Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.

Patents

  1. Advanced Patent Search
Publication numberUS3674050 A
Publication typeGrant
Publication dateJul 4, 1972
Filing dateMay 4, 1970
Priority dateJul 15, 1969
Also published asCA934260A1, DE2021871A1
Publication numberUS 3674050 A, US 3674050A, US-A-3674050, US3674050 A, US3674050A
InventorsKuffer Francois, Strub Dietrich
Original AssigneeStrub Dietrich, Kuffer Francois
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Check valve for drainage of fluid into the vascular system or into a body cavity for the treatment of hydrocephalus internus and externus
US 3674050 A
Abstract
The check valve for drainage of fluid into the vascular system or into a body cavity for the treatment of hydrocephalus internus and externus is fabricated of synthetic material and has a body with screw thread on each side. On the proximal side of the valve is screwed a connector, which has a cone and a cylindrical part to receive a proximal catheter, in addition to a screw thread for the fixing of a screw cap. On the connector is a shoulder serving as a stop for the screw cap and preventing shearing of the proximal catheter. The connector has a longitudinal bore which drains the fluid into the catheter, the bore widens to a cone and this cone is obturated by a piston, which possesses four longitudinal slots. A spring lays in the bore and can be adjusted by a regulating screw for the purpose of pressure calibration of the fluid.
Images(1)
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

United States Patent [is] 3,674,050 Kutfer et al. July 4, 1972 541 CHECK VALVE FOR DRAINAGE, 0F 3,233,610 2/1966 Wade ..128/350 v FLUID INTO THE VASCULAR SYSTEM OR INTO A BODY CAVITY FOR THE TREATMENT OF IIYDROCEPIIALUS INTERNUS AND EXTERNUS Inventors: Francois Kuffer, Holligenstrasse 33, 3000 Bern; Dietrich Strub, Schanzlistr. 38, 4500 Solothurn, both of Switzerland Filed: May 4, 1970 Appl. No.: 34,389

Int. Cl. ..A6lm 27/00 Field of Search ..l28/350 V; 137/536 References Cited UNITED STATES PATENTS Becker ..137/536 X Hakim Svenson et al.

....l28/350 V ..l37/536 X AttorneyLinton & Linton ABSTRACT The check valve for drainage of fluid into the vascular system or into a body cavity for the treatment of hydrocephalus internus and extemus is fabricated of synthetic material and has a body with screw thread on each side. On the proximal side of the valve is screwed a connector, which has a cone and a cylindrical part to receive a proximal catheter, in addition to a screw thread for the fixing of a screw cap. On the connector is a shoulder serving as a stop for the screw cap and preventing shearing of the proximal catheter. The connector has a longitudinal bore which drains the fluid into the catheter, the bore widens to a cone and this cone is obturated by a piston, which possesses four longitudinal slots. A spring lays in the bore and can be adjusted by a regulating screw for the purpose of pressure calibration of the fluid.

3 Claims, 2 Drawing Figures The present invention relates to a check valve for drainage of fluid into the vascular system or into a body cavity for the treatment of hydrocephalus intemus and extemus.

In the various treatment principles of hydrocephalus internus and extemus the draining of the fluid into the vascular system or into a body cavity is effected by the insertion of a valve. For this purpose three types of valves have been developed. Two of them present some now well-known disadvantages; The third valve has been developed on the basis of the disadvantageous experienced with the first two valves and has only recently been on the market; experiences with this valve type are not yet available and only few scientific publications have yet appeared on this matter in the literature. The well-known disadvantage of the above first two mentioned valves can be summarized as follows:

a. lnsufficient and unconstant calibration of pressure.

b. Dead spaces in the system relative to the flow of fluid and resulting there from, stasis of the fluid.

c. Slipping off and shearing off of the catheter from the valve connectors following the increase, respectively of softening and tensile stress at the points of ligature.

d. Electrostatic charging of the material; slit valve and pumping device are made of silicone so that in the case of infection the bacteria adhere to the valve and make this a source of infection.

e. lnsufficient sterilizability in the autoclave of the material employed.

f. Inadequate performance of the valve, resulting in the necessity of valve replacement.

g. Internal gumming up of the valve device if the protein content of the fluid is too high.

h. Pressure necrosis as a consequence of the valve diameter size.

