|Publication number||US3818511 A|
|Publication date||Jun 25, 1974|
|Filing date||Nov 17, 1972|
|Priority date||Nov 17, 1972|
|Publication number||US 3818511 A, US 3818511A, US-A-3818511, US3818511 A, US3818511A|
|Inventors||S Bazell, E Goldberg, R Ostensen|
|Original Assignee||Medical Prod Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (4), Non-Patent Citations (1), Referenced by (181), Classifications (13)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent [191 Goldberg et al.
[ MEDICAL PROSTHESIS FOR DUCTS OR CONDUITS  Inventors: Edward M. Goldberg, Glencoe;
Seymour Bazell, Skokie; Ralph G. Ostensen, Morton Grove, all of I11.
 Assignee: Medical Products Corporation,
22 Filed: Nov. 17, 1972 211 Appl. N01: 307,641
 US. Cl 3/1, 3/DIG. 1, 128/214 R, 128/334 R, 128/348, 264/257  Int. Cl..... A6lf 1/24, A6lm 5/00, A6lm 25/00  Field of Search 3/1, DIG. 1; 128/214 R, 128/214 B, 348, 334 R, 334 C, l R
 References Cited v UNITED STATES PATENTS 3,646,616 3/1972 Keshin 3/1 3,667,069 6/1972 Blackshear et a1. 3/1 3,713,441 1/1973 Thomas 128/214 R FOREIGN PATENTS OR APPLICATIONS 1,546,118 10/1968 France 3/1 OTHER PUBLICATIONS A Large-Vessel Applique A-V Shunt For Hemodial- June 25,1974
Primary Examiner-Richard A. Gaudet Assistant Examiner-Ronald L. Frinks Attorney, Agent, or Firm-Molinare, Allegretti, Newitt & Witcoff 5 7 ABSTRACT Medical prosthesis for ducts or conduits and method of manufacture. An exemplary embodiment is an arteriovenous shunt having a cannula terminated in a funnel in which the interior included angle ranges from 15 The funnel is of an implantable, resilient silicone rubber into which a woven, flexible Dacron skirt is molded to enable suturing and tissue ingrowth at the anastomotic juncture. The silicone is of a medical type which is body tissue-compatible, and has sufficient elasticity and resilience to permit compliance during pulsatile fluid flow, storage and return of fluid kinetic energy, and accommodation to various sizes of vessels, ducts, or conduits. Actual experimental use shows improved results compared to prior types of tip-type cannulae.
9 Claims, 7 Drawing Figures 24(CLOTH SKIRT) 6 (SHANK) (PUMA/5L 7 (CONNECTOR) 2 (cA/v/vuLA) MEDICAL PROSTHESIS FOR DUCTS OR CONDUITS FIELD OF THE INVENTION This invention is directed to an improved prosthesis for access to, and transport of ducted fluids, such as the vascular, lymphatic, reproductive, regulatory (e.g. glandular) or excretory systems, and repair, extension or access to other body ducts or tubes, such as tracheal, esophagogastrointestinal systems and the like. The invention also includes methods of manufacture of the prosthetic devices. More specifically, the invention is directed to a tipless, funnel-terminated, tubular prosthesis in which the interior angle of the funnel ranges from 30, which funnel is molded of high compliance, body tissue-compatible, flexible, resilient silicone rubber, and has molded therein a Dacron skirt for tissue ingrowth at the anastomotic junctions.
BACKGROUND OF THE INVENTION There is a clear need for artificial, implantable duct prosthesis for treatment or cure of various medical conditions in animals and humans. Examples include artificial veins or arteries used in treatment of circulatory conditions. Likewise repair of, or access to the GI. tract may employ artificial ducting. All of such ducting involves the connecting (anastomosing) of the ducts to body tissue, usually the natural duct which is being replaced or repaired, or connection to the organ or organs which communicate with the natural duct. Frequently the artificial duct prosthesis is led extracorporeally for treatment of the ducted fluid and return to the body, e.g. blood for dialysis in cases of kidney failure.
All such artificial duct prostheses pose serious medical problems at their anastomotic juncture within the body, for example juncture necrosis, chronic infection, leakage, thrombosis, stricture and the like. This invention is directed to an improved juncture prosthesis or duct terminus. The discussion which follows will be with reference to an arteriovenous shunt by way of example, but it is to be understood that the funnel prostheses of this invention may be applied to any artificial implantable duct, or to a natural duct that is being anastomosed to a natural or artificial duct, organ or tissue, as the case may be.
In the United States, approximately 50,000 persons each year suffer some degree of renal (kidney) failure. Of this number, fully percent, or 10,000 patients, can be helped by dialyzing the blood to remove the accumulated urea and other metabolic byproducts.
Kolff introduced direct dialysis of arterial blood, thereby employing arteriostatic pressure to assist in the dialysis. Quinten and Scribner developed an arteriovenous shunt system employing a tipped cannula sutured at 90 to an artery, tunneled subcutaneously, exited through the skin, and connected externally to a similar cannula which analogously was sutured to a vein. When hemodialysis was required, the shunt was disconnected externally and the arterial line was connected to the dialysis machine. The return line from the machine was connected to the venous cannula.
Such Quinten-Scribem shunts are often disfiguring and ineffective, complicated by frequency infections and thrombosis. The tips of the Scriber shunts are very inefficient, with significant turbulence, and low flow rates, which contribute to the thrombosis. The cannula tip is attached to the blood vessel by sutures, and causes juncture necrosis and strictures.
Results of using tip-type cannulae were reported by Baillod et al. at the 1969 meeting of the European Dialysis and Transplant Association, reported at Proc. Europ. Dialysis Transplant Assn., 6:65, 1969. 60 patients treated for more than one year exhibited arterial cannula survival of 13.5 months, during which an average of two and one half cannulae were required. Their venous cannulae survived an average of 8 /2 months, with four cannulae required per patient.
Problems with shunts led Brescia and Cimino to the innovation of the internal arteriovenous fistula which remains post-surgically subcutaneous. In this procedure, the side of an artery is sutured to the side of a vein to form a classical, side-by-side, h-shaped shunt. When dialysis is desired the shunt loop is punctured with hypodermic needles attached to the inlet and return lines of the dialysis machine.
