U.S. patent application number 11/750623 was filed with the patent office on 2007-09-27 for collapsible delivery tool for cardiac support device.
This patent application is currently assigned to Acorn Cardiovascular, Inc.. Invention is credited to Clifton A. Alferness.
Application Number | 20070225547 11/750623 |
Document ID | / |
Family ID | 24894428 |
Filed Date | 2007-09-27 |
United States Patent
Application |
20070225547 |
Kind Code |
A1 |
Alferness; Clifton A. |
September 27, 2007 |
COLLAPSIBLE DELIVERY TOOL FOR CARDIAC SUPPORT DEVICE
Abstract
A cardiac support device and placement tool assembly. The
cardiac support device has a flexible jacket with an open base end.
The placement tool includes a cannula having an open end, a
collapsible support on the end of the cannula releasably connected
to the cardiac support device at a plurality of locations around
the base end, and an acutuator. The collapsible support is movable
between a collapsed state in a retracted position at which the
collapsible support and cardiac support device are within the end
of the cannula, and an open state in an extended position at which
the collapsible support and cardiac support device are outside of
the cannula with the collapsible support holding the base end of
the cardiac support device in an open position for placement onto a
patient's heart. The actuator moves the collapsible support between
the collapsed and open states.
Inventors: |
Alferness; Clifton A.; (Port
Orchard, WA) |
Correspondence
Address: |
FAEGRE & BENSON LLP;PATENT DOCKETING
2200 WELLS FARGO CENTER
90 SOUTH SEVENTH STREET
MINNEAPOLIS
MN
55402-3901
US
|
Assignee: |
Acorn Cardiovascular, Inc.
St. Paul
MN
55112
|
Family ID: |
24894428 |
Appl. No.: |
11/750623 |
Filed: |
May 18, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10810099 |
Mar 26, 2004 |
|
|
|
11750623 |
May 18, 2007 |
|
|
|
10367346 |
Feb 13, 2003 |
6893392 |
|
|
10810099 |
Mar 26, 2004 |
|
|
|
10084806 |
Feb 25, 2002 |
6544168 |
|
|
10367346 |
Feb 13, 2003 |
|
|
|
09696651 |
Oct 25, 2000 |
6375608 |
|
|
10084806 |
Feb 25, 2002 |
|
|
|
09483466 |
Jan 14, 2000 |
6165122 |
|
|
09696651 |
Oct 25, 2000 |
|
|
|
08935723 |
Sep 23, 1997 |
6077218 |
|
|
09483466 |
Jan 14, 2000 |
|
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|
08720556 |
Oct 2, 1996 |
5702343 |
|
|
08935723 |
Sep 23, 1997 |
|
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Current U.S.
Class: |
600/37 |
Current CPC
Class: |
A61F 2/2481 20130101;
A61F 2002/2484 20130101; A61M 60/268 20210101; A61M 60/857
20210101; A61F 2250/0003 20130101; A61M 60/40 20210101; A61M 60/122
20210101 |
Class at
Publication: |
600/037 |
International
Class: |
A61F 2/02 20060101
A61F002/02 |
Claims
1. A placement tool for placing a cardiac support device of the
type having a flexible jacket with an open base end on a patient's
heart, including: a body having an end; and a support on the end of
the body configured to be releasably connected to a cardiac support
device and to hold the base end of the cardiac support device in an
open position for placement on a patient's heart.
2. The placement tool of claim 1 wherein the support is configured
to be releasably connected to the cardiac support device at a
plurality of locations around the base end.
3. The placement tool of claim 1 wherein the support includes a
collapsible structure movable between a retracted position within
the body and an extended position outside of the body.
4. The placement tool of claim 3 wherein the collapsible support is
movable between the retracted and extended positions from an end of
the body.
5. The placement tool of claim 4 wherein the body is a hollow
member, and the collapsible support is within the hollow member
when in the retracted position.
6. The placement tool of claim 5 and further including an actuator
configured to move the collapsible support between a collapsed
state and an open state for holding the end of the cardiac support
device in the open position.
