U.S. patent application number 10/241738 was filed with the patent office on 2003-08-28 for apparatus for the dialysis of blood, method for fabricating the same, and method for the dialysis of blood.
This patent application is currently assigned to Biolink Corporation. Invention is credited to Estabrook, Brian K., Martins, Harold M., Prosl, Frank R., Smith, Paul J..
Application Number | 20030163083 10/241738 |
Document ID | / |
Family ID | 21932032 |
Filed Date | 2003-08-28 |
United States Patent
Application |
20030163083 |
Kind Code |
A1 |
Estabrook, Brian K. ; et
al. |
August 28, 2003 |
Apparatus for the dialysis of blood, method for fabricating the
same, and method for the dialysis of blood
Abstract
Improved apparatus for the dialysis of blood, a method for
fabricating the same, and an improved method for the dialysis of
blood.
Inventors: |
Estabrook, Brian K.;
(Foxboro, MA) ; Smith, Paul J.; (West Kingston,
RI) ; Prosl, Frank R.; (Duxbury, MA) ;
Martins, Harold M.; (Newton, MA) |
Correspondence
Address: |
Mark J. Pandiscio
Pandiscio & Pandiscio
470 Totten Pond Road
Waltham
MA
02154
US
|
Assignee: |
Biolink Corporation
|
Family ID: |
21932032 |
Appl. No.: |
10/241738 |
Filed: |
September 10, 2002 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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10241738 |
Sep 10, 2002 |
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09044372 |
Mar 19, 1998 |
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6447488 |
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Current U.S.
Class: |
604/43 ;
604/526 |
Current CPC
Class: |
A61M 25/005 20130101;
A61M 2025/0031 20130101 |
Class at
Publication: |
604/43 ;
604/526 |
International
Class: |
A61M 003/00 |
Claims
What is claimed is:
1. A catheter comprising at least one flexible tubular element,
said at least one tubular element having an open proximal end, an
open distal end and a side wall defining a lumen extending between
said open proximal end and said open distal end, said side wall (1)
being formed of a biocompatible material, (2) encasing a
reinforcing means therein for reinforcing said side wall, and (3)
having a smooth interior surface for defining said lumen, said
smooth interior surface being sufficiently smooth that said at
least one tubular element may be used for hemodialysis applications
with good results.
2. A catheter according to claim 1 wherein the average variation in
the local surface profile of said lumen is less than about 0.0015
inch.
3. A catheter according to claim 1 wherein said biocompatible
material comprises silicone rubber.
4. A catheter according to claim 3 wherein said biocompatible
material comprises silicone rubber having a hardness of
approximately 80 durometer.
5. A catheter according to claim 1 wherein said reinforcing means
are formed out of a material stiffer than the material used to form
said side wall.
6. A catheter according to claim 5 wherein said reinforcing means
are formed out of metal.
7. A catheter according to claim 6 wherein said reinforcing means
are formed out of titanium.
8. A catheter according to claim 6 wherein said reinforcing means
are formed out of stainless steel.
9. A catheter according to claim 5 wherein said reinforcing means
are formed out of plastic.
10. A catheter according to claim 1 wherein said reinforcing means
comprise a coil spring.
11. A catheter according to claim 10 wherein the wire forming said
coil spring has a thickness of approximately 0.006 inch and a coil
rate of approximately 0.031-0.038 pitch.
12. A catheter according to claim 10 wherein said coil spring
comprises titanium.
13. A catheter according to claim 12 wherein the wire forming said
coil spring has a thickness of approximately 0.006 inch and a coil
rate of approximately 0.031-0.038 pitch.
14. A catheter according to claim 1 wherein said reinforcing means
comprise a plurality of ring-like elements.
15. A catheter according to claim 1 wherein said reinforcing means
are formed out of a radio-opaque material.
16. A catheter according to claim 1 wherein said side wall has a
thickness of approximately 0.015 inch.
17. A catheter according to claim 1 wherein said at least one side
wall comprises a smooth outer surface.
18. A catheter according to claim 1 further comprising a support
structure attached to said side wall adjacent to said open distal
end of said at least one flexible tubular element.
19. A catheter according to claim 18 wherein said support structure
is at least partially embedded in said side wall.
20. A catheter according to claim 16 wherein said support structure
is formed out of a radio-opaque material.
21. A catheter according to claim 18 wherein said at least one
tubular element is substantially cylindrical, and further wherein
said support structure comprises a ring-shaped element formed of a
material more rigid than the biocompatible material forming said at
least one tubular element.
22. A catheter according to claim 18 wherein said at least one
tubular element is substantially cylindrical, and further wherein
said support structure comprises a substantially cylindrical
element having an outer diameter, a distal end, a proximal end, a
first inner diameter portion adjacent to said distal end, a second
inner diameter portion adjacent to said proximal end, and a
proximally-facing shoulder connecting said first and second inner
diameter portions.
23. A catheter according to claim 18 wherein said at least one
tubular element is substantially cylindrical, and further wherein
said support structure comprises a substantially cylindrical
element defining at least one opening therethrough.
24. A catheter according to claim 23 wherein said at least one
opening comprises a slot extending to said proximal end of said
support structure.
25. A catheter according to claim 1 further comprising a support
structure attached to said side wall adjacent to, but spaced from,
said open distal end of said at least one flexible tubular
element.
26. A catheter according to claim 1 wherein said side wall defines
at least one opening therethrough in proximally-spaced, proximate
relation to said open distal end of said at least one flexible
tubular element.
27. A catheter according to claim 26 wherein said at least one
opening comprises a substantially circular hole.
28. A catheter according to claim 26 wherein said at least one
opening comprises a longitudinally-extending slit.
29. A catheter according to claim 28 wherein said slit is normally
substantially closed, but is capable of opening when a positive
internal pressure is established in said lumen.
