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Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants

OBJECTIVE: To examine the association between exposure to newer antidepressants and risk of gastrointestinal (GI) and other bleeding complications among individuals with major depressive disorder (MDD). DESIGN: This study uses an incident user cohort design to compare associations between incidence...

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Autores principales: Castro, Victor M, Gallagher, Patience J, Clements, Caitlin C, Murphy, Shawn N, Gainer, Vivian S, Fava, Maurizio, Weilburg, Jeffrey B, Churchill, Susanne E, Kohane, Isaac S, Iosifescu, Dan V, Smoller, Jordan W, Perlis, Roy H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3330255/
https://www.ncbi.nlm.nih.gov/pubmed/22466034
http://dx.doi.org/10.1136/bmjopen-2011-000544
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author Castro, Victor M
Gallagher, Patience J
Clements, Caitlin C
Murphy, Shawn N
Gainer, Vivian S
Fava, Maurizio
Weilburg, Jeffrey B
Churchill, Susanne E
Kohane, Isaac S
Iosifescu, Dan V
Smoller, Jordan W
Perlis, Roy H
author_facet Castro, Victor M
Gallagher, Patience J
Clements, Caitlin C
Murphy, Shawn N
Gainer, Vivian S
Fava, Maurizio
Weilburg, Jeffrey B
Churchill, Susanne E
Kohane, Isaac S
Iosifescu, Dan V
Smoller, Jordan W
Perlis, Roy H
author_sort Castro, Victor M
collection PubMed
description OBJECTIVE: To examine the association between exposure to newer antidepressants and risk of gastrointestinal (GI) and other bleeding complications among individuals with major depressive disorder (MDD). DESIGN: This study uses an incident user cohort design to compare associations between incidence of vascular/bleeding events and the relative affinity (low, moderate or high) of the antidepressant for the serotonin transporter during an exposure risk period for each patient. SETTING: New England healthcare system electronic medical record database. PARTICIPANTS: 36 389 individuals with a diagnosis of MDD and monotherapy with a selective serotonin reuptake inhibitor, serotonin–norepinephrine reuptake inhibitor or other new-generation antidepressant were identified from among 3.1 million patients in a New England healthcare system. PRIMARY AND SECONDARY OUTCOME MEASURES: Rates of bleeding or other vascular complications, including acute liver failure, acute renal failure, asthma, breast cancer and hip fractures. RESULTS: 601 GI bleeds were observed in the 21 462 subjects in the high-affinity group versus 333 among the 14 927 subjects in the lower affinity group (adjusted RR: 1.17, 95% CI 1.02 to 1.34). Similarly, 776 strokes were observed in the high-affinity group versus 434 in the lower affinity treatment group (adjusted RR: 1.18, 95% CI 1.06 to 1.32). No significant association with risk for a priori negative control outcomes, including acute liver failure, acute renal failure, asthma, breast cancer and hip fractures, was identified. CONCLUSIONS: Use of antidepressants with high affinity for the serotonin transporter may confer modestly elevated risk for GI and other bleeding complications. While multiple methodologic limitations must be considered, these results suggest that antidepressants with lower serotonin receptor affinity may be preferred in patients at greater risk for such complications.
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spelling pubmed-33302552012-04-23 Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants Castro, Victor M Gallagher, Patience J Clements, Caitlin C Murphy, Shawn N Gainer, Vivian S Fava, Maurizio Weilburg, Jeffrey B Churchill, Susanne E Kohane, Isaac S Iosifescu, Dan V Smoller, Jordan W Perlis, Roy H BMJ Open Pharmacology and Therapeutics OBJECTIVE: To examine the association between exposure to newer antidepressants and risk of gastrointestinal (GI) and other bleeding complications among individuals with major depressive disorder (MDD). DESIGN: This study uses an incident user cohort design to compare associations between incidence of vascular/bleeding events and the relative affinity (low, moderate or high) of the antidepressant for the serotonin transporter during an exposure risk period for each patient. SETTING: New England healthcare system electronic medical record database. PARTICIPANTS: 36 389 individuals with a diagnosis of MDD and monotherapy with a selective serotonin reuptake inhibitor, serotonin–norepinephrine reuptake inhibitor or other new-generation antidepressant were identified from among 3.1 million patients in a New England healthcare system. PRIMARY AND SECONDARY OUTCOME MEASURES: Rates of bleeding or other vascular complications, including acute liver failure, acute renal failure, asthma, breast cancer and hip fractures. RESULTS: 601 GI bleeds were observed in the 21 462 subjects in the high-affinity group versus 333 among the 14 927 subjects in the lower affinity group (adjusted RR: 1.17, 95% CI 1.02 to 1.34). Similarly, 776 strokes were observed in the high-affinity group versus 434 in the lower affinity treatment group (adjusted RR: 1.18, 95% CI 1.06 to 1.32). No significant association with risk for a priori negative control outcomes, including acute liver failure, acute renal failure, asthma, breast cancer and hip fractures, was identified. CONCLUSIONS: Use of antidepressants with high affinity for the serotonin transporter may confer modestly elevated risk for GI and other bleeding complications. While multiple methodologic limitations must be considered, these results suggest that antidepressants with lower serotonin receptor affinity may be preferred in patients at greater risk for such complications. BMJ Group 2012-03-30 /pmc/articles/PMC3330255/ /pubmed/22466034 http://dx.doi.org/10.1136/bmjopen-2011-000544 Text en © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Pharmacology and Therapeutics
Castro, Victor M
Gallagher, Patience J
Clements, Caitlin C
Murphy, Shawn N
Gainer, Vivian S
Fava, Maurizio
Weilburg, Jeffrey B
Churchill, Susanne E
Kohane, Isaac S
Iosifescu, Dan V
Smoller, Jordan W
Perlis, Roy H
Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
title Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
title_full Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
title_fullStr Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
title_full_unstemmed Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
title_short Incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
title_sort incident user cohort study of risk for gastrointestinal bleed and stroke in individuals with major depressive disorder treated with antidepressants
topic Pharmacology and Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3330255/
https://www.ncbi.nlm.nih.gov/pubmed/22466034
http://dx.doi.org/10.1136/bmjopen-2011-000544
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