7. The placement tool of claim 1 wherein: the support is movable
between a collapsed state and an open state for holding the end of
the cardiac support device in the open position; and the tool
further includes an actuator configured to move the support between
the collapsed and open states.
8. A cardiac support device and placement tool assembly, including:
a cardiac support device having a flexible jacket with an open base
end; a placement tool, including: a cannula having an end; and a
collapsible support on the end of the cannula releasably connected
to the cardiac support device at a plurality of locations around
the base end, the collapsible support movable between a collapsed
state in a retracted position at which the collapsible support and
cardiac support device are within the end of the cannula and an
open state in an extended position at which the collapsible support
and cardiac support device are outside of the cannula with the
collapsible support holding the base end of the cardiac support
device in an open position for placement onto a patient's heart;
and an actuator to move the collapsible support between the
collapsed and open states.
9. A method for placing a cardiac support device of the type having
a flexible jacket with an open base end on a patient's heart,
including: making an incision in the patient's body to provide
access to the pericardial space around the patient's heart; causing
the cardiac support device to be in a collapsed state and
releasably mounted at a plurality of locations around the base end
to a placement tool; inserting the placement tool and cardiac
support device into the pericardial space, and manipulating the
tool to position the cardiac support device adjacent to the
patient's heart, while the cardiac support device is in the
collapsed state; operating the placement tool to cause the cardiac
support device to be in an open state with the base end of the
cardiac support device in an open position for placement onto a
patient's heart; manipulating the placement tool to maneuver the
cardiac support device into position on the patient's heart;
releasing the cardiac support device from the placement tool; and
removing the tool through the incision.
10. The method of claim 9 wherein: causing the cardiac support
device to be in a collapsed state and mounted to a placement tool
includes: mounting the cardiac support device to a collapsible
support; and causing the collapsible support to be in a collapsed
state; and operating the placement tool to cause the cardiac
support device to be in an open state includes causing the
collapsible support to assume an open state.
11. The method of claim 10 and further including causing the
collapsible support to return to the collapsed state before
removing the tool through the incision.
12. The method of claim 11 wherein causing the collapsible support
to assume an open state includes operating an actuator on the
placement tool.
13. The method of claim 10 wherein causing the collapsible support
to assume an open state includes operating an actuator on the
placement tool.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present application is a continuation of U.S. Ser. No.
10/810,099, filed Mar. 26, 2004, which is a continuation of U.S.
Ser. No. 10/367,346, filed Feb. 13, 2003, now U.S. Pat. No.
6,893,392, which is a continuation of U.S. Ser. No. 10/084,806,
filed Feb. 25, 2002, now U.S. Pat. No. 6,544,168, which is a
continuation of U.S. Ser. No. 09/696,651, filed Oct. 25, 2000, now
U.S. Pat. No. 6,375,608, which is a continuation of U.S. Ser. No.
09/483,466, filed Jan. 14, 2000, now U.S. Pat. No. 6,165,122, which
is a continuation of U.S. Ser. No. 08/935,723, filed Sep. 23, 1997,
now U.S. Pat. No. 6,077,218, which is a continuation of U.S. Ser.
No. 08/720,556, filed Oct. 2, 1996, now U.S. Pat. No. 5,702,343,
which applications and issued patents are incorporated herein by
reference.
BACKGROUND OF THE INVENTION
[0002] The present invention is generally directed to a device and
method for reinforcement of the cardiac wall. The invention is
particularly suited for the treatment of cardiac disease which
result in atrial or ventricular dilation. The invention provides
reinforcement of the cardiac wall during diastolic chamber filling
to prevent or reduce cardiac dilation in patients known to have
experienced such dilation or who have a predisposition for such
dilation occurring in the future. The cardiac reinforcement
structure is typically applied to the epicardial surface of the
heart.
