|Publication number||US3707967 A|
|Publication date||Jan 2, 1973|
|Filing date||Oct 1, 1970|
|Priority date||Oct 1, 1970|
|Also published as||DE2149040A1|
|Publication number||US 3707967 A, US 3707967A, US-A-3707967, US3707967 A, US3707967A|
|Inventors||Kitrilakis S, Robinson T|
|Original Assignee||Tecna Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (4), Non-Patent Citations (3), Referenced by (119), Classifications (12), Legal Events (8)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1-19 Kitrilakis et al. [4 1 Jan. 2, 1973 s41 STEADY FLOW REGENERATIVE 3,520,298 7/1970 Lange ..l28/213 PERITONEAL DIALYSIS SYSTEM AN 3,545,438 12/1910 De Vries ..12s/21s METHOD OTHER PUBLICATIONS  Inventors: soflfis Kimhkis' Berkele Thom Gordon et 21]., Trans. Amer. Soc. Artif. Inter. Organs Charles Robinson, E1 Cemto, both of Calif Vol. XV, 1969 (June) pp. 347-352.
Shinaberger et al., Trans. Amer. Soc. Artif. Inter. Or-  Assignee: Teena Corporation, Berkeley, Calif. gang Vol, X1, 1965 pp, 76-81.  Filed: Oct 1, 1970 Ersek et al., Trans. Amer. Soc. Artif. lnter. Organs 4 Vol. XV, 1969, pp. 267-271.  Appl. No.: 77,240
' Primary Examiner-Dalton L. Truluck  US. Cl. ..128/213, 128/348 y Hohbach, Test, Albritton & Herbert  Int. Cl. ..A6lm 5/00 58 Field of Search ..128/213, 214 R, 348, 1 R; 7] ABST 210/32 A steady-flow regenerative peritoneal dialysis system and method making use of permanent percutaneous  References cued tubes extending into the abdominal cavity and means UNITED STATES PATENTS for circulating a dialysate through the abdominal cavity and reconstituting the dialysate. 3,314,420 4/1967 Smith et al ..l28/92 C 3,605,123 9/1971 Hahn .311 9 Claims, 4 Drawing Figures REGENERATION 22 1? INFLOW [I I l 19 '1 PUMP f f OUTFLO u.v. STERILIZER UREA REMOVAL COLUMN FILTER FLOW REOUIATOR ORIFICE ACTIVATED CARBON I //7/1, 36v 29- I9 I 32 l I II A l SOTIRIS KITRILAKIS THOMAS C. ROBINSON INVENTORS BY 224, M 721, 4 4125 "4%:
ATTORNEYS quantity of dialysing STEADY FLOW REGENERATIVE PERITONEAL DIALYSIS SYSTEM AND METHOD BACKGROUND OF THE INVENTION for treatment of chronic kidney disease. Two types of lo dialysis are currently in use; hemodialysis and peritoneal dialysis. In hemodialysis the blood is removed from an artery or vein, dialyzed in an artifical kidney machine external of the body and returned to a vein usually through cannulas in the arm or leg. This type if dialysis involves permanent connectors to major blood vessels for attachment of the device and also requires the handling of blood in an external prothesis.
The second type of dialysis which does not involve handling of blood directly in a prosthesis is peritoneal dialysis. In this method, dialysing fluid is introduced in the abdominal cavity either through a puncture in the abdominal wall or through a permanently installed percutaneous tube. The dialysate resides in the cavity for a period of time minutes to 1 hour) and is then removed. While the fluid is in the cavity, it picks up urea and other metabolic wastes from the blood stream by diffusion through the walls of the blood vessels within the abdominal cavity. This scheme of dialysis avoids the requirement of handling the blood and invasion of the vascular system but requires the penetration of the abdominal wall. Both types of dialysis require that the blood stream be brought directly or indirectly in chemical equilibrium with a very large quantity of dialysate. In addition to the waste material picked up by the dialysate, a certain amount of proteins and inorganic constituents capable of diffusing through the hemodialysis membrane or the blood vessel walls are dissolved in the dialysate fluid and lost. The systemic replacement capacity for these substances may or may not be capable of maintaining physiologic levels. When certain of these materials are depleted by chronic dialysis over long periods of time, characteristic pathologic symptoms often appear. The depletion of important trace components is proportional to the total quantity of dialysate used.
