Suppr超能文献

全膝关节置换术治疗慢性血友病性关节病。

Total knee arthroplasty for the treatment of chronic hemophilic arthropathy.

作者信息

Figgie M P, Goldberg V M, Figgie H E, Heiple K G, Sobel M

机构信息

Hospital for Special Surgery, New York, NY 10021.

出版信息

Clin Orthop Relat Res. 1989 Nov(248):98-107.

PMID:2805504
Abstract

Total knee arthroplasty (TKA) for hemophilic (factor VIII deficiency) arthropathy is a complex and demanding procedure with a high complication rate. However, the long-term benefits have not previously been reported. This study reviews 19 TKAs performed for hemophilic arthropathy that were followed for a minimum of 5.5 years and an average of 9.5 years. At present, 13 knees have good or excellent results, and six knees rate as poor or failures. Those patients with excellent results have maintained good pain relief and function. Four of the six failures were among the first seven arthroplasties performed, when only 80% factor VIII coverage was used during the perioperative period. Since the use of 100% factor VIII coverage was instituted, the failure rate has declined. Ten of the 19 knees suffered complications, including one deep infection, six superficial skin necroses, three nerve palsies, seven postoperative bleedings, and one transfusion reaction. Six of the seven knees operated on under 80% factor VIII coverage had complications. Once 100% factor VIII coverage was instituted, the only complications included one skin necrosis and three postoperative bleedings. The roentgenographic failure rate has remained high with progressive roentgenographic lucencies in 13 of 19 tibial components, associated with component shift in three knees. While these roentgenographic findings have not necessarily correlated with clinical results, they are disturbing and may portend future failures. However, pain relief and improved function are maintained at longer follow-up times. The best results were obtained under 100% factor VIII coverage using a posterior stabilized prosthesis and patellar resurfacing.

摘要

全膝关节置换术(TKA)用于治疗血友病性(因子VIII缺乏)关节病是一项复杂且要求高的手术,并发症发生率高。然而,此前尚未报道其长期益处。本研究回顾了19例因血友病性关节病而进行的全膝关节置换术,随访时间至少为5.5年,平均为9.5年。目前,13个膝关节效果良好或极佳,6个膝关节效果较差或置换失败。那些效果极佳的患者疼痛得到了很好的缓解,功能良好。6例失败病例中有4例出现在最初进行的7例关节置换术中,当时围手术期仅使用了80%的因子VIII覆盖。自从采用100%因子VIII覆盖后,失败率有所下降。19个膝关节中有10个出现并发症,包括1例深部感染、6例浅表皮肤坏死、3例神经麻痹、7例术后出血和1例输血反应。7例在因子VIII覆盖低于80%情况下进行手术的膝关节中有6例出现并发症。一旦采用100%因子VIII覆盖,仅出现1例皮肤坏死和3例术后出血并发症。X线片显示失败率仍然很高,19个胫骨假体中有13个出现进行性X线透亮区,3个膝关节出现假体移位。虽然这些X线表现不一定与临床结果相关,但令人不安,可能预示着未来会失败。然而,在更长的随访时间内疼痛缓解和功能改善得以维持。使用后稳定型假体和髌骨表面置换,在100%因子VIII覆盖下可获得最佳效果。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验