[0003] Cardiac dilation occurs with different forms of cardiac
disease, including heart failure. In some cases, such as
post-myocardial infarction, the dilation may be localized to only a
portion of the heart. In other cases, such as hypertrophic
cardiomyopathy, there is typically increased resistance to filling
of the left ventricle with concomitant dilation of the left atria.
In dilated cardiomyopathy, the dilation is typically of the left
ventricle with resultant failure of the heart as a pump. In
advanced cases, dilated cardiomyopathy involves the majority of the
heart.
[0004] With each type of cardiac dilation, there are associated
problems ranging from arrhythmias which arise due to the stretch of
myocardial cells, to leakage of the cardiac valves due to
enlargement of the valvular annulus. Devices to prevent or reduce
dilation and thereby reduce the consequences of dilation have not
been described. Patches made from low porosity materials, for
example Dacron.TM., have been used to repair cardiac ruptures and
septal defects, but the use of patches to support the cardiac wall
where no penetrating lesion is present has not been described.
[0005] Drugs are sometimes employed to assist in treating problems
associated with cardiac dilation. For example, digoxin increases
the contractility of the cardiac muscle and thereby causes enhanced
emptying of the dilated cardiac chambers. On the other hand, some
drugs, for example, beta-blocking drugs, decrease the contractility
of the heart and thus increase the likelihood of dilation. Other
drugs including angiotensin-converting enzyme inhibitors such as
enalopril help to reduce the tendency of the heart to dilate under
the increased diastolic pressure experienced when the contractility
of the heart muscle decreases. Many of these drugs, however, have
side effects which make them undesirable for long-term use.
[0006] Accordingly, there is a need for a device that can reduce or
prevent cardiac dilation and reduce the problems associated with
such dilation.
SUMMARY OF THE INVENTION
[0007] The present invention is an improved placement tool and
method for use with a cardiac support device having a flexible
jacket with an open base end. A placement tool in accordance with
one embodiment of the invention includes a body having an end and
support on the end of the body for releasable connection to a
cardiac support device. The support holds the base end of the
cardiac support device in an open position for placement on a
patient's heart. In another embodiment of the invention, the
support is a collapsible support movable between a retracted
position within the body and an extended position outside the
body.
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] FIG. 1 is a frontal view of one embodiment of a cardiac
reinforcement patch.
[0009] FIG. 2 is a perspective view of the cardiac reinforcement
patch of FIG. 1 in place on the epicardium of a heart.
[0010] FIG. 3 is a perspective view of one embodiment of a cardiac
reinforcement jacket according to the invention.
[0011] FIG. 4 is a second embodiment of a cardiac reinforcement
jacket according to the invention.
[0012] FIG. 5 is a perspective view of the embodiment of the
cardiac reinforcement jacket shown in FIG. 3 in place around the
heart.
[0013] FIG. 6 is a schematic cross sectional view of one embodiment
of a mechanism for selectively adjusting the predetermined size of
a cardiac reinforcement jacket.
[0014] FIG. 7 is a perspective view of a placement tool which can
be used for applying a cardiac reinforcement jacket.
[0015] FIG. 8 is a perspective view of a placement tool being
employed to place a cardiac reinforcement jacket over the
heart.
DETAILED DESCRIPTION
[0016] The present invention is directed to reinforcement of the
heart wall during diastolic filling of a chamber of the heart. The
invention is particularly suited for use in cardiomyopathies where
abnormal dilation of one or more chambers of the heart is a
component of the disease.
[0017] As used herein, "cardiac chamber" refers to the left or
right atrium or the left or right ventricle. The term "myocardium"
refers to the cardiac muscle comprising the contractile walls of
the heart. The term "endocardial surface" refers to the inner walls
of the heart. The term "epicardial surface" refers to the outer
walls of the heart.
[0018] The heart is enclosed within a double walled sac known as
the pericardium. The inner layer of the pericardial sac is the
visceral pericardium or epicardium. The outer layer of the
pericardial sac is the parietal pericardium.
