Suppr超能文献

系统评价与荟萃分析:血管活性药物治疗 1 型肝肾综合征。

Systematic review with meta-analysis: vasoactive drugs for the treatment of hepatorenal syndrome type 1.

机构信息

Department of Hepatology, Royal Infirmary of Edinburgh, Edinburgh, UK.

Division of Epidemiology and Public Health, School of Medicine, University of Nottingham, Nottingham, UK.

出版信息

Aliment Pharmacol Ther. 2017 Mar;45(5):593-603. doi: 10.1111/apt.13912. Epub 2017 Jan 4.

Abstract

BACKGROUND

Hepatorenal syndrome type 1 (HRS1) is a functional, rapidly progressive, potentially reversible form of acute kidney injury occurring in patients with cirrhosis. Characterised by intense renal arterial vasoconstriction, it carries a very poor prognosis. There is a significant unmet need for a widely approved, safe and effective pharmacological treatment.

AIM

To re-evaluate efficacy and safety of pharmacological treatments for HRS1, in the light of recently published randomised controlled trials (RCTs).

METHODS

MEDLINE (OvidSP), EMBASE, PubMed and Cochrane registers were searched for RCTs reporting efficacy and adverse events related to pharmacological treatment of HRS1. Search terms included: 'hepatorenal syndrome', 'terlipressin', 'noradrenaline', 'octreotide', 'midodrine', 'vasopressin', 'dopamine', 'albumin' and synonyms. Comparison of vasoactive drugs vs. placebo/no treatment, and two active drugs were included. Meta-analysis was performed for HRS1 reversal, creatinine improvement, mortality and adverse events.

RESULTS

Twelve RCTs enrolling 700 HRS1 patients were included. Treatment with terlipressin and albumin led to HRS1 reversal more frequently than albumin alone or placebo (RR: 2.54, 95% CI: 1.51-4.26). Noradrenaline was effective in reversing HRS1, but trials were small and nonblinded. Overall, there was mortality benefit with terlipressin (RR: 0.79, 95% CI: 0.63-1.01), but sensitivity analysis including only trials with low risk of selection bias weakened this relationship (RR: 0.87, 95% CI: 0.71-1.06). Notably, there was a significant risk of adverse events with terlipressin therapy (RR: 4.32, 95% CI: 0.75-24.86).

CONCLUSIONS

Terlipressin treatment is superior to placebo for achieving HRS1 reversal, but mortality benefit is less clear. Terlipressin is associated with significant adverse events, but infusion regimens may be better tolerated. There is continued need for safe and effective treatment options for hepatorenal syndrome.

摘要

背景

1 型肝肾综合征(HRS1)是一种在肝硬化患者中发生的功能性、快速进展且潜在可逆转的急性肾损伤形式。其特征为强烈的肾动脉血管收缩,预后极差。目前迫切需要一种广泛认可、安全有效的药物治疗方法。

目的

根据最近发表的随机对照试验(RCT),重新评估 HRS1 的药物治疗的疗效和安全性。

方法

在 MEDLINE(OvidSP)、EMBASE、PubMed 和 Cochrane 登记处检索报告 HRS1 药物治疗疗效和不良反应的 RCTs。检索词包括:“肝肾综合征”、“特利加压素”、“去甲肾上腺素”、“奥曲肽”、“米多君”、“加压素”、“多巴胺”、“白蛋白”及其同义词。将血管活性药物与安慰剂/无治疗进行比较,并纳入两种活性药物进行比较。对 HRS1 逆转、肌酐改善、死亡率和不良反应进行荟萃分析。

结果

纳入了 12 项纳入 700 例 HRS1 患者的 RCT。与单独使用白蛋白或安慰剂相比,特利加压素和白蛋白治疗更频繁地导致 HRS1 逆转(RR:2.54,95%CI:1.51-4.26)。去甲肾上腺素在逆转 HRS1 方面有效,但试验规模较小且未设盲。总体而言,特利加压素治疗具有降低死亡率的获益(RR:0.79,95%CI:0.63-1.01),但包括低选择偏倚风险的试验进行敏感性分析后削弱了这种关系(RR:0.87,95%CI:0.71-1.06)。值得注意的是,特利加压素治疗与不良反应风险显著相关(RR:4.32,95%CI:0.75-24.86)。

结论

与安慰剂相比,特利加压素治疗更有利于实现 HRS1 逆转,但死亡率获益不太明确。特利加压素与显著的不良反应相关,但输注方案可能更耐受。仍然需要安全有效的肝肾综合征治疗选择。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验