U.S. patent number RE45,760 [Application Number 14/195,385] was granted by the patent office on 2015-10-20 for coaxial guide catheter for interventional cardiology procedures.
This patent grant is currently assigned to Vascular Solutions, Inc.. The grantee listed for this patent is VASCULAR SOLUTIONS, INC.. Invention is credited to Jason M. Garrity, Howard C. Root, Gregg Sutton, Jeffrey M. Welch.
United States Patent |
RE45,760 |
Root , et al. |
October 20, 2015 |
**Please see images for:
( Certificate of Correction ) ** |
Coaxial guide catheter for interventional cardiology procedures
Abstract
A coaxial guide catheter to be passed through guide catheter
having a first lumen, for use with interventional cardiology
devices that are insertable into a branch artery that branches off
from a main artery. The coaxial guide catheter is extended through
the lumen of the guide catheter and beyond the distal end of the
guide catheter and inserted into the branch artery. The device
assists in resisting axial and shear forces exerted by an
interventional cardiology device passed through the second lumen
and beyond the flexible distal tip portion that would otherwise
tend to dislodge the guide catheter from the branch artery.
Inventors: |
Root; Howard C. (Tonka Bay,
MN), Sutton; Gregg (Plymouth, MN), Welch; Jeffrey M.
(Maple Grove, MN), Garrity; Jason M. (Lima, NY) |
Applicant: |
Name |
City |
State |
Country |
Type |
VASCULAR SOLUTIONS, INC. |
Minneapolis |
MN |
US |
|
|
Assignee: |
Vascular Solutions, Inc.
(Minneapolis, MN)
|
Family
ID: |
38662076 |
Appl.
No.: |
14/195,385 |
Filed: |
March 3, 2014 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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14070161 |
Nov 1, 2013 |
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12824734 |
Mar 27, 2012 |
8142413 |
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11416629 |
Nov 1, 2011 |
8048032 |
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Reissue of: |
13359059 |
Jan 26, 2012 |
8292850 |
Oct 23, 2012 |
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Reissue of: |
13359059 |
Jan 26, 2012 |
8292850 |
Oct 23, 2012 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61M
25/0052 (20130101); A61M 25/0069 (20130101); A61M
25/01 (20130101); A61M 25/0026 (20130101); A61M
25/0662 (20130101); A61M 2025/0081 (20130101); A61M
25/008 (20130101); A61M 25/0051 (20130101); A61M
25/0068 (20130101) |
Current International
Class: |
A61M
5/178 (20060101); A61M 25/00 (20060101); A61M
25/06 (20060101) |
Field of
Search: |
;604/103.04,103.09,160-162,164.01,164.02,164.09-164.11,525 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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0313558 |
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Jan 1988 |
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EP |
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0365993 |
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May 1990 |
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EP |
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0380873 |
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Aug 1990 |
|
EP |
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WO 84/03633 |
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Sep 1984 |
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WO |
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Other References
Judgment and Order Granting Termination of Proceedings, Paper 10,
Entered Aug. 11, 2014, in Case No. IPR2014-00759; Case No.
IPR2014-00760; Case No. IPR2014-00761; Case No. IPR2014-00762; and
Case No. IPR2014-00763. cited by applicant .
Joint Motion to Terminate Filed Aug. 8, 2014, in Case No.
IPR2014-00759. cited by applicant .
Joint Motion to Terminate Filed Aug. 8, 2014, in Case No.
IPR2014-00760. cited by applicant .
Joint Motion to Terminate Filed Aug. 8, 2014, in Case No.
IPR2014-00761. cited by applicant .
Joint Motion to Terminate Filed Aug. 8, 2014, in Case No.
IPR2014-00762. cited by applicant .
Joint Motion to Terminate Filed Aug. 8, 2014, in Case No.
IPR2014-00763. cited by applicant .
Joint Request to File Settlement Agreement as Business Confidential
Information, Filed Aug. 8, 2014, in Case No. IPR2014-00759. cited
by applicant .
Joint Request to File Settlement Agreement as Business Confidential
Information, Filed Aug. 8, 2014, in Case No. IPR2014-00760. cited
by applicant .
Joint Request to File Settlement Agreement as Business Confidential
Information, Filed Aug. 8, 2014, in Case No. IPR2014-00761. cited
by applicant .
Joint Request to File Settlement Agreement as Business Confidential
Information, Filed Aug. 8, 2014, in Case No. IPR2014-00762. cited
by applicant .
Joint Request to File Settlement Agreement as Business Confidential
Information, Filed Aug. 8, 2014, in Case No. IPR2014-00763. cited
by applicant .
Defendant, Boston Scientific Corporation's Prior Art Statement,
Dated Dec. 20, 2013, cited in Civil No. 0:13-cv-01172-JRT-SER.
cited by applicant .
Defendant, Boston Scientific Corporation's First Amended Prior Art
Statement, Dated Apr. 25, 2014, cited in Civil No.
0:13-cv-01172-JRT-SER. cited by applicant .
Plaintiff, Vascular Solutions, Inc.'s Response to Defendant Boston
Scientific Corporation's Prior Art Statement, Dated Jan. 23, 2014,
Civil No. 0:13-cv-01172-JRT-SER. cited by applicant .
Plaintiff, Vascular Solutions, Inc.'s Response to Defendant Boston
Scientific Corporation's First Amended Prior Art Statement, Dated
Jul. 1, 2014, Civil No. 0:13-cv-01172-JRT-SER. cited by applicant
.
Saeko Takahashi, et al., "New Method to Increase a Backup Support
Of A 6 French Guiding Coronary Catheter", Catheterization and
Cardiovascular Interventions, 63:452-456 (2004), 5 Pages; Published
online in Wiley InterScience (www.interscience.wiley.com). cited by
applicant .
Complaint, Jury Trial Demanded, Dated May 15, 2013, Filed in
District Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions,
Inc., v. Boston Scientific Corporation, 18 Pgs. cited by applicant
.
Amended Complaint, Jury Trial Demanded, Dated May 28, 2013, Filed
in District Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions,
Inc., v. Boston Scientific Corporation, 20 Pgs. cited by applicant
.
Plaintiff's Memorandum in Support of Motion for Preliminary
Injunction, dated Jun. 10, 2013, Filed in District Court Case
0:13-cv-01172 (JRT-SER), Vascular Solutions, Inc., v. Boston
Scientific Corporation, 40 Pgs. cited by applicant .
Declaration of Howard Root in Support of Plaintiff's Motion for
Preliminary Injunction, Dated Jun. 10, 2013, Filed in District
Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions, Inc., v.
Boston Scientific Corporation, 55 Pgs. cited by applicant .
Declaration of Anthony C. Vrba, Dated Jul. 8, 2013, Filed in
District Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions,
Inc., v. Boston Scientific Corporation, 4 Pgs. cited by applicant
.
Declaration of Tony J. Demartini, M.D., Dated Jul. 8, 2013, Filed
in District Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions,
Inc., v. Boston Scientific Corporation, 3 Pgs. cited by applicant
.
Placeholder for Declaration of Sam Rasmusen, Dated Jul. 8, 2013,
Filed in District Court Case 0:13-cv-01172 (JRT-SER), Vascular
Solutions, Inc., v. Boston Scientific Corporation, 1 Pg. cited by
applicant .