[0019] According to the present invention, a cardiac reinforcement
device (CRD) limits the outward expansion of the heart wall during
diastolic chamber filling beyond a predetermined size. The
expansion constraint applied to the heart by a CRD is predetermined
by the physician based on, for example, cardiac output performance
or cardiac volume. In contrast to known ventricular assist devices
which provide cardiac assistance during systole, a CRD according to
the present disclosure provides cardiac reinforcement during
diastole.
[0020] A CRD is made from a biomedical material which can be
applied to the epicardial surface of the heart. As used herein, a
"biomedical material" is a material which is physiologically inert
to avoid rejection or other negative inflammatory response. A CRD
can be prepared from an elastic or substantially non-elastic
biomedical material. The biomedical material can be inflexible, but
is preferably sufficiently flexible to move with the expansion and
contraction of the heart without impairing systolic function. The
biomedical material should, however, constrain cardiac expansion,
during diastolic filling of the heart, to a predetermined size.
Examples of suitable biomedical materials include perforate and
non-perforate materials. Perforate materials include, for example,
a mesh such as a polypropylene or polyester mesh. Non-perforate
materials include, for example, silicone rubber.
[0021] A biomedical material suitable for a device of the invention
generally has a lower compliance than the heart wall. Even though
the biomedical material is less compliant than the heart wall, some
limited expansion of an elastic biomedical material can occur
during cardiac filling.
[0022] In an alternative embodiment, the biomedical material can be
substantially non-elastic. According to this embodiment, the term
"substantially non-elastic" refers to a material which constrains
cardiac expansion during diastole at a predetermined size, but
which has substantially no elastic properties.
[0023] Regardless if the biomedical material is elastic or
non-elastic, advantageous to a CRD according to the present
disclosure is cardiac reinforcement which is provided during
diastole. Moreover, a CRD as disclosed herein does not provide
cardiac assistance through active pumping of the heart.
[0024] I. CRD Patch
[0025] In one embodiment, a cardiac reinforcement device (CRD)
provides for local constraint of the heart wall during cardiac
expansion. According to this embodiment, a CRD is a "patch" that
provides reinforcement of the heart wall at a localized area, such
as a cardiac aneurysm or at an area of the myocardium which has
been damaged due to myocardial infarction. When discussing a
"patch", "predetermined size" of the patch means that the size of
the patch is selected to cover an area of the epicardial surface of
the heart in need of reinforcement without completely surrounding
the circumference of the heart.
[0026] A CRD patch can be prepared from the biomedical materials
described above. In a preferred embodiment, the patch is an open
mesh material.
[0027] A CRD patch can be applied to the epicardial surface of the
heart over or under the parietal pericardium. A patch is typically
applied to the epicardial surface by suturing around the periphery
of the patch. The peripheral edge of the patch can include a
thickened "ring" or other reinforcement to enhance the strength of
the patch at the point of suture attachment to the epicardium.
Generally, a patch is applied to the epicardium through a
thoracotomy or other incision providing sufficient exposure of the
heart.
[0028] II. CRD Jacket
[0029] In another embodiment, a CRD is a jacket that
circumferentially surrounds the epicardial surface of the heart.
When applied to the heart, a CRD jacket can be placed over or under
the parietal pericardium.
[0030] A CRD applied to the epicardium is fitted to a
"predetermined size" for limitation of cardiac expansion. According
to a jacket embodiment, "predetermined size" refers to the
predetermined expansion limit of the jacket which circumferentially
constrains cardiac expansion during diastolic filling of the heart.
In practice, for example, a physician could measure cardiac output
and adjust the jacket size to an optimal size for the desired
effect. In this example, the optimal size is the "predetermined
size". In one embodiment, the predetermined size can be adjusted
for size reduction as the cardiac size is reduced.
[0031] In one embodiment, the CRD jacket is a cone-shaped tube,
having a base broader than the apex, which generally conforms to
the external geometry of the heart. When applied to the epicardial
surface of the heart, the base of the jacket is oriented towards
the base of the heart, and the apex of the jacket is oriented
towards the apex of the heart. Typically, the base of the jacket
includes an opening for applying the jacket by passing the jacket
over the epicardial surface of the heart. The apical end of the
jacket can be a continuous surface which covers the apex of the
heart. Alternatively, the apex of the jacket can have an opening
through which the apex of the heart protrudes.
