
posterior occluder 406 and a separate lumen may extend from an
optional second connector 410, through distal tubular extension 412
and through an opening 414 such that matter may also be aspirated
from the area distal to the posterior occluder 406. A port body 418
is formed on the proximal end of the intranasal tube 402. An
insertion port 420 extends through port body 418 into the lumen 422
of the intranasal tube. A side suction port 416 may also be
connected to the lumen 422 of the intranasal tube 402. In routine
operation, the intranasal tube 402 is inserted through the nostril
into one nasal cavity and advanced to a position where its distal
end is within or near the posterior choanae or nasopharynx. With
the posterior occluder 406 in a collapsed (e.g., deflated)
configuration, the occluder catheter 404 is advanced through the
lumen 422 of the intranasal catheter 402 to a position where the
posterior occluder is located in the posterior choanae, nasopharynx
or pharynx posterior to the nasal septum (but typically superior to
the glottis). Thereafter, the posterior occluder 406 may be
expanded (e.g., inflated) such that it occludes or blocks the
posterior choanae, nasopharynx or pharynx posterior to the nasal
septum (but typically superior to the glottis), thereby
substantially preventing blood, other fluid or debris from draining
into the patient's esophagus or trachea during the procedure.
Thereafter, suction may be applied to suction port 416 to suction
blood, other fluid or debris from the area proximal to the
posterior occluder 406. During such suctioning, the intranasal tube
402 may be moved back and/or forth as indicated by arrows on FIG.
20, while the occluder catheter 404 remains stationary. Such
ability to move the intranasal catheter 402 during the suctioning
process may facilitate complete removal of blood, other fluid
and/or debris from the operative field.
[0207] FIGS. 2Q and 2R show a modified posterior occluder system
430, which includes the same elements and components as the
posterior occluder system 400 described above, but wherein the
distal end 434 of the intranasal tube 402a is tapered and wherein a
plurality of side apertures 432 are formed in the intranasal tube
402a such that blood, other fluid or debris may be aspirated into
the lumen 422a of the intranasal tube 402a through such side
apertures 432.
[0208] B. Variations in Occluder Design and Suction Apparatus:
[0209] Although the above-described examples of occluder/access
devices 10, 12, 300, 400 show occluders that are in nature of
inflatable balloons, it will be appreciated that these occluders
are not limited to balloons and may be of various other designs and
types. Further, it is to be understood that various arrangements of
access and/or suction tubing/port(s) may be used to facilitate in
complete removal of blood, fluid or other debris from the areas
adjacent to the occluder(s) and/or elsewhere in the operative field
or optimal positioning of working devices within the operative
field. In fact, certain occluder and/or suction-access tubing/port
designs may be more desirable for certain procedures than others
depending on a number of factors including the positioning of the
patient's head during surgery, whether the patient will be under a
general anesthetic, whether an endotracheal tube will be inserted,
etc., In some cases, where a posterior occluder is positioned
within the posterior choanae, nasopharynx or pharynx posterior to
the nasal septum the completeness with which blood, other fluid or
debris may be suctioned out of the area adjacent to that posterior
occluder may depend on the shape and/or design of the occluder
itself as well as the shape and location of the suction lumen(s)
and port(s) through which the blood, fluid or debris is to be
suctioned. Beyond optimized fluid control, the posterior occluder
and/or associated access tubing may also serve as an essential
guiding element for devices, and alternative shapes and
trajectories may be particularly useful to access specific
structures. FIGS. 3A-3K show examples of varied occluder types and
variations in the arrangements of suction lumen(s) and port(s)
through which the blood, fluid or debris may be suctioned from
areas adjacent to the occluder or elsewhere within the operative
field. The examples shown in FIGS. 3A and 3K may be incorporated
into the occluder & access devices shown in FIGS. 2A-2R, when
appropriate.
[0210] FIG. 3A shows an occluder 446 mounted on a tube 442, wherein
a generally "U" shaped curve is formed in the distal end of the
tube such that a distal portion of the tube 442 passes beneath the
upper surface 449 of the occluder 446 and curves upwardly such that
the distal end of the tube 442 terminates in an opening 444 that is
flush with the upper surface 449 of occluder 446. In this manner,
any fluid that has accumulated adjacent to the upper surface 449 of
occluder 446 may be suctioned into opening 444 and through tube
442. In embodiments where the occluder comprises a balloon, a
balloon inflation lumen may extend through the tube and open
through an opening 447 into the interior of the balloon, to permit
inflation/deflation of the balloon. Optionally, a working device
448, such as a flexible catheter or elongate apparatus examples of
which are shown in FIGS. 5A-5T and described herebelow, may also be
advanced through the suction lumen of tube 442 and out of opening
444 as indicated on FIG. 3A.
[0211] FIG. 3B shows another alternative wherein an occluder 450
has a depression or well 454 formed in its upper surface. A tube
452 is attached to the occluder by attachment members 456 and the
distal end of the tube 452 protrudes into well 454 such that any
blood, fluid or debris that collects within the well 454 may be
suctioned through the tube 452. In embodiments where the occluder
450 comprises a balloon, the tube 452 may incorporate a balloon
inflation/deflation lumen which may extend through an
inflation/deflation side tube 458 into the interior of the balloon
to facilitate inflation and deflation of the balloon.
[0212] FIGS. 3C and 3C.sup.1 show another alternative wherein an
occluder 460 had a depression or well 462 formed in its upper
surface and a tube 464 is attached to the occluder 460, as shown. A
lumen of the tube 464 is in communication with the area adjacent
the floor of the well to facilitate suctioning of blood, fluid or
debris that collects within the well. In embodiments where the
occluder 460 comprises a balloon, the tube 464 may incorporate a
suction lumen 468 and a balloon inflation/deflation lumen 470. A
small curved (e.g., generally "U" shaped) suction tube 466 may be
connected in a sealed connection to the distal end of suction lumen
468 and the interior of the well 462 such that blood, other fluid
or debris may be suctioned from the well 462, through suction tube
466 and through suction lumen 468.
[0213] FIG. 3D shows a concave occluder 471 that comprises a self
expanding concave structure 472 such as a basket formed of a
superelastic or resilient mesh material (e.g., nickel titanium
alloy wire mesh). The expanding concave structure 472 is covered by
a fluid impermeable flexible covering 474 such as a skin formed of
flexible polymer (e.g., expanded polytetrafluoroethylene,
polyurethane, polyethylene teraphthalate, etc.). When fully
expanded the concave occluder 471 occludes the body lumen in which
it is positioned (e.g., the nasal cavity, posterior choanae,
nasopharynx, pharynx, etc.) and forms a concave well 479. A tube
480 extends into the well 479 of the concave occluder 471 and may
be used to suction blood, fluid or debris from the well 479. The
occluder 471 may be advanced from and withdrawn into a delivery
catheter 478. Struts 472 may connect the concave occluder 471 to a
delivery member (not shown) within the delivery catheter 478, such
delivery member being advanceable to push the occluder 471 out of
the delivery catheter 478 and retractable to withdraw the occluder
471 into the delivery catheter 478. When inside the delivery
catheter, the occluder 471 may be in a collapsed configuration but
when expelled out of the delivery catheter the occluder will
resiliently spring or self-expand to its expanded concave
configuration, as shown in FIG. 3D. The suction catheter 480 may
advance from and/or retract into the delivery catheter 478
concurrently with, or separately from, the occluder 471.
[0214] FIGS. 3E.sup.1-3E.sup.111 show yet another occluder/suction
arrangement wherein the occluder 484 comprises an everting tubular
member that is advanceable from a delivery/suction catheter 486.
The everting tubular member comprises a frame 488 that is covered
with a covering 500. Initially the everting tubular member is in a
substantially cylindrical configuration within the lumen of the
delivery/suction catheter 486. The frame may be a resilient or
superelastic material that is biased to the everted shape shown in
FIG. 3E.sup.111. Such frame 488 may be formed of mesh material
(e.g., nickel titanium alloy wire mesh). The covering 500 may be
formed of flexible polymer (e.g., expanded polytetrafluoroethylene,
polyurethane, polyethylene teraphthalate, etc.) In operation, the
delivery/suction catheter 486 is advanced to the position where it
is desired to place the occluder 484. Then, the everting tube is
advanced from the distal end opening of the delivery/suction tube
486, as shown in FIGS. 3E.sup.1 and 3E.sup.11. As it advances out
of the catheter 486, the everting tube member assumes its everted
configuration, forming a concave occluder 484 as shown in FIG.
3E.sup.111. The occluder 484, when fully everted, occludes the body
lumen in which it is positioned (e.g., the nasal cavity, posterior
choanae, nasopharynx, pharynx, etc.) and creates a concave well
504. The delivery/suction catheter 486 may be advanced into the
concave well 504 such that any blood, fluid or debris that collects
within concave well 504 may be suctioned through suction ports 502
and through the distal end of the delivery/suction catheter
486.
[0215] FIGS. 3F-3F.sup.111 show another embodiment wherein an
occluder 510 is positioned on the end of a tube 512. The occluder
510 has an arched upper surface such that a generally "V" shaped
annular collection space 518 is created in the region of the
coaptation between the occluder 510 and the adjacent wall of the
body lumen in which it is positioned (e.g., a nasal cavity,
posterior choanae, nasopharynx, pharynx, etc.). A suction tube 516
extends from tube 512 into the annular collection space 518 and
blood, other fluid or debris that collects in the annular
collection space 518 may be suctioned through suction tube 516 and
through a lumen of tube 512, thereby providing for maintenance of a
substantially dry environment adjacent to the upper surface of the
occluder 510. The occluder 510 may comprise a balloon or any other
suitable occlusion member as described herein or known in the art.
As shown in FIGS. 3F.sup.1-3F.sup.111 the suction tube 516 may
comprise a simple tube having an open distal end or, alternatively,
the device may incorporate a suction tube 516a that has a plurality
of side apertures 520 formed near its distal end and/or a suction
tube 516 that has a guard member 522, such as a screen, formed over
its suction ports or openings to deter solid matter (e.g., blood
clots or other debris) from clogging the suction ports or
openings.
[0216] FIG. 3G shows an occluder 530 attached to a tube 532 that
has a curved (e.g., generally "U" shaped) distal end that does not
protrude into the interior of the occluder. Suction apertures 536
are formed in the distal portion of the tube 532 to permit blood,
fluid or debris that collects adjacent to the upper surface of the
occluder 530 to be suctioned through the tube 532. In embodiments
where the occluder is a balloon a balloon/inflation lumen may
extend through tube 532 and a small balloon inflation tube 538 may
extend into the interior of the balloon to permit the balloon to be
inflated and deflated. Optionally, in some embodiments, a separate
tube 540 may extend through tube 532 and trough occluder 530 to
provide access to the area distal to the occluder 530 for purposes
of suctioning, introduction of instruments, or other purposes.
[0217] FIG. 3H shows another embodiment wherein the occluder 546 is
connected to a tube or elongate member 550 and a suction tube 548
having an expanded (e.g., trumpet shaped) distal end is useable to
suction blood, fluid or debris from the area adjacent to the upper
surface of the occluder. As can be seen from FIG. 3H, where the
upper surface of the occluder is arched and annular collection
space may be created around the perimeter of the occluder 546 where
the occluder 546 coapts with the wall of the anatomical structure
in which it is positioned (e.g., a nasal cavity, posterior choanae,
nasopharynx, pharynx, etc.) and the expanded end 552 of the suction
tube 548 may be sized and shaped to receive the arched upper
surface of the occluder 546 and to suction any blood, fluid or
debris from that annular collection space. In embodiments where the
occluder is a balloon a balloon/inflation lumen may extend through
tube 548 and a small balloon inflation tube may extend into the
interior of the balloon to permit the balloon to be inflated and
deflated. Optionally, in some embodiments, a separate tube 550 may
extend through tube 548 and through occluder 546 to provide access
to the area distal to the occluder 546 for purposes of suctioning,
introduction of instruments or fluid injectors, or other
purposes.
[0218] FIG. 3I shows an embodiment wherein the occluder 570
comprises a mass of absorbent material such as a tampon (e.g.,
cotton, gauze, hydrogel or other material or composite of materials
that will absorb fluid and occlude the desired body lumen). In the
particular example shown, the occluder is advanced out of an
aperture 578 formed in a tube 572 that has a curved (e.g.,
generally "U" shaped) tip. Suction apertures 576 are formed in the
distal portion of the tube 572 to permit blood, fluid or debris
that collects adjacent to the upper surface of the occluder 570 to
be suctioned through the tube 572. After the procedure is complete
or the occlusion is no longer required, the tube 572 and
fluid-soaked occluder 570 may be withdrawn from the body without
retraction of the occluder 570 into the tube 572. Optionally, a
distal end opening 574 may be formed in tube 572 and such distal
end opening may be connected to the same lumen as openings 576 or a
separate lumen to the optional distal end opening 574 to be used
for suctioning, irrigation or introduction of a working device 580
such those shown in FIGS. 5A-5Y.sup.11111 and described
herebelow.
[0219] FIG. 3J shows an occluder embodiment similar to that of the
device shown in FIGS. 2O and 2P and described hereabove. In this
embodiment, an occluder 600 is attached to a tube or elongate
member 604 and a suction tube 602 is movable back and forth over
the tube or elongate member 604 to suction blood, fluid or debris
from the area adjacent to the upper surface of the occluder 600 or
elsewhere in the body lumen in which the occluder 600 is
positioned. In embodiments where the occluder 600 is a balloon, a
balloon/inflation lumen may extend through tube or elongate member
604 and into the balloon to permit the balloon to be inflated and
deflated. Optionally, in some embodiments, a separate tube 606 may
extend trough tube or elongate member 604 and through occluder 600
to provide access to the area distal to the occluder 600 for
purposes of suctioning, introduction of instruments, or other
purposes.
[0220] FIG. 3K shows an occluder embodiment similar to that
incorporated into the device shown in FIGS. 2Q and 2R and described
hereabove. In this embodiment, an occluder 610 is attached to a
tube or elongate member 614 and a tapered suction tube 612 having
one or more suction apertures 616 formed therein is movable back
and forth over the tube or elongate member 614 to suction blood,
fluid or debris from the area adjacent to the upper surface of the
occluder 610 or elsewhere in the body lumen in which the occluder
600 is positioned. Of course, irrigation solution or other fluids
may also be delivered through such apertures 616 or through a
separate irrigation/infusion lumen that opens through separate
irrigation/infusion aperture(s) (not shown). In embodiments where
the occluder 610 is a balloon, a balloon/inflation lumen may extend
through tube or elongate member 614 and into the balloon to permit
the balloon to be inflated and deflated. Optionally, in some
embodiments, a separate 10 tube 618 may extend trough tube or
elongate member 614 and through occluder 610 to provide access to
the area distal to the occluder 610 for purposes of suctioning,
introduction of instruments, or other purposes.
[0221] FIGS. 3L.sup.1-3L.sup.11 show yet another occluder/tubing
device 1000 comprising an outer tube 1002 and an inner tube 1004
disposed coaxially within the outer tube 1002. An outwardly
bendable region 1006 is formed in the wall of the outer tube 1002
near its distal end. The distal end of the outer tube 1002 is
affixed to the inner tube 1004. A passageway 1010 extends between
the outer tube 1002 and inner tube 1004 and openings 1008 are
formed in the wall of the outer tube 1002. In routine operation,
this device 1000 is initially disposed in the configuration shown
in FIG. 3L.sup.1 and is inserted into the desired passageway.
Thereafter, the inner tube 1004 is pulled in the proximal direction
while the outer tube 1002 is held stationary, thereby causing the
outwardly bendable region 1006 to protrude outwardly as shown in
FIG. 3L.sup.11 and resulting in occlusion of the body lumen in
which the distal portion of the device 1000 is positioned. Suction
may be applied to passageway 1010 to remove blood, fluid or other
debris from the area adjacent to the upper surface of 1007 of the
outwardly protruding bendable region 1006. In this regard, the
openings 1008 may be formed close to and/or even in the upper
surface 1007 of the outwardly protruding bendable region 1006.
[0222] FIGS. 3M.sup.1 and 3M.sup.11 show another occluder/tubing
device 1020 comprising an outer tube 1022 an inner tube 1024. The
inner tube 1024 is advanceable out of the distal end of the outer
tube 1022 and a distal portion of the inner tube 1024 expands as it
emerges from the inner tube, thereby forming an occluder that
occludes the body lumen or passageway in which it is positioned, as
shown in FIG. 3M.sup.11. Blood, other fluid or debris may be
suctioned from the area adjacent to the upper surface of the
occluder through the open distal end of the outer tube 1022 and/or
through optional side apertures 1026.
[0223] FIG. 4 shows a nasopharyngeal occluder/endotracheal tube
device 620 of the present invention inserted through the right
nasal cavity and Into the trachea. This device 620 comprises a
curved tube 622 having a posterior occluder 626 positioned at or
near the distal end of the tube 622 and, optionally an anterior
occluder (shown in dotted lines on FIG. 4) formed near the proximal
end of the tube 622. An endotracheal tube 624 extends through
curved tube 622, through the posterior occluder and into the
patient's trachea. Optionally, a cuff 628 may be formed on
endotracheal tube 624 to provide a second substantially fluid tight
seal within the patient's trachea, inferior to the glottis. A hub
630 is formed on the proximal end of tube 622. A ventilator tube
634 extends from the hub and is connected to endotracheal tube 624
and is attachable to a ventilator, anesthesia machine, t-tube,
Ambu-bag, etc., In embodiments where the posterior occluder 626 is
a balloon, a posterior occluder inflation/deflation connector 632
extends from hub 630 and is connected to an inflation/deflation
lumen that extends through tube 622 for inflation/deflation of the
posterior occluder 626. A cuff inflation/deflation connector 634
may also extend from hub 630 and through the endotracheal tube 624
for inflation/deflation of the endotracheal tube cuff 628.
Optionally, suction and/or device insertion ports may also be
formed in hub 630, as described above in connection with other
occluder/access devices. In routine operation, this device 620 is
inserted to a position where the posterior occluder 626 occludes
the posterior choanae, nasopharynx or pharynx posterior to the
nasal septum (but typically superior to the glottis) and the
endotracheal tube 624 extends into the patient's trachea with the
optional cuff positioned in the trachea inferior to the
glottis.