Boston Scientific Corporation's Answer to Amended Complaint and
Counterclaims, Dated Jul. 11, 2013, Filed in District Court Case
0:13-cv-01172 (JRT-SER), Vascular Solutions, Inc., v. Boston
Scientific Corporation, 22 Pgs. cited by applicant .
Plaintiff's Reply Memorandum in Support of Motion for Preliminary
Injunction ***Redacted***, Filed Jul. 24, 2013, Filed in District
Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions, Inc., v.
Boston Scientific Corporation, 27 Pgs. cited by applicant .
Second Declaration of Howard Root in Support of Plaintiff's Motion
for Preliminary Injunction, Dated Jul. 24, 2013, Filed in District
Court Case 0:13-cv-01172 (JRT-SER), Vascular Solutions, Inc., v.
Boston Scientific Corporation, 22 Pgs. cited by applicant .
U.S. Appl. No. 11/416,629, filed Jun. 28, 2010; Howard Root et al.
cited by applicant .
U.S. Appl. No. 12/824,734, filed Jun. 28, 2010, Howard Root et al.
cited by applicant.
|
Primary Examiner: Mehta; Bhisma
Assistant Examiner: Osinski; Bradley
Attorney, Agent or Firm: Patterson Thuente Pedersen,
P.A.
Parent Case Text
RELATED APPLICATIONS
This application is .Iadd.a reissue of application Ser. No.
13/359,059, filed Jan. 26, 2012 which issued as U.S. Pat. No.
8,292,850 entitled "Coaxial Guide Catheter for Interventional
Cardiology Procedures" and a continuation of application Ser. No.
14/070,161 entitled "Coaxial Guide Catheter for Interventional
Cardiology Procedures" which is an application for reissue of U.S.
Pat. No. 8,292,850 which is .Iaddend.a divisional of application
Ser. No. 12/824,734, filed Jun. 28, 2010 entitled "Coaxial Guide
Catheter for Interventional Cardiology Procedures", which is
divisional of application Ser. No. 11/416,629, filed May 3, 2006
now U.S. Pat. No. 8,048,032 entitled "Coaxial Guide Catheter for
Interventional Cardiology Procedures": .Iadd.now U.S. Pat. No.
8,142,413: more than one reissue application has been filed for the
reissue of U.S. Pat. No. 8,292,850; the reissue applications are
application Ser. No. 14/070,161, this application and continuation
reissue application Ser. Nos. 14/195,413 and 14/195,435 filed Mar.
3, 2014, the same day as this application.Iaddend..
Claims
The invention claimed is:
.[.1. A system for use with interventional cardiology devices
adapted to be insertable into a branch artery, the system
comprising: a guide catheter having a continuous lumen extending
for a predefined length from a proximal end at a hemostatic valve
to a distal end adapted to be placed in the branch artery, the
continuous lumen of the guide catheter having a circular
cross-sectional inner diameter sized such that interventional
cardiology devices are insertable into and through the continuous
lumen of the guide catheter; and a device adapted for use with the
guide catheter, including: a flexible tip portion defining a
tubular structure and having a circular cross-section and a length
that is shorter than the predefined length of the continuous lumen
of the guide catheter, the tubular structure having a
cross-sectional outer diameter sized to be insertable through the
cross-sectional inner diameter of the continuous lumen of the guide
catheter and defining a coaxial lumen having a cross-sectional
inner diameter through which interventional cardiology devices are
insertable; and a substantially rigid portion proximal of and
operably connected to, and more rigid along a longitudinal axis
than the flexible tip portion and defining a structure without a
lumen having a maximal cross-sectional dimension at a proximal
portion that is smaller than the cross-sectional outer diameter of
the flexible tip portion and having a length that, when combined
with the length of the flexible distal tip portion, defines a total
length of the device along the longitudinal axis that is longer
than the length of the continuous lumen of the guide catheter, such
that when at least a distal portion of the flexible tip portion is
extended distally of the distal end of the guide catheter, at least
a portion of the proximal portion of the substantially rigid
portion extends proximally through the hemostatic valve in common
with interventional cardiology devices that are insertable into the
guide catheter..].
.[.2. The system of claim 1, wherein the tubular structure includes
a distal portion adapted to be extended beyond the distal end of
the guide catheter while a proximal portion remains within the
lumen of the guide catheter, such that the device assists in
resisting axial and shear forces exerted by the interventional
cardiology device passed through and beyond the coaxial lumen that
would otherwise tend to dislodge the guide catheter from the branch
artery..].
.[.3. The system of claim 2, wherein the proximal portion of the
tubular structure further comprises structure defining a proximal
side opening extending for a distance along the longitudinal axis,
and accessible from a longitudinal side defined transverse to the
longitudinal axis, to receive the interventional cardiology devices
into the coaxial lumen while the proximal portion remains within
the lumen of the guide catheter..].
.[.4. The system of claim 3, wherein the proximal side opening
includes structure defining a full circumference portion and
structure defining a partially cylindrical portion..].
.[.5. The system of claim 1, wherein the tubular structure includes
a flexible cylindrical distill tip portion and a flexible
cylindrical reinforced portion proximal to the flexible distal tip
portion..].
.[.6. The system of claim 5, wherein the flexible cylindrical
reinforced portion is reinforced with metallic elements in a
braided or coiled pattern..].
.[.7. The system of claim 2, wherein the flexible cylindrical
distal tip portion further comprises a radiopaque marker proximate
a distal tip..].
.[.8. The system of claim 1, wherein the cross-sectional inner
diameter of the coaxial lumen of the tubular structure is not more
than one French smaller than the cross-sectional inner diameter of
the guide catheter..].
.[.9. The system of claim 1, wherein the substantially rigid
portion includes from distal to proximal direction, a
cross-sectional shape having a full circumference portion, a
hemicylindrical portion and an arcuate portion..].
.[.10. The system of claim 1, wherein the predefined length of the
guide catheter is about 100 cm and the total length of the device
is about 125 cm..].
.[.11. The system of claim 1, further comprising a kit that
includes the guide catheter and the device in a common sterile
package..].
.[.12. A system for use with interventional cardiology devices
adapted to be insertable into a branch artery, the system
comprising: a guide catheter having a continuous lumen extending
for a predefined length from a proximal end at a hemostatic valve
to a distal end adapted to be placed in the branch artery, the
continuous lumen of the guide catheter having a circular
cross-section and a cross-sectional inner diameter sized such that
interventional cardiology devices are insertable into and through
the continuous lumen of the guide catheter; and a device adapted
for use with the guide catheter, including: an elongate structure
having an overall length that is longer than the predefined length
of the continuous lumen of the guide catheter, the elongate
structure including: a flexible tip portion defining a tubular
structure and having a circular cross-section that is smaller than
the circular cross-section of the continuous lumen of the guide
catheter and a length that is shorter than the predefined length of
the continuous lumen of the guide catheter, the flexible tip
portion having a cross-sectional outer diameter sized to be
insertable through the cross-sectional inner diameter of the
continuous lumen of the guide catheter and defining a coaxial lumen
having a cross-sectional inner diameter through which
interventional cardiology devices are insertable; a reinforced
portion proximal to the flexible tip portion; and a substantially
rigid portion proximal of, connected to, and more rigid along a
longitudinal axis rail than the flexible tip portion and defining a
structure without a lumen having a maximal cross-sectional
dimension at a proximal portion that is smaller than the
cross-sectional outer diameter of the flexible tip portion, such
that when at least a distal portion of the flexible tip portion is
extended distally of the distal end of the guide catheter with at
least proximal portion of the reinforced portion remaining within
the continuous lumen of the guide catheter, at least a portion of
the proximal portion of the substantially rigid portion extends
proximally through the hemostatic valve in common with
interventional cardiology devices that are insertable into the
guide catheter..].
