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Slowly absorbable mesh in contaminated incisional hernia repair: results of a French multicenter study

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Abstract

Purpose

To analyze the postoperative morbidity and 1-year recurrence rate of incisional hernia repair using a biosynthetic long-term absorbable mesh in patients at higher risk of surgical infection in a contaminated surgical field.

Methods

All patients undergoing incisional hernia repair in a contaminated surgical field with the use of a biosynthetic long-term absorbable mesh (Phasix®) between May 2016 and September 2018 at six participating university centers were included in this retrospective cohort and were followed-up until September 2019. Regarding the risk of surgical infection, patients were classified according to the modified Ventral Hernia Working Group classification. Preoperative, operative and postoperative data were collected. All patients’ surgical site infections (SSIs) and occurrences (SSOs) and recurrence rates were the endpoints of the study.

Results

Two hundred and fifteen patients were included: 170 with mVHWG grade 3 (79%) and 45 with mVHWG grade 2 (21%). The SSI and SSO rates at 12 months were 22.3% and 39.5%, respectively. According to the Dindo–Clavien classification, 43 patients (20.0%) had at least one minor complication, and 57 patients (26.5%) had at least one major complication. Among the 121 patients (56.3%) having at least 1 year of follow-up, the clinical recurrence rate was 12.4%. Multivariate analysis showed that a concomitant gastrointestinal procedure was an independent risk factor for surgical infection (OR = 2.61), and an emergency setting was an independent risk factor for major complications (OR = 11.9).

Conclusion

The use of a biosynthetic absorbable mesh (Phasix®) is safe in a contaminated surgical field, with satisfying immediate postoperative and 1-year results.

Trial registration

The study is registered on Clinical Trial ID: NCT04132986.

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Availability of data and material

The study is registered on Clinical Trial ID: NCT04132986.

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Correspondence to D. Charleux-Muller.

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Conflict of interest

Ortega Deballon P., received grants from Bard/Beckton-Dickinson within the past 5 years. Dubuisson V., received grants from Bard/Beckton-Dickinson within the past 5 years. Renard Y., received grants from Bard/Beckton-Dickinson within the past 5 year. Bard/Beckton-Disckinson didn’t influence analysis and writing process of the study. D. Charleux-Muller, R. Hurel, T. Fabacher, C. Brigand, S. Rohr, S. Manfredelli, G. Passot, B. Romain authors declare that they have no conflict of interest.

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All participants gave their permission to participate to the study.

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Charleux-Muller, D., Hurel, R., Fabacher, T. et al. Slowly absorbable mesh in contaminated incisional hernia repair: results of a French multicenter study. Hernia 25, 1051–1059 (2021). https://doi.org/10.1007/s10029-020-02366-5

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  • DOI: https://doi.org/10.1007/s10029-020-02366-5

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