Abstract
Background: Depressive disorders are common in children and adolescents. Antidepressants, psychotherapies, and their combination are often used in routine clinical practice; however, available evidence on the comparative efficacy and safety of these interventions is inconclusive. Therefore, we sought to compare and rank all available treatment interventions for the acute treatment of depressive disorders in children and adolescents. Methods: We did a systematic review and network meta-analysis. We searched PubMed, Embase, the Cochrane Central Register of Controlled Trials, Web of Science, PsycINFO, ProQuest, CINAHL, LiLACS, international trial registries, and the websites of regulatory agencies for published and unpublished randomised controlled trials from database inception until Jan 1, 2019. We included placebo-controlled and head-to-head trials of 16 antidepressants, seven psychotherapies, and five combinations of antidepressant and psychotherapy that are used for the acute treatment of children and adolescents (≤18 years old and of both sexes) with depressive disorder diagnosed according to standard operationalised criteria. Trials recruiting participants with treatment-resistant depression, bipolar disorder, psychotic depression, treatment duration of less than 4 weeks, or an overall sample size of fewer than ten patients were excluded. We extracted data following a predefined hierarchy of outcome measures, and assessed risk of bias and certainty of evidence using validated methods. Primary outcomes were efficacy (change in depressive symptoms) and acceptability (treatment discontinuation due to any cause). We estimated summary standardised mean differences (SMDs) or odds ratios (ORs) with credible intervals (CrIs) using network meta-analysis with random effects. This study was registered with PROSPERO, number CRD42015020841. Findings: From 20 366 publications, we included 71 trials (9510 participants). Depressive disorders in most studies were moderate to severe. In terms of efficacy, fluoxetine plus cognitive behavioural therapy (CBT) was more effective than CBT alone (–0·78, 95% CrI −1·55 to −0·01) and psychodynamic therapy (–1·14, −2·20 to −0·08), but not more effective than fluoxetine alone (–0·22, −0·86 to 0·42). No pharmacotherapy alone was more effective than psychotherapy alone. Only fluoxetine plus CBT and fluoxetine were significantly more effective than pill placebo or psychological controls (SMDs ranged from −1·73 to −0·51); and only interpersonal therapy was more effective than all psychological controls (–1·37 to −0·66). Nortriptyline (SMDs ranged from 1·04 to 2·22) and waiting list (SMDs ranged from 0·67 to 2·08) were less effective than most active interventions. In terms of acceptability, nefazodone and fluoxetine were associated with fewer dropouts than sertraline, imipramine, and desipramine (ORs ranged from 0·17 to 0·50); imipramine was associated with more dropouts than pill placebo, desvenlafaxine, fluoxetine plus CBT, and vilazodone (2·51 to 5·06). Most of the results were rated as “low” to “very low” in terms of confidence of evidence according to Confidence In Network Meta-Analysis. Interpretation: Despite the scarcity of high-quality evidence, fluoxetine (alone or in combination with CBT) seems to be the best choice for the acute treatment of moderate-to-severe depressive disorder in children and adolescents. However, the effects of these interventions might vary between individuals, so patients, carers, and clinicians should carefully balance the risk-benefit profile of efficacy, acceptability, and suicide risk of all active interventions in young patients with depression on a case-by-case basis. Funding: National Key Research and Development Program of China.