[0224] C. Working Devices for Delivering Substances or for Cutting,
Ablating, Remodeling or Expanding Bone or Soft Tissue
[0225] The present invention provides a variety of apparatus that
may be inserted into the nasal cavity, paranasal sinus, nasopharynx
or middle ear to perform diagnostic or therapeutic procedures.
These devices may be delivered through or incorporated into
flexible catheters or flexible rod-like shafts. Such flexible
construction allows these devices to be delivered and positioned to
perform the desired diagnostic or therapeutic procedures with
minimal trauma to other tissues, as can result from the insertion
of rigid scopes and rigid instruments in accordance with the
methodology of the prior art. It is within the scope of this
approach that these devices may be partially flexible or have rigid
portions and flexible portions to facilitate their control and
guidance to the appropriate region. Further, they may be used in
conjunction or combination with other standard rigid apparatus
(scopes, etc.) during some part of the procedure, if desired.
[0226] Also, in some but not necessarily all procedures, these
working devices (and/or the catheters used to deliver them) may be
inserted through lumens of the occluder & access devices 10,
12, 300, 301, 400, 430, etc., as shown in FIGS. 2A-2R and described
above. As stated earlier, it may also be desirable to focus the
access and occlusion to an even smaller territory, through
stand-alone guide catheters or subselective guide catheters with or
without balloons or other occluders.
[0227] Optionally, any of the working devices and guide catheters
described herein may be configured to receive or be advanced over a
guidewire unless to do so would render the device inoperable for
its intended purpose. Some of the specific examples described
herein include guidewires, but it is to be appreciated that the use
of guidewires and the incorporation of guidewire lumens is not
limited to only the specific examples in which guidewires or
guidewire lumens are shown. The guidewires used in this invention
may be constructed and coated as is common in the art of
cardiology. This may include the use of coils, tapered or
non-tapered core wires, radiopaque tips and/or entire lengths,
shaping ribbons, variations of stiffness, PTFE, silicone,
hydrophilic coatings, polymer coatings, etc., For the scope of this
inventions, these wires may possess dimensions of length between 5
and 75 cm and outer diameter between 0.005'' and 0.050''.
[0228] Also, some of the working devices shown in FIGS.
5A-5Y.sup.11111 and described herein incorporate assemblies,
components or mechanisms (e.g., rotating cutters, radiofrequency
electrodes, electrocautery devices, receptacles for capturing
matter, cryosurgical apparatus, balloons, stents, radioactive or
substance-eluting coatings, snares, electro-anatomical mapping and
guidance, optical fibers, lenses and other endoscopic apparatus,
seals, hemostatic valves, etc., The designs and constructions of
such components and assemblies are well known in the art.
Non-limiting examples of some such designs and constructions are
set forth in U.S. Pat. No. 5,722,984 (Fischell et al.), U.S. Pat.
No. 5,775,327 (Randolph et al.), U.S. Pat. No. 5,685,838 (Peters,
et al.), U.S. Pat. No. 6,013,019 (Fischell et al.), U.S. Pat. No.
5,356,418 (Shturman), U.S. Pat. No. 5,634,908 (Loomas), U.S. Pat.
No. 5,255,679 (Imran), U.S. Pat. No. 6,048,299 (Hoffman), U.S. Pat.
No. 6,585,794 (Wright et al.), U.S. Pat. No. 6,503,185 (Waksman),
U.S. Pat. No. 6,669,689 (Lehmann et al.), U.S. Pat. No. 6,638,233
(Corvi et al.), U.S. Pat. No. 5,026,384 (Fan et al.), U.S. Pat. No.
4,669,469 (Gifford et al.), U.S. Pat. No. 6,685,648 (Flaherty et
al.), U.S. Pat. No. 5,250,059 (Andreas et al.), U.S. Pat. No.
4,708,834 (Tsuno), U.S. Pat. No. 5,171,233 (Amplatz), U.S. Pat. No.
6,468,297 (Williams et al.) and U.S. Pat. No. 4,748,869
(Wardle).
[0229] As shown in the examples of FIGS. 5A-5Y.sup.111 these
working devices include guide catheters, substance delivery
catheters, scopes, injectors, cutters, bone breaking apparatus,
balloons and other dilators, laser/thermal delivery devices,
braces, implants, stents, snares, biopsy tools, forceps, etc.
[0230] FIG. 5A shows a side suction and/or cutting catheter 70
comprising a flexible catheter body 72 having a side opening 74.
The catheter 72 is advanced into a passageway such as a nostril,
nasal cavity, meatus, ostium, interior of a sinus, etc., and
positioned so that the opening 74 is adjacent to matter (e.g., a
polyp, lesion, piece of debris, tissue, blood clot, etc.) that is
to be removed. Suction may be applied through a lumen of the
catheter 72 to suction the matter through the opening 74, and into
the catheter 72. In some cases, a cutter such as a rotating cutter,
linear slicer, pincher, laser beam, electrosurgical cutter, etc.,
may be incorporated into the catheter 72 to assist in severing or
ablating tissue or other matter that has been positioned in the
side opening 74. This catheter may incorporate a deflectable tip or
a curved distal end which may force the opening of the catheter
against the tissue of interest. Further, this device 70 may have an
optional stabilizing balloon (similar to that shown in FIG. 5M and
described herebelow) incorporated on one side of the catheter 72 to
press it against the tissue of interest and may also contain one or
more on-board imaging modalities such as ultrasound, fiber or
digital optics, OCT, RF or electromagnetic sensors or emitters,
etc.
[0231] FIG. 5B shows an injector catheter 76 that comprises a
flexible catheter shaft 78 having one or more injector(s) 80 that
are advanceable into tissue or other matter that is located in or
on the wall of the body lumen in which the catheter 78 is
positioned. The catheter 78 is advanced, with the injector(s)
retracted into the catheter body, through a passageway such as a
nostril, nasal cavity, meatus, ostium, interior of a sinus, etc.,
and positioned adjacent the area to which a diagnostic or
therapeutic substance is to be injected. Thereafter, the
injector(s) are advanced into the adjacent tissue or matter and the
desired substance is injected. Energy, such as laser, RF, thermal
or other energy may be delivered through these injectors 80 or
energy emitting implants (such as gamma or beta radioactive seeds)
may also be delivered through these injectors 80, either alone or
in combination with a fluid carrier or other substance such as a
diagnostic or therapeutic substance (as defined herein). It will be
noted that this device 76 as well as other working devices and
methods of the present invention (including the various implantable
devices described herein) are useable to deliver diagnostic or
therapeutic substances. The term "diagnostic or therapeutic
substance" as used herein is to be broadly construed to include any
feasible drugs, prodrugs, proteins, gene therapy preparations,
cells, diagnostic agents, contrast or imaging agents, biologicals,
etc., For example, in some applications where it is desired to
treat or prevent a microbial infection, the substance delivered may
comprise pharmaceutically acceptable salt or dosage form of an
antimicrobial agent (e.g., antibiotic, antiviral, antiparasitic,
antifungal, etc.).
[0232] Some nonlimiting examples of antimicrobial agents that may
be used in this invention include acyclovir, amantadine,
aminoglycosides (e.g., amikacin, gentamicin and tobramycin),
amoxicillin, amoxicillin/Clavulanate, amphotericin B, ampicillin,
ampicillin/sulbactam, atovaquone, azithromycin, cefazolin,
cefepime, cefotaxime, cefotetan, cefpodoxime, ceftazidime,
ceftizoxime, ceftriaxone, cefuroxime, cefuroxime axetil,
cephalexin, chloramphenicol, clotrimazole, ciprofloxacin,
clarithromycin, clindamycin, dapsone, dicloxacillin, doxycycline,
erythromycin, fluconazole, foscarnet, ganciclovir, atifloxacin,
imipenem/cilastatin, isoniazid, itraconazole, ketoconazole,
metronidazole, nafcillin, nafcillin, nystatin, penicillin,
penicillin G, pentamidine, piperacillin/tazobactam, rifampin,
quinupristin-dalfopristin, ticarcillin/clavulanate,
trimethoprim/sulfamethoxazole, valacyclovir, vancomycin, mafenide,
silver sulfadiazine, mupirocin, nystatin, triamcinolone/nystatin,
clotrimazole/betamethasone, clotrimazole, ketoconazole,
butoconazole, miconazole, tioconazole, detergent-like chemicals
that disrupt or disable microbes (e.g., nonoxynol-9, octoxynol-9,
benzalkonium chloride, menfegol, and N-docasanol); chemicals that
block microbial attachment to target cells and/or inhibits entry of
infectious pathogens (e.g., sulphated and sulponated polymers such
as PC-515 (carrageenan), Pro-2000, and Dextrin 2 Sulphate);
antiretroviral agents (e.g., PMPA gel) that prevent retroviruses
from replicating in the cells; genetically engineered or naturally
occurring antibodies that combat pathogens such as anti-viral
antibodies genetically engineered from plants known as
"plantibodies;" agents which change the condition of the tissue to
make it hostile to the pathogen (such as substances which alter
mucosal pH (e.g., Buffer Gel and Acidform) or non-pathogenic or
"friendly" bacteria or other microbes that cause the production of
hydrogen peroxide or other substances that kill or inhibit the
growth of pathogenic microbes (e.g., lactobacillus). As may be
applied to any of the substances listed previously or below, these
substances may be combined with any one or more drug-releasing
devices or molecular constructs such as polymers, collagen, gels,
implantable osmotic pump devices, etc., to permit their release
over an extended period of time once deposited. Further, these
substances may also be combined with any of the implantable
structural devices described below (stents, expanders, etc.) to
reduce Infection, encrustation, or encapsulation of the implant
itself, or to allow the drug to be deposited in the optimal
location mucosally, sub-mucosally or into the bone. Examples of
Implantable substance delivery devices useable in this invention
include those shown in FIGS. 5Y.sup.1-5Y.sup.11111 and described
herebelow.
[0233] Additionally or alternatively, in some applications where it
is desired to treat or prevent inflammation the substances
delivered in this invention may include various steroids. For
example, corticosteroids that have previously administered by
intranasal administration may be used, such as beclomethasone
(Vancenase.RTM. or Beconase.RTM.), flunisolide (Nasalideft
fluticasone (Flonase.RTM.), triamcinolone (Nasacort.RTM.) and
mometasone (Nasonex.RTM.). Also, other steroids that may be useable
in the present invention include but are not limited, to
aclometasone, desonide, hydrocortisone, betamethasone,
clocortolone, desoximetasone, fluocinolone, flurandrenolide,
mometasone, prednicarbate; amcinonide, desoximetasone, diflorasone,
fluocinolone, fluocinonide, halcinonide, clobetasol, augmented
betamethasone, diflorasone, halobetasol, prednasone, dexamethasone
and methylprednisolone,
[0234] Additionally or alternatively, in some applications, such as
those where it is desired to treat or prevent an allergic or immune
response, the substances delivered in this invention may include a)
various cytokine inhibitors such as humanized anti-cytokine
antibodies, anti-cytokine receptor antibodies, recombinant (new
cell resulting from genetic recombination) antagonists, or soluble
receptors; b) various leucotriene modifiers such as zaflrlukast,
montelukast and zileuton; c) immunoglobulin E (IgE) inhibitors such
as Omalizumab (an anti-IgE monoclonal antibody formerly called rhu
Mab-E25) and secretory leukocyte protease inhibitor).
[0235] Additionally or alternatively, in some applications, such as
those where it is desired to shrink mucosal tissue, cause
decongestion or effect hemostasis, the substances delivered in this
invention may include various vasoconstrictors for decongestant and
or hemostatic purposes including but not limited to
pseudoephedrine, xylometazoline, oxymetazoline, phenylephrine,
epinephrine, etc.
[0236] Additionally or alternatively, in some applications, such as
those where it is desired to facilitate the flow of mucous, the
substances delivered in this invention may include various
mucolytics or other agents that modify the viscosity or consistency
of mucous or mucoid secretions, including but not limited to
acetylcysteine (Mucomyst.TM., Mucosil.TM.) and guaifenesin.
[0237] Additionally or alternatively, in some applications such as
those where it is desired to prevent or deter histamine release,
the substances delivered in this invention may include various mast
cell stabilizers or drugs which prevent the release of histamine
such as cromolyn (e.g., Nasal Chrom.RTM.) and nedocromil.
[0238] Additionally or alternatively, in some applications such as
those where it is desired to prevent or inhibit the effect of
histamine, the substances delivered in this invention may include
various antihistamines such as azelastine (e.g., Astylin.RTM.),
diphenhydramine, loratidine, etc.
[0239] Additionally or alternatively, in some embodiments such as
those where it is desired to dissolve, degrade, cut, break or
remodel bone or cartilage, the substances delivered in this
invention may include substances that weaken or modify bone and/or
cartilage to facilitate other procedures of this invention wherein
bone or cartilage is remodeled, reshaped, broken or removed. One
example of such an agent would be a calcium chelator such as EDTA
that could be injected or delivered in a substance delivery implant
next to a region of bone that is to be remodeled or modified.
Another example would be a preparation consisting of or containing
bone degrading cells such as osteoclasts. Other examples would
include various enzymes of material that may soften or break down
components of bone or cartilage such as collagenase (CGN), trypsin,
trypsin/EDTA, hyaluronidase, and tosyllysylchloromethane
(TLCM).
[0240] Additionally or alternatively, in some applications, the
substances delivered in this invention may include other classes of
substances that are used to treat rhinitis, nasal polyps, nasal
inflammation, and other disorders of the ear, nose and throat
including but not limited to anticolinergic agents that tend to dry
up nasal secretions such as ipratropium (Atrovent Nasal.RTM.), as
well as other agents not listed here.
[0241] Additionally or alternatively, in some applications such as
those where it is desired to draw fluid from polyps or edematous
tissue, the substances delivered in this invention may include
locally or topically acting diuretics such as furosemide and/or
hyperosmolar agents such as sodium chloride gel or other salt
preparations that draw water from tissue or substances that
directly or indirectly change the osmolar content of the mucous to
cause more water to exit the tissue to shrink the polyps directly
at their site.
[0242] Additionally or alternatively, in some applications such as
those wherein it is desired to treat a tumor or cancerous lesion,
the substances delivered in this invention may include antitumor
agents (e.g., cancer chemotherapeutic agents, biological response
modifiers, vascularization inhibitors, hormone receptor blockers,
cryotherapeutic agents or other agents that destroy or inhibit
neoplasia or tumorigenesis), such as alkylating agents or other
agents which directly kill cancer cells by attacking their DNA
(e.g., cyclophosphamide, isophosphamide), nitrosoureas or other
agents which kill cancer cells by inhibiting changes necessary for
cellular DNA repair (e.g., carmustine (BCNU) and lomustine (CCNU)),
antimetabolites and other agents that block cancer cell growth by
interfering with certain cell functions, usually DNA synthesis
(e.g., 6-mercaptopurine and 5-fluorouracil (5FU), antitumor
antibiotics and other compounds that act by binding or
intercalating DNA and preventing RNA synthesis (e.g., doxorubicin,
daunorubicin, epirubicin, idarubicin, mitomycin-C and bleomycin)
plant (vinca) alkaloids and other anti-tumor agents derived from
plants (e.g., vincristine and vinblastine), steroid hormones,
hormone inhibitors, hormone receptor antagonists and other agents
which affect the growth of hormone-responsive cancers (e.g.,
tamoxifen, herceptin, aromatase ingibitors such as
aminoglutethamide and formestane, trriazole inhibitors such as
letrozole and anastrazole, steroidal inhibitors such as
exemestane), antiangiogenic proteins, small molecules, gene
therapies and/or other agents that inhibit angiogenesis or
vascularization of tumors (e.g., meth-1, meth-2, thalidomide),
bevacizumab (Avastin), squalamine, endostatin, angiostatin,
Angiozyme, AE-941 (Neovastat), CC-5013 (Revimid), medi-522
(Vitaxin), 2-methoxyestradiol (2ME2, Panzem), carboxyamidotriazole
(CAI), combretastatin A4 prodrug (CA4P), SU6668, SU11248,
BMS-275291, COL-3, EMD 121974, IMC-1C11, IM862, TNP-470, celecoxib
(Celebrex), rofecoxib (Vioxx), interferon alpha, interleukin-12
(IL-12) or any of the compounds identified in Science Vol. 289,
Pages 1197-1201 (Aug. 17, 2000) which is expressly incorporated
herein by reference, biological response modifiers (e.g.,
interferon, bacillus calmette-guerin (BCG), monoclonal antibodies,
interluken-2, granulocyte colony stimulating factor (GCSF), etc.),
PGDF receptor antagonists, herceptin, asparaginase, busulphan,
carboplatin, cisplatin, carmustine, cchlorambucil, cytarabine,
dacarbazine, etoposide, flucarbazine, flurouracil, gemcitabine,
hydroxyurea, ifosphamide, irinotecan, lomustine, melphalan,
mercaptopurine, methotrexate, thioguanine, thiotepa, tomudex,
topotecan, treosulfan, vinblastine, vincristine, mitoazitrone,
oxaliplatin, procarbazine, streptocin, taxol, taxotere,
analogs/congeners and derivatives of such compounds, as well as
other antitumor agents not listed here.
[0243] Additionally or alternatively, in some applications such as
those where it is desired to grow new cells or to modify existing
cells, the substances delivered in this invention may include cells
(mucosal cells, fibroblasts, stem cells or genetically engineered
cells), as well as genes and gene delivery vehicles like plasmids,
adenoviral vectors or naked DNA, mRNA, etc., injected with genes
that code for anti-inflammatory substances, etc., and, as mentioned
above, osteoclasts that modify or soften bone when so desired.
[0244] Additionally or alternatively to being combined with a
device and/or a substance releasing modality, it may be ideal to
position the device in a specific location upstream in the mucous
flow path (i.e., frontal sinus or ethmoid cells). This could allow
the deposition of fewer drug releasing devices, and permit the
"bathing" of all the downstream tissues with the desired drug. This
utilization of mucous as a carrier for the drug may be ideal,
especially since the concentrations for the drug may be highest in
regions where the mucous is retained; whereas non-diseased regions
with good mucous flow will be less affected by the drug. This could
be particularly useful in chronic sinusitis, or tumors where
bringing the concentration of drug higher at those specific sites
may have greater therapeutic benefit. In all such cases, local
delivery will permit these drugs to have much less systemic impact.
