Department of Orthopedic Surgery, NYU Langone Health , New York , NY.
J Bone Joint Surg Am. 2021 May 19;103(10):900-904. doi: 10.2106/JBJS.20.01226.
Tranexamic acid (TXA) is increasingly used to minimize blood loss during total joint arthroplasty (TJA). Although TXA has been shown to be highly effective in reducing operative blood loss, many surgeons believe that it places patients with coronary artery disease (CAD) or a history of coronary stents at an increased risk for myocardial infarction. The purpose of this study was to determine if TXA is safe to use in patients with a history of CAD or coronary stents.
We performed a retrospective analysis at a single, tertiary academic medical center identifying consecutive total hip and knee arthroplasty cases over an 8-year period. From this cohort who received TXA intraoperatively, we identified patients with a history of CAD or coronary stents and determined the total myocardial infarction and venous thromboembolism (VTE) rates within a 90-day postoperative period. Chi-square analyses were used to identify differences in VTE rates between cohorts. A post hoc power analysis was also performed to determine whether our results were powered to detect a difference in VTE rates.
In the 26,808 identified at-risk patients, there were no postoperative myocardial infarctions. No significant differences were observed for VTE rates compared with the control cohort using either topical or intravenous TXA, with regard to CAD (0.29% compared with 0.76%; p = 0.09) or coronary stents (0% compared with 0.76%; p = 0.14). Moreover, there was no significant difference observed in VTE rates when administration was subcategorized into intravenous and topical methods with regard to CAD (0.13% compared with 0.72%; p = 0.12) or coronary stents (0% compared with 0%; p = 1.0).
In our series, topical and intravenous TXA were equally safe when used in patients with a history of CAD and coronary stents in comparison with the control cohort. With equal efficacy and risk of adverse events, we recommend intravenous TXA, which may enable easier institutional implementation.
Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.
氨甲环酸(TXA)在全关节置换术中(TJA)越来越多地被用于减少失血。尽管 TXA 已被证明在减少手术失血量方面非常有效,但许多外科医生认为,它会使患有冠状动脉疾病(CAD)或冠状动脉支架史的患者心肌梗死的风险增加。本研究的目的是确定 TXA 是否可安全用于患有 CAD 或冠状动脉支架史的患者。
我们在一家单一的三级学术医疗中心进行了回顾性分析,确定了 8 年内连续接受全髋关节和膝关节置换术的病例。从接受术中 TXA 的队列中,我们确定了有 CAD 或冠状动脉支架史的患者,并确定了术后 90 天内的总心肌梗死和静脉血栓栓塞(VTE)发生率。卡方分析用于确定队列之间 VTE 发生率的差异。还进行了事后功效分析,以确定我们的结果是否有能力检测 VTE 发生率的差异。
在 26808 名确定有风险的患者中,无术后心肌梗死。与对照组相比,使用局部或静脉 TXA 的 CAD(0.29%比 0.76%;p=0.09)或冠状动脉支架(0%比 0.76%;p=0.14)的 VTE 发生率无显著差异。此外,在 CAD 方面(0.13%比 0.72%;p=0.12)或冠状动脉支架(0%比 0%;p=1.0)方面,根据静脉和局部给药将给药方式细分为亚类时,VTE 发生率也无显著差异。
在我们的系列中,与对照组相比,局部和静脉 TXA 在有 CAD 和冠状动脉支架史的患者中使用时同样安全。鉴于疗效和不良事件风险相等,我们建议使用静脉 TXA,这可能使机构更容易实施。
治疗性 III 级。请参阅作者说明,以获取完整的证据水平描述。