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Convalescent Plasma Treatment in Patients with Covid-19: A Systematic Review and Meta-Analysis

Jorda et al., Frontiers in Immunology, doi:10.3389/fimmu.2022.817829
Feb 2022  
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Meta-analysis of 16 RCTs with 16,317 COVID-19 patients showing no significant difference in mortality, mechanical ventilation, time to clinical improvement, or time to discharge with convalescent plasma treatment. Subgroup analyses in critically ill, non-critically ill, and seronegative patients also showed no significant difference in mortality. Authors note that the high certainty evidence does not support routine use of convalescent plasma in COVID-19 patients.
Currently there are 54 convalescent plasma studies and meta analysis shows:
OutcomeImprovement
Mortality2% higher [-3‑7%]
Ventilation0% higher [-11‑14%]
ICU admission9% higher [-6‑27%]
Hospitalization2% higher [-11‑16%]
Jorda et al., 7 Feb 2022, peer-reviewed, 7 authors. Contact: georg.gelbenegger@meduniwien.ac.at.
This PaperConv. PlasmaAll
Convalescent Plasma Treatment in Patients with Covid-19: A Systematic Review and Meta-Analysis
Anselm Jorda, Manuel Kussmann, Nebu Kolenchery, Jolanta M Siller-Matula, Markus Zeitlinger, Bernd Jilma, Georg Gelbenegger
Frontiers in Immunology, doi:10.3389/fimmu.2022.817829
Convalescent plasma is a suggested treatment for Coronavirus disease 2019 , but its efficacy is uncertain. We aimed to evaluate whether the use of convalescent plasma is associated with improved clinical outcomes in patients with Covid-19.In this systematic review and meta-analysis, we searched randomized controlled trials investigating the use of convalescent plasma in patients with Covid-19 in Medline, Embase, Web of Science, Cochrane Library, and medRxiv from inception to October 17 th , 2021. Two reviewers independently extracted the data. The primary efficacy outcome was all-cause mortality. The Cochrane Risk of Bias Tool and GRADE (Grading of Recommendations Assessment, Development and Evaluation) method were used. This study was registered with PROSPERO, CRD42021284861. Of the 8874 studies identified in the initial search, sixteen trials comprising 16 317 patients with Covid-19 were included. In the overall population, the all-cause mortality was 23.8% (2025 of 8524) with convalescent plasma and 24.4% (1903 of 7769) with standard of care (risk ratio (RR) 0.97, 95% CI 0.90-1.04) (high-certainty evidence). All-cause mortality did not differ in the subgroups of noncritically ill (21.7% [1288 of 5929] vs. 22.4% [1320 of 5882]) and critically ill (36.9% [518 of 1404] vs. 36.4% [455 of 1247]) patients with Covid-19. The use of convalescent plasma in patients who tested negative for anti-SARS-CoV-2 antibodies at baseline was not associated with significantly improved survival (RR 0.94, 95% CI 0.87-1.02). In the overall study population, initiation of mechanical ventilation (RR 0.97, 95% CI 0.88-1.07), time to clinical improvement (HR 1.09, 95% CI 0.91-1.30), and time to discharge (HR 0.95, 95% CI 0.89-1.02) were similar between the two groups. In patients with Covid-19, treatment with convalescent plasma, as compared with control, was not associated with lower all-cause mortality or improved disease progression, irrespective of disease severity and baseline antibody status. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/, identifier PROSPERO (CRD42021284861).
AUTHOR CONTRIBUTIONS GG conceived the idea. AJ and GG performed the research, interpreted the results, and drafted the manuscript. All authors critically revised the manuscript and approved the final version for publication. SUPPLEMENTARY MATERIAL The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2022.817829/ full#supplementary-material Conflict of Interest: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Publisher's Note: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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DOI record: { "DOI": "10.3389/fimmu.2022.817829", "ISSN": [ "1664-3224" ], "URL": "http://dx.doi.org/10.3389/fimmu.2022.817829", "abstract": "<jats:p>Convalescent plasma is a suggested treatment for Coronavirus disease 2019 (Covid-19), but its efficacy is uncertain. We aimed to evaluate whether the use of convalescent plasma is associated with improved clinical outcomes in patients with Covid-19.In this systematic review and meta-analysis, we searched randomized controlled trials investigating the use of convalescent plasma in patients with Covid-19 in Medline, Embase, Web of Science, Cochrane Library, and medRxiv from inception to October 17<jats:sup>th</jats:sup>, 2021. Two reviewers independently extracted the data. The primary efficacy outcome was all-cause mortality. The Cochrane Risk of Bias Tool and GRADE (Grading of Recommendations Assessment, Development and Evaluation) method were used. This study was registered with PROSPERO, CRD42021284861. Of the 8874 studies identified in the initial search, sixteen trials comprising 16 317 patients with Covid-19 were included. In the overall population, the all-cause mortality was 23.8% (2025 of 8524) with convalescent plasma and 24.4% (1903 of 7769) with standard of care (risk ratio (RR) 0.97, 95% CI 0.90-1.04) (high-certainty evidence). All-cause mortality did not differ in the subgroups of noncritically ill (21.7% [1288 of 5929] vs. 22.4% [1320 of 5882]) and critically ill (36.9% [518 of 1404] vs. 36.4% [455 of 1247]) patients with Covid-19. The use of convalescent plasma in patients who tested negative for anti-SARS-CoV-2 antibodies at baseline was not associated with significantly improved survival (RR 0.94, 95% CI 0.87-1.02). In the overall study population, initiation of mechanical ventilation (RR 0.97, 95% CI 0.88-1.07), time to clinical improvement (HR 1.09, 95% CI 0.91-1.30), and time to discharge (HR 0.95, 95% CI 0.89-1.02) were similar between the two groups. 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to Prevent Severe Covid-19 in Older Adults", "author": "Libster", "doi-asserted-by": "publisher", "journal-title": "N Engl J Med", "key": "B20", "volume": "384", "year": "2021" }, { "DOI": "10.1172/JCI150646", "article-title": "A Randomized Double-Blind Controlled Trial of Convalescent Plasma in Adults With Severe COVID-19", "author": "O’Donnell", "doi-asserted-by": "publisher", "journal-title": "J Clin Invest", "key": "B21", "volume": "131", "year": "2021" }, { "DOI": "10.1056/NEJMoa2031304", "article-title": "A Randomized Trial of Convalescent Plasma in Covid-19 Severe Pneumonia", "author": "Simonovich", "doi-asserted-by": "publisher", "journal-title": "N Engl J Med", "key": "B22", "volume": "384", "year": "2021" }, { "DOI": "10.1097/CCM.0000000000005066", "article-title": "Severe Acute Respiratory Syndrome Coronavirus 2 Convalescent Plasma Versus Standard Plasma in Coronavirus Disease 2019 Infected Hospitalized Patients in New York: A Double-Blind Randomized Trial", "author": 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Please send us corrections, updates, or comments. c19early involves the extraction of 100,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. FLCCC and WCH provide treatment protocols.
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