30. A catheter according to claim 1 wherein said catheter comprises
a pair of said flexible tubular elements longitudinally joined
together in side-by-side relation to one another.
31. Apparatus for use in the dialysis of the blood of a patient,
said apparatus comprising a connector portion and a catheter
portion; said connector portion comprising an outlet adapted for
communication with a line connected to the input port of a dialysis
machine, and an inlet adapted for communication with a line
connected to the output port of a dialysis machine; and said
catheter portion comprising a catheter element comprising: a
suction line and a return line, each said line comprising a
flexible tubular element, said tubular element having an open
proximal end, an open distal end and a side wall defining a lumen
extending between said open proximal end and said open distal end,
said side wall (1) being formed of a biocompatible material, (2)
encasing reinforcing means therein for reinforcing said side wall,
and (3) having a smooth interior surface for defining said lumen,
said smooth interior surface being sufficiently smooth that said
tubular element may be used for hemodialysis applications with good
results; said proximal end of said suction line being connected to
said connector portion and in communication with said outlet, and
said distal end of said suction line terminating in a suction line
mouth; said proximal end of said return line being connected to
said connector portion and in communication with said inlet, and
said distal end of said return line terminating in a return line
mouth; said suction line and said return line being adapted for
disposition within the body of the patient so that said suction
line mouth and said return line mouth are both disposed in the
vascular system of the patient.
32. Apparatus according to claim 31 wherein said connector portion
comprises an extracorporeal connector element adapted for
attachment against an outside surface of the body of the
patient.
33. Apparatus according to claim 31 wherein said connector portion
comprises a subcutaneous port element adapted for implantation
within the body of the patient.
34. A method for making a catheter, said method comprising the
steps of: (a) providing an elongated, removable molding core; (b)
forming a tubular element of biocompatible material on said molding
core; (c) positioning reinforcing means for reinforcing said
tubular element on the outer surface of said tubular element; (d)
forming an overlayer of biocompatible material over said tubular
element and said reinforcing means; and (e) removing said molding
core from the coated tubular element.
35. A method according to claim 34 wherein said tubular element is
formed on said molding core by co-extruding said tubular element
about the outer surface of said molding core.
36. A method according to claim 34 wherein said step of removing
said molding core from said coated tubular element comprises
reducing the transverse cross-section of said molding core.
37. A method according to claim 36 wherein reducing the transverse
cross-section of said elongated molding core comprises stretching
said molding core longitudinally.
38. A method according to claim 36 wherein reducing the transverse
cross-section of said elongated molding core comprises melting said
core.
39. A method according to claim 36 wherein reducing the transverse
cross-section of said elongated molding core comprises dissolving
said core.
40. A method according to claim 34 wherein said step of removing
said molding core from said coated tubular element comprises
pulling said molding core longitudinally out of said coated tubular
element.
41. A method according to claim 34 comprising the further steps of,
prior to step (d), forming at least one side opening through said
tubular element in proximally-spaced, proximate relation to the
distal end thereof, and inserting a molding pin therein.
42. A method according to claim 34 comprising the further step of,
prior to step (d), locating a support structure at the distal end
of said tubular element.
43. A method for the dialysis of the blood of a patient, said
method comprising the steps of: (a) providing a dialysis machine,
and providing apparatus comprising a connector portion and a
catheter portion; said connector portion comprising an outlet
adapted for communication with a line connected to the input port
of said dialysis machine, and an inlet adapted for communication
with a line connected to the output port of said dialysis machine;
and said catheter portion comprising a catheter element comprising:
a suction line and a return line, each said line comprising a
flexible tubular element, said tubular element having an open
proximal end, an open distal end and a side wall defining a lumen
extending between said open proximal end and said open distal end,
said side wall (1) being formed of a biocompatible material, (2)
encasing a reinforcing means therein for reinforcing said side
wall, and (3) having a smooth interior surface for defining said
lumen, said smooth interior surface being sufficiently smooth that
said tubular element may be used for hemodialysis applications with
good results; said proximal end of said suction line being
connected to said connector portion and in communication with said
outlet, and said distal end of said suction line terminating in a
suction line mouth; said proximal end of said return line being
connected to said connector portion and in communication with said
inlet, and said distal end of said return line terminating in a
return line mouth; said suction line and said return line being
adapted for disposition within the body of the patient so that said
suction line mouth and said return line mouth are both disposed in
the vascular system of the patient; (b) placing said suction line
mouth and said return line mouth in the vascular system of the
patient; (c) connecting said outlet to the input port of said
dialysis machine, and connecting said inlet to the output port of
said dialysis machine; and (d) operating said dialysis machine.
44. A method according to claim 43 wherein said connector portion
comprises an extracorporeal connector element attached against an
outside surface of the body of the patient.
45. A method according to claim 43 wherein said connector portion
comprises a subcutaneous port element implanted within the body of
the patient.
46. A method according to claim 43 wherein, in step (a), said
suction line and said return line are field trimmed to size prior
to being connected to said connector portion.
47. A catheter comprising at least one flexible tubular element,
said at least one tubular element having an open proximal end, an
open distal end and a side wall defining a lumen extending between
said open proximal end and said open distal end, said side wall
being formed of a biocompatible material and having a smooth
interior surface for defining said lumen, said smooth interior
surface being sufficiently smooth that said at least one tubular
element may be used for hemodialysis applications with good
results, and said catheter further comprising a support structure
attached to said side wall adjacent to said open distal end of said
at least one flexible tubular element.
48. A method according to claim 34 wherein said step of removing
said molding core from said coated tubular element comprises
blowing said molding core longitudinally out of said coated tubular
element.
49. A catheter according to claim 1 wherein said reinforcing means
comprise a tubular, braided mesh reinforcer.
Description
FIELD OF THE INVENTION
[0001] This invention relates to the dialysis of blood in general,
and more particularly to apparatus and methods for use in the
same.