.[.13. The system of claim 12, wherein, when the distal portion of
the flexible tip portion is insertable through the continuous lumen
of the guide catheter and beyond the distal end of the guide
catheter, the device assists in resisting axial and shear forces
exerted by an interventional cardiology device passed through and
beyond the coaxial lumen that would otherwise tend to dislodge the
guide catheter from the branch artery..].
.[.14. The system of claim 12, wherein the substantially rigid
portion further includes a partially cylindrical portion defining
an opening extending for a distance along a side thereof defined
transverse to a longitudinal axis that is adapted to receive an
interventional cardiology device passed through continuous lumen of
the guide catheter and into the coaxial lumen while the device is
inserted into the continuous lumen, the opening extending
substantially along at least a portion of a length of the
substantially rigid portion..].
.[.15. The system of claim 12, wherein, after the device is
inserted into the continuous lumen of the guide catheter, the
device presents an overall effective length of a coaxial lumen
through which an interventional cardiology device may be inserted
while utilizing only a single hemostatic valve and without any
telescoping structure preassembled prior to the device being
inserted into the continuous lumen of the guide catheter..].
.[.16. The system of claim 12, the device further comprising a
radiopaque marker proximate the distal portion of the flexible tip
portion..].
.[.17. The system of claim 12, wherein the reinforced portion of
the device is reinforced with metallic elements in a braided or
coiled pattern..].
.[.18. The system of claim 12, wherein the cross-sectional inner
diameter of the coaxial lumen of the flexible distal portion is not
more than one French smaller than the cross-sectional inner
diameter of the guide catheter..].
.[.19. The system of claim 12, wherein the substantially rigid
portion includes, from distal to proximal, a cross-sectional shape
having a full circumference portion, a hemicylindrical portion and
an arcuate portion..].
.[.20. The system of claim 12, wherein the elongate structure
includes, starting at the distal portion of the flexible distal
portion, at least a first portion having a first flexural modulus,
a second portion having a second flexural modulus greater than the
first flexural modulus, and a third portion having a third flexural
modulus greater than the second flexural modulus..].
.[.21. The system of claim 20, in which the first flexural modulus
is about 13,000 PSI plus or minus 5000 PSI, the second flexural
modulus is about 29,000 PSI plus or minus 10,000 PSI, and the third
portion flexural modulus is about 49,000 PSI plus or minus 10,000
PSI..].
.[.22. The system of claim 20, in which the first portion is about
0.1 cm in length, the second portion is about three cm in length,
and the third portion is about five cm in length..].
.[.23. The system of claim 12, wherein the predefined length of the
guide catheter is about 100 cm and the total length of the device
is about 125 cm..].
.[.24. The system of claim 12, further comprising a kit that
includes the guide catheter and the device in a common sterile
package..].
.Iadd.25. A system, comprising: a guide catheter configured to be
advanceable through a main blood vessel to a position adjacent an
ostium of a coronary artery, the guide catheter having a lumen
extending from a hemostatic valve at a proximal end of the guide
catheter to a distal end of the guide catheter that is adapted to
be positioned adjacent the ostium of the coronary artery; and a
guide extension catheter configured to be partially advanceable
through the guide catheter and into the coronary artery, the guide
extension catheter having a length such that a distal end of the
guide extension catheter is extendable through the lumen and beyond
the distal end of the guide catheter, and a proximal end of the
guide extension catheter is extendable through the hemostatic valve
at the proximal end of the guide catheter, the guide extension
catheter including, in a proximal to distal direction, a
substantially rigid segment, a segment defining a side opening, and
a tubular structure defining a lumen coaxial and in fluid
communication with the lumen of the guide catheter, the lumen of
the tubular structure having a length that is shorter than the
length of the lumen of the guide catheter and having a uniform
cross-sectional inner diameter that is not more than one French
size smaller than the cross-sectional inner diameter of the lumen
of the guide catheter, the side opening extending for a distance
along a longitudinal axis of the segment defining the side opening
and accessible from a longitudinal side defined transverse to the
longitudinal axis, and the side opening and the lumen of the
tubular structure configured to receive one or more stents or
balloon catheters when the segment defining the side opening and a
proximal end portion of the tubular structure are positioned within
the lumen of the guide catheter and the distal end of the guide
extension catheter extends beyond the distal end of the guide
catheter; wherein a material forming the segment defining the side
opening is more rigid than the tubular structure..Iaddend.
.Iadd.26. The system of claim 25, wherein the segment defining the
side opening includes a portion having an arcuate cross-sectional
shape..Iaddend.
.Iadd.27. The system of claim 25, wherein the segment defining the
side opening includes a portion having a hemicylindrical
cross-sectional shape..Iaddend.
.Iadd.28. The system of claim 25, wherein the segment defining the
side opening includes a portion having a full circumference
cross-sectional shape..Iaddend.
.Iadd.29. The system of claim 28, wherein the cross-section of the
guide extension catheter at the portion of the segment defining the
side opening having the full circumference cross-sectional shape
includes a single lumen..Iaddend.
.Iadd.30. The system of claim 25, wherein the segment defining the
side opening defines a concave track configured to guide the one or
more stents or balloon catheters along a length of the concave
track..Iaddend.
.Iadd.31. The system of claim 25, wherein the segment defining the
side opening includes at least one inclined slope..Iaddend.
.Iadd.32. The system of claim 25, wherein the segment defining the
side opening includes at least two inclined slopes..Iaddend.
.Iadd.33. The system of claim 25, wherein the side opening is
formed by a cutout portion of a cylindrical tubular
structure..Iaddend.
.Iadd.34. The system of claim 25, wherein the segment defining the
side opening and the tubular structure comprise a reinforced
portion of the guide extension catheter..Iaddend.
.Iadd.35. The system of claim 25, wherein the distal end of the
guide extension catheter includes a tip portion..Iaddend.
.Iadd.36. The system of claim 35, wherein a flexural modulus of the
tubular structure is greater than a flexural modulus of the tip
portion..Iaddend.
.Iadd.37. The system of claim 25, wherein the uniform
cross-sectional inner diameter of the lumen of the tubular
structure is greater than a largest outer dimension of the
substantially rigid segment..Iaddend.
.Iadd.38. The system of claim 25, wherein the substantially rigid
segment is eccentrically positioned relative to a cross-section of
the tubular structure..Iaddend.
.Iadd.39. The system of claim 38, further comprising a stent
releasably joined to the distal end of the elongate balloon
catheter..Iaddend.
.Iadd.40. The system of claim 25, further comprising an elongate
balloon catheter partially insertable within the guide catheter
alongside the substantially rigid segment, through the side
opening, and through the lumen of the tubular
structure..Iaddend.
.Iadd.41. The system of claim 25, wherein a cross-section of the
substantially rigid segment is sufficiently sized and configured to
permit the tubular structure of the guide extension catheter to be
partially advanced through the guide catheter and into the coronary
artery without blocking use of the guide catheter..Iaddend.
.Iadd.42. The system of claim 25, wherein the substantially rigid
segment and the tubular structure are operably coupled at or
adjacent to the segment defining the side opening..Iaddend.
