EFFECT OF PAXLOVID TREATMENT DURING ACUTE COVID-19 ON LONG COVID ONSET: AN EHR-BASED TARGET TRIAL EMULATION FROM THE N3C AND RECOVER CONSORTIA.
Alexander J PreissAbhishek BhatiaLeyna V AragonJohn M BarattaMonika BaskaranFrank BlanceroM Daniel BrannockRobert F ChewIvan DiazMegan L FitzgeraldElizabeth P KellyAndrea G ZhouThomas W CartonChristopher G ChuteMelissa A HaendelRichard A MoffittEmily Rose PfaffPublished in: medRxiv : the preprint server for health sciences (2024)
Preventing and treating post-acute sequelae of SARS-CoV-2 infection (PASC), commonly known as Long COVID, has become a public health priority. In this study, we examined whether treatment with Paxlovid in the acute phase of COVID-19 helps prevent the onset of PASC. We used electronic health records from the National Covid Cohort Collaborative (N3C) to define a cohort of 426,352 patients who had COVID-19 since April 1, 2022, and were eligible for Paxlovid treatment due to risk for progression to severe COVID-19. We used the target trial emulation (TTE) framework to estimate the effect of Paxlovid treatment on PASC incidence. We estimated overall PASC incidence using a computable phenotype. We also measured the onset of novel cognitive, fatigue, and respiratory symptoms in the post-acute period. Paxlovid treatment did not have a significant effect on overall PASC incidence (relative risk [RR] = 0.98, 95% confidence interval [CI] 0.95-1.01). However, it had a protective effect on cognitive (RR = 0.90, 95% CI 0.84-0.96) and fatigue (RR = 0.95, 95% CI 0.91-0.98) symptom clusters, which suggests that the etiology of these symptoms may be more closely related to viral load than that of respiratory symptoms.
Keyphrases
- coronavirus disease
- sars cov
- public health
- electronic health record
- liver failure
- respiratory failure
- physical activity
- early onset
- sleep quality
- combination therapy
- depressive symptoms
- quality improvement
- aortic dissection
- open label
- smoking cessation
- acute respiratory distress syndrome
- adverse drug
- extracorporeal membrane oxygenation
- phase ii
- clinical decision support