U.S. patent application number 11/303154 was filed with the patent office on 2006-05-04 for methods and apparatus for securing medical instruments to desired locations in a patient's body.
Invention is credited to Fred H. Burbank, Michael L. Jones, Paul Lubock, Richard L. Quick.
Application Number | 20060094983 11/303154 |
Document ID | / |
Family ID | 22516198 |
Filed Date | 2006-05-04 |
United States Patent
Application |
20060094983 |
Kind Code |
A1 |
Burbank; Fred H. ; et
al. |
May 4, 2006 |
Methods and apparatus for securing medical instruments to desired
locations in a patient's body
Abstract
Devices and methods are provided for securely affixing a medical
instrument to desired tissue in a patient's body, using a fixation
agent. Such medical instruments may comprise localization wires or
tissue acquisition instruments, such as biopsy instruments, for
example. In the case of tissue acquisition instruments, the
inventors have discovered significant advantages for securely
affixing the distal end of the tissue acquisition instrument to a
particular tissue target area. For example, such an approach
permits the imaging environment to be uncoupled from the procedural
environment so that expensive and often unavailable imaging
equipment, such as stereotactic imaging equipment, need not be
used. In a preferred embodiment, a bonding agent, such as adhesive,
surgical glue, or a solvent, is used as the fixation agent.
Inventors: |
Burbank; Fred H.; (San Juan
Capistrano, CA) ; Lubock; Paul; (Laguna Niguel,
CA) ; Jones; Michael L.; (Capistrano Beach, CA)
; Quick; Richard L.; (Trabuco Canyon, CA) |
Correspondence
Address: |
Edward J. Lynch;DUANE MORRIS LLP
One Market
Spear Tower, Ste. 2000
San Francisco
CA
94105
US
|
Family ID: |
22516198 |
Appl. No.: |
11/303154 |
Filed: |
December 15, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10010213 |
Dec 4, 2001 |
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11303154 |
Dec 15, 2005 |
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09146185 |
Sep 1, 1998 |
6540693 |
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10010213 |
Dec 4, 2001 |
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09057303 |
Apr 8, 1998 |
6331166 |
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09146185 |
Sep 1, 1998 |
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60076973 |
Mar 3, 1998 |
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Current U.S.
Class: |
600/567 ;
604/164.01 |
Current CPC
Class: |
A61B 2018/00333
20130101; A61B 2018/0091 20130101; A61B 2018/1407 20130101; A61B
2090/3908 20160201; A61B 18/1492 20130101; A61B 2018/1475 20130101;
A61B 18/12 20130101; A61B 10/02 20130101; A61B 2017/320064
20130101; A61B 2018/00898 20130101; A61B 90/37 20160201; A61B
2018/126 20130101; A61B 18/1487 20130101; A61B 18/1477 20130101;
A61B 17/32056 20130101; A61B 90/39 20160201; A61B 2018/162
20130101; A61B 2018/1425 20130101; A61B 2018/00214 20130101; A61B
18/14 20130101; A61B 10/04 20130101; A61B 2018/1253 20130101; A61B
2018/00208 20130101; A61B 17/3417 20130101; A61B 10/0266 20130101;
A61B 2018/00267 20130101; A61B 2017/3488 20130101; A61B 90/17
20160201; A61B 17/320725 20130101; A61B 2090/3987 20160201; A61B
2018/00601 20130101; A61B 10/0241 20130101; A61B 2090/3991
20160201; A61B 2018/00916 20130101; A61B 2018/00577 20130101; A61B
17/00491 20130101 |
Class at
Publication: |
600/567 ;
604/164.01 |
International
Class: |
A61B 10/00 20060101
A61B010/00; A61M 5/178 20060101 A61M005/178 |
Claims
1. A medical device comprising a tube having a distal end, a
proximal end, and a longitudinal axis, the device being adapted for
placement of said distal end into a patient's body at a desired
location, said medical device having a fixation agent disposed on
said distal end, the fixation agent being adapted for affixing the
distal end of said medical device at said desired location.
2-48. (canceled)
49. A medical device for securing a medical instrument to a desired
location within a patient's body comprising: a. a shaft having a
distal end, a proximal end, and a longitudinal axis, and having a
distal tip configured for advancement within a patient's body to a
desired location; and b. a fixation agent for fixing the distal end
at the desired location which is selected from a group of fixation
agents consisting of a bonding agent, an electrical heating agent,
an electrosurgical cauterizing agent, and combinations thereof.
50. The medical device as recited in Clam 49, wherein the distal
end of the device has at least one opening for dispensing bonding
agent into the patient's body to fix the distal end at the desired
location.
51. The medical device as recited in claim 50, wherein the bonding
agent is a surgical adhesive.
52. The medical device as recited in claim 51, wherein the surgical
adhesive is a cyanoacrylate.
53. The medical device as recited in claim 50, wherein the bonding
agent is a fibrin glue.
54. The medical device as recited in claim 50, wherein the bonding
agent is a solvent.
55. The medical device as recited in claim 50, wherein the tube has
a braided outer wall.
56. The device of claim 55 wherein the braided outer wall has an
interstice which forms at least in part the at least one opening
for dispensing the bonding agent.
57. The medical device as recited in claim 50, wherein the shaft
has an outer wall formed at least in part from a coil of material,
which has at least one interstice for dispensing the bonding
agent.
58. The medical device as recited in claim 50 having a tissue
acquisition device with a longitudinal axis about which the medical
device is rotatable, a cutting element disposed on the shaft for
cutting surrounding tissue, and a bushing disposed on the shaft
which has at least one opening and which is rotatable relative to
the shaft, and wherein the bonding agent is dispensed through the
at least one opening and affixes the bushing to the surrounding
tissue, so that the instrument is secured to the desired location
without preventing rotational movement thereof.
59. The medical device as recited in claim 49, wherein the fixation
agent is an electrosurgical element disposed on the distal end of
the shaft, which coagulates tissue surrounding the distal end of
the shaft to affix tissue to the distal end of the shaft.
