US3722500A - Abortive device and method - Google Patents

Abstract

Premature termination of pregnancy is effected by insertion of a hollow, distensible body of elastomeric material into the uterus to stimulate muscular activity sufficiently to induce menstruation and thereby cause spontaneous expulsion of the nonviable embryo. In one form of the invention, after the body is inserted, it is filled with a substance to effect the distension thereof. In another embodiment, the body is provided with an incrustation and then charged with a pressurized substance before insertion. The incrustation dissolves in the uterus, permitting the substance to expand and distend the body to a size which precludes its expulsion until shedding of the endometrium and discharge of the implantation therewith.

Description

0 United States Patent 1 1 1111 3,722,500

Robinson 1 Mar. 27, 1973 [54] ABORTIVE DEVICE AND METHOD [76] Inventor: Ralph R. Robinson, PO. Box 668, f,

Middlesboro, 40965 Attorney-Schmidt, Johnson, Hovey & W1ll1ams [22] Filed: Dec. 29, 1970 57 ABSTRACT PP N03 102,448 Premature termination of pregnancy is effected by insertion of a hollow, distensible body of elastomeric 52 US. 01. ..12s/1 R material into the uterus to stimulate muscular activity 51 1m. 01. ..A61b 19/00, A6lf 5/46 snfficinnflyv o induce menstruation and thereby cause 58 Field of Search ..128/1 R, 127, 129, 130,131, Spontaneous expulsion of the nonviable y In 123 344 one form of the invention, after the body is inserted, it is filled with a substance to effect the distension [56] Referen Cited thereof. In another embodiment, the body is provided with an incrustation and then charged with a pres- UNITED STATES PATENTS surized substance before insertion. The incrustation 3,464,409 9/1969 Murphy ..l28/l29 dissolves in the mus, Pflmming the Substance 3,452,749 7/1969 Riedell ....12s/129 P and distend the y to a Size which precludes 3,401,689 9/1968 Greenwood ..128/129 its expulsion until shedding of the endometrium and 3,512,528 5/1970 Whitehead et al..... ....l28/l29 X discharge of the implantation therewith. 2,063,202 12/1936 Spicer ..l28/l30 2,893,385 7/1959 Millar...... ....l28/l31 9 Claims, 10 Drawing Figures PATENTEDMAR 27 I973 INVENTOR. ph R. RObI/730I7 T NE Y8.

ABORTIVE DEVICE AND METHOD Legalized abortive methods have, for the most part, heretofore been performed by the duly authorized and properly registered physician through use of acurette' or the like in the case of the nonviable embryo and other surgical instruments with respect to the viable fetus. On the other hand, miscarriages for various reasons occur quite frequently, oftentimes without knowledge by the female, particularly within a short period of time following conception. Such spontaneous expulsion may be caused by health, injury or unknown factors which induce menstruation and resultant discharge of the endometrium, together with the fertilized ovum implanted therein.

It is an important object of the instant invention, therefore, to provide the doctor with a safe and simple, yet effective means for duplicating such premature expulsion of the nonviable embryo during the early stages of pregnancy without need for the usual uterus scraping procedures or any other type of surgical techniques.

Another important object of my present invention is to cause naturopathic abortion by virtue of the fact that the uterus tends to expel foreign objects, causing miscarriage, and eliminating the need for surgical discomfort or the risk of ill after effects.

Still another object of the present invention is to provide an abortive device which may be easily and quickly inserted into the uterus by the physician, following which the fertilized ovum is expelled through natural process of muscular activity and induced menstruation.