However, the Brescia-Cimino internal A-V fistula is not without its serious problems. The use of the fistula requires training and skill in venipuncture, which frequently mitigates against home dialysis by the patient or other unskilled persons. After repeated punctures with large bore needles, hematomas, scarring, induration and false aneurysms-develop.
There is,therefore, a great need for improved juncture prostheses for ducts and conduits of all types, both internal and external shunts to provide for vascular access, and access to the lymphatic system, reproductive system, regulatory system, excretory system. G. I. system and the like or to other organs or implanted prostheses to or from which fluid (gas or liquid) transmittal is desired. The ducts should be readily established and perform continuously as long as needed. They must allow adequate fluid (e.g., blood) flow, be nonthrombogenic and free of infection. They should be easily declottable, and should be large enough to provide adequate fluid volume exit or input.
THE INVENTION OBJECTS It is among the objects of this invention to provide an improved duct juncture prosthesis which overcomes the above-described problems of the prior art tips and achieves the goals set forth for improved medical ducts, e.g., A-V shunts and the like.
It is another object to provide a juncture prosthesis for ducts which has fluid dynamics advantages, and presents improved survival expectancy.
It is another object to provide a funnel juncture prosthesis for ducts which may be used internally or externally, and which may be used for access to any body organ or tissue from any other, or from the exterior, and for transport of any fluid (gas or liquid) which is input, withdrawn, administered or monitored.
It is another object of this invention to provide a funnel juncture for a shunt prosthesis which exhibits low incidence of late failure, thrombosis, provides smooth transition from body organ, duct or tissue to the prosthesis, is simple to declot, has excellent flow rates, an absence of major clinical complications, and exhibits long survival.
Still other objects will be evident from the following summary and detailed description.
SUMMARY Our juncture prosthesis employs a tipless" cannula having a dacron-skirted silicone rubber funnel at an end for transmitting fluids across an anastomotic site. We have discovered that best hemodynamic and medical properties are obtained when the included angle of the funnel ranges from about 30, whether the funneledorifice is anastomosed end-to-end or at an acute angle to a body duct, organ or tissue. The flexibility, resilience and compliance of the silicone rubber is selected to permit sufficient elasticity to be responsive to natural pulsatile flow, and to store and return fluid kinetic energy. The funnel is also sufficiently elastic to be self-compensating within small angles, thus permitting anastomosis to vessels or ducts of varying size. The Dacron skirt permits tissue ingrowth with a pseudoendothelium and a fibrous adventitia which prevents buildup of fibrin at the anastomotic juncture. The juncture funnel prostheses of this invention are applicable to internal A.V. fistulae, arterialized vein shunts, external shunts, or to any situation where fluid (gas or liquid) is to be transferred to or from any body duct, organ or tissue to another, or to or from the exterior. Improved results are demonstrated by the prostheses of this invention.
BRIEF DESCRIPTION OF THE DRAWINGS The following detailed description makes reference to the FIGURES in which:
FIG. 1 illustrates in sectional view the funnel assembly for a cannula prosthesis in accordance with this invention;
FIG. 2 illustrates in sectional view a molding apparatus employed in the method of manufacture of the prostheses of this invention;
FIG. 3 shows in perspective a funnel assembly in accordance with this invention particularly useful for end-to-end anastomosis;
FIG. 4 shows in perspective a funnel assembly in accordance with this invention for acute angle anastomosis;
FIG. 5 shows an exemplary prosthesis of this invention in use; and
FIGS. 6a and 6b compare flow with the funnel prosthesis of this invention to prior art tipped" cannulae.
DETAILED DESCRIPTION Referring to FIGS. 1, 3 and 4, the prosthesis of this invention comprises a funnel assembly I mounted on a cannula tube 2. The funnel assembly in turn includes a cloth skirt 3, typically a sterile polyester (Dacron) cloth, for example, one about 0.007 inch thick, embedded in the walls of the funnel mouth portion 4 as at 5. The Dacron cloth may be flat or formed into a conical shape. Shank portion 6 connects the funnel mouth portion 4 with connector portion 7, into which is seated a cannula 2. The cannula 2 may be secured into connector portion 7 with cannula tip 8 abutting against shoulder 9 in a manner to provide a smooth interior passage at 10. We prefer to use a silicone cement 11 to join the tube 2 to the funnel assembly. The funnel walls may be tapered so that the mouth edge 4 is thinner and more flexible than the shank end portion 6. This flexibility permits a range of fit for various sized ducts or blood vessels, and compensates for pulsatile fluid flow by storage and return of kinetic energy.
Critical to our invention is the fact that the included angle 6, defined as the angle lying between the inner surfaces l2, 12' of the funnel mouth, is in the range of about 15 30. This provides a smooth transition of flow of fluids, e.g., blood, lymph, urine, oxygen or the like in either direction through the tipless cannula prosthesis, and improves system survival. In addition, the entrance energy loss using our prosthesis is tenfold less than a constant diameter orifice anastomosed end-toend to a duct. In such constant diameter juncture, the entrance loss is 0.5 (V /2g), where V is flow velocity and g is gravity. In our tipless funnel juncture prosthesis, the entrance loss is one tenth, that is, 0.05 (V /2g) for the same flow velocity.
In addition to the end-to-end anastomosis, we have found that the same type of funnel transition provided for by our tipless funnel cannulae is beneficial when anastomosing vessels end-to-end to ducts or cannulae. As seen in FIG. 6a in the prior art techniques employing tip-type cannulae 28, there is almost always a stric ture or sudden reduction 29 of the internal diameter of the vessel which is anastomosed to the body vessel or duct 30. This abrupt narrowing of the diameter results in frictional energy losses and boundary layer separation 31 contributing to hemolysis and the formation of thrombi whether the flow is converging or diverging. In addition, there is a pressure drop with up to 50 percent velocity head loss, occasioned by the use of such tiptype cannula. In contrast, as seen in FIG. 6b, end-toend anastomosis using the tipless funnel-type cannula l of this invention for either converging or diverging flow affords a smooth translation and flow 32, improves system survival, promotes more effective declotting, helps eliminate the buildup of fibrin at the junction of the cannula and vessel, and generally exhibits an absence of major clinical complications. We have been able to observe cannula survival of over two years, using the cannula of this invention.
