U.S. patent application number 10/724342 was filed with the patent office on 2004-04-22 for delivery system for a stentless valve bioprosthesis.
This patent application is currently assigned to 3f Therapeutics, Inc.. Invention is credited to Quijano, Rodolfo C., Tu, Hosheng.
Application Number | 20040078072 10/724342 |
Document ID | / |
Family ID | 25316098 |
Filed Date | 2004-04-22 |
United States Patent
Application |
20040078072 |
Kind Code |
A1 |
Tu, Hosheng ; et
al. |
April 22, 2004 |
Delivery system for a stentless valve bioprosthesis
Abstract
The current invention discloses a catheter and a method for
delivering a stentless bloprosthesis in a body channel, the method
comprising percutaneously introducing a catheter into the body
channel, wherein the catheter contains said stentless bloprosthesis
at a retracted state; and disengaging said stentless bioprosthesis
out of a distal opening of the catheter by a pulling mechanism
associated with the catheter structure.
Inventors: |
Tu, Hosheng; (Tustin,
CA) ; Quijano, Rodolfo C.; (Laguna Hills,
CA) |
Correspondence
Address: |
JONES DAY
555 WEST FIFTH STREET, SUITE 4600
LOS ANGELES
CA
90013-1025
US
|
Assignee: |
3f Therapeutics, Inc.
Lake Forest
CA
|
Family ID: |
25316098 |
Appl. No.: |
10/724342 |
Filed: |
November 26, 2003 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10724342 |
Nov 26, 2003 |
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09853463 |
May 10, 2001 |
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6682558 |
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Current U.S.
Class: |
623/1.23 |
Current CPC
Class: |
A61F 2/2475 20130101;
A61F 2/2436 20130101; A61F 2/2412 20130101 |
Class at
Publication: |
623/001.23 |
International
Class: |
A61F 002/06 |
Claims
What is claimed is:
1. A method for delivering a longitudinally collapsible prosthesis
to an anatomical site in a body channel, the method comprising:
introducing a catheter into the body channel, wherein the catheter
contains a longitudinally collapsible prosthesis in a retracted
state; advancing the catheter to an anatomical site; maintaining a
distal portion of the longitudinally collapsible prosthesis in
place relative to the anatomical site by attaching the distal
portion of the prosthesis to the interior of the anatomical site;
disengaging the longitudinally collapsible prosthesis from said
catheter, wherein the collapsible prosthesis expands from the
retracted state to a non-retracted state; and withdrawing said
catheter from the body channel.
2. The method according to claim 1, wherein the longitudinally
collapsible prosthesis is a vascular graft.
3. The method according to claim 1, wherein the longitudinally
collapsible prosthesis is a biological vascular graft.
4. The method according to claim 1, wherein the longitudinally
collapsible prosthesis is a stentless cardiac valve.
5. The method according to claim 1, wherein the longitudinally
collapsible prosthesis is a valved conduit.
6. The method according to claim 1, wherein the longitudinally
collapsible prosthesis is a venous valve.
7. The method according to claim 1, wherein the step of attaching
the distal portion of the prosthesis to the interior of the
anatomical site further comprises a step of stapling said
prosthesis into the tissue of the body channel.
8. The method according to claim 1, wherein the step of attaching
the distal portion of the prosthesis to the interior of the
anatomical site further comprises a step of adhering said
prosthesis into the tissue of the body channel.
9. The method according to claim 1, wherein the step of attaching
the distal portion of the prosthesis to the interior of the
anatomical site further comprises a step of coupling said
prosthesis into the tissue of the body channel.
10. The method according to claim 1, wherein said distal portion of
the longitudinally collapsible prosthesis is maintained in place at
a position relative to the anatomical site by an elongated delivery
member located within a lumen of the catheter, said elongated
delivery member having an engagement element at a distal end of the
said elongated delivery member, where in the engaging element is
adapted for engaging and digging ht distal portion of said
longitudinally collapsible prosthesis. a therapeutic fluid is
introduced into the lumen of the catheter shaft.
11. A method for delivering a stentless longitudinally collapsible
bioprosthesis in a body channel, the method comprising
percutaneously introducing a catheter into the body channel,
wherein the catheter contains said stentless longitudinally
collapsible bioprosthesis at a retracted state; and disengaging
said stentless bioprosthesis out of a distal opening of the
catheter by pulling the distal end of the stentless
bioprosthesis.
12. The method according to claim 11, wherein said pulling
mechanism further comprises an engaging element coupling to a
distal portion of the stentless longitudinally collapsible
bioprosthesis from said engaging element.