[0032] A cardiac reinforcement jacket, as disclosed herein, is not
an inflatable device that surrounds the heart. Rather, the device
is typically a single layer of biomedical material. In one
embodiment discussed below, an inflatable member can be included
with the device, but the inflatable member serves to reduce the
volume within a localized region of the jacket and does not follow
the entire jacket to surround the epicardial surface of the
heart.
[0033] In one embodiment, the CRD jacket can be secured to the
epicardium by a securing arrangement mounted at the base of the
jacket. A suitable securing arrangement includes, for example, a
circumferential attachment device, such as a cord, suture, band,
adhesive or shape memory element which passes around the
circumference of the base of the jacket. The ends of the attachment
device can be fastened together to secure the jacket in place.
Alternatively, the base of the jacket can be reinforced for
suturing the base of the jacket to the epicardium.
[0034] Various sized CRD jackets can be prepared such that
different sized jackets are used for different predetermined
cardiac expansion sizes or expansion ranges. Alternatively, a CRD
jacket can include a mechanism for selectively adjusting the size
of the jacket. A mechanism for selectively adjusting the volumetric
size of the jacket theoretically provides for a "one size fits all"
device. More importantly, however, an adjustable jacket provides
the ability to titrate (readjust) the amount of cardiac
reinforcement by graded reduction in jacket size as therapeutic
reduction of cardiac expansion occurs.
[0035] A mechanism for selectively adjusting the size of the jacket
can include a slot which opens at the base of the jacket and
extends toward the apex end of the CRD. If the apex end of the CRD
jacket is open, the apical extent of the slot can be continuous
with the apex opening. The slot includes opposing lateral edges. By
adjusting the proximity of the opposing lateral edges, the overall
size of the jacket can be varied. Moving the opposing edges of the
slot closer together narrows the slot and reduces the volumetric
size of the jacket. The opposing edges of the slot can be fastened
together at a predetermined proximity by, for example, one or more
lateral attachment devices, such as a cord, suture, band, adhesive
or shape memory element attached to each lateral edge.
[0036] In another embodiment, a mechanism for selectively adjusting
the size of the jacket can be an inflatable member. According to
this embodiment, the inflatable member is mounted between the
jacket and the epicardium. The volumetric size of the jacket can be
reduced by inflating the inflatable member through an inflation
port with, for example, a gas or liquid. As cardiac expansion
volume responds to cardiac constraint by size reduction, the
predetermined size of the jacket can then be reduced by inflating
the inflatable member within the jacket. Once inflated, the size of
the inflatable member is preferably maintained until therapeutic
response causes a need for further inflation. According to the
invention, the inflation of the inflatable member provides a
reduction in the predetermined size of the jacket by a fixed
increase in volume of the inflatable member. The inflatable member
is not rhythmically inflated and deflated to provide assistance to
cardiac contraction during systole.
[0037] The biomedical material of the invention can be radioluscent
or radiopaque. In one embodiment, the material of the jacket can be
made radiopaque by inclusion of radiopaque markers for
identification of the outside surface of the heart, the expansion
slot or inflation port. As used herein, radiopaque means causing
the CRD to be visible on x-ray or fluoroscopic viewing. Suitable
radiopaque markers include, for example, platinum wires, titanium
wires and stainless steel wires.
[0038] A CRD according to the present disclosure provides a new
method for the treatment of cardiac disease. As used herein,
cardiac disease includes diseases in which dilation of one of the
chambers of the heart is a component of the disease. Examples
include heart failure or cardiomyopathy. Heart failure can occur as
a result of cardiac dilation due to ventricular hypertrophy or
secondary to, for example, valvular incompetency, valvular
insufficiency or valvular stenosis. Cardiomyopathy, according to
the invention, can be primary or secondary to infection, ischemia,
metabolic disease, genetic disorders, etc.
