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Langenbeck's Archives of Surgery

, Volume 403, Issue 2, pp 255–263 | Cite as

Comparison of biological and alloplastic meshes in ventral incisional hernia repair

  • A. Koscielny
  • S. Widenmayer
  • T. May
  • J. Kalff
  • P. Lingohr
ORIGINAL ARTICLE
First Online:
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Accepted:
  • 224 Downloads

Abstract

Purpose

The aim of our retrospective analysis was to compare the results of incisional hernia repair by porcine small intestinal submucosa-derived (SIS) meshes with those obtained by alloplastic polypropylene-based (PP) meshes in comparable surgical indications by matched-pair design. We hypothesized that in incisional hernia, SIS mesh repair is associated with fewer recurrences and SSO than PP mesh repair in incisional hernias.

Methods

Twenty-four matched pairs (SIS vs. PP mesh repair between 1 January 2005 and 31 December 2013) were identified by matching criteria: gender, age, comorbidities, body mass index, EHS hernia classification, mesh implantation technique, CDC wound classification, and source of contamination/primary surgery leading to incisional hernia. Minimal follow-up time was 24 months. Means and standard deviations were compared by paired t test; categorial data were compared by McNemar’s test. Poisson’s distribution and negative binominal distribution were employed to detect significant correlation.

Results

There were no statistically significant differences between both groups in the pre- and perioperative factors and the follow-up times. There were significantly more wound complications (19 vs. 12, p = 0.041), longer hospital stay (22.0 ± 6.3 vs. 12.0 ± 3.1 days, p = 0.010), and significantly more recurrent hernias (25 vs. 12.5%, p = 0.004) after SIS mesh repair. Both the Poisson’s distribution and the negative binominal distribution unveiled significantly more complication points (3–6 vs. 1–2) per month after SIS mesh repair.

Conclusion

There is no advantage of SIS meshes compared to PP meshes in incisional hernia repair with different degrees of wound contamination in this matched-pair analysis. Further prospective and randomized trials or at least registry studies such as the EHS register with standardized and defined conditions are warranted.

Keywords

Ventral incisional hernia Biologic mesh Alloplastic mesh Cross-matched pair 
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Notes

Acknowledgements

Dr. Ralf Fimmers, deputy head of the institute of medical biometry, informatics, and epidemiology at the University of Bonn Medical School, deserves our acknowledgment for his highly appreciated assistance in the statistical analyses.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Supplementary material

423_2017_1639_MOESM1_ESM.doc (78 kb)
ESM 1 (DOC 78 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2017

Authors and Affiliations

  • A. Koscielny
    • 1
  • S. Widenmayer
    • 1
  • T. May
    • 1
  • J. Kalff
    • 1
  • P. Lingohr
    • 1
  1. 1.Klinik und Poliklinik für Allgemein-, Viszeral-, Thorax- und GefäßchirurgieRheinische Friedrich-Wilhelms-Universität BonnBonnGermany

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