Role of intravenous aspirin versus oral aspirin in the treatment of acute coronary syndrome: Answering a clinical query by systematic review and meta-analysis of randomized controlled trials.

IF 1.4 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Hardeep Kaur, Phulen Sarma, Anusuya Bhattacharyya, Manojkumar Rohit, Manisha Prajapat, Subodh Kumar, Ajay Prakash, Bikash Medhi
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引用次数: 0

Abstract

Background: Aspirin is indicated in the emergency management of acute coronary syndrome. However, oral aspirin has erratic bioavailability compared to i.v. formulation.

Objective: The objective of this study was to evaluate the comparative efficacy and safety of intravenous (IV) and oral aspirin in acute coronary syndrome.

Study design: This was a systematic review and meta-analysis.

Results: Two randomized controlled trials were included. Compared to oral aspirin, lower platelet aggregability was seen with IV aspirin at 5 min and 20 min. Lower thromboxane B2 and lower platelet CD-62p levels were noted in the IV group; however, no significant difference was observed in terms of "composite cardiovascular death, stroke, and myocardial infarction (MI) at 4-6 weeks," "any cause mortality," "cardiovascular mortality," "occurrence of stroke," and "occurrence of MI/reinfarction." However, no difference was noted in terms of the occurrence of serious adverse events.

Conclusion: IV aspirin showed some advantages in terms of platelet aggregability biomarkers at 20 min and 1 week with comparable safety to oral aspirin. No difference was seen in terms of clinical outcomes (at 24 h, 7, and 30 days) and the occurrence of serious adverse events.

Abstract Image

静脉注射阿司匹林与口服阿司匹林在治疗急性冠脉综合征中的作用:通过随机对照试验的系统评价和荟萃分析回答临床问题。
背景:阿司匹林适用于急性冠状动脉综合征的急诊治疗。然而,与静脉注射制剂相比,口服阿司匹林具有不稳定的生物利用度。目的:本研究的目的是评价静脉注射(IV)和口服阿司匹林治疗急性冠脉综合征的疗效和安全性。研究设计:这是一项系统综述和荟萃分析。结果:纳入两项随机对照试验。与口服阿司匹林相比,静脉注射阿司匹林在5分钟和20分钟时血小板聚集性较低。静脉注射组血栓素B2和血小板CD-62p水平较低;然而,在“复合心血管死亡、卒中和心肌梗死(MI) 4-6周”、“任何原因死亡率”、“心血管死亡率”、“卒中发生率”和“MI/再梗死发生率”方面,没有观察到显著差异。然而,在严重不良事件的发生方面没有发现差异。结论:静脉注射阿司匹林在20分钟和1周的血小板聚集性生物标志物方面具有一定优势,且安全性与口服阿司匹林相当。在临床结果(24小时、7天和30天)和严重不良事件的发生方面没有发现差异。
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来源期刊
CiteScore
4.00
自引率
4.20%
发文量
53
审稿时长
4-8 weeks
期刊介绍: Indian Journal of Pharmacology accepts, in English, review articles, articles for educational forum, original research articles (full length and short communications), letter to editor, case reports and interesting fillers. Articles concerning all aspects of pharmacology will be considered. Articles of general interest (e.g. methods, therapeutics, medical education, interesting websites, new drug information and commentary on a recent topic) are also welcome.
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