An additional serious difficulty with both types of dialysis is the danger of infection, either at the sites of cannulation of arteries and veins in the case of hemodialysis, or the penetrations through the abdominal wall, temporary or permanent, in the case of peritoneal dialysis. The large quantities of dialysate involved must be maintained sterile during preparation and throughout the diffusion process to avoid infecting the blood stream or the peritoneal cavity.
As a consequence, elaborate cleaning and sterilization procedures must be followed by hospital personnel or the patient himself while connecting the cannulas or percutaneous in-flow out-flow tubes to the dialysis equipment. Any laxities during the procedure can lead to serious infection.
The equipment involved in both types dialysis is bulky and expensive, primarily because of the large fluid and the handling of blood. In both types the patient must be attached to the equipment and remains essentially immobilized for the duration of the dialysis process. The complexity and high risks associated with currently used dialysis equipment and methods have resulted in the administration of treatments as infrequently as possible, usually about 2-3 times weekly. In the time period between treatments the concentration of metabolic wastes in the patients blood stream continuously increases reaching levels which normally cause discomfort and often clebilitation prior to the next dialysis treatment.
The discomfort and incapacity prior and during treatments often impairs the patients ability to lead a normal, productive life and may also lead to serious psychological problems.
OBJECTS AND SUMMARY OF THE INVENTION It is a general object of the present invention to provide a steady-flow regenerative peritoneal dialysis system and method which overcomes a number of the drawbacks of presently used systems and methods.
It is another object of the present invention to provide a peritoneal dialysis system and method which employs a small amount of dialysate fluid which is circulated at low, steady flow rates through the peritoneal cavity via in-flow and out-flow tubes extending through the abdominal wall.
\ It is another object of the present invention to provide a regenerative peritoneal dialysis system and method wherein the fluid employed is regenerated and the amount retained in the abdomen is minimized whereby the abdominal cavity is not distended by a large amount of fluid and virtually no discomfort results from'the presence of the fluid within the cavity.
It is a further object of the present invention to provide a peritoneal dialysis system and method in which the dialysis is performed at steady flow rates and approaches continuous use thereby eliminating excessive concentrations or urea and other metabolic wastes which would otherwise build up in the blood stream and thereby avoid abrupt changes in waste concentration resulting from present dialysis processes.
It is a further object of the present invention to provide a continuous regenerative peritoneal dialysis system and method in which the in-flow and out-flow tubes extending through the abdominal wall into the peritoneal cavity are permanently affixed and are formed whereby the tissue may readily grow to the surface of the tubes to form a living seal to prevent bacterial infection.
The foregoing and other objects of the invention are achievedby a dialysis system including in-flow and outflow conduits extending through the abdominal wall and provided with a surface which permits the growing and attachment of tissue to the surface of the conduits. The conduits provide means for introducing and removing fluid from the peritoneal cavity which communicates with means for circulating the dialysate fluid through the cavity and regenerative means for regenerating the fluid. The cavity, associated conduits, and circulating and regenerating means are connected in a closed fluid system whereby the fluid is continuously reconstituted and circulated through the peritoneal cavity.
BRIEF DESCRIPTION OF THE DRAWINGS I FIG. 1 is a schematic diagram of the regenerative peritoneal dialysis system in accordance with the present invention shown connected to supply fluid to the cavity.
FIG 2 is an enlarged view of the abdominal wall showing the skin, subcutaneous tissue and peritoneum together with a conduit anchored in the wall by tissue growth.
