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Link to original content: https://pubmed.ncbi.nlm.nih.gov/12728375/
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Clinical Trial
. 2003 Jul;17(7):1105-9.
doi: 10.1007/s00464-002-9167-1. Epub 2003 May 6.

Comparison of biomaterials in the early postoperative period

Affiliations
Clinical Trial

Comparison of biomaterials in the early postoperative period

M R Langenbach et al. Surg Endosc. 2003 Jul.

Abstract

Background: Laparoscopic hernia repair necessitates the use of biocompatible materials. A prospective, double-blind study was conducted to compare two different polypropylene meshes.

Methods: The study included 40 men with primary inguinal hernia undergoing transabdominal preperitoneal polypropylene mesh repair. In 20 of these men, a monofile, heavy-weight, rigid mesh was implanted (group A), and in the remaining 20 men, a smooth, heavy-weight variant of polypropylene mesh was implanted (group B). Complications, pain development, inability to work, physical conditions, testicular volume, and blood circulation were documented.

Results: Reconvalescence in group A was slower than in group B. In group A, the postoperative values of the visual scales for pain development were higher; inability to work was 7.3 days longer; urologic disorders were worse; activities of everyday life were more reduced; and SF-36 data showed a significant reduction of physical problems ( p < 0.05).

Conclusions: The polypropylene mesh variant seems to be more compatible with the human organism than conventional mesh. Not only the material, but also the structure seems to influence the comfort of the mesh.

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