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德瑞蒂斯比值升高与COVID-19的不良预后相关:一项系统评价和荟萃分析

Elevated De Ritis Ratio Is Associated With Poor Prognosis in COVID-19: A Systematic Review and Meta-Analysis.

作者信息

Pranata Raymond, Huang Ian, Lim Michael Anthonius, Yonas Emir, Vania Rachel, Lukito Antonia Anna, Nasution Sally Aman, Siswanto Bambang Budi, Kuswardhani Raden A Tuty

机构信息

Faculty of Medicine, Universitas Pelita Harapan, Tangerang, Indonesia.

Faculty of Medicine, Department of Internal Medicine, Hasan Sadikin General Hospital, Universitas Padjadjaran, Bandung, Indonesia.

出版信息

Front Med (Lausanne). 2021 Dec 22;8:676581. doi: 10.3389/fmed.2021.676581. eCollection 2021.

Abstract

This meta-analysis aims to assess whether elevated De Ritis ratio is associated with poor prognosis in patients with coronavirus 2019 (COVID-19). A systematic literature search was performed using PubMed, Embase, and EuropePMC databases up until September 17, 2021. De Ritis ratio is also known as Aspartate aminotransferase/alanine transaminase (AST/ALT) ratio. The main outcome was poor prognosis, a composite of mortality, severity, the need for ICU care, and intubation. The effect measure was odds ratios (ORs) and mean differences. We generated sensitivity and specificity, negative and positive likelihood ratio (NLR and PLR), diagnostic odds ratio (DOR), and area under curve (AUC). There were eight studies with 4,606 patients. De Ritis ratio was elevated in 44% of the patients. Patients with poor prognosis have higher De Ritis ratio [mean difference 0.41 (0.31, 0.50), < 0.001; : 81.0%] and subgroup analysis showed that non-survivors also have higher De Ritis Ratio [mean difference 0.47 (0.46, 0.48), < 0.001; : 0%]. Elevated De Ritis ratio was associated with poor prognosis [OR 3.28 (2.39, 4.52), < 0.001; : 35.8%]. It has a sensitivity of 55% (36-73), specificity of 71% (52-85), PLR 1.9, NLR.63, DOR of 3 (2-4), and AUC of.67 (0.63-0.71). The posterior probability of poor prognosis was 38% if De Ritis is elevated, while 17% if De Ritis is not elevated. Elevated De Ritis ratio is associated with poor prognosis in patients with COVID-19. PROSPERO ID: CRD42020216634.

摘要

本荟萃分析旨在评估2019冠状病毒病(COVID-19)患者中升高的德瑞蒂斯比值是否与预后不良相关。截至2021年9月17日,使用PubMed、Embase和欧洲生物医学中心数据库进行了系统的文献检索。德瑞蒂斯比值也称为天冬氨酸转氨酶/丙氨酸转氨酶(AST/ALT)比值。主要结局为预后不良,是死亡率、严重程度、入住重症监护病房的需求和插管的综合指标。效应量为比值比(OR)和均值差。我们计算了敏感性和特异性、阴性和阳性似然比(NLR和PLR)、诊断比值比(DOR)和曲线下面积(AUC)。共有八项研究,涉及4606例患者。44%的患者德瑞蒂斯比值升高。预后不良的患者德瑞蒂斯比值更高[均值差0.41(0.31,0.50),<0.001;I²:81.0%],亚组分析显示非幸存者的德瑞蒂斯比值也更高[均值差0.47(0.46,0.48),<0.001;I²:0%]。德瑞蒂斯比值升高与预后不良相关[OR 3.28(2.39,4.52),<0.001;I²:35.8%]。其敏感性为55%(36 - 73),特异性为71%(52 - 85),PLR为1.9,NLR为0.63,DOR为3(2 - 4),AUC为0.67(0.63 - 0.71)。如果德瑞蒂斯比值升高,预后不良的后验概率为38%,而如果德瑞蒂斯比值未升高,则为17%。德瑞蒂斯比值升高与COVID-19患者的预后不良相关。PROSPERO注册号:CRD42020216634。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc2/8729881/99de20e7ff55/fmed-08-676581-g0001.jpg

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