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Clozapine treatment and risk of severe COVID‐19 infection
OBJECTIVE: To investigate whether patients with clozapine treatment are at an increased risk of a more severe COVID‐19 infection as compared with patients on other antipsychotic drugs. METHODS: In this register‐based cohort study, all residents (age 18 or older) in the Stockholm Region with a psycho...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653206/ https://www.ncbi.nlm.nih.gov/pubmed/34676888 http://dx.doi.org/10.1111/acps.13379 |
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author | Ohlis, Anna Sörberg Wallin, Alma Sarafis, Anna Sjöqvist, Hugo MacCabe, James H. Ahlen, Johan Dalman, Christina |
author_facet | Ohlis, Anna Sörberg Wallin, Alma Sarafis, Anna Sjöqvist, Hugo MacCabe, James H. Ahlen, Johan Dalman, Christina |
author_sort | Ohlis, Anna |
collection | PubMed |
description | OBJECTIVE: To investigate whether patients with clozapine treatment are at an increased risk of a more severe COVID‐19 infection as compared with patients on other antipsychotic drugs. METHODS: In this register‐based cohort study, all residents (age 18 or older) in the Stockholm Region with a psychotic disorder diagnosis and antipsychotic treatment were included (N = 8 233) and followed from 1 March 2020 to 14 January 2021. The exposure was defined as clozapine treatment and the outcome measures (indicating a more severe COVID‐19 infection) were: inpatient care, care within intensive care unit or death due to COVID‐19 infection. Differences in outcome rates between exposed (n = 966) and unexposed (other antipsychotics; n = 7 267) were examined using Cox proportional hazards models and expressed as hazard ratios (HR) with 95% confidence intervals (CI). RESULTS: No statistically significant differences in outcome rates were found between the two groups of patients after adjusting for age, sex and residence in retirement homes. The adjusted HR for the exposed compared to the unexposed was 0.96 (95% CI: 0.54, 1.70) for inpatient care; 1.69 (0.48, 5.93) for care in intensive care unit (ICU); and 0.86 (0.26, 2.80) for death. Regarding inpatient care, additional adjusting for country of birth, living in socioeconomically vulnerable areas, number of care visits during the previous year, and comorbid medical illnesses did not alter the results. CONCLUSIONS: Our results may add support to the present guidelines, recommending sustained clozapine treatment during the current COVID‐19 pandemic with careful monitoring and readiness to alter drug doses as needed. |
format | Online Article Text |
id | pubmed-8653206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86532062021-12-08 Clozapine treatment and risk of severe COVID‐19 infection Ohlis, Anna Sörberg Wallin, Alma Sarafis, Anna Sjöqvist, Hugo MacCabe, James H. Ahlen, Johan Dalman, Christina Acta Psychiatr Scand Original Articles OBJECTIVE: To investigate whether patients with clozapine treatment are at an increased risk of a more severe COVID‐19 infection as compared with patients on other antipsychotic drugs. METHODS: In this register‐based cohort study, all residents (age 18 or older) in the Stockholm Region with a psychotic disorder diagnosis and antipsychotic treatment were included (N = 8 233) and followed from 1 March 2020 to 14 January 2021. The exposure was defined as clozapine treatment and the outcome measures (indicating a more severe COVID‐19 infection) were: inpatient care, care within intensive care unit or death due to COVID‐19 infection. Differences in outcome rates between exposed (n = 966) and unexposed (other antipsychotics; n = 7 267) were examined using Cox proportional hazards models and expressed as hazard ratios (HR) with 95% confidence intervals (CI). RESULTS: No statistically significant differences in outcome rates were found between the two groups of patients after adjusting for age, sex and residence in retirement homes. The adjusted HR for the exposed compared to the unexposed was 0.96 (95% CI: 0.54, 1.70) for inpatient care; 1.69 (0.48, 5.93) for care in intensive care unit (ICU); and 0.86 (0.26, 2.80) for death. Regarding inpatient care, additional adjusting for country of birth, living in socioeconomically vulnerable areas, number of care visits during the previous year, and comorbid medical illnesses did not alter the results. CONCLUSIONS: Our results may add support to the present guidelines, recommending sustained clozapine treatment during the current COVID‐19 pandemic with careful monitoring and readiness to alter drug doses as needed. John Wiley and Sons Inc. 2021-10-29 2022-01 /pmc/articles/PMC8653206/ /pubmed/34676888 http://dx.doi.org/10.1111/acps.13379 Text en © 2021 The Authors. Acta Psychiatrica Scandinavica published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Ohlis, Anna Sörberg Wallin, Alma Sarafis, Anna Sjöqvist, Hugo MacCabe, James H. Ahlen, Johan Dalman, Christina Clozapine treatment and risk of severe COVID‐19 infection |
title | Clozapine treatment and risk of severe COVID‐19 infection |
title_full | Clozapine treatment and risk of severe COVID‐19 infection |
title_fullStr | Clozapine treatment and risk of severe COVID‐19 infection |
title_full_unstemmed | Clozapine treatment and risk of severe COVID‐19 infection |
title_short | Clozapine treatment and risk of severe COVID‐19 infection |
title_sort | clozapine treatment and risk of severe covid‐19 infection |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653206/ https://www.ncbi.nlm.nih.gov/pubmed/34676888 http://dx.doi.org/10.1111/acps.13379 |
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