U.S. patent application number 11/894467 was filed with the patent office on 2007-12-27 for energy based devices and methods for treatment of patent foramen ovale.
This patent application is currently assigned to Cierra, Inc.. Invention is credited to Jose Alejandro, Mark E. Deem, Dan Francis, Hanson S. III Gifford, Kenneth Horne, William Malecki.
Application Number | 20070299434 11/894467 |
Document ID | / |
Family ID | 32996390 |
Filed Date | 2007-12-27 |
United States Patent
Application |
20070299434 |
Kind Code |
A1 |
Malecki; William ; et
al. |
December 27, 2007 |
Energy based devices and methods for treatment of patent foramen
ovale
Abstract
Methods and apparatus for treatment of patent foramen ovale
(PFO) provide for applying energy to tissues adjacent the PFO with
a catheter device to substantially close the PFO acutely. Apparatus
generally includes a catheter device having at least one energy
transmission member at or near its distal end configured to apply
energy to PFO tissues to acutely, substantially close the PFO.
Applied energy may be monopolar or bipolar radiofrequency energy or
any other suitable energy, such as laser, microwave, ultrasound,
resistive heating or the like. Some embodiments of a catheter
device further include one or more tissue apposition members near
the distal end for helping bring PFO tissues together, such as a
PFO covering member, a vacuum applying member and/or the like. PFO
closure via energy-based approaches of the invention may help
prevent stroke, treat migraine headache, and possibly treat or
prevent other medical conditions.
Inventors: |
Malecki; William; (San
Francisco, CA) ; Francis; Dan; (Mountain View,
CA) ; Horne; Kenneth; (Palo Alto, CA) ; Deem;
Mark E.; (Mountain View, CA) ; Gifford; Hanson S.
III; (Woodside, CA) ; Alejandro; Jose;
(Sunnyvale, CA) |
Correspondence
Address: |
CIERRA, INC. &TOWNSEND & TOWNSEND AND CREW, LLP
TWO EMBARCADERO CENTER
EIGHTH FLOOR
SAN FRANCISCO
CA
94111-3834
US
|
Assignee: |
Cierra, Inc.
2761 Fair Oaks Ave
Redwood City
CA
94063
|
Family ID: |
32996390 |
Appl. No.: |
11/894467 |
Filed: |
August 20, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11249566 |
Oct 12, 2005 |
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11894467 |
Aug 20, 2007 |
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10958533 |
Oct 4, 2004 |
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11249566 |
Oct 12, 2005 |
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10679245 |
Oct 2, 2003 |
6939348 |
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10958533 |
Oct 4, 2004 |
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60490082 |
Jul 24, 2003 |
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60478035 |
Jun 11, 2003 |
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60458854 |
Mar 27, 2003 |
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Current U.S.
Class: |
606/27 |
Current CPC
Class: |
A61B 2018/00351
20130101; A61B 2018/00285 20130101; A61B 2018/0063 20130101; A61B
2018/00875 20130101; A61B 18/1492 20130101; A61B 2018/00791
20130101; A61B 2017/306 20130101; A61B 2090/3614 20160201; A61B
2018/00898 20130101; A61B 2018/00214 20130101; A61B 2017/00867
20130101; A61B 17/3439 20130101; A61B 2018/1472 20130101; A61B
2018/00702 20130101; C08L 2201/12 20130101; A61B 2018/00261
20130101; A61B 2017/3445 20130101; A61B 2018/00619 20130101; A61B
18/1445 20130101; A61B 17/0057 20130101; A61B 2018/00291 20130101;
A61B 2017/00575 20130101 |
Class at
Publication: |
606/027 |
International
Class: |
A61B 18/18 20060101
A61B018/18 |
Claims
1. A method for closing a patient's patent foramen ovale,
comprising: drawing at least one of the patient's primum and
secundum toward the other, the primum and the secundum being
portions of the patient's atrial septum; applying energy to the
primum and secundum; and welding at least a portion of the primum
and a portion of the secundum together to at least partially seal
the patent foramen ovale.
2. The method of claim 1 wherein welding includes welding at a
first location of the atrial septum, and wherein the method further
includes welding at least one additional location of the atrial
septum.
3. The method of claim 1 wherein welding includes spot welding the
atrial septum.
4. The method of claim 1, further comprising at least partially
sealing the patent foramen ovale without leaving an implantable
sealing device in the patient's heart.
5. The method of claim 1 wherein applying energy includes applying
RF energy.
6. The method of claim 1 wherein applying energy includes applying
sonic energy.
7. The method of claim 1 wherein drawing at least one of the
patient's primum and secundum toward the other includes clamping
the primum and secundum between a first electrode and a second
electrode.
8. The method of claim 1 wherein welding the tissue includes
melting the tissue.
9. The method of claim 1, further comprising applying a vacuum to
bring atrial septal tissue into contact with an electrode.
10. The method of claim 1, further comprising puncturing the atrial
septum.
11. The method of claim 1, further comprising: puncturing the
atrial septum; and passing at least one electrode through the
punctured septum.
12. The method of claim 1 wherein applying energy to the primum and
the secundum includes shrinking at least one of the primum and the
secundum.
13. The method of claim 1 wherein welding the tissue includes
fusing the tissue acutely.
14. The method of claim 1 wherein welding the tissue includes
fusing the tissue acutely to at least partially seal the patent
foramen ovale, and wherein the method further comprises allowing
the patient's healing process to further seal the patent foramen
ovale.
15. The method of claim 1, the method comprising closing the
patient's patent foramen ovale without piercing the patient's
atrial septum tissues.
16. A method for closing a patient's patent foramen ovale,
comprising: applying a vacuum to the patient's atrial septum, the
atrial septum including a primum and a secundum; applying energy to
the primum and secundum; and welding at least a portion of the
primum and a portion of the secundum together to at least partially
seal the patent foramen ovale.
17. The method of claim 16 wherein welding includes welding at a
first location of the atrial septum, and wherein the method further
includes welding at least one additional location of the atrial
septum.
18. The method of claim 16 wherein welding includes spot welding
the atrial septum.
19. The method of claim 16, further comprising at least partially
sealing the patent foramen ovale without leaving an implantable
sealing device in the patient's heart.
20. The method of claim 16 wherein applying energy includes
applying RF energy.
21. The method of claim 16 wherein welding the tissue includes
melting the tissue.
22. The method of claim 16 wherein applying energy to the primum
and the secundum includes shrinking at least one of the primum and
the secundum.
23. The method of claim 16 wherein welding the tissue includes
fusing the tissue acutely.
24. The method of claim 16 wherein welding the tissue includes
fusing the tissue acutely to at least partially seal the patent
foramen ovale, and wherein the method further comprises allowing
the patient's healing process to further seal the patent foramen
ovale.
25. The method of claim 16, the method comprising closing the
patient's patent formamen ovale without piercing the primum or
secundum tissues.
26. A method for closing a patient's patent foramen ovale,
comprising: drawing at least one of the patient's primum and
secundum tissues toward the other as to bring the tissues together,
the primum and the secundum being portions of the patient's atrial
septum; applying energy to the primum and secundum; and welding at
least a portion of the primum and a portion of the secundum
together to at least partially seal the patent foramen ovale.
27. The method of claim 26, the method comprising closing the
patient's patent formamen ovale without piercing the primum or
secundum tissues.