The funnel juncture prosthesis, anastomosed to the arterial limb ofa fistula or any afferent flow duct, is the converging channel with a short graduated contraction of diameter. The converging channel or nozzle" refers to a channel system in which the velocity of the fluid is increased and the pressure is reduced. The fluid is accelerated in the converging channel and some pressure head is converted into velocity head. In general, this conversion is a stable process and can be made with few losses.
The prosthesis anastomosed to the venous limb of the fistula or any efferent flow duct is the diverging channel with a short gradual enlargement of diameter. The diverging channel or diffuser refers to a channel in which the velocity of fluid is decreased and the pressure is increased. The flow involves a conversion of velocity head to pressure head. As the fluid moves down stream, a greater boundary layer forms and grows in thickness. The fluid may not fill the channel completely, but separates by breaking away from the walls. This results in eddy formation and dissipation of energy by turbulent mixing. Flow in a diverging channel is more troublesome than flow in a converging nozzle and can be an unstable inefficient process.
In evaluating the efficiency of a diverging channel, it is necessary to consider the velocity variations across the channel. The diverging channel efficiency can be considered as a function of the total included angle of divergence (0). Theta represents a particular expansion ratio or ratio of final area to initial area. The efficiency is high (75 90 percent) in the region between 0 and 30. Beyond about 30, the efficiency decreases with an increase in the included angle.
We further have improved the system by the provision of flexibility and compliance so that in pulsatile flow, the juncture expands upon systoly storing kinetic energy, and delivers the energy to the fluid on diastoly.
Turning now to FIG. 2, this figure illustrates the method of construction of the funnel assembly of our invention. Mold 13 comprises a skirt holder plate 16 and body-forming plate 17. In manufacture, a core, ring or washer of Dacron cloth, a medical grade such as US. Catheter& Instrument Corp. No. 6103, is centered over the central aperture 19 in the body-forming plate 17. The Dacron cloth may be of any type which has sufficiently large mesh to permit complete inpregnation of the silicone rubber around the fibers. Thereafter, the skirt holder plate 16 is placed thereover to securely retain the Dacron skirt in position during molding. The skirt holder is shown as flat, but may be conical. Centering pins l8, 18 are inserted to secure the mold parts together, and the mold is then positioned on the bottom plate of the molding press. Centering pins 18 and 18 extend into recesses 20, 20 in the bottom plate of the press for proper centering of the shoulder-forming projection 21 in the mold aperture. A tubular slug of vinyl type silicone rubber molding compound, such as a Dow-Corning *Silastic" brand rubber MDX-445l2, is dropped into the mold aperture 19, and top press plate 14 is lowered into position to compression-mold the silicone rubber, for ten minutes at 260F. In the alternative, 21 fluorosilicone may be used; this type silicone rubber exhibits lesser clotting characteristics under dynamic flow conditions. The mold pin 22 projecting from the top press plate 14 forces the gum-like silicone rubber into the mold cavity. Optionally, the amount of the silicone rubber slug may be chosen so that there may be very small excess of the silicone rubber which extrudes into the cloth skirt beyond the outward edge of the funnel mount portion 4. This is best illustrated in FIG. 1 as zone 23. The extrusion of this silicone provides a zone for anchoring the sutures when anastomising the funnel mouth to the body vessel or duct. The funnel mouth walls 12, 12 are thus free of turbulence-causing sutures, yet there is a sufficient feather edge of silastic-impregnated Dacron to provide for proper suture anchorage while at the same time sealing against fluid loss. The outer edge of the Dacron skirt 24 is open mesh which providesfor tissue ingrowth. The excess skirt may be trimmed as desired to fit any given duct size. For a tipless funnel juncture prosthesis of 0.125 inch ID. and a funnel mouth opening of 0.250 inches, we employ approximately 0.1 gram of a silicone rubber slug for the molding.
After the compressionmolding for ten minutes at 260F., the funnel assembly part is extracted from the mold and inspected. Thereafter, the molded funnel assembly part is post-cured for four hours at 350F. All flashing is trimmed from the part, and after final inspection and washing, it is ready for assembly on a cannula tube. In assembling the cannula tube, a clean, transversely cut end of a cannula is painted on its exterior surface with a medical grade silicone rubber adhesive, such as Dow-Corning medical grade Silastic brand adhesive Type A, and inserted into the connector portion of the funnel assembly. Excess may build up and form a smooth transition shoulder, as 11, seen in FIG. 1. The final tipless funnel cannula prosthesis is best seen in FIGS. 3 and 4. FIG. 3 illustrates a prosthesis either for end-to-end anastomosis with a body vessel, duct, tissue or organ, or for end-to-side anastomosis. FIG. 4 shows a tipless funnel cannula prosthesis having an oval or eliptical-shaped funnel mouth which is oriented at an angle to the longitudinal axis of the shank and connector portions. This oblique funnel is particularly adapted for acute angle end-to-side anastomosis to body vessels, ducts, tissues or organs.
The method of employing the tipless funnel cannula of this invention may be seen with reference to FIG. 5. This description is in reference to providing vascular access to an arterialized vein although it should be understood that vascular access is merely exemplary of the more general use of the cannula of this invention. FIG. 5 shows the use, in a 2-step procedure, of our tipless funnel cannula where external access is required.
A suitably dilated arterialized vein 33 is selected for cannulation. This vessel is severed transversely at 34 and each end 35, 36 directly anastomosed to a tipless, funnel-shaped skirted cannula 37, 38 of this invention. The cannulae may be buried in subcutaneous tunnels 39 with open cell silicone rubber cuffs for fixation and seal. The exterior loop 40 of the cannula tube 2 may be adapted to come apart at collar 25 for attachment of the outlet segment 26 and inlet segment 27 to the inlet tube 41 and outlet tube 42 of the dialyzer 43.
