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Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review

BACKGROUND: Millions of people are treated with antidepressants like selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs). This clinical practice is based on short-term trials that have exaggerated the benefits and underestimated the harms. We also...

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Autores principales: Danborg, P.B., Valdersdorf, M., Gøtzsche, P.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839490/
https://www.ncbi.nlm.nih.gov/pubmed/30714974
http://dx.doi.org/10.3233/JRS-180046
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author Danborg, P.B.
Valdersdorf, M.
Gøtzsche, P.C.
author_facet Danborg, P.B.
Valdersdorf, M.
Gøtzsche, P.C.
author_sort Danborg, P.B.
collection PubMed
description BACKGROUND: Millions of people are treated with antidepressants like selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs). This clinical practice is based on short-term trials that have exaggerated the benefits and underestimated the harms. We also know too little about long-term harms. AIM: To assess harms of SSRIs and SNRIs that persist after end of drug intake. METHODS: Systematic review of placebo-controlled randomised trials of any length in patients with a psychiatric diagnosis and a follow-up of at least six months. Our primary outcomes were mortality, functional outcomes, quality of life and core psychiatric events. We searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials and checked the references for eligible articles. One researcher extracted data and another checked the data extraction. RESULTS: Our searches returned 9,153 unique records. We included 22 papers for 12 trials on SSRIs. Median intervention and follow-up periods were 15 and 52 weeks, respectively. Median number of randomised participants was 51; only two trials had a drop-out rate below 20%. Outcome reporting was less thorough during follow-up than for the intervention period and only two trials maintained the blind during follow-up. All authors concluded that the drugs were not beneficial in the long term. All trials reported harms outcomes selectively or did not report any. Only two trials reported on any of our primary outcomes (school attendance and number of heavy drinking days). CONCLUSION: The randomised trials currently available cannot be used to investigate persistent harms of antidepressants.
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spelling pubmed-68394902019-11-20 Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review Danborg, P.B. Valdersdorf, M. Gøtzsche, P.C. Int J Risk Saf Med Review BACKGROUND: Millions of people are treated with antidepressants like selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs). This clinical practice is based on short-term trials that have exaggerated the benefits and underestimated the harms. We also know too little about long-term harms. AIM: To assess harms of SSRIs and SNRIs that persist after end of drug intake. METHODS: Systematic review of placebo-controlled randomised trials of any length in patients with a psychiatric diagnosis and a follow-up of at least six months. Our primary outcomes were mortality, functional outcomes, quality of life and core psychiatric events. We searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials and checked the references for eligible articles. One researcher extracted data and another checked the data extraction. RESULTS: Our searches returned 9,153 unique records. We included 22 papers for 12 trials on SSRIs. Median intervention and follow-up periods were 15 and 52 weeks, respectively. Median number of randomised participants was 51; only two trials had a drop-out rate below 20%. Outcome reporting was less thorough during follow-up than for the intervention period and only two trials maintained the blind during follow-up. All authors concluded that the drugs were not beneficial in the long term. All trials reported harms outcomes selectively or did not report any. Only two trials reported on any of our primary outcomes (school attendance and number of heavy drinking days). CONCLUSION: The randomised trials currently available cannot be used to investigate persistent harms of antidepressants. IOS Press 2019-07-26 /pmc/articles/PMC6839490/ /pubmed/30714974 http://dx.doi.org/10.3233/JRS-180046 Text en © 2019 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Danborg, P.B.
Valdersdorf, M.
Gøtzsche, P.C.
Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review
title Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review
title_full Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review
title_fullStr Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review
title_full_unstemmed Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review
title_short Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review
title_sort long-term harms from previous use of selective serotonin reuptake inhibitors: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839490/
https://www.ncbi.nlm.nih.gov/pubmed/30714974
http://dx.doi.org/10.3233/JRS-180046
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