Description
RELATED APPLICATIONS
[0001] This application claims priority to U.S. Utility application
Ser. No. 09/853,463, filed May 10, 2001, the entirety of which is
hereby incorporated by reference.
TECHNICAL INVENTION
[0002] The present invention generally relates to a tubular
prosthesis and methods for delivery into a body channel. More
particularly, the present invention relates to an improved delivery
system for delivering a stentless bioprosthesis comprising a
collapsible elastic valve or a biological graft at a desired
anatomical site of the body channel for implantation.
BACKGROUND OF THE INVENTION
[0003] A prosthetic heart valve may be used to replace a diseased
natural heart valve in a human patient. Similarly, a prosthetic
venous valve may be used to replace a dysfunctional natural venous
valve in a patient. Mechanical heart valves typically have a rigid
orifice ring and rigid hinged leaflets coated with a blood
compatible substance such as pyrolytic carbon. Other
configurations, such as ball-and-cage assemblies, have also been
used for such mechanical valves. A mechanical heart valve cannot be
retracted radially and delivered by a catheter-based delivery
system.
[0004] In contrast to mechanical heart valves, bioprosthetic heart
valves comprise valve leaflets formed of biological material. Many
bioprosthetic valves include a support structure, or stent, for
supporting the leaflets and maintaining the anatomical structure of
the valve. Stented bioprosthetic valves generally are prepared by
chemically cross-linking a retrieved pig's heart valve, followed by
attaching it to a stent. The stent provides structural support to
the valve and, with a sewing cuff, facilitates attachment of the
valve to the patient by suturing. Gabbay in U.S. Pat. No. 5,935,163
discloses a natural tissue heart valve prosthesis with a
substantially flexible annular ring to provide additional support,
the entire contents of which are incorporated herein by
reference.
[0005] One of the major functions of stents is to serve as a
framework for attachment of the valve and for suturing the valve
into place in the human patient. Various stent designs have been
implemented in a continuing effort to render valve implantation
simpler and more efficient. Inevitably, however, a stent limits
interactions with aortic wall dynamics and tends to inhibit natural
valve movement. This results in post-operative transvalvular
gradients with resultant additional work burden on the heart. In
addition, a stent causes a reduction in size of the bioprosthetic
valve that can be placed in a particular location, since the stent
and sewing cuff occupy space that otherwise would be available for
blood flow. Recently biodegradable stents are disclosed, for
example, U.S. Pat. No. 5,895,420 to Mirsch II, et al. and U.S. Pat.
No. 5,489,297 to Duran, to limit disadvantage of the valve stenting
to a shorter time of implantation until it is biodegraded. Both
patents are incorporated herein by reference.
[0006] Some bioprosthetic valve manufacturers have attempted to
develop methods and systems to ease the implantation of stented
valves, including special catheter-based delivery system. Both of
U.S. Pat. No. 5,840,081 and U.S. Pat. No. 6,168,614 to Andersen et
al. disclose a minimally invasive percutaneous delivery system with
a balloon catheter. A stented valve prosthesis is contractively
mounted within a lumen of the catheter during delivery. At a
desired anatomical site, the prosthesis is pushed out of the
catheter tip and self expands. Lutter et al. reported an
experimental study on percutaneous transluminal replacement of the
aortic valve (81.sup.st American Association for Thoracic Surgery
Program Book pp. 174, May 6-9, 2001, San Diego, Calif.). They
concluded that aortic valve stents with a self-expandable metallic
stent can be successfully implanted by transluminal catheter
technique without the need of opening the chest.
[0007] Porter in U.S. Pat. No. 5,064,435 discloses a catheter-based
apparatus and methods for releasing a self-expandable prosthesis by
a conventional pushing mechanism. The above-mentioned approaches
are satisfactory for delivering a stented prosthesis having an
external rigid support adapted for receiving the pushing force. A
self expanding prosthesis often is preferred over a plastically
deformed device. Resilient prosthesis can be deployed without
dilatation balloons or other stent expanding means. A
self-expanding prosthesis can be preselected in accordance with the
diameter of the body channel or other anatomic site for fixation.
While deployment requires skill in positioning the prosthesis, the
added skill of properly dilating the balloon to plastically expand
a prosthesis to a selected diameter is not required. Also, the
self-expanding prosthesis remains at least slightly compressed
after fixation, and thus has a restoring force which facilitates
acute fixation.