Optionally, a direct fistula can be created by directly anastomising a cannula terminated at each end with a funnel prosthesis of this invention and utilizing a vein graft for juncture to the small artery. First, one end of a vein graft is anastomosed to an artery and the other end anastomised to the mouth of the funnel prosthesisterminated cannula. A vein is then selected for return flow to the heart and the distal branch of this vein anastomised to the funnel prosthesis at the other end of the cannula.
It is also possible to make a vein-to-vein shunt, as in a porto-canal shunt to reduce portal hypertension. In the same manner an artery-to-artery shunt can be performed (artery bypass). As above, for access to small vessels, we use a vein graft anastomosed to a funnel mouth, and for large vessels, we can directly anastomose our funnel juncture prosthesis thereto.
Fourteen or our new external fistula systems using tipless, funnel-skirted prostheses of this invention have been created for external circulatory access useful in chronic hemodialysis. The treatment periods range from 2 to 34 months. In all 14 patients flow exceeded 300 ml/min. Taken as a whole 13 of 14 systems have survived to date, representing an experience of 213 months with a mean survival of 15.2 months. The 14 arterial prostheses had a mean survival of 15.0 months; the 13 venous prostheses had a mean survival of [2.4 months. All arterial and venous prosthesis replacements have not been included in the above analysis. Expression of data in this manner, however, is unsatisfactory. Any series, with a number of patients having a short period of observation will, when calculated in this manner, result in spuriously low survival times. Thus, the survival times will actually be greater than the number of months calculated in the above manner.
If survival data are computed only from patients observed for more than 12 months, (including all failures even under 12 months), the recalculated mean survival times are as follows: for an arterial prosthesis 19.3 months, and for a venous prosthesis 15 months. This compares to 13.5 months (arterial) and 8.5 months (venous) for tipped cannulae of the prior art.
A more meaningful representation of circulatory access survival data would be to express it in terms of estimated survival curves calculated by standard life table techniques described by Merrell and Shulman Determination of Prognosis of Chronic Disease Illustrated by Systemic Lupus Erythematosus, .1. Chronic Dis. 1, (1955). The logarithm of the percent surviving is plotted against the duration in months. These curves are of course provisional since the numbers are small. They show the expected survival of an arterial prosthesis is 80 percent, and for the venous prosthesis about 50 percent under these circumstances.
It is to be understood that various modifications within the scope of this invention can be made by one of ordinary skill in the art without departing from the spirit thereof. We therefore wish our invention to be defined by the scope of the appended claims as broadly as the prior will permit, and in view of this specification if need be.
1. A medical prosthesis for providing vascular access to an arterialized vein which comprises:
a. a cannula;
b. a funnel assembly secured to an end of said cannula, said funnel assembly comprising: i. a connector portion connected to said cannula;
ii. a funnel portion with walls having an included interior angle ranging from about 15 to 30, said walls tapering to a smaller thickness at the mouth 8 of the funnel;
c. said funnel assembly being a tissue compatible, silicone rubber with sufficient flexibility and compliance so that in pulsatile flow, the funnel walls expand upon systole and deliver energy during diastole;
d. a flexible fabric skirt embedded in the walls of said funnel portion and extending outward from the edges of the funnel mouth a distance sufficient to provide for tissue growth therein and to connect the prosthesis through the skirt to a vein or artery.
2. A prosthesis as in claim 1 wherein a plane defined by the distal edge of said funnel mouth portion is ori ented at an angle to the longitudinal axis of said connector portion to provide an elliptical funnel mouth.
3. A prosthesis as in claim 1 wherein a plane defined by the distal edge of said funnel mouth is oriented at substantially a angle to the longitudinal axis of said connector portion.
4. A prosthesis as in claim 1 where a portion of said fabric adjacent said funnel mouth is impregnated with silicone rubber to provide suture anchorage for anastomosis.
5. A prosthesis as in claim 1 wherein said connector portion comprises a collar having an inner diameter suitable for fitting over said cannula and a shoulder to abut the end of said cannula,
6. A prosthesis as in claim 1 wherein said cannula is a body tissue compatible tube.
7. A prosthesis as in claim 6 wherein each end of said cannula has a funnel assembly secured thereto.
8. A prosthesis as in claim 6 wherein said cannula is silicone rubber.