In the drawing:

FIG. 1 is an elevational view of one type of tubular instrument which may be used to carry out one of the methods of my present invention, illusfiating in phantom a first example of an abortive device which may be inserted thereby;

FIG. 2 is an enlarged, fragmentary, longitudinal cross-sectional view of the instrument and device shown in FIG. 1;

FIG. 3 is a view similar to FIG. 2, still further enlarged, showing the device projected beyond the tubular portion of the instrument;

FIG. 4 is a fragmentary cross-sectional view of a portion of the device and of the proximal end of the plunger of the instrument;

FIG. 5 is a' fragmentary cross-sectional view, enlarged still further, of the device after the same is detached from the plunger;

FIGS. 6, 7 and 8 are fragmentary cross-sectional views showing the successive steps of inserting the device and its position in the uterus after withdrawal of the instrument from the cervix;

FIG. 9 is a cross-sectional view of a modified form of abortive device made pursuant to my present invention; and

FIG. 10 is an enlarged view of the device of FIG. 9 showing the same within the uterus.

In FIGS. 1-8 of the drawing there is illustrated an abortifacient (abortion inducing means) denoted by the numeral 10 in the nature of an elongated,hollow body 12 which may be made from a silicone rubber or other essentially nonporous, distensible, elastomeric material capable of preventing escape therefrom of a body-distendingsubstance 14. While the precise shape of thebody 12 is of no special importance, ease of insertion intouterus 16 through the cervix l8, and proper fitting ofbody 12 within theuterus 16 suggests, to some extent at least, choice of the generally elliptical configuration ofbody 12 as illustrated. Moreover, the size of thebody 12 is not particularly critical, but generally, depending somewhat on the size and condition of theuterus 16 andcervix 18, it may measure from about 1 1% to 2 A inches long and from about 15 to 1 inch in diameter in theuterus 16 after expansion ofbody 12 bysubstance 14.

For insertion purpose, and by way of example, theabortive device 10 may be placed in one end of atube 20 forming part of a manuallymanipulable tool 22 which is also equipped with aplunger 24.Tool 22 may be further provided with a separate or anintegral syringe 26 or other apparatus that includes acylinder 28 communicating withbore 30 inplunger 24 and having areciprocable piston 32 used to force thesubstance 14 fromcylinder 28 throughbore 30 and intobody 12 after thedevice 10 is disposed theuterus 16 as shown in FIG. 6.

Shoulder 34 oncylinder 28 engagesabutment 36 onenlarged portion 38 oftube 20 to indicate that thedevice 10 has been fully ejected from thetube 20, whereupon the doctor usesfinger tabs 40 oncylinder 28 to facilitate depression ofthumb piece 41 onpiston 32.Boss 42 onplunger 24 engagesshoulder 44 inportion 38 oftube 20 to limit the extent of retraction ofplunger 24.Ribs 46 and 48 ontube 20 andpiston 32 respectively slide within corresponding grooves (not shown) inportion 38 andcylinder 28 respectively to prevent relative rotation of the component parts of thetool 22. Plunger 24 terminates in ashort nozzle 50 that fits within an orifice provided with a check valve or a self-sealingorifice 52 in that end of thebody 12 which abuts a shoulder 54 onplunger 24.

In use, theplunger 24 is extended until shoulder'34 engages abutment 36 so as to projectnozzle 50 out of the proximal end oftube 20, permitting insertion ofnozzle 50 intoorifice 52 as seen best in FIG. 4.Plunger 24 isthen retracted to pull thedevice 10 into thetube 20 as shown in FIGS. 1 and 2.Piston 32 is thereupon removed,cylinder 28 is filled with the substance 14 (FIG. 2) andpiston 32 is then replaced as shown in FIG. 1.

The physician thereupon inserts thetube 20 through the vagina (not shown) and into thecervix 18, following which he depresses theplunger 24 untilshoulder 34 engages theabutment 36 to fully eject thedevice 10 into theuterus 16 as shown in FIG. 6. g I

Thebody 12 is then charged with thesubstance 14 by depression ofplunger 24, causing thebody 12 to expand as shown in FIGS. 3 and 7. Theplunger 24 is then retracted untilboss 42 engagesshoulder 44, causing withdrawal ofnozzle 50 from theorifice 52 as the enlargeddevice 10 is held against movement into thetube 20 by abutment against the proximal end oftube 20.