28. A method for closing a patient's patent foramen ovale,
comprising: applying a vacuum to the patient's atrial septum
tissues as to bring the tissue together, the atrial septum
including a primum and a secundum; applying energy to the primum
and secundum; and welding at least a portion of the primum and a
portion of the secundum together to at least partially seal the
patent foramen ovale
29. The method of claim 28, the method comprising closing the
patient's patent foramen ovale without piercing the patient's
atrial septum tissues.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 11/249,566 (Attorney Docket No.
022128-000202US), filed Oct. 12, 2005, which is a continuation of
U.S. patent application Ser. No. 10/958,533 (Attorney Docket No.
022128-000201US), filed Oct. 4, 2004, which was a divisional of
U.S. patent application Ser. No. 10/679,245 (Attorney Docket No.
022128-000200US), filed Oct. 2, 2003, now U.S. Pat. No. 6,939,348,
which claimed priority to U.S. Provisional Patent Application Nos.
60/458,854 (Attorney Docket No. 022128-000100US (formerly
020979-002100US)), filed Mar. 27, 2003; 60/478,035 (Attorney Docket
No. 022128-000110US (formerly 020979-002110US)), filed Jun. 11,
2003; and 60/490,082 (Attorney Docket No. 022128-000120US (formerly
020979-002120US)), filed Jul. 24, 2003, the full disclosures of
which are incorporated herein by reference. This application is
related to U.S. patent application Ser. No. 10/665,974 (Attorney
Docket No. 022128-000300US (formerly 020979-002600US)), filed Sep.
18, 2003, the full disclosure of which is incorporated herein by
reference.
BACKGROUND OF THE INVENTION
[0002] The invention generally relates to medical devices and
methods. More specifically, the invention relates to energy based
devices and methods for treatment of patent foramen ovale.
[0003] Fetal blood circulation is much different than adult
circulation. Because fetal blood is oxygenated by the placenta,
rather than the fetal lungs, blood is generally shunted away from
the lungs to the peripheral tissues through a number of vessels and
foramens that remain patent (i.e., open) during fetal life and
typically close shortly after birth. For example, fetal blood
passes directly from the right atrium through the foramen ovale
into the left atrium, and a portion of blood circulating through
the pulmonary artery trunk passes through the ductus arteriosus to
the aorta. This fetal circulation is shown in attached FIG. 1.
[0004] At birth, as a newborn begins breathing, blood pressure in
the left atrium rises above the pressure in the right atrium. In
most newborns, a flap of tissue closes the foramen ovale and heals
together. In approximately 20,000 babies born each year in the US,
the flap of tissue is missing, and the hole remains open as an
atrial septal defect (ASD). In a much more significant percentage
of the population (estimates range from 5% to 20% of the entire
population), the flap is present but does not heal together. This
condition is known as a patent foramen ovale (PFO). Whenever the
pressure in the right atrium rises above that in the left atrium,
blood pressure can push this patent channel open, allowing blood to
flow from the right atrium to the left atrium.
[0005] Patent foramen ovale has long been considered a relatively
benign condition, since it typically has little effect on the
body's circulation. More recently, however, it has been found that
a significant number of strokes may be caused at least in part by
PFO. In some cases, stroke may occur because a PFO allows blood
containing small thrombi to flow directly from the venous
circulation to the arterial circulation and into the brain, rather
than flowing to the lungs where the thrombi can become trapped and
gradually dissolved. In other cases, thrombi might form in the
patent channel of the PFO itself and become dislodged when the
pressures cause blood to flow from the right atrium to the left
atrium. It has been estimated that patients with PFOs who have
already had cryptogenic strokes have a 4% risk per year of having
another stroke.
[0006] Further research is currently being conducted into the link
between PFO and stroke. At the present time, if someone with a PFO
has two or more strokes, the healthcare system in the U.S. may
reimburse a surgical or other interventional procedure to
definitively close the PFO. It is likely, however, that a more
prophylactic approach would be warranted to close PFOs to prevent
the prospective occurrence of a stroke. The cost and potential
side-effects and complications of such a procedure must be low,
however, since the event rate due to PFOs is relatively low. In
younger patients, for example, PFOs sometimes close by themselves
over time without any adverse health effects.
[0007] Another highly prevalent and debilitating condition--chronic
migraine headache--has also been linked with PFO. Although the
exact link has not yet been explained, PFO closure has been shown
to eliminate or significantly reduce migraine headaches in many
patients. Again, prophylactic PFO closure to treat chronic migraine
headaches might be warranted if a relatively non-invasive procedure
were available.
[0008] Currently available interventional therapies for PFO are
generally fairly invasive and/or have potential drawbacks. One
strategy is simply to close a PFO during open heart surgery for
another purpose, such as heart valve surgery. This can typically be
achieved via a simple procedure such as placing a stitch or two
across the PFO with vascular suture. Performing open heart surgery
purely to close an asymptomatic PFO or even a very small ASD,
however, would be very hard to justify.
[0009] A number of interventional devices for closing PFOs
percutaneously have also been proposed and developed. Most of these
devices are the same as or similar to ASD closure devices. They are
typically "clamshell" or "double umbrella" shaped devices which
deploy an area of biocompatible metal mesh or fabric (ePTFE or
Dacron, for example) on each side of the atrial septum, held
together with a central axial element, to cover the PFO. This
umbrella then heals into the atrial septum, with the healing
response forming a uniform layer of tissue or "pannus" over the
device. Such devices have been developed, for example, by companies
such as Nitinol Medical Technologies, Inc. (Boston, Mass.) and AGA
Medical, Inc. (White Bear Lake, Minn.). U.S. Pat. No. 6,401,720
describes a method and apparatus for thoracoscopic intracardiac
procedures which may be used for treatment of PFO.
[0010] Although available devices may work well in some cases, they
also face a number of challenges. Relatively frequent causes of
complications include, for example, improper deployment, device
embolization into the circulation and device breakage. In some
instances, a deployed device does not heal into the septal wall
completely, leaving an exposed tissue which may itself be a nidus
for thrombus formation. Furthermore, currently available devices
are generally complex and expensive to manufacture, making their
use for prophylactic treatment of PFO impractical. Additionally,
currently available devices typically close a PFO by placing
material on either side of the tunnel of the PFO, compressing and
opening the tunnel acutely, until blood clots on the devices and
causes flow to stop.
[0011] Research into methods and compositions for tissue welding
has been underway for many years. Of particular interest are
technologies developed by McNally et. al., (as shown in U.S. Pat.
No. 6,391,049) and Fusion Medical (as shown in U.S. Pat. Nos.
5,156,613, 5,669,934, 5,824,015 and 5,931,165). These technologies
all disclose energy delivery to tissue solders and patches to join
tissue and form anastamoses between arteries, bowel, nerves, etc.
Also of interest are a number of patents by inventor Sinofsky,
relating to laser suturing of biological materials (e.g., U.S. Pat.
Nos. 5,725,522, 5,569,239, 5,540,677 and 5,071,417). None of these
disclosures, however, show methods or apparatus suitable for
positioning the tissues of the PFO for welding or for delivering
the energy to a PFO to be welded.
[0012] Causing thermal trauma to a patent ovale has been described
in two patent applications by Stambaugh et al. (PCT Publication
Nos. WO 99/18870 and WO 99/18871). The devices and methods
described, however, cause trauma to PFO tissues to hopefully
eventually cause scar tissue formation which will close the PFO.
Using such devices and methods, the PFO actually remains patent
immediately after the procedure and only closes sometime later.