.Iadd.43. The system of claim 25, further comprising means for
releasably joining the proximal end of the guide catheter and the
proximal end of the guide extension catheter..Iaddend.
.Iadd.44. The system of claim 25, wherein a flexural modulus of the
segment defining the side opening is greater than a flexural
modulus of the tubular structure..Iaddend.
.Iadd.45. The system of claim 25, wherein the guide extension
catheter is configured such that the proximal end of the tubular
structure cannot be advanced to or past the distal end of the guide
catheter..Iaddend.
.Iadd.46. The system of claim 25, wherein the segment defining the
side opening includes one or more cuts and wherein a first cut is
spaced approximately 0.010 inches apart from a second
cut..Iaddend.
.Iadd.47. The system of claim 25, wherein a distal portion of the
guide extension catheter is configured to anchor within the ostium
of the coronary artery and resist axial and shear forces exerted by
the one or more received stents or balloon catheters that would
otherwise tend to dislodge the distal portion..Iaddend.
.Iadd.48. A system, comprising: a guide catheter configured to be
advanceable through a main blood vessel to a position adjacent an
ostium of a coronary artery, the guide catheter having a lumen
extending from a hemostatic valve at a proximal end of the guide
catheter to a distal end of the guide catheter that is adapted to
be positioned adjacent the ostium of the coronary artery; and a
guide extension catheter configured to be partially advanceable
through the guide catheter and into the coronary artery, the guide
extension catheter having a length such that a distal end of the
guide extension catheter is extendable through the lumen and beyond
the distal end of the guide catheter, and a proximal end of the
guide extension catheter is extendable through the hemostatic valve
at the proximal end of the guide catheter, the guide extension
catheter including, in a proximal to distal direction, a
substantially rigid segment, a segment defining a side opening, and
a tubular structure defining a lumen coaxial and in fluid
communication with the lumen of the guide catheter, the lumen of
the tubular structure having a length that is shorter than the
length of the lumen of the guide catheter and having a uniform
cross-sectional inner diameter that is not more than one French
size smaller than the cross-sectional inner diameter of the lumen
of the guide catheter, the side opening extending for a distance
along a longitudinal axis of the segment defining the side opening
and accessible from a longitudinal side defined transverse to the
longitudinal axis, and the side opening and the lumen of the
tubular structure configured to receive one or more stents or
balloon catheters when the segment defining the side opening and a
proximal end portion of the tubular structure are positioned within
the lumen of the guide catheter and the distal end of the guide
extension catheter extends beyond the distal end of the guide
catheter; wherein the segment defining the side opening comprises a
portion of the guide extension catheter that is more rigid than a
distal end portion of the tubular structure..Iaddend.
.Iadd.49. The system of any one of claims 25, 31, 32, 48, 38, 40,
41 or 43, wherein the segment defining the side opening includes
one or more cuts..Iaddend.
.Iadd.50. The system of claim 49, wherein at least one cut includes
two circumferential cuts along a single line and separated by a
section of uncut structure..Iaddend.
.Iadd.51. A system, comprising: a guide catheter configured to be
advanceable through a main blood vessel to a position adjacent an
ostium of a coronary artery, the guide catheter having a lumen
extending from a hemostatic valve at a proximal end of the guide
catheter to a distal end of the guide catheter that is adapted to
be positioned adjacent the ostium of the coronary artery; and a
guide extension catheter configured to be partially advanceable
through the guide catheter and into the coronary artery, the guide
extension catheter having a length such that a distal end of the
guide extension catheter is extendable through the lumen and beyond
the distal end of the guide catheter, and a proximal end of the
guide extension catheter is extendable through the hemostatic valve
at the proximal end of the guide catheter, the guide extension
catheter including, in a proximal to distal direction, a
substantially rigid segment, a segment defining a side opening, and
a tubular structure defining a lumen coaxial and in fluid
communication with the lumen of the guide catheter, the lumen of
the tubular structure having a length that is shorter than the
length of the lumen of the guide catheter and having a uniform
cross-sectional inner diameter that is not more than one French
size smaller than the cross-sectional inner diameter of the lumen
of the guide catheter, the side opening extending for a distance
along a longitudinal axis of the segment defining the side opening
and accessible from a longitudinal side defined transverse to the
longitudinal axis, and the side opening and the lumen of the
tubular structure configured to receive one or more stents or
balloon catheters when the segment defining the side opening and a
proximal end portion of the tubular structure are positioned within
the lumen of the guide catheter and the distal end of the guide
extension catheter extends beyond the distal end of the guide
catheter; wherein the tip portion includes an atraumatic bumper
formed from a flexible material and having a lumen continuous with
the lumen of the tubular structure; and wherein the tubular
structure includes a reinforcing braid or coil, and wherein the tip
portion includes a marker band positioned distal to the distal end
of the reinforcing braid or coil..Iaddend.
.Iadd.52. The system of claim 51, wherein a longitudinal length of
the reinforcing braid or coil is between 20 to 30 cm..Iaddend.
.Iadd.53. A system, comprising: a guide catheter configured to be
advanceable through a main blood vessel to a position adjacent an
ostium of a coronary artery, the guide catheter having a lumen
extending from a hemostatic valve at a proximal end of the guide
catheter to a distal end of the guide catheter that is adapted to
be positioned adjacent the ostium of the coronary artery; and a
guide extension catheter configured to be partially advanceable
through the guide catheter and into the coronary artery, the guide
extension catheter having a length such that a distal end of the
guide extension catheter is extendable through the lumen and beyond
the distal end of the guide catheter, and a proximal end of the
guide extension catheter is extendable through the hemostatic valve
at the proximal end of the guide catheter, the guide extension
catheter including, in a proximal to distal direction, a
substantially rigid segment, a segment defining a side opening, and
a tubular structure defining a lumen coaxial and in fluid
communication with the lumen of the guide catheter, the lumen of
the tubular structure having a length that is shorter than the
length of the lumen of the guide catheter and having a uniform
cross-sectional inner diameter that is not more than one French
size smaller than the cross-sectional inner diameter of the lumen
of the guide catheter, the side opening extending for a distance
along a longitudinal axis of the segment defining the side opening
and accessible from a longitudinal side defined transverse to the
longitudinal axis, and the side opening and the lumen of the
tubular structure configured to receive one or more stents or
balloon catheters when the segment defining the side opening and a
proximal end portion of the tubular structure are positioned within
the lumen of the guide catheter and the distal end of the guide
extension catheter extends beyond the distal end of the guide
catheter; wherein a material forming the segment defining the side
opening is more rigid than the tubular structure; wherein a
flexural modulus of the substantially rigid segment is greater than
a flexural modulus of the tubular structure..Iaddend.
Description
FIELD OF THE INVENTION
The present invention relates generally to catheters used in
interventional cardiology procedures. More particularly the present
invention relates to methods and apparatus for increasing backup
support for catheters inserted into the coronary arteries from the
aorta.
BACKGROUND OF THE INVENTION
Interventional cardiology procedures often include inserting
guidewires or other instruments through catheters into coronary
arteries that branch off from the aorta. For the purposes of this
application, the term "interventional cardiology devices" is to be
understood to include but not be limited to guidewires, balloon
catheters, stents and stent catheters. In coronary artery disease
the coronary arteries may be narrowed or occluded by
atherosclerotic plaques or other lesions. These lesions may totally
obstruct the lumen of the artery or may dramatically narrow the
lumen of the artery. Narrowing is referred to as stenosis. In order
to diagnose and treat obstructive coronary artery disease it is
commonly necessary to pass a guidewire or other instruments through
and beyond the occlusion or stenosis of the coronary artery.
