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Maximizing mesh mileage: evaluating the long-term performance of a novel hybrid mesh for ventral hernia repair

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Abstract

Purpose

The objective of this study is to evaluate the safety and long-term outcomes of GORE Synecor™ in ventral hernia repair (VHR).

Methods

This retrospective, single-center case review analyzed outcomes in patients who underwent VHR with Synecor from May 2016 to December 2022. Primary outcomes were hernia recurrence and mesh infection rates. Secondary outcomes were 30-day morbidity, 30-day mortality, 30-day readmission, re-operation, surgical-site infection (SSI) and occurrence (SSO) rates, and occurrences requiring intervention (SSOI).

Results

278 patients were identified. Mean follow-up was 24.1 (0.2–87.1) months. Mean hernia defect size was 63.4 (± 77.2) cm2. Overall hernia recurrence and mesh infection rates were 5.0% and 1.4% respectively. No mesh infections required full explantation. We report the following overall rates: 13.3% 30-day morbidity, 4.7% 30-day readmission, 2.9% re-operation, 7.2% SSI, 6.1% SSO, and 2.9% SSOI. 30-day morbidity was significantly higher in non-clean (42.1% vs 11.2%, p < 0.01), onlay (OL) mesh (37.0% vs preperitoneal (PP) 16.4%, p = 0.05 vs retrorectus (RR) 15.0%, p < 0.05 vs intraperitoneal (IP) 5.2%, p < 0.001), and open cases (23.5% vs 3.1% laparoscopic vs 4.4% robotic, p < 0.01). SSI rates were significantly higher in non-clean (31.6% vs 5.4%, p < 0.001), OL mesh (29.6% vs RR 11.3%, p < 0.05 vs PP 5.5%, p < 0.01 vs IP 0.0%, p < 0.001), and open cases (15.2% vs 0% laparoscopic vs 0% robotic, p < 0.05).

Conclusion

Long-term performance of a novel hybrid mesh in VHR demonstrates a low recurrence rate and favorable safety profile in various defect sizes and mesh placement locations.

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Data availability

The data presented in this study is available upon request from the corresponding author.

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Funding

No funding information to disclose for this project.

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Authors and Affiliations

Authors

Contributions

Conceptualization: Jonathan Z Li, Ryan C Broderick, Garth R Jacobsen; Formal analysis and investigation: Graham J Spurzem, Jonathan Li; Writing—original draft preparation: Graham J Spurzem, Jonathan Z Li; Writing—review and editing: Graham J Spurzem, Ryan C Broderick, Santiago Horgan, Garth R Jacobsen; Supervision: Bryan J Sandler, Santiago Horgan, Garth R Jacobsen.

Corresponding author

Correspondence to G. J. Spurzem.

Ethics declarations

Ethical approval

This retrospective case review study was approved by the University of California, San Diego Institutional Review Board.

Human and animal rights

This research study was conducted retrospectively from data obtained for clinical purposes. All procedures were performed as part of standard routine care. There were no procedures involving animals.

Informed consent

A waiver of informed consent was granted for this study by the University of California, San Diego Institutional Review Board.

Conflict of interest

Dr. Broderick is a consultant for Stryker Corporation. Dr. Sandler is a consultant for Intuitive Surgical and Boston Scientific. Dr. Horgan is a consultant for Stryker Corporation, Intuitive Surgical, Fortimedix Surgical, and Alume Biosciences. Dr. Jacobsen is a consultant for Gore Medical and Viacyte. Drs. Spurzem & Li have no disclosures.

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Spurzem, G.J., Broderick, R.C., Li, J.Z. et al. Maximizing mesh mileage: evaluating the long-term performance of a novel hybrid mesh for ventral hernia repair. Hernia (2024). https://doi.org/10.1007/s10029-024-02995-0

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