60. The medical device as recited in claim 49, wherein the fixation
agent is an electrical heating element disposed on the shaft distal
end which cauterizes tissue surrounding the shaft distal end and
thereby causes the tissue to be affixed to the distal end of the
shaft.
61. The medical device of claim 49, wherein the fixation agent is
a, bonding agent selected from the group consisting of adhesives,
solvents, and combinations thereof.
62. A medical device for securing medical instruments to a desired
location in a patient's body comprising: a. a shaft having a distal
end configured for advancement within a patient's body to a desired
location, a proximal end, a localization wire, and a longitudinal
axis; b. a fixation agent disposed on the distal end of the shaft
which is adapted for affixing the distal end of the medical device
at the desired location; and c. a catheter having a lumen through
which the localization wire is introduced into the patient's
body.
63. The medical device as recited in claim 62, wherein the fixation
agent is a bonding agent, and the catheter has a second lumen which
accommodates the bonding agent.
64. A medical device for securing medical instruments to a desired
location in a patient's body comprising: a. a shaft having a distal
end configured for advancement within a patient's body to a desired
location, a proximal end, and a longitudinal axis and b. an
expandable mechanical fixation agent which is configured for
affixing the distal end of the shaft to the desired location.
65. The medical device as recited in claim 64, wherein the
mechanical fixation agent is a Mallicot structure.
66. The medical device as recited in claim 64, wherein the
mechanical fixation agent is a rolled stent and an axially movable
sleeve, and the stent is exposed and unrolls to engage surrounding
tissue and affix the distal end of the device when the sleeve is
moved proximal to the stent.
67. The medical device as recited in claim 64, wherein the
mechanical fixation agent is a radially expandable and retractable
basket which is actuatable to extend outwardly into tissue
surrounding the distal end of the device to engage the tissue and
thereby anchor the distal end of the shaft to the desired
location.
68. The medical device as recited-in claim 64, wherein the
mechanical fixation agent is a wire.
69. The medical device as recited in claim 64, wherein the
mechanical fixation agent is an anchor.
70. A tissue acquisition instrument for retrieving tissue at a body
site comprising a. a longitudinal axis; b. a distal end with a
distal tip configured for advancement within a patient's body; c. a
cutting element having a contracted configuration for delivery to
the body site and an expanded configuration for separating tissue
from the body site; d. a lumen containing a bonding agent and at
least one opening disposed at the distal end for dispensing the
bonding agent to surrounding tissue; and e. a mechanical fixation
element disposed proximal to the distal end which has an expanded
configuration for securing the tissue acquisition instrument at a
predetermined desired location, in order to insure that the tissue
acquisition instrument remains in place during a tissue acquisition
procedure and which has a fully retracted configuration with a
transverse dimension of the bendable legs which is smaller than the
expanded configuration.
71. The tissue acquisition instrument as recited in claim 70,
wherein the instrument is rotatable about the longitudinal axis and
wherein a bushing is disposed on the instrument which is rotatable
relative to the instrument and which has an electrical heating
element disposed on the bushing which cauterizes and bonds to the
bushing when the electrical heating element is energized so that
the instrument is secured to a location without preventing
rotational movement thereof.
72. The tissue acquisition instrument as recited in claim 70,
wherein the instrument is rotatable about the longitudinal axis and
wherein the instrument has a bushing disposed on the instrument
which is rotatable relative to the instrument and wherein the
bonding agent dispensed through the at least one opening affixes
the bushing to the surrounding tissue, so that the instrument is
secured in a desired location without preventing rotational
movement thereof.
73. The tissue acquisition instrument as recited in claim 70,
wherein the bonding agent comprises a surgical adhesive.
74. The tissue acquisition instrument as recited in claim 73,
wherein the surgical adhesive is a cyanoacrylate.
75. The tissue acquisition instrument as recited in claim 70,
wherein the bonding agent is a fibrin glue.
76. The tissue acquisition as recited in claim 70 wherein the
bonding agent is a solvent.
77. A tissue acquisition instrument for retrieving tissue at a body
site comprising: a. a longitudinal axis; b. a distal end with a
distal tip configured for advancement within a patient's body; c. a
cutting element which has a contracted configuration for delivery
to the body site and an expanded configuration for separating
tissue from the body site; d. and a mechanical fixation element
which is a Mallicot structure, which is disposed proximal to the
distal end, which has an expanded configuration for securing the
tissue acquisition instrument at a predetermined desired location,
in order to insure that the tissue acquisition instrument remains
in place during a tissue acquisition procedure and which has a
fully retracted configuration with a transverse dimension of the
bendable legs which is smaller than the expanded configuration.
78. The tissue acquisition instrument as recited in claim 77,
wherein the mechanical fixation agent is a rolled stent and an
axially movable sleeve and wherein the stent is exposed and unrolls
to engage the surrounding tissue and affix to the distal end of the
medical device when the sleeve is moved proximally to the
stent.
79. The tissue acquisition instrument as recited in claim 77,
wherein the tissue specimen has a transverse dimension and the
Mallicot structure is configured to have a transverse dimension
smaller than the transverse dimension of the tissue specimen.
80. The tissue acquisition instrument as recited in claim 77,
wherein the cutting element has a transverse dimension and the
Mallicot structure is configured to have a transverse dimension
smaller than the transverse dimension of the cutting element.
81. A tissue acquisition instrument for retrieving a tissue
specimen at a body site comprising: a. a longitudinal axis; b. a
distal end with a distal tip configured for advancement within a
patient's body; c. a cutting element which has a contracted
configuration for delivery to the body site and an expanded
configuration for separating tissue from the body site and d. a
mechanical fixation element which is a radially expandable and
retractable basket, which is disposed proximal to the distal end,
which has an expanded configuration for securing the tissue
acquisition instrument at a predetermined desired location, in
order to insure that the tissue acquisition instrument remains in
place during a tissue acquisition procedure and which has a fully
retracted configuration with a transverse dimension which is
smaller than the expanded configuration.
82. The tissue acquisition instrument as recited in claim 81,
wherein the tissue specimen has a transverse dimension and the
radially expandable and retractable basket is configured to have a
transverse dimension smaller than the transverse dimension of the
tissue specimen.