| Original language | English |
|---|---|
| Pages (from-to) | 581-601 |
| Number of pages | 21 |
| Journal | The Lancet. Psychiatry |
| Volume | 7 |
| Issue number | 7 |
| Early online date | 18 Jun 2020 |
| DOIs | |
| Publication status | Published - Jul 2020 |
Funding
XZ reports travel and accommodation expenses from the Chinese Society of Psychiatry (CSP) for lectures delivered for CSP, outside the submitted work. TAF reports grants and personal fees from Mitsubishi-Tanabe and personal fees from MSD and Shionogi and has a pending patent (2018-177688), outside the submitted work. DC reports grants and personal fees from Shire-Takeda and personal fees from Medice, Servier, and Oxford University Press, outside the submitted work. SEH reports that she is the joint coordinating editor of the Cochrane Common Mental Disorders Group and manages the Children and Young People Satellite. She has funding from the Royal Society, the Faculty of Medical and Health Sciences at the University of Auckland, and Cochrane to pursue this work, including systematic reviews in the area of children and young people's mental health. She is funded by the Auckland Medical Research Foundation to develop and test an application that delivers goal setting for young people with mental health and related difficulties, such as self-harm. She is a CureKids Research Fellow, working on developing digital tools to support parents to support children with mental health and related difficulties. SL reports personal fees from LB Pharma, Otsuka, Lundbeck, Boehringer Ingelheim, LTS Lohmann, Janssen, Johnson & Johnson, TEVA, Merck Sharp & Dohme, Sandoz, Sanofi-Aventis, Angelini, Recordati, and Gedeon Richter, outside the submitted work. AVR reports grants and non-financial support from Janssen Canada and personal fees from Abilify Maintena, MDD National Advisory Board, Mental Health National Advisory, Allergan National Advisory Board, Brexpiprazole Advisory Board, and Bipolar Disorder Advisory Board, outside the submitted work. AC reports personal fees from the CARIPLO Foundation, Angelini Pharma for consultancy and paid peer reviewing of grant applications, and Italian Network for Paediatric Clinical Trials, outside the submitted work. PX reports speaker's honoraria from Janssen, outside the submitted work. All other authors declare no competing interests. This study was funded by the National Key Research and Development Program of China (2017YFA0505700), We thank Sofia Dias (Health Technology Assessment, University of York, UK), Alex Sutton (Department of Health Sciences, College of Life Sciences, University of Leicester, UK) and Nicky Welton (Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK) for providing statistical guidance. We are grateful to Mehmet Eskin (Department of Psychology, College of Social Sciences and Humanities, Koc University, Turkey), Graham J Emslie (Department of Psychiatry, University of Texas Southwestern Medical Center, USA), and Taryn Mayes (Department of Psychiatry, University of Texas Southwestern Medical Center, USA) for providing unpublished data in this review, and Salvatore Gentile (Department of Neurosciences, University of Naples, Italy) for his valuable advice. We also thank Ian M Goodyer (Department of Psychiatry, University of Cambridge, UK), Giovanna Porta (Department of Psychiatry, University of Pittsburgh School of Medicine, USA), David Brent (Department of Psychiatry, University of Pittsburgh School of Medicine, USA), Greg Clarke (Kaiser Permanente Center for Health Research, Portland), Paul Wilkinson (Department of Psychiatry, University of Cambridge, UK), and Glenn Melvin (School of Psychology, University of Deakin, Australia) for replying to our requests. PX is supported by the National Key Research and Development Program of China (2017YFA0505700), the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences (2019PT320002), and the Natural Science Foundation Project of China (81820108015). XZ is supported by the National Natural Science Foundation of China (81873800 and 81701342), High-level Talents Special Support Plan of Chongqing (T04040016), and Science and Technology Research Project of Chongqing Education Commission (KJQN201800415). AC is supported by the NIHR Oxford Cognitive Health Clinical Research Facility, by an NIHR Research Professorship (RP-2017-08-ST2-006), by the NIHR Collaboration for Leadership in Applied Health Research and Care Oxford, now recommissioned as NIHR Applied Research Collaboration Oxford and Thames Valley, and by the NIHR Oxford Health Biomedical Research Centre (BRC-1215-20005). The views expressed are those of the authors and not necessarily those of the UK National Health Service, the NIHR, or the UK Department of Health and Social Care.
| Funders | Funder number |
|---|---|
| Bristol Medical School, University of Bristol, UK | |
| College of Life Sciences | |
| Department of Health Sciences | |
| Department of Population Health Sciences | |
| Glenn Melvin | |
| High-level Talents Special Support Plan of Chongqing | T04040016 |
| National Health Service | |
| Natural Science Foundation Project of China | 81820108015 |
| Nicky Welton | |
| Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences | 2019PT320002 |
| Science and Technology Research Project of Chongqing Education Commission | KJQN201800415 |
| Thames Valley | |
| University of Leicester, UK) | |
| University of Pittsburgh School of Medicine | |
| University of Texas Southwestern Medical Center | |
| Janssen Canada | |
| National Institute for Health Research | RP-2017-08-ST2-006 |
| Department of Health and Social Care | |
| Royal Society | |
| Deakin University | |
| National Natural Science Foundation of China | 81701342, 81873800 |
| Fondazione Cariplo | |
| Faculty of Medical and Health Sciences, University of Auckland | |
| Angelini Pharma | |
| National Key Research and Development Program of China | 2017YFA0505700 |
| NIHR Oxford Biomedical Research Centre | BRC-1215-20005 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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