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Symptom Duration and Resolution With Early Outpatient Treatment of Convalescent Plasma for Coronavirus Disease 2019:
Sheriza N Baksh1, Sonya L Heath2, Yuriko Fukuta3
1Department of Epidemiology Bloomberg Johns Hopkins School of Public Health, Baltimore, Maryland, USA.
Insights
COVID-19 convalescent plasma (CCP) did not speed up symptom resolution in outpatients. Early treatment with CCP showed no significant difference in symptom recovery compared to control plasma.
Area of Science:
- Infectious Diseases
- Immunology
- Clinical Medicine
Background:
- Coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) is known to reduce hospitalizations in early outpatient treatment.
- The effect of CCP on the time to symptom resolution in outpatients remains unclear.
Purpose of the Study:
- To evaluate if COVID-19 convalescent plasma (CCP) accelerates symptom resolution in outpatients with early COVID-19.
- To compare the prevalence of symptom clusters at day 14 between CCP and control plasma recipients.
Main Methods:
- An adjusted subdistribution hazard model was used to assess symptom resolution at day 14, with hospitalization as a competing risk.
- Symptom clusters were defined based on biologic clustering, impact on work, and algorithmic analysis.
- 1070 outpatients were followed up after transfusion.
Main Results:
- At day 14, symptom resolution rates were similar between CCP (70.8%) and control plasma (71.6%) groups.
- No significant difference in symptom resolution by day 14 was observed between CCP and control groups after adjusting for baseline characteristics (aSHR, 0.99; P = .62).
- The most common symptom cluster (cough, fatigue, shortness of breath, headache) showed no significant difference in prevalence between groups (57.2% vs 61.1%, P = .16).
Conclusions:
- COVID-19 convalescent plasma (CCP) was not associated with faster symptom resolution compared to control plasma in outpatients with early COVID-19.
- No significant differences in the prevalence of individual symptoms or symptom clusters were found between treatment groups at day 14.
Background:
Coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) reduces hospitalizations among outpatients treated early after symptom onset. It is unknown whether CCP reduces time to symptom resolution among outpatients.
Methods:
We evaluated symptom resolution at day 14 by trial arm using an adjusted subdistribution hazard model, with hospitalization as a competing risk. We also assessed the prevalence of symptom clusters at day 14 between treatments. Clusters were defined based on biologic clustering, impact on ability to work, and an algorithm.
Results:
Among 1070 outpatients followed up after transfusion, 381 of 538 (70.8%) receiving CCP and 381 of 532 (71.6%) receiving control plasma were still symptomatic (P = .78) at day 14. Associations between CCP and symptom resolution by day 14 did not differ significantly from those in controls after adjustment for baseline characteristics (adjusted subdistribution hazard ratio, 0.99; P = .62). The most common cluster consisted of cough, fatigue, shortness of breath, and headache and was found in 308 (57.2%) and 325 (61.1%) of CCP and control plasma recipients, respectively (P = .16).
Conclusions:
In this trial of outpatients with early COVID-19, CCP was not associated with faster resolution of symptoms compared with control. Overall, there were no differences by treatment in the prevalence of each symptom or symptom clusters at day 14.
Clinical Trials Registration:
NCT04373460.
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