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COVID-19 Convalescent Plasma Therapy: Long-term Implications
Hyunah Yoon1, Yi Li2, Keith S Goldfeld2
1Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York, USA.
Insights
COVID-19 convalescent plasma (CCP) did not improve long-term post-acute sequelae (PASC) symptoms. Demographic factors like sex, age, and infection timing significantly influenced PASC symptom reporting 18 months after hospitalization.
Area of Science:
- Infectious Diseases
- Immunology
- Public Health
Background:
- The long-term effects of COVID-19 treatments on Post-Acute Sequelae of SARS-CoV-2 infection (PASC) remain largely unknown.
- Investigating the impact of COVID-19 convalescent plasma (CCP) on PASC symptoms and general health is crucial for understanding long-term recovery.
Purpose of the Study:
- To evaluate the 18-month efficacy of COVID-19 convalescent plasma (CCP) therapy in mitigating Post-Acute Sequelae of SARS-CoV-2 infection (PASC) symptoms.
- To assess the long-term impact of CCP on general health and Patient-Reported Outcomes Measurement Information System (PROMIS) scores in hospitalized COVID-19 patients.
Main Methods:
- The CONTAIN-Extend study followed 281 participants from the CONTAIN COVID-19 trial for 18 months post-hospitalization.
- Data collection included symptom surveys, global health assessments, and biospecimen analysis.
- Multivariable regression analyses were used to assess associations between CCP treatment arms and PASC symptoms, adjusting for relevant covariates.
Main Results:
- No significant differences in PASC symptoms or PROMIS scores were observed between the CCP and placebo groups.
- Female sex, age between 45-64 years, and enrollment during April-June 2020 were associated with increased general symptoms and poorer physical health.
- Hispanic and Black participants reported poorer physical health outcomes compared to White participants.
Conclusions:
- COVID-19 convalescent plasma (CCP) therapy showed no lasting benefit for Post-Acute Sequelae of SARS-CoV-2 infection (PASC) symptoms or overall health at 18 months.
- Demographic factors including sex, age, and the timing of acute infection are significant predictors of long-term symptom reporting and health outcomes after COVID-19 hospitalization.
Background:
The long-term effect of coronavirus disease 2019 (COVID-19) acute treatments on postacute sequelae of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (PASC) is unknown. The CONTAIN-Extend study explores the long-term impact of COVID-19 convalescent plasma (CCP) therapy on postacute sequelae of SARS-CoV-2 infection (PASC) symptoms and general health 18 months following hospitalization.
Methods:
The CONTAIN-Extend study examined 281 participants from the original CONTAIN COVID-19 trial (CONTAIN-RCT, NCT04364737) at 18 months post-hospitalization for acute COVID-19. Symptom surveys, global health assessments, and biospecimen collection were performed from November 2021 to October 2022. Multivariable logistic and linear regression estimated associations between the randomization arms and self-reported symptoms and Patient-Reported Outcomes Measurement Information System (PROMIS) scores and adjusted for covariables, including age, sex, race/ethnicity, disease severity, and CONTAIN enrollment quarter and sites.
Results:
There were no differences in symptoms or PROMIS scores between CCP and placebo (adjusted odds ratio [aOR] of general symptoms, 0.95; 95% CI, 0.54-1.67). However, females (aOR, 3.01; 95% CI, 1.73-5.34), those 45-64 years (aOR, 2.55; 95% CI, 1.14-6.23), and April-June 2020 enrollees (aOR, 2.39; 95% CI, 1.10-5.19) were more likely to report general symptoms and have poorer PROMIS physical health scores than their respective reference groups. Hispanic participants (difference, -3.05; 95% CI, -5.82 to -0.27) and Black participants (-4.48; 95% CI, -7.94 to -1.02) had poorer PROMIS physical health than White participants.
Conclusions:
CCP demonstrated no lasting effect on PASC symptoms or overall health in comparison to the placebo. This study underscores the significance of demographic factors, including sex, age, and timing of acute infection, in influencing symptom reporting 18 months after acute hypoxic COVID-19 hospitalization.
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