Further, it may be ideal to configure the composition of the drug
or delivery system such that it maintains a loose affinity to the
mucous permitting it to distribute evenly in the flow. Also, in
some applications, rather than a drug, a solute such as a salt or
other mucous soluble material may be positioned at a location
whereby mucous will contact the substance and a quantity of the
substance will become dissolved in the mucous thereby changing some
property (e.g., pH, osmolarity, etc.) of the mucous. In some cases,
this technique may be used to render the mucous hyperosmolar so
that the flowing mucous will draw water from polyps, edematous
mucosal tissue, etc., thereby providing a desiccating therapeutic
effect.
[0245] Additionally or alternatively to substances directed towards
local delivery to affect changes within the sinus cavity, the nasal
cavities provide unique access to the olfactory system and thus the
brain. Any of the devices and methods described herein may also be
used to deliver substances to the brain or alter the functioning of
the olfactory system. Such examples include, the delivery of energy
or the deposition of devices and/or substances and/or substance
delivering implant(s) to occlude or alter olfactory perception, to
suppress appetite or otherwise treat obesity, epilepsy (e.g.,
barbiturates such as phenobarbital or mephoobarbital;
iminostilbenes such as carbamazepine and oxcarbazepine;
succinimides such as ethylsuximide; valproic acid; benzodiazepines
such as clonazepam, clorazepate, diazepam and lorazepam,
gabapentin, lamotrigine, acetazolamide, felbamate, levetiraceam,
tiagabine, topiramate, zonisamide, etc.), personality or mental
disorders (e.g., antidepressants, anti-anxiety agents,
antipsychotics, etc.), chronic pain, Parkinson's disease (e.g.,
dopamine receptor agonists such as bromocriptine, pergolide,
ropinitrol and pramipexole; dopamine precursors such as levodopa;
COMT inhibitors such as tolcapone and entacapone; selegiline;
muscarinic receptor antagonists such as trihexyphenidyl,
benztropine and diphenhydra mine) and Alzheimer's, Huntington's
Disease or other dementias, disorders of cognition or chronic
degenerative diseases (e.g., tacrine, donepezil, rivastigmine,
galantamine, fluoxetine, carbamazepine, clozapine, clonazepam and
proteins or genetic therapies that inhibit the formation of
beta-amyloid plaques), etc.
[0246] FIG. 5C shows a device 82 that comprises a rotating shaft 84
having a drill, auger or burr 86 that is useable to drill, bore,
grind or cut through tissue, bone, cartilage or other matter. This
device 82 may deployed as shown or, alternatively, the device 82
may be inserted through a small mucosal incision to preserve the
overlying mucosal lining while removing or boring Into the bone or
cartilage below the mucosal lining.
[0247] FIG. 5D shows a guided injector catheter device 88 for
delivering a diagnostic or therapeutic substance as defined above.
This device 88 comprises a flexible catheter 90 having an imaging
apparatus 96 thereon and an injector 92 that is advanceable from
and retractable into the catheter 90. The imaging apparatus 96 is
useable to image the target location 94 at which the substance is
to be deposited and to enable orientation of the catheter 88 such
that, when the injector 92 is advanced from the catheter 88, the
injector 92 will travel to the desired target location 94. Examples
of such catheter 88 are described in U.S. Pat. No. 6,195,225
(Makower), U.S. Pat. No. 6,544,230 (Flaherty et al.), U.S. Pat. No.
6,375,615 (Flaherty et al.), U.S. Pat. No. 6,302,875 (Makower et
al), U.S. Pat. No. 6,190,353 (Makower et al.) and U.S. Pat. No.
6,685,648 (Flaherty et al.), the entireties of which are expressly
incorporated herein by reference.
[0248] FIG. 5E shows a balloon catheter device 98 comprising a
flexible catheter 100 having a balloon 102 thereon. The catheter
device 98 is advanced, with balloon 102 deflated, into a passageway
such as a nostril, nasal cavity, meatus, ostium, interior of a
sinus, etc., and positioned with the deflated balloon 102 situated
within an ostium, passageway or adjacent to tissue or matter that
is to be dilated, expanded or compressed (e.g., to apply pressure
for hemostasis, etc.). Thereafter, the balloon 102 may be inflated
to dilate, expand or compress the ostium, passageway, tissue or
matter. Thereafter the balloon 102 may be deflated and the device
98 may be removed. This balloon 102 may also be coated, impregnated
or otherwise provided with a medicament or substance that will
elute from the balloon into the adjacent tissue (e.g., bathing the
adjacent tissue with drug or radiating the tissue with thermal or
other energy to shrink the tissues in contact with the balloon
102). Alternatively, in some embodiments, the balloon may have a
plurality of apertures or openings through which a substance may be
delivered, sometimes under pressure, to cause the substance to
bathe or diffuse into the tissues adjacent to the balloon.
Alternatively, in some embodiments, radioactive seeds, threads,
ribbons, gas or liquid, etc., maybe advanced into the catheter
shaft 100 or balloon 102 or a completely separate catheter body for
some period of time to expose the adjacent tissue and to achieve a
desired diagnostic or therapeutic effect (e.g., tissue shrinkage,
etc.).
[0249] FIG. 5F shows a balloon/cutter catheter device 104
comprising a flexible catheter 106 having a balloon 108 with one or
more cutter blades 110 formed thereon. The device 104 is advanced,
with balloon 108 deflated, into a passageway such as a nostril,
nasal cavity, meatus, ostium, interior of a sinus, etc., and
positioned with the deflated balloon 108 situated within an ostium,
passageway or adjacent to tissue or matter that is to be dilated,
expanded or compressed and in which it is desired to make one or
more cuts or scores (e.g., to control the fracturing of tissue
during expansion and minimize tissue trauma, etc.). Thereafter, the
balloon 108 may be inflated balloon to dilate, expand or compress
the ostium, passageway, tissue or matter and causing the cutter
blade(s) 110 to make cut(s) in the adjacent tissue or matter.
Thereafter the balloon 108 may be deflated and the device 104 may
be removed. The blade may be energized with mono or bi-polar RF
energy or simply be thermally heated to part the tissues in a
hemostatic fashion, as well as cause contraction of collagen fibers
or other connective tissue proteins, remodeling or softening of
cartilage, etc.
[0250] FIGS. 5G.sup.1-5G.sup.111 show a device 160 and method for
delivery of a pressure expandable stent 166. This device 160
comprises a flexible catheter 162 having a balloon 164 thereon.
Initially, as shown in FIG. 5G.sup.1, the balloon 164 is deflated
and the stent 166 is radially compressed to a collapsed
configuration, around the deflated balloon 164. The catheter 162
with the balloon 164 deflated and the collapsed stent 166 mounted
thereon is advanced into a passageway such as a nostril, nasal
cavity, meatus, ostium, interior of a sinus, etc., that is to be
stented. Thereafter, the balloon 164 is inflated causing the stent
166 to expand to a size that frictionally engages the surrounding
tissue so as to hold the stent 166 in place, as shown in FIG.
5G.sup.11. In some instances the procedure will be performed for
the purpose of enlarging a passageway (e.g., an ostium, meatus,
etc.) and the stent 166 will be expanded to a diameter that is
sufficiently large to cause the desired enlargement of the
passageway and the stent will then perform a scaffolding function,
maintaining the passageway in such enlarged condition. After the
stent 166 has been fully expanded and implanted, the balloon 164
may be deflated and the catheter 162 removed as shown in FIG.
5G.sup.111. In some applications, the stent may contain a
diagnostic or therapeutic substance as defined herein and such
substance may elute from the stent 166 into the surrounding tissue
to bring about a desired diagnostic or therapeutic effect. In some
cases, the stent 166 may be permanently implanted. In other cases
the stent 166 may be temporarily implanted. In cases where the
stent 166 is temporarily implanted, it may be removed in a second
procedure conducted to retrieve the stent 166 or the stent 166 may
be made of bio-absorbable or biodegradable material such that it
degrades or is absorbed within a desired period of time after
implantation. In some cases, such as when the stent is to be placed
within the ostium of a paranasal sinus, the stent and/or the
balloon may be specifically shaped to facilitate and/or cause the
stent 166 to seat in a desired position and to prevent unwanted
slippage of the stent 166. For example, the stent 166 and/or
balloon 164 may have an annular groove formed about the middle
thereof or may be hourglass or venture shaped, to facilitate
seating of the stent 166 within an ostium or orifice without
longitudinal slippage of the stent 166. In some cases it may be
desirable to leave a tether or suture attached to the stent 166 to
allow for simple removal of the stent 166 in the physician's office
or other suitable location. In some cases the procedure may be
intended to actually break bone (e.g., where the stent is intended
to dilate or enlarge a sinus ostium). Thus, the balloon 164 may be
made of polymeric material including, but not limited to flexible
polyvinyl chloride (PVC), polyethylene terephthalate (PET),
cross-linked polyethylene, polyester, polyamide, polyolefin,
polyurethane and silicone. Various balloon properties (strength,
flexibility, thickness, etc.) may be modified by, but not limited
to, blending, layering, mixing, co-extruding, irradiating, and
other means of engineering balloon material(s). This allows for the
use of compliant balloons that can conform to the surrounding
structure or non-compliant balloons that can deform or break the
surrounding structures (e.g., bone).
[0251] FIG. 5H shows an electrosurgical device 208 comprising a
flexible shaft 210 (e.g., a catheter or solid shaft) having arched
strut members 214 attached thereto. Electrodes 216 are located on
the strut members 214. In some cases, the strut members may be of
fixed configuration and in other cases the strut members 214 may be
collapsible and expandable. In operation, the device 208 is
advanced into a passageway such as a nostril, nasal cavity, meatus,
ostium, interior of a sinus, etc., Thereafter, current is applied
to the electrodes 216 causing tissue adjacent to the struts 214 to
be cauterized or heated. The electrodes 216 may be bipolar,
monopolar or facilitated by any other suitable form of energy such
as a gas or plasma arc. Additionally, sensing elements may also be
attached to the catheter and/or strut members to monitor various
parameters of the catheter and/or surrounding tissue (e.g.,
temperature, etc.). In instances where monopolar electrodes are
used, a separate antenna electrode (not shown) will be applied to
the patient's body in accordance with processes and techniques that
are well known in the art.
[0252] FIG. 5I shows a device 218 that delivers a flow 222 of
material (e.g., cryogenic material, diagnostic or therapeutic
agent, etc.) or energy (laser light, infrared light, etc.) to the
tissues adjacent to the passage or body cavity in which the device
218 is positioned. This device comprises a flexible catheter 220
with an outlet aperture or lens at or near its distal end, through
which the flow of material or energy is delivered. This device may
be used to cryogenically freeze polyps or other tissues or to
deliver laser energy to turbinates or other tissues for the purpose
of ablating the tissue or to heat the tissue to a temperature that
results in shrinking of the tissue.
[0253] FIG. 5J shows an implantable pressure exerting device 224
that is implantable within a passageway such as a nostril, nasal
cavity, meatus, ostium, interior of a sinus, etc., to exert
pressure on bone, cartilage, soft tissue, etc., Examples of
situations where it is desirable to apply such pressure to an
anatomical structure include those wherein it is desired to splint
or maintain approximation of a broken bone or those wherein it is
desired to cause remodeling or gradual repositioning or reshaping
of bone, cartilage, soft tissue or other structures. This
implantable device 224 comprises a pressure exerting member 228 and
two or more plate members 226. The device 224 is initially
constrained in a collapsed configuration wherein the pressure
exerting member 228 is compressed or collapsed and the device 224
is advanced into a passageway such as a nostril, nasal cavity,
meatus, ostium, interior of a sinus, etc., where it is desired to
apply pressure to an anatomical structure. When the device 224 is
in the desired position, the pressure exerting member 228 is
expanded or elongated to exert outward pressure on the plate
members 226 and onto the anatomical structures against which the
plate members 226 are positioned. In some embodiments, the pressure
exerting member may comprise a spring. In other embodiments, the
pressure exerting member may comprise a ratchet, hydraulic cylinder
or other mechanical apparatus that may be adjusted to create a
desired amount of pressure on the plate members 226. In some
applications, the pressure exerting member 228 may be adjustable in
situ (i.e., with the device implanted in the body) so as to allow
the operator to periodically change the amount of pressure being
applied to the anatomical structures of interest (e.g., the
operator may change to position of a ratchet or add fluid to a
hydraulic cylinder) thereby bringing about gradual remodeling or
movement of an anatomical structure in a manner similar to that
achieved during dental orthodontia. Thus, this pressure exerting
device 224 has broad applicability in a variety of procedures,
including those intended to enlarge a sinus ostium or to straighten
an intranasal septum.
[0254] FIGS. 5K-5K.sup.1 and 5L show a forward rotary cutting
catheter device 700 that comprises a flexible outer tube 702 and a
flexible inner tube 704 disposed coaxially and rotatably mounted
within the outer tube 702. One or more bearings 708 (e.g., a
helical bearing or a series of individual cylindrical bearings) may
be disposed between the outer tube 702 and inner tube 704, as
shown. Alternatively, one or both apposing tube surfaces may be
made of, lined with, or be coated by etc., a lubricious material
such as silicone or PTFE to facilitate movement. A rotating cutter
706 is positioned on the distal end of the inner tube 704. In
operation, as shown in FIG. 5K.sup.1, the device 700 is advanced
through a passageway such as a nostril, nasal cavity, meatus,
ostium, interior of a sinus, etc., to a position where the distal
end of the device 700 is positioned just behind some obstructive
matter, such as a polyp P. The inner tube 704 and its cutter 706
are rotated as the device is advanced into the obstructive matter P
and/or suction is applied through the lumen of the inner tube 704
and/or through the lumen of the outer tube 702 to draw the
obstructive matter P into contact with the rotating cutter 706. It
is to be appreciated that, although this embodiment shows a
rotating cutter 706, various other types of cutters such as lasers,
radiofrequency cutters and other mechanical cutters, etc., may be
used instead. As the obstructive matter P is severed by the
rotating cutter 706 the obstructive matter P or pieces thereof may
be suctioned through the lumen of the inner tube 704 and/or through
the lumen of the outer tube 702. In some applications, as shown in
FIG. 5L, a scope or guidewire 710 may extend through the lumen of
the inner tube to facilitate advancement and positioning of the
device 700 prior to the removal of the obstructive matter P.
[0255] FIGS. 5M and 5N show a side rotary cutting device 714
comprising a flexible outer tube 718 and a flexible inner tube 722
that is disposed coaxially and rotatably mounted within the outer
tube 718. One or more bearings 730 (e.g., a helical bearing or a
series of individual cylindrical bearings) may be disposed between
the outer tube 718 and inner tube 722, as shown. Alternatively, one
or both apposing tube surfaces may be made of, lined with, or be
coated by etc., a lubricious material such as silicone or PTFE to
facilitate movement. A rotating cutter 724 is positioned on the
distal end of the inner tube 722. A side opening 720 is formed in
the outer tube 718 and the cutter 724 is positioned proximal to the
side opening 720. A pull member 728 extends through the inner tube
722 and is attached to a retractor head 726. In operation, the
device 714 is advanced and/or torqued to a position where the side
opening 720 is near a polyp, tissue or other obstructive matter to
be removed. The inner tube 722 and its cutter 724 are rotated. In
some applications, suction may be applied through the inner tube
722 and/or through the lumen of the outer tube 718 to draw the
obstructive matter into the side opening 720. The pull member 728
is pulled in the proximal direction, causing the retractor head 726
to retract or pull the obstructive matter into contact with the
rotating cutter 724. As the obstructive matter is severed by the
rotating cutter, the severed obstructive matter or pieces thereof
may be suctioned through the lumen of the inner tube 722 and/or
through the lumen of the outer tube 718. The pull member 728 may
then be advanced in the distal direction to return the refractor
head 726 to its original position as shown in FIGS. 5M and 5N. An
optional balloon 719 or other laterally extendable member may be
located on the side of the catheter 718 opposite the side opening
720 to push the side opening 720 against a lumen wall or into the
direction of a polyp or other tissue to be removed. Alternatively,
the catheter may incorporate a deflectable tip or a curved distal
end that may force the side opening of the catheter against a lumen
wall or into the direction of a polyp or other tissue to be
removed. With specific reference to FIG. 5N, there is shown a side
rotary cutting device 714a that includes all of the elements of the
device 714 shown in FIG. 5M, but includes a side lumen 731. A scope
may be permanently positioned within this side lumen 731 or a scope
may be temporarily inserted into (or through) the side lumen 731 to
enable the operator to view the area near the side opening 720 and
to facilitate the advancement and positioning of the device 714A.
Also, the side lumen 731 may function as a guidewire lumen to allow
the device 714A to be advanced over a guidewire.
[0256] It is to be understood that any of the devices described
within this document may be further modified to include any one of
the following devices within its structure: electromagnetic
positioning sensor/detector (Biosense/JNJ, Surgical Navigation
Technologies/Medtronic, Calypso Medical), RF sensor/transmitter,
magnetic direction localizer (Stereotaxis, Inc.), thermal sensor,
radiopaque composition, radioactive detection emitter/sensor,
ultrasonic scanner/transmitter/receiver, Doppler scanner,
electrical stimulator, fiber optic, digital optic, local diagnostic
chip containing elements responsive to the presence or absence of
certain substances and therefore having the ability to diagnose the
presence of fungus, microbes, viruses, blood, abnormal mucous
content, cancer cells, drugs of abuse, genetic abnormalities,
metabolic bi-products, etc.
[0257] It is to be further understood that any and all of the
devices described in this patent application may incorporate, or
may be used in conjunction with, endoscopes. Such endoscopes will
typically include light transmitting optical fibers for casting
light in the area to be viewed by the scope and image transmitting
optical fibers for carrying an image received by the scope to an
eyepiece or monitor device located outside the patient's body. In
some embodiments a scope, such as a disposable and/or flexible
scope, may be affixed to the working device. Examples of such
endoscopes that are suitable for incorporation into the working
devices of this invention include that described in U.S. Pat. Nos.
4,708,434; 4,919,112; 5,127,393; 5,519,532; 5,171,233, 5,549,542,
6,551,239 and 6,572,538; as well as published United States Patent
Application No. 2001/0029317A1, the entireties of which are
expressly incorporated herein by reference.
