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      Association of Antidepressant Use With Adverse Health Outcomes : A Systematic Umbrella Review

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          Abstract

          Is antidepressant use associated with adverse health outcomes, and how credible is the evidence behind this association in published meta-analyses of real-world data? In this systematic umbrella review of 45 meta-analyses of observational studies, convincing evidence was found for the associations between antidepressant use and suicide attempt or completion among individuals younger than 19 years and between antidepressant use and autism risk among the offspring. However, none of these associations remained at the convincing evidence level after a sensitivity analysis that adjusted for confounding by indication. This study’s findings suggest that claimed adverse health outcomes associated with antidepressants may not be supported by strong evidence and may be exaggerated by confounding by indication; no absolute contraindication to the use of antidepressants was found to be currently supported by convincing evidence. This umbrella review searches PubMed, Scopus, and PsycINFO to summarize and grade the strength of evidence of the associations between antidepressants and adverse outcomes reported in multiple meta-analyses. Antidepressant use is increasing worldwide. Yet, contrasting evidence on the safety of antidepressants is available from meta-analyses, and the credibility of these findings has not been quantified. To grade the evidence from published meta-analyses of observational studies that assessed the association between antidepressant use or exposure and adverse health outcomes. PubMed, Scopus, and PsycINFO were searched from database inception to April 5, 2019. Only meta-analyses of observational studies with a cohort or case-control study design were eligible. Two independent reviewers recorded the data and assessed the methodological quality of the included meta-analyses. Evidence of association was ranked according to established criteria as follows: convincing, highly suggestive, suggestive, weak, or not significant. Forty-five meta-analyses (17.9%) from 4471 studies identified and 252 full-text articles scrutinized were selected that described 120 associations, including data from 1012 individual effect size estimates. Seventy-four (61.7%) of the 120 associations were nominally statistically significant at P  ≤ .05 using random-effects models. Fifty-two associations (43.4%) had large heterogeneity ( I 2  > 50%), whereas small-study effects were found for 17 associations (14.2%) and excess significance bias was found for 9 associations (7.5%). Convincing evidence emerged from both main and sensitivity analyses for the association between antidepressant use and risk of suicide attempt or completion among children and adolescents, autism spectrum disorders with antidepressant exposure before and during pregnancy, preterm birth, and low Apgar scores. None of these associations remained supported by convincing evidence after sensitivity analysis, which adjusted for confounding by indication. This study’s findings suggest that most putative adverse health outcomes associated with antidepressant use may not be supported by convincing evidence, and confounding by indication may alter the few associations with convincing evidence. Antidepressant use appears to be safe for the treatment of psychiatric disorders, but more studies matching for underlying disease are needed to clarify the degree of confounding by indication and other biases. No absolute contraindication to antidepressants emerged from this umbrella review.

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          Most cited references55

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          The Lancet Psychiatry Commission: a blueprint for protecting physical health in people with mental illness

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            Comparative efficacy and tolerability of antidepressants for major depressive disorder in children and adolescents: a network meta-analysis

            Major depressive disorder is one of the most common mental disorders in children and adolescents. However, whether to use pharmacological interventions in this population and which drug should be preferred are still matters of controversy. Consequently, we aimed to compare and rank antidepressants and placebo for major depressive disorder in young people.
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              Suicidality in pediatric patients treated with antidepressant drugs.

