直接口服抗凝药与华法林对低体重心房颤动患者的有效性和安全性比较:系统回顾与元分析》。

IF 2.8 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Mohamed Nabil Elshafei, Ahmed El-Bardissy, Muhammad Salem, Mohamed S. Abdelmoneim, Ahmed Khalil, Sherine Elhadad, Mohammed Danjuma
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引用次数: 0

摘要

导言:口服抗凝剂(DOAC)正在成为大多数临床风险的首选抗凝策略。然而,对于低体重[< 60 kg 或体重指数 (BMI) < 18 kg/m2]患者使用 DOAC 预防卒中仍存在不确定性。我们对已发表的研究进行了汇总系统分析,以确定与华法林相比,这些药物在低体重患者中预防卒中的有效性和安全性:我们对电子数据库进行了全面检索,检索时间从开始到 2023 年 6 月,检索对象为符合条件的研究,这些研究报告了直接口服抗凝药与华法林相比对低体重心房颤动患者的疗效和安全性。这些数据库包括 PubMed、EMBASE、Cochrane 系统综述数据库、科学引文索引和有效性综述文摘数据库。使用随机效应模型,得出了低体重心房颤动患者队列中使用直接口服抗凝药与华法林相比的死亡率结果的奇数比(及其相应的置信区间):我们的荟萃分析纳入了九项研究(n = 159,514 例患者)。与华法林相比,DOAC 类似物可降低中风复发率[几率比 (OR) 0.66,95% 置信区间 (CI) 0.49-0.9];但在综合结果(OR 0.81,95% CI 0.59-1.09)和死亡率(OR 0.82,95% CI 0.48-1.41)方面没有显著差异。此外,与华法林相比,DOAC类似物显著减少了30%的大出血事件(OR为0.70,95% CI为0.62-0.80):在这项汇集了真实世界和随机对照数据的荟萃分析综合研究中,与稳定接受华法林治疗的患者队列相比,房颤和低体重(< 60 kg 或 BMI < 18 kg/m2)患者使用 DOAC 类似物可显著降低中风和大出血风险。这两种抗凝策略的复合结果和死亡率点估计值存在不确定性。这一发现有助于解决在该队列中使用 DOACs 的不确定性。此外,它还表明有必要进行确证性非劣效随机对照试验,评估 DOACs 与华法林在该组患者中的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative Effectiveness and Safety of Direct Oral Anticoagulants Compared with Warfarin in Patients with Low Bodyweight who have Atrial Fibrillation: A Systematic Review and Meta-analysis

Comparative Effectiveness and Safety of Direct Oral Anticoagulants Compared with Warfarin in Patients with Low Bodyweight who have Atrial Fibrillation: A Systematic Review and Meta-analysis

Introduction

oral anticoagulant (DOAC) agents are becoming the anticoagulation strategy of choice for most clinical risks for which they are indicated. However, residual uncertainty remains regarding their use in preventing stroke in patients with low bodyweight [< 60 kg or body mass index (BMI) < 18 kg/m2]. We have carried out pooled systematic analyses of published studies to determine the efficacy and safety of these agents compared with warfarin in stroke prevention in patients with low bodyweight.

Methods

We carried out a comprehensive search of electronic databases from inception to June 2023 for eligible studies reporting on the efficacy and safety of direct oral anticoagulants versus warfarin in patients with atrial fibrillation who had low bodyweight. These include PubMed, EMBASE, the Cochrane Database of Systematic Reviews, the Science Citation Index, and the Database of Abstracts of Reviews of Effectiveness. Using the random effects model, derived pooled odd ratios (with their corresponding confidence intervals) of mortality outcomes in patient cohorts exposed to direct oral anticoagulants versus warfarin in patients with atrial fibrillation who had low bodyweight.

Results

Nine studies (n = 159,514 patients) were included in our meta-analysis. DOAC analogs were associated with lower stroke recurrence compared with warfarin [odds ratio (OR) 0.66, 95% confidence interval (CI) 0.49–0.9]; however, there was no significant difference in the composite outcome (OR 0.81, 95% CI 0.59–1.09) and mortality (OR 0.82, 95% CI 0.48–1.41). Additionally, DOAC analogs showed a significant reduction in major bleeding events by 30% compared with warfarin (OR 0.70, 95% CI 0.62–0.80).

Conclusion

In this pooled meta-analytical synthesis of studies comprising both real-world and randomized controlled data, the use of DOAC analogs in patients with atrial fibrillation and low bodyweight (< 60 kg or BMI < 18 kg/m2) was associated with a significant reduction in risks of stroke and major bleeding compared with patient cohorts stabilized on warfarin-based therapy. There was uncertainty regarding the composite outcome and mortality point estimate between these two anticoagulation strategies. This finding helps to resolve the uncertainty associated with the use of DOACs in this cohort. Additionally, it suggests the need for confirmatory non-inferiority randomized controlled trials evaluating DOACs versus warfarin in this cohort of patients.

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来源期刊
CiteScore
6.70
自引率
3.30%
发文量
38
审稿时长
>12 weeks
期刊介绍: Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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