The first two mentioned valves are slit valves of silicone rubber, which allow an excess pressure in the valve an out flow and inhibit a back flow on an excess pressure outside the valve. The principle and the materials used do not allow an exact calibration. On storage and later after application of the valves, changes occur and in the course of time the elasticity and thereby the calibrated pressure of the silicone rubber change.

The inlet and outlet catheters are, in all the valves described till now, fixed by means of ligatures on metal connectors of the valve. There is the danger of these connections being severed by the ligatures cutting into the catheter, by slipping off of the end of the catheter and by shearing off the catheter and may lead in this manner sooner or later to serious complications.

The above-mentioned valves are constructed with materials which take up electrostatic charges and therefore, in the event of infection, bacteria adhere to the valve and cleaning can only be effected in rare cases by self-rinsing or active antibiotic rinsing by puncture.

The three valves previously mentioned, are valves for a single use and if they are to be removed for renewal they can never be replaced, because they cannot be sterilized or are not dismountable.

In the case of new-born infants and especially for premature births some of said valves are large and lead frequently to pressure necrosis.

A complication to be feared and caused by the valves known until now is the above-mentioned pressure-necrosis above the valve or in the region of the wound on the neck and by the sepsis which occurs. This danger is particularly great in the case of nursing infants whose scalps have bad blood circulations, because some of the valves are rigid and relatively large.

The object of the invention is to effect draining of cerebrospinal fluid by means of a check valve, with which it is sought to overcome the above mentioned inadequacies.

The valveaccording to the invention is characterized by the fact, that it is made of synthetic material and consists of a body which has a threaded end part, on each side, that on the proximal side of the valve is screwed a connector, which has a cone and a cylindrical part to receive a proximal catheter, and has also a threaded part, for the fixing of a cap, which has a cone different from the connector and clamps in this manner the proximal catheter on the connector, that on the connector is formed a shoulder which serves as a stop for the cap and prevents shearing of the proximal catheter, that the connector has a longitudinal bore which conducts the fluid from the catheter, that the bore enlarges to a cone and that this cone is obturated by a piston which possesses on its circumference four longitudinal slots for the flow of the fluid, that inside the piston'a spring is disposed, which is situated outside the stream of fluid, that the spring can be adjusted with a regulating screw for calibrating the pressure of the fluid, which screw possesses a cylindrical part that serves as a stop for the spring on the one hand and as a slideway for the piston on the other hand, that in the threaded part of the regulating screw four longitudinal slots are to be found, which enable the flow of fluid, that on the distal end of the valve a connector is screwed in, the diameter of which is slightly smaller that the diameter of the proximal connector, in order to take into consideration the dimensions of the distal catheter.

For a better understanding of the invention the annexed drawing in conjunction with the following description, shows, by way of illustrative but non-limiting example, one embodi ment of the invention.

In the drawing:

FIG. 1 shows a longitudinal section through the embodiment of the invention;

FIG. 2 shows a cross section along the line A-B of FIG. 1.

in the embodiment shown in FIGS. 1 and 2, the valve consists of a body 1 of a cylindrical shape and which has in both end portions a screw thread 2, each of which receives a connector 3 and 4 which, preferably, are made of polyphenylenoxide, since this material is physiologically neutral, possesses good mechanical qualities, is stable to changes in temperature, is easily sterilized, has very good dimensional stability, is insensitive to electrostatic charges, has good chemical resistance to most of acids, bases, alcohols and water, and guarantees a constant flow of the cerebrospinal fluid. The proximal connector 3 consists of an internal conical part 3b, a shoulder 30, that serves as a stop to a screw cap 13, a threaded part 3d, on which, the cap 13 is screwed, a cylindrical part 32, a conical part 3f and a bore 33. The catheter 16 is disposed on the cylindrical piece 32 and the conical part 3f The distal connector 4 is constituted by the same elements and parts 4b-f.

