• Annals of surgery · Sep 2024

    Prophylactic Mesh-related Reoperations and Mesh-related Problems During Subsequent Relaparotomies: Long-term Results From the PRIMA Trial.

    • Rudolf van den Berg, van den DopL MatthijsLMDepartment of Surgery, Erasmus University Medical Centre, Rotterdam, The Netherlands., Lucas Timmermans, Michiel van den Berg, PierikRobert E G J MREGJMDepartment of Surgery, Isala Clinic, Zwolle, The Netherlands., Willem A R Zwaans, Daniel Reim, Steven E Buijk, Jerome P van Brussel, Johan F Lange, Johannes J Jeekel, and Pieter J Tanis.
    • Department of Surgery, Erasmus University Medical Centre, Rotterdam, The Netherlands.
    • Ann. Surg. 2024 Sep 6.

    ObjectiveThis study aimed to evaluate all mesh-related problems during reoperations after mesh-reinforcement 15 years after the start of the PRIMA trial. SUMMARY BACKGROUND DATA Prophylactic mesh reinforcement during closure of a midline laparotomy has proven to reduce the incidence of incisional hernia, especially in high-risk patients, but long-term mesh-related morbidity is largely unknown.MethodsPatients receiving a prophylactic onlay or retro-rectus mesh in the PRIMA trial between 2009 and 2012 were included on an as-treated basis from participating centers that made reoperation notes available. Main outcomes were the incidences of complications requiring mesh explantation, mesh-related ileus, and mesh-related problems during laparotomy for other diagnoses.MethodsOut of 373 patients randomized to prophylactic mesh reinforcement, 242 were included: 127 with onlay and 115 patients with retrorectus mesh. Median follow-up is 27 months (IQR 12-78). Thirty-four patients underwent reoperation for any reason during entire follow-up, 22 after onlay (17.3%) and 12 after retrorectus mesh (10.4%). Reoperation rate for complications that required mesh explantation was 4/127 (3.1%) after onlay and 0/115 (0%) after retrorectus mesh. Mesh-related ileus occurred in none of the onlay group, and 3/115 (2.6%) in the retrorectus group. During subsequent laparotomies for other primary diagnoses, adhesions to the mesh were noted in 3/10 patients in the onlay group and 1/5 patients in the retro-rectus group. Overall, the mesh was removed in 10/127 (7.9%) in the onlay group and 7/115 (6.1%) patients in the retro-rectus group.ConclusionsIn high-risk patients receiving a prophylactic mesh during midline laparotomy closure, low incidences of mesh-related complications requiring reoperation and mesh-related problems during unrelated subsequent laparotomies were found, for both the onlay and retrorectus techniques.Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

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