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DC Field | Value | Language |
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dc.contributor.author | Chiraphat Kloypan | en_US |
dc.contributor.author | Matthanaporn Saesong | en_US |
dc.contributor.author | Juthamat Sangsuemoon | en_US |
dc.contributor.author | Prawat Chantharit | en_US |
dc.contributor.author | Pajaree Mongkhon | en_US |
dc.date.accessioned | 2022-10-16T07:00:30Z | - |
dc.date.available | 2022-10-16T07:00:30Z | - |
dc.date.issued | 2021-11-01 | en_US |
dc.identifier.issn | 13652362 | en_US |
dc.identifier.issn | 00142972 | en_US |
dc.identifier.other | 2-s2.0-85112686321 | en_US |
dc.identifier.other | 10.1111/eci.13663 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112686321&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/75526 | - |
dc.description.abstract | Background: There is still a lack of consensus on the efficacy of convalescent plasma (CP) treatment in COVID-19 patients. We performed a systematic review and meta-analysis to investigate the efficacy of CP vs standard treatment/non-CP on clinical outcomes in COVID-19 patients. Methods: Cochrane Library, PubMed, EMBASE and ClinicalTrials.gov were searched from December 2019 to 16 July 2021, for data from clinical trials and observational studies. The primary outcome was all-cause mortality. Risk estimates were pooled using a random-effect model. Risk of bias was assessed by Cochrane Risk of Bias tool for clinical trials and Newcastle-Ottawa Scale for observational studies. Results: In total, 18 peer-reviewed clinical trials, 3 preprints and 26 observational studies met the inclusion criteria. In the meta-analysis of 18 peer-reviewed trials, CP use had a 31% reduced risk of all-cause mortality compared with standard treatment use (pooled risk ratio [RR] = 0.69, 95% confidence interval [CI]: 0.56-0.86, P =.001, I2 = 50.1%). Based on severity and region, CP treatment significantly reduced risk of all-cause mortality in patients with severe and critical disease and studies conducted in Asia, pooled RR = 0.61, 95% CI: 0.47-0.81, P =.001, I2 = 0.0%; pooled RR = 0.67, 95% CI: 0.49-0.92, P =.013, I2 = 0.0%; and pooled RR = 0.62, 95% CI: 0.48-0.80, P <.001, I2 = 20.3%, respectively. The meta-analysis of observational studies showed the similar results to the clinical trials. Conclusions: Convalescent plasma use was associated with reduced risk of all-cause mortality in severe or critical COVID-19 patients. However, the findings were limited with a moderate degree of heterogeneity. Further studies with well-designed and larger sample size are needed. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.title | CONVALESCENT plasma for COVID-19: A meta-analysis of clinical trials and real-world evidence | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | European Journal of Clinical Investigation | en_US |
article.volume | 51 | en_US |
article.stream.affiliations | University of Phayao | en_US |
article.stream.affiliations | Charité – Universitätsmedizin Berlin | en_US |
article.stream.affiliations | Faculty of Medicine Ramathibodi Hospital, Mahidol University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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