Therefore, a physician may not know whether the treatment has
worked until long after the treatment procedure has been performed.
Frequently, scar tissue may fail to form or may form incompletely,
resulting in a still patent PFO.
[0013] Therefore, it would be advantageous to have improved methods
and apparatus for treating a PFO. Ideally, such methods and
apparatus would help seal the PFO during, immediately after or soon
after performing a treatment procedure. Also ideally, such devices
and methods would leave no foreign material (or very little
material) in a patient's heart. Furthermore, such methods and
apparatus would preferably be relatively simple to manufacture and
use, thus rendering prophylactic treatment of PFO, such as for
stroke prevention, a viable option. At least some of these
objectives will be met by the present invention.
BRIEF SUMMARY OF THE INVENTION
[0014] The present invention generally provides devices and methods
for treating patent foramen ovale (PFO). More specifically, the
devices and methods involve advancing a catheter device to a
position in the heart for treating the patent foramen ovale and
applying energy to (or removing energy from) tissues adjacent a PFO
to substantially close the PFO acutely. By "substantially," it is
meant that a stable tissue bridge will be formed across the PFO,
which will withstand physiologic pressures. A substantially closed
PFO, however, may still have one or more small gaps or openings,
which will in at least some cases close over time via the healing
process. By "acutely," it is meant that the PFO is substantially
closed when the closure procedure is completed. Thus, acute closure
distinguishes devices and methods of the present invention from
prior protocols, which rely on delayed PFO closure via tissue
healing and scarring. "Acutely," for purposes of this application,
does not mean temporarily, since devices and methods of the present
invention will typically provide for permanent (or at least
long-term) PFO closure.
[0015] The phrase "tissues adjacent a PFO," or simply "PFO
tissues," for the purposes of this application, means any tissues
in, around or in the vicinity of a PFO which may be used or
manipulated to help close the PFO. For example, tissues adjacent a
PFO include septum primum tissue, septum secundum tissue, atrial
septal tissue lateral to the septum primum or septum secundum,
tissue within the tunnel of the PFO, tissue on the right atrial
surface or the left atrial surface of the atrial septum and the
like. By "application or removal" of energy, it is meant that
energy may be transferred either to or from PFO tissues. In various
embodiments, any of a number of energy transfer devices and forms
of energy may be used to provide such energy transfer. Types of
energy used may include, for example, radiofrequency energy,
cryogenic energy, laser energy, ultrasound energy, resistive heat
energy, microwave energy and the like.
[0016] Application of energy to (or removal of energy from) tissues
to substantially close the PFO acutely may sometimes be referred to
as "tissue welding." Preferably, tissue welding methods of the
present invention will be performed without using tissue soldering
material or other foreign material. In some embodiments, however,
it may be advantageous to use one or more solder materials. Various
solders and other tissue soldering matrices are described more
fully in U.S. patent application Ser. No. 10/665,974 (Attorney
Docket No. 022128-000300US), which was previously incorporated by
reference. Examples of tissue solders or adhesives which may be
used include, but are not limited to, autologous blood, albumin,
collagen, fibrin, cyanoacrylates, mussel byssus adhesives, polymer
hot melt adhesives and the like.
[0017] In some embodiments of the present invention, devices and
methods further provide for bringing tissues adjacent a PFO
together (or "apposing" tissues). In various embodiments, tissues
may be apposed before, during and/or after application or removal
of energy to the tissues. Generally, energy application or removal
will act to denature collagen in the PFO tissues. If the tissues
are apposed before and/or during denaturation and/or while the
collagen in the tissues is allowed to renature, the collagen in
once-separated tissues binds together to bring the tissues
together. Therefore, although not required, some embodiments of the
invention include one or more devices for bringing (and possibly
holding) tissues together before, during and/or after energy
application or removal. Such devices include, for example, PFO
tissue covering members, which may also be suction or vacuum
application members, expandable members within the PFO tunnel,
distal tip members for contacting a left atrial surface of PFO
tissue and the like. By providing for substantial, acute closure of
a PFO, devices and methods of the invention may be advantageous for
preventing stroke, treating migraine headaches and/or preventing or
treating other medical conditions caused or exacerbated by PFO.
[0018] In one aspect of the present invention, a method of treating
a PFO in a heart involves advancing a catheter device to a position
in the heart for treating the PFO and applying energy to the
tissues with the catheter device to substantially close the PFO
acutely. In some embodiments, as just mentioned, the method further
includes bringing the tissues at least partially together,
preferably using the catheter device but in some embodiments using
a separate device. For example, in some embodiments the tissues are
brought together before applying the energy. Optionally, the
tissues may then be held together while applying the energy. In
some embodiments, the tissues are held together after the energy
has been applied as well. The method may also involve cooling the
tissues after the energy has been applied.
[0019] Bringing the tissues at least partially together may be
accomplished by any of a number of suitable devices and methods. In
one embodiments, for example, the tissues are contacted with a
tissue covering member adjacent a distal end of the catheter
device. The tissue covering member may cause blood pressure in a
left atrium of the heart to bring the tissues at least partially
together. In some embodiments, the tissue covering member may be
further used to apply vacuum force to the tissues.
[0020] Although the catheter device may be positioned in a number
of different locations for treating a PFO, in some embodiments
advancing the catheter involves positioning a distal end of the
catheter in a right atrium of the heart. Advancing the catheter may
also include advancement over a guide catheter or guidewire
extending into the PFO. Optionally, the guide catheter or guidewire
may extend through the PFO into a left atrium of the heart.
[0021] In some embodiments, the method further includes retracting
a sheath portion of the guide catheter to expose an expanding
member within the PFO, the exposed expanding member bringing the
tissues adjacent the PFO at least partially together. Such an
expanding member may provide lateral force to the tissues adjacent
the PFO, for example, and in some embodiments will do so without
extending into the left atrium. As is explained further below, such
expanding members may comprise "fishmouth," two-pronged members in
one embodiment, and may be constructed of shape memory materials,
spring-loaded materials or the like. By spreading PFO tissues
laterally between two prongs (for example), the tissues come
together in the area between the prongs. Optionally, the method may
also include contacting a left atrial surface of at least one of a
septum primum and a septum secundum with a distal portion of the
expanding member and retracting the expanding member to bring the
tissues adjacent the PFO together. For example, the distal portion
may contact the septum primum and pull it toward the right side of
the heart, into contact with the septum secundum. At some point
after the expanding member has been used to appose the tissues
adjacent the PFO, it may be advantageous to retract the expanding
member to a position within the guide catheter. For example, the
expanding member may be retracted in some embodiments before
removing the guide catheter through the main catheter device.
[0022] As mentioned, in some embodiments the catheter device may be
advanced over a guidewire rather than a guide catheter. The
guidewire typically extends through the PFO and may include an
expanding portion along its length for expanding within the PFO.
Optionally, the guidewire may extend into the left atrium, and the
method may optionally include contacting a left atrial surface of
at least one of a septum primum and a septum secundum with a distal
portion of the guidewire and retracting the guidewire to bring the
tissues adjacent the PFO together.
[0023] Any suitable type of energy may be applied to the PFO
tissues to provide acute PFO closure. In some embodiments, for
example, monopolar or bipolar radiofrequency energy is applied,
while in alternative embodiments cryogenic, resistive heat,
ultrasound, microwave, or laser energy, heat energy in the form of
heated fluid such as saline, or the like may be applied. Energy may
be applied by energizing a single conductive member of the catheter
device or multiple conductive members, in various embodiments.