In treating a stenosis, a guide catheter is inserted through the
aorta and into the ostium of the coronary artery. This is sometimes
accomplished with the aid of a guidewire. A guide catheter is
typically seated into the opening or ostium of the artery to be
treated and a guidewire or other instrument is passed through the
lumen of the guide catheter and inserted into the artery beyond the
occlusion or stenosis. Crossing tough lesions can create enough
backward force to dislodge the guide catheter from the ostium of
the artery being treated. This can make it difficult or impossible
for the interventional cardiologist to treat certain forms of
coronary artery disease.
Prior attempts to provide support to the guiding catheter to
prevent backward dislodgement from the coronary ostium (referred to
as "backup support") fall generally into four categories.
First are guiding catheters that, through a combination of shape
and stiffness, are configured to draw backup support from engaging
the wall of the aortic arch opposing the ostium of the coronary
artery that is being accessed. Examples of this approach can be
found in U.S. Pat. No. 6,475,195 issued to Voda and U.S. Pat. No.
5,658,263 issued to Dang et al. These guiding catheters all share
the common limitation that a guide catheter stiff enough to provide
adequate backup support is often too stiff to be safely inserted
into the aorta without the possibility of causing damage to the
aortic wall. In addition, attempts to deep seat the guide catheter
have been made but the rigid nature of the guide catheter creates
the risk that the guide catheter may damage the coronary artery
wall or that the guide catheter may occlude the coronary artery and
interfere with blood flow to the heart muscle.
Second are guiding catheters that include a retractable appendage.
The appendage in these catheters can be extended to engage the
opposing wall of the aortic arch to provide backup support or the
appendage may be placed under tension to stiffen a bend in the
catheter to provide backup support. Examples of this approach may
be found in U.S. Pat. No. 4,813,930 issued to Elliot; U.S. Pat. No.
5,098,412 issued to Shiu; and U.S. Pat. No. 6,860,876 issued to
Chen. These guiding catheters tend to be somewhat mechanically
complex and have not been widely adopted by practitioners.
Third are guide catheters that have a portion that seeks to expand
laterally to grip the interior wall of the ostium of the coronary
artery to provide a force acting in opposition to the backward
forces created when trying to maneuver a therapeutic device past a
lesion or blockage in the coronary artery. These devices can
include a balloon secured to a guidewire or a catheter or another
device for expanding to grip the walls of the coronary artery from
within. Examples of this approach may be found in U.S. Pat. No.
4,832,028 issued to Patel; U.S. Pat. No. 6,595,952 issued to
Forsberg; and U.S. Published Application No. 2005/0182437 by
Bonnette et al. Again, these devices tend to be mechanically
complex and can completely occlude the coronary ostium thus
stopping perfusion of the coronary artery.
A fourth technique includes the placement of a smaller guide
catheter within a larger guide catheter in order to provide added
support for the crossing of lesions or for the distal delivery of
balloons and stents. This technique has been described in an
article by Takahashi entitled "New Method to Increase a Backup
Support of Six French Guiding Coronary Catheter," published in
Catheterization and Cardiovascular Interventions, 63:452-456
(2004). This technique is used in order to provide a method of deep
seating the guide catheter within the ostium of the coronary
artery. Deep seating refers to inserting the catheter more deeply
into the ostium of the coronary artery than typically has been done
before. Unfortunately, deep seating by this technique with a
commonly available guide catheter creates the risk that the
relatively stiff, fixed curve, guide catheter will damage the
coronary artery. This damage may lead to dissection of the coronary
artery when the catheter is advanced past the ostium.
Several other problems arise when using a standard guide catheter
in this catheter-in-a-catheter fashion. First, the inner catheters
must be substantially longer than the one hundred centimeter guide
catheter. Second, a new hemostasis valve must be placed on the
inner guide catheter which prevents the larger guide catheter from
being used for contrast injections or pressure measurements. Third,
the smaller guide catheter still must be inserted into the coronary
vessel with great care since the smaller guide catheter has no
tapered transition or dilator at its tip and does not run over a
standard 0.014 inch guidewire.
Thus, the interventional cardiology art would benefit from the
availability of a system that would be deliverable through standard
guide catheters for providing backup support by providing the
ability to effectively create deep seating in the ostium of the
coronary artery.
SUMMARY OF THE INVENTION
The present invention is a coaxial guide catheter that is
deliverable through standard guide catheters by utilizing a
guidewire rail segment to permit delivery without blocking use of
the guide catheter. The coaxial guide catheter preferably includes
a tapered inner catheter that runs over a standard 0.014 inch
coronary guidewire to allow atraumatic placement within the
coronary artery. This feature also allows removal of the tapered
inner catheter after the coaxial guide catheter is in place. The
tapered inner catheter provides a gradual transition from the
standard 0.014 inch diameter guidewire to the diameter of the
coaxial guide catheter which is typically five to eight French.
The coaxial guide catheter preferably can be delivered through
commonly existing hemostatic valves used with guide catheters while
still allowing injections through the existing Y adapter. In
addition, the coaxial guide catheter preferably has an inner
diameter that is appropriate for delivering standard coronary
treatment devices after it is placed in the coronary artery.
In one embodiment, the coaxial guide catheter is made in at least
three sizes corresponding to the internal capacity of 8 French, 7
French, and 6 French guide catheters that are commonly used in
interventional cardiology procedures. An 8 French catheter has an
internal diameter greater than or equal to 0.088 inches. A 7 French
catheter has an internal diameter greater than or equal to 0.078
inches. A 6 French guide catheter has an internal diameter greater
than or equal to 0.070 inches. Thus, for three exemplary sizes the
effective internal diameter of the coaxial guide catheter may be as
follows. For a 7 French in 8 French coaxial guide catheter, the
internal diameter should be greater than or equal to 0.078 inches.
For a 6 French in 7 French coaxial guide catheter the internal
diameter should be greater than or equal to 0.070 inches. For a 5
French in 6 French coaxial guide catheter the internal diameter
should be greater than or equal to 0.056 inches.
Interventional cardiology procedures are typically carried out
under fluoroscopy or another x-ray or imaging technique. Therefore,
one embodiment of the coaxial guide catheter of the present
invention includes a radiopaque marker at its distal tip to
facilitate positioning and manipulation of the coaxial guide
catheter.
The present invention generally includes the coaxial guide catheter
and a tapered inner catheter. The coaxial guide catheter includes a
tip portion, a reinforced portion. and a substantially rigid
portion. The coaxial guide catheter will generally have an overall
length of preferably approximately 125 cm, though this should not
be considered limiting.
In one embodiment, the tip portion may include a soft tip and a
marker band. The soft tip is tapered and may be formed from a low
durometer polymer or elastomer material such as polyether block
amide polymer, (PEBA, Pebax.RTM.) the marker band may be formed
from a platinum iridium alloy sandwiched between the Pebax.RTM.
that extends from the bump tip and a PTFE liner.
In one embodiment, the reinforced portion may be reinforced,
preferably with metallic fibers in a braided or coiled pattern. The
braided or coiled portion is lined by a PTFE liner and may be
covered on its exterior with Pebax.RTM.. The braided or coiled
portion may extend approximately 20 to 110 cm in length. In one
exemplary embodiment, the braided portion extends approximately 32
to 36 cm.