9. A prosthesis as in claim 1 wherein said silicone rubber is a fluorosilicone rubber.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3646616 *||Jul 23, 1969||Mar 7, 1972||Jesse G Keshin||Prosthesis for implanting around a body duct such as the urethra and method of treating urinary incontinence|
|US3667069 *||Mar 27, 1970||Jun 6, 1972||Univ Minnesota||Jet pump cardiac replacement and assist device and method of at least partially replacing a disabled right heart|
|US3713441 *||Oct 22, 1970||Jan 30, 1973||Battelle Development Corp||Method of using an artery vein shunt applique|
|FR1546118A *||Title not available|
|1||*||A Large Vessel Applique A V Shunt For Hemodialysis by G. I. Thomas, Transactions Amer. Soc. Artif. Internal Organs, Vol. 15, 1969, pages 288 292.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3882862 *||Jan 11, 1974||May 13, 1975||Olga Berend||Arteriovenous shunt|
|US4217664 *||Feb 2, 1979||Aug 19, 1980||Faso Joseph M||Prosthesis and method for creating a stoma|
|US4318401 *||Apr 24, 1980||Mar 9, 1982||President And Fellows Of Harvard College||Percutaneous vascular access portal and catheter|
|US4405305 *||Feb 17, 1981||Sep 20, 1983||University Of Utah Research Foundation||Subcutaneous peritoneal injection catheter|
|US4557724 *||Aug 12, 1983||Dec 10, 1985||University Of Utah Research Foundation||Apparatus and methods for minimizing cellular adhesion on peritoneal injection catheters|
|US4559033 *||Aug 12, 1983||Dec 17, 1985||University Of Utah Research Foundation||Apparatus and methods for minimizing peritoneal injection catheter obstruction|
|US4693704 *||Oct 12, 1983||Sep 15, 1987||Sumitomo Bakelite Company Limited||Cervical canal catheter|
|US4719916 *||Sep 19, 1986||Jan 19, 1988||Biagio Ravo||Intraintestinal bypass tube|
|US4854316 *||Oct 3, 1986||Aug 8, 1989||Davis Emsley A||Apparatus and method for repairing and preventing para-stomal hernias|
|US4905693 *||Nov 16, 1988||Mar 6, 1990||Biagio Ravo||Surgical method for using an intraintestinal bypass graft|
|US5084064 *||Jun 15, 1989||Jan 28, 1992||Abiomed Cardiovascular, Inc.||Surgical cuff|
|US5234006 *||Jan 18, 1991||Aug 10, 1993||Eaton Alexander M||Adjustable sutures and method of using the same|
|US5236446 *||Mar 2, 1989||Aug 17, 1993||Dumon Jean Francois||Tubular endoprosthesis for anatomical conduits|
|US5389088 *||Nov 13, 1992||Feb 14, 1995||Hageman; Marinus J.||Grommet|
|US5413597 *||Apr 15, 1993||May 9, 1995||Krajicek; Milan||Three-layer vascular prostheses|
|US5425739 *||Dec 17, 1992||Jun 20, 1995||Avatar Design And Development, Inc.||Anastomosis stent and stent selection system|
|US5425761 *||Nov 21, 1990||Jun 20, 1995||Lundgren; Dan||Implant with a through passage|
|US5456712 *||Oct 18, 1993||Oct 10, 1995||Maginot; Thomas J.||Graft and stent assembly|
|US5480434 *||Jul 13, 1993||Jan 2, 1996||The University Of Miami||Method and device for connecting biological duct to a prosthesis|
|US5667486 *||Apr 26, 1994||Sep 16, 1997||Ams Medinvent, S.A.||Prostatic stent|
|US5676696 *||May 3, 1996||Oct 14, 1997||Intervascular, Inc.||Modular bifurcated intraluminal grafts and methods for delivering and assembling same|
|US5683449 *||Feb 24, 1995||Nov 4, 1997||Marcade; Jean Paul||Modular bifurcated intraluminal grafts and methods for delivering and assembling same|
|US5693088 *||Jun 7, 1995||Dec 2, 1997||Lazarus; Harrison M.||Intraluminal vascular graft|
|US5911757 *||Jun 7, 1995||Jun 15, 1999||Seare, Jr.; William J.||Methods and apparatus for transcutaneous access|
|US5922019 *||Dec 29, 1995||Jul 13, 1999||Schneider (Europe) A.G.||Conical stent|
|US5934286 *||Jun 4, 1998||Aug 10, 1999||Maginot Vascular Systems||Bypass grafting method which uses a number of balloon catheters to inhibit blood flow to an anastomosis site|
|US5979455 *||May 5, 1998||Nov 9, 1999||Maginot Vascular Systems||Method for directing blood flow in the body of a patient with a graft and stent assembly|
|US5989287 *||May 6, 1998||Nov 23, 1999||Av Healing Llc||Vascular graft assemblies and methods for implanting same|
|US6022312 *||May 1, 1996||Feb 8, 2000||Chaussy; Christian||Endosphincter, set for releasable closure of the urethra and method for introduction of an endosphincter into the urethra|
|US6086553 *||Jul 1, 1999||Jul 11, 2000||Akbik; Mohamad J.||Arteriovenous shunt|
|US6261255 *||Nov 6, 1998||Jul 17, 2001||Ronald Jay Mullis||Apparatus for vascular access for chronic hemodialysis|
|US6283992||Jul 9, 1999||Sep 4, 2001||Schneider (Europe) Gmbh||Conical stent|
|US6338724 *||Mar 29, 1999||Jan 15, 2002||Christos D. Dossa||Arterio-venous interconnection|
|US6355020 *||Oct 29, 1999||Mar 12, 2002||Gerald G. Bousquet||Transcutaneous access device|
|US6371981||Nov 2, 1999||Apr 16, 2002||Av Healing Llc||Vascular graft assemblies and methods for implanting same|
|US6395019||Aug 14, 1998||May 28, 2002||Trivascular, Inc.||Endovascular graft|
|US6401721||Nov 8, 1999||Jun 11, 2002||Cardiothoracic Systems, Inc.||Endoscopic bypass grafting method utilizing an inguinal approach|
|US6533810||Sep 4, 2001||Mar 18, 2003||Schneider (Europe) Ag||Conical stent|
|US6582409 *||Jan 24, 2000||Jun 24, 2003||Graftcath, Inc.||Hemodialysis and vascular access systems|
|US6585762||Nov 1, 2000||Jul 1, 2003||Paul Stanish||Arteriovenous grafts and methods of implanting the same|
