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围手术期低分子量肝素治疗对既往冠状动脉支架植入超过12个月的老年患者行非心脏手术临床事件的影响:一项随机、安慰剂对照试验。

Impact of perioperative low-molecular-weight heparin therapy on clinical events of elderly patients with prior coronary stents implanted > 12 months undergoing non-cardiac surgery: a randomized, placebo-controlled trial.

作者信息

Wang Bin, Su Yanhui, Ma Cong, Xu Lining, Mao Qunxia, Cheng Wenjia, Lu Qingming, Zhang Ying, Wang Rong, Lu Yan, He Jing, Chen Shihao, Chen Lei, Li Tianzhi, Gao Linggen

机构信息

Department of Comprehensive Surgery, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese PLA General Hospital, Beijing, 100853, China.

Health Management Institute, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese PLA General Hospital, Beijing, China.

出版信息

BMC Med. 2024 Apr 23;22(1):171. doi: 10.1186/s12916-024-03391-2.

Abstract

BACKGROUND

Little is known about the safety and efficacy of discontinuing antiplatelet therapy via LMWH bridging therapy in elderly patients with coronary stents implanted for > 12 months undergoing non-cardiac surgery. This randomized trial was designed to compare the clinical benefits and risks of antiplatelet drug discontinuation via LMWH bridging therapy.

METHODS

Patients were randomized 1:1 to receive subcutaneous injections of either dalteparin sodium or placebo. The primary efficacy endpoint was cardiac or cerebrovascular events. The primary safety endpoint was major bleeding.

RESULTS

Among 2476 randomized patients, the variables (sex, age, body mass index, comorbidities, medications, and procedural characteristics) and percutaneous coronary intervention information were not significantly different between the bridging and non-bridging groups. During the follow-up period, the rate of the combined endpoint in the bridging group was significantly lower than in the non-bridging group (5.79% vs. 8.42%, p = 0.012). The incidence of myocardial injury in the bridging group was significantly lower than in the non-bridging group (3.14% vs. 5.19%, p = 0.011). Deep vein thrombosis occurred more frequently in the non-bridging group (1.21% vs. 0.4%, p = 0.024), and there was a trend toward a higher rate of pulmonary embolism (0.32% vs. 0.08%, p = 0.177). There was no significant difference between the groups in the rates of acute myocardial infarction (0.81% vs. 1.38%), cardiac death (0.24% vs. 0.41%), stroke (0.16% vs. 0.24%), or major bleeding (1.22% vs. 1.45%). Multivariable analysis showed that LMWH bridging, creatinine clearance < 30 mL/min, preoperative hemoglobin < 10 g/dL, and diabetes mellitus were independent predictors of ischemic events. LMWH bridging and a preoperative platelet count of < 70 × 10/L were independent predictors of minor bleeding events.

CONCLUSIONS

This study showed the safety and efficacy of perioperative LMWH bridging therapy in elderly patients with coronary stents implanted > 12 months undergoing non-cardiac surgery. An alternative approach might be the use of bridging therapy with half-dose LMWH.

TRIAL REGISTRATION

ISRCTN65203415.

摘要

背景

对于植入冠状动脉支架超过12个月的老年患者在接受非心脏手术时通过低分子肝素桥接治疗停用抗血小板治疗的安全性和有效性知之甚少。本随机试验旨在比较通过低分子肝素桥接治疗停用抗血小板药物的临床益处和风险。

方法

患者按1:1随机分组,接受皮下注射达肝素钠或安慰剂。主要疗效终点是心脏或脑血管事件。主要安全终点是大出血。

结果

在2476例随机分组的患者中,桥接组和非桥接组之间的变量(性别、年龄、体重指数、合并症、用药情况和手术特征)以及经皮冠状动脉介入治疗信息无显著差异。在随访期间,桥接组的复合终点发生率显著低于非桥接组(5.79%对8.42%,p = 0.012)。桥接组心肌损伤的发生率显著低于非桥接组(3.14%对5.19%,p = 0.011)。非桥接组深静脉血栓形成更频繁(1.21%对0.4%,p = 0.024),肺栓塞发生率有升高趋势(0.32%对0.08%,p = 0.177)。两组在急性心肌梗死发生率(0.81%对1.38%)、心源性死亡(0.24%对0.41%)、中风(0.16%对0.24%)或大出血(1.22%对1.45%)方面无显著差异。多变量分析显示,低分子肝素桥接、肌酐清除率<30 mL/min、术前血红蛋白<10 g/dL和糖尿病是缺血事件的独立预测因素。低分子肝素桥接和术前血小板计数<70×10⁹/L是轻微出血事件的独立预测因素。

结论

本研究显示了围手术期低分子肝素桥接治疗在植入冠状动脉支架超过12个月的老年非心脏手术患者中的安全性和有效性。另一种方法可能是使用半剂量低分子肝素进行桥接治疗。

试验注册

ISRCTN65203415

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0328/11036782/1883e97d0168/12916_2024_3391_Fig1_HTML.jpg

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