[0258] It is to be further understood that any catheters or
elongate flexible devices of this invention may include design
elements that impact performance features, which include but are
not limited to, durability, flexibility, stiffness, length,
profile, lubricity, trackability, steerability, torqueability,
deflectability, guidance, and radiopacity. Design elements can
include, but are not limited to, use of various polymers and
metals, use of varying durometer materials to establish a desired
flexibility gradient along the device,
blending/mixing/layering/co-extruding etc., various materials,
using bearings or lubricious coatings or lubricious materials
(e.g., silicone, PTFE, parylene, polyethene, etc.) where two or
more surfaces will move relative to each other (e.g., guidewire or
instrument lumen, deflecting tendon in lumen, etc.), use of
braiding or springs to increase torque control over the device,
using materials (e.g., barium, tantalum, etc.) to increase polymer
radiopacity, and use of elements to predictably deflect various
sections of the catheter (e.g., tension straps or wires, shape
memory alloys such as nitinol, etc.).
[0259] It is to be further understood that any of the catheters,
scopes, elongate working devices or other devices disclosed in this
patent application may be rendered steerable or volitionally
bendable, unless to do so would make such device inoperative for
its intended purpose. Steerable catheters and scopes are well known
in the art and may utilize mechanical steering assemblies (e.g.,
pull wires, hinges, etc.) or shape memory materials (e.g., nickel
titanium alloys, shape memory polymers, etc.) to induce the device
to undergo the desired bending or curvature after it has been
inserted into the body. Examples of apparatus and construction that
may be used to render these devices steerable or volitionally
bendable include but are not limited to those described in U.S.
Pat. No. 5,507,725 (Savage et al.); U.S. Pat. No. 5,656,030 (Hunjan
et al.); U.S. Pat. No. 6,183,464 (Webster); U.S. Pat. No. 5,251,092
(Qin et al.); U.S. Pat. No. 6,500,130 (Kinsella et al.); U.S. Pat.
No. 6,571,131 (Nguyen); U.S. Pat. No. 5,415,633 (Lazarus et al.);
U.S. Pat. No. 4,998,916 (Hammerslag et al.); U.S. Pat. No.
4,898,577 (Badger et al.); U.S. Pat. No. 4,815,478 (Buchbinder et
al.); and published United States Patent Application Nos.
2003/0181827A1 (Hojeibane et al.) and 2003/0130598A1 (Manning et
al.), the entireties of which are expressly incorporated herein by
reference.
[0260] FIG. 5O shows a flexible catheter 733 having a working lumen
734 that extends though the catheter 732 and terminates in a distal
end opening. Optionally, a second lumen 736 may also extend though
the catheter 732 and terminate in a distal end opening, as shown.
An endoscope 738 may be permanently positioned within this lumen
736 or such endoscope 738 may be temporarily inserted into (or
through) the lumen 736 to enable the operator to view the area
distal to the catheter 732. Additionally or alternatively, a side
scope or lumen 740 may be located on the catheter 732. and an
endoscope may be permanently embodied by or positioned in or
temporarily inserted into (or through) such side scope or lumen 740
to enable the operator to view the area distal to the catheter 732
and, in at least some cases, the distal end of the catheter 732
itself. In any devices which incorporate such optional side scope
or lumen 740, the side scope or lumen 740 may be of any suitable
length and may terminate distally at any suitable location and such
side scope or lumen 740 is not limited to the specific positioning
and the specific distal end location shown in the drawings. Also,
in embodiments that incorporate a side scope or lumen 740 such side
lumen may be employed as a guidewire or working lumen to permit the
catheter to be advanced over a guidewire or for other working
devices to be inserted therethrough.
[0261] FIG. 5P shows a balloon catheter and pressure expandable
stent system 744 which includes all of the elements of the balloon
expandable stent system shown in FIGS. 5G.sup.1-5G.sup.111 and, in
addition, may incorporate an endoscope or side lumen. Specifically,
referring to FIG. 5P, there is shown a balloon catheter and
pressure expandable stent system 744 that comprises a flexible
catheter 746 having a balloon 750 and pressure expandable stent 748
thereon. A side lumen 756 may be located on the catheter 746 and an
endoscope may be permanently positioned in or temporarily inserted
into (or through) such side lumen 756 to enable the operator to
view the balloon 750 and 0 stent 748 and to advance the catheter
749 to its desired position. Also, in embodiments that incorporate
a side lumen 756 such side lumen may be employed as a guidewire
lumen to permit the catheter 746 to be advanced over a guidewire.
Optionally, a lumen may extend through the catheter 746 and through
an opening 752 in the distal end of the catheter 749 and a
straight, curved, bendable, deflectable or steerable scope and/or
stent 754 may be passed through or received in that lumen to
facilitate over the wire and/or scope assisted and/or guided and/or
manipulated advancement of the catheter 749 to an intended
location. In routine use, the balloon 750 is initially deflated and
the stent 748 is radially compressed to a collapsed configuration,
around the deflated balloon 750. The catheter 746 with the balloon
750 deflated and the collapsed stent 748 mounted thereon is
advanced, under endoscopic guidance or over a guidewire, to a
position within a passageway such as a nostril, nasal cavity,
meatus, ostium, interior of a sinus, etc., that is to be stented.
Thereafter, the balloon 750 is inflated causing the stent 748 to
expand to a size that frictionally engages the surrounding tissue
so as to hold the stent 748 in place. In some instances the
procedure will be performed for the purpose of enlarging a
passageway (e.g., an ostium, meatus, etc.) and the stent 748 will
be expanded to a diameter that is sufficiently large to cause the
desired enlargement of the passageway and the stent 748 will then
perform a scaffolding function, maintaining the passageway in such
enlarged condition. After the stent 748 has been fully expanded and
implanted, the balloon 750 may be deflated and the catheter 748
removed. In some applications, the stent 748 may contain a
diagnostic or therapeutic substance as defined herein and such
substance may elute from the stent 748 into the surrounding tissue
to bring about a desired diagnostic or therapeutic effect. In some
cases, the stent 748 may be permanently implanted. In other cases
the stent 748 may be temporarily implanted. In cases where the
stent 748 is temporarily implanted, it may be removed in a second
procedure conducted to retrieve the stent 748 or the stent 748 may
be made of bio-absorbable or biodegradable material such that it
degrades or is absorbed within a desired period of time after
implantation. As shown in the examples of FIGS. 5R' and 5R'', in
some cases, such as when a stent is to be placed within the ostium
of a paranasal sinus, the stent and/or the balloon may be
specifically shaped to facilitate and/or cause the stent to seat in
a desired position and to prevent unwanted slippage of the stent.
For example, FIG. 5R' shows a device 1040 comprising a catheter
1042 having a balloon 1044 and stent 1046 mounted thereon as
described above. However, in this embodiment, the balloon 1044 and
stent 1046 are of a configuration where one end of the balloon 1044
and stent 1046 is larger in diameter than the other end.
[0262] As described above in connection with other embodiments such
as those shown in FIGS. 5P and 5Q, a side scope or side lumen 1048
may optionally be formed on the catheter 1042 and/or a scope or
guidewire 1050 may optionally be passed through a lumen of the
catheter 1042 and out of its distal end. FIG. 5R.sup.11 shows
another device 1052 comprising a catheter 1054 having a balloon
1056 and stent 1058 mounted thereon as described above. However, in
this embodiment, the balloon 1056 and stent 1058 are of a
configuration where both ends of the balloon 1056 and stent 1058
are larger in diameter than the middle of the balloon 1056 and
stent 1058. As a result, the stent 1058 has an annular groove or
indentation formed circumferentially or about the mid-portion
thereof or may be hourglass or venture shaped, to facilitate
seating of the stent 1058 within an ostium or orifice without
longitudinal slippage of the stent 1058. Again, as described above
in connection with other embodiments such as those shown in FIGS.
5P and 5Q, a side scope or side lumen 1060 may optionally be formed
on the catheter 1052 and/or a scope or guidewire 1062 may
optionally be passed through a lumen of the catheter 1054 and out
of its distal end. In cases where the procedure is intended to
actually break bone (e.g., where the stent 1046, 1058 is intended
to dilate or enlarge a sinus ostium) the specially shaped balloon
1044, 1056 may be made of strong polymeric material as described
hereabove to enable it to exert bone-breaking pressure on the
adjacent or surrounding bone as it is inflated.
[0263] FIGS. 5Q and 5Q.sup.1 show a self-expanding stent and
delivery system 760 comprising a flexible outer sheath 762, a
flexible inner tube 764 and a stent 768. This stent differs from
the stent 748 of FIG. 5P only in that it is resilient and
self-expanding rather than pressure expandable. The stent 768 is
biased to an expanded configuration. Initially, it is compressed to
a radially collapsed configuration on the outer surface of the
inner tube 764 and the outer sheath 762 is advanced over the stent
768 to constrain the stent 768 in its collapsed configuration, as
can be seen in the cross-sectional showing of FIG. 5Q.sup.1. A
scope and/or guidewire 770 may be inserted through the lumen of the
inner tube 764. Additionally or alternatively, a side lumen 772 may
be located on the outer sheath 762 and an endoscope may be
permanently positioned in or temporarily inserted into (or through)
such side lumen 772 to enable the operator to view the 0 distal
portion of the system 760 and the area ahead of the distal end of
the sheath 762 as the system is advanced. Also, in embodiments that
incorporate a side lumen 772 such side lumen 772 may be employed as
a guidewire lumen to permit the system 760 to be advanced over a
guidewire. In routine operation the system 760, with its sheath 762
in a distally advanced position such that it surrounds and
constrains the collapsed stent 768, is advanced, under endoscopic
guidance and/or over a guidewire, to a position within a passageway
such as a nostril, nasal cavity, meatus, ostium, interior of a
sinus, etc., that is to be stented. Thereafter, when the stent 768
is positioned at the location to be stented, the sheath 762 is
withdrawn, allowing the self-expanding stent 768 to spring or self
expand to a radially expanded configuration in which it
frictionally engages the surrounding anatomical structure.
Thereafter, the remainder of the system 760 is removed, leaving the
stent 768 implanted in the body. The stent 768 may perform dilation
and scaffolding and/or substance delivery function(s) as described
hereabove with respect to the pressure expandable stent 748 of FIG.
5P.
[0264] FIG. 5S shows a snare apparatus 780 comprising a flexible
catheter 782 having a lumen 784 extending therethrough. A snare 786
having a general loop shape is advanceable out of the lumen 784 of
the device 780. In some embodiments, the snare 786 may optionally
be charged with electrical current or otherwise heated so that it
performs a cauterization function as it cuts through tissue.
Additionally or alternatively, in some embodiments, the snare 786
may be of variable diameter (e.g., a noose that may be tightened or
loosened by the operator). Also, optionally, a scope or side lumen
788 may be located on the catheter 782 and a stationary or moveable
endoscope may be permanently embodied in or temporarily inserted
into (or through) such side lumen 788 to enable the operator to
view the distal portion of the device 780 and the area of the snare
786. Also, in embodiments where the scope or side lumen 780
comprises a side lumen, such side lumen 788 may be employed as a
guidewire lumen to permit the device 780 to be advanced over a
guidewire. Alternatively, multiple lumens may run through catheter
782 such that they can accommodate a snare, a guidewire and/or an
endoscope. In routine operation, the snare 786 is initially
retracted within lumen 784 and the device 780 is advanced under
endoscopic guidance and/or over a guidewire, to a position within a
passageway such as a nostril, nasal cavity, meatus, ostium,
interior of a sinus, etc., where a polyp or other matter to be
snared or cut away is located. The snare 786 is advanced out of
lumen 784 and positioned around the polyp or other matter and,
thereafter, the snare may be pulled or moved, heated (if equipped
for heating) and/or tightened (if equipped for tightening) so as to
sever or cut the polyp or other matter. In some cases, the severed
polyp or other matter bay be suctioned through the lumen 784. In
other cases, a separate catheter or device may be introduced to
retrieve the severed polyp or other matter. After completion of the
procedure, the snare 786 may be retracted into lumen 784 and the
device 780 may be removed. Also, in some embodiments, the snare 786
may be replaced by a basket, bag or other retrieval receptacle that
is useable to capture and retrieve tissue or other matter and to
withdraw it into the lumen of the catheter 782.
[0265] FIG. 5T shows a forceps device 790 which comprises a
flexible shaft 792 having jaws or forceps 794 thereon. The jaws or
forceps 794 may be volitionally opened and closed by the operator.
A scope or side lumen 796 may be located on the flexible shaft 792,
as shown. In embodiments where the scope or side lumen 792
comprises a scope, such scope may be fixed or moveable and may be
used to observe or view the advancement of the device 790 and/or
the use of the forceps 794. In embodiments where the scope or side
lumen 796 comprises a side lumen, a stationary or moveable
endoscope may be permanently embodied in or temporarily inserted
into (or through) such side lumen 796 to enable the operator to
view the distal portion of the device 790 and the area of the
forceps 794. Also, in embodiments where the scope or side lumen 796
comprises a side lumen, such side lumen 796 may be employed as a
guidewire lumen to permit the device 790 to be advanced over a
guidewire. In routine operation, the device 790 is advanced, either
alone or through the lumen of a catheter, and possibly under
endoscopic guidance and/or over a guidewire, to a position within a
passageway such as a nostril, nasal cavity, meatus, ostium,
interior of a sinus, etc., where matter is to be grasped by the
forceps. Thereafter, under optional endoscopic guidance and
observation, the forceps 794 are used to grasp the intended matter.
In some embodiments, a distal portion of the flexible shaft 792 may
be bendable or steerable as indicated by dotted lines on the
example of FIG. 5T. In some embodiments, the jaws of the forceps
794 may be designed to sever and retain a specimen of tissue for
biopsy or other tissue sampling applications or the forceps 794 may
comprise scissors for cutting tissue, cartilage, bone, etc.
Alternatively, a lumen may pass through flexible shaft 792 and exit
through or next to the forceps 794 and allow the passage of a
guidewire or endoscope through such lumen.
[0266] FIGS. 5U and 5U.sup.1 show a telescoping system 800
comprising a flexible catheter 802, a flexible scope 804 and a
guidewire 806. The flexible scope 804 comprises a plurality of
light transmitting pathways 808 (e.g., optical fibers) that
transmit light in the distal direction from a light source (not
shown) and out of the distal end of the scope 804 such that the
light is cast onto the object or anatomical structure to be viewed.
Also, the scope comprises an image transmitting pathway 810 (e.g.,
optical fiber and lens) that carries reflected light from distal
end of the scope to an eyepiece or monitor on which the image may
be viewed. The scope also has a guidewire lumen 805 extending
therethrough and opening through its distal end. The scope 804 is
advanceable through the flexible catheter 802 and a guidewire 806
that is advanceable through a guidewire lumen 805 of the scope, as
shown. In routine operation, the telescoping system 800 may be
inserted into the nose and the scope 804 may be utilized to view an
anatomical structure, such as the ostium of a paranasal sinus, and
facilitate advancement of the guidewire into that anatomical
structure. Thereafter, the scope may be advanced over the guidewire
and into the anatomical structure (e.g., though the ostium and into
the interior of the paranasal sinus). The scope may then be used to
examine the anatomical structure (e.g., to view the condition of
the mucosa lining the paranasal sinus and to look for signs of
infection, tumors, etc.). The catheter 802 may then be advanced
over the scope 804 and into the anatomical structure (e.g., the
catheter tip may be advanced through the ostium and into the
paranasal sinus). Thereafter, the scope 804 may be removed and a
diagnostic or therapeutic substance as defined hereabove may be
infused through the catheter 802 and/or another working device,
including but not limited to the working devices shown in FIGS.
5A-5T and 5V-5Y.sup.11111, may be advanced through the catheter 802
and into the anatomical structure where it is used to perform a
diagnostic or therapeutic function.
[0267] FIG. 5V shows a side port suction/cutting device 820 which
comprises a flexible outer tube 822, a flexible inner tube 830 is
disposed coaxially and rotatably mounted within the outer tube 822.
One or more bearings 834 (e.g., a helical bearing or a series of
individual cylindrical bearings) may be disposed between the outer
tube 822 and inner tube 830, as shown. Alternatively, one or both
apposing tube surfaces may be made of, lined with, or be coated by
etc. a lubricious material such as silicone or PTFE to facilitate
movement. A rotating cutter 832 is positioned on the distal end of
the inner tube 830. A side opening 828 is formed in the outer tube
822 and the cutter 832 is positioned proximal to the side opening
828. Optionally, a tapered atraumatic distal tip 824 may be formed
on the distal end of the outer tube 822 and the side opening 828
may be configured to form a ramp or chute through which matter may
pass into the area immediately distal to the cutter 832. Also
optionally, an opening maybe formed in the distal end of the distal
tip such that a guidewire or scope 826 may pass through the lumen
of the inner tube 830 and out of the opening in the distal tip, as
shown. In operation, the device 820 is advanced to a position where
the side opening 828 is near a polyp, tissue or other obstructive
matter to be removed. The inner tube 830 and cutter 832 are
rotated. Suction may be applied through the lumen of the inner tube
830 and/or through the lumen of the outer tube 822 to draw the
obstructive matter into the side opening 828 and into contact with
the rotating cutter 832. As the obstructive matter is severed by
the rotating cutter 832, the severed obstructive matter or pieces
thereof may be suctioned through the lumen of the inner tube 830
and/or through the lumen of the outer tube. 822. Of course, as in
any of the working devices described in this patent application, a
scope or side lumen of any size or length, into which a scope may
be inserted (not shown in FIG. 5U but shown in various other
figures such as FIGS. 5O, 5P, 5Q, 5R, 5S and 5T) may be attached to
the outer tube 822 at a position which allows a scope to be used to
view the side opening 828 and matter entering the side opening 828.
Alternatively, the catheter may incorporate a deflectable tip or a
curved distal end which may force the side opening of the catheter
against a lumen wall or into the direction of a polyp or other
tissue to be removed.
[0268] In some applications of the invention, it may be desirable
to break bone, such as the thin bone that forms the periphery of a
sinus ostium. FIGS. 5W-5X.sup.11111 show devices that may be used
to break bones at specific locations. For example, FIGS. 5W-5W''
show a device 840 that comprises a flexible catheter 842 having a
rigid cylindrical member 847 located on the distal end thereof. An
advanceable and retractable member 846 extends through the catheter
842 and is connected to a distal tip member 844. The distal tip
member 844 has a cylindrical proximal end 849 that is sized to be
received within the cylindrical member 847. As shown in FIGS.
