Massimo Franchini , Mario Cruciani , Carlo Mengoli , Arturo Casadevall , Claudia Glingani , Michael J. Joyner , Liise-anne Pirofski , Jonathon W. Senefeld , Shmuel Shoham , David J. Sullivan , Matteo Zani , Daniele Focosi
{"title":"住院 COVID-19 患者的康复血浆和死亡率预测因素:系统回顾和荟萃分析。","authors":"Massimo Franchini , Mario Cruciani , Carlo Mengoli , Arturo Casadevall , Claudia Glingani , Michael J. Joyner , Liise-anne Pirofski , Jonathon W. Senefeld , Shmuel Shoham , David J. Sullivan , Matteo Zani , Daniele Focosi","doi":"10.1016/j.cmi.2024.07.020","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Plasma collected from recovered patients with COVID-19 (COVID-19 convalescent plasma [CCP]) was the first antibody-based therapy employed to fight the COVID-19 pandemic. While the therapeutic effect of early administration of CCP in COVID-19 outpatients has been recognized, conflicting data exist regarding the efficacy of CCP administration in hospitalized patients.</div></div><div><h3>Objectives</h3><div>To examine the effect of CCP compared to placebo or standard treatment, and to evaluate whether time from onset of symptoms to treatment initiation influenced the effect.</div></div><div><h3>Data sources</h3><div>Electronic databases were searched for studies published from January 2020 to January 2024.</div></div><div><h3>Study eligibility criteria</h3><div>Randomized clinical trials (RCTs) investigating the effect of CCP on COVID-19 mortality in hospitalized patients with COVID-19.</div></div><div><h3>Participants</h3><div>Hospitalized patients with COVID-19.</div></div><div><h3>Interventions</h3><div>CCP versus no CCP.</div></div><div><h3>Assessment of risk of bias</h3><div>Cochrane risk of bias tool for RCTs.</div></div><div><h3>Methods of data synthesis</h3><div>The random-effects model was used to calculate the pooled risk ratio (RR) with 95% CI for the pooled effect estimates of CCP treatment. The Grading of Recommendations Assessment, Development and Evaluation was used to evaluate the certainty of evidence.</div></div><div><h3>Results</h3><div>Twenty-seven RCTs were included, representing 18,877 hospitalized patients with COVID-19. When transfused within 7 days from symptom onset, CCP significantly reduced the risk of death compared to standard therapy or placebo (RR, 0.76; 95% CI, 0.61–0.95), while later CCP administration was not associated with a mortality benefit (RR, 0.98; 95% CI, 0.90–1.06). The certainty of the evidence was graded as moderate. Meta-regression analysis demonstrated increasing mortality effects for longer interval to transfusion or worse initial clinical severity.</div></div><div><h3>Conclusions</h3><div>In-hospital transfusion of CCP within 7 days from symptom onset conferred a mortality benefit.</div></div>","PeriodicalId":10444,"journal":{"name":"Clinical Microbiology and Infection","volume":"30 12","pages":"Pages 1514-1522"},"PeriodicalIF":8.7000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Convalescent plasma and predictors of mortality among hospitalized patients with COVID-19: a systematic review and meta-analysis\",\"authors\":\"Massimo Franchini , Mario Cruciani , Carlo Mengoli , Arturo Casadevall , Claudia Glingani , Michael J. Joyner , Liise-anne Pirofski , Jonathon W. Senefeld , Shmuel Shoham , David J. Sullivan , Matteo Zani , Daniele Focosi\",\"doi\":\"10.1016/j.cmi.2024.07.020\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Plasma collected from recovered patients with COVID-19 (COVID-19 convalescent plasma [CCP]) was the first antibody-based therapy employed to fight the COVID-19 pandemic. While the therapeutic effect of early administration of CCP in COVID-19 outpatients has been recognized, conflicting data exist regarding the efficacy of CCP administration in hospitalized patients.</div></div><div><h3>Objectives</h3><div>To examine the effect of CCP compared to placebo or standard treatment, and to evaluate whether time from onset of symptoms to treatment initiation influenced the effect.</div></div><div><h3>Data sources</h3><div>Electronic databases were searched for studies published from January 2020 to January 2024.</div></div><div><h3>Study eligibility criteria</h3><div>Randomized clinical trials (RCTs) investigating the effect of CCP on COVID-19 mortality in hospitalized patients with COVID-19.</div></div><div><h3>Participants</h3><div>Hospitalized patients with COVID-19.</div></div><div><h3>Interventions</h3><div>CCP versus no CCP.</div></div><div><h3>Assessment of risk of bias</h3><div>Cochrane risk of bias tool for RCTs.</div></div><div><h3>Methods of data synthesis</h3><div>The random-effects model was used to calculate the pooled risk ratio (RR) with 95% CI for the pooled effect estimates of CCP treatment. The Grading of Recommendations Assessment, Development and Evaluation was used to evaluate the certainty of evidence.</div></div><div><h3>Results</h3><div>Twenty-seven RCTs were included, representing 18,877 hospitalized patients with COVID-19. When transfused within 7 days from symptom onset, CCP significantly reduced the risk of death compared to standard therapy or placebo (RR, 0.76; 95% CI, 0.61–0.95), while later CCP administration was not associated with a mortality benefit (RR, 0.98; 95% CI, 0.90–1.06). The certainty of the evidence was graded as moderate. 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Convalescent plasma and predictors of mortality among hospitalized patients with COVID-19: a systematic review and meta-analysis
Background
Plasma collected from recovered patients with COVID-19 (COVID-19 convalescent plasma [CCP]) was the first antibody-based therapy employed to fight the COVID-19 pandemic. While the therapeutic effect of early administration of CCP in COVID-19 outpatients has been recognized, conflicting data exist regarding the efficacy of CCP administration in hospitalized patients.
Objectives
To examine the effect of CCP compared to placebo or standard treatment, and to evaluate whether time from onset of symptoms to treatment initiation influenced the effect.
Data sources
Electronic databases were searched for studies published from January 2020 to January 2024.
Study eligibility criteria
Randomized clinical trials (RCTs) investigating the effect of CCP on COVID-19 mortality in hospitalized patients with COVID-19.
Participants
Hospitalized patients with COVID-19.
Interventions
CCP versus no CCP.
Assessment of risk of bias
Cochrane risk of bias tool for RCTs.
Methods of data synthesis
The random-effects model was used to calculate the pooled risk ratio (RR) with 95% CI for the pooled effect estimates of CCP treatment. The Grading of Recommendations Assessment, Development and Evaluation was used to evaluate the certainty of evidence.
Results
Twenty-seven RCTs were included, representing 18,877 hospitalized patients with COVID-19. When transfused within 7 days from symptom onset, CCP significantly reduced the risk of death compared to standard therapy or placebo (RR, 0.76; 95% CI, 0.61–0.95), while later CCP administration was not associated with a mortality benefit (RR, 0.98; 95% CI, 0.90–1.06). The certainty of the evidence was graded as moderate. Meta-regression analysis demonstrated increasing mortality effects for longer interval to transfusion or worse initial clinical severity.
Conclusions
In-hospital transfusion of CCP within 7 days from symptom onset conferred a mortality benefit.
期刊介绍:
Clinical Microbiology and Infection (CMI) is a monthly journal published by the European Society of Clinical Microbiology and Infectious Diseases. It focuses on peer-reviewed papers covering basic and applied research in microbiology, infectious diseases, virology, parasitology, immunology, and epidemiology as they relate to therapy and diagnostics.