|US6589278||May 15, 1998||Jul 8, 2003||Impra, Inc.||Vascular prosthesis|
|US6599313||Dec 30, 1999||Jul 29, 2003||Cardiothoracic Systems, Inc.||Extravascular bypass grafting method utilizing an intravascular approach|
|US6746480 *||Jul 3, 2001||Jun 8, 2004||Bard Peripheral Vascular, Inc.||Flanged graft for end-to-side anastomosis|
|US6818015||Mar 3, 2003||Nov 16, 2004||Schneider (Europe) Gmbh||Conical stent|
|US6821295 *||Jun 26, 2000||Nov 23, 2004||Thoratec Corporation||Flared coronary artery bypass grafts|
|US7044962||Jun 25, 2002||May 16, 2006||Scimed Life Systems, Inc.||Implantable prosthesis with displaceable skirt|
|US7081129||Apr 24, 2002||Jul 25, 2006||Boston Scientific Santa Rosa Corp.||Endovascular graft|
|US7147660||Dec 20, 2002||Dec 12, 2006||Boston Scientific Santa Rosa Corp.||Advanced endovascular graft|
|US7147661||Dec 20, 2001||Dec 12, 2006||Boston Scientific Santa Rosa Corp.||Radially expandable stent|
|US7195646 *||Oct 28, 2002||Mar 27, 2007||Oded Nahleili||Polymeric stent useful for the treatment of the salivary gland ducts and method for using the same|
|US7252680||Apr 5, 2002||Aug 7, 2007||Alveolus, Inc.||Removable essentially cylindrical implants|
|US7390317||Dec 2, 2002||Jun 24, 2008||Applied Medical Resources Corporation||Universal access seal|
|US7507258||Mar 5, 2007||Mar 24, 2009||Oded Nahleili||Polymeric stent useful for the treatment of the salivary gland ducts and method for using the same|
|US7527644||Nov 5, 2002||May 5, 2009||Alveolus Inc.||Stent with geometry determinated functionality and method of making the same|
|US7547321||Jul 5, 2002||Jun 16, 2009||Alveolus Inc.||Removable stent and method of using the same|
|US7553316||Jun 30, 2009||Bard Peripheral Vascular, Inc.||Flanged graft for end-to-side anastomosis|
|US7597697 *||Jul 11, 2001||Oct 6, 2009||Boston Scientific Scimed, Inc.||Bypass grafting method|
|US7615071||Mar 28, 2006||Nov 10, 2009||Trivascular2, Inc.||Endovascular graft|
|US7637942||Sep 24, 2003||Dec 29, 2009||Merit Medical Systems, Inc.||Coated stent with geometry determinated functionality and method of making the same|
|US7686845||Oct 24, 2006||Mar 30, 2010||Devax, Inc.||Noncylindrical stent deployment system for treating vascular bifurcations|
|US7731654||May 13, 2005||Jun 8, 2010||Merit Medical Systems, Inc.||Delivery device with viewing window and associated method|
|US7753946 *||Jul 13, 2010||Boston Scientific Scimed, Inc.||Bypass grafting system and apparatus|
|US7762977||Aug 31, 2005||Jul 27, 2010||Hemosphere, Inc.||Device and method for vascular access|
|US7766954||Aug 3, 2010||Trivascular2, Inc.||Advanced endovascular graft|
|US7780720 *||Oct 24, 2003||Aug 24, 2010||Scimed Life Systems, Inc.||Bifurcated endoluminal prosthesis|
|US7803178||Sep 28, 2010||Trivascular, Inc.||Inflatable porous implants and methods for drug delivery|
|US7875068||Sep 30, 2003||Jan 25, 2011||Merit Medical Systems, Inc.||Removable biliary stent|
|US7887579||Feb 15, 2011||Merit Medical Systems, Inc.||Active stent|
|US7896846||Mar 1, 2011||Tyco Healthcare Group Lp||Trocar seal system|
|US7901449||Jul 18, 2007||Mar 8, 2011||Scimed Life Systems, Inc.||Bifurcated endoluminal prosthesis|
|US7942919||Feb 23, 2004||May 17, 2011||Scimed Life Systems, Inc.||Bifurcated endoluminal prosthesis|
|US7959671||Jun 14, 2011||Merit Medical Systems, Inc.||Differential covering and coating methods|
|US7993386||Aug 9, 2011||Boston Scientific Scimed, Inc.||Implantable prosthesis with displaceable skirt|
|US8002934||Aug 25, 2009||Aug 23, 2011||Tyco Healthcare Group Lp||Trocar seal system|
|US8047986 *||Nov 1, 2011||Applied Medical Technology, Inc.||Molded and undivided medical penetrating device|
|US8066755||Nov 29, 2011||Trivascular, Inc.||System and method of pivoted stent deployment|
|US8079973||Dec 20, 2011||Hemosphere Inc.||Vascular access system|
|US8079986||Dec 20, 2011||Applied Medical Resources Corporation||Universal access seal|
|US8083789||Dec 27, 2011||Trivascular, Inc.||Securement assembly and method for expandable endovascular device|
|US8096966 *||Jun 21, 2010||Jan 17, 2012||Gi Dynamics, Inc.||Eversion resistant sleeves|
|US8109911||Nov 30, 2007||Feb 7, 2012||Applied Medical Resources Corporation||Universal access seal|
|US8118767||Sep 2, 2008||Feb 21, 2012||Laufer Michael D||Gastrointestinal implant and methods for use|
|US8192405||Jun 5, 2012||Tyco Healthcare Group Lp||Trocar seal system|
|US8206436||Jun 26, 2012||Merit Medical Systems, Inc.||Coated stent with geometry determinated functionality and method of making the same|
|US8226701||Jul 24, 2012||Trivascular, Inc.||Stent and delivery system for deployment thereof|
|US8231667||May 9, 2005||Jul 31, 2012||Jacques Séguin||Endoprosthesis for vascular bifurcation|
|US8236041||Aug 7, 2012||Biosensors International Group, Ltd.||Noncylindrical stent deployment system for treating vascular bifurcations|
|US8267898||Sep 18, 2012||Tyco Healthcare Group Lp||Trocar seal system|
|US8267989||Aug 20, 2010||Sep 18, 2012||Trivascular, Inc.||Inflatable porous implants and methods for drug delivery|
|US8282591||Oct 9, 2012||Iftikhar Khan||Hybrid arteriovenous shunt|
