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Publication numberUS3625198 A
Publication typeGrant
Publication dateDec 7, 1971
Filing dateMay 9, 1969
Priority dateMay 9, 1969
Also published asCA973651A1, DE2022576A1, DE2022576B2, DE2022576C3, DE2065370A1
Publication numberUS 3625198 A, US 3625198A, US-A-3625198, US3625198 A, US3625198A
InventorsCharles H Sparks
Original AssigneeCharles H Sparks
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Die and holder for implanting in a living body to grow tissue grafts
US 3625198 A
Abstract  available in
Images(3)
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Claims  available in
Description  (OCR text may contain errors)

United States Patent [56] References Cited UNITED STATES PATENTS 9/1966 Artandietal.................

[72] Inventor Charlesl'l. Sparks 3725 SE. Martins St., Portland, Oreg. 97202 3,272,204 3,479,670 1l/l969 Medell.........................

OTHER REFERENCES 211 AppLNo. 823,287 22 Filed May9, 1969 45 Patented Dec.7,197l

wBm 94k u n S m a m v n a H v. a .mmw Vw C u. 258 M .4 6 ME .I o h N a m gfia l mM m m 30% b .3 eLP Wm nY r eslN e 1: u s .3 MmN 0C ,3 MnL3 i w h PMm A30 Continuation-impart of application Ser. No. 655,838, July 25, 1967, now Patent No. 3,514,791. This application May 9, 1969, Ser. No. 823,287

Primary Examiner-Richard A. Gaudet [54] DIE AND HOLDER FOR IMPLANTING IN A LIVING BODY TO GROW TISSUE GRAFTS 11 Claims, 13 Drawing Figs.

ABSTRACT: Method and apparatus for growing a graft structure, particularly in a patients own body. A die cluster is disclosed comprising a plurality of dies for growing graft tubes whereby such graft tubes may be connected together end to end to make a tube of desired length. The invention also includes an improved method for implanting the die cluster in the body.

7 4. O8 ma B H WHMQQ l 1 D .D 2 6 6 H A 3R "n" "1.2 m m W m mum u 5 mm m M m m NW mWm m4M mzm 1. m m mm 0 W w m mm m NR MZW WM m N m m "G" I9 MI 8 mm "MW L3" 2 v 01. M .m U .m F l l m 2 l 5 5 5 PATENTEU HEB 7 l97| SHEET 1 (IF 3 I NVENTOR BYCHARLES H. SPARKS I Hobie PATENTED DEC 7 |97I SHEET 2 BF 3 PECTORALI S SERRATUS ANTERIOR MUSCLE PATENTEDUEC 71971 3 52519 SHEET 3 OF 3 INVENTOR CHARLES H. SPARKS ZbM DIE AND HOLDER FOR IMPLANTING IN A LIVING BODY TO GROW TISSUE GRAFIS CROSS-REFERENCE TO RELATED APPLICATION This application is a continuation-in-part of my copending application, Ser. No. 655,838, filed July 25, 1967, for TISSUE GRAFTS now US. Pat. No. 3,514,791.

BACKGROUND OF THE INVENTION This invention relates to a novel method and apparatus for growing tissue grafts and has particular reference to a die cluster for growing a plurality of grafts and to a novel method of implantation of the die cluster in the body.

My prior application, identified above, discloses a number of individual dies for growing grafts for different purposes. It is often desired to grow a plurality of grafts at the same time, as for example, when a graft tube is needed of greater length than can be provided in a single implantable die. Also, the need may arise to grow different sizes or types of grafts simultaneously.

Further, an improved technique for implantation is desired. It would be advantageous to obviate the necessity for tying the die or dies to the bone structure of the body and to provide a method of implantation which would not require a large inci- SIOII.

Objects of the invention are. therefore, to provide an improved tissue graft, to provide an improved cloth reinforcement for a tissue graft. to provide an improved arrangement of a cloth reinforcement within a die cavity, to provide an improved die for forming a tissue graft, to provide a novel die cluster for growing a plurality of tissue grafts simultaneously, and to provide an improved method for implanting a die or die cluster for growing the grafts.

