| Literature DB >> 33256141 |
Hoyt Burdick1,2, Carson Lam3, Samson Mataraso3, Anna Siefkas3, Gregory Braden4, R Phillip Dellinger5, Andrea McCoy6, Jean-Louis Vincent7, Abigail Green-Saxena3, Gina Barnes3, Jana Hoffman3, Jacob Calvert3, Emily Pellegrini3, Ritankar Das3.
Abstract
Therapeutic agents for the novel coronavirus disease 2019 (COVID-19) have been proposed, but evidence supporting their use is limited. A machine learning algorithm was developed in order to identify a subpopulation of COVID-19 patients for whom hydroxychloroquine was associated with improved survival; this population might be relevant for study in a clinical trial. A pragmatic trial was conducted at six United States hospitals. We enrolled COVID-19 patients that were admitted between 10 March and 4 June 2020. Treatment was not randomized. The study endpoint was mortality; discharge was a competing event. Hazard ratios were obtained on the entire population, and on the subpopulation indicated by the algorithm as suitable for treatment. A total of 290 patients were enrolled. In the subpopulation that was identified by the algorithm, hydroxychloroquine was associated with a statistically significant (p = 0.011) increase in survival (adjusted hazard ratio 0.29, 95% confidence interval (CI) 0.11-0.75). Adjusted survival among the algorithm indicated patients was 82.6% in the treated arm and 51.2% in the arm not treated. No association between treatment and mortality was observed in the general population. A 31% increase in survival at the end of the study was observed in a population of COVID-19 patients that were identified by a machine learning algorithm as having a better outcome with hydroxychloroquine treatment. Precision medicine approaches may be useful in identifying a subpopulation of COVID-19 patients more likely to be proven to benefit from hydroxychloroquine treatment in a clinical trial.Entities:
Keywords: COVID-19; SARS-Cov-2; drug treatment; hydroxychloroquine; machine learning; mortality; prediction
Year: 2020 PMID: 33256141 PMCID: PMC7760047 DOI: 10.3390/jcm9123834
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241