Orifice 52 seals automatically (FIG. 5) trapping thesubstance 14 within thebody 12, whereupon thetube 20 is withdrawn from the cervix 1s and the vagina, leaving thedevice 10 in theuterus 16 as shown in FIG. 8.

As is well known, the presence ofdevice 10 in the uterus causes natural muscular activity in an effort to expel thedevice 10 from theuterus 16 through thecervix 18. The size of device is such that expulsion does not occur until the muscular action becomes sufficiently forceful to induce menstruation. This results in shedding of the endometrium of the uterus l6 and its discharge from thecervix 18 along with the fertilized ovum implanted therein as well as thedevice 10.

lt follows then that the wall ofbody 12 should be sufficiently thin and pliable as to cause it to distend readily under the pressure of thesubstance 14 forced therein by use of thetool 22 in the manner above described, yet be strong and tough enough to withstand the pressure and not burst. Moreover, the material chosen forbody 12 must be resistant not only to the physical forces of movement into and out oftube 20 but to the extraction ofnozzle 50 from within theorifice 52. Still further, the elastomeric material from whichbody 12 is made must be capable of resisting all chemical reaction while subjected to the fluids within theuterus 16 and not in any manner become an irritant to the internal uterus tissues.

Consideration should also be given to proper choice of thesubstance 14 such that no deleterious chemical reaction will occur between the material chosen forbody 12 and thesubstance 14 used for its distension. Many types of fluids may be used but a weak saline solution or other liquid is satisfactory because there should be no risk of injury to the patient in the event of accidental spillage by the doctor or leakage from thebody 12.

Theabortive device 56 illustratedin FIGS. 9 and 10 includes abody 58 which may have the same characteristics as thebody 12 except that it is precoated with an incrustation 60 capable of being softened or dissolved inuterus 62 after insertion of thedevice 56 thereinto throughcervix 64. Moreover, afterbody 58 is so coated and prior to insertion ofdevice 56 into theuterus 62,body 58 is charged with a pressurized substance which will distend thebody 58 after the incrustation 60 has softened or dissolved away, it being understood, of course, that incrustation 60 be capable of preventing distension ofbody 58 by the substance therein while the incrustation 60 remains in a hardened condition onbody 58.

A check valve or self-sealingorifice 66 may be provided for thebody 58 the same as in thebody 12 but theplunger 24 of theinsertion tool 22 need not be provided with thebore 30 or thenozzle 50, and there will be no need forsyringe 26 if thebody 58 is charged with a compressible fluid or the like, such asv air or other elastic gas, beforedevice 56 is loaded into the outer end oftube 20.

The pressure of the substance inbody 58 should be sufficient only to balloon thebody 58, after softening or dissolution of incrustation 60, to approximately the expanded size ofbody 12 as above specified and as shown in FIGS. 8 and 10, butdevice 56, prior to insertion, as shown in FIG. 9, should be about the same size as unexpanded device 10 (compare with FIG. 2) for ease of direction throughcervix 64.

Proper selection of the ingredients for the incrustation 60 will assure its softening by body heat of the patient and/0r dissolution by the uterus fluids, sufficient to releasebody 58 for expansion by the compressed substance precharged therein, all without/injury or harmful effects to the patient. Such ingredients may include an admixture of a filler, a binder for increasing the strength and cohesive properties of incrustation 60, and a disintegrating agent for increasing its speed of solution.

Powdered milk, powdered cocoa, or sugar (powdered or granular) may be used as the filler, whereas the binder may be selected from glucose, an acacia or gelatine solution, a heavy sugar syrup, or a starch paste. Lactose may also be used to serve both as a filler and as a binder. If a disintegrating agent is believed necessary or desirable, the use of corn or potato starch will make it unnecessary to rely entirely on the heat ofuterus 62 to releasebody 58 for expansion as shown in FIG..10.

While it is not contemplated that the devices or methods above described will necessarily be satisfactory in an effort to efifect miscarriage of the viable fetus beyond the first 12 to 28 weeks of gestation, its use to induce abortion of the nonviable embryo during at least the first 8 weeks of pregnancy will, in most cases, cause no ill effects and constitute a decided improvement over devices and methods heretofore used or suggested.