SUMMARY OF THE INVENTION According to the present invention a clothreinforcing member is impregnated with a stiffening agent so that the cloth may be preshaped and will maintain itself in a position in a die cavity where it will be located adjacent the outer surface of the graft tissue. When a plurality of grafts are needed a number of dies are assembled in a die cluster for implantation as a unit.

Instead of tying the die or die cluster to the rib cage to avoid movement in the body, it is inserted under a layer of muscles overlying the rib cage. The muscles themselves hold the die or die cluster in fixed position against the ribs whereby the dies are easily insertable and removable through a relatively small II'ICISIOII.

Other objects and advantages will become apparent and the invention will be better understood with reference to the following description of the preferred embodiment illustrated in the accompanying drawings. Various changes may be made, however, in the details of the method and in the form of construction of the dies and certain features may be used without others. The invention is of particular advantage in growing autogenous grafts within the body of the same patient who is to receive the grafts but the invention may also be used in growing homografts and heterografts if desired.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a perspective view of a die cluster embodying the principles of the invention;

FIG. 2 is an exploded view of the die cluster in FIG. 1 with parts removed and parts broken away;

FIG. 3 is a sectional view on the line 3-3 in FIG. 1;

FIG. 4 is a sectional view on the line 4-4 in FIG. 1;

FIG. 5 is a fragmentary front elevation view of a patient, showing the die cluster of FIG. 1 implanted;

FIG. 6 is an enlarged view of a portion of FIG. 5 showing the use of a pathfinder for preparing an opening to receive the die cluster;

FIG. 7 is a view similar to FIG. 6 showing a first step in the removal of the dies;

FIG. 8 is a view similar to FIG. 7 showing a subsequent step in removal of the dies;

FIG. 9 is an enlarged view of a portion of FIG. 8 with parts in section;

FIGS. 10 and 11 are views similar to FIGS. 7 and 8 showing subsequent steps in removal of the die cluster;

FIG. 12 is a fragmentary perspective view showing a preliminary step in removal of a graft from a die; and

FIG. 13 is a similar view showing the final step in removal of a graft from a die.

DESCRIPTION OF THE PREFERRED EMBODIMENT FIG. I shows a die cluster 10 containing a plurality of dies 11 for implantation as a unit. By way of example, tubular dies are illustrated for growing artery grafts and the like. Each die comprises essentially an outer cylindrical metal tube 12 containing perforations I3 and an inner cylindrical metal mandrel 14 of smaller diameter. The annular space between the outer surface of the mandrel and the inner surface of tube 12 forms a die cavity 15 for growing a tube graft. Tube 12 and mandrel 14 may be made of a suitable plastic if desired.

Each tube 12 and mandrel 14 is supported at its front end on a plastic ferrule 20 and at its rear end on a plastic ferrule 21. In the middle die of the cluster these ferrules are mounted on an anchor rod 22 while in the two outside dies the ferrules are mounted on removable rods 23. The two ferrules 21 on rods 23 are secured thereto by pins 24 while the other ferrules are not attached to their supporting rods. Each ferrule has a stepped end flange portion 25 to support tube 12 and an interior shoulder portion 26 supporting mandrel 14 in concentric position within tube 12. Flange 25 on each ferrule 20 has the same diameter as the outside diameter of tube 12 while flange 25 on each ferrule 21 is of larger diameter for a purpose which will presently appear.

Mounted on the rear end of anchor rod 22 is a head 30 having hinge pins 31 for pivotal connection with crossbars 32. The outer end of each crossbar 32 is provided with a threaded hole 33 and its intermediate portion is provided with a smooth hole 34. The rear ends of rods 23 are received in the holes 34 and a pair of tie rods 35 have threaded engagement with the end holes 33.