83. The tissue acquisition instrument as recited in claim 81,
wherein the cutting element has a transverse dimension and the
radially expandable and retractable basket is configured to have a
transverse dimension smaller than the transverse dimension of the
cutting element.
84. A tissue acquisition instrument for retrieving tissue at a body
site comprising: a. a longitudinal axis; b. a distal end with a
distal tip configured for advancement within a patient's body; c.
a-cutting element which has a contracted configuration for delivery
to the body site and an expanded configuration for separating
tissue from the body site; d. a mechanical fixation element
disposed proximal to the distal end which has an expanded
configuration for securing the tissue acquisition instrument at a
predetermined desired location, in order to insure that the tissue
acquisition instrument remains in place during a tissue acquisition
procedure and which has a contracted configuration with a
transverse dimension which is smaller than the expanded
configuration for delivery to a target site; and e. a bushing which
is disposed on the instrument, which is rotatable relative to the
instrument, and which has an electrosurgical element disposed on
the bushing which coagulates and bonds surrounding tissue to the
bushing when the electrosurgical element is energized so that the
instrument is secured in a desired location without preventing
movement thereof.
85. A tissue acquisition instrument for retrieving tissue at a body
site comprising: a. an elongated shaft having a distal portion, a
proximal portion and a longitudinal axis; b. a distal end with a
distal tip configured for advancement within a patient's body; c. a
cutting element which has a contracted configuration for delivery
to the body site and an expanded configuration for separating
tissue from the body site; and d. a mechanical fixation element
disposed proximal to the distal end which has an expanded
configuration for securing the tissue acquisition instrument at a
predetermined desired location, in order to insure that the tissue
acquisition instrument remains in place during a tissue acquisition
procedure, and which has a fully retracted configuration with a
transverse dimension which is smaller than the expanded
configuration and a hinged linkage configured to have a transverse
dimension smaller than a transverse dimension of a tissue
specimen.
86. A method for performing a tissue acquisition procedure
comprising the steps of: a.) providing a tissue acquisition
instrument having a distal end, a proximal end, a longitudinal
axis, and a cutting element; b) placing the distal end of the
instrument in a patient's body, so that the distal end is disposed
in a desired tissue location and c) affixing the distal end of the
instrument to the desired tissue location by performing a step
selected from the group consisting of dispensing a bonding agent
from the distal end into surrounding tissue, activating an
electrosurgical element, activating an electrical heating element,
and combinations thereof.
87. The method as recited in claim 86, wherein the step of affixing
the distal end of the instrument is performed by dispensing a
bonding agent from the distal end into surrounding tissue.
88. The method of claim 87, wherein the bonding agent is selected
from the group consisting of adhesives, solvents, and combinations
thereof.
89. The method as recited in claim 86, wherein the step of affixing
the distal end of the instrument is performed by activating an
electrosurgical element and operating it to coagulate tissue
surrounding the distal end of the instrument, to an extent that the
tissue bonds to the instrument distal end.
90. The method as recited in claim 86, wherein the step of affixing
the distal end of the instrument is performed by activating an
electrical heating element and operating it to cauterize tissue
surrounding the distal end of the instrument, to an extent that the
tissue bonds to the instrument distal end.
91. A biopsy device for separating a tissue specimen from a target
site within a patient, comprising: a. an elongated shaft having a
distal shaft portion, a proximal shaft portion, a tissue
penetrating distal tip and a longitudinal axis; b. a radially
expandable, longitudinally oriented tissue cutting component which
is secured to the distal shaft portion proximal to the distal tip,
which has a distal end and a proximal end and which has a
contracted configuration for delivery to the target site and an
expanded configuration for cutting the tissue specimen from
supporting tissue at the target site; and c. a tissue fixation
component disposed on the elongated shaft between the proximal and
distal ends of the tissue cutting component to be fixed to the
tissue specimen.
92. The device of claim 91 wherein the tissue fixation component
includes a bushing which is disposed on the shaft between the ends
of the tissue cutting component, which has at least one discharge
opening and which is rotatable relative to the shaft, and wherein a
bonding agent is dispensed through the at least one opening to
affix the bushing to the tissue specimen.
93. The device of claim 91, wherein the bonding agent is at least
in part a surgical adhesive.
94. The device of claim 93 wherein the surgical adhesive is at
least in part a cyanoacrylate.
95. The device of claim 91, wherein the bonding agent is at least
in part a fibrin glue.
96. The device of claim 91 wherein the bonding agent is at least in
part a solvent.
97. The device of claim 91, wherein the tissue fixation component
includes a Mallicot structure.
98. The device of claim 91, wherein the tissue fixation component
includes an expandable stent.
99. The device of claim. 98 wherein an axially movable sleeve is
disposed about the expandable stent, and removal of the sleeve
allows the stent to expand and thereby be fixed to the tissue
specimen.
100. The device of claim 91, wherein the tissue fixation component
includes a radially expandable and retractable basket.
101. The device of claim 91 wherein the tissue fixation component
has at least one expandable band.
102. The device of claim 101 wherein the at least one expandable
band is split at its center to form a tissue engaging protruding
portion.
103. The device of claim 102 wherein the tissue engaging protruding
portion extends distally.
104. The device of claim 103 wherein the tissue engaging protruding
portion extends proximally.
105. The device of claim 101 wherein the tissue fixation component
has a plurality of protruding portions, with at least one
protruding portion extending distal and at least one protruding
portion extending proximal.
106. The device of claim 105 wherein the protruding portions are
part of split bands.
107. The device of claim 91 wherein the penetrating distal tip has
an electrosurgical tissue cutting element.
108. The device of claim 107 wherein the electrosurgical tissue
cutting element lies in a plane perpendicular to the longitudinal
axis of the elongated shaft.
109. The device of claim 107 wherein the electrosurgical tissue
cutting element is configured for connection to a RF power source.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to methods and devices for
ensuring that a medical instrument remains in a desired location
within a patient's body during a medical procedure, and more
particularly to methods and devices for affixing a distal end of
the medical instrument to the desired location using adhesives.
