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单药及双联抗血小板和抗凝药物预处理联合静脉溶栓治疗老年急性缺血性卒中:TTT-AIS研究经验

Pre-treatment of Single and Double Antiplatelet and Anticoagulant With Intravenous Thrombolysis for Older Adults With Acute Ischemic Stroke: The TTT-AIS Experience.

作者信息

Lin Sheng-Feng, Hu Han-Hwa, Ho Bo-Lin, Chen Chih-Hung, Chan Lung, Lin Huey-Juan, Sun Yu, Lin Yung-Yang, Chen Po-Lin, Lin Shinn-Kuang, Wei Cheng-Yu, Lin Yu-Te, Lee Jiunn-Tay, Chao A-Ching

机构信息

School of Public Health, College of Public Health, Taipei Medical University, Taipei, Taiwan.

Department of Critical Care Medicine, Taipei Medical University Hospital, Taipei, Taiwan.

出版信息

Front Neurol. 2021 Feb 22;12:628077. doi: 10.3389/fneur.2021.628077. eCollection 2021.

Abstract

This study aimed to investigate the safety and efficacy of single antiplatelet, anticoagulant and Dual Antiplatelet pre-treatment (DAPP) in older, moderate to high severity acute ischemic stroke patients treated with intravenous thrombolysis (IVT). A prospective cohort study was conducted to monitor the development of symptomatic intracranial hemorrhage (SICH) and functional outcomes at 90 days. Two different dosages of alteplase were used for IVT. Logistic regression models were used for analysis of the safety and efficacy outcomes. A total of 1,156 patients were enrolled and categorized into six groups based on their pre-treatment medications: (1) aspirin (n = 213), (2) clopidogrel ( = 37), (3) DAPP of aspirin + clopidogrel (= 27), (4) warfarin ( = 44), (5) any of the above pre-medications ( = 331), and (6) none of these medications as controls ( = 825). The DAPP group showed significantly increased SICH by the NINDS (adjusted OR: 4.90, 95% CI 1.28-18.69) and the ECASS II (adjusted OR: 5.09, 95% CI: 1.01-25.68) standards. The aspirin group was found to significantly improve the favorable functional outcome of the modified Rankin Scale (mRS) of 0-1 (adjusted OR: 1.91, 95% CI, 1.31.2.78), but no significance for mRS of 0-2 (adjusted OR: 1.39, 95% CI, 0.97-1.99). The DAPP group also significantly increased mortality (adjusted OR: 4.75, 95% CI: 1.77-12.72). A significant interaction between different dosages for IVT and the functional status was noted. Compared to standard dose, the DAPP group showed higher proportions of disability and mortality with low dose of IVT. For older adults with higher baseline severity of acute ischemic stroke, DAPP may increase the risk of SICH and mortality post IVT. However, DAPP is still not an indication to withdraw IVT and to prescribe low-dose IVT for older adults.

摘要

本研究旨在调查单药抗血小板、抗凝及双联抗血小板预处理(DAPP)在接受静脉溶栓(IVT)治疗的老年中重度急性缺血性卒中患者中的安全性和有效性。开展一项前瞻性队列研究,以监测症状性颅内出血(SICH)的发生情况及90天时的功能转归。IVT使用两种不同剂量的阿替普酶。采用逻辑回归模型分析安全性和有效性结果。共纳入1156例患者,根据其预处理用药分为六组:(1)阿司匹林组(n = 213),(2)氯吡格雷组(= 37),(3)阿司匹林+氯吡格雷DAPP组(= 27),(4)华法林组(= 44),(5)上述任何一种预处理用药组(= 331),以及(6)无上述任何用药作为对照组(= 825)。根据美国国立神经疾病与卒中研究所(NINDS)标准(校正比值比:4.90,95%可信区间1.28 - 18.69)和欧洲急性卒中协作研究II(ECASS II)标准(校正比值比:5.09,95%可信区间:1.01 - 25.68),DAPP组SICH显著增加。发现阿司匹林组改良Rankin量表(mRS)评分为0 - 1的良好功能转归显著改善(校正比值比:1.91,95%可信区间,1.31 - 2.78),但mRS评分为0 - 2时无显著差异(校正比值比:1.39,95%可信区间,0.97 - 1.99)。DAPP组死亡率也显著增加(校正比值比:4.75,95%可信区间:1.77 - 12.72)。注意到IVT不同剂量与功能状态之间存在显著交互作用。与标准剂量相比,DAPP组在低剂量IVT时残疾和死亡率比例更高。对于基线严重程度较高的老年急性缺血性卒中患者,DAPP可能增加IVT后SICH和死亡风险。然而,DAPP仍不是老年患者停用IVT和给予低剂量IVT的指征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e07/7937707/eff58956067c/fneur-12-628077-g0001.jpg

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