BACKGROUND OF THE INVENTION
[0002] A healthy kidney removes toxic wastes and excess water from
the blood. In End Stage Renal Disease ("ESRD"), or chronic kidney
failure, the kidneys progressively stop performing these essential
functions over a long period of time. When the kidneys fail, a
patient dies within a short period of time unless that patient
receives dialysis treatment for the rest of that patient's life or
undergoes transplantation of a healthy, normal kidney. Since
relatively few kidneys are currently available for transplantation,
the overwhelming majority of patients with ESRD receive dialysis
treatment.
[0003] Hemodialysis therapy is an extracorporeal (i.e., outside the
body) process which removes toxins and water from a patient's
blood. A hemodialysis machine pumps blood from the patient, through
a dialyzer, and then back to the patient. The dialyzer removes the
toxins and water from the blood by a membrane diffusion process.
Typically, a patient with chronic kidney disease requires
hemodialysis three times per week, for 3-6 hours per session.
Removing blood from the body requires a vascular access to the
patient's blood system.
[0004] One common method for accessing a patient's blood system for
hemodialysis involves the use of a percutaneous catheter assembly.
The percutaneous catheter assembly is inserted into a major vein,
such as the femoral, subclavian or jugular vein. For long term
maintenance dialysis, the jugular vein is generally the preferred
insertion site. The catheter assembly is percutaneous, with one end
external to the body and the other end dwelling in either the
superior vena cava or the right atrium of the heart. The external
portion of the catheter assembly has connectors permitting
attachment of blood lines leading to and from the hemodialysis
machine.
[0005] FIGS. 1 and 2 show the traditional manner of positioning a
percutaneous catheter assembly 5 relative to the body. More
particularly, percutaneous catheter assembly 5 generally comprises
a catheter portion 10 comprising a dual-lumen catheter element 15,
and a connector portion 20 comprising an extracorporeal connector
element 25. The catheter assembly's extracorporeal connector
element 25 is disposed against the chest 30 of the patient, and the
distal end 35 of catheter element 15 is passed into the patient's
internal jugular vein 40 (FIG. 2) and then down into the patient's
superior vena cava 45. More particularly, the distal end 35 of
catheter element 15 is positioned within the patient's superior
vena cava 45 such that the mouth 50 of suction line 55, and the
mouth 60 of return line 65, are both located between the patient's
right atrium 70 and the patient's left subclavia vein 75 and right
subclavia vein 80. Alternatively, the distal end 35 of catheter
element 15 may be positioned so that mouth 50 of suction line 55,
and mouth 60 of return line 65, are located within the patient's
right atrium 70. The percutaneous catheter assembly 5 is then left
in this position relative to the body, waiting to be used during an
active dialysis session.
[0006] When hemodialysis is to be performed on the patient, the
catheter assembly's extracorporeal connector element 25 is
appropriately connected to a dialysis machine (not shown), i.e.,
suction line 55 is connected to the input port (i.e., the suction
port) of the dialysis machine, and return line 65 is connected to
the output port (i.e., the return port) of the dialysis machine.
The dialysis machine is then activated (i.e., the dialysis
machine's blood pump is turned on and the flow rate set), whereupon
the dialysis machine will withdraw relatively "dirty" blood from
the patient through suction line 55 and return relatively "clean"
blood to the patient through return line 65.
[0007] It has also been proposed to use a subcutaneous port and
catheter assembly to provide vascular access for hemodialysis.
[0008] More particularly, a subcutaneous port and catheter assembly
82 is shown in FIGS. 3-5. Looking first at FIG. 3, subcutaneous
port and catheter assembly 82 generally comprises a connector
portion 84 comprising a subcutaneous port element 86, and the
aforementioned catheter portion 10 comprising the dual-lumen
catheter element 15. As noted above, the catheter element 15 in
turn comprises the suction line 55 and the return line 65.
Subcutaneous port element 86 includes a needle port 88 which is
connected to suction line 55, and a needle port 90 which is
connected to return line 65. The distal end of suction line 55
terminates in the aforementioned mouth 50, and the distal end of
return line 65 terminates in the aforementioned mouth 60.
[0009] FIGS. 4 and 5 show subcutaneous port and catheter assembly
82 positioned within the body. More particularly, the assembly's
port element 86 is disposed under the skin of the patient (e.g., in
the chest area of the patient), and the assembly's catheter element
15 is passed into the patient's internal jugular vein 40 and then
down into the patient's superior vena cava 45. The distal end of
the assembly's catheter element 15 may be positioned within the
patient's superior vena cava 45 such that mouth 50 of suction line
55, and mouth 60 of return line 65, are both located approximately
between the patient's right atrium 70 and the patient's left
subclavia vein 75 and right subclavia vein 80. Alternatively, the
distal end of catheter element 15 may be positioned so that mouth
50 of suction line 55, and mouth 60 of return line 65, are located
within the patient's right atrium 70. The subcutaneous port and
catheter assembly 82 is then left in this position within the body,
waiting to be used during an active dialysis session.
[0010] When hemodialysis is to be performed on the patient, the
assembly's subcutaneous port element 86 is appropriately connected
to a dialysis machine, i.e., needle port 88 is connected to the
input port (i.e., the suction port) of the dialysis machine with an
appropriate percutaneous needle (not shown), and the assembly's
needle port 90 is connected to the output port (i.e., the return
port) of the dialysis machine with an appropriate percutaneous
needle (not shown). The dialysis machine is then activated,
whereupon it will withdraw relatively "dirty" blood from the
patient through suction line 55 and return relatively "clean" blood
to the patient through return line 65.
[0011] It will be appreciated that both percutaneous catheter
assembly 5 (FIGS. 1 and 2) and subcutaneous port and catheter
assembly 82 (FIGS. 3-5) comprise the catheter portion 10, which in
turn comprises the dual-lumen catheter element 15, with the distal
end of the catheter element normally dwelling in the patient's
vascular system.
