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Clinical Trial
. 2004 Dec;139(12):1356-8.
doi: 10.1001/archsurg.139.12.1356.

Preventing parastomal hernia with a prosthetic mesh

Affiliations
Clinical Trial

Preventing parastomal hernia with a prosthetic mesh

Arthur Jänes et al. Arch Surg. 2004 Dec.

Abstract

Hypothesis: Parastomal hernia is a common complication following colostomy. The lowest recurrence rate has been produced when repair is with a prosthetic mesh. This study evaluated the effect on stoma complications of using a mesh during the primary operation.

Design: Randomized clinical study.

Methods: Patients undergoing permanent colostomy were randomized to have either a conventional stoma or the addition of a mesh placed in a sublay position. The mesh used was a large-pore lightweight mesh with a reduced polypropylene content and a high proportion of absorbable material.

Results: Twenty-seven patients had a conventional stoma, and in 27 patients the mesh was used. No infection, fistula formation, or pain occurred (observation time, 12-38 months). At the 12-month follow-up, parastomal hernia was present in 13 of 26 patients without a mesh and in 1 of 21 patients in whom the mesh was used.

Conclusions: A lightweight mesh with a reduced polypropylene content and a high proportion of absorbable material placed in a sublay position at the stoma site is not associated with complications and significantly reduces the rate of parastomal hernia.

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