首页|序贯器官衰竭评分各项衍生指标预测脓毒症患者转归效能的Meta分析

序贯器官衰竭评分各项衍生指标预测脓毒症患者转归效能的Meta分析

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目的 系统性回顾评估序贯器官衰竭评分(SOFA)各项衍生指标在脓毒症患者病死率方面的预测效能.方法 在PubMed、Embase、Cochrane Library 3 个数据库中检索关于脓毒症、SOFA评分的相关文献,检索时间限定为建库至 2023 年 2 月.主要结局指标包括 28d病死率、30d病死率、院内病死率、重症监护病房(ICU)病死率和远期病死率.由 2 名研究者独立进行文献筛选、资料提取和质量评价.使用Revman 5.3.5、Meta-DiSc及Stata软件进行数据分析.采用Deek漏斗图评估纳入研究是否存在发表偏倚.结果 共纳入40篇文献,包含51项试验研究.其中英文文献32篇,中文文献8篇;前瞻性研究17项,回顾性研究34项;初始SOFA相关研究 38 项,SOFA评分变化值(ΔSOFA)相关研究 9 项;共纳入 59 962 例患者.① 初始SOFA、ΔSOFA预测脓毒症患者转归的汇总受试者工作特征曲线下面积(AUC)分别为 0.773、0.787(Z=0.115,P>0.05),表明两种指标在预测脓毒症患者转归效能方面无明显差异.②亚组分析中,因文献篇数限制,将28d病死率与30d病死率合并讨论,ΔSOFA对 28d或 30d病死率的预测效能明显高于初始SOFA(AUC分别为 0.854、0.787,Z=2.603,P≤0.01).③ΔSOFA在预测脓毒症患者院内病死率、ICU病死率及远期病死率方面的研究较少;初始SOFA预测上述研究终点的AUC分别为:ICU病死率(0.814)>28 d或 30d病死率(0.787)>院内病死率(0.697)>远期病死率(0.646).④非汉族来源脓毒症患者的初始SOFA和ΔSOFA预测转归效能好且两者间无明显差异(AUC分别为 0.766、0.811),但其ΔSOFA预测转归的合并敏感度较高(92%).⑤前瞻性研究中,初始SOFA对脓毒症患者转归的预测效能较好(AUC为 0.804,合并敏感度为 64%),ΔSOFA预测脓毒症患者转归的敏感度明显高于初始SOFA(78%比 64%).漏斗图结果显示,所纳入的文献无明显发表偏倚.结论 ΔSOFA在预测脓毒症患者短期(28d或 30d)病死率方面有相对较高的诊断效能.
Meta analysis of the predictive efficacy of various derived indicators of sequential organ failure assessment in outcomes of patients with sepsis
Objective To systematically review and evaluate the predictive efficacy of various derived indicators of sequential organ failure assessment(SOFA)in mortality rate of sepsis patients.Methods Literature on sepsis and SOFA scores were searched in PubMed,Embase and Cochrane Library.The retrieval time will be set to the time of database-building to February,2023.The main outcome measures included 28-day mortality,30-day mortality,in-hospital mortality,intensive care unit(ICU)mortality and long-term mortality.Literature screening,data extraction and quality evaluation were carried out independently by 2 researchers.Data were analyzed by Revman 5.3.5,Meta-disc and Stata software.Deek funnel plots were used to assess publication bias in the included studies.Results A total of 40 articles including 51 trials were included.Of these,32 were in English and 8 in Chinese,17 were in prospective trials and 34 were in retrospective trials,38 were in initial SOFA-related trials and 9 were in the change of SOFA score(ΔSOFA)-related studies,a total of 59962 patients were enrolled.①The area under the receiver operator characteristic curve(AUC)of initial SOFA and ΔSOFA for predicting outcome in sepsis was 0.773 and 0.787(Z = 0.115,P>0.05),respectively.There was no significant difference between the two indexes in predicting the outcome of patients with sepsis.② In subgroup analysis,due to limitations in the number of literature articles,the 28-day mortality rate and 30-day mortality rate were merged for discussion.The predictive power of ΔSOFA for 28-day or 30-day mortality was significantly higher than that of initial SOFA(AUC was 0.854,0.787,Z = 2.603,P≤0.01).③There were few studies onΔSOFA in predicting in-hospital mortality,ICU mortality and long-term mortality of sepsis patients.The AUC of the initial SOFA for predicting the study endpoints described above was:ICU mortality(0.814)>28-day or 30-day mortality(0.787)>in-hospital mortality(0.697)>long-term mortality(0.646).④Initial SOFA and ΔSOFA in patients with sepsis of non-Han original had good predictive performance and there was no significant difference between them(AUC was 0.766,0.811,respectively).However,the pooled sensitivity of ΔSOFA was higher(92%).⑤In prospective studies,initial SOFA was better at predicting outcomes in patients with sepsis(AUC was 0.804,pooled sensitivity 64%).The sensitivity of ΔSOFA indicators in predicting the outcome of sepsis patients was significantly higher than the initial SOFA(78%vs.64%).The funnel plot showed that there was no significant publication bias in the included literature.Conclusion ΔSOFA has a relatively high diagnostic efficacy in predicting short-term(28-day or 30-day)mortality in patients with sepsis.

SepsisSequential organ failure assessmentMortality

李雯、赵志伶、周庆涛、葛庆岗

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北京大学第三医院危重医学科,北京 100191

脓毒症 序贯器官衰竭评分 病死率

北京市自然科学基金

L222019

2024

中华危重病急救医学
中华医学会

中华危重病急救医学

CSTPCD北大核心
影响因子:3.049
ISSN:2095-4352
年,卷(期):2024.36(3)
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