[0012] Inasmuch as a substantial portion of catheter element 15
dwells in the patient's vascular system (e.g., within internal
jugular vein 40 and superior vena cava 45), it is desirable for the
catheter element to have the smallest possible outside diameter so
as to minimize interference with normal blood flow. At the same
time, however, it is also desirable for the catheter element to
have the largest possible inside diameter so that maximum dialysis
blood flow can be achieved. Thus, from the standpoint of blood flow
alone, it is desirable for the catheter element to have the
thinnest possible wall thickness.
[0013] Unfortunately, however, other considerations also come into
effect. For one thing, it is also important that the catheter
element have the highest possible burst strength so that it will
not fail when passing blood under pressure. In addition, it is also
important that the catheter element be able to withstand high
negative pressures without collapsing, so that blood can be
withdrawn from the body at a rapid rate. Furthermore, it is
important that the catheter element be capable of being bent at a
substantial angle without kinking, such as, for example, at the
point where the catheter element undergoes a large deflection in
order to enter internal jugular vein 40 (see FIGS. 1 and 4). These
and other considerations tend to significantly limit the degree to
which the catheter element's wall thickness can be reduced.
[0014] Furthermore, the choice of materials for forming the
catheter element is also limited, since the element is typically
deployed in the patient's body for substantial periods of time.
Currently, silicone rubber is the accepted material for forming
catheter elements for use in percutaneous catheter assemblies and
subcutaneous port and catheter assemblies.
[0015] The foregoing factors have, collectively, tended to limit
either (1) the degree to which the outside diameter of the catheter
element can be reduced, and/or (2) the degree to which the inside
diameter of the catheter element can be enlarged, and/or (3) the
rate at which blood can be introduced into the patient's body
through the catheter element, and/or (4) the rate at which blood
can be withdrawn from the patient's body through the catheter
element, and/or (5) the degree to which the catheter element can be
bent without kinking.
[0016] In U.S. Pat. No. 5,041,098, issued Aug. 20, 1991 to
Loiterman et al., it was suggested that a helically wound
reinforcement wire could be incorporated into the side wall of the
catheter element. Such a suggestion could appear to be
advantageous, since it could enable the walls of the catheter
element to be made thinner yet stronger.
[0017] Unfortunately, in practice, Applicants have found that
commercially-available coil-reinforced silicone rubber tubes lack
the smooth interior lumen desirable for hemodialysis
applications.
[0018] More particularly, Applicants have discovered that in
hemodialysis applications, smooth lumen walls are important for (1)
providing the laminar blood flows required for high volume blood
transfer, (2) avoiding the creation of irregular blood currents and
the creation of blood stagnation areas, (3) avoiding the formation
of blood clots, (4) eliminating breeding areas for bacteria, and
(5) facilitating flush-cleaning of the apparatus after dialysis has
taken place.
[0019] Unfortunately, Applicants have also found that
commercially-available coil-reinforced silicone rubber tubes lack
the smooth interior lumen desirable for hemodialysis
applications.
[0020] It is believed that this may be due to the facts that (1)
commercially-available coil-reinforced silicone rubber tubes are
generally used for purposes other than dialysis applications, and
(2) the importance of smooth interior lumens has not yet been
discovered by the dialysis industry.
[0021] It is also believed that commercially-available
coil-reinforced silicone rubber tubes may lack the smooth interior
lumen desirable for hemodialysis applications due to the manner in
which such tubes are typically formed.
[0022] More particularly, it is believed that
commercially-available coil-reinforced silicone rubber tubes are
generally formed by (1) creating an outer tube out of silicone
rubber, (2) forcing that tube open, (3) inserting the coil spring
inside the forced-open silicone rubber tube, (4) releasing the
outer tube so that it contracts back on the coil spring, and (5)
dip molding an interior layer of silicone rubber onto the spring
and the interior lumen is of the outer tube. While such a process
is generally adequate for capturing the coil spring within a body
of silicone rubber material, it also results in an undulating
interior lumen, since the process essentially covers the coil
spring and the interior lumen of the outer tube with a
substantially constant-thickness dip layer. Coil-reinforced
silicone rubber tubes formed with the aforementioned process are
not smooth enough for good hemodialysis applications.
OBJECTS OF THE INVENTION
[0023] Accordingly, one object of the present invention is to
provide improved apparatus for use in the dialysis of blood.
[0024] Another object of the present invention is to provide an
improved catheter element for use in the dialysis of blood, wherein
the catheter element may be used in either a percutaneous catheter
assembly or a subcutaneous port and catheter assembly.
[0025] And another object of the present invention is to provide an
improved catheter element which has the largest possible interior
diameter and the smallest possible exterior diameter, yet is
resistant to bursting, collapse and kinking.
[0026] Still another object of the present invention is to provide
an improved catheter element which incorporates reinforcing means
within the side wall of the catheter, yet has an interior lumen
which is sufficiently smooth that the catheter element may be used
in hemodialysis applications with good results.
[0027] And another object of the present invention is to provide a
support structure at the distal end of the catheter element to help
maintain openness of the flow path through the catheter
element.
[0028] Yet another object of the present invention is to provide an
improved method for fabricating apparatus for use in the dialysis
of blood.
[0029] And another object of the present invention is to provide an
improved method for the dialysis of blood.
SUMMARY OF THE INVENTION
[0030] These and other objects are addressed by the present
invention, which comprises improved apparatus for the dialysis of
blood, a method for making the same, and an improved method for the
dialysis of blood.
[0031] In one preferred embodiment, the present invention comprises
a catheter comprising at least one flexible tubular element, the at
least one tubular element having an open proximal end, an open
distal end and a side wall defining a lumen extending between the
open proximal end and the open distal end, the side wall (1) being
formed of a biocompatible material, (2) encasing reinforcing means
therein for reinforcing the side wall, and (3) having a smooth
interior surface for defining the lumen, the smooth interior
surface being sufficiently smooth that the at least one tubular
element may be used for hemodialysis applications with good
results.
