U.S. patent number 3,630,207 [Application Number 04/848,510] was granted by the patent office on 1971-12-28 for pericardial catheter.
This patent grant is currently assigned to Cutter Laboratories, Inc.. Invention is credited to Mogens L. Bramson, Paul Kahn.
United States Patent |
3,630,207 |
Kahn , et al. |
December 28, 1971 |
PERICARDIAL CATHETER
Abstract
The pericardial catheter has a main tube, flat in cross section,
open at one end and closed at the other. The top wall is flat and
the bottom wall is generally flat, having a plurality of openings
near to but spaced from the closed end. A plurality of lengthwise
extending ridges lie between successive openings and on each end of
them. A round collapse-prevention member is inside the main tube
and has an outer diameter at least as great as the inner distance
between the top and bottom walls.
Inventors: |
Kahn; Paul (San Francisco,
CA), Bramson; Mogens L. (San Francisco, CA) |
Assignee: |
Cutter Laboratories, Inc.
(Berkeley, CA)
|
Family
ID: |
25303477 |
Appl.
No.: |
04/848,510 |
Filed: |
August 8, 1969 |
Current U.S.
Class: |
604/524 |
Current CPC
Class: |
A61M
1/3659 (20140204); A61M 27/00 (20130101) |
Current International
Class: |
A61M
27/00 (20060101); A61M 1/36 (20060101); A61m
027/00 () |
Field of
Search: |
;128/348-351 |
References Cited
[Referenced By]
U.S. Patent Documents
Other References
Miller et al.-Jour. Thorac. & Card. Surg., Vol. 56 No. 4, Oct.
68, pp. 607-608.
|
Primary Examiner: Truluck; Dalton L.
Claims
We claim:
1. A pericardial catheter, including in combination, a main tube of
flexible plastic, flat in cross section open at one end and closed
at the other and having a flat top wall, a generally flat bottom
wall, and shallow sidewalls, said bottom wall having entrance
opening means spaced from the closed end of the tube, said bottom
wall also having a plurality of lengthwise extending ridges
adjacent the longitudinal ends of said opening means, and
a collapse-prevention member, round in cross section, inside said
main tube along the longitudinal centerline thereof and having an
outer diameter at least as great as the inner distance between said
top and bottom walls.
2. The catheter of claim 1 having a plurality of entrance opening
means spaced apart from each other by a plurality of lengthwise
extending ridges.
3. The catheter of claim 1 wherein said collapse-prevention member
is a hollow tube.
4. A pericardial catheter, including in combination,
a main flexible plastic tube, flat in cross section open at one end
and closed at the other and having a generally flat bottom wall, a
flat top wall, and shallow sidewalls, said bottom wall having a
plurality of entrance openings spaced from each other and from the
closed end of the tube, said bottom wall also having a plurality of
lengthwise extending ridges between said openings and adjacent
their distal ends, and
a collapse-prevention tube, round in cross section inside said main
tube along the longitudinal outerline thereof and slightly larger
in outer diameter than the inner distance between said top and
bottom walls.
5. The catheter of claim 4 wherein said entrance openings are
generally rectangular.
6. The catheter of claim 5 wherein there are two said entrance
openings and wherein there are three said ridges in each location
of said ridges.
7. The catheter of claim 6 wherein said entrance openings are
approximately as wide as the width across said ridges.
Description
This invention relates to an improved pericardial catheter or
drainage tube.
Among the serious problems that remain in the field of surgery
requiring extracorporeal circulation are intraoperative hemolysis
and postoperative tamponade.
While there are many possible causes of hemolysis, it has been
found that one of the major causes relates to blood lying in
extracardiac spaces (pericardial or pleural) for prolonged periods
of time before being returned to the pump oxygenator. As this blood
pools, it is contaminated by tissue fluid and fat droplets, and
drying occurs at the blood-air-membrane junction. Further, cell
trauma has been found to occur when this mixture is returned to the
venous reservoir by a suction source that mixes great amounts of
air with the blood. Together, these factors appear to be a major
source of hemolysis, at least in some systems of extracorporeal
circulation.
It has been found that these factors can be largely eliminated by
the continuous evacuation of the pericardial space by means of a
gentle source of suction, thereby reducing to a minimum the time
for tissue fluid to mix with the blood, for drying to occur, and
for the blood and air to mix in the cardiotomy suction. In
considering these problems of intraoperative hemolysis and
postoperative tamponade, it became apparent that a drainage or
catheter tube placed in a dependent position in the pericardium
would effectively remove the blood during the procedure and could
be placed or left in place postoperatively as a means of dependent
pericardial drainage, so long as it would not cause cardiac
irritability or otherwise interfere with cardiac contraction.