FIG. 3 is an enlarged view of the portion of the conduit of FIG. 2 showing the surface microcavities into which the tissue grows.
FIG. 4 is a detailed drawing of the fluid circulating flow control and regeneration means.
DESCRIPTION OF THE PREFERRED EMBODIMENTS vide microcavities which have a depth in the range of 0.002 to 0.020 inches. These microcavities permit the subcutaneous tissue to grow around the outside walls and become permanently affixed or anchored to the walls. Thus, the track along the peritoneal penetrations is completely sealed by the tissue which grows into the microcavities and is nourished from adjacent cells.
The tubes are preferably very small in diameter, for example, 1 to 3 mm. in diameter, and are very flexible because of the very low flow rates required in steady flow dialysis in accordance with another feature of the present invention. Both of these characteristics greatly facilitate the permanent fixation of the tubes into the abdominal wall. The conduits 11 and 12 each have a portion 16 and 17, respectively, which extend into the abdominal cavity. The other end of the conduit 12 is connected to means for removing the fluid from the abdominal cavity comprises a conduit 18 which, in turn, connects the pump 19 which serves to transport fluid from the upper portion of the abdominal cavity and pumps the fluid along the conduit2l to the reconstitution system 22 which reconstitutes the dialysate fluid and forms a means for supplying the fluid to the abdominal cavity. The fluid then flows through the conduit 23 through the conduit 11 and into'the lower portionof the abdominal cavity at the tube 16. Thus, it is seen that there is formed a closed system in which the dialysate fluid is circulated and reconstituted.
The out-flow from'the peritoneal cavity flows along the line 18 to the fluid pump 19. The pump 19 may include a cup-shaped chamber 26 provided with a cap 27 which is suitably secured to the portion 26 as, for example, by screws. Piston 28 which includes a pair of spaced ports 29 provided with one-way valves 31 is disposed in the chamber 26. The piston is urged in one as by a ring 36 and its other end suitably secured to the cup by being sandwiched between the cap 27 and the side walls 26; Thus, fluid is drawn into the chamber 33 as the springs urge the piston in one direction. At the same time as fluid is being drawn into chamber 33, the fluid in the upper chamber 39, which is defined by the other side of the piston, the flexible seal membrane 34 and a second sealing membrane 40, is moved through the conduit 21 into the reconstitution system. The upper chamber 39 is defined by the upper wall of the pump together with the flexible seal 36 which has one end affixed to the upper wall by means of a ring 41 and to the piston rod by means of a second ring 42.
The reconstitution system may be one of two general types. In a first type, illustrated in FIGS. 1 and 4, the fluid travelling along the conduit 21 passes through a urea removal column 46, an activated carbonor charcoal column 47, a transparent conduit portion 48 which is irradiated by an ultra-violet source 49, and a conventional flow regulator 50 which regulates the flow and finally through a filter 51. The reconstituted fluid leaving the reconstitution system is thenapplied along the conduit 23 to the in-flow conduit 11. The rate of flow through the system is controlledby flow regulator 50.
After the piston P reaches the top of the stroke, the chamber 33 is full and, of course, chamber 39 is basically empty. The piston is then depressed and fluid is transferred from the lower chamber 33 to the upper chamber 34, through valve means 31. When the piston reaches its lowest stroke, the piston is released and the springs urge thepiston upwardly pumping fluid into the chamber and expelling fluid from the chamber 39.
Although rolling diaphragms or seals are indicated and are preferable since there is minimal leakage and a reliable method of knowing the piston displacement and rate and minimal friction, it is, of course, apparent that other seals such as O-ring seals or the like could be employed. In any event, the pump is entirely sealed and remains sterile. v
The urea removal column includes material which serves to absorb urea or converts the urea to ammonia enzymatically as with the enzyme, urease, and then absorbs the ammonia. Such columns are known.
