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Suture fixation versus self-gripping mesh for open inguinal hernia repair: a systematic review with meta-analysis and trial sequential analysis.
Bullen, N L; Hajibandeh, S; Hajibandeh, S; Smart, N J; Antoniou, S A.
Affiliation
  • Bullen NL; Department of Colorectal Surgery, Royal Devon and Exeter NHS Foundation Trust, Royal Devon and Exeter Hospital, Barrack Road, Exeter, EX2 5DW, UK. n.bullen@nhs.net.
  • Hajibandeh S; Department of General Surgery, Sandwell and West, Birmingham Hospitals NHS Trust, Birmingham, UK.
  • Hajibandeh S; Department of General Surgery, North Manchester General Hospital, Manchester, UK.
  • Smart NJ; Department of Colorectal Surgery, Royal Devon and Exeter NHS Foundation Trust, Royal Devon and Exeter Hospital, Barrack Road, Exeter, EX2 5DW, UK.
  • Antoniou SA; Surgical Service, Mediterranean Hospital of Cyprus, Limassol, Cyprus.
Surg Endosc ; 35(6): 2480-2492, 2021 06.
Article in En | MEDLINE | ID: mdl-32444971
ABSTRACT

INTRODUCTION:

Morbidity following open inguinal hernia repair is mainly related to chronic pain. ProGrip™ is a self-gripping mesh which aims to reduce rates of chronic pain. The aim of this study is to perform an update meta-analysis to consolidate the non-superiority hypothesis in terms of postoperative pain and recurrence and perform a trial sequential analysis.

METHODS:

Systematic review of randomised controlled trials performed according to PRISMA guidelines. Pooled odds ratios with 95% confidence intervals (CI) were calculated using the Mantel-Haenszel (M-H) method. The primary outcome measure was postoperative pain and secondary outcomes were recurrence, operative time, wound complications, length of stay, re-operation rate, and cost. Trial sequential analysis was performed.

RESULTS:

There were 14 studies included in the quantitative analysis with 3180 patients randomised to self-gripping mesh (1585) or standard mesh (1595). At all follow-up time points, there was no significant difference in the rates of chronic pain between the self-gripping and standard mesh (risk ratio, RR 1.10, 95% confidence interval, CI 0.83-1.46). There were no significant differences in recurrence rates (RR 1.13, CI 0.84-2.04). The mean operating time was significantly shorted in the ProGrip™ mesh group (MD - 7.32 min, CI - 10.21 to - 4.44). Trial sequential analysis suggests findings are conclusive.

CONCLUSION:

This meta-analysis has confirmed no benefit of a ProGrip™ mesh when compared to a standard sutured mesh for open inguinal hernia repair in terms of chronic pain or recurrence. No further trials are required to address this clinical question.
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Full text: 1 Collection: 01-internacional Health context: 1_ASSA2030 / 2_ODS3 Database: MEDLINE Main subject: Hernia, Inguinal Type of study: Clinical_trials / Etiology_studies / Guideline / Systematic_reviews Limits: Humans Language: En Journal: Surg Endosc Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 1_ASSA2030 / 2_ODS3 Database: MEDLINE Main subject: Hernia, Inguinal Type of study: Clinical_trials / Etiology_studies / Guideline / Systematic_reviews Limits: Humans Language: En Journal: Surg Endosc Year: 2021 Document type: Article