[0032] In another preferred embodiment, the present invention
comprises apparatus for use in the dialysis of the blood of a
patient, the apparatus comprising a connector portion and a
catheter portion; the connector portion comprising an outlet
adapted for communication with a line connected to the input port
of a dialysis machine, and an inlet adapted for communication with
a line connected to the output port of a dialysis machine; and the
catheter portion comprising a catheter element comprising: a
suction line and a return line, each such line comprising a
flexible tubular element, the tubular element having an open
proximal end, an open distal end and a side wall defining a lumen
extending between the open proximal end and the open distal end,
the side wall (1) being formed of a biocompatible material, (2)
encasing reinforcing means therein for reinforcing the side wall,
and (3) having a smooth interior surface for defining the lumen,
the smooth interior surface being sufficiently smooth that the
tubular element may be used for hemodialysis applications with good
results; the proximal end of the suction line being connected to
the connector portion and in communication with the outlet, and the
distal end of the suction line terminating in a suction line mouth;
the proximal end of the return line being connected to the
connector portion and in communication with the inlet, and the
distal end of the return line terminating in a return line mouth;
the suction line and the return line being adapted for disposition
within the body of the patient so that the suction line mouth and
the return line mouth are both disposed in the vascular system of
the patient.
[0033] In yet another preferred embodiment, the present invention
comprises a method for making a catheter, the method comprising the
steps of: (a) providing an removable molding core; (b) forming a
tubular element of biocompatible material on the molding core; (c)
positioning reinforcing means for reinforcing the tubular element
on the outer surface of the tubular element; (d) forming an
overlayer of biocompatible material over the tubular element and
the reinforcing means; and (e) removing the molding core from the
coated tubular element.
[0034] In another preferred embodiment, the present invention
comprises a method for the dialysis of the blood of a patient, the
method comprising the steps of:
[0035] (a) providing a dialysis machine, and providing apparatus
comprising a connector portion and a catheter portion; the
connector portion comprising an outlet adapted for communication
with a line connected to the input port of the dialysis machine,
and an inlet adapted for communication with a line connected to the
output port of the dialysis machine; and the catheter portion
comprising a catheter element comprising: a suction line and a
return line, each such line comprising a flexible tubular element,
the tubular element having an open proximal end, an open distal end
and a side wall defining a lumen extending between the open
proximal end and the open distal end, the side wall (1) being
formed of a biocompatible material, (2) encasing a reinforcing
means therein for reinforcing the side wall, and (3) having a
smooth interior surface for defining the lumen, the smooth interior
surface being sufficiently smooth that the tubular element maybe
used for hemodialysis applications with good results; the proximal
end of the suction line being connected to the connector portion
and in communication with the outlet, and the distal end of the
suction line terminating in a suction line mouth; the proximal end
of the return line being connected to the connector portion and in
communication with the inlet, and the distal end of the return line
terminating in a return line mouth; the suction line and the return
line being adapted for disposition within the body of the patient
so that the suction line mouth and the return line mouth are both
disposed in the vascular system of the patient;
[0036] (b) placing the suction line mouth and the return line mouth
in the vascular system of the patient;
[0037] (c) connecting the outlet to the input port of the dialysis
machine, and connecting the inlet to the output port of the
dialysis machine; and
[0038] (d) operating the dialysis machine.
BRIEF DESCRIPTION OF THE DRAWINGS
[0039] These and other objects and features of the present
invention will be more fully disclosed or rendered obvious by the
following detailed description of the preferred embodiments of the
invention, which are to be considered together with the
accompanying drawings wherein:
[0040] FIG. 1 is a schematic view of a percutaneous catheter
assembly installed in a patient;
[0041] FIG. 2 is a schematic view showing the distal end of the
catheter element of the percutaneous catheter assembly of FIG. 1
installed in a patient, with the direction of blood flow being
indicated by appropriate arrows;
[0042] FIG. 3 is a schematic view of a subcutaneous port and
catheter assembly;
[0043] FIG. 4 is a schematic view showing the subcutaneous port and
catheter assembly of FIG. 3 installed in a patient;
[0044] FIG. 5 is an enlarged schematic view showing the
subcutaneous port and catheter assembly of FIG. 3 installed in a
patient;
[0045] FIG. 6 is a schematic view, partially in section, of novel
catheter apparatus formed in accordance with the present
invention;
[0046] FIG. 7 is a perspective view of a support structure
incorporated into the novel catheter apparatus shown in FIG. 6;
[0047] FIGS. 8-10 are schematic views illustrating how the local
surface profile of the central lumen of the catheter apparatus may
vary along the length of the lumen;
[0048] FIGS. 11-17 illustrate process steps for fabricating the
novel catheter apparatus shown in FIG. 6;
[0049] FIG. 18 illustrates the distal end of an alternative form of
catheter apparatus formed in accordance with the present
invention;
[0050] FIG. 19 is a perspective view of the support structure
incorporated into the catheter apparatus shown in FIG. 18;
[0051] FIGS. 20 and 21 illustrate still other forms of support
structures which may be incorporated into catheter apparatus formed
in accordance with the present invention;
[0052] FIG. 22 illustrates an alternative manner for incorporating
the support structure of FIG. 21 into catheter apparatus formed in
accordance with the present invention;
[0053] FIG. 22A illustrates an alternative manner for forming side
openings near the distal end of the catheter apparatus, wherein the
side openings are in the form of relatively narrow,
longitudinally-extending slits;
[0054] FIG. 23 illustrates catheter apparatus utilizing an
alternative form of reinforcing means; and
[0055] FIG. 23A schematically illustrates an alternative form of
reinforcing means, wherein the reinforcing means comprise a
tubular, braided mesh reinforcer.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0056] Looking next at FIG. 6, novel catheter apparatus 100 is
shown. Catheter apparatus 100 comprises a silicone rubber tube 105
having a side wall 110, a distal end wall 115 and a proximal end
wall 120. The outer surface 125 of side wall 110 has a smooth
configuration so as to minimize interference with blood flow when
catheter apparatus 100 is disposed in the vascular system of a
patient.