[0008] Stentless valves have demonstrated better hemodynamic
function than stented valves. This is because a stentless valve is
sewn directly into the host tissues, without the need for
extraneous structure such as a sewing cuff. Such extraneous
structures inevitably compromise hemodynamics. A stentless valve
closely resembles a native valve in its appearance and function,
and rely upon the patient's tissues to supply the structural
support normally provided by a stent. Quintero et al. in U.S. Pat.
No. 5,197,979, Nguyen Thien-Nhon in PCT W.O. No. 99/33412, and
Vrandecic Peredo in PCT W.O. No. 00/00107 all disclose stentless
valve structure and function, the entire contents of which are
incorporated herein by reference.
[0009] The main disadvantage to stentless valves has been in their
difficulty of deployment and implantation, particularly in a
catheter-based percutaneous route. With recent scientific
advancements in robotics, instrumentation and computer technology,
a minimally invasive catheter-based delivery system for a stentless
bioprosthesis is imminent. There is currently a clinical need for
deploying a tubular stentless prosthesis, such as a stentless valve
or a vascular graft without a rigid support, into a body channel,
preferably by a percutaneous approach. The catheter-based
percutaneous delivery system as compared to an open-cavity surgery
will greatly reduce the patient's hospital stay and improve
recovery.
SUMMARY OF THE INVENTION
[0010] It is an object of the present invention to provide a method
for delivering a stentless bioprosthesis in a body channel, the
method comprising percutaneously introducing a catheter into the
body channel, wherein the catheter contains the radially elastic
stentless bloprosthesis at a retracted state; and disengaging said
stentless bloprosthesis out of a distal opening of the catheter by
a pulling mechanism. In one embodiment, the pulling mechanism
further comprises an engaging element coupling to a distal portion
of the stentless bioprosthesis. In another embodiment, the method
further comprises separating the stentless bioprosthesis from said
engaging element.
[0011] The stentless bioprosthesis of the present invention has the
common characteristics of soft, collapsible radially, collapsible
longitudinally, and without any rigid support onto or around the
bioprosthesis.
[0012] It is another object of the present invention to provide a
catheter for delivering a tubular prosthesis to an anatomical site
in a body channel, the catheter comprising an elongated delivery
member located inside the lumen of the catheter, the elongated
delivery member having an engaging element at the distal end of the
elongated delivery member, wherein the engaging element is adapted
for engaging and disengaging a distal portion of the tubular
prosthesis. In one embodiment, the catheter further comprises a
delivery mechanism at the handle that is coupled to the elongated
delivery member. The delivery mechanism is adapted for pulling the
distal portion of the tubular prosthesis out of the catheter shaft
during a deployment or releasing stage. In another embodiment, the
engaging element comprises a plurality of releasable sutures,
gripping jaws or bio adhesives.
[0013] It is still another object of the present invention to
provide a method for delivering a tubular stentless prosthesis to
an anatomical site in a body channel, the method comprising the
steps of introducing a catheter into the body channel, wherein the
catheter contains the tubular stentless prosthesis at a retracted
state; advancing the catheter to the anatomical site; maintaining a
distal portion of the tubular stentless prosthesis in place
relative to the anatomical site; disengaging the catheter from the
tubular stentless prosthesis adapted for self-expanding said
prosthesis from the retracted state; and withdrawing said catheter
from the body channel.
[0014] The tubular stentless prosthesis of the present invention
generally includes, but not limited to, a vascular graft, a
synthetic vascular graft, a biological vascular graft, a cardiac
valve, a valved conduit, a venous valve, and other stentless
implantable devices. The "tubular stentless prosthesis" is
essentially synonymous with the "longitudinally collapsible
prosthesis" in the invention.
[0015] In a further embodiment, the method comprises another step
of coupling the prosthesis into tissue of the body channel, wherein
the coupling means may include stapling, adhering, stenting,
anchoring and the like.
BRIEF DESCRIPTION OF THE DRAWINGS
[0016] Additional objects and features of the present invention
will become more apparent and the invention itself will be best
understood from the following Detailed Description of Exemplary
Embodiments, when read with reference to the accompanying
drawings.
[0017] FIG. 1 is an overall view of a delivery catheter of the
present invention for delivering a tubular stentless prosthesis
into a body channel.
[0018] FIG. 2 is an enlarged distal portion view of the catheter
showing a first stage of the delivery sequences in accordance to
the principles of the present invention.
[0019] FIG. 2A is a transverse view of the section 1-1 of FIG. 2
showing the relative location of the catheter shaft and the
prosthesis inside the shaft.
[0020] FIG. 3 is an enlarged distal portion view of the catheter
showing a second stage of the delivery sequences in accordance to
the principles of the present invention.
