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Prophylactic, Synthetic Intraperitoneal Mesh Versus No Mesh Implantation in Patients with Fascial Dehiscence.
Jakob, Manuel O; Spari, Daniel; Zindel, Joel; Pinworasarn, Tawan; Candinas, Daniel; Beldi, Guido.
Afiliação
  • Jakob MO; Department of Visceral Surgery and Medicine, Bern University Hospital, Bern, Switzerland.
  • Spari D; Department of Visceral Surgery and Medicine, Bern University Hospital, Bern, Switzerland.
  • Zindel J; Department of Visceral Surgery and Medicine, Bern University Hospital, Bern, Switzerland.
  • Pinworasarn T; Department of Visceral Surgery and Medicine, Bern University Hospital, Bern, Switzerland.
  • Candinas D; Department of Visceral Surgery and Medicine, Bern University Hospital, Bern, Switzerland.
  • Beldi G; Department of Visceral Surgery and Medicine, Bern University Hospital, Bern, Switzerland. guido.beldi@insel.ch.
J Gastrointest Surg ; 22(12): 2158-2166, 2018 12.
Article em En | MEDLINE | ID: mdl-30039450
ABSTRACT

BACKGROUND:

Primary closure of post-operative facial dehiscence (FD) is associated with a high incidence of recurrence, revisional surgery, and incisional hernia. This retrospective study compares outcomes of implantation of non-absorbable intra-abdominal meshes with primary closure of FD. The outcomes of different mesh materials were assessed in subgroup analysis.

METHODS:

A total of 119 consecutive patients with FD were operated (70 mesh group and 49 no mesh group) between 2001 and 2015. Primary outcome parameter was hernia-free survival. Secondary outcome parameters include re-operations of the abdominal wall, intestinal fistula, surgical site infections (SSI), and mortality. Kaplan-Meier analysis for hernia-free survival, adjusted Poisson regression analysis for re-operations and adjusted regression analysis for chronic SSI was performed.

RESULTS:

Hernia-free survival was significantly higher in the mesh group compared to the no mesh group (P = 0.005). Fewer re-operations were necessary in the mesh group compared to the no mesh group (adjusted incidence risk ratio 0.44, 95% confidence interval [CI] 0.20-0.93, P = 0.032). No difference in SSI, intestinal fistula, and mortality was observed between groups. Chronic SSI was observed in 7 (10%) patients in the mesh group (n = 3 [6.7%] with polypropylene mesh and 4 [28.6%] with polyester mesh). The risk for chronic SSI was significantly higher if a polyester mesh was used when compared to a polypropylene mesh (adjusted odds ratio 8.69, 95% CI 1.30-58.05, P = 0.026).

CONCLUSION:

Implantation of a polypropylene but not polyester-based mesh in patients with FD decreases incisional hernia with a low rate of mesh-related morbidity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Telas Cirúrgicas / Deiscência da Ferida Operatória / Implantação de Prótese / Hérnia Incisional / Hérnia Ventral Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Telas Cirúrgicas / Deiscência da Ferida Operatória / Implantação de Prótese / Hérnia Incisional / Hérnia Ventral Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article