Department of Orthopedic Surgery, NYU Langone Health, New York, NY.
Department of Orthopedic Surgery, Brigham and Women's Hospital, Boston, MA.
J Arthroplasty. 2020 Aug;35(8):2182-2187. doi: 10.1016/j.arth.2020.03.040. Epub 2020 Mar 30.
Currently, there is no established universal standard of care for prophylaxis against venous thromboembolism (VTE) in orthopedic patients undergoing revision total hip arthroplasty (rTHA). The aim of this study is to determine whether a protocol of 81-mg aspirin (ASA) bis in die (BID) is safe and/or effective in preventing VTE in patients undergoing rTHAs vs 325-mg ASA BID.
In 2017, a large academic medical center adopted a new protocol for VTE prophylaxis in arthroplasty patients at standard risk. Initially, patients received 325-mg ASA BID but switched to 81-mg ASA BID. A retrospective review (2011-2019) was performed to identify 1361 consecutive rTHA patients and their associated 90-day postoperative complications such as VTE, including pulmonary embolism (PE) and/or deep vein thrombosis (DVT), as the primary outcome; and gastrointestinal and wound bleeding, acute periprosthetic joint infection, and mortality as the secondary outcome.
From 2011 to 2017, 973 rTHAs were performed and 13 total VTE cases were diagnosed (1.34%). From 2017 to 2019, 388 rTHAs were performed with 3 total VTE cases identified (0.77%). Chi-squared analyses and logistic regression models showed no differences in rates or odds in postoperative PE (P = .09), DVT (P = .79), PE and DVT (P = .85), and total VTE (P = .38) using either dose. There were also no differences between bleeding complications (P = .14), infection rate (P = .46), and mortality (P = .53).
Using a protocol of 81-mg of ASA BID is noninferior to 325-mg ASA BID and may be safe and effective in maintaining low rates of VTE in patients undergoing rTHA.
目前,对于接受翻修全髋关节置换术(rTHA)的骨科患者,尚无预防静脉血栓栓塞症(VTE)的既定通用标准护理。本研究旨在确定 81mg 阿司匹林(ASA)每日两次(BID)方案在预防 rTHA 患者 VTE 方面是否安全和/或有效,与 325mg ASA BID 相比。
2017 年,一家大型学术医疗中心为标准风险的关节置换术患者采用了一种新的 VTE 预防方案。最初,患者接受 325mg ASA BID,但改为 81mg ASA BID。进行了回顾性研究(2011-2019 年),以确定 1361 例连续 rTHA 患者及其相关的 90 天术后并发症,如 VTE,包括肺栓塞(PE)和/或深静脉血栓形成(DVT),作为主要结局;胃肠道和伤口出血、急性假体周围关节感染和死亡率作为次要结局。
2011 年至 2017 年,共进行了 973 例 rTHA,诊断出 13 例总 VTE 病例(1.34%)。2017 年至 2019 年,共进行了 388 例 rTHA,发现 3 例总 VTE 病例(0.77%)。卡方分析和逻辑回归模型显示,术后 PE(P=0.09)、DVT(P=0.79)、PE 和 DVT(P=0.85)以及总 VTE(P=0.38)的发生率或比值无差异。出血并发症(P=0.14)、感染率(P=0.46)和死亡率(P=0.53)之间也无差异。
使用 81mg ASA BID 方案不劣于 325mg ASA BID,并且可能在维持 rTHA 患者低 VTE 发生率方面是安全有效的。