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Publication numberUS2579113 A
Publication typeGrant
Publication dateDec 18, 1951
Filing dateJun 18, 1948
Priority dateJun 18, 1948
Publication numberUS 2579113 A, US 2579113A, US-A-2579113, US2579113 A, US2579113A
InventorsGardner Herman L
Original AssigneeGardner Herman L
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
US 2579113 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

Dec. 18, 1951 H. L. GA DNER 2,579,113

INSUF'FLATOR Filed Jlgne 18, 1948 I I I I I I I I I I I I I I I I I I I I I I I I I I r I I Herman L. Gardner INVENTOR.

Patented Dec. 18, 1951 UNITED STATES PATENT OFFICE INSUFFLATOR Herman L. Gardner, Houston, Tex.

Application June 18, 1948, Serial No. 33,886

1 Claim.

This invention relates to a medical device to be used for determination of patency or nonpatency of human Fallopian tubes.

Another object of the invention is to provide a device that is adapted to make readily available a source of carbon dioxide.

Still another object of the invention is to eliminate danger of fatality occurring in the prior use of air as a source of gas, by the utilization of carbon dioxide.

Yet another object of the invention is to provide an even and controlled flow of gas, with a change in pressure quickly discernible by the operator.

.And yet another object of the invention is to avoid wide fluctuations of pressure as are normally incurred when improvised office apparatuses are used.

And still another object of. the invention is to provide a simple, compact and comparatively light device, with no complicated structures to adjust and in which no extremes of pressure are possible.

And it is a further object of the invention to provide a reservoir of sufiicient capacity for the carbon dioxide whereby pressure can be reduced to the desired level without the use of a pressure reducing valve.

The invention accordingly comprises the features of construction, combination of elements and relations of parts, which are exemplified in the structure hereinafter in connection with the accompanying drawings, and in the scope of the application of which will be indicated in the following claim.

In the accompanying drawings, in which is illustrated one of the various possible embodiments of the invention:

Figure 1 is a perspective view of the device of the invention; and

Figure 2 is a diagrammatic showing of the device of Figure 1.

Referring to the figures, the device of the invention is generally indicated at l and consists of a gas-holding cartridge l2, a gas reservoir M, a fiow meter [6 controlled by means of a valve [8, and a manometer 20.

Gas container 12 is of the pierceable cartridge type and in this preferred embodiment contains carbon dioxide rather than the usual air. Cartridge I2 is removably replaceable on a threaded nipple 22 on reservoir [4, nipple 22 being axially bored at 24 and containing therein a piercing pin 26. Piercing pin 26 punctures the end of the cartridge l2 and allows carbon dioxide to below the water level therein.

2 pass into reservoir It. The reservoir is of metal construction, corrosion resistant and is preferably of a capacity of 4900 cc. and contains carbon dioxide at a pressure of 520 mm. of mercury. Conduit 28 extends from a suitable aperture 30 at the lower end of reservoir l4 and includes regulating valve l8 therein. Conduit 28 is bent as illustrated and terminates in flow meter 16 To obtain a maximum efiiciency in operation, conduit 28 is drawn out to taper to a fine point at 32 and thereby produce a fine stream of gas through the water 34 within the flow meter. Manometer 20 includes the usual mercury indicating means 36 as well as the upwardly extending leg 38. Leg 38 terminates in an enlarged emergency reservoir 40 to act as an escape should the pressure rise exceed a predetermined upper limit. Flexible hose 42 connects with passage 44 extending from flow meter [6 and terminating in manometer 20 as the source of supply of gas to the patient. A cervical cannula 46 is connected to the open end of conduit 42 and fluid flow is regulated by means of a suitable valve 48. Since the cervical cannula is not a part of the invention, it is believed that it is not necessary to describe the function thereof in greater detail.

The operation of the device is as follows: The device is preferably used after menstruation has ceased for about 3 to '7 days. The patient is prepared by introducing a small uterine sound in order to ascertain the direction and the patency of the cervical canal. The position of the uterus should already have been determined by manual examination. By knowing the position of the uterine cavity and the direction of the cervical canal the cervical cannula is easily inserted with little pain, and there is less likelihood of forcing the end of the cannula into the wall of the uterus or cervix. The cervix should be prepared after the introduction of a bivalve speculum by drying and applying an antiseptic solution.

The cannula 46 is inserted into the tubing 42. Carbon dioxide has been supplied to reservoir M and some of it is now allowed to flow through the apparatus for a few seconds to eliminate any air and water that may be present in the cannula. The cannula is then inserted into the cervical canal with the rubber olive having already been adjusted at a predetermined distance. The olive should fit snugly into the external cervical os. Of course, it is understood that occasionally it is necessary to dilate the cervix slightly before introducing the cannula or, if

the cervix is high and the uterus is anteflexed, it may be necessary to grasp the anterior cervical lip with a tenaculum. When the cannula is in proper position, valve [8 is slowly opened to allow a steady flow of gas. This flow of gas is observed through the water 34 in meter I6 and the manometer indicates a gradual increase in pressure. The rate of flow should be regulated to permit a pressure not in excess of 50 mm. of mercuryin seconds, as too rapid an introduction of the carbon dioxide causes spasm which will cause manometer 213 to indicate a false reading. It is important not to exceed a pressure of 200 mm. of mercury.

