急性呼吸窘迫综合征后急性肾损伤的时间关系和临床结果:系统回顾与元分析》。

Q4 Medicine
Critical care explorations Pub Date : 2024-02-12 eCollection Date: 2024-02-01 DOI:10.1097/CCE.0000000000001054
Mariam Charkviani, Hong Hieu Truong, Nasrin Nikravangolsefid, Jacob Ninan, Larry J Prokop, Swetha Reddy, Kianoush B Kashani, Juan Pablo Domecq Garces
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引用次数: 0

摘要

目的:对急性呼吸窘迫综合征(ARDS)后急性肾损伤(AKI)的发生率和时间及其与死亡率的关系进行系统回顾和荟萃分析:进行系统综述和荟萃分析,评估急性呼吸窘迫综合征(ARDS)后急性肾损伤(AKI)的发生率、发生时间及其与死亡率的关系:数据来源:Ovid MEDLINE(R)、Ovid Embase、Ovid Cochrane Central Register of Controlled Trials、Ovid Cochrane Database of Systematic Reviews、Ovid PsycINFO 数据库、Scopus 和 Web of Science(认为 2023 年 4 月):对标题和摘要进行一式两份的独立筛选,以确定符合条件的研究。数据提取:两名审稿人使用预先试用的摘要表独立提取数据。我们使用 Review Manager 5.4 软件(英国牛津 Cochrane 图书馆)和 Open Meta 软件(美国罗得岛州普罗维登斯布朗大学)进行统计分析:在已确定和筛选的 3646 项研究中,有 17 项研究(包括 9359 名 ARDS 患者)符合资格标准,并被纳入荟萃分析。3287名患者(40%)在确诊ARDS后发生了AKI。在确诊 ARDS 后至少 48 小时内发生 AKI 的比例为 20%(95% CI,0.18-0.21%)。在发生 AKI 的 ARDS 患者中,住院(或 30 天)死亡率的汇总风险比 (RR) 为 1.93(95% CI,1.71-2.18)。ARDS后发生AKI被认为是导致ARDS患者死亡的一个独立风险因素,多变量分析的汇总风险比为3.69(95% CI,2.24-6.09)。此外,有两项研究比较了 ARDS 后晚期与早期 AKI 患者的死亡率,结果显示晚期 AKI 患者的死亡率更高,RR 为 1.46(95% CI,1.19-1.8)。然而,大多数结果的证据确定性较低或很低:虽然我们的研究结果突显了ARDS与后续发生AKI之间的重要关联,但证据的确定性较低或非常低,这强调了谨慎解释的必要性。本系统综述发现了一个重要的知识缺口,因此有必要开展进一步研究,以更明确地了解这种关系及其临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Temporal Relationship and Clinical Outcomes of Acute Kidney Injury Following Acute Respiratory Distress Syndrome: A Systematic Review and Meta-Analysis.

Objectives: Conduct a systematic review and meta-analysis to assess prevalence and timing of acute kidney injury (AKI) development after acute respiratory distress syndrome (ARDS) and its association with mortality.

Data sources: Ovid MEDLINE(R), Ovid Embase, Ovid Cochrane Central Register of Controlled Trials, Ovid Cochrane Database of Systematic Reviews, Ovid PsycINFO database, Scopus, and Web of Science thought April 2023.

Study selection: Titles and abstracts were screened independently and in duplicate to identify eligible studies. Randomized controlled trials and prospective or retrospective cohort studies reporting the development of AKI following ARDS were included.

Data extraction: Two reviewers independently extracted data using a pre piloted abstraction form. We used Review Manager 5.4 software (Cochrane Library, Oxford, United Kingdom) and Open Meta software (Brown University, Providence, RI) for statistical analyses.

Data synthesis: Among the 3646 studies identified and screened, 17 studies comprising 9359 ARDS patients met the eligibility criteria and were included in the meta-analysis. AKI developed in 3287 patients (40%) after the diagnosis of ARDS. The incidence of AKI at least 48 hours after ARDS diagnosis was 20% (95% CI, 0.18-0.21%). The pooled risk ratio (RR) for the hospital (or 30-d) mortality among ARDS patients who developed AKI was 1.93 (95% CI, 1.71-2.18). AKI development after ARDS was identified as an independent risk factor for mortality in ARDS patients, with a pooled odds ratio from multivariable analysis of 3.69 (95% CI, 2.24-6.09). Furthermore, two studies comparing mortality between patients with late vs. early AKI initiation after ARDS revealed higher mortality in late AKI patients with RR of 1.46 (95% CI, 1.19-1.8). However, the certainty of evidence for most outcomes was low to very low.

Conclusions: While our findings highlight a significant association between ARDS and subsequent development of AKI, the low to very low certainty of evidence underscores the need for cautious interpretation. This systematic review identified a significant knowledge gap, necessitating further research to establish a more definitive understanding of this relationship and its clinical implications.

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CiteScore
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