Gillinov Stephen M, Burroughs Patrick J, Moore Harold G, Rubin Lee E, Frumberg David B, Grauer Jonathan N
Yale School of Medicine, New Haven, CT.
MedStar Health/Georgetown University Hospital Program, Washington DC.
J Arthroplasty. 2022 Jul;37(7):1333-1337. doi: 10.1016/j.arth.2022.02.107. Epub 2022 Mar 4.
Patients with classic hemophilia can develop joint hemarthroses, degenerative changes, and eventually require total hip arthroplasty (THA). Little data exist concerning THA outcomes in this population, and evidence-based guidelines specifically addressing venous thromboembolism (VTE) prophylaxis in this population are lacking.
A retrospective study was conducted using the 2010-2020 PearlDiver MHip database. Patients undergoing primary THA were identified, and those with classic hemophilia were matched 1:10 with non-hemophilia patients based on age, gender, and Elixhauser Comorbidity Index. Ninety-day serious adverse events, minor adverse events, and any adverse events were compared with multivariate analysis. Reoperation at 5 years was assessed using Kaplan-Meier analysis.
Five hundred eighteen classic hemophilia THA patients were matched 1:10 with 5,193 non-hemophilia patients. On multivariate analysis, those with classic hemophilia had greater odds of aggregated any adverse events (odds ratio [OR] 1.76), serious adverse events (OR 2.30), and minor adverse events (OR 1.52) (P < .001 for each). Patients with classic hemophilia had greater odds of bleeding issues (transfusion, OR 1.98; hematoma, OR 4.23; P < .001 for both), VTE (deep vein thrombosis, OR 2.67; pulmonary embolism, OR 4.01; P < .001 for both), and acute kidney injury (OR 1.63; P = .03). Five-year implant survival was lower in hemophilia patients (91.9%) relative to matched controls (95.3%; P = .009).
Hemophilia patients undergoing THA had elevated risks of both 90-day bleeding complications (transfusion and hematoma) and VTE (deep vein thrombosis and pulmonary embolism) relative to matched controls. These findings emphasize the need to balance factor replacement and VTE prophylaxis. Although the 5-year implant survival was lower in hemophilia patients, this represented a difference of 3.4% at 5 years, suggesting that THA remains effective in this cohort.
典型血友病患者可出现关节积血、退行性改变,最终需要进行全髋关节置换术(THA)。关于该人群全髋关节置换术的结果,现有数据较少,且缺乏专门针对该人群静脉血栓栓塞(VTE)预防的循证指南。
使用2010 - 2020年PearlDiver MHip数据库进行一项回顾性研究。确定接受初次全髋关节置换术的患者,并根据年龄、性别和埃利克斯豪泽合并症指数,将典型血友病患者与非血友病患者按1:10进行匹配。采用多变量分析比较90天严重不良事件、轻微不良事件和任何不良事件。使用Kaplan - Meier分析评估5年时的再次手术情况。
518例典型血友病全髋关节置换术患者与5193例非血友病患者按1:10进行匹配。多变量分析显示,典型血友病患者发生任何不良事件(优势比[OR] 1.76)、严重不良事件(OR 2.30)和轻微不良事件(OR 1.52)的几率更高(每项P < .001)。典型血友病患者发生出血问题(输血,OR 1.98;血肿,OR 4.23;两者P < .001)、VTE(深静脉血栓形成,OR 2.67;肺栓塞,OR 4.01;两者P < .001)和急性肾损伤(OR 1.63;P = .03)的几率更高。血友病患者5年植入物生存率(91.9%)低于匹配对照组(95.3%;P = .009)。
与匹配对照组相比,接受全髋关节置换术的血友病患者90天出血并发症(输血和血肿)和VTE(深静脉血栓形成和肺栓塞)风险升高。这些发现强调了平衡凝血因子替代和VTE预防的必要性。虽然血友病患者5年植入物生存率较低,但5年时差异为3.4%,表明全髋关节置换术在该队列中仍然有效。