5W.sup.1 and 5W.sup.11, in routine operation, the advanceable and
retractable member 846 is advanced to separate the distal tip
member 844 from the rigid cylindrical member 847. The device 840 is
advanced to a position adjacent to a bony structure, such as a
structure formed by bone B covered with mucosal tissue M. The
device is positioned such that the bony structure is between the
cylindrical proximal end 849 of the distal tip member 844 and the
cylindrical member 847. The advanceable and retractable member 846
is then retracted, pulling the distal tip member 844 in the
proximal direction and capturing the bony structure between the
cylindrical proximal end 849 of the distal tip member 844 and the
cylindrical member 847, thereby breaking the bone B. The shape or
configuration of the distal tip member 844 and/or cylindrical
member 847 may be varied depending on the shape and pattern of
break desired to be made in the bone B. In this regard, FIGS.
5X-5X.sup.11111 show alternative constructions or configurations
that may be used to produce different shapes and patterns of bone
breaks. FIG. 5X.sup.1 shows an assembly 850 comprising a distal tip
member 852 that has three (3) projections on its proximal side and
a proximal member 854 that has three (3) notches in its distal
surface, such notches being configured to receive the three
projections of the distal tip member 852 when the distal tip member
852 is retracted. FIG. 5W.sup.11 shows an assembly 860 comprising a
distal tip member that forms a pincher for breaking bone. FIG.
5X.sup.111 shows an assembly 870 comprising a collapsible distal
tip member 872 and a cylindrical proximal member 874. The distal
tip member 872 may be initially deployed in a collapsed
configuration that allows it to be advanced through an opening such
as the ostium of a sinus. Then, it may be expanded to a size that
is too large in diameter to pass through that opening, thereby
causing it to strike the periphery of the opening as it Is
retracted in the proximal direction. In this manner, the assembly
5X.sup.111 may be used to break bone B all the way around an ostium
or aperture. FIG. 5X.sup.1111 shows another assembly 880 comprising
a distal tip 882 that has two projections on its proximal side and
a proximal member 884 that has one projection on its distal side.
The projection on the distal side of the proximal member 884 is
received between the projections formed on the proximal side of the
distal member 882 when the distal member 882 is retracted in the
proximal direction.
[0269] FIGS. 5Y.sup.1-5Y.sup.11111 show various substance delivery
implants that may be implanted into the nasal cavities, paranasal
sinuses, middle or inner ear, nasopharynx, etc., to deliver a
diagnostic or therapeutic substance as defined herein. These
devices may be formed of permanent or bio-absorbable material. In
many instances, these devices will be formed of a polymer (e.g.,
Hydron, hydrogel, collagen, etc.) within which the diagnostic or
therapeutic substance is contained or a polymer or metal that is
coated with or otherwise contains the substance. FIG. 5Y.sup.1
shows an implant 1070 that comprises a bead or pellet. FIG.
5Y.sup.11 shows an implant 1072 that comprises a wafer. FIG.
5Y.sup.111 shows an implant 1074 that comprises a brad or staple.
FIG. 5Y.sup.1111 shows an implant 1076 that comprises a screw or
helical coil. FIG. 5Y.sup.11111 shows an implant 1078 that
comprises a strand or coil, another example of which is shown in
FIG. 7E and described herebelow.
[0270] D. Pre-Shaped Guide Catheters
[0271] FIGS. 6A-6E show various guide catheters that may be used in
the methods of the present invention.
[0272] FIG. 6A shows a sphenoid sinus guide catheter 120 that
incorporates three preformed curves 122, 124, 126. The three
dimensional shape of the catheter 120 is such that, when advanced
through a nasal cavity, the distal end of the catheter 120 will
tend to enter the ostium of the sphenoid sinus.
[0273] FIG. 6B shows a frontal sinus guide catheter 128 that
incorporates two preformed curves 130, 133. The shape of the
catheter 128 is such that, when advanced through a nasal cavity,
the distal end of the catheter 128 will tend to enter the ostium of
the frontal sinus.
[0274] FIG. 6C shows a maxillary sinus guide catheter 136 that
incorporates three preformed curves 138, 140, 142. The three
dimensional shape of the catheter 136 is such that, when advanced
through a nasal cavity, the distal end of the catheter 136 will
tend to enter the ostium of the maxillary sinus.
[0275] FIG. 6D shows an ethmoid sinus guide catheter 144 that
incorporates two preformed curves 146,148. The three dimensional
shape of the catheter 144 is such that, when advanced through a
nasal cavity, the distal end of the catheter 144 will tend to enter
the ostium of the ethmoid sinus.
[0276] In some of the methods of the invention, it will be
desirable to plug the ostium of a sinus or another opening such as
the nasolacrimal duct or the nasopharyngeal opening into the
Eustachian tube. Thus, any of the above described guide catheters
120, 128, 136, 144 may be equipped with a plug on its distal tip
such that when its distal end enters the sinus ostium it will plug
the sinus thereby preventing fluid from exiting the sinus through
the ostium. An example of one such procedure is shown in FIG. 7B
and described herebelow.
[0277] FIG. 6E shows a plug guide catheter 149 that is useable for
temporarily plugging the opening into a nasolacrimal duct. This
plug guide catheter 149 has two preformed curves 150, 152 and a
plug 154 at its distal tip. The three dimensional configuration of
this catheter 149 is such that, when advanced through a nasal
cavity the distal tip plug 154 will tend to enter the opening into
the nasolacrimal duct. The plug may consist of, but is not limited
to, a semi-rigid plug or a balloon on the end of the catheter. It
will be appreciated that a different shaped plug guide catheter
(not shown) may be used to plug the Eustachian tube.
[0278] E. Devices and Methods for Treatment within Paranasal
Sinuses:
[0279] FIGS. 7A-7G provide examples of devices and methods for
performing diagnostic or therapeutic procedures within the
paranasal sinuses. In the methods of the prior art, rigid or
flexible scopes are sometimes used to visualize the ostia of
sinuses but, typically, such scopes have not actually been advanced
into the interior of the sinuses. As described hereabove, the
present invention does provide devices and methods for placing
endoscopes inside the paranasal sinuses and such methods may or may
not be used in conjunction with any of the diagnostic or
therapeutic devices and methods shown in FIGS. 7A-7G.
[0280] FIG. 7A shows an electrode network delivery device 168 being
used to deliver radiofrequency or electrical current to the lining
of the sphenoid sinus SS. This device 168 comprises a flexible
catheter 168 that has been inserted through the sphenoidal sinus
ostium SSO. An expandable electrode network such as a cage 170 is
advanced out of the distal end of the catheter 169. Electrodes 172
are positioned at spaced apart locations on the cage. As the cage
170 expands, it places the electrodes in contact with the lining of
the sinus SS. Current is delivered to the electrodes 172 to ablate
all mucous producing tissue within the sinus in preparation for the
sinus to be functionally isolated or embolized, or to ablate tumors
or polyps located within the sinus.
[0281] FIG. 7B shows a procedure where a flowable substance, such
as a diagnostic or therapeutic substance as defined above, is
introduced into the sphenoid sinus SS and the ostium SSO has been
plugged by a sphenoid sinus plug guide catheter device 174. This
device 174 comprises a flexible catheter 176 having the shape shown
in FIG. 6A and described above and a plug member 178 at its distal
tip. The fluid is maintained in the sphenoid sinus SS until the
plug catheter device 174 is removed, allowing the fluid to then
drain through the sphenoid sinus ostium SSO. This procedure may be
particularly useful when it is desired to fill a sinus with
radiographic contrast agent to visualize the entire sinus or to
apply a therapeutic agent to the entire lining of the sinus by
entirely filling the sinus with the agent and maintaining such
fully filled state for a desired period of time to allow the agent
to act on the entire lining of the sinus. Imaging materials may be
mixed with viscous agents so that they simulate mucous or if simple
structural imaging is desired it may be preferable to have
substances of lower viscosity. It may be also desirable to use
imaging agents which bind with the surface of the mucosa to
minimize the amount of injected contrast.
[0282] FIG. 7C shows a balloon catheter device 180 which comprises
a flexible catheter 182 having a balloon 184 that is positioned in
the sphenoid sinus ostium SSO and inflated to hold the catheter 182
in position while a quantity of a diagnostic or therapeutic
substance 186 (as defined above) is introduced into the interior of
the sinus SS. This therapeutic substance may be one or more of any
of the drug delivery materials and drugs selected from the previous
list, or may additionally include a sclerotic agent such as alcohol
to uniformly kill all the tissues within the cavity. Other
materials such as capasian or other neurotoxic substances may be
considered to eliminate the pain and other sensation within the
cavity.
[0283] FIG. 7D shows a sensor equipped catheter device 190 that
comprises a flexible catheter 192 having a sensor 194 thereon for
3-dimensional mapping or navigation. This procedure may be used to
map the precise configuration of the interior of the sphenoid sinus
SS. Examples of the construction and use of such sensor 194 and
associated systems/computers are found in U.S. Pat. Nos. 5,647,361;
5,820,568; 5,730,128; 5,722,401; 5,578,007; 5,558,073; 5,465,717;
5,568,809; 5,694,945; 5,713,946; 5,729,129; 5,752,513; 5,833,608;
5,935,061; 5,931,818; 6,171,303; 5,931,818; 5,343,865; 5,425,370;
5,669,388; 6,015,414; 6,148,823 and 6,176,829, the entireties of
which are expressly incorporated herein by reference.
[0284] FIG. 7E shows an implant delivery device 196 which comprises
a flexible catheter 198 that is inserted through the sphenoid sinus
ostium SSO and into the sphenoid sinus SS and is being used to
implant a coil 200 within the sphenoid sinus. Such coil 200 may
comprise an elongate fiber or other elongate member that may
contain a diagnostic or therapeutic substance as defined herein.
This coil 200 may be constructed to embolize the sinus for the
purpose of to permanently close off the sinus and to prevent any
further mucous production, trapping of secretions or infection
and/or to deliver a diagnostic or therapeutic substance to the
tissues lining the sinus. For example, a coil for sustained
delivery of an antimicrobial agent may be implanted in a sinus to
treat an acute or chronic infection of that sinus. In some cases,
the coil may be bio-absorbable.
[0285] FIG. 7F shows an over-the-wire endoscopic system 240 being
used to view the interior of the sphenoid sinus SS. A flexible
catheter 242 is positioned in or near the sphenoid sinus ostium SSO
and a guidewire 248 is advanced through the sphenoid sinus ostium
SSO and into the sphenoid sinus SS. An over-the-wire endoscope 246
(such as a 2.2 mm over-the-wire scope available commercially as
Model #AF-28C from Olympus America, Melville, N.Y.) is advanced
over the guidewire 248 and is used to examine the interior of the
sphenoid sinus SS.
[0286] FIG. 7G shows a biopsy system 250 being used to obtain a
biopsy specimen from a lesion L within the sphenoid sinus SS. A
flexible catheter 242 is positioned in or near the sphenoid sinus
ostium SSO and an endoscope 246 is advanced through the catheter
242 and into the interior of the sinus SS. A biopsy instrument 252
is inserted through a working channel of the endoscope 246 and is
used, under endoscopic visualization and guidance, to obtain a
specimen of the lesion L.
[0287] F. General Examples of Interventions Using the Occluder
& Access Devices and/or Working Devices
[0288] FIGS. 8A-8D show two of many possible examples of methods
wherein the occluder & access devices 10, 12 of FIGS. 2A and 2B
and/or various working devices such as those shown in FIGS.
5A-5Y.sup.1111 are used to perform diagnostic and/or therapeutic
procedures within the nose, nasopharynx or paranasal sinuses.
[0289] In general, diagnostic interventions in accordance with this
invention may include: a) anatomic studies where obstructions,
sizes, parameters or abnormalities in anatomy are visualized and/or
identified, b) dynamic studies where gas, mucous or fluid is
introduced into the nose, sinus, nasal cavity, nasopharynx,
Eustachian tube, inner or middle ear, etc. and the movement of such
materials is monitored to assess drainage or gas flow issues, and
c) perturbation studies where an agent (e.g., an allergen,
irritant, agent that induces mucous production, etc.) is introduced
into the nose, sinus, nasal cavity, nasopharynx, Eustachian tube,
inner or middle ear, etc., and the patient's response and/or flow
of the endogenously produced mucous or other secretions is
assessed. Examples of procedures that may be used to perform these
types of diagnostic interventions include, but are not limited to,
the following:
[0290] 1. Gaining Access to Sinus:
[0291] Access to one of more of the paranasal sinuses is gained by
advancement of catheter(s) into the sinus or sinuses of interest. A
guidewire may be inserted into the sinus first and the catheter may
then be advanced over the guidewire and into the sinus. In some
cases, a sinus ostium guide catheter of the type shown in FIGS.
6A-6E may be inserted into the ostium of the sinus and a smaller
catheter may be advanced through the guide catheter. One or more
scopes may be used to visualize the sinus ostium and to guide the
guidewire and/or catheter into the sinus ostium. In some cases, a
steerable guidewire, catheter and/or scope may be used to gain
entry into the sinus. In some cases, occlusion & access
device(s) such as those shown in FIGS. 2A-2R, may be inserted and
the guidewire(s), catheter(s) and/or scope(s) used to access the
sinus may be inserted through a device insertion port on the
occluder & access device.
[0292] 2. Mucous Flow Study:
[0293] Optionally, after catheter access to the sinus has been
gained, an imageable contrast substance or radioactive material
such as microbeads or a flowable contrast medium (e.g., an
iodinated contrast solution with or without a thickening agent to
adjust its viscosity to that of mucous) that may have a consistency
similar to that of mucous may be injected into the sinus. An
imaging or scanning technique (e.g., X-ray, fluoroscopy, CT scan,
ultrasound, MRI, radiation detector, gamma camera, etc.) may then
be used to observe the flow of the contrast medium through and out
of the sinus. In some cases a fluoroscope with a C-arm may be used
in a fashion similar to that used in coronary artery
catheterization and angiography procedures to allow the clinician
to view the movement of the contrast medium from different vantage
points or angles. To facilitate flow of the contrast medium from
the sinus, the previously inserted catheter(s) and/or guidewires
and/or scope(s) may be backed out of the sinus and ostium or
removed completely, to allow normal flow to occur. The patient's
head and/or other body parts may be repositioned to observe
different postural drainage effects. In this manner, the clinician
may specifically locate and identify which anatomical structures
are obstructing or interfering with normal mucous flow from the
sinus.
[0294] 3. Air Flow Study:
[0295] Optionally, after access to the sinus has been gained as
described in No. 1, above, an imageable or traceable gas, such as a
radiolabled gas, radiopaque gas or a gas with imageable or
radioactive microbeads therein, may be injected through a catheter
and into the sinus. An imaging device or tracing device (e.g.,
radiation detector, gamma camera, X-ray, fluoroscopy, CT scan,
ultrasound, MRI) may then be used to observe subsequent movement or
dissipation of the gas as it passes out of the sinus and/or
equilibrates with other sinus cavities. In this manner, the
clinician may determine whether normal gas exchange in the sinus is
occurring and may locate and identify any anatomical structures or
irregularities that are obstructing or interfering with normal gas
flow and/or gas exchange.
[0296] 4. Anatomic Dimension Study:
[0297] An entire paranasal sinus or other anatomical passageway or
structure may be filled with an imageable substance or otherwise
measured to determine its actual dimensions and/or configuration.
In some such studies, access to a paranasal sinus will be gained as
described in No. 1, above, and the sinus may be filled with an
imageable substance (e.g., contrast medium). A suitable imaging
technique (e.g., X-ray, fluoroscopy, CT scan, ultrasound, MRI,
radiation detector, gamma camera, etc.) may then be used to
determine the size and shape of the sinus. Again, in such
procedure, a moveable imaging apparatus such as a fluoroscope with
a C-arm may be used to view and measure the contrast filled sinus
from different vantage points or angles. One example of such a
procedure is shown in FIG. 7B and described hereabove.
[0298] 5. Endoscopic Study:
[0299] A flexible and/or steerable endoscope, as described above,
may be inserted into the nose, sinus, nasal cavity, nasopharynx,
Eustachian tube, inner or middle ear, etc., and used to visually
examine the anatomy and/or to observe a treatment and/or to assess
the efficacy or completeness of a previously rendered treatment. In
cases where it is desired to view the interior of a paranasal
sinus, access to the sinus may be gained as described in No. 1,
above, and the endoscope may be advanced into the interior of the
sinus either directly or over a guidewire.
[0300] 6. Transillumination Study:
[0301] A flexible light emitting instrument (e.g., a catheter
having a powerful light emitting apparatus at its distal end) may
be advanced into the nose, paranasal sinus, nasal cavity,
nasopharynx, Eustachian tube, inner or middle ear, etc., and used
to illuminate anatomical structures. Direct or endoscopic
observation may then be made from outside the body and/or from
other locations within the nose, sinus, nasal cavity, nasopharynx,
Eustachian tube, inner or middle ear, orbit, cranial vault, etc.,
to observe anatomical structures and/or to detect aberrant openings
or leaks through which the light passes. In cases where the light
emitter and/or the viewing instrument (e.g., endoscope) is/are
positioned within paranasal sinus(es) access to the sinus(es) may
be gained as described in No. 1, above, and the light emitter
and/or viewing instrument may then be advanced into the sinus(es)
either directly or over guidewire(s).
[0302] 7. Other Imaging Studies:
[0303] Other imaging techniques such as MRI, CT, etc., in
combination with any of the modalities set forth in Nos. 1-6,
above, and modifications may be made to any of those techniques to
adjust for sinus anatomy or other pathology.
[0304] After any or all of the elected diagnostic studies have been
completed, one or more working devices, such as the flexible
devices described herein and shown in FIGS. 5A-5Y.sup.11 may be
inserted and used to perform therapeutic procedure(s).