BACKGROUND OF THE INVENTION
[0002] It is often desirable and frequently necessary to sample or
remove a portion of tissue from humans and other animals,
particularly in the diagnosis and treatment of patients with
cancerous tumors, pre-malignant conditions, and other diseases or
disorders.
[0003] Typically, in the case of cancer, particularly cancer of the
breast, there is a great emphasis on early detection and diagnosis
through the use of screening modalities, such as physical
examination, and particularly mammography, which is capable of
detecting very small-abnormalities, often nonpalpable. When the
physician establishes by means of a mammogram or other screening
modality, such as ultrasound, that suspicious circumstances exist,
a biopsy must be performed to capture tissue for a definitive
diagnosis as to whether the suspicious lesion is cancerous. Biopsy
may be done by an open or percutaneous technique. Open biopsy is a
surgical procedure using a scalpel and involving direct vision of
the target area, for removing the entire mass (excisional biopsy)
or a part of the mass (incisional biopsy). Percutaneous biopsy, on
the other hand, is usually done with a needle-like instrument
through a relatively small incision, blindly or with the aid of an
artificial imaging device, and may be either a fine needle
aspiration (FNA) or a core biopsy. In FNA biopsy, individual cells
or clusters of cells are obtained for cytologic examination and may
be prepared such as in a Papanicolaou smear. In core biopsy, as the
term suggests, a core or fragment of tissue is obtained for
histologic examination which may be done via a frozen section or
paraffin section.
[0004] The type of biopsy utilized depends in large part on
circumstances present with respect to the patient, including the
location of the lesion(s) within the body, and no single procedure
is ideal for all cases. However, core biopsy is extremely useful in
a number of conditions and is being used more frequently by the
medical profession.
[0005] When an open surgical biopsy procedure is indicated, current
practice dictates the use of lesion localization needles and
devices, commonly referred to as "localization wires", for use in
localizing or marking non-palpable lesions and tumors within the
body. These devices generally comprise a hypodermic needle or
cannula which is inserted into the body under local anesthesia to
the lesion or tissue of interest. The wire marker, or localization
wire, is then passed through the cannula and extends through the
lesion of interest so that the distal end thereof is anchored
beyond the lesion. Thus, the lesion is marked for subsequent
surgical procedures such as excision or biopsy. The anchoring
procedure is typically accomplished by means of mechanical
structure disposed at the distal end of the wire marker, such as a
barb, hook, or the like, which is attached to surrounding tissue.
After marking the lesion with the wire marker, the cannula is
usually removed from the body, leaving the wire in place and
extending from the body, for subsequent use by the surgeon during
the biopsy procedure in identifying the lesion location. However,
it often occurs that the barb or hook at the distal end of the wire
marker attaches to something other than the tumor or lesion. For
example, in the case of breast biopsies, the breast will typically
be placed in compression during the imaging procedure in order to
properly identify the location of the target lesion and place the
localization wire. However, breast tissue is comprised of fibrous
bands which, in compression, may be close to the target lesion and
inadvertently engaged by the barb of the localization wire. Later,
when the breast is released from compression prior to the surgical
procedure, the fibrous bands will move away from the target lesion,
and the distal end of the localization wire may thus move a
substantial distance away from the target lesion.
[0006] It would be desirable, therefore, to develop a localization
wire system and method wherein the distal end of the localization
wire could be positively attached to the target lesion in order to
minimize the possibility of migration of the distal end of the
localization wire away from the target lesion between the imaging
and surgical procedures.
[0007] In circumstances where a core biopsy procedure is indicated,
various systems are available. Such systems are shown, for example,
in U.S. Pat. No. 5,526,822 to Burbank et al, which discloses a
probe having a laterally disposed tissue receiving port at the
distal end thereof for acquiring relatively small tissue samples,
and in U.S. Pat. No. 5,111,828 to Kornberg et al., which discloses
a probe having an axially disposed tissue receiving port at the
distal end thereof for acquiring relatively large intact tissue
samples. Both of these patents are expressly incorporated by
reference herein.
[0008] U.S. application Ser. No. 09/057,303 to Burbank et al.,
commonly assigned with the present application and expressly
incorporated by reference herein, discloses still another core
biopsy apparatus, which advantageously permits the acquisition of
tissue samples which are larger in diameter than the diameter of
the instrument lumen, thereby greatly increasing the chances of
completely removing the target lesion and leaving "clean" margins
thereabout.
[0009] As in the case of localization wires, there is some risk in
using any of the foregoing devices that the distal end of the
instrument will migrate away from the target lesion during the
biopsy procedure, thereby reducing the likelihood of removing
target tissue. Heretofore, in the case of core biopsy procedures,
the risk of this occurrence is minimized by employing image
guidance techniques during the entire tissue removal procedure. For
example, in the case of the '822 Burbank et al. patent, a
stereotactic imaging guidance system is typically utilized during
the disclosed procedure. One disadvantage of this approach,
however, is that the patient's breast must remain in compression
during the entire procedure, with attendant discomfort and
increased procedural difficulty, in order to properly utilize the
imaging equipment. Furthermore, stereotactic imaging equipment or
other suitable alternatives can cost as much as $400,000 or more
and is not in the usual inventory of a typical community hospital.
It would therefore be quite advantageous if a method and apparatus
could be developed which would permit the uncoupling of the imaging
environment from the procedural environment without undue risk that
the active or cutting end of the core biopsy instrument would
migrate away from the target lesion during the interval between the
imaging procedure and the biopsy procedure.
SUMMARY OF THE INVENTION
[0010] The present invention solves the problems outlined above by
describing devices and methods for securely affixing a localization
wire to desired tissue in a patient's body, so that after the
patient is moved from the imaging environment to the procedural
environment, the practitioner will have assurance that the
localization wire is still accurately placed. Additionally, devices
and methods are described for ensuring that the distal end of a
tissue acquisition instrument, such as a biopsy instrument, is
securely affixed to a particular target area, such as a lesion, in
a patient's body, thereby advantageously permitting the imaging
environment to be uncoupled from the procedural environment so that
expensive and often unavailable imaging equipment, such as
stereotactic imaging equipment, need not be used.