[0039] It is foreseen that constraint of cardiac expansion by a
device of the invention can provide reduced cardiac dilation.
Reduced cardiac dilation can cause reduction in the problems
associated with cardiac dilation such as arrhythmias and valvular
leakage. As reduction of cardiac dilation occurs, selective
reduction of the predetermined size of the jacket also provides
continued reinforcement for the size reduced heart.
[0040] A CRD jacket can also be used to measure cardiac
performance. According to this embodiment, the CRD jacket is
rendered radiopaque by use of a radiographic marker. The
radiographic markers are distributed throughout the jacket over the
surface of the heart. By evaluation of the markers relative to one
another with each heart beat, cardiac performance may be measured.
As such, evaluation of cardiac performance may assist in adjusting
the predetermined size of a CRD jacket.
[0041] A CRD as described herein can be applied to the epicardium
of a heart through a thoracotomy or through a minimally invasive
procedure. For a minimally invasive procedure a CRD placement tool
can be used to apply the CRD over the epicardium of the heart
through a thorascopic incision. According to this embodiment, a CRD
placement tool includes a cannula, a stiff rod or wire and a guide
tube. For placement of a CRD, the wire is threaded through the
guide tube which is passed around the circumference of the base of
the jacket. The CRD with wire and guide tube passed through the
base opening are then passed into the cannula. The cannula is of
sufficient length and diameter to enclose the CRD, wire and guide
tube during passage of the placement tool through a thorascopic
incision. The placement tool is passed into the thoracic cavity and
positioned at a point near the apex of the heart. When in position,
the wire and guide tube are pushed out of the cannula away from the
operator. Once outside the cannula, the wire and guide tube
sufficiently expand the opening of the base of the CRD jacket to
pass over the epicardial surface of the heart. When the CRD jacket
is in position over the epicardial surface, the wire, guide tube
and cannula can be removed. A second incision can then be made to
provide access for suitable surgical instruments to secure or
adjust the size of the CRD.
[0042] The invention will now be further described by reference to
the drawings.
[0043] FIG. 1 is a frontal view of one embodiment of a cardiac
reinforcement patch 1. The CRD patch 1 shown here is a mesh
biomedical material 2 having a thickened peripheral ring 3 which
reinforces the peripheral edge 4 of the patch for attachment of the
patch to the epicardial surface of the heart.
[0044] FIG. 2. is a perspective view of a CRD patch 10 in place on
the epicardial surface of a heart 11, for example, over a cardiac
aneurysm (not shown) of the heart. In one preferred embodiment, the
patch 10 is sized to cover the extent of the cardiac aneurysm and
is placed on the epicardial surface of the heart 11. In practice,
the thorax is surgically opened and the region of the heart 11 with
the aneurysm (not shown) is located and exposed. The patch 10 is
placed over the aneurysm and sutured in place around the periphery
12 of the patch to provide sufficient constraint to prevent further
dilation of the aneurysm.
[0045] FIG. 3 is a perspective view of one embodiment of a CRD
jacket 15 according to the invention. According to the embodiment
shown, the jacket 15 is a mesh material 16, and includes a
circumferential attachment device 17 at the base end 18 of the CRD
jacket. The apex end 24 of the jacket 15 is closed. The jacket 15
shown also includes a slot 19 having opposing lateral edges 20 and
21, and fasteners (e.g. lateral attachment device 22 and 23) for
selectively adjusting the volumetric size of the jacket 15. The CRD
jacket 15 shown also includes radiopaque markers 25 for visualizing
the surface of the heart through radiographic study.
[0046] FIG. 4 is an alternative embodiment of a CRD jacket 30.
