Patent Application
20150025552
The present invention relates to the field of surgery and, in particular, to devices and techniques for reattachment and reinforcement of tissue such as bone, tendon or ligament.
Fracture healing is a proliferative physiological process in which the body facilitates the repair of a bone fracture. In the process of fracture healing, several phases of recovery facilitate the proliferation and protection of the areas surrounding fractures and dislocations. The length of the process depends on the extent of the injury, the angle of dislocation or fracture, and the extent of immobilization after the fracture surgery repair.
Ligaments and tendons are soft collagenous tissues that play a significant role in musculoskeletal biomechanics. Ligaments connect bone to bone and tendons connect muscles to bone. Repairing torn ligaments poses significant challenges for physicians. Some of the repairs include grafting tissue or placing artificial prostheses to replace ligaments. Often patients have to undergo multiple surgeries to maintain a repair, or have to have prostheses replaced.
Treatment of a torn ligament/tendon depends on the severity of the injury but often includes surgery with bracing and/or casting and immobilization. Bracing may cause complications such as stiffness or adhesions from limiting normal knee range of motion.
Successful and less invasive acute repairs that reduce progression to chronic instabilities and reconstruction procedures are needed. Also needed are devices and less invasive repairs for tissue reconstruction that improve primary repair outcomes without the cost of bracing, casting and/or delayed rehabilitation, for both fracture and soft tissue repairs. Systems and devices that are designed to hold bone grafts and other biologics, and then to further hold these bone grafts and biologics at a repair site (fracture, ligament, tendon repair site, etc.) are needed, as well as devices that reduce fracture fragments for comminuted fractures and that could be also used as an adjunct to ORIF (Open Reduction Internal Fixation) surgical procedures.
The present invention provides minimally invasive techniques and devices for reattachment of tissue (such as bone or soft tissue) and reinforcing such reattached tissue with accelerated recovery and optimal length for bone/ligament healing.
The present invention provides a tissue net or brace and associated techniques according to which acute injury of tissue (for example, bone fracture or ligament repair) is treated with a reinforcement construct in the form of a mesh or netting of a woven/braided/knitted/interlinked material (for example, a suture tape or any flexible material that can be knitted, woven, linked, braided, etc.).
The reinforcement construct can be used as a netting to hold bone grafts and/or biologic material and to allow placement of such bone grafts and/or biologic material at a repair site (for example, soft tissue or bone fracture repair site). The reinforcement construct may be used as a sling to help reduce fracture fragments or may be used to provide a net to hold bone graft and augment fracture repair. The reinforcement construct (netting or FiberNet or sling) may be used to augment fracture repair of comminuted fractures, and may be employed as an aid in a fracture repair and care product line. The construct may be used as a sling to help reduce fracture segments or provide a simple net to hold bone graft. The reinforcement construct may be designed to be tied over bone or a button and/or incorporated into a bone plate, or used with any additional devices such as adjustable loop constructs (for example, adjustable knotless suture loop/button constructs, among many others). The reinforcement construct may be impregnated with biologics to aid in biological healing. An exemplary-only “sling” or FiberNet is designed to go around a bone and hold bone graft material and ACP to a fracture site.
The reinforcement construct acts as a “brace” that may be used for internal or external applications, eliminating the need of a post operative brace or cast in post-injury treatment, allowing immediate motion and rehabilitation, accelerating wound healing, and reinforcing the reattached soft tissue resulting in an early return to daily living and sports.
a) illustrate an exemplary flexible material of the reinforcement construct of the present invention (showing woven ultra-high molecular weight polyethylene (UHMWPE) core with a braided jacket of polyester and UHMWPE).
a) illustrate a reinforcement construct in accordance with another exemplary embodiment of the present invention (a fixed option with loops which may be used with additional cinching loops or constructs).
The present invention provides a “tissue brace” or reconstruction system (FiberNet or sling) and associated techniques for treatment of acute injury of tissue (for example, bone or soft tissue repairs such as tendon or ligament repair).
