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Use of Inguinal Hernia Mesh (Dynamesh-Endolap) in Immediate Implant-Based Breast Reconstruction Publisher Pubmed



Omranipour R1, 2 ; Mohammadizavieh M1, 3 ; Alipour S1, 3
Authors
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Authors Affiliations
  1. 1. Breast Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Surgical Oncology, Cancer Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Surgery, Arash Women’s Hospital, Tehran University of Medical Sciences, Tehran, Iran

Source: Aesthetic Plastic Surgery Published:2022


Abstract

Introduction: The rate of immediate implant-based breast reconstruction after mastectomy is increasing, and providing enough coverage for the implant is mandatory; however the choice of appropriate mesh for implant coverage is controversial. Considering the high cost and the limited availability of breast-dedicated meshes in our country, we conducted this study to investigate the consequences of using a polyvinylidene fluoride (PVDF) mesh designed for endoscopic and laparoscopic hernia repair (ENDOLAP) as a coverage for breast prostheses in breast reconstruction. Materials and Methods: A retrospective cross-sectional study was performed on data of patients who had underwent immediate implant-based breast reconstruction between 2012 and 2019. After skin sparing mastectomy and subpectoral implant insertion, the exposed lower and lateral parts were covered with the mesh. Results: Seventy-nine reconstructions were performed on 62 patients. The average follow-up was 31.9 months (ranges 6–102 months). Postoperative complications including small flap necrosis (3.8%), seroma (8.9%), infection (5.1%), hematoma (3.8%), malposition (1.3%), rippling (1.3%), grade two and three capsular contracture (2.5%), and chronic pain (1.3%) occurred in 19% of the operated breasts. The complication rate requiring intervention was 5.3%, and no implant loss was observed. None of the patients who received radiation developed complications. Conclusion: ENDOLAP mesh is a cost-effective and safe option for implant coverage in immediate implant-based breast reconstruction, with an acceptable complication rate. Level of evidence III: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266. © 2021, Springer Science+Business Media, LLC, part of Springer Nature and International Society of Aesthetic Plastic Surgery.