[0011] More particularly, in one aspect of the invention a medical
device is provided comprising a tube having a distal end, a
proximal end, and a longitudinal axis, wherein the device is
adapted for placement of the distal end thereof into a patient's
body at a desired location. The medical device includes a fixation
agent, which may comprise any one of a bonding agent, a mechanical
fixation agent, or an electrosurgical coagulation element, disposed
on the distal end thereof, which is adapted for affixing the distal
end of the medical device at the desired location.
[0012] The medical device may comprise for example, a localization
wire for use in connection with an open biopsy procedure.
Alternatively, the device may comprise a tissue acquisition
instrument, such as a biopsy instrument. In the preferred
embodiment, the fixation agent is a bonding agent, comprising a
surgical adhesive, glue, or solvent.
[0013] In another aspect of the invention, a tissue acquisition
instrument is provided for retrieving body tissue, having a
longitudinal axis and which comprises a distal end adapted for
entry into a patient's body, a cutting element disposed on the
instrument for cutting surrounding tissue, and structure disposed
on the distal end for securing the tissue acquisition instrument at
a predetermined desired location, in order to ensure that the
tissue acquisition instrument remains in place during a tissue
acquisition procedure so that desired tissue is properly
acquired.
[0014] In yet another aspect of the invention, a method of
performing a medical procedure is provided, using a medical device
comprising a tube having a distal end, a proximal end, and a
longitudinal axis. The method first comprises the step of placing
the distal end of the tube in a patient's body, so that the distal
end is disposed in a desired tissue location. Then, a bonding agent
is dispensed for the tube into tissue surrounding the distal end,
so that the distal end of the tube becomes affixed to the desired
tissue location.
[0015] In still another aspect of the invention, a method is
provided for performing a tissue acquisition procedure using a
tissue acquisition instrument having a distal end, a proximal end,
a longitudinal axis, and a cutting element. In this method, the
distal end of the instrument is placed into a patient's body, so
that the distal end is disposed in a desired tissue location. Then,
the distal end of the instrument is affixed to the desired tissue
location, so that the instrument does not move relative to the
desired tissue location during the tissue acquisition procedure.
The cutting element is then actuated to acquire one or more tissue
samples.
[0016] The invention, together with additional features and
advantages thereof, may best be understood by reference to the
following description taken in conjunction with the accompanying
illustrative drawing.
BRIEF DESCRIPTION OF THE DRAWING
[0017] FIG. 1 is a schematic plan view of a first embodiment of the
present invention, illustrating a catheter for a localization wire
introduction and infusion system wherein an introducer needle for
introducing the localization wire into a patient's body remains in
place during securement of the localization wire to surrounding
tissue using a bonding agent;
[0018] FIG. 2 is a schematic plan view of the introducer needle
used in conjunction with the catheter of FIG. 1;
[0019] FIG. 3 is a schematic plan view of one embodiment of a
localization wire which may be used in conjunction with the
infusion system shown in FIGS. 1 and 2;
[0020] FIG. 3a is a perspective view of the distal end of the
embodiment shown in FIGS. 1-3, wherein the introducer needle is
inserted through the lumen of the catheter;
[0021] FIG. 3b is a perspective view of the distal end of the
embodiment shown in FIGS. 1-3, wherein the introducer needle is
inserted through the lumen of the catheter, and its position within
the catheter lumen is shown in phantom for illustrative
purposes;
[0022] FIG. 3c is a perspective view similar to FIG. 3a, wherein
the localization wire is inserted through the lumen of the
catheter;
[0023] FIG. 4 is a perspective view of a second embodiment of the
present invention, illustrating a second embodiment of a
localization wire introduction and infusion system, wherein an
introducer needle for introducing the localization wire into a
patient's body is removed during securement of the localization
wire to surrounding tissue using a bonding agent;
[0024] FIG. 5 is schematic plan view of the catheter for the system
illustrated in FIG. 4;
[0025] FIG. 6 is a schematic plan view of the introducer needle for
the system illustrated in FIGS. 4 and 5;
[0026] FIG. 6a is a perspective view of the distal end of the
embodiment shown in FIGS. 4-6, wherein the localization wire is
inserted through a lumen of the catheter;
[0027] FIG. 7 is a schematic plan view of a second embodiment of a
localization wire which may be utilized in conjunction with either
of the embodiments of FIGS. 1-3 or 4-6;
[0028] FIG. 8 is a schematic view in isolation illustrating one
embodiment of the present invention for storing and releasing a
bonding agent which is dispensed from a medical instrument for
affixing the medical instrument to surrounding tissue in a
patient's body;
[0029] FIG. 9 is a perspective view of a third embodiment of the
present invention, illustrating a catheter which may be used as a
localization wire and infusion system;
[0030] FIG. 10 is an enlarged perspective view of the distal end of
the cannula illustrated in FIG. 9, showing in greater detail the
perforations in the distal end for infusing a bonding agent to
surrounding tissue;
[0031] FIG. 11 is a perspective view of a modified version of the
embodiment shown in FIGS. 9 and 10, wherein the cannula is
comprised of a braided polymer tubing and the interstices between
the braids function as the infusion openings for infusing bonding
agent to surrounding tissue;
[0032] FIG. 12 is a perspective view of another modified version of
the embodiment shown in FIGS. 9 and 10, wherein the cannula is
comprised of a coil and the interstices between expanded coils
function as the infusion openings for infusing bonding agent to
surrounding tissue;
[0033] FIG. 13 is a perspective view of a biopsy instrument
constructed in accordance with the principles of the present
invention;
[0034] FIG. 14 is a perspective view of a second modified
embodiment of a biopsy instrument having an expandable Mallicot
structure at its distal end for anchoring the instrument at a
particular tissue site;
[0035] FIG. 15 is a perspective view of a third modified embodiment
of a biopsy instrument having a modified expandable Mallicot
structure at its distal end for anchoring the instrument at a
particular tissue site;
[0036] FIG. 16 is a perspective view of a fourth modified
embodiment of a biopsy instrument having an expandable linkage
structure at its distal end for anchoring the instrument at a
particular tissue site, wherein the linkage structure is shown in
its retracted position;
[0037] FIG. 17 is a perspective view of the embodiment shown in
FIG. 16, wherein the linkage structure is shown in its expanded
position;
[0038] FIG. 18 is a perspective view of a fourth modified
embodiment of a biopsy instrument having an extendable "bottle
brush" structure at its distal end for anchoring the instrument at
a particular tissue site;
[0039] FIG. 19 is a perspective view of a fifth modified embodiment
of a biopsy instrument having a nitinol flap structure at its
distal end, expandable upon retraction of a surrounding sleeve, for
anchoring the instrument at a particular tissue site;
[0040] FIG. 20 is a perspective view of a sixth modified embodiment
of a biopsy instrument having a rolled stent structure at its
distal end which unrolls upon retraction of a surrounding sleeve,
for anchoring the instrument at a particular tissue site;
[0041] FIG. 21 is a perspective view of a seventh modified
embodiment of a biopsy instrument having expandable spiral wires at
its distal end for anchoring the instrument at a particular tissue
site; and
[0042] FIG. 22 is a perspective view of an eighth modified
embodiment of a biopsy instrument having an expandable basket at
its distal end for anchoring the instrument at a particular tissue
site.