Generally, any suitable devices for energy delivery are
contemplated.
[0024] Some embodiments of the method may further involve
monitoring an amount of energy applied to the tissues. For example,
monitoring the energy may involve monitoring a temperature of the
tissues, an impedance of the tissues and/or the like. Such a method
may further involve determining when a sufficient amount of energy
has been applied to the tissues to acutely close the PFO.
Optionally, the method may also include discontinuing the
application of energy when the sufficient amount of energy has been
applied.
[0025] Any of the above methods may also involve directly
visualizing the PFO and the adjacent tissues using at least one
visualization device coupled with the catheter device. Such a
visualization device may include a fiber optic device, an
ultrasound device or any other suitable visualization device.
[0026] In another aspect of the invention, a method of treating a
PFO in a heart involves advancing a catheter device to a position
in the heart for treating the patent foramen ovale and removing
energy from tissues adjacent the patent foramen ovale with the
catheter device to substantially close the patent foramen ovale
acutely. Removing energy from the tissues may be achieved using any
suitable device(s), such as by contacting the tissues with one or
more cryogenic energy members. Any of the additional or alternative
method steps described above may be applied to this aspect of the
invention.
[0027] In another aspect of the invention, apparatus for treating a
PFO in a heart includes a catheter device having a proximal end and
a distal end and at least one energy transmission member adjacent
the distal end for applying energy to, or removing energy from,
tissues adjacent a PFO to acutely close the PFO. Some embodiments
further include at least one tissue apposition member adjacent the
distal end for at least partially bringing the tissues together. In
some embodiments, the tissue apposition member comprises a tissue
covering member. The tissue covering member may have any suitable
configuration and be constructed from any suitable material(s). In
some embodiments, for example, the tissue covering member has a
suction cup or cone shape.
[0028] In some embodiments, the tissue covering member fully covers
the opening of the PFO to allow blood pressure in a left atrium of
the heart to bring the tissues together. Additionally, the tissue
covering member may comprise a suction member for applying vacuum
force to the tissues to bring the tissues together. Optionally, the
tissue covering member may be expandable from a first delivery
dimension to a second treatment dimension. In some embodiments, the
catheter further comprises a flexible isolation portion disposed
between the tissue covering member and the catheter device to
prevent unwanted movement of the tissue covering member during use.
In some embodiments, the at least one energy transmission member is
coupled with the tissue covering member.
[0029] Some embodiments of the apparatus further include a guide
member for advancing through the PFO, with the catheter device
being slidably disposed over the guide member. The guide member may
include, for example a guide catheter and at least one expandable
member disposed within the guide catheter, wherein the guide
catheter is retractable to expose the expandable member to allow it
to expand within the PFO. The expandable member, in turn, may have
any suitable configuration, but in some embodiments it includes at
least two members that expand apart to provide lateral force to the
tissues adjacent the PFO, such as a "fishmouth" or two-prong
expandable member. When exposed, the expanding member may also
provide dilatory force to the tissues adjacent the PFO. To provide
expandability, the expandable member may be made of shape memory
material, may be spring loaded, and/or the like.
[0030] In alternative embodiments, the guide member may comprise a
guidewire having an expandable portion along its length. For
example, the expandable portion may be a divided portion, the
divided portion comprising expandable shape memory material.
Optionally, the guide member may include at least one tip for
contacting a left atrial surface of the tissues adjacent the PFO.
Such a tip may be conformable to the left atrial surface. The guide
member may be retractable to engage the at least one tip with the
left atrial surface.
[0031] In any of the above embodiments, one or more guide members,
or component parts of a guide member, may act as one or more energy
transmission members. In some embodiments, for example, an
expanding member may act as a monopolar or bipolar radiofrequency
electrode.
[0032] The at least one energy transmission member of the catheter
device may comprise any suitable energy transmission device or
combination of devices. For example, the transmission member may
transmit radiofrequency energy, cryogenic energy, resistive heat
energy, ultrasound energy, microwave energy, laser energy or any
other form of energy for treating PFO tissues. In preferred
embodiments, the energy transmission member comprises a monopolar
or two bipolar radiofrequency transmission members. Such a
transmission member, for example, may be curved to approximate the
curvature of the PFO. In other embodiments, straight transmission
members, mesh or braided transmission members, multiple pin-point
transmission members or the like may be used.
[0033] In some embodiments, the energy transmission member(s) are
coupled with the tissue apposition member. Thus, tissues may be
brought into apposition and energy may be applied using the tissue
apposition member. In some embodiments, energy transmission member
is movable along at least part of a circumference of the at least
one tissue apposition member. In alternative embodiments, the
energy transmission member comprises a guide member for advancing
through the PFO, with the catheter device being slidably disposed
over the guide member. Again, the guide member typically includes
at least one expandable portion for expanding within the PFO to at
least partially bring together the tissues adjacent the PFO, and in
some embodiments the expandable member acts as the energy
transmission member(s). In still other embodiments, energy
transmission members may be coupled with both the tissue apposition
member and the guide member/expandable member.
[0034] Apparatus of the invention may further include at least one
sensor coupled with the catheter device for sensing an amount of
energy delivered to the tissues by the at least one energy
transmission member. Sensors, for example, may be infrared sensors,
thermistors, thermocouples or the like, though any sensors may be
used. Optionally, a microprocessor may be coupled with the at least
one sensor for processing sensed data to determine when the amount
of delivered energy has reached a desired amount of energy.
[0035] These and other embodiments are described in further detail
in the following description related to the appended drawing
figures.
BRIEF DESCRIPTION OF THE DRAWING FIGURES
[0036] FIG. 1 is a diagram of the fetal circulation;
[0037] FIG. 2 is a diagram of a catheter apparatus according to an
embodiment of the present invention, having a conductive element
and closure device, the catheter passing through the inferior vena
cava and right atrium and through the PFO;
[0038] FIG. 3 is a perspective view of a catheter apparatus
according to an embodiment of the present invention;
[0039] FIGS. 3A and 3B are cross-sectional views of the catheter
apparatus in FIG. 3;
[0040] FIG. 4 is a perspective view of a catheter apparatus
according to another embodiment of the present invention;
[0041] FIGS. 5A and 5B are perspective views of a catheter
apparatus according to another embodiment of the present
invention;
[0042] FIG. 6 is a perspective view of a catheter apparatus
according to another embodiment of the present invention;
[0043] FIG. 7 is a perspective view of a catheter apparatus
according to another embodiment of the present invention; and
[0044] FIGS. 8A-8E demonstrate a method for treating a PFO using a
catheter apparatus according to an embodiment of the present
invention.
[0045] FIGS. 9A-9B illustrate a catheter apparatus including a
backstop and inflatable member for treating a PFO according to one
embodiment of the present invention.
[0046] FIG. 10 illustrates a backstop device according to another
embodiment of the present invention.
[0047] FIG. 11 illustrates a coil version of a backstop device
according to another embodiment of the present invention.
[0048] FIG. 12 illustrates a balloon version of a backstop device
according to another embodiment of the present invention.
[0049] FIGS. 13A-13C illustrate a flower petal version of a
backstop device according to another embodiment of the present
invention.
[0050] FIGS. 14A-14D demonstrate treating a PFO using a spring coil
closure device according to another embodiment of the present
invention.
[0051] FIG. 15 demonstrates treating a PFO using a spring coil
closure device according to another embodiment of the present
invention.
