Tay Yu Ting, Purcell Elisha, Seth Ishith, Marcaccini Gianluca, Rozen Warren M
Department of Plastic and Reconstructive Surgery, Eastern Health, Melbourne, VIC 3128, Australia.
Faculty of Medicine, Peninsula Clinical School, Monash University, Melbourne, VIC 3199, Australia.
J Pers Med. 2025 Jun 17;15(6):257. doi: 10.3390/jpm15060257.
Fibroproliferative disorders (FPDs), such as Dupuytren's contracture, scleroderma, capsular contracture, rhinophyma, and keloid scars, are characterised by excessive fibroblast activity and collagen deposition. These conditions are frequently encountered in plastic and reconstructive surgery and remain therapeutically challenging. Cyclooxygenase (COX) inhibitors have emerged as a potential adjunct therapy to modulate fibrotic pathways and improve clinical outcomes. This systematic review aims to evaluate the efficacy and safety profile of COX inhibitors in the management of plastic-surgery-related FPDs. In doing so, it explores how phenotype-guided and route-specific COX-inhibitor use may contribute to precision, patient-centred care. To identify eligible studies, a comprehensive search was conducted in MEDLINE, Embase, and the Cochrane Library. Data were synthesised using both tabular summaries and narrative analysis. The certainty of evidence was appraised according to the GRADE guidelines. Thirteen studies from 1984 to 2024 met inclusion criteria, addressing FPDs such as hypertrophic scarring, Dupuytren's contracture, and desmoid tumours, representing 491 patients. Of those, five studies were related to Dupuytren contracture, three studies were related to hypertrophic scar, and one study each was on topics related to scleroderma, keloid scar, osteogenesis imperfecta, actinic keloidalis nuchae/dissecting cellulitis of the scalp, and desmoid tumours. Nine studies reported clinical improvements (four demonstrating statistically significant outcomes), three showed no difference, and one did not assess outcomes. The thirteen studies show minor side effects from oral and topical COX inhibitors. The overall certainty of evidence was graded as "low." COX inhibitors demonstrate promising efficacy with minimal adverse effects in the management of plastic-surgery-related FPDs. Their accessibility, safety, and potential to reduce fibrosis underscore the need for future high-quality, large-scale studies to establish definitive clinical recommendations.
纤维增生性疾病(FPDs),如杜普伊特伦挛缩症、硬皮病、包膜挛缩、酒渣鼻和瘢痕疙瘩,其特征是成纤维细胞活性过高和胶原蛋白沉积。这些病症在整形和重建手术中经常遇到,并且在治疗上仍然具有挑战性。环氧合酶(COX)抑制剂已成为一种潜在的辅助治疗方法,用于调节纤维化途径并改善临床结果。本系统评价旨在评估COX抑制剂在治疗与整形手术相关的FPDs中的疗效和安全性。在此过程中,探讨了如何根据表型指导和特定途径使用COX抑制剂可能有助于实现精准、以患者为中心的护理。为了确定符合条件的研究,我们在MEDLINE、Embase和Cochrane图书馆进行了全面检索。数据使用表格摘要和叙述性分析进行综合。根据GRADE指南评估证据的确定性。1984年至2024年的13项研究符合纳入标准,涉及增生性瘢痕、杜普伊特伦挛缩症和硬纤维瘤等FPDs,共491例患者。其中,5项研究与杜普伊特伦挛缩症相关,3项研究与增生性瘢痕相关,1项研究分别涉及硬皮病、瘢痕疙瘩、成骨不全、颈部光化性瘢痕疙瘩/头皮穿掘性蜂窝织炎和硬纤维瘤。9项研究报告了临床改善情况(4项显示有统计学意义的结果),3项显示无差异,1项未评估结果。这13项研究表明口服和局部使用COX抑制剂有轻微副作用。证据的总体确定性被评为“低”。COX抑制剂在治疗与整形手术相关的FPDs中显示出有前景的疗效且副作用最小。它们的可及性、安全性以及减少纤维化的潜力突出了未来进行高质量、大规模研究以建立明确临床建议的必要性。