DETAILED DESCRIPTION OF THE INVENTION
[0043] Referring now more particularly to the drawings, FIGS. 1-3c
illustrate a first embodiment of the invention, wherein a medical
instrument 10 (FIGS. 3a-3c) comprises a catheter 12 (FIGS. 1,
3a-3c), an introducer needle 14 (FIGS. 2, 3a, and 3b), and a
localization wire 16 (FIGS. 3, 3c). In this embodiment, which may
be styled as a "needle in" infusion system, the introducer needle
14 comprises a sharp distal end 18, which is inserted through an
entry hole 20 in the catheter 12 (FIG. 1), so that its tip 18
extends beyond the distal end 22 of the catheter 12, as shown in
FIGS. 3a and 3b. The introducer needle 14 may include a stop 24
having an enlarged diameter, which is adapted to engage the
distally tapering inner sidewall of the catheter 12 at a
predetermined point, as generally shown particularly in FIG. 3b, to
ensure that the tip 18 properly extends beyond the distal end 22 of
the catheter 12. The introducer needle 14 and catheter 12 together
are then introduced into a patient's body (not shown), using known
imaging techniques for guiding localization wires to the site of
tissue to be excised ("target tissue").
[0044] Once the catheter 12 and introducer needle 14 are in
position relative to the target tissue, the introducer needle 14 is
removed proximally from the catheter 12, and the localization wire
16 is inserted distally through the entry hole 20 and pushed
distally through the lumen in the catheter 12, so that the distal
end of the localization wire 16 extends distally of the distal end
of the introducer needle and catheter, as shown in FIG. 3b.
Indicator marks 25 preferably assist the practitioner in ensuring
that the localization wire is properly inserted to the required
depth.
[0045] Localization wires such as the wire 16 typically include
some-type of mechanical anchoring means, such as a barb or hook 26,
for securing the distal end of the localization wire 16 in position
behind the target tissue. However, this approach is often
inadequate, as discussed supra in the Background portion of the
specification, because the tissue to which the hook 26 becomes
attached will often shift relative to the target tissue between the
imaging step of the medical procedure, which is usually a biopsy,
such as a breast biopsy, and the ensuing surgical step, which
usually takes place in a different area of the hospital and
requires transportation and resultant jostling of the patient from
the radiology department to the operating room. The present
invention, therefore, contemplates an advantageous additional step
of employing a bonding agent, which may comprise any known material
which is capable of creating a bond between the distal end of the
medical instrument 10 and surrounding tissue. Once the localization
wire is properly placed at the desired target tissue site, under
imaging guidance, the bonding agent is dispensed from the distal
end of the medical instrument to the surrounding tissue to create
the desired bond. In the embodiment of FIGS. 1-3a, a plurality of
infusion ports 28 are disposed along the length of the distal end
of the catheter 12. Any number of infusion ports (one or more) may
be employed in order to optimize the flow of bonding agent to the
tissue, and they are preferably staggered circumferentially about
the catheter in order to evenly deliver bonding agent about the
circumference of the instrument 10. Various delivery means may be
employed as well. For example, in the illustrated embodiment, the
catheter 12 comprises a proximal hub 30 (FIG. 1), including a
stopcock 32 which is engageable with a syringe (not shown)
containing the bonding agent. When the localization wire is
properly positioned, the practitioner injects the bonding agent
into the lumen (not shown) of the catheter using the syringe with
sufficient pressure that it flows distally through the lumen and is
infused into surrounding body tissue through the infusion ports 28.
The resultant bonding of the distal end of the localization wire 16
to the surrounding target tissue ensures with much greater
certainty than the use of mechanical attachment means alone, such
as the hook 26, that the localization wire will be properly
positioned when the surgical procedure commences, thereby improving
the likelihood that the proper target tissue will be excised with a
minimum incision and resultant trauma to the patient.
[0046] Preferred bonding agents include any known effective
biocompatible bonding materials, such as surgical adhesives,
including cyanoacrylate, fibrin glue, and solvents.
[0047] An alternative to injection of the bonding agent through the
lumen of the medical instrument 10 is illustrated in FIG. 8. The
bonding agent 33 may be stored in a rupturable container 34 which
is disposed in the distal end of the medical instrument 10,
adjacent to the infusion ports 28. When it is desired to release
the bonding agent 33 through the infusion ports, a puncturing
device 36 may be actuated by the practitioner to rupture the
container 34. In the illustrated embodiment, the device 36
comprises a simple "spear" which is actuated distally to rupture
the container, but it may alternatively comprise any suitable
configuration for functioning equivalently. Additionally, it is
within the scope of the invention to employ a chamber for
containing the bonding agent which includes a valved port, wherein
the valve is actuated to an open position by the practitioner to
release the bonding agent. Various other embodiments for
accomplishing this function, as would be known to one of ordinary
skill in the art, are deemed to fall within the scope of the
invention as well.