[0052] FIG. 16 demonstrates treating a PFO using a spring coil
closure device according to another embodiment of the present
invention.
DETAILED DESCRIPTION OF THE INVENTION
[0053] Devices and methods of the present invention generally
provide for patent foramen ovale (PFO) treatment through
application or removal of energy. Methods involve advancing a
catheter device to a position in the heart for treating the PFO and
applying energy to (or removing energy from) tissues adjacent a PFO
to substantially close the PFO acutely. Terms such as
"substantially," "acutely," and "tissues adjacent the PFO" are
defined above in the Brief Summary of the Invention. Devices of the
invention generally include a catheter device having a proximal end
and a distal end and at least one energy transmission member
adjacent the distal end for applying energy to or removing energy
from tissues adjacent the PFO.
[0054] As mentioned above in the background section, FIG. 1 is a
diagram of the fetal circulation. The foramen ovale is shown, with
an arrow demonstrating that blood passes from the right atrium to
the left atrium in the fetus. After birth, if the foramen ovale
fails to close (thus becoming a PFO), blood may travel from the
right atrium to the left atrium or vice versa, causing increased
risk of stroke, migraine and possibly other adverse health
conditions, as discussed above.
[0055] With reference to FIG. 2, one embodiment of a PFO-treatment
apparatus 100 may be advanced through the vasculature of a patient
to a position in the heart for treating a PFO. In this embodiment,
apparatus 100 includes an elongate catheter device 110 having one
or more tissue apposition members 112 and one or more energy
transmission members 114 at or near its distal end. Optionally,
catheter device 110 may be slidably disposed over a guide member
120, such as a guide catheter (as in FIG. 1), a guidewire, or the
like. Guide member 120 may include, for example, one or more
expanding members 122 or other similar devices for deploying within
the PFO to help appose the adjacent tissues. In some embodiments,
as described further below, expanding members 122 may comprise (or
be coupled with) one or more energy transmission members 114.
Generally, apparatus 100 may be used to bring together tissues
surrounding and/or adjacent the PFO and to transmit energy to the
tissues to close the PFO.
[0056] Although the embodiment in FIG. 2 and many of the
embodiments described below include one or more tissue apposition
members, devices of the present invention do not require such
members. In some embodiments, as mentioned above and as set forth
in the claims, devices may include a catheter device having one or
more energy transmission members for applying or removing energy,
without any components designed for bringing the tissues together.
Therefore, although much of the following discussion focuses on
embodiments including tissue apposition members and the like, such
members are not required.
[0057] Referring now to FIG. 3, one embodiment of a PFO-treatment
apparatus 200 suitably includes a catheter device 210 coupled with
a tissue apposition member 212 at its distal end. One or more
energy transmission members 214 may be disposed through or within
catheter device 210 and/or coupled with tissue apposition member
212. In some embodiments, catheter device 210 is slidably disposed
over a guide catheter 220. Guide catheter 220 may contain one or
more expandable elements 222, such as a guide wire or the like. One
or more radiopaque markers 224, 226 may be included on catheter
device 210, guide catheter 220 or both. Catheter device 210 may
also include an isolation portion 228 for helping to stabilize
tissue apposition member 212 during use, so that it is not caused
to move due to the flexibility of catheter device 210.
[0058] FIGS. 3A and 3B show cross-sectional views of apparatus 200
from the perspective of lines A and B in FIG. 3, respectively. In
FIG. 3A, catheter device 210 is shown, having a guide catheter
lumen 232, two energy transmission member lumens 234 and a vacuum
lumen 236. As shown in FIG. 3B, guide catheter 220 includes an
expandable element lumen 238. Guide catheter lumen 232 may
sometimes be configured with an inner diameter (or "profile") that
is shaped (or "keyed") to allow guide catheter 220 to pass easily
through lumen 232. This feature is demonstrated in FIGS. 3A and 3B,
where guide catheter 220 and guide catheter lumen 232 each have an
ovoid shape.
[0059] In general, catheter device 210 comprises an elongate,
flexible catheter which may be advanced through the vasculature of
a patient to a position in the heart for treating a PFO. Thus,
catheter device 210 may have any suitable length, diameter,
cross-sectional profile and the like, and may be constructed of any
suitable material. Tissue apposition member 212 (or multiple tissue
apposition members in some embodiments) is disposed at or near the
distal end of catheter device 210. Although many different types of
devices may be used to bring tissues of the PFO together, in one
embodiment (shown in FIG. 2) tissue apposition member 212 comprises
a PFO-covering member. PFO-covering tissue apposition member 212
may be positioned to contact adjacent PFO tissues to fully cover,
or block, the opening of the PFO. This blocking of the PFO may
prevent right-to-left shunting of blood and may allow blood
pressure in the left atrium to bring the septum primum and septum
secundum at least partially together to close the PFO. Therefore,
simply by forming a seal or blockage over the PFO, tissue
apposition member 212 may help bring the PFO tissues together to
assist in PFO closure.
[0060] In this and other embodiments, tissue apposition member 212
may also include one or more vacuum members for applying vacuum to
the PFO tissues. In one embodiment, for example, suction lumen 236
(FIG. 3A) may extend from the proximal end to the distal end of
catheter device 210, opening into one or more vacuum-application
apertures at the distal end of tissue apposition member 212. The
vacuum-application aperture(s) may have any suitable configuration,
such as a continuous aperture encircling tissue apposition member
212, multiple apertures encircling tissue apposition member 212 or
in any other suitable configuration at or near its distal end, or
the like. In still another embodiment, vacuum may be applied via a
large, central lumen in tissue apposition member 212. In any case,
vacuum force may be used to bring PFO tissues together and/or to
secure tissue apposition member 212 and thus catheter device 210 to
the PFO tissues.
[0061] Tissue apposition member 212, especially when configured as
a PFO-covering member, may be collapsible/expandable to facilitate
advancement and delivery of catheter device 210. For example,
tissue apposition member 212 may comprise a collapsible polymeric
cover disposed over an expandable/collapsible frame. In other
embodiments, tissue apposition member 212 may be constructed of a
shape memory material, such as nitinol or another shape memory
metal, spring stainless steel or the like, to allow catheter device
210 to be delivered through vasculature and then allow tissue
apposition member 212 to expand to contact and appose the PFO
tissues. In some embodiments, catheter device 210 and tissue
apposition member 212 may be delivered to a location for PFO
treatment through an introducer sheath. To further enhance the use
of apparatus 200, an angle between catheter device 210 and tissue
apposition member 212 may be selected to approximate a convenient
angle for delivery and/or deployment. In one embodiment, for
example, the angle between catheter device 210 and tissue
apposition member 212 may approximate the angle between the
inferior vena cava and the interatrial septum. Any other
configuration, combination of angles and the like is contemplated,
however. In some embodiments, for example, direct steering of the
angle of tissue apposition member 212 relative to catheter device
210 may be employed to enhance delivery of catheter device 210 to a
treatment site.
[0062] To further facilitate use of apparatus 200, catheter device
210 may include one or more radiopaque markers 226 for facilitating
visualization of the device 210. Catheter device 210 may also
include a "flexible isolation portion" 228, which in some
embodiments comprises a rigid but shapeable portion disposed toward
the distal end of catheter device 210, between tissue apposition
member 212 and the generally flexible proximal portion of catheter
device 210. Flexible isolation portion 228 may help to isolate
tissue apposition member 212 from some or all movement experienced
by the more flexible, proximal portion of catheter device 210, thus
allowing a PFO treatment procedure to be performed without
significant movement of tissue apposition member 212. In other
embodiments, flexible isolation portion 228 may be more flexible
than the more proximal portion of catheter device 210, thus
enhancing maneuverability, shapability or the like of the position
of tissue apposition member 212 relative to the more proximal
portion.
