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成人患者的急性肾损伤与万古霉素/哌拉西林/他唑巴坦:系统评价。

Acute kidney injury and vancomycin/piperacillin/tazobactam in adult patients: a systematic review.

机构信息

Hospital of Marcianise, ASL Caserta, Marcianise, Italy.

Department of Biomedical Sciences and Human Oncology, University of Bari, Bari, Italy.

出版信息

Intern Emerg Med. 2020 Mar;15(2):327-331. doi: 10.1007/s11739-020-02287-2. Epub 2020 Feb 10.

Abstract

The aim of this systematic review was to assess AKI (acute kidney injury) in adult patients, treated with vancomycin (V) + piperacillin/tazobactam (PT) compared to V monotherapy. Studies were found in Pubmed, Web of Science and Scopus databases. Articles not in English, pediatric studies and case reports were excluded. A study is eligible for inclusion if the adjusted Odds ratio (aOR) for AKI in V + PT compared to V monotherapy groups, could be extracted or determined from available data. Six retrospective cohort studies were eligible for inclusion criteria and so they were included in the analysis. All studies separately showed a significant higher risk of developing AKI (OR > 1, p < 0.05) in V + PT group compared to V monotherapy group. Considering the methodological difference of included studies, a random effect model was preferred. The model showed a pooled significant higher risk of developing AKI [OR 2.77 (95% CI 1.94, 3.96), p < 0.0001] in V + PT group compared to V group. Association of V and PT appears to be associated with a greater risk of AKI compared to V in monotherapy. These results may serve as the impetus for further evaluation into true mechanisms behind this additive nephrotoxic effect and its potential implications on mortality.

摘要

本系统评价的目的是评估与万古霉素(V)单药治疗相比,在接受 V +哌拉西林/他唑巴坦(PT)治疗的成年患者中急性肾损伤(AKI)的情况。研究在 Pubmed、Web of Science 和 Scopus 数据库中进行。排除非英文文章、儿科研究和病例报告。如果可以从可用数据中提取或确定 V + PT 与 V 单药治疗组相比 AKI 的调整后优势比(aOR),则该研究有资格纳入。有 6 项回顾性队列研究符合纳入标准,因此被纳入分析。所有研究均单独显示 V + PT 组与 V 单药治疗组相比,发生 AKI 的风险显著更高(OR>1,p<0.05)。考虑到纳入研究的方法学差异,首选随机效应模型。该模型显示,与 V 单药治疗组相比,V + PT 组发生 AKI 的风险显著更高[OR 2.77(95%CI 1.94,3.96),p<0.0001]。V 和 PT 的联合使用似乎与 AKI 的风险增加有关,与 V 单药治疗相比。这些结果可能为进一步评估这种附加性肾毒性作用的真正机制及其对死亡率的潜在影响提供动力。

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