The assemblage thus far described is retained in the cluster by a front crossbar 40. Crossbar 40 has a central hole 41 to receive anchor rod 22, end holes 42 to receive tie rods 35, and intermediate holes 43 to receive the removable rods 23, all of these holes being smooth bore. The front ends of rods 22 and 35 are threaded at 44 to receive nuts 45. Nuts 45 hold all the parts in place and immobilize the hinged joints at 31 to form a rigid relatively flat unit for implantation. Crossbars 32 and 40 and rods 22 and 35 form a frame or die holder which contains the dies 11 in side-by-side relation.

In order to prevent adherence of the graft to the mandrel 14 the outer surface of the mandrel is preferably coated with a suitable release agent such as Dow Corning resin R-671 or Teflon. To strengthen the graft a cloth-reinforcing member 50 is inserted in die cavity 15. Member 50 is preferably made of woven or knitted seamless tubular construction having such diameter that it will lie against or substantially adjacent outer tube 12 in spaced relation to mandrel 14. The structural advantages and disadvantages of both woven and knitted materials are well understood by persons skilled in the art. Tube 50 is preferably made of a suitable synthetic fiber such as Dacron. This reinforcement is most effective to prevent leakage or rupture of the graft under arterial blood pressure if the reinforcement is located adjacent the outer surface of the graft tube and relatively remote from the inner surface or lumen.

In order to make the cloth tube 50 support itself and lie substantially smoothly against the inside of tube 12, the cloth is preferably impregnated with a suitable stiffening agent such as silicone rubber. A preferred procedure is to dip the tube several times in a 1:5 suspension of crude (unvulcanized) silicone rubber in xylene. The tube is hung to dry between dips. It is then stretched on a glass rod having a diameter equal to the inside diameter of tube 12 and vulcanized in stretched condition. This accomplishes a desirable sizing operation. When the cloth tube is removed from the glass rod it holds its diameter, and when installed in the die it automatically positions itself snugly against the inner surface of tube 12. Impregnation and vulcanization in the manner described also causes the cloth tube to hold its length and causes the junc tures of the threads to become locked together, both of which stabilizing factors are especially advantageous with a knitted type of cloth.

Before implantation of the die cluster the die cavities are preferably filled with a suitable nutrient. A preferred method of preparing the nutrient will be described. The quantities given in the following example are not intended to limit the invention but will serve to define the preferred proportions of the ingredients used. First, 50 cc. of the patients blood is drawn from a vena puncture into a syringe containing 2 cc. of a solution of one million units of penicillin and one gram of streptomycin dissolved in 20 cc. of normal saline solution. Then an assembled and sterile die cluster as shown in FIG. 1 is placed in a metal laboratory boat and covered with the blood solution just described. The die cluster is allowed to remain in the blood solution for about 25 minutes so that a strong, firm clot forms, filling the die cavities 15.

FIGS. 5 and 6 illustrate the method of implantation of the prepared die cluster. A transverse incision A is made in the skin immediately above the costal margin across the mid clavicular line as shown in FIG. 5. This incision is carried down to the serratus anterior muscle. If the patient is righthanded this incision is made on the left side, as shown; if the patient is left-handed the incision would be made on the right side. In instances where two long graft tubes are needed, a die cluster is implanted on each antrolateral chest wall.

After incision A has been made in the skin, the serratus anterior muscle is incised in the direction of its fibers as indicated at B in FIG. 5. A flat spatula-shaped pathfinder 60 is inserted and passed on the rib cage superomedially, aiming at the junction of the middle and medial thirds of the clavicle as shown in FIG. 6. In the proximal one-half of the passage considerable resistance is met as a result of the origins of the serratus anterior muscle. These must be pushed forcefully off the ribs. Essentially no resistance is met as the instrument passes beneath the pectoralis major muscle in the upper half of the passage. Then the pathfinder 60 is withdrawn.