[0063] Energy transmission members 214 may comprise any of a number
of devices and may transmit any suitable type of energy for closing
a PFO. Some types of energy which may be used, for example, include
radiofrequency, cryogenic, resistive heat, ultrasound, microwave
and laser energy. Radiofrequency energy transmission members 214
may be either monopolar or bipolar, with monopolar catheter devices
also including a grounding member. Energy transmission members 214
may have any suitable configuration. For example, they may have a
curved shape to approximate a radius of curvature of the PFO, as
shown in FIG. 3, or they may be configured as points for
spot-welding the PFO tissues, as a circular member for welding
around the circumference of PFO tissues, as one or more mesh or
braided members disposed within the orifice of tissue apposition
member 212 or the like. In some embodiments, energy transmission
members 214 are fixedly coupled with tissue apposition member 212,
while in other embodiments energy transmission members 214 are
movable within tissue apposition member, for example to move about
the circumference of the PFO to weld PFO tissues at multiple
locations.
[0064] As mentioned earlier, the phrase "tissue welding" herein is
used to mean application of energy to (or removal of energy from)
PFO tissues to substantially and acutely close the PFO. Energy
transmission members 214 generally provide for transfer of energy
to or from PFO tissues to denature collagen in the tissues, and
when the collagen is allowed to renature, with the tissues apposed,
the once separated tissues bind together to form a stable tissue
bridge. This stable tissue bridge substantially and acutely closes
the PFO, preferably permanently. PFO tissues may, in some
embodiments, be brought and held together by one or more tissue
apposition members 212. Energy transmission members 214 provide
sufficient energy transfer, for a sufficient time, to weld the
tissues. The time span of energy transmission may be, for example,
from about 0.5 seconds to about 15 minutes, and more preferably
from about 30 seconds to about 5 minutes. Energy transmission, in
some embodiments, may be from about 0.5 Watts to about 100 Watts,
and more preferably from about 2 Watts to about 20 Watts. Any other
suitable energy and timing combination may also be used. In one
experimental example, a PFO in a section of pig heart tissue used
ex-vivo in a flowing saline test fixture was closed by applying
suction to appose the PFO tissues and applying RF energy at
approximately 25 watts for 7 minutes. RF energy application was
then discontinued, but suction was continued for an additional 1
minute to keep tissues in apposition while the tissue cooled, to
allow collagen in the tissues to reorganize and bind together to
form a stable tissue bridge. Many other energy amounts, energy
application times, tissue apposition times and the like are
contemplated, however.
[0065] Although any type of energy may be transmitted by energy
transmission members 214, some embodiments will make use of
monopolar or bipolar radiofrequency (RF) energy. Devices may use
monopolar radiofrequency energy, for example, wherein energy is
applied simultaneously to all conductive elements, completing the
circuit through an external ground pad affixed to the skin of the
patient. Alternatively, bipolar energy may be applied to all
conductive elements simultaneously, and the circuit completed
through a ground element incorporated elsewhere on apparatus 200.
Further embodiments may include applying bipolar energy between two
or more energy transmission members 214, which are electrically
isolated from one another within catheter device 210.
[0066] Control systems coupled with energy transmission members 214
or tissue apposition member 212, or otherwise disposed within
apparatus 200, may sense an amount of energy delivered to PFO
tissues and, optionally, may automatically stop energy delivery
upon detecting a change in condition of energy delivery, for
instance an increase in electrical resistance or impedance in PFO
tissues or in apparatus 200, an increased energy draw from the
treatment apparatus, and/or the like. In some embodiments, energy
delivery may be automatically stopped when an amount of delivered
energy reaches a desired level, such as an amount of energy
sufficient to substantially close the PFO. The amount of delivered
energy may be monitored by any suitable method, such as monitoring
temperature or impedance in PFO tissues or the like. In some
embodiments, one or more sensors coupled with tissue apposition
member 212, energy transmission members 214, or any other part of
apparatus 200 may be used for monitoring such indicia. Examples of
sensor devices include but are not limited to infrared sensing
devices, thermistors and thermocouples. A control system may also
include a microprocessor coupled with the sensors to determine when
a desired amount of energy has been delivered and/or to
automatically stop energy transmission. In alternative embodiments,
a microprocessor may be included in apparatus 200 which can sense,
monitor and control energy delivery, thus not requiring separate
sensors.
[0067] With continued reference to FIG. 3, some embodiments of
apparatus 200 include guide catheter 220, or an alternative guide
member as discussed further below. Guide catheter 220 is generally
a flexible catheter along which catheter device 210 may be slidably
advanced to a position for PFO treatment. Guide catheter 210 is
configured to fit at least partially within a PFO and optionally
through a PFO into the left atrium of the heart. Optionally, one or
more radiopaque markers 224 may be included on guide catheter.
[0068] Guide catheter 220 may contain one or more expandable
members 222 or other similar devices for expanding within the PFO
to help bring the PFO tissues together, anchor catheter device to
the PFO tissues, or both. As shown in FIG. 3, for example, a "fish
mouth" or two-prong expandable member 222 may be deployed within a
PFO. When the two arms of the fish mouth separate, PFO-adjacent
tissues are stretched laterally such that they tend to come
together in the middle. In some embodiments, expandable members 222
may assist in PFO tissue apposition either while extending into the
left atrium, while in other embodiments expandable members 22 do
not extend into the left atrium.
[0069] Expandable member 222 may have any suitable configuration
and may be constructed from any suitable materials. For example,
expandable member 222 may be spring loaded, made of shape memory
material, such as nitinol or spring stainless steel or the like.
Alternatively, expandable member 222 may be expanded mechanically
by one or more expansion members coupled with expandable member 222
and controlled via an actuator at the proximal end of guide
catheter 220. During delivery of guide catheter 220, expandable
member 222 reside within guide catheter 220. Guide catheter 220 may
then be withdrawn to deploy expandable member 222 either within the
PFO or within the left atrium to be drawn back into the PFO. In
some embodiments, expandable member 222 has one or more pre-shaped
or shapeable distal tips 223. Tips 223 may be used, for example, to
help locate and cross the PFO. Tips 223 may also be used to contact
a left atrial surface of the septum primum or other PFO tissue, so
that when the expandable member 222 is pulled proximally tips 223
help bring the PFO tissues together and/or anchor apparatus
200.
[0070] In some embodiments, one or more expandable members 222 may
include or be coupled with one or more energy transmission members.
For example, expandable member 222 may include one or more
radiofrequency transmission members for monopolar or bipolar RF
transmission. A fish mouth expandable member 222, for example, may
include a bipolar RF transmission member on each prong of the fish
mouth. In some embodiments, energy transmission members may be
included in or coupled with both expandable member 222 and tissue
apposition member 212. In any such embodiments, some portions of
the energy transmission member(s) may be insulated, to prevent
unwanted energy transmission to tissues. For example, in some
embodiments a distal tip extending to contact a left atrial surface
of PFO tissues may be insulated to prevent energy transmission from
the tip.
