Laparoscopic ventral hernia repair with primary fascial closure versus bridged repair: a risk-adjusted comparative

John Emil Wennergren1, Erik P Askenasy2, Jacob A Greenberg3

  • 1Department of Surgery, University of Kentucky, C-225 Chandler Medical Center, 800 Rose Street, Lexington, KY, 40536, USA. john.wennergren@gmail.com.

Surgical Endoscopy
|November 19, 2015
PubMed
Abstract

Insights

Primary fascial closure (PFC) in laparoscopic ventral hernia repair (LVHR) did not reduce recurrence or surgical site infections compared to bridged mesh repair. Further research is needed to assess patient outcomes like pain and satisfaction.

Area of Science:

  • General Surgery
  • Minimally Invasive Surgery

Background:

  • Laparoscopic ventral hernia repair (LVHR) is common, with bridged mesh techniques widely used.
  • While laparoscopy reduces surgical site infections (SSI), hernia recurrence rates remain a concern.
  • Primary fascial closure (PFC) is proposed to decrease recurrence in LVHR.

Purpose of the Study:

  • To test the hypothesis that laparoscopic primary fascial closure (PFC) decreases hernia recurrence rates compared to bridged mesh repair in LVHR patients.
  • To compare recurrence, surgical site infection (SSI), and seroma formation between PFC and bridged repair groups.

Main Methods:

  • A retrospective analysis of 1594 patients undergoing LVHR with mesh from 2010-2012.
  • Comparison of 97 patients with PFC versus 99 patients with bridged repairs.
  • Propensity score analysis controlled for multiple patient and surgical factors.

Main Results:

  • No significant statistical differences were found between PFC and bridged repair groups for recurrence, seroma, SSI, reoperation, or readmission.
  • Subgroup analysis and propensity score analysis confirmed these findings.
  • Mean follow-up was 17.5 months.

Conclusions:

  • PFC during LVHR did not reduce recurrence, seroma, or SSI compared to bridge repairs in this multi-institutional study.
  • Further research, including randomized controlled trials, is needed to evaluate patient-reported outcomes such as pain, function, and cosmesis.

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