An activated carbon column may be used to absorb creatinine, uric acid and other toxic substances. The ultraviolet sterilizer is used to sterilize the dialysate and prevent bacterial growth. The filter may be of a type which can or cannot pass bacteria depending upon the effectiveness of the ultra-violet sterilizer and sterilizing procedures. It, of course, will trap larger particles and prevent them from entering into the abdominal cavity where they may be a source of tissue irritation and adhesions. The filter, flow regulator, sterilizer, transparentwindow and reconstitution columns form a selfcontained package which may or may not include the pump and which can easily be replaced. The fact that a very small amount of dialysate is used, of the order of one liter or less,'and the fact that this same'amount of dialysate is continuously reconstituted permits use of a steady flow and possibly a continuous dialysis process. Further, the system is of relatively small size because of the small volume of dialysate fluid being used which makes it possible to devise a system which can be made portable and worn in the vicinity of the patients waist.
Thus, the patient can be completely rehabilitated by wearing such a system. He can continue to perform his normal tasks while dialysis is taking place. This is very much like a physiologic process performed by the kidneys.
In a second type of reconstitution system, not shown, which is conventional in the dialysis field, essentially all of the material removed from the abdominal cavity is non-selectively eliminated from the dialysate fluid. Those components removed during dialysis which are desirable to replace, such as glucose, the ions of sodium, calcium and potassium are supplied to the in-flow conduit from a source external to the reconstitution system. Such systems include the electrolytic type as described in S. B. Tuwiner, Research Design and Development of an Improved Water Reclamation System for Manned Space Vehicles (April 1966), Report No. NASA CR66323, and the ion exchange type as described in R. D. Fall et al., Feasibility of Microcapsule System for Artifical Kidney Applications, Annual Report by Battelle Memorial Institute (Dec. 1968).
A simplified technique for supplying dialysate fluid to the abdominal cavity and removing the fluid from the same eliminates the need for any reconstitution system. In this technique the dialysate fluid is supplied from a fresh external source along with the aforementioned desirable components removed during dialysis. The fluid removed from the abdominal cavity is directed to a waste sink.
In summary, the features that make this system possible and of considerable advantage over prior art systems are the use of the permanently implanted conduits which allow fluid to be introduced and removed from the peritoneal cavity, the reconstitution system which permits the same fluid to be recycled after the waste that is picked up in the peritoneal cavity has been removed, and the simple system for sterilizing and pumping the fluid through the regeneration system and back to the abdominal cavity.
The use of small amounts of fluid which are recycled has added advantages. Many of the abnormal side effects resulting from either hemodialysis or peritoneal dialysis with large volumes of fluid are avoided since this same fluid can be saturated with all those constituents which are normally depleted from the blood stream when a large amount of dialysate is used. Low
flow rate also permits effective ultra-violet sterilization and ultrafiltration to be accomplished.
1. A steady flow peritoneal dialysis system including in-flow and out-flow conduits adapted to extend through the abdominal wall into the abdominal cavity whereby dialysate fluid may be introduced into and removed from the cavity, each of said conduits including an external surface portion at the interface between the abdominal wall and the conduits which is compatible with the skin, subcutaneous tissue and other tissue, said surface including a plurality of adjacent substantially discrete pockets having openings which face in the direction of said skin and tissue, the walls of said pocket extending inwardly to a depth in the range of 0.002 to 0.020 inches and being of such shape and size as to provide means to accommodate a number of living cells sufficient to provide anchorin but not solarge as to prevent essentially normal trans er of nutrients o the living cells in said pockets from adjacent skin and tissue, means for supplying the dialysate fluid to said inflow conduit, means for causing the dialysate fluid to flow through the cavity, and means for removing the dialysate fluid from said out-flow conduit.
2. A system as in claim I in whichsaid means for causing fluid to flow comprises a sealed pump.
3. A system as in claim 1 in which said supply and removal means includes a flow regulator.
4. A system as in claim 1 in whichsaid supply means includes a dialysate fluid source and said removal means includes a sink.