[0071] Referring now to FIG. 4, an alternative embodiment of a
PFO-treatment apparatus 300 suitably includes a catheter device 310
having a tissue apposition member 312, radiopaque marker 326 and
flexible isolation portion 328. For exemplary purposes only, this
embodiment is shown having one energy transmission member 314, such
as a monopolar RF transmission member. As shown, apparatus 300 may
also include a guidewire 320, over which catheter device 310 may be
advanced. Guidewire 320 includes a split, expandable portion 322,
which may be released from catheter device 310 to expand within a
PFO to bring PFO tissues together. Guidewire 320 also suitably
includes a distal tip 323 for locating and crossing a PFO and/or
for contacting a left atrial surface of the septum primum or other
PFO tissue.
[0072] Apparatus 300 of FIG. 4 may include any of the features
described above in relation to FIG. 3. In the embodiment in FIG. 4,
apparatus 300 does not include a guide catheter, but instead
includes guidewire 320. Guidewire 320 may serve many or all of the
functions of the guide catheter and expanding member described
above in reference to FIG. 3. Split portion 322 of guidewire 320
may be constructed of shape memory material or other suitable
materials to allow it to expand when released from catheter device
310. Additionally, split portion 322 may include or be coupled with
one or more energy transmission members instead of or in addition
for energy transmission member(s) 314 coupled with tissue
apposition member 312. Guidewire 320 may also include one or more
distal tips 323, which again may be used to locate and cross a PFO
and/or to help appose PFO tissues. In some embodiments, tip 323 may
also include or be coupled with one or more energy transmission
members.
[0073] Referring now to FIGS. 5A and 5B, another embodiment of a
PFO-treatment apparatus 400 suitably includes a catheter device 410
having a tissue apposition member 412, radiopaque markers 426 and
flexible isolation portion 428. As shown, apparatus 400 may also
include a guidewire 420, over which catheter device 410 may be
advanced. Guidewire 420 includes a split, expandable portion 422,
which may be released from catheter device 410 to expand within a
PFO to bring PFO tissues together. Guidewire 420 also suitably
includes a distal tip 423 for helping locate and cross the PFO
and/or for contacting a left atrial surface of the septum primum or
other PFO tissue to help bring the PFO tissues together. In this
embodiment, catheter device 410 also includes a braided portion 430
which includes the proximally-disposed tissue apposition member 412
and a more distal energy transmission portion 432, the latter of
which is coupled with energy transmission members 414. Tissue
apposition member 412 and energy transmission portion 432 may be a
unitary braided member, with tissue apposition member 412
configured to cover energy transmission portion 432 in a retracted
position and to provide vacuum force application.
[0074] In use, catheter device 410 is typically advanced over
guidewire 420 to a treatment location. Split portion 422 and
optionally distal tip 423 are then used to help appose the tissues
adjacent the PFO. Before, during or after retraction of guidewire
420, energy transmission portion 432 is retracted into tissue
apposition member 412. PFO tissue is then brought together using
tissue apposition member 412, and energy is transmitted to the
tissues using energy transmission portion 432. In some embodiments,
tissue apposition member 412 provides for application of vacuum
energy to the tissues to suction the tissues at least partially
into tissue apposition member 412, thus enhancing contact of the
tissues with energy transmission portion 432. Energy transmission
portion 432 may comprise, for example an electrode mesh material,
while tissue apposition member 412 may comprise an elastic coated
mesh or other material. Again, any features described above in
reference to other embodiments may be applied to the embodiment
shown in FIGS. 5A and 5B.
[0075] With reference now to FIG. 6, another embodiment of a
PFO-treatment apparatus 500 suitably includes a catheter device 510
having a tissue apposition member 512, energy transmission members
514, radiopaque marker 526 and flexible isolation portion 528. For
simplicity, apparatus 500 is shown without a guide catheter or
guidewire, though either may be included. In this embodiment,
tissue apposition member 512 includes ribs or "bellows" 540 to
facilitate placement and/or alignment of tissue apposition member
512 relative to the septal wall tissues to be treated and/or to
enhance adherence of apparatus 500 to the septal wall. For example,
ribs 540 may allow catheter device 510 to move relatively freely
relative to tissue apposition member 512, without displacing tissue
apposition member 512 from the PFO tissues.
[0076] Referring now to FIG. 7, another embodiment of a
PFO-treatment apparatus 600 suitably includes a catheter device 610
having a tissue apposition member 612, energy transmission members
614, radiopaque marker 626 and flexible isolation portion 628.
Apparatus 600 is shown without a guide catheter or guidewire,
though either may be included. In this embodiment, tissue
apposition member 612 includes multiple struts 650 covered by a
covering 652, which may comprise a polymeric covering or any other
suitable material. Struts 650 may be self-expanding or may open via
a mechanical opening actuator coupled with struts 650, such as
opening apparatus used to open an umbrella. Energy transmission
members 614 are coupled with self-expanding struts 650 on the
internal surface of tissue apposition member 612, so as to contact
PFO tissue that is pulled within tissue apposition member 612, such
as by applied vacuum force and/or by blood pressure from the left
atrium.
[0077] FIGS. 8A-8E demonstrate a method for treating a PFO
according to one embodiment of the present invention. It should be
emphasized that this is merely one possible embodiment, and that
many alternative methods are contemplated. For example, steps may
be modified, repeated, added or deleted from the method, the order
of steps may be changed, and/or the like, without departing from
the scope of the invention as defined by the appended claims.
Therefore, the foregoing description should not be interpreted to
limit the scope of the invention in any way.
[0078] That being said, in one embodiment, a PFO treatment method
includes advancing a guide catheter 720 through the PFO, between
tissues T adjacent the PFO, the guide catheter 720 containing an
expandable member (FIG. 8A). Guide catheter 720 is then retracted
(proximally pointing arrow) to expose expanding member 722 (FIG.
8B). Expanding member 722 may be exposed/expanded within the PFO,
or may alternatively be exposed/expanded within the left atrium and
pulled back into the tunnel of the PFO. Expanding member 722 may
also include one or more distal tips 723, which may help to locate
the PFO, cross the PFO, appose the tissues T and/or to anchor guide
catheter 720 to the tissues T.
[0079] Once guide catheter 720 is in place and expandable member
722 is deployed, catheter device 710 may be advanced over guide
catheter 720 to a position for treatment of the PFO (FIG. 8C).
Catheter device 710 typically includes a tissue apposition member
712 (shown here in cross-section for clarity) and one or more
energy transmission members 714. Suction may be applied using
tissue apposition member 712, left atrial pressure may be used, or
both, to bring tissues T adjacent the PFO together (FIG. 8D). Once
tissue apposition member 712 is placed and/or activated, guide
catheter 720 and expandable member 722 may be removed through
catheter device 710, leaving the tissues T apposed and catheter
device in place, as in FIG. 8D. Alternatively, guide catheter 720
and expandable member 722 may be left in place during a first
welding to close the majority of the PFO and then removed. The
small patent portions of the PFO remaining after the guide catheter
720 and expandable member 722 are removed may then be closed by a
second weld or may be left open and allowed to close via healing or
scarring. Tissue apposition member 712 may be used to hold tissues
T together before, during and/or after energy transmission members
714 weld the tissues T together. Such holding of the tissues
together and application of energy to weld the tissues may be
performed for any suitable time, such as for less than one second
to many minutes. Once a sufficient amount of energy has been
applied to the tissues T to acutely close the PFO, catheter device
710 is removed, leaving a closed PFO, as in FIG. 8E.