However, for a tube to be suitable for this use, there must be
means to insure against its collapse, because if it should
collapse, or if anything should rest on it, serious problems might
result.
I have found that these problems can be solved by employing a tube
or catheter which is rather flat in shape, is quite flexible, and
is kept open at all times by means of a small round inner tube of
substantially the same material and about the same diameter, or
slightly larger in minimum exterior diameter than the smallest
interior dimension of the flat tube to be used. The inner tube
included in the lumen of the catheter prevents collapse even when
bending occurs. Another feature of the tube or catheter of my
invention is that the surface of the dependent end of the tube,
which lies against the pericardium, has smooth, interrupted ridges;
these serve to prevent the suction opening from being drawn against
the pericardium, and they also provide multiple channels for the
progression of the blood into the catheter. The tube or catheter is
provided with a pair of generally rectangular entrance openings on
the surface having the ridges.
Further objects and advantages of the invention will appear from
the following description of the preferred embodiment.
In the drawings:
FIG. 1 is a bottom plan view of a tube or catheter embodying the
principles of the invention.
FIG. 2 is a view in section taken along the line 2--2 in FIG.
1.
FIG. 3 is a view in section taken along the line 3--3 in FIG.
1.
FIG. 4 is a view in section taken along the line 4--4 in FIG.
1.
A catheter 10 embodying the principles of the invention is shown in
the drawings; typically, the catheter 10 may be approximately 12
inches long, three-fourths of an inch wide, and one-fourth of an
inch thick. It comprises a flattened flexible tube 11 made from a
suitable plastic, such as a silicone which does not introduce
problems of infection. It should be, in other words, inert, so far
as the body fluids are concerned. The tube 11 has a generally flat
top surface 12 and rather shallow sidewalls 13 and 14. The largest
proportion of its bottom surface 15 comprises a flat portion 16,
but adjacent the dependent end 17 of the tube 11 there is a
plurality of ridges 20, 21, and 22 of about the proportion shown in
the drawings. Between the ridges 20 and 21 there is an entrance
opening 23, and between the ridges 20 and 22 there is an entrance
opening 24. These entrance openings 23 and 24 are preferably
approximately rectangular and serve to take in the fluid. The
smooth ridges 20, 21, and 22 prevent the suction openings 23 and 24
from being drawn against the pericardium and at the same time they
provide between them multiple channels 25, 26, 27, 28, 29, and 30
for the progression of the blood into the openings 23 and 24.
The interior or lumen 31 of the tube 11 is quite flat in cross
section as shown in FIGS. 3 and 4 and is featured by containing an
interior collapse-preventing tube 32 which is nominally round in
cross section and is preferably slightly larger in outer diameter
than the interior diameter of the lumen 31 in its narrowest
direction. This tube 32 need not be cemented in place if so made
slightly larger, for it will then be held by the natural elasticity
of the outer flat tube 11, slightly compressing the walls of the
round tube 32, and making the lumen 31 seek to regain its shaped
and thus hold the tube 32 in place. In place of the tube 32, a rod
may be used, but a tube is better because it distorts more easily
and therefore is more easily retained in place; moreover a tube 32
provides an additional lumen for suction. Cement or welding may be
used to hold the tube 32 in place, but as stated, this is usually
unnecessary.
Wherever bending should occur, the tube 32 prevents collapse of the
tube 11 and even substantial weights do not collapse the tube 11
made in this manner.
The relationship of the heart to the pericardial space is such that
if approached by way of a median sternotomy, the oblique sinus is
slightly cephalad to the angle formed by the diaphragmatic and
posterior parietal pericardium. This anatomic feature thus
necessitates only a very slight bend in the catheter 10 for the
lowermost hole 24 to be in its dependent position. In clinical use,
it has appeared to work best if it enters the pericardial space by
a stab wound in the right subcostal space just lateral to the lower
end of the median sternotomy skin incision.
In clinical use, the catheter 10 is placed just as bypass is
instituted and is connected by a wired connector to a cardiotomy
suction source. At the completion of bypass it is connected to the
usual chest suction and remains so during postoperative period,
until drainage has ceased. It is removed in the same way as any
other chest tube.
The catheter 10 has been used on many patients without any ill
effects. So long as used in the described manner, the catheter 10
does not interfere with operative manipulations and has been noted
to keep the pericardium free of blood. In the postoperative period,
there has been no evidence of cardiac irritability, the tube 11 is
drained well, and the milking of the tube 11 by the left venticular
action prevents clotting. Frequently, the blood level will be seen
moving back and forth with the heart action.
To those skilled in the art to which this invention relates, many
changes in construction and widely differing embodiments and
applications of the invention will suggest themselves without
departing from the spirit and scope of the invention. The
disclosures and the description herein are purely illustrative and
are not intended to be in any sense limiting.
* * * * *