Sutureless fixation with fibrin glue of lightweight mesh in open inguinal hernia repair: Effect on postoperative pain: A double-blind, randomized trial versus standard heavyweight mesh

Background Open inguinal hernia repair is associated with a low incidence of complications that can be influenced by the type of mesh and its method of fixation. Our aim was to investigate the frequency and severity of postoperative pain and other complications when lightweight, large-pore meshes, c...

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Veröffentlicht in:Surgery 2013, Vol.153 (1), p.126-130
Hauptverfasser: Canonico, Silvestro, MD, Benevento, Raffaella, MD, Perna, Giuseppe, MD, Guerniero, Raffaella, MD, Sciaudone, Guido, MD, PhD, Pellino, Gianluca, MD, Santoriello, Antonio, MD, Selvaggi, Francesco, MD, EBSQ
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Sprache:eng
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Zusammenfassung:Background Open inguinal hernia repair is associated with a low incidence of complications that can be influenced by the type of mesh and its method of fixation. Our aim was to investigate the frequency and severity of postoperative pain and other complications when lightweight, large-pore meshes, compared with heavyweight, small-pore meshes, are fixed with human fibrin glue (HFG) during open inguinal hernia repair. Methods A cohort of 80 patients undergoing open inguinal repair were enrolled. Forty patients received a lightweight and large porous mesh and 40 a standard heavyweight mesh with small pores. In all patients, HFG was used for mesh fixation. Results Patients who received lightweight, large-pore mesh reported less pain than those in the control group both postoperatively (2.8 ± 1.1 vs 4.9 ± 1.1; P = .0003) and at 1-month follow-up (1.7 ± 1.0 vs 3.1 ± 1.0; P = .0038), and took fewer analgesics. There was no difference in days off work/activity. No differences were observed concerning postoperative complications. After 6 months there was no difference in groin pain between groups. Conclusion Patients who underwent open inguinal hernia repair with lightweight, large-pore mesh fixed with HFG experienced less pain throughout the first month after operation compared with those receiving standard mesh.
ISSN:0039-6060
1532-7361
DOI:10.1016/j.surg.2012.06.024