Department of Cardiology, The Key Laboratory of Cardiovascular Disease of Wenzhou (D.L., Q.L., Q.Z., X.Z., Y.F., L.W., G.X., W.H., P.S.), the First Affiliated Hospital of Wenzhou Medical University, Zhejiang, China.
NAFLD Research Center, Department of Hepatology (K.I.Z.), the First Affiliated Hospital of Wenzhou Medical University, Zhejiang, China.
Circ Cardiovasc Interv. 2022 Apr;15(4):e011555. doi: 10.1161/CIRCINTERVENTIONS.121.011555. Epub 2022 Mar 23.
Adequate procedural anticoagulation is crucial for radial artery occlusion (RAO) prevention in patients undergoing transradial access coronary catheterization, although the effect of postprocedural anticoagulation lack thorough investigation. The aim of this study was to evaluate the clinical value of short-term postoperative anticoagulation with rivaroxaban for 24 hours and 1-month RAO prevention in patients who received transradial coronary procedures.
A total of 382 patients were randomized to receive either placebo (control group) or rivaroxaban 10 mg once daily for a period of 7 days (rivaroxaban group) to evaluate the effect of the rivaroxaban in the prevention of 24 hours and 1-month RAO assessed by Doppler ultrasound.
There was no significant difference in the incidence of 24-hour RAO (8.9% versus 11.5%; =0.398) between the rivaroxaban group and control group (odds ratio, 0.75 [95% CI, 0.39-1.46]; =0.399). In contrast, the 1-month RAO (3.8% versus 11.5%; =0.011) was significantly reduced in patients who received rivaroxaban as compared with those who did placebo (odds ratio, 0.22 [95% CI, 0.08-0.65]; =0.006). For patients with 24-hour RAO, the rivaroxaban group was associated with higher recanalization rate of the radial artery (69.2% versus 30.0%; =0.027) compared with the control group. No significant differences can be observed between the 2 groups for access-site complications or bleeding events.
Short-term postoperative anticoagulation with rivaroxaban did not reduce the rate of 24-hour RAO but improved 1-month RAO, because of higher recanalization of the radial artery. However, larger clinical trials are needed to prove our results.
URL: https://www.chictr.org.cn; Unique identifier: ChiCTR1900026974.
经桡动脉入路行冠状动脉介入治疗时,充分的抗凝是预防桡动脉闭塞(RAO)的关键,但术后抗凝的效果仍需深入研究。本研究旨在评估经桡动脉入路行冠状动脉介入治疗后短期应用利伐沙班抗凝 24 小时和 1 个月对预防 RAO 的临床价值。
共 382 例患者随机分为安慰剂(对照组)或利伐沙班 10 mg 每日 1 次治疗 7 天(利伐沙班组),通过多普勒超声评估利伐沙班对 24 小时和 1 个月 RAO 的预防效果。
利伐沙班组和对照组 24 小时 RAO 发生率分别为 8.9%和 11.5%(=0.398),差异无统计学意义(比值比,0.75[95%CI,0.391.46];=0.399)。相反,与对照组相比,利伐沙班组患者 1 个月 RAO 发生率(3.8%与 11.5%;=0.011)显著降低(比值比,0.22[95%CI,0.080.65];=0.006)。对于 24 小时 RAO 患者,利伐沙班组桡动脉再通率高于对照组(69.2%与 30.0%;=0.027)。两组患者的血管入路并发症或出血事件发生率无显著差异。
经桡动脉入路行冠状动脉介入治疗后短期应用利伐沙班不能降低 24 小时 RAO 发生率,但可改善 1 个月 RAO,因为桡动脉再通率更高。然而,还需要更大规模的临床试验来证实我们的结果。