[0021] FIG. 3A is a transverse view of the section 2-2 of FIG. 3
showing the relative location of the catheter shaft and the
prosthesis inside the shaft. FIG. 4 is an enlarged distal portion
view of the catheter showing a third stage of the delivery
sequences in accordance to the principles of the present
invention.
[0022] FIG. 5 is an enlarged distal portion view of the catheter
showing a fourth stage of the delivery sequences in accordance to
the principles of the present invention.
DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS
[0023] Referring to FIGS. 1 to 5, what is shown is an embodiment of
the device delivery system and methods, comprising a delivery
catheter adapted particularly for delivering a tubular stentless
prosthesis to an anatomical site in a body channel.
[0024] FIG. 1 shows an overall view of a delivery catheter of the
present invention for delivering a tubular stentless prosthesis
into a body channel. A tubular stentless prosthesis is a prosthesis
without a support or stent. Typically such a prosthesis is soft,
flexible and very compressible or collapsible either radially or
longitudinally. The best handling method is to hold it in its
natural position without buckling, compression, or "spaghetti-like"
twisting. When such a prosthesis 31 is held horizontally, the best
way to move it in an essentially straight manner is to pull the
distal section 32 forward rather than push its proximal end 33.
[0025] The catheter 11 of the present invention comprises a
catheter shaft 17, the catheter shaft having a distal end 12, a
distal opening 16, a proximal end 13, and a lumen 22 between the
distal end 12 and the proximal end 13. The catheter also comprises
a distal section 14 that is used to hold the retracted prosthesis
31B during the catheter delivery stage. A fully un-retracted (free
from constraint) prosthesis 31 in the present invention is the one
prior to being inserted into the lumen 22 or after fully
deployed/released from the lumen.
[0026] The catheter also comprises a handle 15 that is attached to
the proximal end 13 of the catheter shaft 17. There is an elongated
delivery member 21 located inside said lumen 22 (see FIG. 2),
wherein the delivery member can be deployed forward or backward
axially. The elongated delivery member has an engaging element 35A,
35B at a distal end 26 of the elongated delivery member 21, wherein
the engaging element 35A, 35B is adapted for engaging and
disengaging a distal portion 32 of said tubular prosthesis 31B (see
FIG. 3). The tubular prosthesis is characterized by its softness
and collapsibility radially and/or longitudinally.
[0027] The engaging element may comprise a plurality of releasable
sutures, wherein the sutures may be released from the engaging
element by, for example a cutting instrument. The engaging element
may also comprise a plurality of releasably gripping jaws, wherein
the gripping jaws may be released after the stentless prosthesis is
deployed into place. Further, the engaging element may comprise a
plurality of heat-disengageable wires, for example the fuse-like
safety wires. A moderate heat can be provided through
radiofrequency, ultrasound, electromagnetic or the like to
disengage the wires from the prosthesis.
[0028] The catheter further comprises a delivery mechanism 18 at
the handle 15, the delivery mechanism 18 is coupled to the
elongated delivery member 21, wherein the delivery mechanism 18 is
adapted for pulling the distal portion 32 of the tubular prosthesis
31B out of the catheter shaft 17 during a prosthesis releasing
stage.
[0029] The catheter of the present invention may be in the 8 French
to 20 French size in diameter. However, the dimension outside this
range is also applicable depending on the anatomic site and
application. The material for catheters is generally biocompatible
and flexible for inserting purposes.
[0030] The method for delivering a tubular stentless prosthesis 31
to an anatomical site in a body channel may comprise several major
steps of (a) introducing a catheter into the body channel, wherein
the catheter contains the tubular stentless prosthesis at a
retracted state; (b) advancing the catheter to the anatomical site;
(c) maintaining a distal portion of said tubular stentless
prosthesis in place relative to the anatomical site; (d)
disengaging the catheter from the tubular stentless prosthesis
adapted for self-expanding said prosthesis from the retracted
state; and (c) withdrawing the catheter from the body channel.
[0031] FIG. 2 shows an enlarged distal portion 14 of the catheter
11 showing a first stage of the delivery sequences in accordance to
the principles of the present invention. A tubular stentless
prosthesis 31 can be crimped, compressed, constricted, constrained,
contracted, or retracted radially to form a retracted prosthesis
31B so as to snugly fit into a narrow lumen 22 of the catheter
shaft 17 at its distal section for delivering to the anatomical
site.