|US8328861||Nov 16, 2007||Dec 11, 2012||Trivascular, Inc.||Delivery system and method for bifurcated graft|
|US8361136||Sep 25, 2009||Jan 29, 2013||Trivascular, Inc.||Endovascular graft|
|US8366651||Aug 4, 2008||Feb 5, 2013||Bioconnect Systems, Inc.||Implantable flow connector|
|US8376981||Feb 19, 2013||Michael D. Laufer||Gastrointestinal implant and methods for use|
|US8382664||Oct 27, 2011||Feb 26, 2013||Applied Medical Technology, Inc.||Molded and undivided medical penetrating device|
|US8603157||Jun 22, 2007||Dec 10, 2013||Biosensors International Group, Ltd.||Endoprosthesis deployment methods for treating vascular bifurcations|
|US8663309||Sep 26, 2007||Mar 4, 2014||Trivascular, Inc.||Asymmetric stent apparatus and method|
|US8690815||Jul 6, 2010||Apr 8, 2014||Hemosphere, Inc.||Device and method for vascular access|
|US8690816 *||Aug 4, 2008||Apr 8, 2014||Bioconnect Systems, Inc.||Implantable flow connector|
|US8702657||Feb 23, 2012||Apr 22, 2014||Covidien Lp||Trocar seal system|
|US8709069||Apr 21, 2006||Apr 29, 2014||C. R. Bard, Inc.||Flanged graft with trim lines|
|US8728143||Nov 11, 2002||May 20, 2014||Biosensors International Group, Ltd.||Endoprosthesis deployment system for treating vascular bifurcations|
|US8801769||Jan 9, 2013||Aug 12, 2014||Trivascular, Inc.||Endovascular graft|
|US8821507 *||Jul 6, 2007||Sep 2, 2014||Howmedica Osteonics Corp.||Augmentation delivery device|
|US8864817||Jul 9, 2012||Oct 21, 2014||Jacques Séguin||Endoprosthesis for vascular bifurcation|
|US8961446||Dec 16, 2012||Feb 24, 2015||Bioconnect Systems Inc.||Implantable flow connector|
|US8961448 *||Jan 28, 2009||Feb 24, 2015||Peter Forsell||Implantable drainage device|
|US8992595||Mar 13, 2013||Mar 31, 2015||Trivascular, Inc.||Durable stent graft with tapered struts and stable delivery methods and devices|
|US9028539||Sep 30, 2005||May 12, 2015||Bard Peripheral Vascular, Inc.||Flanged graft for end-to-side anastomosis|
|US9055946 *||Nov 25, 2009||Jun 16, 2015||Phraxis Inc.||Anastomotic connector|
|US9101501||Mar 30, 2010||Aug 11, 2015||Biosensors International Group, Ltd.||Bifurcation stent and method of positioning in a body lumen|
|US9277921||Feb 15, 2013||Mar 8, 2016||Michael D. Laufer||Gastrointestinal implant and methods for use|
|US9278172||Sep 6, 2012||Mar 8, 2016||Cryolife, Inc.||Vascular access system with connector|
|US9282967||Mar 9, 2013||Mar 15, 2016||Bioconnect Systems, Inc.||Implantable flow connector|
|US9282968||Nov 22, 2010||Mar 15, 2016||Treus Medical, Inc.||Applicator for endoscopic treatment of biliary disease|
|US9308311||Jun 15, 2012||Apr 12, 2016||Phraxis, Inc.||Arterial venous spool anchor|
|US9345485||Jan 31, 2015||May 24, 2016||Bioconnect Systems, Inc.||Implantable flow connector|
|US9381101 *||Mar 15, 2013||Jul 5, 2016||The Charlotte-Mecklenburg Hospital Authority||Hybrid graft for therapy of aortic pathology and associated method|
|US20030139804 *||Mar 3, 2003||Jul 24, 2003||Schneider (Europe) Ag, A/K/A Schneider (Europe) Gmbh||Conical stent|
|US20030236567 *||Jun 25, 2002||Dec 25, 2003||Scimed Life Systems, Inc.||Implantable prosthesis with displaceabe skirt|
|US20040064181 *||Jun 25, 2003||Apr 1, 2004||Impra, Inc., A Subsidiary Of C.R. Bard, Inc.||Vascular prosthesis|
|US20040073282 *||Aug 6, 2001||Apr 15, 2004||Paul Stanish||Distally-narrowed vascular grafts and methods of using same for making artery-to-vein and artery-to-artery connections|
|US20040098086 *||Oct 24, 2003||May 20, 2004||George Goicoechea||Bifurcated endoluminal prosthesis|
|US20040098115 *||Nov 7, 2003||May 20, 2004||George Goicoechea||Bifurcated endoluminal prosthesis|
|US20040106942 *||Dec 2, 2002||Jun 3, 2004||Applied Medical Resources Corporation||Universal access seal|
|US20040111060 *||Nov 20, 2003||Jun 10, 2004||Racenet David C.||Trocar seal system|
|US20040210302 *||May 10, 2004||Oct 21, 2004||Bard Peripheral Vascular||Flanged graft for end-to-side anastomosis|
|US20050125071 *||Oct 28, 2002||Jun 9, 2005||Oded Nahleili||Polymeric stent useful for the treatment of the salivary gland ducts and method for using the same|
|US20050137614 *||Oct 8, 2004||Jun 23, 2005||Porter Christopher H.||System and method for connecting implanted conduits|
|US20060030935 *||Sep 30, 2005||Feb 9, 2006||Bard Peripheral Vascular, Inc.||Flanged graft for end-to-side anastomosis|
|US20060064159 *||Aug 31, 2005||Mar 23, 2006||Porter Christopher H||Device and method for vascular access|
|US20060161173 *||Mar 13, 2006||Jul 20, 2006||Maginot Thomas J||Endoscopic bypass grafting method utilizing an inguinal approach|
|US20060184229 *||Apr 6, 2006||Aug 17, 2006||Scimed Life Systems, Inc.||Implantable prosthesis with displaceable skirt|
|US20060225747 *||May 23, 2006||Oct 12, 2006||Maginot Thomas J||Vessel grafting method|
|US20070005128 *||Apr 21, 2006||Jan 4, 2007||C. R. Bard, Inc.||Flanged graft with trim lines|
|US20070100425 *||Oct 24, 2006||May 3, 2007||Jacques Sequin||Noncylindrical stent deployment system for treating vascular bifurcations|
|US20070129662 *||Feb 9, 2007||Jun 7, 2007||Maginot Thomas J||Bypass Grafting System and Apparatus|
