U.S. patent number 3,810,471 [Application Number 05/236,947] was granted by the patent office on 1974-05-14 for surgical aspirating cannula.
Invention is credited to Andrew Truhan.
United States Patent |
3,810,471 |
Truhan |
May 14, 1974 |
SURGICAL ASPIRATING CANNULA
Abstract
A surgical aspirating or draining device having means
maintaining a zone of contamination free gas about the surgical
site to reduce a minimum introduction of contaminated particulate
and gaseous matter into the surgical site, cavity or wound.
Inventors: |
Truhan; Andrew (Somerset,
NJ) |
Family
ID: |
22891676 |
Appl.
No.: |
05/236,947 |
Filed: |
March 22, 1972 |
Current U.S.
Class: |
604/45;
604/902 |
Current CPC
Class: |
A61M
1/85 (20210501); Y10S 604/902 (20130101) |
Current International
Class: |
A61M
1/00 (20060101); A61m 001/00 () |
Field of
Search: |
;128/276-278,240-241,350,184 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Rosenbaum; Charles F.
Attorney, Agent or Firm: Stowell; Harold L.
Claims
I claim:
1. A surgical aspirating or draining device comprising a first
aspirating cannula, means connecting one end of said first cannula
to a source of reduced pressure, the other end of said aspirating
cannula being open to its environment at a surgical site, a second
cannula fixed relative to the first cannula in substantially
parallel relationship therewith, means connecting one end of the
second cannula to a source of pressurized contamination-free gas at
a pressure greater than the pressure of the environment of the open
end of the first aspirating cannula, a plurality of outlets for the
pressurized gas, at least one of the outlets being adjacent the
zone of the surgical site of the open end of the first cannula
whereby the zone of aspiration of said first aspirating cannula is
bathed in gas issuing from said second cannula to thereby reduce
introduction of contaminated particulate and gaseous matter into
the surgical site.
2. A surgical aspirating or draining device comprising a first
aspirating cannula, means connecting one end of said first cannula
to a source of reduced pressure, the other end of said aspirating
cannula being open to its environment at a surgical site, a second
cannula maintained in proximity to the first cannula, means
connecting one end of the second cannula to a source of pressurized
contamination-free gas at a pressure greater than the pressure of
the environment of the open end of the first aspirating cannula, a
plurality of outlets for the pressurized gas, at least one of the
outlets being adjacent the zone of the environment of the surgical
site of the open end of the first cannula whereby the zone of
aspiration of said first aspirating cannula is bathed in gas
issuing from said second cannula to thereby reduce introduction of
contaminated particulate and gaseous matter into the surgical site,
the first and second cannulae having concentric bores.
3. A surgical aspirating or draining device as defined in claim 1
wherein the area of the outlets in the second cannula progressively
decrease in size from adjacent the open end of the first cannula
toward said one end thereof.
Description
THE INVENTION
This invention relates to an improved surgical instrument and in
particular to an aspirating or draining device for use during
surgical procedures wherein means are provided to direct a
contamination-free pressure fluid to the zone of the aspirating or
draining tip of the device to thereby reduce to a minimum the
introduction of contaminating gaseous and particulate matter into
the surgical site.
The use of a aspirating or draining cannulae comprises accepted
surgical procedures in the treatment of wounds and during and
following surgery, particularly in the cavity areas of a being. It
has been found, however, that the operation of conventional
aspirating devices causes the in-flow of the surrounding, often
contaminated atmosphere, together with contaminated particulate
material suspended in the atmosphere.
It is a primary object of the present invention to provide a device
which will permit operation of aspirating or drainage devices with
a minimum of environmental contamination of the surgical site.
It is a further object of the present invention to provide such a
device wherein at least the zone of the aspirating or drainage tip
of the drainage cannula is continuously provided with a sterile,
particle free gas, atmosphere, gas and humidifying liquid, or gas
and suspended antiseptic or combinations thereof.
