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Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study

BACKGROUND: Many older patients have chronic kidney disease (CKD), and a lower dose of anti-depressants paroxetine, mirtazapine and venlafaxine is recommended in patients with CKD to prevent drug accumulation from reduced elimination. Using information available in large population-based healthcare...

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Autores principales: Dev, Varun, Dixon, Stephanie N, Fleet, Jamie L, Gandhi, Sonja, Gomes, Tara, Harel, Ziv, Jain, Arsh K, Shariff, Salimah Z, Tawadrous, Davy, Weir, Matthew A, Garg, Amit X
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024017/
https://www.ncbi.nlm.nih.gov/pubmed/24884589
http://dx.doi.org/10.1186/1471-2369-15-79
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author Dev, Varun
Dixon, Stephanie N
Fleet, Jamie L
Gandhi, Sonja
Gomes, Tara
Harel, Ziv
Jain, Arsh K
Shariff, Salimah Z
Tawadrous, Davy
Weir, Matthew A
Garg, Amit X
author_facet Dev, Varun
Dixon, Stephanie N
Fleet, Jamie L
Gandhi, Sonja
Gomes, Tara
Harel, Ziv
Jain, Arsh K
Shariff, Salimah Z
Tawadrous, Davy
Weir, Matthew A
Garg, Amit X
author_sort Dev, Varun
collection PubMed
description BACKGROUND: Many older patients have chronic kidney disease (CKD), and a lower dose of anti-depressants paroxetine, mirtazapine and venlafaxine is recommended in patients with CKD to prevent drug accumulation from reduced elimination. Using information available in large population-based healthcare administrative databases, we conducted this study to determine if ignoring the recommendation and prescribing a higher versus lower dose of anti-depressants associates with a higher risk of adverse events. METHODS: We conducted a population-based cohort study to describe the 30-day risk of delirium in older adults who initiated a higher vs. lower dose of these three anti-depressants in routine care. We defined delirium using the best proxy available in our data sources - hospitalization with an urgent head computed tomography (CT) scan. We determined if CKD status modified the association between anti-depressant dose and outcome, and examined the secondary outcome of 30 day all-cause mortality. We used multivariable logistic regression analyses to estimate adjusted odds ratios (relative risk (RR)) and 95% confidence intervals. RESULTS: We identified adults (mean age 75) in Ontario who started a new study anti-depressant at a higher dose (n = 36,651; 31%) or lower dose (n = 81,160; 69%). Initiating a higher vs. lower dose was not associated with an increased risk of hospitalization with head CT (1.09% vs. 1.27% (adjusted RR 0.90; 95% CI, 0.80 to 1.02), but was associated with a lower risk of all-cause mortality (0.76% vs. 0.97% RR 0.82; 95% CI, 0.71 to 0.95). Neither of these relative risks were modified by the presence of CKD (p = 0.16, 0.68, respectively). CONCLUSIONS: We did not observe an increase in two adverse outcomes when study anti-depressants were initiated at a higher dose in elderly patients with moderate CKD. Contrary to our hypothesis, the 30-day risk of mortality was lower when a higher versus lower dose of anti-depressant was initiated in these patients, a finding which requires corroboration and further study.
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spelling pubmed-40240172014-05-17 Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study Dev, Varun Dixon, Stephanie N Fleet, Jamie L Gandhi, Sonja Gomes, Tara Harel, Ziv Jain, Arsh K Shariff, Salimah Z Tawadrous, Davy Weir, Matthew A Garg, Amit X BMC Nephrol Research Article BACKGROUND: Many older patients have chronic kidney disease (CKD), and a lower dose of anti-depressants paroxetine, mirtazapine and venlafaxine is recommended in patients with CKD to prevent drug accumulation from reduced elimination. Using information available in large population-based healthcare administrative databases, we conducted this study to determine if ignoring the recommendation and prescribing a higher versus lower dose of anti-depressants associates with a higher risk of adverse events. METHODS: We conducted a population-based cohort study to describe the 30-day risk of delirium in older adults who initiated a higher vs. lower dose of these three anti-depressants in routine care. We defined delirium using the best proxy available in our data sources - hospitalization with an urgent head computed tomography (CT) scan. We determined if CKD status modified the association between anti-depressant dose and outcome, and examined the secondary outcome of 30 day all-cause mortality. We used multivariable logistic regression analyses to estimate adjusted odds ratios (relative risk (RR)) and 95% confidence intervals. RESULTS: We identified adults (mean age 75) in Ontario who started a new study anti-depressant at a higher dose (n = 36,651; 31%) or lower dose (n = 81,160; 69%). Initiating a higher vs. lower dose was not associated with an increased risk of hospitalization with head CT (1.09% vs. 1.27% (adjusted RR 0.90; 95% CI, 0.80 to 1.02), but was associated with a lower risk of all-cause mortality (0.76% vs. 0.97% RR 0.82; 95% CI, 0.71 to 0.95). Neither of these relative risks were modified by the presence of CKD (p = 0.16, 0.68, respectively). CONCLUSIONS: We did not observe an increase in two adverse outcomes when study anti-depressants were initiated at a higher dose in elderly patients with moderate CKD. Contrary to our hypothesis, the 30-day risk of mortality was lower when a higher versus lower dose of anti-depressant was initiated in these patients, a finding which requires corroboration and further study. BioMed Central 2014-05-10 /pmc/articles/PMC4024017/ /pubmed/24884589 http://dx.doi.org/10.1186/1471-2369-15-79 Text en Copyright © 2014 Dev et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dev, Varun
Dixon, Stephanie N
Fleet, Jamie L
Gandhi, Sonja
Gomes, Tara
Harel, Ziv
Jain, Arsh K
Shariff, Salimah Z
Tawadrous, Davy
Weir, Matthew A
Garg, Amit X
Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
title Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
title_full Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
title_fullStr Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
title_full_unstemmed Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
title_short Higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
title_sort higher anti-depressant dose and major adverse outcomes in moderate chronic kidney disease: a retrospective population-based study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024017/
https://www.ncbi.nlm.nih.gov/pubmed/24884589
http://dx.doi.org/10.1186/1471-2369-15-79
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