This is a prospective, open-label, non-randomized interventional feasibility study with a nested qualitative analysis. The study exploratively verifies the feasibility of targeted prophylactic closed incision negative pressure wound therapy (ciNPWT) in clinical practice for patients with a high predicted risk of wound healing complications and compares the 30-day incidence of postoperative complications with standard dressing.
Participants will:
* Get ciNPWT or standard dressing after planned laparotomy
* Answer the questionairs about qualite of life
* Will visit the clinic 30 days after surgery to see the final result