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Observational Study of Chlorpromazine in Hospitalized Patients with Covid-19
Nicolas Hoertel; Marina Sanchez Rico; Raphael Vernet; Anne-Sophie Jannot; Antoine Neuraz; Carlos Blanco; Cedric Lemogne; Guillaume Airagnes; Nicolas Paris; Christel Daniel; Alexandre Gramfort; Guillaume Lemaitre; Melodie Bernaux; Ali Bellamine; Nathanael Beeker; Frederic Limosin.
Affiliation
  • Nicolas Hoertel; Universite de Paris
  • Marina Sanchez Rico; Universidad Complutense de Madrid
  • Raphael Vernet; AP-HP
  • Anne-Sophie Jannot; AP-HP
  • Antoine Neuraz; AP-HP
  • Carlos Blanco; NIDA
  • Cedric Lemogne; Universite de Paris
  • Guillaume Airagnes; Universite de Paris
  • Nicolas Paris; AP-HP
  • Christel Daniel; AP-HP
  • Alexandre Gramfort; INRIA
  • Guillaume Lemaitre; INRIA
  • Melodie Bernaux; AP-HP
  • Ali Bellamine; AP-HP
  • Nathanael Beeker; AP-HP
  • Frederic Limosin; Universite de Paris
Preprint in En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20154310
Journal article
A scientific journal published article is available and is probably based on this preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT
On the grounds of its anti-inflammatory and potential antiviral effects, chlorpromazine has been suggested to be effective treatment for Covid-19. We examined the association between chlorpromazine use and respiratory failure among all hospitalized adults with Covid-19 at the 39 Greater Paris University hospitals since the beginning of the epidemic. Study baseline was defined as the date of hospital admission. The primary endpoint was a composite of intubation or death in a time-to-event analysis adjusting for numerous potential confounders. We used a multivariable Cox model with inverse probability weighting according to the propensity score. Of the 12,217 adult inpatients with a positive Covid-19 RT-PCR test included in the analyses, 57 (0.47%) received chlorpromazine. Over a mean follow-up of 20.8 days, the primary endpoint occurred in 29 patients (50.9%) exposed to chlorpromazine and 1,899 patients (15.6%) who were not. In the main analysis, there was a positive significant association between chlorpromazine use and the outcome (HR, 1.67; 95% CI, 1.09 to 2.56, p=0.019), while a Cox regression in a matched analytic sample yielded non-significant association (1.38; 95% CI, 0.91 to 2.09, p=0.123). These findings suggest that chlorpromazine is unlikely to have a clinical efficacy for Covid-19.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Type of study: Cohort_studies / Observational_studies / Prognostic_studies Language: En Year: 2020 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Type of study: Cohort_studies / Observational_studies / Prognostic_studies Language: En Year: 2020 Document type: Preprint