The die cluster I0 prepared as above described is lifted from the boat and the back end having the jointed crossbar 32 is inserted in the same manner as pathfinder 60 in FIG. 6. The die cluster is pushed up along the path made by pathfinder 60 until the lower end of the die cluster lies above incision A as shown in FIG. 5. Finally, the incision is closed in layers using interrupted sutures and a light sterile dressing is applied. The patient is maintained on penicillin and streptomycin until hospital discharge. The patient is normally discharged from the hospital I or 2 days after implantation of the dies and resumes normal activity. The die cluster may be made to contain fewer or more than three dies if desired.

The serratus anterior muscle and the pectoralis major muscle clamp the die cluster firmly and rigidly against the ribs and prevent any movement of the die cluster, making it unnecessary to provide any mechanical attachment to the ribs. This makes it possible to insert and remove the die cluster endwise through a relatively small incision which heals quickly. While the die cluster is implanted, body tissue from the patient grows through holes 13 into the die cavity replacing the blood nutrient and encapsulating the reinforcing cloth tube 50. This ingrowth of tissue completely fills the die cavity and forms the ultimate graft. Mandrel I4 casts a smooth surface on the lumen of the graft tube.

Two or 3 months later the patient is readmitted to the hospital for the grafting procedure. The grafts are usually complete in 2 months and are consistently complete at 3 months. The procedure for removing the dies is shown in FIGS. 7 to 11. A 3 inch incision C is made over the lower end of the die cluster and perpendicular to its long axis. This incision is carried down through the muscle to the dies. Lower crossbar 40 and the lower 1 cm. of the dies are exposed by sharp dissection. Nuts 45 are removed and crossbar 40 is removed as shown in FIG. 7, and tie rods 35 are unscrewed from threaded holes 33 in hinged crossbar 32.

Then a cylindrical cutter 65 is passed onto the exposed end of a die and, using a rotary oscillating motion, is passed up over the entire length of the die as shown in FIGS. 8 and 9. The larger diameter flanges 25 on plastic ferrules 21 provide stops for the cutter. This operation severs the necks of tissue 66 which have ingrown through the holes 13 in tube 12. The cutter and die are then removed and the die containing the graft is removed from the cutter. The remaining two dies are removed in the same manner. In removing the dies, rods 23 come out with the dies while anchor rod 22 remains in the patient.

At this stage only the center anchor rod 22 and the upper jointed crossbar 32 remain in the patient as shown in FIG. I0.

These parts are removed by firm traction on the anchor rod as shown in FIG. 11, causing the ends of crossbar 32 to pivot back to trailing position, as shown. Incision C is closed in layers using interrupted silk sutures.

Using a surgical knife, the outer surface of each tube 12 is completely cleansed of all fragments of tissue and the mandrel 14 is extracted from each die. This is done by pushing the mandrel from one end to expose its other end which is then grasped with a small hemostat and extracted.

A gall bladder probe 70 is then passed between the graft G and the inner surface of tube 12 at several points around the circumference as shown in FIG. 12. With each pass, it is passed throughout the length of the die, releasing the graft from the outer tube by withdrawing the necks of tissue 66 inwardly through the holes 13. After the graft is completely freed from tube 12 in this manner, it may be grasped at one end with a hemostat and extracted as shown in FIG. 13.

When a long graft tube is needed, the individual grafts from the three dies may be sutured together end to end over a glass rod, the ends of the grafts preferably being cut on a 45 angle for each anastomosis. In this manner a graft tube approximately l9 inches long may be made.

When only a short graft is needed, a single die similar to the central die is used with a modified form of die holder. In such case, crossbar 40 and hinged crossbars 32 are made shorter and holes 34 and 43 are omitted. This makes a narrower and more compact unit placing the tie rods 35 adjacent opposite sides of the single die on anchor rod 22. When the die is round, the die holder prevents rotation in the body. When the die and die holder are of small size, the unit may simply be inserted in a stab wound directed as explained in connection with FIGS. 5 and 6.

The invention is not limited to tube grafts. Dies for other graft members may also be implanted essentially as described in connection with FIGS. 5 and 6. When the die is not round, the die holder may be eliminated if desired but a die holder may still be desirable for convenience in handling a single die or cluster of dies.

