人白蛋白输注降低肝硬化患者低钠血症和循环功能障碍:最新荟萃分析。

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Hui-Juan Zhou, Zi-Qiang Li, Da-Er Dili, Qing Xie
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引用次数: 0

摘要

背景:肝硬化是一种高发病率和死亡率的进行性疾病,需要有效的治疗策略来改善患者的预后。各种治疗方法包括白蛋白输注、容量扩张剂(VEs)和血管活性药物用于治疗肝硬化患者。尽管有大量的临床试验,比较白蛋白输注与其他治疗方法的有效性的综合荟萃分析是有限的。本研究提供了当前和全面的综合证据,为优化肝硬化患者的治疗策略提供了关键见解。目的:为了系统地更新肝硬化治疗的现有数据,我们进行了一项荟萃分析,以评估和比较白蛋白输注与其他VEs和血管活性药物在肝硬化患者中的临床疗效。方法:从PubMed和Embase数据库(建立至2024年6月)检索文献,重点研究低钠血症(主要结局)和胃肠道出血、肝性脑病、严重感染、穿刺后诱发循环功能障碍(PICD)、腹水再现、自发性细菌性腹膜炎、肝肾综合征、肾损害、住院时间、死亡率和安全性等各种结局。初步分析汇集了比较白蛋白输注与对照组的研究。在亚组分析中,对包括在对照组中的分层治疗类别进行比较。结果:在检索到的2957项研究中,纳入了31项研究(27项随机对照试验和4项观察性研究),包括6255名患者。使用白蛋白可显著降低低钠血症的发生率[比值比(OR) = 0.67;95%可信区间(95% ci) = 0.53-0.85]和PICD (OR = 0.38;95%CI = 0.20-0.71),而严重感染的减少(OR = 0.55;95%CI = 0.28-1.07),差异无统计学意义。在亚组分析中,与不活跃/标准药物治疗相比,白蛋白在降低低钠血症发生率方面表现出有利的改善(OR = 0.54;95%ci = 0.27-1.09)。对于PICD,与其他VEs相比,白蛋白的使用具有显著性(OR = 0.31;95%CI = 0.11-0.85),但与血管收缩剂无关(OR = 0.63;95%ci = 0.21-1.91)。在整个亚组分析中,观察到低钠血症显著降低(OR = 0.67;95%CI = 0.53-0.85)和PICD (OR = 0.38;95%ci = 0.20-0.71)。结论:人白蛋白已被证明可显著降低肝硬化患者低钠血症和PICD的发生率,而其对严重感染的作用仍有提示作用,但无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human albumin infusion for reducing hyponatremia and circulatory dysfunction in liver cirrhosis: A meta-analysis update.

Background: Liver cirrhosis is a progressive disease with high morbidity and mortality requiring effective management strategies to improve patient outcomes. Various therapies including albumin infusion, volume expanders (VEs), and vasoactive agents are used to manage patients with cirrhosis. Despite numerous clinical trials, a comprehensive meta-analysis comparing the effectiveness of albumin infusion against alternative treatments is limited. This study provides the current and comprehensive synthesis of evidence, offering key insights for optimizing therapeutic strategies in patients with liver cirrhosis.

Aim: To systematically update available data on therapies of liver cirrhosis, we performed a meta-analysis to evaluate and compare the clinical efficacy of albumin infusion vs other VEs and vasoactive agents in patients with liver cirrhosis.

Methods: A literature search from the PubMed and Embase databases (inception till June 2024) focused on hyponatremia (primary outcome) and various outcomes such as gastrointestinal bleeding, hepatic encephalopathy, severe infection, post-paracentesis-induced circulatory dysfunction (PICD), ascites reappearance, spontaneous bacterial peritonitis, hepatorenal syndrome, renal impairment, hospital stay, mortality, and safety was performed. The primary analysis pooled studies that compared albumin infusion with control. In the subgroup analysis, comparisons were made within the stratified treatment categories included in the control group.

Results: Of the 2957 studies retrieved, 31 studies (27 randomized controlled trials and 4 observational studies) comprising 6255 patients were included. Albumin use was significant in reducing odds of hyponatremia [odds ratio (OR) = 0.67; 95% confidence interval (95%CI) = 0.53-0.85] and PICD (OR = 0.38; 95%CI = 0.20-0.71), whereas the reduction in severe infection (OR = 0.55; 95%CI = 0.28-1.07) did not reach statistical significance. In the subgroup analysis, albumin demonstrated a favorable improvement in lowering the incidence of hyponatremia vs inactive/standard medical therapy (OR = 0.54; 95%CI = 0.27-1.09). For PICD, albumin use was significant compared with other VEs (OR = 0.31; 95%CI = 0.11-0.85) but not with vasoconstrictors (OR = 0.63; 95%CI = 0.21-1.91). In the overall subgroup analysis, a significant reduction was observed in hyponatremia (OR = 0.67; 95%CI = 0.53-0.85) and PICD (OR = 0.38; 95%CI = 0.20-0.71).

Conclusion: Human albumin has been shown to significantly reduce the incidence of hyponatremia and PICD in patients with liver cirrhosis, whereas its effect on severe infection remains suggestive but not statistically significant.

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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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