[0057] A central lumen 130 extends between distal end wall 115 and
proximal end wall 120. Central lumen 130 has a smooth interior
surface so that blood can be passed through that lumen during a
hemodialysis session with good results.
[0058] Catheter apparatus 100 also comprises reinforcing means 135
encapsulated within side wall 110 for reinforcing the side wall. In
one preferred form of the invention, reinforcing means 135 comprise
a coil spring 140. Reinforcing means 135 may extend along the
entire length of tube 105, or reinforcing means 135 may extend
along only one or more selected portions of tube 105, as preferred.
For example, reinforcing means 135 might extend along only an
intermediate portion of tube 105. In one form of the invention,
reinforcing means 135 are formed out of a radio-opaque material,
where by catheter apparatus 100 may be visualized while within the
body of the patient through the use of appropriate imaging
equipment, whereby to aid in the proper deployment of the apparatus
within the body.
[0059] Preferably, but not necessarily, at least one side opening
145 is formed in side wall 110 adjacent to, but spaced from, distal
end wall 115. The at least one side opening 145 communicates with
central lumen 130, whereby blood may enter and/or exit the distal
end of catheter apparatus 100 via either the distal end of central
lumen 130 and/or the at least one side opening 145. Preferably the
at least one side opening 145 is in the form of a substantially
circular hole.
[0060] And preferably, but not necessarily, a support structure 150
(FIGS. 6 and 7) is disposed at the intersection of central lumen
130 and distal end wall 115 so as to provide a stiffening element
at the distal end of catheter apparatus 100. This member can help
maintain openness of the flow path through catheter apparatus 100.
In one form of the invention, shown in FIGS. 6 and 7, support
structure 150 is formed with a cylindrical configuration, with a
bore 155 opening on the support structure's distal end surface 160,
a counterbore 165 opening on the support structure's proximal end
surface 170, and with an annular shoulder 175 formed at the
intersection of bore 155 and counterbore 165. In one preferred form
of the invention, support structure 150 is mounted to the distal
end of tube 105 so that the support structure's distal end surface
160 lies flush with the tube's distal end surface 115, and so that
the support structure's bore 155 is aligned with the tube's central
lumen 130 (FIG. 6).
[0061] In one preferred form of the invention, tube 105 is formed
out of 80 durometer silicone rubber, and has an outside diameter of
approximately 0.135 inch, an inside diameter of approximately 0.105
inch, and a wall thickness of approximately 0.015 inch; and coil
spring 140 is formed out of titanium, with the wire forming the
coil spring being approximately 0.006 inch thick and having a coil
rate of approximately 0.031-0.038pitch. Support structure 150 is
preferably formed out of a radio-opaque material, whereby the
distal end of catheter apparatus 100 may be visualized while within
the body of the patient through the use of appropriate imaging
equipment, whereby to aid in the proper deployment of the apparatus
within the body.
[0062] It is an important feature of the present invention that
central lumen 130 be formed smooth enough that catheter apparatus
100 may be used for hemodialysis applications with good results.
However, the presence of reinforcing means 135 in the side wall 110
of catheter apparatus 100, and/or the manner of encapsulating
reinforcing means 135 within side wall 110, and/or a variety of
other factors, may cause variations in the diameter of central
lumen 130.
[0063] More particularly, as seen in FIG. 8, the presence of
reinforcing means 135 may cause central lumen 130 to vary outwardly
(as shown at 130A) in the region between adjacent occurrences of
reinforcing means 135; or, as seen in FIGS. 9 and 10, the presence
of reinforcing means 135 may cause central lumen 130 to vary
inwardly (as shown at 130B) in the region between adjacent
occurrences of reinforcing means 135. Such variations in the local
surface profile of central lumen 130 can have a detrimental effect
when catheter apparatus 100 is used for hemodialysis
applications.
[0064] In accordance with the present invention, central lumen 130
of catheter apparatus 100 is formed smooth enough so that catheter
apparatus 100 may be used for hemodialysis applications with good
results.
[0065] In other words, central lumen 130 of catheter apparatus 100
is formed smooth enough to (1) substantially provide the laminar
blood flows required for high volume blood transfer, (2)
substantially avoid the creation of irregular blood currents and
the creation of blood stagnation areas, (3) substantially avoid the
creation of blood clots, (4) substantially eliminate breeding areas
for bacteria, and (5) facilitate flush-cleaning of catheter
apparatus 100 after dialysis has taken place.
[0066] In one particular aspect of the present invention,
Applicants have discovered that the cumulative effects of
variations in the local surface profile of central lumen 130 can
have a significant detrimental effect on the utility of that lumen
for hemodialysis applications.
[0067] Applicants have further discovered that good hemodialysis
results can be achieved if variations in the local surface profile
of central lumen 130 average less than about 0.0015 inch and
preferably less than about 0.0005 inch (as measured between
adjacent occurrences of reinforcing means 135) along the length of
central lumen 130. In other words, if catheter apparatus 100 is
constructed with a 20 turn helical element, there will be 19 local
variation measuring points along any path of measurement taken
parallel to the axis of the apparatus. The measurements at these
measuring points are then averaged, whereby to provide an average
variation in the local surface profile of central lumen 130.
Applicants have determined that good hemodialysis results can be
achieved where the average variation in the local surface profile
of central lumen 130 is less than about 0.0015 inch, and preferably
less than about 0.0005 inch.
