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Closed-wound negative pressure therapy dressing after loop ostomy closure: a retrospective comparative study.
Curchod, P; Clerc, D; Jurt, J; Hubner, M; Hahnloser, D; Demartines, N; Grass, F.
Afiliación
  • Curchod P; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse.
  • Clerc D; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse.
  • Jurt J; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse.
  • Hubner M; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse. Martin.hubner@chuv.ch.
  • Hahnloser D; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse.
  • Demartines N; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse.
  • Grass F; Department of Visceral Surgery, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 26, Rue du Bugnon, 1010, Lausanne, Suisse.
Sci Rep ; 12(1): 7790, 2022 05 12.
Article en En | MEDLINE | ID: mdl-35550575
ABSTRACT
Closed-wound negative pressure wound therapy (NPWT) dressings were recently introduced with the purpose to reduce incisional surgical site infections (iSSI) in high-risk wounds. The aim of this study was to compare iSSI rates in patients after ostomy closure with and without additional application of a closed-wound NPWT dressing. Single-center retrospective analysis of consecutive patients undergoing ileo- or colostomy closure over an 8-year period (January 2013-January 2021). Intradermal non-purse string technique with absorbable sutures were used in all patients. Since November 2018, all patients (study group) received a NPWT device for a maximum of 5 days postoperatively (PICO, SMITH AND NEPHEW). Primary outcome was iSSI rate within 30 days of surgery. SSI was defined in accordance with the Center of Disease Control (CDC) classification and included superficial and deep incisional SSI. Data was retrieved from the institutional enhanced recovery after surgery (ERAS) database, with standardized complication assessment by trained abstractors. In total, 85 patients (25%) in the study group were comparable with 252 (75%) patients in the control group regarding demographics (age, gender, body mass index, ASA score), ostomy type and anastomotic technique (all p > 0.05), but not wound contamination class (class III 5% vs 0%, p < 0.001). Median time to NPWT removal was 4 (IQR 3-5) days. Incisional SSI were observed in 4 patients (4.7%) in the study group and in 27 patients (10.7%) in the control group (p = 0.097). These preliminary results suggest a potential benefit of systematic application of the NPWT device after loop ostomy closure. A randomized controlled study is needed.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Estomía / Terapia de Presión Negativa para Heridas Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Estomía / Terapia de Presión Negativa para Heridas Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Suiza