Having now described my invention and in what manner the same may be used, what I claim as new and desire to protect by Letters Patent is:

l. A die for forming a tissue graft comprising an outer perforated tube and a mandrel therein defining an annular die cavity for growing a graft tube, and a reinforcing member in said annular die cavity positioned adjacent said outer tube and remote from said mandrel for encapsulation by connective tissue growing through the perforations in said outer tube. said reinforcing member comprising a cloth tube impregnated with silicone rubber vulcanized in situ.

2. A die cluster comprising a holder and a plurality of tissue dies whereby said cluster may be implanted as a unit in a living body for growing tissue grafts in said dies, and means securing said dies in said holder arranged for individual removal of the dies from said holder while said holder remains implanted,

said dies comprising perforated tubes and said holder comprising an anchor rod having cross bars on its opposite ends supporting said die tubes for said individual removal.

3. A die cluster as defined in claim 2, one of said crossbars being removable from said anchor rod and the other crossbar having hinged end portions.

4. A die cluster as defined in claim 3, said anchor rod interconnecting central portions of said crossbars and additional removable tie rods interconnecting the ends of said crossbars.

5. A die cluster as defined in claim 4 including additional rods supported by said crossbars between said anchor rod and tie rods, a mandrel in each die tube defining an annular die cavity in the tube, and ferrules on said anchor rod and additional rods supporting said mandrels and die tubes.

6. In an apparatus for growing a tissue graft, a die holder comprising an anchor rod, a hinged crossbar mounted on one end of said anchor rod, a pair of tie rods detachably connected at one end with the opposite ends of said crossbar, and a second crossbar detachably connected with the opposite ends of said rods.

7. An apparatus as defined in claim 6 including perforated die mounted on said anchor rod, and a pair of additional perforated dies supported by said crossbars between said first die and said tie rods.

8. A die for growing a tubular tissue graft comprising a tube having perforations in the wall thereof for the ingrowth of connective tissue from a living body when said die is implanted in said body, an axial mandrel in said tube defining an annular die cavity in the tube, and a stifi cloth tube reinforcing member in said die cavity disposed adjacent said tube and spaced from said mandrel to allow said connective tissue to grow through said cloth and fill the space between the cloth and said mandrel to fonn a graft tube having said reinforcing member encapsulated adjacent the outer surface of the graft tube and spaced outwardly from the lumen of the graft tube.

