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The AAPS 103rd Annual Meeting 2025

May 24-27, 2025 | Austin, Texas

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D102

A Comparative Analysis Of Retrorectus Ventral Hernia Repair In Clean Wounds Using Biosynthetic Or Synthetic Mesh With Three-year Follow-up  

Part of Topic

General Reconstruction

Biosynthetic vs. Synthetic Mesh in Retrorectus Ventral Hernia Repair: A Matched Analysis with Three-Year Outcomes

Background

Ventral hernias are a common surgical issue, with over 600,000 repairs performed annually in the U.S. Surgical repair with mesh reinforcement significantly reduces recurrence rates compared to suture repair alone. Synthetic meshes provide strong reinforcement but are associated with complications such as infection, chronic pain, and adhesions. In contrast, biologic meshes were developed to reduce foreign body response, but they are significantly more expensive and may have higher recurrence rates. Biosynthetic meshes aim to combine the strength of synthetic materials with the biocompatibility of biologics. These include fully resorbable polymers like poly-4-hydroxybutyrate (P4HB), offering potential benefits in tissue integration and infection resistance. However, comparative data between biosynthetic and synthetic meshes remain limited, especially regarding long-term outcomes such as recurrence and complications. The evidence is often conflicting, with heterogeneity in study designs, indications, and follow-up durations. This study compares long-term outcomes of retrorectus ventral hernia repair (VHR) using uncoated polypropylene synthetic mesh vs. P4HB biosynthetic mesh in clean wounds, focusing on:Hernia recurrence, Surgical site occurrences (SSOs), Reoperation/Readmission/ED visit rates

Methods: This single-center, retrospective cohort study included patients who underwent retrorectus VHR with biosynthetic or synthetic mesh in clean wounds between 2015 and 2021, who were followed up to hernia recurrence or three years. Optimal full matching using Mahalanobis distance, incorporating age, BMI, transversus abdominus release (TAR), and American Society of Anesthesiologists classification was performed.  

Results:  A total of 160 patients (49 synthetic, 111 biosynthetic) were included, with a median age and BMI of 62 years old (IQR 52.8-72.0), and 33.7 kg/m2 (28.4-39.1) respectively. Following match, baseline characteristics, comorbidities, and TAR utilization rates were comparable between groups, however biosynthetic group had a greater average defect size (220 cm2 vs 141 cm2, p=0.010). Hernia recurrence at three years did not differ significantly between the biosynthetic and synthetic mesh groups (3.3% vs. 7.0%, respectively; log-rank p=0.4). Similarly, there were no significant differences in SSOs (27% vs. 37%, p=0.3), readmission rates (17% vs. 21%, p=0.6), SSOs requiring procedural intervention (11% vs. 14%, p=0.7), or all-cause reoperation rates (17% vs. 18%, p=0.9).  

Conclusion
In clean retrorectus ventral hernia repair, P4HB biosynthetic mesh demonstrates comparable 3-year recurrence and complication rates to uncoated polypropylene synthetic mesh, supporting its use as a viable alternative in this setting. While no short-term clinical advantage was observed, the resorbable nature of biosynthetic mesh may offer potential benefits for patients where permanent foreign material is a concern. Given its higher cost and the need to assess long-term outcomes, future studies should incorporate extended follow-up, patient-reported outcomes, and cost-effectiveness analyses to better define its role in ventral hernia repair.
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