[0305] As shown in the example of FIG. 8A, an anterior/posterior
occluder & access device 10 is inserted through the right nasal
cavity NC, The device's anterior occluder 14 is positioned to
occlude the nostril on the right side while its posterior occluder
(not seen in FIGS. 8A-8E) occludes the posterior choanae or
nasopharynx. An anterior occluder & access device 12 is
inserted into the left nasal cavity and its occluder 40 occludes
the left nostril. In this manner, a sealed operative field is
established between the posterior occluder positioned in the
posterior choanae or nasopharynx and the anterior occluders 14, 40
positioned in the right and left nostrils or anterior nasal
cavities.
[0306] FIGS. 8B-8C show an example of a method for performing a
diagnostic and/or therapeutic procedure in the right frontal sinus
FS in the patient in whom the occluder & access devices 10, 14
have been inserted. In FIG. 8B, a frontal sinus guide catheter 128
is inserted into the working device insertion port 30 and advanced
through tube 16 and out of outlet aperture 22. The guide catheter
128 is then advanced to a position where its distal end is in the
right frontal sinus ostium.
[0307] In FIG. 8C, a working device 202 is inserted through the
guide catheter 128 and into the frontal sinus FS. This working
device 202 may comprise any of the devices shown in FIGS.
5A-5Y.sup.11111 or 7A-7G. In some procedures, it may be desired to
initially introduce a contrast agent into the frontal sinus FS and
pull back the guide catheter 128 to allow the contrast agent to
drain from the sinus. Imaging of the draining contrast agent may be
used to diagnose drainage impairment and to identify the specific
anatomical structures that are causing the impairment of drainage.
Thereafter, the guide catheter may be reinserted into the frontal
sinus ostium and the working device(s) 202 may be used to modify
the structures that have been identified and impairments to
drainage. Thereafter, the contrast injection and imaging steps may
be repeated to assess whether the procedure(s) performed have
overcome or corrected the drainage problem that had been initially
diagnosed. A suction device 206 is connected by way of suction line
204 to port 36 to suction blood, other fluid or debris from the
operative field during the procedure.
[0308] FIGS. 8D and 8E show an example of a treatment rendered to
the left maxillary sinus MS, in the same patient in whom the
occluder & access devices 10, 14 have been inserted. In FIG.
8D, a guide catheter 136 is inserted into device insertion aperture
44 and advanced through tube 41 to a position where the distal end
of the guide catheter 136 is positioned in the ostium of the
maxillary sinus MS.
[0309] Thereafter, as shown in FIG. 8E, a working device 202 is
inserted through the guide catheter 136 and into the maxillary
sinus MS. This working device 202 may comprise any of the devices
shown in FIGS. 5A-Y.sup.11111 or 7A-7G. In some procedures, it may
be desired to initially introduce a contrast agent into the
maxillary sinus MS by the same procedure described above in
reference to FIGS. 8B and 8C.
[0310] After all of the desired procedures have been completed, the
anterior occluders 14, 40 and posterior occluder (not shown on
FIGS. 8A-8E) are collapsed (e.g., deflated) and the occluder &
access devices as well as the guide catheters and working devices
are removed (except for implants such as stents, embolic coils,
substance delivery implants, etc.).
[0311] G. Cochlear Implant Procedure
[0312] FIGS. 9A-9C show a procedure for installation of a cochlear
implant in accordance with the present invention. In this
procedure, the nasopharyngeal opening into the Eustachian tube ET
is located and a guidewire is initially advanced into the
Eustachian tube ET. A catheter 900 is advanced over the guidewire
to a location where the distal end of the catheter 900 is in or
near the tympanic cavity TC of the middle ear. Thereafter, if
deemed necessary, a forceps device 790 and/or other devices are
advanced through the catheter 900 and used to remove the small
bones of the sear (i.e., the malleus, incur and stirrup) as shown
in FIG. 9A. This optional removal of the bones of the middle ear
may be done under endoscopic visualization using an endoscope
equipped device such as the endoscope equipped forceps device 790
shown in FIG. 5T and described above. As shown in FIG. 9B, a
cochlear guide catheter 904 having a "J"-shaped distal tip 905 is
advanced through the catheter 900 to a position where the tip 905
of the cochlear guide catheter 904 is directed into or inserted
into the cochlea C. In some applications, the cochlear guide
catheter 904 may be configured to advance into the round window of
the cochlea and through the secondary tympanic membrane that covers
the round window. If necessary, a penetrator such as a needle,
drill or cutter may be advanced through or formed or positioned on
the distal end of the cochlear guide catheter 904 to penetrate
through the secondary tympanic membrane. In other applications, the
cochlear guide catheter 904 may be positioned adjacent to the
cochlea and a cochleostomy device (e.g., a penetrator such as a
drill, needle or cutter) may be advanced through or formed or
positioned on the distal end of the cochlear guide catheter 904 and
used to form a cochleostomy through which the distal end of the
guide catheter 904 is advanced into the cochlea C. Thereafter, a
cochlear electrode array 906 is advanced through the cochlear guide
catheter 904 and into the cochlea, as seen in FIG. 9B. One example
of a commercially available cochlear electrode array is the Nucleus
24 Contour device manufactured by Cochlear Corporation.
[0313] Thereafter, a sound receiving device or transducer 908 is
advanced through the catheter 900 and positioned in the tympanic
cavity TC. The sound receiving device or transducer 908 may be of
any type that is a) sufficiently small to pass through the
Eustachian tube ET and into the tympanic cavity TC, and b) useable
to perform the desired function of converting sound waves to
electrical impulses and delivering such electrical impulses to the
cochlear electrode array 906. A microphone/power/electronics device
910 may be positioned in the outer ear canal, as shown in FIG. 9C
or may be implanted subcutaneously or in any other way that is
acceptable. Certain non-limiting examples of devices 906, 908, 910
that may be useable for this procedure are set forth in PCT
International Patent Publication No. WO 2004/018980 A2, designating
the United States, the entirety of which is expressly incorporated
herein by reference.
[0314] Turning now to FIG. 10, an illustration of a patient being
treated by a system for catheter-based minimally invasive sinus
surgery is shown. A C-arm fluoroscope 1.0001 that is useable to
visualize a first introducing device 1.002 (e.g., a sinus guide,
guide catheter or guide tube), a second introducing device 1.004
(e.g., a guidewire or elongated probe) and a working device 1.006
(e.g., a balloon catheter, other dilatation catheter, debrider,
cutter, etc.). The sinus guide, guide catheter or guide tube 1.002
may be introduced under direct visualization, visualization
provided by fluoroscope 1.0001 and/or from endoscopic
visualization, to place the distal end of catheter or tube 1.002 at
a location approaching an ostium of a sinus to be treated.
[0315] Next guidewire or elongated probe 1.004 is inserted through
catheter or tube 1.002 and distally advanced to extend the distal
end of guidewire or elongated probe through the ostium to be
treated and into the sinus that the ostium opens to. Proper
placement often involves advancement and retraction of the distal
end of guidewire or elongated probe, under fluoroscopic
visualization, until it has been visually confirmed that the distal
end of the guidewire or elongated probe is located where the
surgeon believes the appropriate sinus to be located, relative to
the other features of the patient's head that are visualized under
fluoroscopy.
[0316] Once guidewire or elongated probe 1.004 has been properly
placed, working device 1.006 is next passed over the guidewire or
elongated probe 1.006, under visualization via fluoroscope 1.0001
and/or an endoscope (not shown) that has been inserted adjacent
catheter or tube 1.002, to place the working end of working device
1.006 in the target location where a surgical procedure is to be
performed. Typically, the guidewire or elongated probe remains in
place during the procedure. Under the same type(s) of
visualization, the working (distal) end of working device is then
actuated to perform the desired surgical procedure. In the case of
a dilatation catheter, the balloon at the distal end portion of
catheter 1.006 is expanded once it has been located across the
ostium. This expansion acts to open the ostium to allow proper
mucus flow, as was described in more detail above.
[0317] After performance of the desired surgical procedure, the
working device 1.006 is deactivated and withdrawn from the patient,
after which the remaining devices are withdrawn to complete the
procedure.
[0318] By using the devices and methods described herein, at least
the need for fluoroscopic visualization of the placement of the
guidewire/elongated probe can be reduced or eliminated. Further
optionally, all fluoroscopic visualization needs may be eliminated
in some surgical circumstances.
[0319] It is to be appreciated that the devices and methods of the
present invention relate to the accessing and dilatation or
modification of sinus ostia or other passageways within the ear,
nose and throat. These devices and methods may be used alone or may
be used in conjunction with other surgical or non-surgical
treatments, including but not limited to the delivery or
implantation of devices and drugs or other substances as described
in co-pending U.S. patent application Ser. No. 10/912,578.
[0320] FIGS. 11A through 11D are illustrations of partial sagittal
sectional views through a human head showing various steps of a
method of gaining access to a paranasal sinus using a sinus guide.
In FIG. 11A, a first introducing device in the form of a sinus
guide 1.002 is introduced through a nostril and through a nasal
cavity 1.012 to a location close to an ostium 1.014 of a sphenoid
sinus 1.016. Sinus guide 1.002 may be straight, malleable, or it
may incorporate one or more preformed curves or bends as further
described in U.S. Patent Publication Nos. 2006/004323;
2006/0063973; and 2006/0095066, for example, each of which are
incorporated herein, in their entireties, by reference thereto. In
embodiments where sinus guide 1.002 is curved or bent, the
deflection angle of the curve or bend may be in the range of up to
about 135 degrees.
[0321] In FIG. 11B, a second introduction device comprising a
guidewire 1.01 is introduced through the first introduction device
(i.e., sinus guide 1.002) and advanced so that the distal end
portion of guidewire 1.01 enters the sphenoid sinus 1.016 through
the ostium 1.014.
[0322] In FIG. 11C, a working device 1.006, for example a balloon
catheter, is introduced over guidewire 1.01 and advanced to extend
the distal end portion of device 1.006 into the sphenoid sinus
1.016. Thereafter, in FIG. 11D, working device 1.006 is used to
perform a diagnostic or therapeutic procedure. In this particular
example, the procedure is dilatation of the sphenoid sinus ostium
1.014, as is illustrated in FIG. 11D, where the balloon of device
1.006 is expanded to enlarge the opening of the ostium 1.014. After
completion of the procedure, sinus guide 1.002, guidewire 1.01 and
working device 1.006 are withdrawn and removed. It will be
appreciated that the present invention may also be used to dilate
or modify any sinus ostium or other man-made or naturally occurring
anatomical opening or passageway within the nose, paranasal
sinuses, nasopharynx or adjacent areas. As will also be appreciated
by those of ordinary skill in the art, in this or any of the
procedures described in this patent application, the operator may
additionally advance other types of catheters, and that guidewire
1.01 may be steerable (e.g. torquable, actively deformable) or
shapeable or malleable.
[0323] FIGS. 11B-11D show an optional scope 1.008 in dotted lines,
that may be inserted to provide visualization of advancement of
sinus guide 1.002 and/or inserted alongside catheter 1.002 to
provide visualization of all or at least a portion of working tool
1.006. It is to be appreciated that optional scope 1.008 may
comprise any suitable types of rigid or flexible endoscope and such
optional scope may be separate from or incorporated into the
working devices and/or introduction devices of the present
invention.
[0324] Although scope 1.008 may be useful to reduce or eliminate
the need for fluoroscopic visualization during placement of sinus
guide 1.002 and/or for visualization of the procedure performed by
working device 1.006, it does not provide stand-alone capability to
see inside the sinus (e.g., sphenoid sinus 1.016 or other sinus of
interest), and therefore cannot provide sufficient visual feedback
for use in guiding guidewire 1.01 into the desired sinus (e.g.,
frontal sinus, or some other sinus of interest) or sufficient
visual image confirmation of correct placement of guidewire 1.01
into the desired sinus.
[0325] Further, depending upon the particular configuration of the
sinus passageways to be traversed to gain access to a target
ostium, the scope 1.008, due to physical limitations (e.g., outside
diameter, degree of rigidity, etc.) may be unable to visualize as
deep as the location of the ostium of interest. For example, FIG.
12 illustrates a situation where scope 1.008 has been inserted as
far as possible without causing significant trauma to the patient.
The range of adequately illuminated visibility in this case does
not extend all the way to ostium 1.0201, as indicated schematically
by the rays 1.009 shown extending distally from scope 1.008. In
this case, adequately illuminated visualization of guidewire 1.01
into ostium 1.0201 would not be possible via scope 1.008.
Additionally, if sinus guide 1.002 is physically capable of being
extended further distally to place the distal end thereof at the
approach to ostium 1.0201, scope 1.008 would also not be capable of
adequately visualizing this. Thus, prior to the current invention,
fluoroscopic or other x-ray visualization of these procedures was
required, in order to ensure that the devices approach (and extend
through) the appropriate ostium 1.0201 and not another adjacent
opening, such as opening 1.024.
[0326] In order to overcome these and other problems, the guidewire
devices 1.01 of the present invention include their own light
emitting capability. By illuminating a distal end portion of
guidewire 1.01, a process known as transillumination occurs as
guidewire 1.01 traverses through the sinus passageways, passes
through an ostium and enters a sinus cavity. Transillumination
refers to the passing of light through the walls of a body part or
organ. Thus, when guidewire 1.01 is located in a sinus, the light
emitted from guidewire 1.01 passes through the facial structures
and appears as a glowing region on the skin (e.g., face) of the
patient. It is noted that the light emitted from scope 1.008, such
as positioned in FIG. 12, for example, results in transillumination
as well, but the resultant glow is much more diffuse and larger in
area. As the light source in guidewire 1.01 gets closer to the
surface of the structure that it is inserted into (e.g., the
surface of the sinus), the transillumination effect becomes
brighter and more focused (i.e., smaller in area). Additionally,
the movements of the guidewire 1.01 can be tracked by following the
movements of the transillumination spot produced on the skin of the
patient.
[0327] FIG. 13 shows an illuminating guidewire 1.01 according to
one embodiment of the present invention. Device 1.01 includes a
flexible distal end portion 1.0d that provides a similar degree of
flexibility to a standard, non-illuminating type of guidewire.
Distal end portion 1.0d may include a coil 1.0c as an exterior
portion thereof, to help provide the desired flexibility to this
portion. The proximal end portion 10p of device 1.01 extends the
device to provide a sufficient length so that device 1.01 extends
proximally out of the patient (and, when inserted through another
device, such as a sinus guide, proximally out of the device into
which guidewire 1.01 is inserted), at all times, including the
deepest location into which the distal end of device 1.01 is
placed. The proximal end portion 1.0p can have visible markings,
preferably spaced at equal intervals, that can be observed by the
user to confirm how far the guidewire 1.01 has been placed in the
patient. Proximal end portion 1.0p also provides the necessary
mechanical properties required to make the guidewire function
properly. These mechanical properties include torquability, i.e.,
the ability to torque the proximal end portion 10.p from a location
outside of the patient and have that torque transmitted to the
distal end portion 10.p; pushability, i.e., sufficient rigidity, so
that when an operator pushes on the proximal end portion 10.p from
a location outside of the patient, the pushing force transmits to
the distal portion 10.d to advance the distal portion 1.0p without
buckling the device 1.0; and tensile strength so that an operator
can pull on the proximal end portion 1.0p from a location outside
of the patient and withdraw device 1.01 from the patient without
significant plastic deformation or any disintegration of the
device.
[0328] Coil 1.0c may be formed from a stainless steel wire, for
example. The diameter of the coil wire can be between about 0.004
and about 0.008 inches, typically about 0.006 inches. Alternative
materials from which coil 1.0c may be formed include, but are not
limited to: ELGILOY.RTM., CONICHROME.RTM. or other biocompatible
cobalt-chromium-nickel alloy; nickel-titanium alloys, or other
known biocompatible metal alloys having similar characteristics.
Further alternatively, distal end portion may comprise a braided
metallic construction of any of the aforementioned materials in
lieu of a coil.
[0329] The external casing of the proximal portion 1.0p can be made
from a polyimide sheath, a continuous coil (optionally embedded in
polymer or having polymer laminated thereon), a hypotube (e.g.,
stainless steel hypotube), a laser-cut hypotube, a cable tube, or a
tube made from PEBAX.RTM. (nylon resin) or other medical grade
resin. In any of these cases the construction needs to meet the
required torquability, pushability and tensile requirements of the
device.
[0330] In the example shown, coil 1.0c is joined to proximal
portion 1.0p by solder, epoxy or other adhesive or mechanical
joint. One or more illumination channels 1.0i are provided in
device 1.01 and extend the length thereof. Illumination channels
1.0i are configured to transport light from the proximal end of
device 1.01 to and out of the distal end of device 1.01. In the
example shown, two illumination channels are provided, each
comprising a plastic illumination fiber. The plastic used to make
the illumination fibers is compounded for light transmission
properties according to techniques known and available in the art.
As one example, ESKA.TM. (Mitsubishi Rayon), a high performance
plastic optical fiber may be used, which has a concentric
double-layer structure with high-purity polymethyl methacrylate
(PMMA) core and a thin layer of specially selected transparent
fluorine polymer cladding. In one example, illumination fibers each
have an outside diameter of about 0.010''. The illumination fibers
can have an outside diameter in the range of about 0.005 inches to
about 0.010 inches. Alternatively, a single plastic illumination
fiber 1.0i may be used that has an outside diameter of about
0.020''. Further alternatively, glass illumination fibers may be
substituted which are much smaller in outside diameter, e.g., about
0.002''. In this case, more illumination fibers may be provided in
a bundle, e.g., about six to fifty glass fibers 1.0i may be
provided.
[0331] The distal end of device 1.01 is sealed by a transparent (or
translucent) seal 1.0s which may be in the form of epoxy or other
transparent or translucent adhesive or sealing material. Seal 1.0s
maintains the distal ends of illumination fibers 1.0i coincident
with the distal end of device 1.01 and also provides an atraumatic
tip of the device 1.01. Further, seal 1.0s prevents entrance of
foreign materials into the device. The distal end can be designed
to either focus or distribute the light as it emanates therefrom,
to achieve maximum transillumination effects. In this regard, the
distal end can include a lens, prism or diffracting element.