[0068] Thus, in one preferred form of the invention, catheter
apparatus 100 is formed so that the average variation in the local
surface profile of central lumen 130 is less than about 0.0015
inch, and preferably less than about 0.0005 inch.
[0069] The present invention also includes a novel method for
fabricating catheter apparatus 100.
[0070] In the preferred embodiment of the invention, the novel
catheter apparatus 100 is formed as follows.
[0071] First, an elongated molding core 200 is provided (FIG. 11).
Molding core 200 is formed so that it is removable from a structure
which will be molded over the core, as will hereinafter be
discussed. In one preferred form of the invention, molding core 200
is formed so that it has a reducible transverse cross-section,
whereby the molding core is removable from a structure which will
be molded over the core, as will hereinafter be discussed. Molding
core 200 has a polished finish so that its outer surface 205 is
smooth and free from burrs and other surface irregularities. In one
preferred form of the invention, molding core 200 is formed out of
a teflon extrusion which may have its transverse cross-section
reduced by stretching it along its longitudinal axis. Preferably
the teflon extrusion is formed out of virgin teflon stock which is
capable of reducing its diameter by approximately 5-10% when
subjected to longitudinal stretching. Preferably the virgin stock
is homogenous, so that stretching occurs relatively evenly over the
entire body of the teflon.
[0072] Next, a silicone rubber element 210 is formed about molding
core 200 (FIG. 12). Preferably this is done by co-extruding
silicone rubber element 210 about the outer surface 205 of molding
core 200. Inasmuch as molding core 200 has a smooth outer surface
205, the inner surface 215 of silicone rubber element 210 will
therefore also be smooth and free from burrs and other surface
irregularities.
[0073] Then reinforcing means 135, preferably in the form of coil
spring 140, is loaded over silicone rubber element 210 (FIG.
13).
[0074] Next, support structure 150 (FIGS. 6, 7, and 14) is fit over
the distal end of molding core 200 and the distal end of silicone
rubber element 210. More particularly, support structure 150 is fit
over the distal end of molding core 200 and the distal end of
silicone rubber element 210 so that the distal end of silicone
rubber element 210 rests in counterbore 165 of support structure
150 and against shoulder 175 of support structure 150, and so that
molding core 200 extends out through bore 155 of support structure
150 (FIG. 14). One or more side openings 220 are then formed in
silicone rubber element 210 (FIG. 14), and corresponding molding
pins (not shown) are inserted into the one or more side openings
220.
[0075] Next, a silicone rubber overlayer 225 is molded over
reinforcing means 135 (e.g., coil spring 140) and silicone rubber
element 210 (FIG. 15). Preferably silicone rubber overlayer 225 is
applied so that it is seamlessly integrated with silicone rubber
element 210. Preferably the distal end surface 230 of silicone
rubber overlayer 225 is aligned with the distal end surface 160 of
support structure 150. The molding pins (not shown) located in the
one or more side openings 220 extend out through silicone rubber
overlayer 225.
[0076] Once this has been done, molding core 200 is removed.
[0077] In one preferred form of the invention, where molding core
200 has a reducible transverse cross-section, the molding core
first has its transverse cross-section reduced, causing it to
separate away from the inside wall 215 of silicone rubber element
210 (FIG. 16). Then molding core 200 is removed.
[0078] And in one preferred form of the invention, where molding
core 200 is formed out of a teflon extrusion such that stretching
the teflon extrusion longitudinally will cause it to reduce in
diameter, molding core 200 is first stretched longitudinally,
causing the molding core to separate away from the inside wall 215
of silicone rubber element 210 (FIG. 16). Then molding core 200 is
removed (FIG. 17.).
[0079] After molding core 200 has been removed, the molding pins
located in the one or more side openings 220 are withdrawn, thereby
yielding the finished catheter apparatus 100. Alternatively, the
molding pins located in the one or more side openings 220 may be
withdrawn prior to removing molding core 200.
[0080] In one preferred form of the invention, silicone rubber
element 210 and silicone rubber overlayer 225 are both formed out
of 80 durometer silicone rubber; silicone rubber element 210 has a
wall thickness of approximately 0.005 inch; and silicone rubber
overlayer 225 has a wall thickness (between adjacent occurrences of
reinforcing means 135) of approximately 0.010 inch.
[0081] It is to be appreciated that, when fabricating catheter
apparatus 100 by means of the foregoing process, silicone rubber
element 210 and silicone rubber overlayer 225 together form the
side wall 110 of catheter apparatus 100. Furthermore, inasmuch as
molding core 200 has a smooth outer surface 205, the inside wall
215 of silicone rubber element 210 (which inside wall 215 defines
the central lumen 130 of catheter apparatus 100) also has a smooth
profile.
[0082] It has been found that, by forming catheter apparatus 100 by
means of the foregoing process, the central lumen 130 of that
apparatus will have an interior surface which is sufficiently
smooth that blood can be passed through that lumen during a
hemodialysis session with good results.
[0083] Among other things, it has been found that, by forming
catheter apparatus 100 by means of the foregoing process, the
average variation in the local surface profile of central lumen 130
will be less than about 0.0015 inch, and preferably less than about
0.0005 inch.
[0084] Two of the catheter apparatus 100 can be attached together
in ways well known in the art so as to form a complete dual-lumen
catheter element 15.
[0085] This complete dual-lumen catheter element 15 can then be
combined with the connector portion 20 of a percutaneous catheter
assembly so as to form a complete percutaneous catheter assembly
such as is schematically shown in FIGS. 1 and 2. Such a
percutaneous catheter assembly may then be used in the conventional
manner in the hemodialysis of a patient.
[0086] Alternatively, the complete dual-lumen catheter element 15
can be combined with the connector portion 84 of a subcutaneous
port and catheter assembly so as to form a complete subcutaneous
port and catheter assembly such as is schematically shown in FIGS.