In the cylindrical bore 5 of the valve 1 is situated the valvepiston 6. This piston consists of a conical part 8 and a bore 7, which receives a steel spring 11. The valve piston 6 has four longitudinal slots 10 through which flow the fluid to be drained. The conical part 8 enters the conical part of the connector 3a and closes the latter. The spring 11 is positioned in the bore 7 away from the fluid being drained and presses the valve piston 6 into the inner cone 3a. The pressure regulation is effected by means of the regulating screw 12. This consists of a threaded part 124, four longitudinal slots 12b and a cylindrical part which extends into the bore 7 and regulates the spring 11. By this means the pressure can be regulated to within 2 cm of water.

On the proximal connector 3 the catheter is fixed with the screw cap 13 and no ligature is disposed there. This screw cap consists of a conical part 13a the slope of which is different from that of the conical part 3f, a cylindrical part 13b, which clamps the catheter l6 and a threaded part 13c, which is screwed on the threaded part 3d. On the distal connector 4 the catheter 17 is fixed with the screw cap 14 which is constituted by the parts 14a -l4c in an analogous manner. The fluid to be drained is led by means of the bore 43 in the connector 4 to the distal catheter l7. lf the fluid is now flowing through the catheter 16 in the direction of the arrow through the bore 33,

to the piston 6, the latter is pushed back and the fluid can continue to flow through the four longitudinal slots and 12b and also through the bore 4g into the catheter 17. The piston remains open until the pressure falls to the value regulated by the regulating screw 12. A back flow is impossible, because the fluid will accumulate in the chamber 18, charges the ring area 19 and will in this manner move the piston again into its initial position, that is to say fully into the cone 3a.

The above-described novel valve is so constructed, that by means of regulation of a spring, the pressure may be regulated individually for each valve. The spring is situated outside the stream of fluid. The stream itself is wide and has no dead spaces. No parts are intercalated in the fluid path on which fragments of tissue, fibrin and coagula may adhere and could introduce occlusions. Even storage for many years or multiple sterilizations do not alter the pressure calibration.

The novel valve is provided with conical connectors by which the catheter is fixed by a conical screwed cap; ligatures are no longer utilized. Slipping off of the catheters is impossible. In order that the fixing may be optimal and that shearing by a too severe tightening may be avoided, the connection is constructed so that the screwed cap is drawn on to a shoulder. In this manner it is ensured that the surgeons connection is made correctly. This means of connection is rapid and positive and also offers great advantages at the time of subsequent recatherizations.

The above-described novel valve, which, except for the spring 11, is constructed entirely of synthetic materials, is in length and in diameter smaller than the known valves. This is mainly based on the fact, that with this valve a pumping device can be dispensed with; if it is taken in consideration that the possibility of pumping was at first developed for control purposes, it is superfluous with a well-installed and well calibrated drainage system. A pumping-system does not ensure freedom of flow and the final diagnosis of a valve connection will always be determined clinicaly or by ventrical puncture by pressure measurement and isotope methods. In other words: the pumping device introduces more disadvantages (size of the valve, dead spaces in the flow path, electrostasis of the silicone) than advantages.

We claim:

