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Preventing Parastomal Hernia with a Prosthetic Mesh: A 5-Year Follow-up of a Randomized Study

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Abstract

Background

Parastomal hernia is a major clinical problem. In a randomized, clinical trial, a prosthetic mesh in a sublay position at the index operation reduced the rate of parastomal hernia at 12-month follow-up, without any increase in the rate of complications. This study was designed to evaluate the rate of complications after 5 years.

Methods

Between January 2001 and April 2003, 54 patients who had a permanent ostomy were randomized to a conventional stoma or to a stoma with the addition of a mesh in a sublay position. A large-pore, lightweight mesh with a reduced polypropylene content and a high proportion of absorbable material was used.

Results

After 5 years, 21 patients with a conventional stoma were alive and parastomal herniation was recorded in 17 patients, of whom repair had been demanded in 5. In 15 patients operated on with the addition of a mesh herniation, that did not require repair, was present in 2 (P < 0.001). No fistulas or strictures developed. No mesh infection was noted and no mesh was removed during the study period.

Conclusions

At stoma formation, a prophylactic low-weight mesh in a sublay position is a safe procedure that reduces the rate of parastomal hernia.

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Correspondence to Arthur Jänes.

Additional information

Leif A. Israelsson is a Consultant for Ethicon Innovation Group Worldwide.

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Jänes, A., Cengiz, Y. & Israelsson, L.A. Preventing Parastomal Hernia with a Prosthetic Mesh: A 5-Year Follow-up of a Randomized Study. World J Surg 33, 118–121 (2009). https://doi.org/10.1007/s00268-008-9785-4

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  • DOI: https://doi.org/10.1007/s00268-008-9785-4

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