[0048] Once the localization wire is securely bonded to the
surrounding tissue, the practitioner may withdraw the catheter and
introducer needle assembly, leaving the localization wire in place
to mark the target tissue for the ensuing surgical step in the
biopsy or other medical procedure.
[0049] FIGS. 4-7 illustrate a second "localization wire"
embodiment, wherein like elements to those shown in the first
embodiment are designated by like reference numerals, succeeded by
the letter "a". This system may be styled as a "needle out"
infusion system. In this embodiment, the catheter 12a comprises a
dual lumen extrusion, including first and second lumens 38 and 40,
respectively (FIG. 6a). The first lumen 38 accommodates the bonding
agent, while the second lumen accommodates the localization wire.
The catheter 12a further includes a dual lumen proximal hub 42,
which comprises a localization wire entry port 44 and a stopcock
32a.
[0050] In operation, the introducer needle 14a is disposed
coaxially outside of the catheter 12a, as illustrated in FIG. 4,
and the instrument 10a is inserted into the patient's body in known
fashion, under conventional imaging guidance. The localization wire
16a is inserted distally through the port 44, either before or
after introduction of the instrument 10a into the patient's body.
As in the first embodiment, once the instrument 10a is placed, the
localization wire 16a is advanced distally until the indicator
marks 25a indicate to the practitioner that the distal hook 26a is
distal of the distal end of the catheter 12a and of the target
lesion, as shown by the imaging equipment. The localization wires
of FIGS. 3 and 7 may be used interchangeably in either of the two
disclosed embodiments, and are substantially identical except that
the localization wire 16a includes filaments 46 near its distal end
which provide additional surface area for bonding.
[0051] As in the previous embodiment, once the localization wire is
in the proper position, bonding agent is injected into the catheter
12a, preferably using a syringe which is engaged with the stopcock
32a, so that the bonding agent flows distally through the first
lumen 38 and is infused through the infusion ports 28a. Again, the
infusion ports may be disposed about the catheter, in rows offset
by 90 degrees with respect to one another, or otherwise staggered
so that the bonding agent is evenly disposed about the catheter.
Alternatively, as in the previous embodiment, the bonding agent may
be stored in the distal end of the instrument 10a using an
apparatus like that illustrated in FIG. 8. It is within the scope
of this invention, as well, to store or inject two or more bonding
agent compounds, comprising a reactant and a catalyst, at the
injection site, and to mix the reactant and catalyst together at
the appropriate time to catalyze a bonding agent.
[0052] Once the bonding agent has been injected, but before it has
solidified, the catheter 12a and introducer needle 14a are
withdrawn from the patient's body, leaving the localization wire in
place.
[0053] Still a third embodiment, which functions in a manner
equivalent to that of a localization wire is illustrated in FIGS. 9
and 10. In this embodiment, a catheter 48, which comprises a
proximal hub 50, a distal end 52, and a lumen 54, is insertable
into a patient's body using conventional image guidance techniques,
so that the distal end 52 is disposed at a desired target tissue
site. Once properly located, a bonding agent 33 is infused through
one or more infusion ports 56 to surrounding target tissue, in
order to bond the distal end of the catheter 48 to the surrounding
tissue. Again, as in the previous embodiments, the bonding agent
may be injected into the lumen 54 of the catheter through the
proximal hub 50, or may alternatively be stored in the distal end
52 of the catheter and selectively released at the desired
time.
[0054] FIGS. 11 and 12 illustrate two alternative embodiments for
the outer tube 58 of the catheter in any of the foregoing
embodiments. In FIG. I 1, the tube 58 comprises a stainless steel
braid, the proximal end 60 of which is encapsulated by a polymer,
such as polyamide, and the distal end 62 of which is exposed. The
exposed distal end is preferably approximately 1-2 centimeter (cm)
in length, though it may be longer or shorter if desired. In
operation, interstices 64 between bands 66 of the exposed braided
portion 62 function as openings for permitting infusion of bonding
agent to surrounding tissue, instead of the infusion ports
disclosed in the preceding embodiments. If the exposed braided
portion is expanded, the interstices will be enlarged and will
permit the flow of more bonding agent therethrough.
[0055] In a manner in some respects similar to the embodiment of
FIG. 11, the FIG. 12 embodiment comprises an outer tube 58 having a
sleeve 68 surrounding a coil 70 of suitable material. In the distal
end of the tube 58, the coil 70 may be stretched to create
interstices 72 between bands 74 of the coil. Bonding material may
be infused, as desired, outwardly through the interstices 72 of the
expanded coil, and then through holes 76 in the sleeve 68 to
surrounding tissue. Alternatively, the sleeve could be retracted to
expose the coil, in which case the sleeve holes 76 would be
unnecessary.
[0056] FIG. 13 illustrates the distal end of a medical instrument
78 which is shown and described in co-pending application Ser. No.
09/057,303, commonly assigned with the present application and
expressly incorporated by reference herein. The instrument 78
comprises a tissue acquisition or biopsy instrument and preferably
includes a tip 80 having an electrosurgical element 82 for entering
tissue, and a shaft 84, on which is disposed a radially extendable
and retractable cutting element or wire 86. The cutting element 86
is preferably energized by RF energy provided by an electrosurgical
generator.
[0057] In operation, the instrument 78 is moved axially to a
position wherein the distal tip 80 is preferably distal to a target
lesion or tissue to be removed, using a suitable imaging technique;
In the prior art, such imaging techniques for biopsy procedures and
the like typically include the use of a stereotactic or sonographic
imaging system, both of which are relatively expensive and not
always available in an average community hospital. This approach is
designed to combine the imaging and cutting steps so that both
occur simultaneously. For example, in the case of a breast biopsy
procedure, the breast is clamped in order to effectively utilize
the imaging equipment, after which the instrument is inserted into
the breast under imaging guidance to the lesion location. Then,
under continued imaging guidance, the cutting element is actuated
and the target tissue removed.