9. A die as defined in claim 8, said cloth tube being stiffened by impregnation with a stiffening agent.

10. A die as defined in claim 9, said stiffening agent comprising silicone rubber.

11. A die as defined in claim 8, said mandrel being tubular, and a rod extending through said mandrel to support said die.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US3272204 *Sep 22, 1965Sep 13, 1966Ethicon IncAbsorbable collagen prosthetic implant with non-absorbable reinforcing strands
US3479670 *Oct 19, 1966Nov 25, 1969Ethicon IncTubular prosthetic implant having helical thermoplastic wrapping therearound
Non-Patent Citations
Reference
1 *Ear Molds, Peer type, Catalog No. 6452, Vitallium Surgical Appliances, Austenal Laboratories, Inc. Surgical Div., 224 E. 39th St., N.Y. N.Y., p. 20, March 1948. Copy available in Group 335, 3 1.
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4108161 *Nov 8, 1976Aug 22, 1978Samuels Peter BGraft forming device
US4301814 *Dec 28, 1979Nov 24, 1981Meer SneerCassette implant
US4629458 *Feb 26, 1985Dec 16, 1986Cordis CorporationReinforcing structure for cardiovascular graft
US5282851 *Feb 18, 1992Feb 1, 1994Jacob Labarre JeanIntraocular prostheses
US5472404 *Feb 21, 1995Dec 5, 1995Volgushev; Valentin E.Method for surgical correction of vascular occlusions
US5873906 *Jul 21, 1997Feb 23, 1999Gore Enterprise Holdings, Inc.Procedures for introducing stents and stent-grafts
US5876432 *Mar 28, 1995Mar 2, 1999Gore Enterprise Holdings, Inc.Self-expandable helical intravascular stent and stent-graft
US5885299 *Mar 14, 1996Mar 23, 1999Surgical Dynamics, Inc.Apparatus and method for implant insertion
US5919225 *Jul 14, 1997Jul 6, 1999Gore Enterprise Holdings, Inc.Procedures for introducing stents and stent-grafts
US5925061 *Jan 13, 1997Jul 20, 1999Gore Enterprise Holdings, Inc.Low profile vascular stent
US6001123 *May 28, 1996Dec 14, 1999Gore Enterprise Holdings Inc.Folding self-expandable intravascular stent-graft
US6015429 *Mar 12, 1996Jan 18, 2000Gore Enterprise Holdings, Inc.Procedures for introducing stents and stent-grafts
US6017362 *Jan 22, 1997Jan 25, 2000Gore Enterprise Holdings, Inc.Folding self-expandable intravascular stent
US6042605 *Jul 18, 1997Mar 28, 2000Gore Enterprose Holdings, Inc.Kink resistant stent-graft
US6045555 *Dec 10, 1997Apr 4, 2000Osteonics Corp.Bone graft delivery system and method
US6142998 *Jan 3, 2000Nov 7, 2000Howmedica Osteonics Corp.Bone graft delivery surgical instruments
US6165210 *Apr 1, 1994Dec 26, 2000Gore Enterprise Holdings, Inc.Self-expandable helical intravascular stent and stent-graft
US6309395Apr 25, 2000Oct 30, 2001Howmedica Osteonics Corp.Bone graft delivery surgical instruments
US6331188Jun 9, 1997Dec 18, 2001Gore Enterprise Holdings, Inc.Exterior supported self-expanding stent-graft
US6352553Jul 18, 1997Mar 5, 2002Gore Enterprise Holdings, Inc.Stent-graft deployment apparatus and method
US6352561Dec 23, 1996Mar 5, 2002W. L. Gore & AssociatesImplant deployment apparatus
US6361637Aug 13, 1999Mar 26, 2002Gore Enterprise Holdings, Inc.Method of making a kink resistant stent-graft
US6517570Jul 21, 1997Feb 11, 2003Gore Enterprise Holdings, Inc.Exterior supported self-expanding stent-graft
US6520986Jun 26, 2001Feb 18, 2003Gore Enterprise Holdings, Inc.Kink resistant stent-graft
US6551350Dec 23, 1996Apr 22, 2003Gore Enterprise Holdings, Inc.Kink resistant bifurcated prosthesis
US6613072Jul 18, 1997Sep 2, 2003Gore Enterprise Holdings, Inc.Procedures for introducing stents and stent-grafts
US6626823 *Aug 20, 1999Sep 30, 2003The University Of Queeland Of St. LuciaImplant material
US7608105Jul 20, 2005Oct 27, 2009Howmedica Osteonics Corp.Methods of inserting conically-shaped fusion cages
US7682380Jul 1, 2002Mar 23, 2010Gore Enterprise Holdings, Inc.Kink-resistant bifurcated prosthesis
US8323328Sep 9, 2002Dec 4, 2012W. L. Gore & Associates, Inc.Kink resistant stent-graft
US8623065Oct 7, 2002Jan 7, 2014W. L. Gore & Associates, Inc.Exterior supported self-expanding stent-graft
WO1982003764A1 *May 5, 1982Nov 11, 1982Massachusetts Inst TechnologyFabrication of living blood vessels and glandular tissues
WO1991000119A1 *Jul 2, 1990Jan 10, 1991Baxter IntImplantable device
Classifications
U.S. Classification600/36, 264/137, 425/89, 606/132, 623/916
International ClassificationA61L27/00, A61F2/06, A61L27/18
Cooperative ClassificationA61L27/18, A61F2/062, A61F2/06, Y10S623/916
European ClassificationA61L27/18, A61F2/06B, A61F2/06