The reconstruction system of the present invention comprises a flexible material in the form of a netting or mesh that may be optionally reinforced/assembled with additional flexible strands, cords or adjustable constructs (for example, additional sutures, high strength FiberTape® suture tape, high strength FiberWire® suture, TigerWire® suture, FiberChain® suture chain and/or FiberLink® loops, or adjustable suture loop/button constructs, among others) to form a resulting construct. The assembly options may be flexible/modular or fixed.
A biological material such as blood, blood components, BMA, BMSCs, PRP, ACP and/or growth factors may be injected into the injury site and small incisions and/or into the reinforcement construct, to further improve and accelerate incision and tissue healing. Alternatively, the reinforcement construct may be impregnated with such biological materials.
The reinforcement construct of the present invention may be employed with fixation devices (for example, screws or anchors such as SwiveLocks® or PushLocks®, or flexible adjustable knotted or knotless button/suture loop constructs) and/or with bone plates and fixation systems to simplify the overall surgical procedure and augment the ligament/tendon/bone repair, while reinforcing the reconnected ligament/tendon/bone. The reinforcement construct of the present invention may be used as a tissue protector/reinforcement construct.
The reinforcement construct of the present invention can be used as a netting to reduce fracture fragments for comminuted fractures, to hold bone graft and other biologics at a fracture site, or to be used as an adjunct to ORIF (Open Reduction Internal Fixation) procedures.
The reinforcement construct of the present invention may be also employed to augment fracture repair of comminuted fractures (as an adjunct to fracture care product lines) or can be used simply as a sling to help reduce fracture fragments or provide a net to hold bone grafts and/or biologics. The reinforcement construct may be tied over bone or a button and incorporated into a bone plate, for example. The reinforcement construct may be impregnated with biologics and may be used to aid in biological healing. A “sling” or FiberNet according to the present invention helps hold bone graft material and ACP to a fracture site. The reinforcement construct of the present invention may be permanently left at a repair site or may be removed.
Referring now to the drawings, where like elements are designated by like reference numerals,
a) illustrate flexible material 10 in the form of an exemplary mat section 10 which may be any flexible material or combination of materials that can be woven, knitted, braided, interlocked, etc. In an exemplary-only and non-limiting embodiment, section 10 is formed of woven ultra-high molecular weight polyethylene (UHMWPE) core with a braided jacket of polyester and UHMWPE. In an exemplary embodiment only shown in
As noted above, at least one additional strand or flexible construct (suture, tape, chain, filaments, yarns, fibrils, loops, adjustable knotless suture/button constructs, etc.) may be added to/through the flexible material (in a fixed and/or non-fixed manner) to provide additional strength and support to the construct.
The materials employed for the formation of the reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f may be loosely braided ultrahigh molecular weight polyethylene (UHMWPE) sutures, which may be braided with at least one other fiber, natural or synthetic, absorbable or resorbable, to form lengths of suture material. The reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f may be also formed of suture tape such as FiberTape® as disclosed in U.S. Pat. No. 7,892,256, the disclosure of which is incorporated by reference in its entirety herewith.
The flexible material 10 may have various forms and geometries (for example, rectangular or square, among many others) that allow at least one addition element to attach thereto (either in a fixed or modular manner). As detailed above, the flexible material 10 of the constructs of the present invention may be formed of suture tape such as FiberTape® (disclosed in U.S. Pat. No. 7,892,256), suture chain such as FiberChain® (disclosed in U.S. Pat. No. 7,803,173), among others, or combination of these materials. Preferably, the flexible material may be a loosely braided UHMWPE suture that can be woven with additional strands/yarns/filaments to provide a braided/woven net (mesh) that can be used with additional reinforcing cords, strands and/or structures.
The reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f may be woven or braided structures, or may be formed of yarns, fibers or similar materials, or combinations of these materials, that are joined/interlocked together by any known method in the art. In the exemplary-only embodiments above, the reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f of the present invention are formed essentially of suture such as braided UHMWPE.
The reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f could be utilized for multiple indications such as, for example, fracture repairs and ligament/tendon repairs such as AC joint reconstruction, syndesmosis reconstruction, quad/patellar tendon rupture repair, hallux-valgus repair, and any other tendon repair to bone. The reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f detailed above may be also employed in conjunction with additional various knotted and/or knotless fixation devices (or combination of such knotted and knotless fixation devices), such as PushLock® anchors and/or SwiveLock® anchors to secure, for example, a medial row on rotator cuff repairs.
The reconstruction constructs and systems of the present invention may be also used in conjunction with any knotless fixation devices which can allow a flexible strand to be attached thereto. The fixation devices may be any of swivel and/or screw-in suture anchors and/or push-in suture anchors a knotless suture anchor such as the two-piece Arthrex PushLock® anchor, disclosed in U.S. Pat. No. 7,329,272, or an Arthrex SwiveLock® anchor, disclosed in U.S. Pat. No. 8,012,174 (the disclosures of which are herein incorporated by reference in their entireties). As detailed in these patents and applications, a knotless suture anchor is formed of an implant with a distal eyelet (which may be closed or forked, and which engages and secures at least one flexible strand) and a fixation device (a cannulated screw) that is advanced over the implant body to secure the implant and the flexible strand into a bone hole or socket, and to approximate soft tissue to bone. The implant may be rotatably attached to (and/or may swivel relative to) a tip of a driver assembly that is pre-loaded with the separate, cannulated fixation device (cannulated screw).
The fixation devices may be also any anchors, implants or screws (such as interference screws or tenodesis screws) or any fixation element that allows attachment/fixation of the constructs to bone. The fixation devices/implants may have various sizes (various diameters and/or lengths) and may be formed of biocompatible materials such as PEEK, biocomposite materials, metals and/or metal alloys, or combination of such materials, among others.
The flexible strands or sutures of the construct of the present invention may be also spliced—at least in part—in a manner similar to an Arthrex ACL TightRope®, such as disclosed in U.S. Pat. Nos. 8,439,976 and 8,460,379, the disclosures of which are incorporated by reference in their entirety herein.
Additional reinforcement constructs may be provided at a repair site (for example, fracture site) dependent upon the size of the tissue defect. Suture passing and knot tying are carried out in the preferred fashion to secure further attachment of soft tissue to bone, and if necessary.
The flexible strands employed for the formation of the reconstruction systems 50a, 50b, 50c, 50d, 50e, 50f may be high-strength sutures, such as the high strength suture sold by Arthrex, Inc. of Naples, Fla. under the registered tradename TigerWire® or FiberWire®, which is disclosed and claimed in U.S. Pat. No. 6,716,234, the entire disclosure of which is incorporated by reference in its entirety herewith. FiberWire® suture is formed of an advanced, high-strength fiber material, namely ultrahigh molecular weight polyethylene (UHMWPE), sold under the tradenames Spectra (Honeywell) and Dyneema (DSM), braided with at least one other fiber, natural or synthetic, to form lengths of suture material. The flexible strands may be also formed of suture tape such as FiberTape® as disclosed in U.S. Pat. No. 7,892,256, or a suture chain such as FiberChain® as disclosed in U.S. Pat. No. 7,803,173.
Biological materials such as blood, blood components, BMA, BMSCs, PRP, ACP and/or growth factors may be directly injected into the bone/ligament injury site and small incisions, to further improve and accelerate incision and tissue healing, or may be provided via the construct (i.e., provided within the flexible material 10 and/or additional cords/tapes, for example).
While the present invention is described herein with reference to illustrative embodiments for particular applications, it should be understood that the invention is not limited thereto. Those having ordinary skill in the art and access to the teachings provided herein will recognize additional modifications, applications, embodiments and substitution of equivalents all fall within the scope of the invention. Accordingly, the invention is not to be considered as limited by the foregoing description.
This application claims the benefit of U.S. Provisional Application No. 61/846,870 filed Jul. 16, 2013, the entire disclosure of which is incorporated by reference in its entirety herein.
| Number | Date | Country | |
|---|---|---|---|
| 61846870 | Jul 2013 | US |