|US20070162148 *||Mar 5, 2007||Jul 12, 2007||Oded Nahlieli||Polymeric stent useful for the treatment of the salivary gland ducts and method for using the same|
|US20070167901 *||Nov 16, 2006||Jul 19, 2007||Herrig Judson A||Self-sealing residual compressive stress graft for dialysis|
|US20080039878 *||Jul 6, 2007||Feb 14, 2008||Williams Michael S||Systems and methods for restoring function of diseased bowel|
|US20080077169 *||Nov 30, 2007||Mar 27, 2008||Applied Medical Resources Corporation||Universal access seal|
|US20080091143 *||Nov 30, 2007||Apr 17, 2008||Applied Medical Resources Corporation||Universal access seal|
|US20080195125 *||Feb 11, 2008||Aug 14, 2008||Hoffman Grant T||Device for heart bypass surgery and anastomosis|
|US20080319258 *||Jul 14, 2006||Dec 25, 2008||Thompson Christopher C||Sterile Access Conduit|
|US20090005802 *||Jun 29, 2007||Jan 1, 2009||Applied Medical Technology, Inc.||Molded and undivided medical penetrating device|
|US20090012521 *||Jul 6, 2007||Jan 8, 2009||Howmedica Osteonics Corp.||Augmentation delivery device|
|US20090036817 *||Aug 4, 2008||Feb 5, 2009||Bio Connect Systems||Implantable flow connector|
|US20090062717 *||Sep 2, 2008||Mar 5, 2009||Laufer Michael D||Gastrointestinal implant and methods for use|
|US20090105841 *||Dec 22, 2008||Apr 23, 2009||Oded Nahlieli||Polymeric stent useful for the treatment of the salivary gland ducts and method for using the same|
|US20090143713 *||Nov 25, 2008||Jun 4, 2009||Jacques Van Dam||Biliary Shunts, Delivery Systems, Methods of Using the Same and Kits Therefor|
|US20090143759 *||Nov 25, 2008||Jun 4, 2009||Jacques Van Dam||Methods, Devices, Kits and Systems for Defunctionalizing the Cystic Duct|
|US20090143760 *||Nov 25, 2008||Jun 4, 2009||Jacques Van Dam||Methods, Devices, Kits and Systems for Defunctionalizing the Gallbladder|
|US20100069819 *||Mar 18, 2010||Laufer Michael D||Minimally invasive gastrointestinal bypass|
|US20100130995 *||Nov 25, 2009||May 27, 2010||Phraxis Inc.||Anastomotic connector|
|US20100191167 *||Dec 22, 2009||Jul 29, 2010||Lytn||Gastrointestinal implant and methods for use|
|US20100256776 *||Jun 21, 2010||Oct 7, 2010||Gi Dynamics, Inc.||Eversion Resistant Sleeves|
|US20100280598 *||Dec 24, 2008||Nov 4, 2010||C.R. Bard, Inc.||Vascular graft prosthesis having a reinforced margin for enhanced anastomosis|
|US20100312163 *||Jan 28, 2009||Dec 9, 2010||Peter Forsell||Implantable fluid movement device|
|US20100312164 *||Jan 28, 2009||Dec 9, 2010||Peter Forsell||Implantable drainage device|
|US20110054381 *||Jun 1, 2010||Mar 3, 2011||Jacques Van Dam||Biliary shunts, delivery systems, and methods of using the same|
|US20110060264 *||Jul 6, 2010||Mar 10, 2011||Hemosphere Inc.||Device and method for vascular access|
|US20110071350 *||Mar 24, 2011||Jacques Van Dam||Applicator for endoscopic treatment of biliary disease|
|US20110184329 *||Jan 22, 2010||Jul 28, 2011||Valentin Kramer||Composite Arterial-Venous Shunt System|
|US20120259157 *||Oct 11, 2012||Spence Paul A||Cannula Systems and Methods|
|US20130282103 *||Mar 15, 2013||Oct 24, 2013||The Charlotte-Mecklenburg Hospital Authority D/B/A Carolinas Healthcare System||Hybrid graft for therapy of aortic pathology and associated method|
|USRE41448||Jul 20, 2010||Hemosphere, Inc.||Squitieri hemodialysis and vascular access systems|
|USRE44639||Jan 15, 2010||Dec 10, 2013||Hemosphere, Inc.||Hemodialysis and vascular access system|
|CN103501735A *||Mar 7, 2012||Jan 8, 2014||W.L.戈尔及同仁股份有限公司||Medical device for use with a stoma|
|CN103501735B *||Mar 7, 2012||Apr 6, 2016||W.L.戈尔及同仁股份有限公司||用于造口的医疗装置|
|CN104394798A *||Apr 23, 2013||Mar 4, 2015||夏洛特-梅克伦堡医院(商业用名:卡罗来纳保健系统)||Hybrid graft for therapy of aortic pathology and associated method|
|EP3031428A1 *||Mar 7, 2012||Jun 15, 2016||W.L. Gore & Associates, Inc||Medical device for use with a stoma|
|WO1991019522A1 *||Jun 12, 1991||Dec 26, 1991||Baxter International Inc.||Needle assembly for reduced coagulation|
|WO1998044869A1 *||Apr 6, 1998||Oct 15, 1998||The Queen's University Of Belfast||Haemodynamic control device|
|WO1998050093A1 *||May 1, 1998||Nov 12, 1998||United States Surgical Corporation||Trocar seal system|
|WO2002054987A2 *||Dec 20, 2001||Jul 18, 2002||Sulzer Carbomedics Inc.||Prosthetic graft device with ventricular apex attachment apparatus|
|WO2002054987A3 *||Dec 20, 2001||Feb 13, 2003||Sulzer Carbomedics Inc||Prosthetic graft device with ventricular apex attachment apparatus|
|WO2007011689A2 *||Jul 14, 2006||Jan 25, 2007||The Brigham And Women's Hospital, Inc.||Sterile access conduit|
|WO2008014752A1 *||Jul 20, 2007||Feb 7, 2008||Michael Heise||Tubular vascular transplant|
|WO2012018917A1 *||Aug 3, 2011||Feb 9, 2012||World Heart Corporation||Conformal cannula device and related methods|
|WO2012122220A1 *||Mar 7, 2012||Sep 13, 2012||W.L. Gore & Associates, Inc.||Medical device for use with a stoma|
|WO2015023460A1 *||Aug 4, 2014||Feb 19, 2015||Cryolife, Inc.||Systems and methods for a fluid carrying conduit of a vascular access system|
|U.S. Classification||623/1.31, 606/153, 264/257, 604/175, 623/9, 623/23.64|
|International Classification||A61M39/10, A61M1/36, A61B17/11|
|Cooperative Classification||A61M1/3655, A61M2001/3659, A61B2017/1139|