Preferably, the rigid portion may be advantageously formed from a
stainless steel or Nitinol tube. The rigid portion may be joined to
the braid or coil portion by welding. The rigid portion may include
a cutout portion and a full circumference portion. For example, the
cutout portion may include a section where about 45% of the
circumference of the cylindrical tubular structure has been
removed. The cutout portion may also include a section where 75-90%
of the circumference of the tubular structure has been removed. In
one exemplary embodiment, the portion having approximately 45%
removed may extend for approximately 75 cm and the portion having
75-90% of the structure removed extends for about 15 cm.
The full circumference portion of the rigid portion is typically
located at the most proximal end of the coaxial guide catheter.
The rigid portion may include a plurality of radially oriented
slits or other cuts in its distal portion to increase and control
the flexibility of the rigid portion
In an exemplary embodiment, the tapered inner catheter generally
includes a tapered inner catheter tip and a cutout portion. The
tapered inner catheter tip includes a tapered portion and a
straight portion. The tapered portion is typically at the most
distal end of the tapered inner catheter. Both the straight portion
and the tapered portion are pierced by a lumen through which a
guidewire may be passed.
The cutout portion supports a track passing along the concave side
thereof that continues from the lumen that passes through the
straight portion and the tapered portion. The tapered inner
catheter may also have a clip or snap attachment at its proximal
end to releasably join the tapered inner catheter to the coaxial
guide catheter.
In operation, the tapered inner catheter is inserted inside and
through the coaxial guide catheter. The tapered inner catheter is
positioned so that the tapered inner catheter tip extends beyond
the tip portion of the coaxial guide catheter. The coaxial guide
catheter-tapered inner catheter combination may then be inserted
into a blood vessel that communicates with the aorta. The coaxial
guide catheter-tapered inner catheter combination may be threaded
over a preplaced 0.014 inch guidewire. The tapered inner
catheter-coaxial guide catheter combination is advanced up the
aorta until the tapered inner catheter is passed into the ostium of
a coronary artery over the guidewire. Once the coaxial guide
catheter-tapered inner catheter combination has been inserted
sufficiently into the ostium of the coronary artery to achieve deep
seating the tapered inner catheter may be removed. During this
entire process at least part of the coaxial guide catheter-tapered
inner catheter combination is located inside of the guide
catheter.
Once the tapered inner catheter is removed a cardiac treatment
device, such as a guidewire, balloon or stent, may be passed
through the coaxial guide catheter within the guide catheter and
into the coronary artery. As described below, the presence of the
coaxial guide catheter provides additional backup support to make
it less likely that the coaxial guide catheter guide catheter
combination will be dislodged from the ostium of the coronary
artery while directing the coronary therapeutic device past a tough
lesion such as a stenosis or a chronic arterial occlusion.
A guide catheter inserted into the ostium of a branch artery where
it branches off from a larger artery is subject to force vectors
that tend to dislodge the distal end of the guide catheter from the
ostium of the branch artery when a physician attempts to direct a
guidewire or other interventional cardiology device past an
occlusive or stenotic lesion in the branch artery. This discussion
will refer to a guide wire but it is to be understood that similar
principles apply to other interventional cardiology devices
including balloon catheters and stent catheters.
One of the forces that act on the guide catheter is an axial force
substantially along the axis of the branch artery and the portion
of the guide catheter that is seated in the ostium. This force
vector is a reactive force created by the pushing back of the guide
wire against the guide catheter as the physician tries to force the
guidewire through or past the lesion. It tends to push the distal
end of the catheter out of the ostium in a direction parallel to
the axis of the branch artery and the axis of the distal end of the
guide catheter.
Another of the force vectors that acts on the guide catheter is a
shearing force that tends to dislodge the distal end of the guide
catheter from the ostium of the branch artery in a direction
perpendicular to the axis of the branch artery and the axis of the
distal end of the guide catheter. This force vector arises from
curvature of the guide catheter near its distal end and the guide
wire pushing on the curved portion of the guide catheter as the
physician applies force to the guidewire. The coaxial guide
catheter of the present invention assists in resisting both the
axial forces and the shearing forces that tend to dislodge a guide
catheter from the ostium of a branch artery.
The system is deliverable using standard techniques utilizing
currently available equipment. The present invention also allows
atraumatic placement within the coronary artery. Further, the
invention is deliverable through an existing hemostatic valve
arrangement on a guide catheter without preventing injections
through existing Y adapters. Finally, the invention has an inner
diameter acceptable for delivering standard coronary devices after
it is placed in the blood vessel.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic depiction of the coaxial guide catheter and a
tapered inner catheter in accordance with the present
invention;
FIG. 2 is schematic depiction of the coaxial guide catheter and
tapered inner catheter assembled in accordance with the present
invention;
FIG. 3 is a plan view of a guide catheter, the coaxial guide
catheter, and a treatment catheter in accordance with the present
invention;
FIG. 4 is a sectional view of the coaxial guide catheter in
accordance with the present invention;
FIG. 5 is a cross sectional view of the coaxial guide catheter and
tapered inner catheter in accordance with the present
invention;
FIG. 6 is another cross sectional view of the coaxial guide
catheter and tapered inner catheter in accordance with the present
invention;
FIG. 7 is a schematic view of a guide catheter and a guidewire
located in an aortic arch and a coronary artery and the guide
catheter and guidewire in a second position depicted in
phantom;
FIG. 8 is a schematic view of a guide catheter, a guidewire, a
coaxial guide catheter in accordance with the present invention and
a tapered inner catheter located in the aortic arch and coronary
artery;
FIG. 9 is a schematic view of a guide catheter, a guidewire and a
coaxial guide catheter in accordance with the present invention
located in the aortic arch and coronary artery;
FIG. 10 is a flat pattern for making relief cuts in a curved rigid
portion of the coaxial guide catheter in accordance with the
present invention;
FIG. 11 is a detailed view taken from FIG. 10;
FIG. 12 is a plan view of the rigid portion in accordance with the
present invention;
FIG. 13 is an elevational view of the rigid portion;
FIG. 14 is a sectional view of the rigid portion taken along
section line 14-14 of FIG. 13; and
FIG. 15 is a sectional view of the rigid portion taken along
section line 15-15 of FIG. 13.
FIG. 16 is a sectional view of the rigid portion taken along
section line 16-16 of FIG. 13.
FIG. 17 is a plan view of a coaxial guide catheter having a longer
rail segment and a tapered inner catheter in accordance with the
present invention.
FIG. 18 is a plan view of the tapered inner catheter as depicted in
the FIG. 17.
FIG. 19 is a cross-sectional view of the tapered inner catheter
taken along section lines 19-19 of FIG. 18.
FIG. 20 is a plan view of a coaxial guide catheter in accordance
with the present invention.
FIG. 21 is an elevational view of a coaxial guide catheter in
accordance with the present invention.
FIG. 22 is a cross-sectional view taken along section line 22-22 of
FIG. 21.
DETAILED DESCRIPTION OF THE DRAWINGS
Referring to FIGS. 1 and 2, coaxial guide catheter assembly 10 of
the present invention generally includes coaxial guide catheter 12
and tapered inner catheter 14.
Coaxial guide catheter 12 generally includes tip portion 16,
reinforced portion 18, and rigid portion 20. The overall length of
the coaxial guide catheter typically can be approximately 125 cm.
This length should not be considered limiting.
Tip portion 16 generally includes bump tip 22 and marker band 24.