As the pressure is slowly built up, the gas will usually pass through the normally open tubes of the patient at a pressure between and 120 mm. of mercury. Disregarding leakage around cannula G5, a sudden drop in pressure indicates gas passing through the tube and if gas is steadily injected-the pressure generally fluctuates between 30 to mm. However, if the tubes are occluded, pressure rises steadily-to 20.0 mm. of mercury without a drop. Pressure should be maintained at this point for a "few seconds. If gas flows through the tubes only after a pressure of mm. or more, it serves to indicate that apartial occlusion :or spasm, has'been present. Thus, it is readily apparent that a sudden fall in pressure indicates normalcy whereas a slow and steady decline in pressure generally means that there is partial occlusion. "If tubal patency is indicated according to pressure of manometer 2d, the gas is permitted .to flow an additional 30 to 45 seconds. This is done in order :to assure a sufficient pneumo peritoneum for production of shoulder pain.

If no :flow of gas occurs with :the first test, "the examination should be repeated after the next menstrual period, and preferably after the patient has .taken atropine about one hour before the test,since occlusion from spasm will be eliminated thereby. Occasionally, patency is established after several insufflations.

By this particular device, many of the disadvantages of the apparatuses now in use are avoided. With the use of carbon dioxide rather than air, the danger of fatal gas embolus is'largely eliminated and the pain resulting from pneumo-peritoneum disappears within a few minutes, whereas such painpersists for several hours or days in the use of air. The control of thefiow of gas in an even and regulated manner is now possible and the drop in pressure is quickly discernable in the manometer. The wide fluctuations of intra-uterine pressure, always present with the use of a sphygnomanometer bulb is eliminated. The use of a safety mercury trap 40 is an additional safety measure against high pressures of gas being inadvertently introduced into the body of the patient. When pressures go above 220 mm., all of the mercury in manometer 20 is forced into the emergency reservoir 40 and gas escapes from the open end 50.

Thus, it is readily apparent that the object of the invention has been sufficiently and simply attained. As many modifications with respect to the embodiment above illustrated might be made without departing from the spirit and scope of'the present invention, it is intended that the above description and accompanying drawings and claim shall be interpreted as illustrative and not in a limited sense.

Having described the claimed as new is:

An insufiiator comprising a relatively large carbon I dioxide "supply tank, .a lcarloon :dioxide cartinvention, what is ridge, means for removably retaining said icartridge on said tank. means carried by said retaining means for piercing .said cartridge, 2. bubble-type flow meter, :a valved conduit interconnecting said ficw meter with said tank, 'a second conduit leading from saidflow meter, a

manometer tube operatively connected to .said

second conduit, and-a branch=conduit connected to said second conduit between said flow meter and said manometer tube and adapted to secure a cannula, said manometer tube inc'l-uding an enlarged reservoir having an escape aperture.


REFERENCES CITED The following references are of record in the fileof this patent:

OTHER REFERENCES Page 1034 of the British Medical Journal for June '9, 1-934.

Page 143 of the American Journal of Surgery for January 1943.

Page :328 of f'Diseases of Women by C-rossentk 'Crossen, 58th edition, published in 1940 by -C. V.

Mosby (30., St. Louis, Mo.

Pages 169, and 171 of the American Journal of :Surgery, for 1937.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1611272 *Mar 13, 1925Dec 21, 1926Hill Thomas ALiquid gauge
US1614215 *Dec 4, 1924Jan 11, 1927Summers John RLiquid gauge
US2441237 *Dec 28, 1946May 11, 1948Charles DaviesTubal insufflator
Referenced by
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US5006109 *Sep 12, 1989Apr 9, 1991Donald D. DouglasMethod and device for controlling pressure, volumetric flow rate and temperature during gas insuffication procedures
US5814012 *Mar 12, 1993Sep 29, 1998Birtcher Medical Systems, Inc.Method and apparatus for relieving excess insufflation pressure
US6976489Jun 29, 2001Dec 20, 2005Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
US7647925Oct 12, 2005Jan 19, 2010Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
US7762251Jan 4, 2007Jul 27, 2010Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
US8091546Nov 30, 2009Jan 10, 2012Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
US8206337Oct 15, 2001Jun 26, 2012Fisher & Paykel Healthcare LimitedApparatus used for the humidification of gases in medical procedures
US8211052Jul 13, 2006Jul 3, 2012Lexion Medical LlcCharged hydrator
US8955511Aug 24, 2011Feb 17, 2015Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
US9095668Jun 22, 2012Aug 4, 2015Fisher & Paykel Healthcare LimitedApparatus used for humidification of gases in medical procedures
US20020072700 *Jun 29, 2001Jun 13, 2002Mantell Robert R.Method and apparatus for humidification and warming of air
US20040102731 *Oct 15, 2001May 27, 2004Blackhurst Michael JosephApparatus used for the humidification of gases in medical procedures
US20060033223 *Oct 12, 2005Feb 16, 2006Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
US20070107726 *Jan 4, 2007May 17, 2007Northgate Technologies, Inc.Method and apparatus for humidification and warming of air
U.S. Classification600/560
International ClassificationA61M31/00
Cooperative ClassificationA61M31/00
European ClassificationA61M31/00