Implantable prosthesis

Abstract

An implantable prosthesis for repairing an anatomical defect, such as a soft tissue and muscle wall defect. The prosthesis is configured to reduce the likelihood that an applied force at the repair site, such as due to intraabdominal pressure or tissue shrinkage, can lead to detrimental effects associated with tension at the anchoring locations between the prosthesis and host tissue and / or contraction of the prosthesis. In this regard, the prosthesis may be configured to limit the amount of tension at the anchoring locations caused by the application of a force or pressure to the prosthesis and / or contraction of the prosthesis. Alternatively, the prosthesis may be configured to compensate for contraction of the prosthesis due to tissue shrinkage at the repair site. The prosthesis may be configured to both limit tension at the anchoring locations and compensate for tissue shrinkage. The prosthesis may facilitate a reduction in postoperative discomfort, a recurrence of the defect, or the creation of a new defect associated with tension and / or prosthetic contraction.

Description

[0001] The present invention relates to an implantable prosthesis and, more particularly, to a prosthesis for use in soft tissue repair and reconstruction.DISCUSSION OF RELATED ART[0002] Various prosthetic materials have been proposed to repair and reinforce anatomical defects, such as tissue and muscle wall hernias. For example, an inguinal hernia is commonly repaired using a sheet of biocompatible fabric, such as a knitted polypropylene mesh (BARD MESH). The fabric is typically sutured, stapled or otherwise provisionally anchored in place over, under or within the defect. Tissue integration with the fabric, such as by tissue ingrowth into and / or along the fabric, eventually completes the repair.[0003] The attachment of the fabric to host tissue adjacent the defect can result in tension at the anchoring locations between the fabric and the tissue when abdominal pressure at the repair site is applied to the fabric, such as when an individual stands or strains, coughs, sneezes and th...

AI Technical Summary

Benefits of technology

[0006] The present invention is an implantable prosthesis and a method of repairing an anatomical defect, such as a tissue or muscle wall defect. The prosthesis is configured to reduce the likelihood that an applied force, such as due to intraabdominal pressure or tissue shrinkage, at the repair site can lead to detrimental effects associated with tension at the anchoring locations of the prosthesis and host tissue and / or contraction of the prosthesis. The prosthesis may reduce postoperative pain, and reduce the likelihood of either a recurrence of the defect or the creation of a new defect associated with tension and / or prosthetic contraction.

[0009] In one embodiment of the invention, the repair fabric may include a preformed region configured to reduce the prospects that an applied force at the repair site will cause detrimental tension at the anchoring location and / or to compensate for contraction of the prosthesis that may occur as a result of tissue shrinkage at the repair site during scarification.

[0010] According to one aspect of the invention, the preformed region has a predetermined amount of laxity that is greater than an amount of laxity at an anchoring portion of the fabric to reduce the prospects that an applied force at the repair site will cause detrimental tension at the anchoring location. According to another aspect of the invention, the preformed region has a predetermined amount of compensation to compensate for contraction of the prosthesis. According to a further aspect of the invention, the preformed region is configured to both reduce detrimental tension at the anchoring portion and to compensate for prosthetic contraction.

Problems solved by technology

The attachment of the fabric to host tissue adjacent the defect can result in tension at the anchoring locations between the fabric and the tissue when abdominal pressure at the repair site is applied to the fabric, such as when an individual stands or strains, coughs, sneezes and the like.

Tension at the anchoring locations may lead to postoperative pain for the patient, a recurrence of the defect, or the formation of a new defect.

For example, a recurrence of the original defect or the creation of a new defect may result from failure of the suture line or other fastener, or tearing of the tissue due to tension at one or more of the anchoring locations.

Tension on the suture line at the anchoring locations may also lead to ischemia of the tissue, resulting in enlargement of the suture holes and an eventual defect.

Scar formation (scarification) associated with the repair of tissue and wall defects may cause tissue shrinkage at the repair site, thereby contracting the repair fabric that has been integrated with tissue.

Contraction of the fabric may cause patient discomfort as the fabric strains against the host tissue at the anchoring locations.

Contraction of the fabric may cause failure of the fasteners and / or tearing of the tissue, in either case potentially leading to a recurrence of the defect, due to the fabric being pulled away from the tissue or muscle at the anchoring locations.

The prosthesis is configured to reduce the likelihood that an applied force, such as due to intraabdominal pressure or tissue shrinkage, at the repair site can lead to detrimental effects associated with tension at the anchoring locations of the prosthesis and host tissue and / or contraction of the prosthesis.

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