Hydroxyzine Use and Mortality in Patients Hospitalized for COVID-19: A Multicenter Observational Study

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Sánchez-Rico, Marina | Limosin, Frédéric | Vernet, Raphaël | Beeker, Nathanaël | Neuraz, Antoine | Blanco, Carlos | Olfson, Mark | Lemogne, Cédric | Meneton, Pierre | Daniel, Christel | Paris, Nicolas | Gramfort, Alexandre | Lemaitre, Guillaume | de La Muela, Pedro | Salamanca, Elisa | Bernaux, Mélodie | Bellamine, Ali | Burgun, Anita | Hoertel, Nicolas

Edité par CCSD ; MDPI -

International audience. Background: Based on its antiviral activity, anti-inflammatory properties, and functional inhibition effects on the acid sphingomyelinase/ceramide system (FIASMA), we sought to examine the potential usefulness of the H1 antihistamine hydroxyzine in patients hospitalized for COVID-19. (2) Methods: In a multicenter observational study, we included 15,103 adults hospitalized for COVID-19, of which 164 (1.1%) received hydroxyzine within the first 48 h of hospitalization, administered orally at a median daily dose of 25.0 mg (SD = 29.5). We compared mortality rates between patients who received hydroxyzine at hospital admission and those who did not, using a multivariable logistic regression model adjusting for patients’ characteristics, medical conditions, and use of other medications. (3) Results: This analysis showed a significant association between hydroxyzine use and reduced mortality (AOR, 0.51; 95%CI, 0.29–0.88, p = 0.016). This association was similar in multiple sensitivity analyses. (4) Conclusions: In this retrospective observational multicenter study, the use of the FIASMA hydroxyzine was associated with reduced mortality in patients hospitalized for COVID-19. Double-blind placebo-controlled randomized clinical trials of hydroxyzine for COVID-19 are needed to confirm these results, as are studies to examine the potential usefulness of this medication for outpatients and as post-exposure prophylaxis for individuals at high risk for severe COVID-19.

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