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重症监护病房中用于血管升压药依赖型休克的辅助性米多君治疗:一项系统评价和荟萃分析

Adjunctive Midodrine Therapy for Vasopressor-Dependent Shock in the ICU: A Systematic Review and Meta-Analysis.

作者信息

Kilcommons Sebastian J, Hammal Fadi, Kamaleldin Mostafa, Opgenorth Dawn L, Fiest Kirsten M, Karvellas Constantine J, Kutsogiannis Demetrios J, Lau Vincent I, MacIntyre Erika J, Rochwerg Bram, Senaratne Janek M, Slemko Jocelyn M, Sligl Wendy I, Wang Xiaoming X M, Bagshaw Sean M, Rewa Oleksa G

机构信息

University of Alberta, Edmonton, AB, Canada.

Department of Critical Care Medicine, University of Alberta, Edmonton, AB, Canada.

出版信息

Crit Care Med. 2025 Feb 1;53(2):e384-e399. doi: 10.1097/CCM.0000000000006519. Epub 2024 Dec 4.

Abstract

OBJECTIVES

To summarize the efficacy of midodrine as an adjunctive therapy in critically ill patients. Safety of midodrine was assessed as a secondary outcome.

DATA SOURCES

We performed a systematic review and meta-analysis using a peer-reviewed search strategy combining the themes of vasopressor-dependent shock, critical care, and midodrine and including MEDLINE, Ovid Embase, CINAHL, and Cochrane library databases until September 14, 2023.

STUDY SELECTION

We included studies if they: 1) included patients with vasopressor-dependent shock, 2) were performed in the ICU, 3) evaluated oral midodrine therapy compared with placebo or usual care, and 4) evaluated one of the outcomes of interest.

DATA EXTRACTION

We extracted data independently in duplicate using standardized data abstraction forms, which included the following specific variables: patient characteristics, age, sex, type of ICU, etiology of shock, number of patients, study inclusion and exclusion criteria, and geographical location. We also captured the type, dose, and duration of IV vasopressors, any cointervention used, and outcome data.

DATA SYNTHESIS

We identified seven randomized controlled trials (six included in the pooled analysis) and ten observational studies (four included in the pooled analysis) that met eligibility criteria. Adjunctive midodrine may decrease ICU length of stay (LOS) and there is low certainty of effect on hospital LOS. Midodrine may decrease IV vasopressor support duration, ICU mortality, and hospital mortality. Pooled observational data was based on very low certainty data for all outcomes of interest. The trial sequential analysis-informed required sample size was not met for ICU LOS or IV vasopressor duration and this contributed to Grading of Recommendations, Assessment, Development, and Evaluations assessments of imprecision for both outcomes.

CONCLUSIONS

Adjunctive midodrine may decrease ICU LOS, duration of IV vasopressor therapy, and mortality in critically ill patients. However, required sample sizes was not met to determine our outcomes of interest. Midodrine may increase risk of bradycardia. While midodrine may provide benefit for patient-centered outcomes, due to increased risk of adverse events, further large-scale studies are needed to inform and guide its routine use in the ICU.

摘要

目的

总结米多君作为重症患者辅助治疗的疗效。将米多君的安全性作为次要结局进行评估。

数据来源

我们采用同行评审的检索策略进行了一项系统评价和荟萃分析,该策略结合了血管升压药依赖型休克、重症监护和米多君等主题,并纳入了MEDLINE、Ovid Embase、CINAHL和Cochrane图书馆数据库,检索截至2023年9月14日。

研究选择

如果研究符合以下条件,我们将其纳入:1)纳入血管升压药依赖型休克患者;2)在重症监护病房进行;3)评估口服米多君治疗与安慰剂或常规治疗的比较;4)评估感兴趣的结局之一。

数据提取

我们使用标准化数据提取表独立进行了两次重复数据提取,该表包括以下特定变量:患者特征、年龄、性别、重症监护病房类型、休克病因、患者数量、研究纳入和排除标准以及地理位置。我们还记录了静脉血管升压药的类型、剂量和持续时间、使用的任何联合干预措施以及结局数据。

数据合成

我们确定了七项随机对照试验(六项纳入汇总分析)和十项观察性研究(四项纳入汇总分析)符合纳入标准。辅助使用米多君可能会缩短重症监护病房住院时间(LOS),但对医院住院时间的影响确定性较低。米多君可能会缩短静脉血管升压药支持时间、降低重症监护病房死亡率和医院死亡率。汇总的观察性数据基于所有感兴趣结局的极低确定性数据。对于重症监护病房住院时间或静脉血管升压药持续时间,试验序贯分析得出的所需样本量未达到,这导致对这两个结局的推荐分级、评估、制定和评价评估存在不精确性。

结论

辅助使用米多君可能会缩短重症患者的重症监护病房住院时间、静脉血管升压药治疗持续时间并降低死亡率。然而,未达到确定我们感兴趣结局所需的样本量。米多君可能会增加心动过缓的风险。虽然米多君可能会为以患者为中心的结局带来益处,但由于不良事件风险增加,需要进一步的大规模研究来为其在重症监护病房的常规使用提供信息并加以指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce4/11801447/ba5aed591196/ccm-53-e384-g001.jpg

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