Efficacy and Safety of Non-Vitamin K Antagonist Oral Anticoagulants Compared with Vitamin K Antagonists in Patients with Atrial Fibrillation and Type 2 Valvular Heart Disease: A Systematic Review and Meta-Analysis.

IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Xiaoyun Liang, Shangyu Liu, Lishuang Ji, Fangfang Ma, Guoyuan Song, Fang Li, Gang Liu
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引用次数: 0

Abstract

Purpose: This meta-analysis aimed to evaluate the efficacy and safety of non-vitamin K antagonist oral anticoagulants (NOACs) compared with vitamin K antagonists (VKAs) in patients with atrial fibrillation (AF) and type 2 valvular heart disease (VHD).

Methods: We searched the PubMed, LILACS, and MEDLINE databases to retrieve, randomized controlled trials (RCTs) comparing NOACs and VKAs in patients with AF and type 2 VHD, excluding mitral stenosis (moderate to severe, of rheumatic origin) or mechanical heart valves. The efficacy outcomes assessed were stroke and systemic embolism (SE), while safety outcomes included major bleeding and intracranial hemorrhage (ICH).

Results: Seven RCTs, including 16,070 patients with AF and type 2 VHD, were included. NOACs reduced the risk of stroke/SE (relative risk [RR], 0.75; 95% confidence interval [CI], 0.64-0.89; P = 0.0005), with no significant difference in major bleeding (RR, 0.88; 95% CI, 0.64-1.21; P = 0.43). The risk of ICH was reduced with NOACs (RR, 0.46; 95% CI, 0.27-0.77; P = 0.003). For patients with AF and bioprosthetic heart valve (five trials, 2805 patients), stroke/SE risks (RR, 0.65, 95% CI, 0.44-0.96) with NOACs were superior to VKAs. Major bleeding risks without ENVISAGE TAVI AF trial (RR, 0.53; 95% CI, 0.30-0.94; P = 0.03) with NOACs were superior to VKAs. The risks of ICH (RR, 0.61; 95% CI 0.34-1.09; P = 0.09) with NOACs were comparable to VKAs.

Conclusions: NOACs demonstrate efficacy and safety in patients with AF and type 2 VHD and reduce the risk of stroke/SE and ICH when compared with those with VKAs.

Abstract Image

心房颤动和 2 型瓣膜性心脏病患者口服非维生素 K 拮抗剂与维生素 K 拮抗剂的疗效和安全性比较:系统回顾与元分析》。
目的:本荟萃分析旨在评估非维生素K拮抗剂口服抗凝药(NOACs)与维生素K拮抗剂(VKAs)相比,对心房颤动(AF)和2型瓣膜性心脏病(VHD)患者的疗效和安全性:我们检索了 PubMed、LILACS 和 MEDLINE 数据库,以检索在房颤和 2 型瓣膜性心脏病患者中比较 NOAC 和 VKAs 的随机对照试验 (RCT),但不包括二尖瓣狭窄(中度至重度,风湿性)或机械心脏瓣膜。评估的疗效结果为中风和全身性栓塞(SE),安全性结果包括大出血和颅内出血(ICH):结果:共纳入了七项 RCT,包括 16,070 名房颤和 2 型 VHD 患者。NOACs 可降低卒中/SE 风险(相对风险 [RR],0.75;95% 置信区间 [CI],0.64-0.89;P = 0.0005),但在大出血方面无显著差异(RR,0.88;95% CI,0.64-1.21;P = 0.43)。使用 NOACs 可降低 ICH 风险(RR,0.46;95% CI,0.27-0.77;P = 0.003)。对于房颤和生物人工心脏瓣膜患者(5 项试验,2805 例患者),NOACs 的卒中/SE 风险(RR,0.65;95% CI,0.44-0.96)优于 VKAs。在没有 ENVISAGE TAVI AF 试验的情况下,NOACs 的大出血风险(RR,0.53;95% CI,0.30-0.94;P = 0.03)优于 VKAs。NOACs的ICH风险(RR,0.61;95% CI,0.34-1.09;P = 0.09)与VKAs相当:结论:NOACs 对房颤和 2 型 VHD 患者具有疗效和安全性,与 VKAs 相比可降低卒中/SE 和 ICH 风险。
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来源期刊
Cardiovascular Drugs and Therapy
Cardiovascular Drugs and Therapy 医学-心血管系统
CiteScore
8.30
自引率
0.00%
发文量
110
审稿时长
4.5 months
期刊介绍: Designed to objectively cover the process of bench to bedside development of cardiovascular drug, device and cell therapy, and to bring you the information you need most in a timely and useful format, Cardiovascular Drugs and Therapy takes a fresh and energetic look at advances in this dynamic field. Homing in on the most exciting work being done on new therapeutic agents, Cardiovascular Drugs and Therapy focusses on developments in atherosclerosis, hyperlipidemia, diabetes, ischemic syndromes and arrhythmias. The Journal is an authoritative source of current and relevant information that is indispensable for basic and clinical investigators aiming for novel, breakthrough research as well as for cardiologists seeking to best serve their patients. Providing you with a single, concise reference tool acknowledged to be among the finest in the world, Cardiovascular Drugs and Therapy is listed in Web of Science and PubMed/Medline among other abstracting and indexing services. The regular articles and frequent special topical issues equip you with an up-to-date source defined by the need for accurate information on an ever-evolving field. Cardiovascular Drugs and Therapy is a careful and accurate guide through the maze of new products and therapies which furnishes you with the details on cardiovascular pharmacology that you will refer to time and time again.
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