Bump tip 22 includes taper 26. Bump tip 24 is relatively flexible
and may be formed, for example, from 4033 Pebax.RTM.. Bump tip 22
may be yellow or another high visibility color for ease of
handling.
Marker band 24 is formed of a radiopaque material such as
platinum/iridium alloy usually at a 90/10 ratio. Marker band 24 may
be sandwiched between an outer Pebax.RTM. material 28 and a PTFE
liner 30. Outer Pebax.RTM. material 28 in this location may be
formed of 5533 Pebax, for example.
Reinforced portion 18 includes braid or coil reinforcement 32.
Braid or coil reinforcement 32 may be formed of metal, plastic,
graphite, or composite structures known to the art. Reinforced
portion 18 may be lined on the interior by PTFE liner 30 and
covered on the exterior by Pebax.RTM. material 28. Tip portion 16
and reinforced portion 18 together form a substantially cylindrical
structure. Braid or coil reinforcement 32 may extend approximately
20 to 30 cm. In one exemplary embodiment, braid or coiled portion
has a length of approximately 32 to 36 cm.
Rigid portion 20 may be secured to braid or coil reinforcement by,
for example, welding or bonding. Rigid portion 20 may be formed
from a hypotube or a section of stainless steel or Nitinol tubing.
Other substantially rigid materials may be used as well. Rigid
portion 20 includes first full circumference portion 34,
hemicylindrical portion 36, arcuate portion 38, and second full
circumference portion 40.
First full circumference portion 34 is joined to braid or coil
reinforcement 32. First full circumference portion 34 extends for a
relatively short distance, for example, 0.25 cm.
Hemicylindrical portion 36 desirably includes 40% to 70% of the
circumference of the tube. Hemicylindrical portion 36 may extend,
for example, approximately 20 to 75 cm in length.
Hemicylindrical portion 36 tapers into arcuate portion 38.
Arcuate portion 38 extends from 25% to 40% of the circumference of
the tube. Arcuate portion 38 may extend linearly, for example, for
about 15 cm.
Arcuate portion 38 connects to second full circumference portion
40. Second full circumference portion 40 may extend for a short
distance, for example, approximately 3 cm.
Tapered inner catheter 14 generally includes tapered inner catheter
tip 42 and cutout portion 44. Tapered inner catheter tip 42 tapers
gradually from the diameter of a guide wire to the diameter of tip
portion 16.
Tapered inner catheter tip 42 includes tapered portion 46 at a
distal end thereof, and straight portion 48. Both tapered portion
46 and straight portion 48 are pierced by lumen 50.
Cutout portion 44 defines a concave track 52 along its length.
Concave track 52 is continuous with lumen 50.
Tapered inner catheter 14 may also include clip 54 at a proximal
end thereof to releasably join tapered inner catheter 14 to coaxial
guide catheter 12. Thus, tapered inner catheter 14 is keyed to
coaxial guide catheter 12.
Coaxial guide catheter 12 may include, starting at its distal end,
a first portion having a flexural modulus of about 13,000 PSI plus
or minus 5000 PSI, a second portion having a flexural modulus of
about 29,000 PSI plus or minus 10,000 PSI, a third portion having a
flexural modulus of about 49,000 PSI plus or minus 10,000 PSI and a
fourth portion having a flexural modulus of about 107,000 PSI plus
or minus 20,000 PSI. Coaxial guide catheter 12 may be formed, for
example, of 4033 Pebax.RTM. at bump tip 22 for the first 0.1 cm.
This portion may followed by a section about three cm long of 5533
Pebax.RTM. that covers marker band 24 and the distal portion of
braid or coil reinforcement 32. Next may come an approximately five
cm portion of 6333 Pebax.RTM. which encloses part of braid or coil
reinforcement 32 followed by an approximately twenty seven cm
portion of 7233 Pebax.RTM. covering the most proximal portion of
braid or coil reinforcement 32. Braid or coil reinforcement 32 is
bonded to rigid portion 20 which may be formed from stainless steel
or a similar biocompatible material. Rigid portion 20 may extend
for approximately ninety cm and include first full circumference
portion 34 (approximately 0.25 cm), hemicylindrical portion 36
(approximately seventy five cm), arcuate portion (approximately
fifteen cm) and second full circumference portion (approximately
three cm.) Rigid portion 20 may be formed from a stainless steel or
Nitinol hypo tube.
FIG. 7 depicts a typical guide catheter 56 passing through aortic
arch 58 into ostium 60 of coronary artery 62. FIG. 7 also depicts
guidewire 64 passing through the guide catheter 56 and into
coronary artery 62. Located in coronary artery 62 is stenotic
lesion 66. In a typical procedure, guidewire 64 is placed through
the aortic arch 58 and into the ostium 60 of the coronary artery.
62. The guide catheter 56 is passed over guidewire 64 until distal
end 68 of guide catheter 56 is seated in ostium 60 of coronary
artery 62. Force is then applied to the guidewire 64 to push
guidewire 64 past stenotic lesion 66 or an occlusive lesion (not
shown). Once the guidewire 64 is pushed past stenotic lesion 66 or
occlusive lesion (not shown), a treating catheter including a stent
or balloon can be passed along the guidewire to stenotic lesion 66
or occlusive lesion (not shown). The lesion can then be
treated.
As can be seen in phantom, in FIG. 7, the application of force to
guidewire 64 can cause guide catheter 56 to dislodge from ostium 60
of coronary artery 62. This can occur in the case of a tough
stenotic lesion 66 or occlusive lesion (not shown) when it is
difficult to pass the guidewire 64 beyond the stenotic lesion 66 or
occlusive lesion (not shown).
Referring the FIG. 8 coaxial guide catheter 12 is depicted as used
with guide catheter 56, guidewire 64, and tapered inner catheter
14. Here, coaxial guide catheter 12 with tapered inner catheter 14
is passed through guide catheter 56 and over guidewire 64 into
coronary artery 62 after the guide catheter 56 has been placed in
the ostium 60 of coronary artery 62, as depicted in FIG. 7. Coaxial
guide catheter 12, with tapered inner catheter 14, provides an
inner support member for proper translation over guidewire 64.
Tapered inner catheter tip 42 provides a distal tapered transition
from guidewire 64 to coaxial guide catheter 12. Once coaxial guide
catheter 12 is in place, tapered inner catheter 14 is removed from
the inside of coaxial guide catheter 12.
Coaxial guide catheter 12 is now ready to accept a treatment
catheter such as a stent or balloon catheter. Referring to FIG. 9,
the combination of guide catheter 56 with coaxial guide catheter 12
inserted into ostium 60 of coronary artery 62 provides improved
distal anchoring of guide catheter 56 and coaxial guide catheter
12. The presence of coaxial guide catheter 12 within guide catheter
56 also provides stiffer back up support than guide catheter 56
alone. The combination of improved distal anchoring and stiffening
of the guide catheter 56/coaxial guide catheter 12 combination
provides additional back up support to resist dislodging of guide
catheter 56 from ostium 60 when force is applied to guidewire 64 to
pass through stenotic lesion 66 or another lesion. In addition, the
improved back up support assists in the positioning of a treating
catheter that may include a stent or balloon.
Referring to FIGS. 10 and 11, in some embodiments of coaxial guide
catheter 12, rigid portion 20 may be perforated by relief cuts 70.
Relief cuts 70 may be classed into first group 72 and second group
74.