The invention will be more particularly described in reference to
the accompanying drawings wherein:
FIG. 1 is a fragmentary partial sectional view of an embodiment of
the present invention;
FIG. 2 is a section on line 2--2 of FIG. 1;
FIG. 3 is a fragmentary sectional view of a portion of the
structures illustrated in FIG. 1; and,
FIG. 4 is a diagrammatic illustration of a use of the improved
aspirating or drainage cannula of the invention.
Referring to the drawings, 10 generally designates the improved
aspirating or drainage surgical cannula of the invention which
generally comprises a first cannula 12 and a second cannula 14
maintained in the proximity of the first cannula 12. Each of the
elements 12 and 14 is constructed of, for example, stainless steel
where the device is manufactured for multiple use requiring
sterilization between uses. The cannulae may also be constructed of
plastic material and be disposed of after a single use.
Cannula 12 is open at end 16 and is provided at the opposite end 18
with a fitting adapted to receive a flexible tube 20 having its
extended end connected to a source of reduced pressure as is well
known in the art. Between fitting 18 and the open end 16, the
cannula 12 may be provided with a manual control valve generally
designated 22 whereby the surgeon or his assistant may regulate the
aspirating affect of the device.
The second cannula 14, in the illustrated form of the invention,
has a greater diameter than the first cannula 12 and the cannula 12
is internally received in the lumen 24 thereof. The upper end 26 of
cannula 14 forms a seal about the external surface of the cannula
12 and a similar seal may be provided at end 28 adjacent the open
end 16 of tube 12. Between ends 26 and 28 an inlet conduit 30
communicates with the lumen 24 of cannula 14. The extended end of
conduit 30 is provided with a fitting 32, adapted to be connected
to a source of pressure fluid as to be more fully described
hereinafter.
The conduit 30 is also provided with a manual flow control valve 34
whereby the surgeon may adjust the release of the pressure fluid
about the surgical site.
The cannula 14 is provided with a number of bores or openings
designated 36a, b . . . g, which permit the flow of pressure gas,
from within the tubular member, about the zone of the outlet tip 16
of cannula 12 and about an extended zone adjacent thereto. The flow
of gases is diagrammatically illustrated by flow arrows A in, for
example, FIGS. 1 and 4. In the illustrated embodiment of the
invention, the openings 36a through 36g progressively vary in area
from the largest adjacent the tip 16 to the smallest designated 36g
as it has been found that such progressive size openings provide a
more desired flow pattern for the contamination-free gases.
As hereinbefore discussed, inlet fitting 32 receives one end of a
flexible conduit 38 having its opposite end connected to a source
of contamination-free pressure gas generally designated 40. The
reference character 40 may designate bottled nitrogen, CO.sub.2, or
compressed contamination-free and sterol air. In order to reduce
fluid losses during operating procedures, humidifying means 42 may
be connected via conduit 44 to the source of pressurized gas 40
and, as hereinbefore set forth, antiseptic fluids may be directed
into the pressure gas directed into the space 24 between the pair
of cannulae.
Referring to FIG. 4, there is diagrammatically illustrated use of
the improved surgical aspirating device to remove blood and body
fluids from the operating site generally designated 50. In FIG. 4,
the tip 16 of the suction cannula 12 is illustrated within the
incision and in close proximity to the surgical knife 54 and the
lowermost of the pressure fluid outlets 36a also being shown below
the outer surface 52 of the patient.
In general, it has been found that the pressure of the pressure
fluid being supplied to the cannula 14 need only be slightly
positive in respect to the environmental pressure and an operating
range of, for example, one to about ten psig has been found to be
useful.
It will be appreciated that aspirating cannula 12, when not needed,
may be inactivated by closing valve 22 and the device may continue
to be used to supply contamination free gas about the surgical
site. Further, the device lends itself to a construction wherein
the outer cannula 14 is in whole or in part formed of porous metal,
glass or plastic as a replacement for the tube with discrete
openings 36a - g, formed therein.
* * * * *