Similar to the embodiment shown in FIG. 3, the embodiment of FIG. 4
includes a base end 31 and an apex 32 end. The base end includes a
circumferential attachment device 33 for securing the CRD jacket 30
to the heart. The CRD jacket 30 of FIG. 4 also includes a slot 34
having opposing lateral edges 35, 36. The lateral edges 35, 36 are
shown pulled together at 37 by a lateral attachment device 38, for
example, a suture. In contrast to the embodiment shown in FIG. 3,
the embodiment shown in FIG. 4 has an opening 39 at the apex end 32
of the CRD jacket 30.
[0047] FIG. 5. is a perspective view of a CRD jacket 40 around a
heart 41. According to the embodiment shown, at the base 42 of the
jacket 40, there is a circumferential attachment device 43 which
secures the CRD jacket 40 near the base of the heart 44. A slot 45,
is shown with opposing lateral edges 46, 47 fastened together by a
lateral attachment device 48. In the embodiment shown, the CRD
jacket 40 has an opening 49 at the apical end 50 of the jacket. The
apex of the heart 51 protrudes through the opening 49 at the apical
end 50 of the jacket 40.
[0048] Still referring to FIG. 5, in a preferred embodiment, if one
or more of the lateral attachment device 48 are made of an elastic
material, such as silicone rubber, the device can provide a way of
applying a graded constraint around the outside of the heart 41 to
reduce cardiac dilation over time. In practice, the jacket would be
placed over the heart 41 as shown, either over or under the
parietal pericardium (not shown). The circumferential attachment
device 43 and lateral attachment device 48 would then be tightened
to cause a constraining effect on the outside of the heart.
[0049] In a preferred embodiment, if one or more of the lateral
attachment cords 48 is made of an elastic material, such as
silicone rubber, surface pressure exerted on the epicardial surface
of the heart varies as a function of the amount of dilation of the
heart. This variable pressure has the effect of reducing the
cardiac dilation to a certain point and then stopping because the
surface pressure drops to a negligible amount. The amount of
constraint or reduction in dilation that is accomplished over time
and the resultant cardiac performance may be monitored
radiographically using techniques known in the art, for example
fluoroscopy, by observing radiographic markers (FIG. 4, 25), if
present.
[0050] FIG. 6 is a schematic cross sectional view of an alternative
embodiment of an arrangement for selectively adjusting the
predetermined size of a jacket 53. According to this embodiment, an
inflatable member 54 is inserted within the jacket 53 between the
jacket 53 and the epicardial surface 55 of the heart 56. The
inflatable member 54 includes a filling apparatus 57 for entry of a
fluid (liquid or gas) to inflate the inflatable member 54 and
reduce the predetermined size of the jacket 53.
[0051] FIG. 7 is a perspective view of a placement tool 60 which
can be used for placement of a CRD jacket 61 around the epicardium
of the heart. As shown here, the base end of the jacket 62 is held
open by guide tube 63 through which is passed a wire or stiffening
rod 64. The wire 64 can be removed from the guide tube 63 by
pulling on the wire extraction grip 66. The placement tool 60
includes a cannula 65 which encloses the jacket 61, guide tube 63
and wire 64 during insertion of the tool into a thorascopic
incision.
[0052] FIG. 8 is a perspective view of a placement tool 70 being
employed to place a jacket 71 over the heart 72 on the outside of
the parietal pericardium 73. The placement tool 70 is guided
through a small incision in the thorax and the jacket 71 is
maneuvered into position over the heart 72. Once the jacket 71 is
in proper position, the wire 74, which is passed through the guide
tube 75 around the base 76 of the jacket 71, is extracted from the
guide tube 75 by pulling on the wire extraction grip 77. The guide
tube 75 is then extracted by pulling on the guide tube extraction
grip 78. The cannula 79 is removed from the chest and the
circumferential attachment cord (not shown in this view), and the
lateral attachment cord 80 can be fastened to secure the jacket
71.
[0053] The above specification and drawings provide a description
of a cardiac reinforcement device and method of using on the heart.
Since many embodiments of the invention can be made without
departing from the spirit and scope of the invention, the invention
resides in the claims hereinafter appended.
* * * * *