Mesh versus acellular dermal matrix in immediate implant-based breast reconstruction – A prospective randomized trial

Abstract Background Comparative studies on the use of meshes and acellular dermal matrices (ADM) in implant-based breast reconstruction (IBBR) have not yet been performed. Methods This prospective, randomized, controlled, multicenter pilot study was performed at four Austrian breast cancer centers. Fifty patients with oncologic or prophylactic indication for mastectomy and IBBR were randomized to immediate IBBR with either an ADM (Protexa ® ) or a titanized mesh (TiLOOP ® Bra). Complications, failed reconstruction, cosmetic outcome, patients' quality of life and the thickness of the overlying tissue were recorded immediately postoperatively and 3 and 6 months after surgery. Results 48 patients participated in the study (Protexa ® group: 23; TiLOOP ® Bra group: 25 patients). The overall complication rate was 31.25% with similar rates in both groups (Protexa ® group: 9 versus TiLOOP ® Bra group: 6; p = 0.188). There was a higher incidence of severe complications leading to failed reconstructions with implant loss in the Protexa ® group than in the TiLOOP ® Bra group (7 versus 2; p  ® (p = 0.037, p = 0.012, respectively). There were no significant differences in patients' satisfaction with cosmetic results (p = 0.632), but surgeons and external specialists graded significantly better outcomes with TiLOOP ® Bra (p = 0.034, p = 0.032). Conclusion This pilot study showed use of TiLOOP ® Bra or Protexa ® in IBBR is feasible leading to good cosmetic outcomes and high patient satisfaction. To validate the higher failure rates in the Protexa ® group, data from a larger trial are required. NCT02562170