[0332] The proximal end of device 1.01 is also sealed by a
transparent (or translucent) seal 1.0ps which may be in the form of
epoxy or other transparent or translucent adhesive or sealing
material. Seal 1.0ps maintains the proximal ends of illumination
fibers 1.0i coincident with the proximal end of device 1.01. The
proximal end of device 1.01 may be further prepared by grinding and
polishing to improve the optical properties at the interface of the
proximal end of device 1.01 with a light source. The illumination
fibers 1.0i at locations intermediate of the proximal and distal
ends need not be, and typically are not fixed, since no mapping of
these fibers is required, as device 1.01 provides only
illumination, not a visualization function like that provided by an
endoscope. Further, by leaving illumination fibers free to move at
locations between the proximal and distal ends, this increases the
overall flexibility and bendability of device 1.01 relative to a
similar arrangement, but where the illumination fibers 10i are
internally fixed.
[0333] The outside diameter of device 1.01 may be in the range of
about 0.025 inches to about 0.040 inches, typically about 0.030 to
0.038 inches, and in at least one embodiment, is about
0.035'':1:0.005''. At least the distal portion 1.0d of device 1.01
is provided with a core support 1.0cw that is contained therein. In
the example shown in FIG. 4, core support 1.0cw is a wire that is
fixed to proximal section 1.0p such as by laser welding, epoxy or
other adhesive or mechanical fixture. Core support 1.0cw may extend
substantially the full length of device 1.01. In any case, core
support 1.0cw is typically formed from stainless steel NITINOL
(nickel-titanium alloy) or other biocompatible nickel-titanium
alloys, cobalt-chromium alloys, or other metal alloys that are
biocompatible and provide the necessary rigidity and torquability.
Core support 1.0cw may be formed as a wire, as in the example shown
in FIG. 13, or alternatively, may be braided from any of the same
materials or combination of materials mentioned above. Core support
1.0cw, when formed as a wire can be ground to different diameters
to provide varying amounts of rigidity and torquability. When
formed as a braid, the braid can be formed to have varying amounts
of rigidity and torquability along the length thereof. For example,
core wire 1.0cw has a larger outside diameter at the proximal end
portion than at the distal end portion so that it is more rigid and
transfers more torque from the proximal portion of device 1.01,
whereas at the distal end portion, core 1.0cw is relatively more
flexible and twistable. For core supports 1.0cw that extend through
proximal portion 1.0p, the portion of core support near the
proximal end of device 1.01 may have an even larger outside
diameter.
[0334] Core support 10cw particularly increases the pushability and
the torquability of coil 1.0c which, by itself, is quite flexible
and twistable. Combined with the core support 1.0cw, the distal
portion is much more effective at transferring pushing and torquing
forces without buckling or twisting. Additionally, core support
1.0cw may be plastically deformed or memory set into a bent shape,
an example of which is shown in FIG. 14. Bend 1.0b provides a
steerability function, allowing an operator to direct the distal
end of device 1.0in different directions by torquing device about
the longitudinal axis of the device, as indicated by the arrows in
FIG. 14. In some embodiments this bending can be performed by an
operator in the midst of a procedure, which can be particularly
useful in combination with a scope 1.008, as viewing through the
scope may make it apparent to the operator that the guidewire 1.01
needs to be inserted or directed at an angle offset from where the
straight direction along the longitudinal axis of the device would
direct it to. In some embodiments, the guidewire 1.01 does not have
a core support or core wire. In these embodiments, the outer jacket
(e.g., a coil, cable tube, laser-cut hypotube, braided polymer
tube, etc.) provides the support for torque, pushability and
tension. An advantage of not having a core wire/core support is
that the full inner diameter of the guidewire is then available to
be filled with illumination fibers.
[0335] The illumination fibers, as noted above, can be free to move
about radially within the device. Further, there is no need to
center the illumination fibers 1.0i with respect to device 1.01
even at the distal and proximal ends of the device. FIG. 15 is a
sectional illustration of a distal end portion of device 1.01
showing core support 1.0cw fixed to coil 1.0c, with illumination
fibers 1.0i residing adjacent to core support 1.0cw, but not fixed
to either core support 10cw or coil 1.0c.
[0336] The plastic or glass illumination fibers 1.0i of the device
shown in FIG. 13 are typically used to transmit light from a light
source such as one provided in a operating room for use by
endoscopes, e.g., xenon light source, halogen light source, metal
halide light source, etc. Alternatively, device 1.01 may be
configured to transmit light from other light sources, such as a
laser light source, wherein laser fibers 1.0f would be substituted
for the illumination fibers described above, and extend through
device 1.01 in a fiber optic bundle as illustrated in the
cross-sectional view of FIG. 16. The fiber optic bundle, like the
illumination fibers 1.0i, contributes to stiffness (in both bending
and torquing motions) of device 1.01, thereby enhancing
trackability, steering and other torquing.
[0337] FIG. 17 illustrates another embodiment of an illuminating
guidewire 1.01. In this example, proximal end portion of device
1.01 is formed externally by a coil with a polymer layer laminated
thereon, but any of the other arrangements described above may be
substituted. In this example, illumination is provided by a high
intensity light emitting diode (LED) 1.0id fitted at the distal end
of device 1.01. The proximal end of device 1.01 may be sealed such
as with epoxy, or any of the other alternatives mentioned above
with regard to the proximal end of device 1.01 in FIG. 13, in order
to prevent pulling on the wires 1.0iw at the connections with LED
1.0id, as well as to seal the proximal end of the device. Grinding
and polishing are not necessary, as the proximal end of device 1.01
in FIG. 17 does not transmit light.
[0338] Device 1.01 in FIG. 17 performs substantially similar to the
device 1.01 of FIG. 13 with regard to the properties of push
ability, torquability and tensile properties. Device 1.01 of FIG.
17, however, does not require illumination fibers or laser fibers.
Instead, a pair of insulated lead wires are electrically connected
to the terminals of LED 1.0id (not shown) and then extend within
device 1.01 over the length of device 1.01 to extend proximally
from the proximal end of device 1.01. The free ends of wires 1.0w
are configured to be connected to a power source that functions as
the source of electrical power, to deliver electrical energy to LED
10id to illuminate it. FIG. 18 illustrates a cross-sectional view
of a distal end portion of device 1.01 of FIG. 17. In this example,
core support 1.0cw is in the form of a flattened distal end core
wire or shaping ribbon as known in the art, that extends between
the two wires 1.0w. FIG. 18 also illustrates the insulation layer
1.0iw over each wire.
[0339] Any of the devices 1.01 described herein may optionally
include one or more radiopaque markers and/or electromagnetic coils
on the tip of the device 1.01 and/or elsewhere along the device for
enhancing visibility by fluoroscopy systems, image guided surgery
(IGS) systems, or other visualization systems.
[0340] FIG. 19 shows an alternative design of device 1.0in which
light is emitted proximally of the distal end of the device. This
configuration may employ any of the various light transmission
means described above (e.g., illumination fibers, laser fibers,
LED). The proximal portion 1.0p may be constructed in any of the
manners described above with regard to other embodiments of device
1.0.
[0341] The distal portion 1.0d includes a transparent proximal end
portion 1.0dp that mounts over the distal end of proximal end
portion 1.0p of the device 1.01. The transparent portion 1.0dp
permits the illumination emitted from illumination member 1.0i or
1.0id to pass out of the device 1.01 at the location of transparent
portion 1.0dp. The illumination member(s) 1.0i or 1.0id thus
terminate at the proximal end portion 1.0dp of the distal end
portion of device 1.01. Distally of this transparent portion 1.0dp,
the distal portion 1.0dd of distal end portion 1.0d of device 1.01
extends as a floppy guidewire leader or tip. This floppy guidewire
leader or tip 1.0dd may include a coiled section 1.0c and may
optionally include a core support 1.0cw in the manner described
above with regard to FIG. 4. The light emitted from illumination
fibers will disperse naturally through the transparent portion
1.0dp. Optionally, a deflector 1.1, such as a convex mirror (e.g.,
parabolic or other convex) shape or other reflective surface may be
provided distally of illumination fibers/light emitting portion
1.0i, 1.0id of device 1.01 to deflect light rays out of the
transparent portion. Additionally, or further alternatively,
illumination fibers 1.0i may be angled at the distal end portions
thereof to direct the emitted light out through the transparent
portion. This configuration may be beneficial in further protecting
the illumination emitter(s) 1.0i, 1.0id from foreign materials
inside the body, as well as from trauma that may be induced by
bumping the illumination emitter up against structures within the
body. Further, a floppy guidewire leader 1.0dd of this type may
provide more flexibility and maneuverability than a device in which
the illumination emitter is located on the distal tip of the
device.
[0342] Transparent portion 1.0dp may be provided as a clear plastic
or glass integral tube, or may have openings or windows 1.0t
provided therein (see the partial view of FIG. 19). Further
alternatively, transparent portion may be formed by a plurality of
struts 1.0st circumferentially arranged to interconnect the distal
floppy tip 1.0dd with the proximal end portion 1.0p of device 1.01
as shown in the partial illustration of FIG. 21. Alternatively
members 1.0st may be intersecting in a criss-crossing cage like
configuration or other cage configuration. In any of these
alternative configurations, members 1.0st may be transparent, but
need not be and could be formed of non-transparent materials, such
as metals or opaque plastics, for example.
[0343] Device 1.01 should be readily connectable to and
disconnectable from a power source to enable attachment for
providing illumination for positioning the guidewire 1.01 and/or
other devices during a procedure, detachment to allow another
device to be slid onto the guidewire 1.01 from a free proximal end
thereof, and reattachment to again provide illumination, to assist
in guidance/visualization of the device being passed over the
guidewire 1.01, for example.
[0344] FIGS. 22A and 22B illustrate one example of a coupler 2.01
that is configured for quick connection and disconnection of an
illumination guidewire 1.01 that employs illumination fibers 1.0i
or laser fibers 1.0f. Coupler 2.01 is connected to a light source
1.0301, such as a conventional endoscope light source, for example,
or other light source capable of delivering preferably at least
10,000 lux through coupler 2.01. Light cable 1.032 optically
connects connector 2.01 with light source 1.0301 to deliver light
from the light source 1.0301 to connector 2.01. Light cable 1.032
can optionally be a fluid-filled light cable, such as the type
provided with DYMAX BLUEWAVE.TM. 200 and ADAC SYSTEMS CURE SPOT.TM.
light cables, for example. A liquid filled light cable comprises a
light conducting liquid core within plastic tubing. The liquid is
non-toxic, non-flammable and transparent from 270 to 720 nm. The
ends of a liquid tilled light cable can be sealed with high quality
quartz glass and metal spiral tubing surrounded by a plastic sleeve
for exterior protection.
[0345] Connector 2.01 includes a proximal channel, slot or bore 2.2
that has an inside dimension or circumference that is slightly
greater than the outside diameter or circumference of device 1.01
at the proximal end portion 1.0p. A quick release locking mechanism
2.4 is provided for locking and unlocking device 1.01 within
connector 2.01. Quick release locking mechanism is biased toward
the locking position shown in FIG. 22B, in which the locking
portion 2.4a of mechanism 2.4 is driven into channel slot or bore
2.2 and may even abut against the opposite wall of the channel,
slot or bore 2.2, when no guidewire 1.01 has been inserted. Locking
mechanism 2.4 may be spring-biased toward the locked position, for
example. Additionally, locking mechanism 2.4 may include a ball and
detent arrangement, or other temporary locking means to maintain
the mechanism 2.4 in the locked configuration. An additional,
similar mechanism may be provided to temporarily fix locking
mechanism 2.4 in the unlocked configuration shown in FIG. 22A.
Alternative locking mechanisms may be employed, such as a pivoting
lock arm, for example, that is manually pivotable between the
locked and unlocked orientations, or other mechanism that would be
apparent to one of ordinary skill in the mechanical arts, such as a
collapsible silicone valve that grips the device, for example.
[0346] Light cable 1.032 generally has a much larger inside
diameter than the inside diameter or combined inside diameters of
the illumination fibers 1.0i. Accordingly, the proximal end portion
of connector 2.01 provides a tapering or funnel shaped pathway 2.6
having a proximal inside diameter that is substantially equivalent
to the inside diameter of cable 1.032 or greater, and which tapers
to a distal inside diameter that is about the same or only slightly
greater than the inside diameter or combined inside diameters of
the illumination fiber(s), or alternatively, that is about the same
or only slightly greater than the outside diameter of the proximal
end of device 1.01. The light cable 1.032 generally has a larger
diameter bundle of illumination fibers than that contained within
the illuminating guidewire 1.01. Accordingly, the tape 2.6 is used
to transition between the larger bundle in the light cable 1.032
and the smaller bundle in the guidewire 1.01. With this
arrangement, light delivered through light cable 1.032 is
concentrated or focused down to a pathway where most of the light
can be transmitted through the illumination fibers.
[0347] To insert device 1.01 into connector 2.01, an operator
retracts quick connect locking mechanism 2.4 to the open position
shown in FIG. 22A. If quick connect mechanism 2.4 is provided with
a temporary locking mechanism as referred to above, then quick
connect locking mechanism 2.4 can be temporarily fixed in the
orientation shown in FIG. 22A, without the operator having to hold
it open. Otherwise, the operator will hold connector 2.4 open in
the position shown in FIG. 22A. The proximal end of device 1.01 is
next inserted into the open channel, slot or bore 2.2 and slid
proximally with respect to connector 2.01 until the proximal end of
device 1.01 abuts against the proximal end of channel, slot or bore
2.2. Quick release mechanism is next released by the operator (in
embodiments when there is no temporary locking mechanism to
maintain the quick release in the open configuration) or released
from the temporary locked open configuration, so that the locking
arm 2.4a is advanced toward the proximal end portion 1.0p of device
1.01, by the biasing of quick connect locking mechanism 2.4
described above. Locking arm 2.4a contacts device 1.01 and holds
device 1.01 under compression between locking arm 2.4a and the
opposite inner wall of channel, slot or bore 2.2, with sufficient
force to prevent device 1.01 from sliding out of connector 2.01
even if the distal tip of device 1.01 is pointed straight down in a
vertical direction. Optionally, locking arm 2.4a may be
additionally temporarily locked in place by a ball and detent
mechanism, or other temporary locking mechanism, as mentioned
above. To remove device 1.01 from connector 2.01, quick connect
locking mechanism 2.4 is repositioned to the open or unlocked
orientation shown in FIG. 22A and the device is slid distally with
respect to the connector until it is free from the connector
2.01.
[0348] FIGS. 23A-23B illustrate an alternative connector 2.01 that
includes a quick release locking mechanism 2.4. In this example,
two or more locking arms 2.4 are provided circumferentially about
the distal end of connector 2.01. Arms 2.4 are biased to the closed
or locked configuration as shown in FIG. 23A. For example, arms 2.4
may be made from resilient spring steel, nickel-titanium alloy or
resilient plastic and formed to assume the configuration shown in
1.4A when mounted to connector 2.01 and when in an unbiased state.
Installation of device 1.01 into connector 2.01 is simplified by
the automatic grasping and temporary locking functions provided by
quick release locking mechanism 2.4. The proximal end of device
1.01 is simply inserted between the two or more arms 2.4. Arms 2.4
included ramped or cammed surfaces 24b that guide the proximal end
of device 1.01 into connector 2.01, and, as device 1.01 is pushed
against these surfaces 2.4b, arms 2.4 are deflected into the
opened, biased configuration shown in FIG. 23B. The
biasing/resiliency of arms 2.4 imparts compressive forces to the
shaft of device 1.01 via temporary locking surfaces 2.4a, so that
device 1.01 is gripped and held in position as shown in FIG. 23B.
To remove device 1.01, the operator needed simply pull on device
1.01, while holding connector 2.01 relatively immobile, with a
force sufficient to overcome the compressive and frictional forces
imparted by surfaces 2.4a. The resilient arms 2.4 then return to
the unbiased configuration shown in FIG. 23A. Optionally, surfaces
2.4a may be coated with, or include a friction enhancing surface,
such as rubber or other elastomer, and/or be roughened, such as by
knurling or other surface roughening technique.
[0349] In the example shown in FIGS. 23A-23B, the light cable 1.032
that is provided has an inside diameter that is about the same as
the diameter of the proximal end of device 1.01 and thus, no
tapering channel 2.6 is required. However, for arrangements where
the light cable 1.032 is much larger, as is usually the case when
using a conventional endoscope light source 1.0301, connector 2.01
may be provided with a tapering light channel 2.6 in the same
manner as described above with regard to the embodiment of FIGS.
22A-22B.
[0350] FIG. 24 illustrates a longitudinal sectional view of a
connector 2.01 that is quickly connectable and releasable from a
guidewire device 1.01 and is also connectable to and releasable
from standard light source cables that are typically found in
operating rooms. Thus, this connector 2.01 functions both as an
adapter to connect to a conventional endoscope light source channel
or cable, and as a quick release locking connector to connect to
and release from a proximal end portion of guidewire 1.0.
[0351] The proximal end of connector 2.01 is provided with a light
post 2.8 that is configured to mate with a connector on the distal
end of a light cable extending from a conventional endoscope light
source. For example, light post 2.8 may be an ACMI light post (ACMI
Corporation) or other standard connector typically used to connect
endoscopes to operating room light sources. Because the cable
extending from an operating room light source generally has a much
larger inside diameter than the inside diameter or combined inside
diameters of the illumination fibers of device 1.01, and larger
than the diameter of the proximal end of guidewire 1.01, the
proximal end portion of connector 2.01 includes a light tapering or
funnel-shaped pathway 2.6 like that described above with regard to
FIG. 22A.
[0352] The quick release locking mechanism 2.4 in this example
includes a collet 2.4c that is configured to center the proximal
end of device 1.01 with the distal end of tapering pathway 2.6. A
threaded cap 2.4d is threaded over mating threads 2.4t on the body
of connector 2.01, so that when cap 2.4d is torqued in a direction
to advance cap 2.4d proximally with respect to the body of
connector 2.01, inner ramped or cammed surfaces 2.4e of cap 2.4d
ride over outer ramped or cammed surfaces 2.4f of collet 2.4c,
thereby functioning as a pin vise and clamping collet 2.4c against
the proximal end portion of device 1.01 to clamp and maintain
device 1.01 in its current position relative to connector 2.01. To
insert device 1.01, cap 2.4d is rotated in a reverse direction from
that described above to open the distal opening of the inner
channel 2.4g of collet 2.4c to a dimension larger than the outside
diameter of the proximal end of device 1.01, so that device 1.01
can be easily slid through the channel 2.4g until the proximal end
of device 1.01 abuts the proximal end portion of collet 2.4c, or
approximates the same. The cap 2.4d is then turned with respect to
the body of connector 2.01 to clamp device 1.01 into position, as
described above. Removal of device 1.01 can be performed by turning
cap 2.4d in a reverse direction relative to connector body 2.01,
thereby loosening the grip of collet 2.4c on device 1.01, after
which device 1.01 can be easily slid out from connection with
connector 2.01. Components of connector 2.01 may be made from
metal, such as stainless steel or other biocompatible metals, or
temperature-resistant thermosetting polymer, for example.