Having thus described the invention, what is claimed as new and desired to be secured by Letters Patent is:

1. An abortifacient comprising:

an essentially nonporous, distensible hollow body of elastomeric material insertable into the uterus through the cervix,

said body containing a substance when the body is in the uterus capable of distending the body to a size sufficient to induce menstruation,

said substance being expansible, said body having an incrustation normally holding the body against distension by said substance, said incrustation softening in the uterus to release the body for distension by the substance.

2. An abortifacient as claimed in claim 1 wherein said substance is a compressible fluid.

3. An abortifacient as claimed in claim 1, said body being provided with a self-sealing orifice through which said substance may be directed after the incrustation is placed thereon. i

4. An abortifacient as claimed in claim 1 wherein said incrustation contains a binder for increasing its strength and cohesive properties.

5. An abortifacient as claimed in claim 1 wherein said incrustation contains a disintegrating agent for increasing the speed of solution.

6. An abortifacient as claimed in claim 1 wherein said incrustation comprises an admixture of a filler, a binder and a disintegrating agent.

7. A method of terminating pregnancy prematurely which comprises insertion of an essentially nonporous, distensible hollow body of elastomeric material into the uterus through the cervix, said body containing a substance when the body is in the uterus capable of distending the body to a size sufficient to induce menstruation, said substance being expansible and being directed into the body under pressure before the latter is inserted into the uterus, said body prior to having the substance directed thereinto being provided with an incrustation which softens when the body is in the uterus, said incrustation holding the body against distension by said substance until the incrustation softens.

8. A method of terminating pregnancy prematurely comprising the steps of:

6 inserting anessentially nonporous, distensible hollow condition from the uterus through the cervix by body into the uterus through the cervix; the force of said uterine muscular activity during injecting a predetermined amount of substance into e ndu enstruat on.

said body when the latter is in the uterus to distend The m th l ime in clairn 8, herein the the body to a size sufficient to induce muscular ac- 5 Substance l l f mm 831d f y llmlted to an tivity of such magnitude as to cause menstruation; f F whlch W111 Produce a m of from to l and ll'lCh 1n the body when the latter is fully distended. expelling the body while still in its fully distended

Claims (8)

1. 2. An abortifacient as claimed in claim 1 wherein said substance is a compressible fluid.
2. 3. An abortifacient as claimed in claim 1, said body being provided with a self-sealing orifice through which said substance may be directed after the incrustation is placed thereon.
3. 4. An abortifacient as claimed in claim 1 wherein said incrustation contains a binder for increasing its strength and cohesive properties.
4. 5. An abortifacient as claimed in claim 1 wherein said incrustation contains a disintegrating agent for increasing the speed of solution.
5. 6. An abortifacient as claimed in claim 1 wherein said incrustation comprises an admixture of a filler, a binder and a disintegrating agent.
6. 7. A method of terminating pregnancy prematurely which comprises insertion of an essentially nonporous, distensible hollow body of elastomeric material into the uterus through the cervix, said body containing a substance when the body is in the uterus capable of distending the body to a size sufficient to induce menstruation, said substance being expansible and being directed into the body under pressure before the latter is inserted into the uterus, said body prior to having the substance directed thereinto being provided with an incrustation which softens when the body is in the uterus, said incrustation holding the body against distension by said substance until the incrustation softens.
7. 8. A method of terminating pregnancy prematurely comprising the steps of: inserting an essentially nonporous, distensible hollow body into the uterus through the cervix; injecting a predetermined amount of substance into said body when the latter is in the uterus to distend the body to a size sufficient to induce muscular activity of such magnitude as to cause menstruation; and expelling the body while still in its fully distended condition from the uterus through the cervix by the force of said uterine muscular activity during the induced menstruation.
8. 9. The method as claimed in claim 8, wherein the substance injected into said body is limited to an amount which will produce a maximum of from 1/2 to 1 inch in the body when the latter is fully distended.

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