l. A check valve for draining fluid into the vascular system or into a body cavity for the treatment of hydrocephalus internus and extemus, comprising a cylindrical body having a longitudinal bore and which has inlet and outlet ends thereof with screw threads in said ends; a proximal connector having first screw threads in threaded engagement with the screw threads in the inlet end of said body and closing said inlet end, said connector having a cone shaped part insertable in an end of a proximal catheter, a cylindrical part with an external screw threads and a shoulder between said cylindrical part and said first screw threads, a screw cap which has a bore with an internal cone shaped portion on a different slant from that of said connector cone shaped part and a cylindrical portion being in threaded engagement with said connector cylindrical part external screw threads whereby said cap can retain said proximal catheter end on said proximal connector, said screw cap being seated on said shoulder which serves as a stop for said screw cap, said connector having a longitudinal bore for the passage of the fluid which bore widens to a cone, a piston slideably mounted in said body bore, having a closed end bore, a conical end slideably in said bore cone for closing the same and four longitudinal slots on its periphery for ensuring the flow of fluid, a spring inside said piston bore away from the fluid, a regulating screw having a cylindrical part providing a stop for said spring and having said piston slideable thereon, said regulating screw having a screw threaded peripheral part in which are situated four longitudinal slots for the flow of fluid and which is in threaded engagement with the screw threads in the outlet end of said body, a distal connector, is threadably mounted in the outlet end of said body, has a end portion insertable in an end of a distal catheter and a longitudinal bore and a second cap detachably connected to said distal connector and capable of retaining said distal catheter end on said distal connector.

2. A check valve according to the claim 1 wherein said body and connectors are of polyphenylenoxide.

3. A check valve according to the claim 1, wherein said body bore has a chamber between said piston and said regulating screw in which the fluid can accumulate and load the piston to avoid a back flow of blood and fiuid and thus to urge the piston into its connector closing position.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2809660 *Apr 24, 1956Oct 15, 1957Aeroquip CorpCushioned streamlined check valve
US3233610 *May 24, 1963Feb 8, 1966Charles Wade StanleyHydrocephalus shunt pump
US3288142 *Apr 27, 1964Nov 29, 1966Salomon HakimHydrocephalus shunt with spring biased one-way valves
US3473561 *Mar 29, 1966Oct 21, 1969Svensson Ivar LCheck valve with supported closure member
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4413985 *Nov 30, 1981Nov 8, 1983The United States Of America As Represented By The Dept. Of Health & Human ServicesHydrocephalic antenatal vent for intrauterine treatment (HAVIT)
US4675003 *Dec 23, 1985Jun 23, 1987Cordis CorporationThree stage pressure regulator valve
US4676772 *Dec 23, 1985Jun 30, 1987Cordis CorporationAdjustable implantable valve having non-invasive position indicator
US4681559 *Dec 23, 1985Jul 21, 1987Cordis CorporationFor controlling the passage of body fluids from location to location
US4714458 *Dec 23, 1985Dec 22, 1987Cordis CorporationFor regulating the flow of fluid from one location to another
US4714459 *Dec 23, 1985Dec 22, 1987Cordis CorporationThree stage intracranial pressure control valve
US4729762 *Dec 23, 1985Mar 8, 1988Cordis CorporationThree stage implantable pressure relief valve with adjustable valve stem members
US4776838 *Jul 10, 1987Oct 11, 1988Cordis CorporationSurgically implantable valve for controlling cerebrospinal fluid
US4776839 *Oct 21, 1986Oct 11, 1988Cordis CorporationThree stage implantable pressure relief valve with improved valve stem member
US4781672 *Oct 21, 1986Nov 1, 1988Cordis CorporationThree stage implantable flow control valve with improved valve closure member
US4861331 *Apr 22, 1988Aug 29, 1989Pudenz-Schulte Medical Research Corp.Implantable shunt system and method of assembly
US4867740 *Mar 24, 1988Sep 19, 1989Pudenz-Schulte Medical Research Corp.Multiple-membrane flow control valve and implantable shunt system
US6146352 *Mar 24, 1997Nov 14, 2000Cordis SaImplantable drainage valve for the treatment of hydrocephalus
US7153296Nov 7, 2003Dec 26, 2006Mitchell Martin SReleasable tubing connector
WO2009127028A2 *Apr 17, 2009Oct 22, 2009Universidade Federal De Minas Gerais-UfmgDevice for controlling and monitoring vacuum pressure in systems for the suction of biological secretions
WO2011098867A1May 20, 2010Aug 18, 2011Debiotech S.A.Passive fluid flow regulator
Classifications
U.S. Classification137/536, 604/9
International ClassificationA61M27/00
Cooperative ClassificationA61M27/006
European ClassificationA61M27/00C2