First group 72 may be located near to the juncture between rigid
portion 20 and reinforced portion 18. First group 72 of relief cuts
70, are relatively closely spaced. For example, first group 72 of
relief cuts 70 may be spaced approximately 0.010 inches apart.
First group 72 of relief cuts 70 extends for a relatively short
distance, for example, approximately 2 inches.
Second group 74 of relief cuts 70 may extend for a relatively long
distance, for example, approximately 30-35 inches. Second group 74
of relief cuts 70 are spaced farther apart than first group 72. For
example, relief cuts 70 of second group 74 may be spaced
approximately 0.020 inches between cuts. Referring particularly to
FIG. 11, relief cuts 70 may include single cuts 76 and double cuts
78. Single cuts 76 may include an individual linear cut, as can be
seen in FIG. 11. Double cuts 78 may include two linear cuts along a
single line but separated by a short section of uncut structure.
Typically, single cuts 76 and double cuts 78 are alternated along
the length of rigid portion 20. Generally, the overall length of
single cut 76 may be less than the overall length of two double
cuts 78.
In an embodiment depicted in FIGS. 12-15, rigid portion includes
full circumference portion 80, greater than 180.degree. portion 82,
and less than 180.degree. portion 84. Greater than 180.degree.
portion 82 may, for example, include structure forming
approximately 300.degree. of the circumference of the cylinder.
Less than 180.degree. portion may include, for example, structure
forming approximately 90.degree. of the circumference of a
cylinder. Greater than 180.degree. portion 82 may extend
approximately 22-25 inches. Greater than 180.degree. portion 82
holds tapered inner catheter 14 within rigid portion 20.
When tapered inner catheter is inserted into coaxial guide catheter
12 greater than 180.degree., portion 82 grips tapered inner
catheter 14 which is exposed through the opening in greater than
180.degree. portion 82. Thus, the overall structure of tapered
inner catheter 14 along with greater than 180.degree. portion 82 is
substantially cylindrical. Accordingly, when inserted through a
guide catheter 56 having a Touhey-Borst style adapter, the
Touhey-Borst style adapter can still seal around rigid portion 20
and enclosed inner tapered catheter 14.
Referring to FIG. 16, another embodiment of coaxial guide catheter
assembly 10 includes coaxial guide catheter 12 and tapered inner
catheter 14. Tapered inner catheter 14 is keyed to coaxial guide
catheter 12 at hub 86.
Referring to FIGS. 17 and 18, tapered inner catheter 14 generally
includes connector hub 88 and catheter tube 90.
Connector hub 88 generally includes connector portion 92, grip
portion 94 and joining portion 96. Connector hub 88 defines funnel
portion 98 therein.
Catheter tube 90 generally includes straight portion 100, tapered
portion 102 and marker band tip 104. Catheter tube 90 is joined to
connector hub 88 at joining portion 96. Tapered inner catheter 14
may be formed in whole or in part from low-density polyethylene
plastic, for example. Other suitable materials known to the
catheter arts may be used as well.
Grip portion 94 desirably includes gripping ears 106. Gripping ears
106 may extend outwardly from grip portion 94 substantially
radially and be shaped for convenient gripping by a physician.
Referring to FIGS. 19 through 21, in this embodiment, coaxial guide
catheter 12 includes interrupted hub 108, hemitube portion 110,
braided portion 112 and tip portion 114.
Interrupted hub 108 defines an opening 116, along a side thereof.
Interrupted hub 108 may be substantially C-shaped or U-shaped in
cross section. Opening 116 is sized so that tapered inner catheter
14 may be passed readily therethrough in a direction perpendicular
to the long axes of both interrupted hub 108 and tapered inner
catheter 14. Hemi-tube portion 110 is immediately distal to
interrupted hub 108. Hemi-tube portion 110 may be formed, for
example, from a metal hypo tube forming approximately 50% of the
circumference of a cylinder. Hemi-tube portion 110 is aligned so
that opening 116 of interrupted hub 108 is coextensive with opening
118 of hemi-tube portion 110. Hemi-tube portion 110 is joined to
braided portion 112, for example, by adhesive, bonding or welding.
The location where hemi-tube portion 110 and braided portion 112
join defines the entire circumference of a cylinder.
Braided portion 112 may be reinforced by a coil or braid, 120. Coil
or braid 120 may be formed of metal or another suitable reinforcing
material.
Tip portion 114 is generally not reinforced and is substantially
soft. Tip portion 114 is similarly structured to tapered inner
catheter tip 42. Tip portion 114 may include a radiopaque marker
band 24.
Beginning at the distal end of coaxial guide catheter 12, tip
portion 114 may be formed substantially of, for example, 2533
Pebax.RTM. This may be followed by a section of 3533 Pebax.RTM.,
then by a section of 5533 Pebax.RTM., then by a further section of
7233 Pebax.RTM.. These Pebax.RTM. portions may all incorporate, for
example, about 20% barium sulfate (BaSO.sub.4).
In one embodiment, tip portion 114 and braided portion 112 may have
an overall length together of approximately one hundred nine
centimeters. Hemi-tube portion 110 and interrupted hub 108 may
together have an overall length of approximately eighteen
centimeters.
In this embodiment, coaxial guide catheter 12 may be lined with a
PTFE liner 122.
In operation, a guide catheter 56 is inserted into a major blood
vessel in the body such as aortic arch 58 over guidewire 64 and the
distal end 68 of guide catheter 56 is brought into proximity of
ostium 60 of a smaller branch blood vessel, such as coronary artery
62, that it is desired to enter. Coaxial guide catheter 12, with
tapered inner catheter 14, is inserted through guide catheter 56
and over guidewire 64. Guide catheter 56, guidewire 64, coaxial
guide catheter 12, and tapered inner catheter 14 are manipulated to
insert tapered inner catheter tip 42 into the ostium 60 of the
blood vessel that branches off from the major blood vessel. The
bump tip 22 of coaxial guide catheter 12 is inserted with tapered
inner catheter tip 42 well into ostium 60 of coronary artery 62 or
other blood vessel until bump tip 22 of coaxial guide catheter 12
achieves a deep seated position. Tapered inner catheter 14 is then
withdrawn from the lumen of coaxial guide catheter 12. An
interventional cardiology treatment device such as a catheter
bearing a stent or a balloon (not shown) is then inserted through
the lumen of coaxial guide catheter 12 which remains inside guide
catheter 56.
When the interventional cardiology device reaches a stenosis or
blockage in coronary artery 62 or another branch blood vessel,
force may be applied to the interventional cardiology device
catheter while reinforced portion 18 and rigid portion 20 of
coaxial guide catheter 12 provide back up support. The back force
that would tend to dislodge bump tip 22 from a deep seated position
in the ostium in the branch blood vessel is transferred through
reinforced portion 18 to rigid portion 20 of coaxial guide catheter
12. A physician may apply a force to the proximal end of the
coaxial guide catheter 12 to resist dislodging of bump tip 22 from
the ostium of the branch artery.
One advantage of the present invention over prior art approaches is
that the present invention does not interfere with the injection of
fluids via the Y-adapter of guide catheter 56 as does the use of a
smaller catheter within a larger catheter.
The present invention may be embodied in other specific forms
without departing from the spirit of the essential attributes
thereof; therefore, the illustrated embodiments should be
considered in all respects as illustrative and not restrictive,
reference being made to the appended claims rather than to the
foregoing description to indicate the scope of the invention.
* * * * *