              There has been concern that widely used antidepressant agents might be associated with an increased risk of suicidal ideation and behavior (suicidality) in pediatric patients. To investigate the relationship between antidepressant drugs and suicidality in pediatric patients participating in randomized, placebo-controlled trials. Data were derived from 23 trials conducted in 9 drug company-supported programs evaluating the effectiveness of antidepressants in pediatric patients and 1 multicenter trial (the Treatment for Adolescents With Depression Study) that evaluated fluoxetine hydrochloride. All placebo-controlled trials submitted to the Food and Drug Administration were eligible for inclusion. Evaluable data were derived from 4582 patients in 24 trials. Sixteen trials studied patients with major depressive disorder, and the remaining 8 studied obsessive-compulsive disorder (n = 4), generalized anxiety disorder (n = 2), attention-deficit/hyperactivity disorder (n = 1), and social anxiety disorder (n = 1). Only 20 trials were included in the risk ratio analysis of suicidality because 4 trials had no events in the drug or placebo groups. Individual patient data were available for all the trials. A meta-analysis was conducted to obtain overall suicidality risk estimates for each drug individually, for selective serotonin reuptake inhibitors in depression trials as a group, and for all evaluable trials combined. There were no completed suicides in any of these trials. The multicenter trial was the only individual trial to show a statistically significant risk ratio (4.62; 95% confidence interval [CI], 1.02-20.92). The overall risk ratio for selective serotonin reuptake inhibitors in depression trials was 1.66 (95% CI, 1.02-2.68) and for all drugs across all indications was 1.95 (95% CI, 1.28-2.98). The overall risk difference for all drugs across all indications was 0.02 (95% CI, 0.01-0.03). Use of antidepressant drugs in pediatric patients is associated with a modestly increased risk of suicidality.
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                Author and article information

                Journal
                JAMA Psychiatry
                JAMA Psychiatry
                American Medical Association (AMA)
                2168-622X
                October 02 2019
                Affiliations
                [1 ]Pain and Rehabilitation Centre, Department of Medicine and Health Sciences, Linköping University, Linköping, Sweden
                [2 ]Department of Hygiene and Epidemiology, School of Medicine, University of Ioannina, University Campus, Ioannina, Greece
                [3 ]Department of Neuroscience, University of Padua, Padua, Italy
                [4 ]Padova Neuroscience Center (PNC), University of Padua, Padua, Italy
                [5 ]Early Psychosis: Interventions and Clinical-Detection (EPIC) Lab, Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom
                [6 ]OASIS Service, South London and Maudsley NHS (National Health Service) Foundation Trust, London, United Kingdom
                [7 ]Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy
                [8 ]Section of Imaging, Neurobiology, and Psychosis, Department of Psychosis Studies, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, United Kingdom
                [9 ]National Institute for Health Research (NIHR) Mental Health Biomedical Research Centre at South London and Maudsley NHS Foundation Trust, London, United Kingdom
                [10 ]Department of Psychology, Social Work and Counselling, University of Greenwich, Greenwich, United Kingdom
                [11 ]Physiotherapy Department, South London and Maudsley NHS Foundation Trust, London, United Kingdom
                [12 ]Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom
                [13 ]NICM Health Research Institute, School of Science and Health, University of Western Sydney, Sydney, Australia
                [14 ]Division of Psychology and Mental Health, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom
                [15 ]Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
                [16 ]Department of Neuroscience, Reproductive Sciences and Dentistry, Federico II University, Naples, Italy
                [17 ]Department of Clinical Physiology, Linköping University, Linköping, Sweden
                [18 ]Centre for Addiction and Mental Health and Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada
                [19 ]Department of Psychiatry and Psychology, Hospital Clinic, Institute of Neuroscience, University of Barcelona, IDIBAPS, the Spanish Ministry of Science and Innovation (CIBERSAM), Barcelona, Catalonia, Spain
                [20 ]South London and Maudsley NHS Foundation Trust, Bethlem Royal Hospital, Beckenham, Kent, United Kingdom
                [21 ]Department of Pediatrics, Yonsei University College of Medicine, Seoul, Republic of Korea
                [22 ]Department of Psychiatry, Zucker Hillside Hospital, Glen Oaks, New York
                [23 ]Department of Psychiatry and Molecular Medicine, Hofstra Northwell School of Medicine, Hempstead, New York
                [24 ]Center for Psychiatric Neuroscience, Feinstein Institute for Medical Research, Manhasset, New York
                [25 ]Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Department of Child and Adolescent Psychiatry, Berlin Institute of Health, Berlin, Germany
                [26 ]Department of Epidemiology and Biostatistics, Imperial College London, London, United Kingdom
                Article
                10.1001/jamapsychiatry.2019.2859
                6777224
                31577342
                4c23c1a9-6807-45c5-a8fb-84902a38eb71
                © 2019
                History

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