An updated systematic review and meta-analysis investigating perihematomal edema and clinical outcome after intracerebral hemorrhage

医学 荟萃分析 改良兰金量表 脑出血 置信区间 优势比 子群分析 内科学 随机效应模型 出版偏见 缺血性中风 蛛网膜下腔出血 缺血
作者
Sarah Marchina,Kun He Lee,Vasileios‐Arsenios Lioutas,Filipa Carvalho,Diego Incontri‐Abraham,Elizabeth Heistand,David Lin,Magdy Selim
出处
期刊:Journal of stroke and cerebrovascular diseases [Elsevier]
卷期号:32 (8): 107204-107204 被引量:2
标识
DOI:10.1016/j.jstrokecerebrovasdis.2023.107204
摘要

The relationship between perihematomal edema (PHE) and intracerebral hemorrhage (ICH) outcomes is uncertain. Given newly published studies, we updated a previous systematic review and meta-analysis assessing the prognostic impact of PHE on ICH outcomes.Databases were searched through September 2022 using pre-defined keywords. Included studies used regression to examine the association between PHE and functional outcome (assessed by modified Rankin Scale [mRS]) and mortality. The study quality was assessed using the Newcastle-Ottawa Scale. The overall pooled effect, and secondary analyses exploring different subgroups were obtained by entering the log transformed odds ratios and their confidence intervals into a DerSimonian-Laird random effects meta-analysis.Twenty-eight studies (n=8655) were included. The pooled effect size for overall outcome (mRS and mortality) was 1.05 (95% CI 1.03, 1.07; p<0.00). In secondary analyses, PHE volume and growth effect sizes were 1.03 (CI 1.01, 1.05) and 1.12 (CI 1.06, 1.19), respectively. Results of subgroup analyses assessing absolute PHE volume and growth at different time points were: baseline volume 1.02 (CI 0.98, 1.06), 72-hour volume 1.07 (CI 0.99, 1.16), growth at 24 hours 1.30 (CI 0.96, 1.74) and growth at 72 hours 1.10 (CI 1.04, 1.17). Heterogeneity across studies was substantial.This meta-analysis indicates that PHE growth, especially within the first 24 hours after ictus, has a stronger impact on functional outcome and mortality than PHE volume. Definitive conclusions are limited by the large variability of PHE measures, heterogeneity, and different evaluation time points between studies.
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