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Prophylactic slowly resorbable mesh in midline laparotomy to limit incisional hernia incidence: the prospective 'Mesh Augmented Reinforcement of Abdominal Wall Suture Line (MARS)' cohort study protocol.
Van Den Dop, Louis Matthijs; Molina-Villar, Jose M; Mäkäräinen, Elisa; Torkington, Jared; Weyhe, Dirk; Koncar, Igor; Lange, Johan F.
Afiliación
  • Van Den Dop LM; Department of Surgery, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Molina-Villar JM; Department of Surgery, Hospital Universitario Ramon y Cajal, Madrid, Spain.
  • Mäkäräinen E; Department of Surgery, Oulu University Hospital, Medical Research Center Oulu, Oulu, Finland.
  • Torkington J; Department of Surgery, Cardiff and Vale University Health Board, University of Wales, Cardiff, Wales.
  • Weyhe D; Department of Surgery, University Hospital for Visceral Surgery, Department of Human Medicine, Carl von Ossietzky University Oldenburg, Oldenburg, Germany.
  • Koncar I; Department of Surgery, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
  • Lange JF; Department of Surgery, Erasmus University Medical Center, Rotterdam, The Netherlands.
Int J Surg Protoc ; 28(2): 58-63, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38854712
ABSTRACT

Background:

Incisional hernia (IH) after abdominal surgery is a frequent surgical complication. Risk factors associated with IH are midline incisions, patients with an abdominal aneurysm of the aorta, and high BMI. Preventive measures include the use of the small-bites suture technique and/or placing a prophylactic mesh for reinforcement of the midline closure. Although recommended for high-risk patients, many surgeons are still reluctant to place a prophylactic mesh due to related complications. To counter these concerns, new synthetic resorbable meshes are being developed, such as the Deternia Self-Gripping Resorbable Mesh ("investigational device"). However, the effectiveness of this mesh in IH prevention has not been proved.

Methods:

The Mesh Augmented Reinforcement of Abdominal Wall Suture Line (MARS) study is a European, multicentre, prospective, single-arm study. A total of 120 patients scheduled for elective midline laparotomy, and for that reason at risk of developing IH, will be recruited in ~12 sites after informed consent. The sample size was estimated based on greater than 80% power, two-sided alpha of 0.05, an expected 12 month IH rate of 8% and a predefined performance goal of 18% (10% clinical margin). Midline incisions will be closed by the small bites closure technique with a minimum 41 suture-to-wound length ratio and reinforced by mesh placement in the retrorectus position. The primary outcome will be IH occurrence at 12-month postoperatively, evaluated both clinically and by ultrasound. Secondary outcomes will include mesh-related and postoperative complications, surgical characteristics, IH incidence at 2 and 3 years after surgery, and quality of life.

Discussion:

Currently, no conclusive evidence is available for synthetic resorbable meshes in a prophylactic setting to prevent IH. The MARS study will be the first prospective cohort study to investigate resorbable synthetic meshes and small bites closure to reduce IH incidence.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Int J Surg Protoc Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Int J Surg Protoc Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos