Antipsychotic use and 28-day mortality in patients hospitalized with COVID-19 : A multicenter observational retrospective study
Copyright © 2023. Published by Elsevier B.V..
Prior research has yielded conflicting results about the potential influence of antipsychotics in patients with COVID-19. In this multicenter retrospective study, we examined the association of antipsychotic use at admission with 28-day all-cause mortality in a sample of 59,021 adult patients hospitalized with COVID-19 from January 2020 to November 2021. In a 1:1 ratio matched analytic sample (N=1,454) accounting for age, sex, hospital, hospitalization period, the Elixhauser Comorbidity Index, other psychotropic medications, medications prescribed according to compassionate use or as part of a clinical trial, current diagnoses of psychiatric disorders, and clinical and biological markers of COVID-19 severity, antipsychotic use was not associated with 28-day mortality [23.5% (N=727) versus 18.6% (N=727); OR=1.16; 95%CI=0.89-1.51; p=0.280]. This association remained non-significant in exploratory analyses across all classes of antipsychotics and individual molecules, except for typical antipsychotics and loxapine, which were significantly linked to increased 28-day mortality, associations likely due to residual indication bias. Contrariwise, antipsychotics prescribed at daily doses higher than 200 mg of chlorpromazine-equivalents might be associated with reduced 28-day mortality when compared to patients not taking antipsychotics in the matched analytic sample [10.4% (N=154) versus 18.6% (N=727); AOR=0.56; 95%CI=0.31-0.96; p=0.040]. These results suggest that antipsychotic use, when prescribed at usual doses, are not be associated with 28-day mortality in patients hospitalized with COVID-19.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:75 |
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Enthalten in: |
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology - 75(2023) vom: 02. Okt., Seite 93-104 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Sánchez-Rico, Marina [VerfasserIn] |
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Links: |
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Themen: |
Acid sphingomyelinase |
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Anmerkungen: |
Date Revised 01.10.2023 published: Print-Electronic Citation Status Publisher |
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doi: |
10.1016/j.euroneuro.2023.06.005 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM362108781 |
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520 | |a Prior research has yielded conflicting results about the potential influence of antipsychotics in patients with COVID-19. In this multicenter retrospective study, we examined the association of antipsychotic use at admission with 28-day all-cause mortality in a sample of 59,021 adult patients hospitalized with COVID-19 from January 2020 to November 2021. In a 1:1 ratio matched analytic sample (N=1,454) accounting for age, sex, hospital, hospitalization period, the Elixhauser Comorbidity Index, other psychotropic medications, medications prescribed according to compassionate use or as part of a clinical trial, current diagnoses of psychiatric disorders, and clinical and biological markers of COVID-19 severity, antipsychotic use was not associated with 28-day mortality [23.5% (N=727) versus 18.6% (N=727); OR=1.16; 95%CI=0.89-1.51; p=0.280]. This association remained non-significant in exploratory analyses across all classes of antipsychotics and individual molecules, except for typical antipsychotics and loxapine, which were significantly linked to increased 28-day mortality, associations likely due to residual indication bias. Contrariwise, antipsychotics prescribed at daily doses higher than 200 mg of chlorpromazine-equivalents might be associated with reduced 28-day mortality when compared to patients not taking antipsychotics in the matched analytic sample [10.4% (N=154) versus 18.6% (N=727); AOR=0.56; 95%CI=0.31-0.96; p=0.040]. These results suggest that antipsychotic use, when prescribed at usual doses, are not be associated with 28-day mortality in patients hospitalized with COVID-19 | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Acid sphingomyelinase | |
650 | 4 | |a Antipsychotic | |
650 | 4 | |a COVID-19 | |
650 | 4 | |a FIASMA | |
650 | 4 | |a Mortality | |
650 | 4 | |a SARS-CoV-2 | |
700 | 1 | |a Edán-Sánchez, Alejandro |e verfasserin |4 aut | |
700 | 1 | |a Olfson, Mark |e verfasserin |4 aut | |
700 | 1 | |a Alvarado, Jesús M |e verfasserin |4 aut | |
700 | 1 | |a Airagnes, Guillaume |e verfasserin |4 aut | |
700 | 1 | |a Rezaei, Katayoun |e verfasserin |4 aut | |
700 | 1 | |a Delcuze, Aude |e verfasserin |4 aut | |
700 | 1 | |a Peyre, Hugo |e verfasserin |4 aut | |
700 | 1 | |a Limosin, Frédéric |e verfasserin |4 aut | |
700 | 1 | |a Hoertel, Nicolas |e verfasserin |4 aut | |
700 | 0 | |a AP-HP / Université Paris Cité / INSERM COVID-19 research collaboration, AP-HP COVID CDR Initiative, and “Entrepôt de Données de Santé” AP-HP Consortium |e verfasserin |4 aut | |
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