[0032] FIG. 2A shows a transverse view of the section 1-1 of FIG. 2
showing the relative location of the catheter shaft 17 and the
prosthesis 31B inside the shaft. The catheter has an optional
guidewire lumen or channel for riding the catheter shaft over a
guidewire 23. In one embodiment, the guidewire lumen 24 is provided
within the elongated delivery member 21. In another embodiment, the
guidewire channel is provided at the distal section of the catheter
shaft as a rapid exchange type guidewire system. The guidewire
lumen is adapted for introducing a guidewire of about 0.014 inch or
smaller.
[0033] FIG. 3 shows an enlarged distal portion 14 view of the
catheter showing a generally second stage of the delivery sequences
in accordance to the principles of the present invention. The
distal portion 32 of the prosthesis 31B is pulled out of the distal
opening 16 of the catheter shaft 17 by a pulling action from the
distal end of the elongated delivery member 21. In one embodiment,
the pulling action is accomplished by an engaging element, wherein
the engaging element 35A, 35B may have its engaging points 37A, 37B
at the distal end 26 of the elongated delivery member 21 and
another engaging points 36A, 36B at the distal section 32 of the
prosthesis 31B. In a relative sense when the distal section 32
remains fixed relative to an anatomical site, the catheter 11 is
viewed as moving backward toward the operator. The distal portion
32 of the prosthesis 31B self-expands radially due to its elastic
feature when the constraint is removed.
[0034] To ensure that the self-expanded prosthesis will stay at a
desired anatomic site within the body channel, the method may
further comprise a step of coupling the prosthesis into tissue of
the body channel whenever feasible. The coupling method may include
stapling, adhering by a bio-adhesive, such as Bio-glue.TM. (from
CryoLife, Inc., Kennesaw, Ga., USA). The stapling step may include
stapling both the distal portion and the proximal portion of the
prosthesis into tissue of the body channel, though more than two
stapling points is also applicable.
[0035] FIG. 3A shows a transverse view of the section 2-2 of FIG. 3
showing the relative location of the catheter shaft 17 and the
prosthesis 31B inside the shaft. In a preferred embodiment, the
guidewire lumen 24 is provided within the elongated delivery member
21 of the catheter 11 for riding the catheter shaft over a
guidewire 23.
[0036] FIG. 4 shows an enlarged distal portion 14 view of the
catheter showing a generally third stage of the delivery sequences
in accordance to the principles of the present invention. The
majority of the prosthesis 31B is pulled out of the distal opening
16 of the catheter shaft 17 by a pulling action from the distal end
of the elongated delivery member 21. At this stage, the distal
portion 32 and the middle portion 39 of the prosthesis 31B
self-expands radially due to its elastic feature when the
constraint is removed.
[0037] FIG. 5 shows an enlarged distal portion 14 view of the
catheter showing a generally fourth stage of the delivery sequences
in accordance to the principles of the present invention. The whole
prosthesis 31A is pulled out of the distal opening 16 of the
catheter shaft 17 by a pulling action from the distal end 26 of the
elongated delivery member 21. At this stage, the distal portion 32,
the middle portion 39, and the proximal end 33 of the prosthesis
31B self-expands radially to form the un-constrained prosthesis 31A
as a result of its elastic feature when the constraint is
completely removed.
[0038] To provide an additional therapeutic therapy to the anatomic
site, a therapeutic fluid is introduced into the lumen of the
catheter shaft. The therapeutic fluid may be selected from a group
consisting of an anti-inflammatory solution, an anti-virus
solution, an antibiotic solution, an angiogenic fluid, heparin
solution, an anti-sense fluid, an anti angiogenic fluid, a
biocompatible adhesive, and a combination thereof. Typically a
fluid inlet port is provided at about the handle of the catheter
and the fluid can be supplied by a syringe or an infusion pump
coupling to the fluid inlet port. The biocompatible adhesive, such
as Bio-glue.TM. (from CryoLife, Inc., Kennesaw, Ga., USA) can be
used to adhere the distal section of the longitudinally collapsible
prosthesis on to the tissue at the anatomic site.
[0039] From the foregoing description, it should now be appreciated
that a method for delivering a stentless bioprosthesis in a body
channel, the method comprising percutaneously introducing a
catheter into the body channel, wherein the catheter contains the
stentless bioprosthesis at a retracted state; and disengaging said
stentless bioprosthesis out of a distal opening of the catheter by
a pulling mechanism has been disclosed. While the invention has
been described with reference to a specific embodiment, the
description is illustrative of the invention and is not to be
construed as limiting the invention. Various modifications and
applications may occur to those who are skilled in the art, without
departing from the true spirit and scope of the invention, as
described by the appended claims.
* * * * *