E Rubens, F VAN Glabbeek, J G DE Man, G Peersman, B Y DE Winter, G Hubens, J Michielsen, P Plaeke
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Subsequently, articles reporting the effects of a preventive pharmacological intervention against arthrofibrosis were included in this review.</p><p><strong>Results: </strong>16 studies investigated the pharmacological prevention of arthrofibrosis of which 13 were conducted in animal models. Several drugs improved the range of motion (ROM) in animal models. Bevacizumab (ROM +39.4 degrees), nonsteroidal anti-inflammatory drugs (ROM +18.0-31.2 degrees), and rosiglitazone (ROM +19.5 degrees) significantly increased the ROM. Artesunate, mitomycin c, bevacizumab, hyaloglide, and botulinum toxin A significantly reduced adhesion scores. None of the drugs tested in humans improved the functional outcomes after joint arthroplasty. Methodological differences limited the ability to compare outcomes and, due to poor reporting of methodology, many studies had an unclear risk of bias.</p><p><strong>Conclusion: </strong>This review identified several drugs as potential candidates for arthrofibrosis prevention. These drugs modulate inflammation or alter the activity of fibroblasts. Most studies are conducted in experimental animal models and none of these results are currently translated into a clinical application. Moreover, the methodology and route of administration varied between studies. Nor were dose dependency studies conducted. Future studies should adopt a standardized approach to determine the effects of preventive pharmacological interventions on arthrofibrosis.</p>","PeriodicalId":7018,"journal":{"name":"Acta orthopaedica Belgica","volume":"90 2","pages":"311-318"},"PeriodicalIF":0.5000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pharmacological prevention of arthrofibrosis: a systematic review.\",\"authors\":\"E Rubens, F VAN Glabbeek, J G DE Man, G Peersman, B Y DE Winter, G Hubens, J Michielsen, P Plaeke\",\"doi\":\"10.52628/90.2.10815\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and aims: </strong>Arthrofibrosis is a complication of intra-articular knee surgery which is caused by intra-articular fibrosis. To date, several preventive therapies for arthrofibrosis have been reported. 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引用次数: 0
摘要
背景和目的:关节纤维化是膝关节内手术的一种并发症,由关节内纤维化引起。迄今为止,已有多种预防关节纤维化的疗法被报道。本系统综述旨在总结目前有关药物预防关节纤维化的知识:方法:以 "关节纤维化和预防 "为检索词,在 Medline、Web of Science 和 Cochrane 图书馆进行了系统性文献检索。结果:16 项研究调查了药物预防关节纤维化的效果:结果:16 项研究对药物预防关节纤维化进行了调查,其中 13 项在动物模型中进行。有几种药物改善了动物模型的活动范围(ROM)。贝伐单抗(ROM +39.4度)、非甾体类抗炎药(ROM +18.0-31.2度)和罗格列酮(ROM +19.5度)能显著增加关节活动度。青蒿琥酯、丝裂霉素 c、贝伐珠单抗、hyaloglide 和肉毒杆菌毒素 A 能明显降低粘连评分。在人体中测试的药物均未改善关节置换术后的功能效果。研究方法上的差异限制了对结果进行比较的能力,而且由于方法报告不完善,许多研究的偏倚风险不明确:本综述确定了几种可用于预防关节纤维化的药物。这些药物可调节炎症或改变成纤维细胞的活性。大多数研究都是在实验性动物模型中进行的,目前还没有一项研究成果能应用于临床。此外,不同研究的方法和给药途径各不相同。也没有进行剂量依赖性研究。未来的研究应采用标准化的方法来确定预防性药物干预对关节纤维化的影响。
Pharmacological prevention of arthrofibrosis: a systematic review.
Background and aims: Arthrofibrosis is a complication of intra-articular knee surgery which is caused by intra-articular fibrosis. To date, several preventive therapies for arthrofibrosis have been reported. This systematic review aims to summarize current knowledge about pharmacological arthrofibrosis prevention.
Methods: A systematic literature search was conducted in Medline, Web of Science, and Cochrane library using the search term 'Arthrofibrosis AND prevention'. Subsequently, articles reporting the effects of a preventive pharmacological intervention against arthrofibrosis were included in this review.
Results: 16 studies investigated the pharmacological prevention of arthrofibrosis of which 13 were conducted in animal models. Several drugs improved the range of motion (ROM) in animal models. Bevacizumab (ROM +39.4 degrees), nonsteroidal anti-inflammatory drugs (ROM +18.0-31.2 degrees), and rosiglitazone (ROM +19.5 degrees) significantly increased the ROM. Artesunate, mitomycin c, bevacizumab, hyaloglide, and botulinum toxin A significantly reduced adhesion scores. None of the drugs tested in humans improved the functional outcomes after joint arthroplasty. Methodological differences limited the ability to compare outcomes and, due to poor reporting of methodology, many studies had an unclear risk of bias.
Conclusion: This review identified several drugs as potential candidates for arthrofibrosis prevention. These drugs modulate inflammation or alter the activity of fibroblasts. Most studies are conducted in experimental animal models and none of these results are currently translated into a clinical application. Moreover, the methodology and route of administration varied between studies. Nor were dose dependency studies conducted. Future studies should adopt a standardized approach to determine the effects of preventive pharmacological interventions on arthrofibrosis.