乙酰唑胺作为急性失代偿性心力衰竭患者的辅助利尿疗法:系统综述与元分析》。

IF 2.8 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS American Journal of Cardiovascular Drugs Pub Date : 2024-02-28 DOI:10.1007/s40256-024-00633-9
Ahmed Kamal Siddiqi, Muhammad Talha Maniya, Muhammad Tanveer Alam, Andrew P. Ambrosy, Marat Fudim, Stephen J. Greene, Muhammad Shahzeb Khan
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引用次数: 0

摘要

背景:最近的证据表明,乙酰唑胺作为急性失代偿性心力衰竭(HF)患者的辅助利尿剂治疗可能是有益的。我们旨在汇总迄今为止进行的所有研究,并提供有关乙酰唑胺在急性失代偿性心力衰竭患者中作为辅助利尿剂的作用的最新证据:方法:检索了 PubMedline/Medline、Cochrane Library 和 Scopus 中从开始到 2023 年 7 月评估乙酰唑胺作为急性失代偿性高血压患者附加利尿剂的随机和非随机研究。提取、汇总并分析了有关利尿、尿量、解除充血和充血临床表现的数据。数据采用随机效应模型进行汇总。结果以风险比 (RR)、几率比 (OR) 或加权平均差 (WMD) 及 95% 置信区间 (95% CI) 表示。证据的确定性采用建议、评估、发展和评价分级法(GRADE)进行评估。在所有情况下,P 值小于 0.05 均被视为有意义:共纳入 5 项研究(n = 684 例患者),中位随访时间为 3 个月。汇总分析表明,尿量(MD 55.07,95% CI 35.1-77.04,P < 0.00001;I2 = 54%;中度确定性)、尿量(MD 1.04,95% CI 0.10-1.97,P = 0.与对照组相比,乙酰唑胺组的尿量(MD 1.04,95% CI 0.10-1.97,P = 0.03;I2 = 79%;中度确定性)和减充血[几率比(OR)1.62,95% CI 1.14-2.31,P = 0.007;I2 = 0%;高度确定性]均高于对照组。腹水(RR 0.56,95% CI 0.23-1.36,P = 0.20;I2 = 0%;低确定性)、水肿(RR 1.02,95% CI 0.52-2.0,P = 0.95;I2 = 45%;极低确定性)、颈静脉压(JVP)升高(RR 0.86,95% CI 0.63-1.17,P = 0.35;I2 = 0%;低确定性)和肺部啰音(RR 0.82,95% CI 0.44-1.51,P = 0.52;I2 = 25%;低确定性):结论:乙酰唑胺作为辅助利尿剂可显著改善减充血治疗的总体替代终点,但不能改善容量超负荷的所有个体症状和体征:本系统综述在 PROSPERO ( https://www.crd.york.ac.uk/PROSPERO/ ) 上进行了前瞻性注册,注册号为 CRD498330。
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Acetazolamide as an Adjunctive Diuretic Therapy for Patients with Acute Decompensated Heart Failure: A Systematic Review and Meta-Analysis

Background

Recent evidence suggests that acetazolamide may be beneficial as an adjunctive diuretic therapy in patients with acute decompensated heart failure (HF). We aim to pool all the studies conducted until now and provide updated evidence regarding the role of acetazolamide as adjunctive diuretic in patients with acute decompensated HF.

Methods

PubMed/Medline, Cochrane Library, and Scopus were searched from inception until July 2023, for randomized and nonrandomized studies evaluating acetazolamide as add-on diuretic in patients with acute decompensated HF. Data about natriuresis, urine output, decongestion, and the clinical signs of congestion were extracted, pooled, and analyzed. Data were pooled using a random effects model. Results were presented as risk ratios (RRs), odds ratios (ORs), or weighted mean differences (WMD) with 95% confidence intervals (95% CIs). Certainty of evidence was assessed using the grading of recommendation, assessment, development, and evaluation (GRADE) approach. A P value of < 0.05 was considered significant in all cases.

Results

A total of 5 studies (n = 684 patients) were included with a median follow-up time of 3 months. Pooled analysis demonstrated significantly increased natriuresis (MD 55.07, 95% CI 35.1–77.04, P < 0.00001; I2 = 54%; moderate certainty), urine output (MD 1.04, 95% CI 0.10–1.97, P = 0.03; I2 = 79%; moderate certainty) and decongestion [odds ratio (OR) 1.62, 95% CI 1.14–2.31, P = 0.007; I2 = 0%; high certainty] in the acetazolamide group, as compared with controls. There was no significant difference in ascites (RR 0.56, 95% CI 0.23–1.36, P = 0.20; I2 = 0%; low certainty), edema (RR 1.02, 95% CI 0.52–2.0, P = 0.95; I2 = 45%; very low certainty), raised jugular venous pressure (JVP) (RR 0.86, 95% CI 0.63–1.17, P = 0.35; I2 = 0%; low certainty), and pulmonary rales (RR 0.82, 95% CI 0.44–1.51, P = 0.52; I2 = 25%; low certainty) between the two groups.

Conclusions

Acetazolamide as an adjunctive diuretic significantly improves global surrogate endpoints for decongestion therapy but not all individual signs and symptoms of volume overload.

Systematic Review Registration

This systematic review was prospectively registered on the PROSPERO (https://www.crd.york.ac.uk/PROSPERO/), registration number CRD498330.

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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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