3-5. Such a subcutaneous port and catheter assembly may then be
used in the conventional manner in the hemodialysis of a
patient.
[0087] In practice, it has been found possible to provide a
dual-lumen catheter element 15, formed out of two of the catheter
apparatus 100, which is flexible; capable of substantial bending
(e.g., capable of being bent so as to enter the patient's internal
jugular vein) without kinking, and resistant to collapse when
subjected to substantial negative pressures (e.g., 500 mm of
mercury negative pressure).
[0088] It should be appreciated that a dual-lumen catheter element
15 formed out of two of the catheter apparatus 100 is easily "field
trimmable" to the desired length. In particular, in one preferred
trimming method, a scalpel or the like is first used to cut through
side wall 110 and expose reinforcing means 135, and then surgical
scissors or the like are used to cut through reinforcing means 135.
Alternatively, surgical scissors could be used to cut completely
through catheter apparatus 100 in a single step.
[0089] Numerous modifications can be made to the apparatus and
method described above without departing from the scope of the
present invention.
[0090] Thus, for example, reinforcing means 135 might be formed out
of stainless steel, or a hard plastic, or some other material which
is harder than the material used to form tube 105.
[0091] Or molding core 200 might be formed out of a material other
than teflon, where the alternative material is also capable of
having its transverse cross-section reduced by longitudinal
stretching. Or molding core 200 might have its transverse
cross-section reduced by a method other than stretching, e.g.,
depending on the material involved, the molding core might be
melted out or dissolved away so as to separate it from silicone
rubber element 210. Furthermore, molding core 200 might be removed
from within the molded structure by a technique other than reducing
its transverse cross-section. By way of example but not limitation,
molding core 200 might comprise a sufficiently lubricious material
such that the molding core could be removed from within the molded
structure by simply pulling the molding core longitudinally out of
the molded structure. Or molding core 200 could be blown out of the
molded structure.
[0092] Also, if desired, the distal end of catheter apparatus 100
can be formed with an alternative geometry.
[0093] By way of example but not limitation, a support structure
180 (FIGS. 18 and 19) can be utilized, wherein support structure
180 is substantially identical to the support structure 150
discussed above, except that side slots 182 are formed in support
structure 180, and appropriate molding pins (not shown) are used in
association with side slots 180 to form semi-circular side openings
184 (FIG. 18) in the distal end of the catheter apparatus.
[0094] Or, as seen in FIG. 20, side windows 186 can be formed in a
support structure 188 which, when covered with appropriate molding
pins during molding, will yield appropriate openings in the distal
end of the catheter apparatus.
[0095] Or a simple ring-shaped support structure 190 (FIG. 21) can
be used, with or without side openings 145. With such a
construction, support structure 190 can be positioned so that its
distal end surface 192 resides flush with distal end wall 115 of
tube 105, in a manner generally analogous to the construction shown
in FIG. 6; or support structure 190 can be encapsulated within the
distal end of tube 105, in the manner shown in FIG. 22.
[0096] It is also possible for the distal support structure to be
attached onto a surface of side wall 110 of tube 105, rather than
embedded into the material of side wall 110.
[0097] And the distal support structure may open on the distal end
of tube 105, and/or open on the inner lumen of tube 105, and/or
open on the outer lumen of tube 105.
[0098] Or the distal support structure may be omitted completely
from the catheter apparatus if desired.
[0099] Furthermore, side openings 145 might comprise relatively
narrow, longitudinally-extending slits rather than holes, in which
case they could act something like a check valve, opening under
positive internal pressure but otherwise remaining substantially
closed. See, for example, FIG. 22A, which shows side openings 145
in the form of such relatively narrow, longitudinally extending
slits, with the slits being shown in their closed position in solid
line and in their open position in dashed, or phantom, line.
[0100] It should also be appreciated that reinforcing means 135 may
take a form other than the coil spring 140 discussed above. For
example, reinforcing means 135 might take the form of a plurality
of ring-like elements 194, such as is shown in FIG. 23.
Alternatively, reinforcing means 135 might comprise a tubular,
braided mesh reinforcer. See, for example, FIG. 23A, where
reinforcing means 135 are shown, schematically, in the form of a
tubular, braided mesh reinforcer 195.
[0101] It should also be appreciated that one might form a catheter
apparatus of the sort generally described above, including a distal
support structure, but omitting reinforcing means 135.
[0102] It will, of course, be appreciated that various other
modifications may be made to the embodiments disclosed above
without departing from the spirit and scope of the present
invention. Accordingly, it is intended that this invention be
limited only by the claims ultimately issued from this patent
application and/or from any patent application(s) claiming priority
therefrom.
ADVANTAGES OF THE INVENTION
[0103] Numerous advantages are achieved through the provision and
use of the present invention.
[0104] For one thing, the present invention provides improved
apparatus for use in the dialysis of blood.
[0105] And the present invention provides an improved catheter
element for use in the dialysis of blood, wherein the catheter
element may be used in either a percutaneous catheter assembly or a
subcutaneous port and catheter assembly.
[0106] Also, the present invention provides an improved catheter
element which has the largest possible interior diameter and the
smallest possible exterior diameter, yet is resistant to bursting,
collapse and kinking.
[0107] And the present invention provides an improved catheter
element which incorporates reinforcing means within the side wall
of the catheter, yet has an interior lumen which is sufficiently
smooth that the catheter element may be used in hemodialysis
applications with good results.
[0108] The present invention also provides a support structure at
the distal end of the catheter element to help maintain openness of
the flow path through the catheter element.
[0109] Furthermore, the present invention provides an improved
method for fabricating apparatus for use in the dialysis of
blood.
[0110] And the present invention provides an improved method for
the dialysis of blood.
[0111] Still other advantages associated with the present invention
will be obvious to a person skilled in the art.
* * * * *