Aziz Joseph, Wang Tzu-Fei, Siegal Deborah, Douketis James, Le Gal Grégoire, Carrier Marc, Shaw Joseph R
Department of Medicine, University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, Canada.
Department of Medicine, McMaster University, Hamilton, ON, Canada.
J Thromb Haemost. 2023 Apr;21(4):933-943. doi: 10.1016/j.jtha.2022.12.016. Epub 2022 Dec 27.
Patients with cancer are at an increased risk of developing atrial fibrillation (AF) and often need to undergo procedures or surgery that requires periprocedural interruption of anticoagulation. Anticoagulated patients with cancer might be at increased risk of postprocedural thromboembolic and bleeding complications. Data on postprocedural outcomes among patients with concurrent active cancer and AF are sparse.
To assess the 30-day risk of postoperative thromboembolic and major bleeding complications after the periprocedural interruption of anticoagulation among patients with AF and active cancer.
We conducted a single-center retrospective cohort study in patients with active cancer and AF who required periprocedural interruption of anticoagulation for invasive procedures between August 2015 and May 2019. The primary endpoints were the 30-day postoperative risks of arterial thromboembolism (ATE) and major bleeding. The secondary endpoints included the 30-day risks of venous thromboembolism, clinically relevant nonmajor bleeding, and overall mortality.
Two hundred sixty-four patients undergoing 302 periprocedural interruptions were included in our study. The 30-day risk of ATE was 0.7% (95% CI, 0.1%-2.4%), and the 30-day risk of major bleeding was 1.7% (95% CI, 0.6%-3.9%). The 30-day risks of venous thromboembolism and clinically relevant nonmajor bleeding were 0.7% (95% CI, 0.1%-2.4%) and 4.3% (95% CI, 2.5%-7.3%), respectively. The overall risk of mortality at 30 days was 1.3% (95% CI, 0.4%-3.4%). There was one fatal postoperative stroke.
Patients with AF and active cancer in this study were at relatively low risk for ATE and postoperative bleeding complications when patients were managed according to commonly applied perioperative management recommendations.
癌症患者发生心房颤动(AF)的风险增加,且常常需要接受手术或操作,而这些手术或操作需要在围手术期中断抗凝治疗。接受抗凝治疗的癌症患者术后发生血栓栓塞和出血并发症的风险可能会增加。关于同时患有活动性癌症和房颤的患者术后结局的数据较为稀少。
评估房颤合并活动性癌症患者在围手术期抗凝治疗中断后30天内发生术后血栓栓塞和大出血并发症的风险。
我们对2015年8月至2019年5月期间因侵入性操作需要在围手术期中断抗凝治疗的活动性癌症合并房颤患者进行了一项单中心回顾性队列研究。主要终点是术后30天内发生动脉血栓栓塞(ATE)和大出血的风险。次要终点包括术后30天内发生静脉血栓栓塞、临床相关非大出血和全因死亡率的风险。
我们的研究纳入了264例接受302次围手术期抗凝治疗中断的患者。术后30天发生ATE的风险为0.7%(95%CI,0.1%-2.4%),大出血风险为1.7%(95%CI,0.6%-3.9%)。术后30天发生静脉血栓栓塞和临床相关非大出血的风险分别为0.7%(95%CI,0.1%-2.4%)和4.3%(95%CI,2.5%-7.3%)。30天全因死亡风险为1.3%(95%CI,0.4%-3.4%)。术后发生了1例致命性卒中。
在本研究中,按照常用的围手术期管理建议对房颤合并活动性癌症患者进行管理时,其发生ATE和术后出血并发症的风险相对较低。