5. A system as in claim 1 in which said supply and removal means includes means for reconstituting the dialysate fluid connected by fluid conduits to said inflow and out-flow conduits.
6. A system as in claim 5 in which said reconstitution means includes a column for the removal of uric acid and creatinine.
7. A system as in claim 5 including means for irradiating the circulatory fluid with ultra-violet radiation.
8. A system as in claim 7 in which said reconstitution means includes a filter adapted to receive the fluid flowing from the irradiation means.
9. A system as in claim 5 in which said system is a closed self-contained fluid system.
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|U.S. Classification||604/29, 604/175|
|International Classification||A61M1/16, A61M1/28|
|Cooperative Classification||A61M2001/284, A61M2001/1674, A61M2001/281, A61M1/285, A61M1/28, A61M1/1696|
|European Classification||A61M1/28, A61M1/28C|
|Feb 16, 1990||AS||Assignment|
Owner name: BELL, CHRISTY W.
Owner name: BRADLEY RESOURCES COMPANY
Owner name: GLENN, PAUL F.
Free format text: SECURITY INTEREST;ASSIGNOR:WELLS FARGO BANK N.A., A NATIONAL BANKING ASSOCIATION;REEL/FRAME:005250/0202
Effective date: 19890628
Owner name: HILL, J. DONALD
|Jul 18, 1988||AS||Assignment|
Owner name: BELL, CHRISTY W., ( BELL )
Owner name: BRADLEY RESOURCES COMPANY ("BRADLEY"), A NEW YORK
Free format text: SECURITY INTEREST;ASSIGNOR:THORATEC LABORATORIES CORPORATION, A CA CORP.;REEL/FRAME:004926/0506
Effective date: 19880616
Owner name: GLENN, PAUL F., ( GLENN )
|Jul 15, 1988||AS||Assignment|
Owner name: BELL, CHRISTY W.
Owner name: BRADLEY RESOURCES COMPANY, A NEW YORK GENERAL PART
Owner name: GLENN, PAUL F.
Free format text: SECURITY INTEREST;ASSIGNOR:THORATEC LABORATORIES CORPORATION, A CORP. OF CA.;REEL/FRAME:005049/0326
Effective date: 19880616
|Jan 30, 1987||AS||Assignment|
Owner name: WELLS FARGO BANK N.A., 420 MONTGOMERY STREET, SAN
Free format text: SECURITY INTEREST;ASSIGNORS:THORATEC LABORATORIES INCORPORATED;THORATEC MEDICAL INCORPORATED;BIOTEXINDUSTRIES INCORPORATED MERCOR INCORPORATED;REEL/FRAME:004681/0966
Effective date: 19870122
|Dec 12, 1984||AS||Assignment|
Owner name: CROCKER NATIONAL BANK ONE MONTGOMERY ST., SAN FRAN
Free format text: SECURITY INTEREST;ASSIGNOR:THORATEC LABORATORIES CORPORATION A CA CORP;REEL/FRAME:004339/0427
Effective date: 19841207
Owner name: CROCKER NATIONAL BANK,CALIFORNIA
|Dec 12, 1984||AS06||Security interest|
Owner name: CROCKER NATIONAL BANK ONE MONTGOMERY ST., SAN FRAN
Effective date: 19841207
Owner name: THORATEC LABORATORIES CORPORATION A CA CORP
|Dec 6, 1982||AS02||Assignment of assignor's interest|
Owner name: CROCKER NATIONAL BANK, ONE MONTGOMERY ST., SAN FRA
Owner name: THORATEC LABORATORIES CORPORATION A CA CORP.
Effective date: 19821201
|Dec 6, 1982||AS||Assignment|
Owner name: CROCKER NATIONAL BANK, ONE MONTGOMERY ST., SAN FRA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:THORATEC LABORATORIES CORPORATION A CA CORP.;REEL/FRAME:004066/0838
Effective date: 19821201