[0353] Light post 2.8 is rotatable with respect to the light cable
1.032 of the light source 1.30 when connector 2.01 is connected to
the distal end connector of the light cable 1.032. This allows
device 1.01, when connected to connector 2.01 in this arrangement,
to be rotated during use without building up significant twisting
or rotational counter forces within the light cable 1.032. For
example, in the light post 2.8 shown, the female receptacle (not
shown) of the light cable 1.032 couples over light post 2.8 and
engages in groove 2.8g, about which the female receptacle is then
rotatable relative to light post 2.8. FIG. 25 is a longitudinal
sectional view of a connector 2.01 that is similar to the connector
2.01 described with regard to FIG. 24 above. One difference in the
example of FIG. 25 is that the tapered light guide 2.6 is provided
in the light post 2.8, as contrasted with being provided in the
proximal end portion of the main body of connector 2.01 in FIG. 24.
However, in both cases, the function is the same.
[0354] Turning now to FIGS. 26A-26E, illustrations of partial
coronal sectional views through a human head showing various steps
of a method for treating an ostium that opens to a frontal sinus
are shown. The methods described here, and all other methods
disclosed herein may also comprise a step of cleaning or lavaging
anatomy within the nose, paranasal sinus, nasopharynx or nearby
structures including but not limited to irrigating and suctioning.
The step of cleaning the target anatomy can be performed before or
after a diagnostic or therapeutic procedure. The methods of the
present invention may also include one or more preparatory steps
for preparing the nose, paranasal sinus, nasopharynx or nearby
structures for the procedure, such as spraying or lavaging with a
vasoconstricting agent (e.g., 0.025-0.5% phenylephyrine or
Oxymetazoline hydrochloride (Neosynephrine or Afrin) to cause
shrinkage of the nasal tissues, an antibacterial agent (e.g.,
provodine iodine (Betadine), etc. to cleanse the tissues, etc.
[0355] In FIG. 26A, a first introducing device in the form of a
sinus guide 1.002 is introduced through a nostril and through a
nasal cavity 1.012 to a location close to an ostium 1.034 of a
frontal sinus 1.036. Sinus guide 1.002 may be as described
previously herein, or as described in the applications incorporated
herein by reference. The advancement of sinus guide 1.002 can be
visualized with a scope inserted into the nasal cavity 1.012 and
advanced as close to the ostium 1.034 as possible without causing
significant trauma to the tissues therein.
[0356] Once the surgeon is satisfied that the distal end of the
sinus guide 1.002 is positioned close enough to the appropriate
ostium 1.034, illuminating guidewire 1.01, connected to a light
source as described by any of the techniques mentioned above, is
inserted through sinus guide 1.002 and advanced therethrough, see
FIG. 26B. There may be some transillumination from the light
emitted from the scope which can be used to confirm that the sinus
guide 1.002 is positioned in the correct general area, which
confirmation can be made even before the distal tip of guidewire
1.01 exits the distal end of sinus guide 1.002. However, much more
specific transillumination effects are produced when the tip of
guidewire 1.01 exits the distal end of guide 1.002 and especially
when the light emitting portion of guidewire 1.01 touches or
approximates an intended target surface, such as an inner wall of a
sinus, for example. As the guidewire 1.01 is advanced,
transillumination on the face of the patient can be observed as a
glowing spot that moves as the distal end portion of device 1.01
moves, thereby making it possible to visibly track the location of
the light emitting portion of device 1.01 without the need to use
radiographic imaging, such as by fluoroscopy, for example.
[0357] While there may be some diffuse transillumination on the
forehead of the patient overlying the frontal sinus 1.036 as the
light emitting portion of device 1.01 approaches the ostium 1.034,
the glow on the forehead becomes brighter and smaller in dimension
(more focused) as the light emitting portion passes through the
ostium 1.034 and enters the frontal sinus 1.036, FIG. 26C. As
device 1.01 is further advanced, the glowing spot becomes most
defined and brightest as the light emitting portion approaches and
contacts a wall of the frontal sinus 1.036. Further, as noted, the
movement of the trans illuminated spot can be visibly followed to
confirm that the guidewire 1.01 is indeed moving within the
location of the frontal sinus, as can be confirmed by the surgeon's
knowledge of the particular anatomy of the patient being treated.
In this regard, a CAT scan or other image of the sinus anatomy can
be performed prior to this procedure and studied by the surgeon, to
apprise the surgeon of any distinctive or unusual patterns in the
individual patient's sinus anatomy which might be useful in
tracking and confirmation of where the guidewire is located, as
indicated by the transillumination.
[0358] Once properly positioned, the proximal end of device 1.01 is
disconnected from connector 2.01, while leaving guidewire 1.01 in
its current position. A working device 1.006, for example a balloon
catheter, is the introduced over guidewire 1.01 and advanced
thereover so that the proximal end of device 1.01 extends
proximally beyond a proximal end of device 1.006. Device 1.01 is
then reconnected to connector 20 so that light is again emitted
from the light emission portion of the distal end portion of device
1.01. Thus it can be visually confirmed, without radiography, that
the distal end portion of the guidewire 1.01 remains properly in
the frontal sinus 1.036 as the working device 1.006 is advanced
toward ostium 1.034 and the balloon of working device 1.006 is
extended across the ostium 1.034. The proper positioning of the
working end (distal end portion) of working device 1.006 can be
visualized with the scope and/or fluoroscopy.
[0359] Once proper placement of the working device 1.006 has been
confirmed, working device 1.006 is used to perform a diagnostic or
therapeutic procedure. In this particular example, the procedure is
dilatation of the frontal sinus ostium 1.034 by expansion of the
balloon thereagainst, to enlarge the opening of the ostium 1.034.
However, it will be appreciated that the present invention may also
be used to dilate or modify any sinus ostium or other man-made or
naturally occurring anatomical opening or passageway within the
nose, paranasal sinuses, nasopharynx or adjacent areas. Further,
other working tools may be inserted and used according to these
same techniques. After the completion of the procedure, sinus guide
1.002, guidewire 1.01 and working device 1.006 are withdrawn and
removed, completing the procedure, see FIG. 26E.
[0360] Illuminating guidewire device 1.01 can also be used to
facilitate visualization and placement of the sinus guide 1.002 in
the procedure described above with regard to FIGS. 26A-26E, or in
another procedure in which a sinus guide, guide catheter or guide
tube is placed in the sinus pathways. FIG. 27 illustrates a
situation, like that described above with regard to FIG. 12, where
scope 1.008 has been inserted as far as possible without causing
significant trauma to the patient. The range of visibility in this
case does not extend all the way to ostium 1.034, as indicated
schematically by the rays 1.009 shown extending distally from scope
1.008. In this case, adequate visualization of sinus guide 1.002 by
scope 1.008 is possible only up to the extent of the rays 1.009
shown. Thus, if sinus guide 1.002 is flexible enough to be advanced
more closely to ostium 1.034, then adequate visualization of this
movement would not be possible via scope 1.008. That is, if sinus
guide 1.002 is physically capable of being extended further
distally to place the distal end thereof at the approach to ostium
1.034, scope 1.008 would not be capable of adequately visualizing
this. However, by inserting illuminating guidewire through sinus
guide 1.002 as shown in FIG. 27, additionally illumination can be
provided distally of the illuminating range of scope 1.008. This
additional illumination can be received by scope 1.008 to enable
visualization up to the illumination portion of device 1.01 and
potentially even extending to illumination range of device 1.01, as
long as there is a straight pathway of the field of view. Thus,
advancement of the sinus guide 1.002 can be visualized further
distally by the scope 1.008 using this technique, and potentially
all the way up to the ostium 1.034.
[0361] Additionally, this technique can be used to visualize
placement of the guidewire 1.01 up to and into the desired ostium
1.034. Alternatively, this can be carried out without the sinus
guide 1.002, wherein the guidewire 1.01 is inserted and the scope
1.008 can be used to visualize placement of guidewire 1.01 into the
target ostium with the assistance of the light emitted by the scope
1.008 in addition to the light emitted by guidewire 1.0.
[0362] In any of these procedures where a scope 1.008 is used for
visualization and an illuminating guide wire is inserted, some
transillumination of the target sinus may occur from the light
emitted by the scope 1.008 alone. However, this transillumination
will be diffuse and show a rather dim, large area of
transillumination on the patient's skin. When the illumination
guidewire is inserted and advanced, as noted earlier, a smaller,
brighter transillumination spot will be visible when the
illuminating portion of the guidewire has entered the sinus.
Additionally, even before entering the sinus, the light emitted
from the guidewire will produce a moving transillumination spot at
guidewire 1.01 is advance, which also helps distinguish the
location of the distal portion of the guidewire, relative to any
diffuse transillumination produced by the scope light.
[0363] If the guidewire 1.01 is advanced into an ostium other than
the target ostium (e.g., ostium 1.035 shown in FIG. 27), this may
be possible to be viewed by scope 1.008, depending upon the line of
sight. However, even if it is not, the transillumination resulting
from entrance into a different sinus than the target sinus will be
evident by the different location on the patient's face. Also, in
the example shown, guidewire 1.01 would not be able to be advanced
very far through ostium 1.35 before it was diverted and curled by
the relatively small sinus space that ostium 1.35 leads into. Thus,
by tracking the movement of the illumination spot produced by
guidewire 1.01, the surgeon could confirm that guidewire 1.01 was
misplaced as the guidewire would be diverted by a much smaller
space then that characterized by the target frontal sinus
1.036.
[0364] Thus, by using an illuminating guidewire device 10in the
methods as described above, the use of fluoroscopy or other X-ray
visualization can be reduced is not required to confirm proper
placement of the guidewire in some cases.
[0365] Similar procedures may be carried out in other sinuses. For
example, a similar procedure to that described above with regard to
FIGS. 26A-26E may be carried out to open or expand an opening of an
ostium leading to a maxillary sinus. In this case, when
illuminating guidewire device 1.01 passes through the ostium that
opens to the target maxillary sinus and enters the maxillary sinus,
a relatively bright, relatively small, defined transillumination
spot can be observed to move across the cheek region of the
patient. As guidewire 1.01 is advance further distally along the
maxillary sinus, the maxillary sinus typically tends to track in an
inferior direction relative to the skull, and the bottom wall of
the maxillary sinus is very close to the palate of the patient.
Therefore as the illuminating portion of guidewire approaches
and/or touches the bottom wall of the maxillary sinus, a
transillumination spot can be observed on the roof of the patient's
mouth by looking into the mouth of the patient. At the same time,
the transillumination spot on the cheek that was caused by the
guidewire will diminish, or not be visible at all at this time.
This viewability on the roof of the mouth is further confirmation
that the guidewire has entered the maxillary sinus. Movement of the
transillumination spot on the roof of the mouth can also be
observed as the guide wire 1.01 is advanced and/or refracted.
[0366] It is further noted that some wavelengths of light may be
more effective in producing the transillumination effects described
herein, for the purpose of locating the position of the guidewire.
In this regard, particular wavelengths of visible light can be
selected for this purpose. Alternatively, or in addition, infrared
wavelengths may be particularly effective. In this regard,
guidewires that employ illuminating fibers may be provided with a
filter 1.2 to define the color/wavelength of the light emitted by
device 1.01. As schematically shown in FIG. 28, filter 1.2 may be
provided distally of the illumination fibers, such as at the distal
tip of device 1.01, proximally of the illumination fibers, such as
at the proximal end of device 1.01, or in the light pathway at a
location within connector 2.01, for example. Multiple filters may
be placed at one or more of these locations. For devices 1.01 that
employ an LED light emitting component, different color LEDs may be
employed to emit different wavelengths of light. For devices 1.01
that employ laser fibers, different types of lasers may be used
that emit different wavelengths of light.
[0367] Another optional feature that guidewire 1.01 may be provided
with is the ability to emit strobed, flashing or flickering light.
The transillumination produced by a flashing light can be further
distinguished from diffuse transillumination produced by other
light sources, such as endoscopes, for example, since the
transillumination produced by the guidewire 1.01 in this case will
flicker or vary in intensity between bright and dim. To produce
this type of light, either a light source having strobing
capability could be connected to the device 1.01, or connector 2.01
may be provided with this capability. When using a laser light
source or an LED as the light emitter, as described in embodiments
above, a blinking or strobing effect can be electronically
generated according to techniques known in the electronics and
lighting arts. FIG. 29A schematically illustrates a connector 2.01
having a rotating shutter 2.7 rotatably mounted therein so that the
vanes 2.7v and gaps 2.7g between the vanes (see plane view in FIG.
29B) become successively aligned with the light pathway through the
connector 2.01 to alternate emission and blocking of light
transmission out of the connector 2.01 and ultimately through
device 1.01 when a device 1.01 is connected thereto. Shutter 2.7
can be powered by a motor 2.9 that is either battery powered or
connectable to an operating room power source, and motor can be
operated by the user via actuator 3.1, which can be configured to
turn the motor on and off, and optionally can be configured to vary
the speed of rotation. Alternatively, shutter can be configured so
that vanes 2.7v extend through a slot in connector 2.01 whereby a
user can manually rotate the shutter to cause the light emitted
from device 1.01 to flicker.
[0368] Other instruments that are designed to be inserted into a
sinus, or at least to be positioned at the ostium of a sinus can
also be provided with illumination capability according to any or
all of the features described above with regard to illumination
guidewires. FIG. 30 shows a frontal ostium seeker 1.001 instrument
that can be used to access a sinus ostium. For example, seeker
1.001 may be provided with a length of about 175 mm to about 250 mm
(about 208 mm in the example shown) and a ball tip at one or both
ends of the instrument. In FIG. 30, seeker 1.001 is also provided
with a light emitter 1.04 at one or both ends of the device 100
that can be used to locate an end of device 1.001 as it is being
advanced to seek an ostium, by the transillumination effects as
discussed above. Light emitters 1.04 may be provided by LED, light
illumination fibers or laser illumination fibers, for example. One
or both end portions of the instrument may include a light fiber
bundle or electrical wires for connection to a light source or
power source in a manner as described above.
[0369] FIG. 31 shows a suction sinus instrument 1.101 that is
configured to evacuate blood and/or other fluids from a target
surgical site, such as the frontal sinus, sphenoid sinus or other
sinus, to improve visibility of a surgical procedure. Instrument
1.101 includes an elongated shaft 1.16 with a distal end that opens
to deliver suction via a suction lumen end 112. Additionally, a
light emitter 1.14 is provided at the distal end of shaft 1.16,
which may be an LED or one or more illumination fibers configured
to transmit light in a manner as described above. Shaft 1.16 is
configured and dimensioned to be inserted into the sinus
passageways and sinuses. The proximal end portion of instrument
1.101 may include a light fiber bundle 1.18 or electrical wires for
connection to a light source or power source in a manner as
described above.
[0370] FIG. 32 shows an integrated wire dilatation catheter 1.201
that includes an elongate, flexible catheter shaft 1.26 having a
balloon 1.28 mounted thereon. A proximal Luer hub 1.22 is attached
to the proximal end of the catheter shaft 1.26. An inflation device
(not shown) may be attached to the Luer hub 1.22 and used to
inflate and deflate the balloon 1.28. A non-removable, integrated
guide member 1.24 extends out of and beyond the distal end of the
catheter shaft 1.26. Guide member 1.24 can extend through the
length of catheter shaft 1.26 and extend proximally thereof as
shown in FIG. 32. The proximal end portion may be configured with a
polished proximal end containing illumination fibers, as described
previously, or may have one or more electrical wires extending
proximally thereof for connection with an electrical power source
to deliver electrical power to an LED, for example. A light emitter
1.25 may be provided at the distal tip of integrated guide member
1.24, as shown in FIG. 32 and may be one or more LEDs or one or
more illumination fibers, according to any of the different
embodiments described above. Alternatively, light emitter 1.25 may
be provided proximally of the distal tip of guide member 1.24, in a
manner like that described with regard to FIG. 19, for example.
Further alternatively, guide member may not extend through the
entire length of catheter 1.26 or may not extend proximally of
balloon member 1.28 at all. In these examples, light emitter may be
an LED, wherein wires can be threaded through or alongside of
catheter 1.26 and into guide member 1.24 to connect with the LED.
Further alternatively, if light emitter 1.25 comprises one or more
illumination fibers, the illumination fibers may extend proximally
of the proximal end of the guide member 1.24, and proximally
through catheter 1.26 where they are not surrounded by an external
sheath in a guidewire formation.
[0371] In one preferred embodiment for adult applications, balloon
catheter 1.201 has an overall length of approximately 43.5 cm and
its shaft 1.26 has an outer diameter of about 0.058 inches. Further
details about integrated wire dilatation catheters that may be
configured with a light emitter in a manner as described herein can
be found in co-pending application Ser. No. 11/438,090 filed May
18, 2006 and titled "Catheters with Non-Removable Guide Members
Useable for Treatment of Sinusitis. Application Ser. No. 11/438,090
is hereby incorporated herein, in its entirety, by reference
thereto.
[0372] While the present invention has been described with
reference to the specific embodiments thereof, it should be
understood by those skilled in the art that various changes may be
made and equivalents may be substituted without departing from the
true spirit and scope of the invention. In addition, many
modifications may be made to adapt a particular situation,
material, composition of matter, process, process step or steps, to
the objective, spirit and scope of the present invention. All such
modifications are intended to be within the scope of the claims
appended hereto. It is to be appreciated that the invention has
been described hereabove with reference to certain examples or
embodiments of the invention but that various additions, deletions,
alterations and modifications may be made to those examples and
embodiments without departing from the Intended spirit and scope of
the invention. For example, any element or attribute of one
embodiment or example may be incorporated into or used with another
embodiment or example, unless to do so would render the embodiment
or example unsuitable for its intended use. All reasonable
additions, deletions, modifications and alterations are to be
considered equivalents of the described examples and embodiments
and are to be included within the scope of the following
claims.
* * * * *