[0058] However, an important advantage of the present invention is
the ability to "uncouple" the imaging environment from the
procedural environment in a typical surgical or biopsy procedure,
and the resultant important ability to utilize unmodified
mammography equipment, readily available in most hospitals, to
position the distal end of the instrument during the imaging step,
rather than expensive and specialized stereotactic equipment. Then,
the procedural step may occur later, in another area of the
hospital. In the case of breast biopsies, this "uncoupling" also
permits the patient's breast to be unclamped for the procedural
step, resulting in increased patient comfort and easier working
conditions for the practitioner.
[0059] These advantages are made possible because the inventive
apparatus and technique permits the securement of the distal end of
the instrument to the target tissue or lesion with sufficient
confidence that the patient may be moved to the procedural
environment without fear of having it slip away from the target
tissue. This securement is accomplished using a fixation agent,
which preferably comprises a bonding agent like that disclosed in
connection with the foregoing localization wire and catheter
embodiments. In a manner similar to those embodiments, once the
instrument is positioned in a desired position, the bonding agent
is injected into a lumen of the instrument, or, alternatively, in a
manner like that described supra, released from a container or
chamber in the distal end of the instrument, so that it may be
infused from one or more infusion ports 88 disposed on the distal
end of the instrument. Preferably, the ports 88 are disposed on a
bushing or sleeve 90 which has a linear slot 92 for permitting
passage of the cutting element 86 as it is extended and retracted
radially, and which is rotatable relative to the shaft 84. Thus,
when the bonding agent is infused to the surrounding tissue, so
that the bushing 90 is affixed in place relative to the surrounding
tissue, the cutting element 86 will still be rotatable on the
underlying shaft 84 in order to permit circumferential cutting of
tissue, as desired, during the later procedural step. Suitable care
is taken that only a sufficient amount of bonding agent is
dispensed to bond the bushing to surrounding tissue, and not the
shaft or tip of the instrument, in order that the shaft and tip
continue to be rotatable relative to the bushing.
[0060] Of course, the bushing 90 may be constructed in number of
alternative ways, as will be apparent to those of ordinary skill in
the art. For example, as shown in FIGS. 11 and 12, the bushing
could be comprised of a braided or coil material, so that
interstices between braids or coils thereof could function as the
infusion openings.
[0061] Rather than using a bonding agent, a mechanical fixation
agent may be utilized to secure the distal end of the instrument to
surrounding tissue. For example, FIG. 14 illustrates an alternative
embodiment to that of FIG. 13, wherein a mechanical fixation
structure 94 is utilized to secure the distal end of the instrument
to surrounding tissue, rather than a bonding agent. In this
embodiment, wherein like elements to those of FIG. 13 are
designated by like reference numerals, succeeded by the letter "b",
the mechanical fixation structure 94 comprises an expandable
Mallicot structure, having a rotatable bushing 90b and a plurality
of expandable bands 96. Actuating pushrods 98, of which there are
preferably four, arranged circumferentially 90 degrees apart, are
provided to actuate the bands 96 between their expanded positions
(as shown), in which they are positioned to anchor the distal tip
80b to the desired tissue site, and their retracted positions.
[0062] FIG. 15 illustrates another modified embodiment which is
similar to that of FIG. 14, and wherein like elements to those of
FIG. 14 are designated by like reference numerals, succeeded by the
letter "c". The only difference between this embodiment and the
FIG. 14 embodiment is that the bands 96c are split at their
centers, to form protruding portions 100, for the purpose of
permitting further radial extension of each band and to also permit
the protruding portions 100 to attach themselves to adjacent
tissue.
[0063] FIGS. 16 and 17 schematically illustrate still another
modified mechanical fixation structure 94d, comprising a linkage,
which may be substituted for the structures 94 and 94c of FIGS. 14
and 15, respectively, wherein FIG. 16 illustrates the linkage in
its retracted configuration and FIG. 17 illustrates it in its
radially expanded configuration.
[0064] FIG. 18 schematically illustrates yet another modified
mechanical fixation structure 94e, comprised of a plurality of
radially retractable and extendable wires 102.
[0065] FIG. 19 schematically illustrates still another modified
mechanical fixation structure 94f, of the bone anchor type,
comprised of a nitinol tube 104 and radially expandable flaps
106.
[0066] In FIG. 20, there is shown another modified mechanical
fixation structure 94g, comprised of a rolled stent which may be
unrolled to expand radially and provide an anchoring function by
axially retracting a sleeve 108.
[0067] FIG. 21 shows still another modified mechanical fixation
structure 94h comprised of a plurality of extendable wires 110.
[0068] FIG. 22 illustrates a modified mechanical fixation structure
94i which comprises a radially expandable and retractable
basket.
[0069] Any of the foregoing mechanical fixation structures may be
interchangeably employed in the embodiments of FIGS. 14 and 15, and
it is within the scope of this invention to also employ other
mechanical fixation structures which are known conventionally for
anchoring medical devices in the body.
[0070] Still another means for bonding the distal end of the
instrument 78 to surrounding tissue, which is within the scope of
the present invention, is to apply RF energy to the tissue, using
an electrosurgical coagulation element. The electrosurgical
coagulation element may comprise one of the existing
electrosurgical elements 82 or 86, or preferably another
coagulation element 112 (FIG. 13) which may be disposed on or near
the bushing 90. Activation of the coagulation element 112 for a
short interval coagulates the tissue surrounding the tissue,
thereby bonding the bushing to the tissue. Alternatively, the
element 112 could comprise a heating rod for cauterizing tissue,
similar to the function of a branding iron, to produce the same
type of bonding effect by "sticking" the cauterized tissue to the
distal end of the instrument.
[0071] This approach may also be utilized in the localization wire
embodiments illustrated in FIGS. 1-12, by employing an
electrosurgical coagulation element on the distal end thereof,
which is connected to a suitable-electrosurgical generator, or,
alternatively, by employing an electrical heating element for
cauterizing tissue.
[0072] While this invention has been described with respect to
various specific examples and embodiments, it is to be understood
that the invention is not limited thereto and that it can be
variously practiced within the scope of the following claims.
* * * * *