Abstract | BACKGROUND: METHODS: We systematically searched PubMed, PMC PubMed Central, Medline, World Health Organization COVID-19 Database, Embase, Web of Science, Cochrane Library, Emcare, and Academic Search Premier (through 30 June 2020). Random effects meta-analysis was used to pool the risk ratios and risk differences of individual studies. Risk of bias was appraised using the Methodological Index for Non-randomized Studies (MINORS) checklist. RESULTS: The search strategy retrieved 743 unique titles, of which 10 studies (all on tocilizumab [TCZ]) comprising 1358 patients were included. Nine of 10 studies were considered to be of high quality. Meta-analysis showed that the TCZ group had lower mortality than the control group. The risk ratio was 0.27 (95% confidence interval [CI], .12-.59) and the risk difference was 12% (95% CI, 4.6%-20%) in favor of the TCZ group. With only a few studies available, there were no differences observed regarding side effects. CONCLUSIONS: Our results showed that mortality was 12% lower for COVID-19 patients treated with TCZ compared with those not treated with TCZ. The number needed to treat was 11, suggesting that for every 11 (severe) COVID-19 patients treated with TCZ, 1 death is prevented. These results require confirmation by randomized controlled trials.
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Authors | Jishnu Malgie, Jan W Schoones, Bart G Pijls |
Journal | Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
(Clin Infect Dis)
Vol. 72
Issue 11
Pg. e742-e749
(06 01 2021)
ISSN: 1537-6591 [Electronic] United States |
PMID | 32964913
(Publication Type: Journal Article, Meta-Analysis, Systematic Review)
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Copyright | © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. |
Chemical References |
- Antibodies, Monoclonal, Humanized
- tocilizumab
|
Topics |
- Antibodies, Monoclonal, Humanized
(adverse effects)
- Humans
- SARS-CoV-2
- COVID-19 Drug Treatment
|