[0080] Apparatus and methods according to the present invention may
rely on energy, in various forms, to seal the PFO, either with or
without an associated implant device. As an alternative to
implant-based devices, systems according to the present invention
can function to weld the PFO closed with no implant left behind. As
illustrated in FIGS. 9A and 9B, in some embodiments, a backstop and
energy delivery catheter are placed in contact with the PFO, and
energy is delivered to disrupt the collagen matrix of the primum
and secundum to cause fusion of the two parts of the PFO. Energy
used can be monopolar or biopolar RF (in which case the backstop
acts as energy return), ultrasound, laser, microwave, or resistance
heating. Protein solder may be introduced to facilitate the
weld.
[0081] Referring to FIG. 9A, one embodiment of a backstop catheter
device 800 for treating a PFO may include an outer catheter element
802, an inner catheter element 804, a backstop 806 coupled with a
portion 808 extending through the inner shaft 804, and energy
delivery arms 810. Energy delivery arms 810 can include ultrasound
transducers, microwave antennae, or RF electrodes. The backstop
catheter device 800 is advanced through the PFO and used to help
advance an energy delivery catheter to the right atrial side of the
PFO. Relative translation of an inner 804 and outer catheter
element 802 deploy a set of arms 810 which carry the energy
delivery elements. The energy delivered breaks down the collagen in
each part of the PFO, and allows the tissues to be welded together.
The energy delivered could take the form of RF, microwave, or
ultrasound. RF energy can either be monopolar, in which the
backstop 806 is electrically insulated such that it is not part of
the energy delivery path, or bipolar, in which case the backstop
806 acts as the energy return electrode. If desired, the inner
catheter 804 of the energy delivery catheter 800 can be used to
infuse liquid albumin to act as a protein solder for the system.
Alternatively, the shaft of the backstop 806 could be covered with
a tube of solid or braided material made of, or soaked in, a tissue
solder. After delivery of the energy and activation and bonding of
the tissue solder to the PFO walls, the backstop 806 is withdrawn
through the PFO and the entire system is withdrawn.
[0082] As illustrated in FIG. 9B, in another embodiment, a catheter
device 820 can include an expandable balloon member 822 and an
expandable backstop 824. The balloon catheter 820 can be outfitted
with sections 826 of piezo film/foil which can be driven
electrically to produce an ultrasound signal to heat and seal a
PFO. The balloon member 822 and expandable backstop 824 are used to
position the catheter device 820 in the desired location and energy
is then applied via the piezo film/foil 826 for treating the
PFO.
[0083] Variations of a backstop device according to the present
invention are illustrated in FIGS. 10 through 13. Referring to FIG.
10, a backstop device 830 can have an inferior bias to
preferentially engage the primum without interfering with the left
atrial wall. Embodiments of the backstop device 830 are shown
including prongs 832 and wire loops 834.
[0084] Referring to FIG. 11, a backstop device can include a coiled
version 840, where a gidewire reforms into a coil 842 when
introduced into the left atrium. The coil can be reverse-bias coil,
so traction causes a former seat, or inferior-bias coil 846, so
there is less contact with the left atrial wall superiorly. A flat
coil version 848 of a backstop device is also shown.
[0085] FIG. 12 shows a balloon version backstop device, with a
soft, low-pressure balloon 852 and a fixed wire 854. The balloon
854 can be concentric to the shaft 856, or inferior-biased for
clearance. The inferior-bias balloon 858 preferentially engages the
primum without hitting the left atrial wall. The device can be
fixed-wire, over-the-wire, or tip-mounted with no central lumen for
a guide wire or for inflation only.
[0086] FIGS. 13A through 13C show a backstop device 860 with a
normally-open flower petal 862, where nitinol petals 862 are biased
open, and attached proximal to an outer catheter 864, distal to a
core wire 866. Translation of the core wire 866 opens and closes
the petals 862. The petals 862 are shown attached to the core wire
866 and the outer catheter 864 (FIG. 13B). The core wire 866 is
advanced to collapse the petals 862 (FIG. 13C).
[0087] In other embodiments, PFO closure systems according to the
present invention may utilize one or more clips to close the PFO.
Such systems can be divided into designs that involve both a right
and left atrial component, and those that are right-sided only.
While they are generally not energized, it may be desirable to add
energy to any of these designs to facilitate adhesion and
sealing.
[0088] Referring now to FIG. 14A through FIG. 14D, another
embodiment of the present invention is described which includes a
catheter device comprising a coil closure device 900. According to
this embodiment, a catheter 902 is used to insert a closure device
900 comprising a pair of flexible, pre-formed coils 904, 906 into
both the left and right atriums. The spring tension in the pair of
coils 904, 906 pulls the primum into the secundum to close the
PFO.
[0089] Referring now to FIG. 15, another embodiment of the present
invention includes a deployable spring coil closure device 910
which may inserted through a small pierced hole in the septum. For
example, a needle tipped catheter (not shown) can be used to pierce
the primum and install the spiral spring coil 910 (e.g., similar to
that described above) through a small hole made in the septum
rather than through the PFO tunnel itself.
[0090] Referring now to FIG. 16, in another embodiment, a spiral
spring coil 920 is inserted through the PFO. The portion 922 of the
wire form that goes through the actual PFO tunnel is shaped to
maximize contact area and flatten the PFO by stretching it closed.
RF energy is then applied to the wire 920 to burn it into the
tissue and promote tissue growth, especially in the area between
the primum and secundum where there is a high contact area. The
flattened PFO combined with tissue healing on adjacent primum and
secundum sides might cause the PFO to heal closed. The spring
tension provided by the spiral spring coil 920 will keep the PFO
closed as the tissue heals. The tissue healing around the wire 920
will help secure it to the tissue and prevent embolization.
[0091] In another embodiment, a patch might also be used on the
right atrial side to provide an additional means to seal the PFO.
If it is desirable to prevent the wire around the patch area from
receiving RF energy, it is possible to electrically insulate the
portion of the wire that is not desired to burn into the tissue
(not shown). In another embodiment, the "zig zag" portion 922 of
the coil 920 located in the flattened passageway between the primum
and secundum might have sharp features (such as needles or barbs)
which cause the adjacent surfaces of the primum and secundum to
bleed and heal together. RF energy might be used in any of the
embodiments of the spiral spring coil described above to buRN some
or all of the device into the tissue and promote rapid healing and
prevent embolization.
[0092] As mentioned above, the foregoing method may be altered in
any number of ways without departing from the scope of the
invention. In some embodiments, for example, tissues adjacent the
PFO are brought at least partially together and energy is applied
to the tissues to acutely close the PFO with fewer steps and/or
fewer device components than just described. For example,
application of suction to appose tissues is not required in all
embodiments. Furthermore, a variety of different types of energy
may be applied to the tissues from a variety of differently
configured energy transmission devices. In some embodiments, one or
more of the steps described above may be repeated one or more
times, such as by repeating a tissue welding step. The above
description, therefore, is provided for exemplary purposes
only.
[0093] Although the foregoing description is complete and accurate,
it has described only exemplary embodiments of the invention.
Various changes, additions, deletions and the like may be made to
one or more embodiments of the invention without departing from the
scope of the invention. Additionally, different elements of the
invention could be combined to achieve any of the effects described
above. Thus, the description above is provided for exemplary
purposes only and should not be interpreted to limit the scope of
the invention as set forth in the following claims.
* * * * *