دورية أكاديمية

Influence of study characteristics, methodological rigour and publication bias on efficacy of pharmacotherapy in obsessive-compulsive disorder: a systematic review and meta-analysis of randomised, placebo-controlled trials.

التفاصيل البيبلوغرافية
العنوان: Influence of study characteristics, methodological rigour and publication bias on efficacy of pharmacotherapy in obsessive-compulsive disorder: a systematic review and meta-analysis of randomised, placebo-controlled trials.
المؤلفون: Cohen SE; Psychiatry, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands s.e.cohen@amsterdamumc.nl.; Amsterdam Neuroscience Research Institute, Amsterdam, The Netherlands., Zantvoord JB; Psychiatry, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.; Amsterdam Neuroscience Research Institute, Amsterdam, The Netherlands., Storosum BWC; Psychiatry, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.; Amsterdam Neuroscience Research Institute, Amsterdam, The Netherlands., Mattila TK; Medicines Evaluation Board, Utrecht, The Netherlands., Daams J; Medical Library, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands., Wezenberg B; Psychiatry, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.; Amsterdam Neuroscience Research Institute, Amsterdam, The Netherlands., de Boer A; Medicines Evaluation Board, Utrecht, The Netherlands.; Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht University, Utrecht, The Netherlands., Denys DAJP; Psychiatry, Amsterdam UMC Locatie AMC, Amsterdam, The Netherlands.; Amsterdam Neuroscience Research Institute, Amsterdam, The Netherlands.
المصدر: BMJ mental health [BMJ Ment Health] 2024 Feb 12; Vol. 27 (1). Date of Electronic Publication: 2024 Feb 12.
نوع المنشور: Meta-Analysis; Systematic Review; Journal Article
اللغة: English
بيانات الدورية: Publisher: BMJ Country of Publication: England NLM ID: 9918521385306676 Publication Model: Electronic Cited Medium: Internet ISSN: 2755-9734 (Electronic) Linking ISSN: 27559734 NLM ISO Abbreviation: BMJ Ment Health
أسماء مطبوعة: Original Publication: London : BMJ, [2023]-
مواضيع طبية MeSH: Obsessive-Compulsive Disorder*/drug therapy , Randomized Controlled Trials as Topic* , Selective Serotonin Reuptake Inhibitors*/therapeutic use , Publication Bias* , Clomipramine*/therapeutic use, Humans ; Treatment Outcome ; Research Design/standards
مستخلص: Question: We examined the effect of study characteristics, risk of bias and publication bias on the efficacy of pharmacotherapy in randomised controlled trials (RCTs) for obsessive-compulsive disorder (OCD).
Study Selection and Analysis: We conducted a systematic search of double-blinded, placebo-controlled, short-term RCTs with selective serotonergic reuptake inhibitors (SSRIs) or clomipramine. We performed a random-effect meta-analysis using change in the Yale-Brown Obsessive-Compulsive Scale (YBOCS) as the primary outcome. We performed meta-regression for risk of bias, intervention, sponsor status, number of trial arms, use of placebo run-in, dosing, publication year, age, severity, illness duration and gender distribution. Furthermore, we analysed publication bias using a Bayesian selection model.
Findings: We screened 3729 articles and included 21 studies, with 4102 participants. Meta-analysis showed an effect size of -0.59 (Hedges' G, 95% CI -0.73 to -0.46), equalling a 4.2-point reduction in the YBOCS compared with placebo. The most recent trial was performed in 2007 and most trials were at risk of bias. We found an indication for publication bias, and subsequent correction for this bias resulted in a depleted effect size. In our meta-regression, we found that high risk of bias was associated with a larger effect size. Clomipramine was more effective than SSRIs, even after correcting for risk of bias. After correction for multiple testing, other selected predictors were non-significant.
Conclusions: Our findings reveal superiority of clomipramine over SSRIs, even after adjusting for risk of bias. Effect sizes may be attenuated when considering publication bias and methodological rigour, emphasising the importance of robust studies to guide clinical utility of OCD pharmacotherapy.
Prospero Registration Number: CRD42023394924.
Competing Interests: Competing interests: None declared.
(© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ.)
References: Nat Struct Mol Biol. 2018 Feb;25(2):170-175. (PMID: 29379174)
BMC Med. 2018 Oct 16;16(1):173. (PMID: 30322399)
JAMA Psychiatry. 2015 May;72(5):500-10. (PMID: 25806940)
J Clin Epidemiol. 2010 Mar;63(3):282-8. (PMID: 19836925)
Stat Med. 2013 Jan 15;32(1):51-66. (PMID: 22806991)
BMJ. 2019 Aug 28;366:l4898. (PMID: 31462531)
Stat Med. 2007 Nov 10;26(25):4544-62. (PMID: 17476644)
Stat Med. 2003 Sep 15;22(17):2693-710. (PMID: 12939780)
Mol Psychiatry. 2010 Jan;15(1):53-63. (PMID: 18725912)
Aust N Z J Psychiatry. 2013 Feb;47(2):121-41. (PMID: 23125399)
Stat Med. 2010 Dec 20;29(29):2969-83. (PMID: 20963748)
J Clin Psychopharmacol. 2002 Jun;22(3):309-17. (PMID: 12006902)
PLoS Med. 2022 Jan 19;19(1):e1003886. (PMID: 35045113)
J Affect Disord. 2019 May 1;250:419-424. (PMID: 30878654)
Cochrane Database Syst Rev. 2008 Jan 23;(1):CD001765. (PMID: 18253995)
Lancet Psychiatry. 2016 Aug;3(8):730-739. (PMID: 27318812)
Campbell Syst Rev. 2022 Jul 01;18(3):e1256. (PMID: 36909879)
Neurol Int. 2021 Aug 05;13(3):387-401. (PMID: 34449705)
BMJ. 2008 Apr 26;336(7650):924-6. (PMID: 18436948)
BMJ. 2017 Mar 3;356:j573. (PMID: 28258124)
Front Psychiatry. 2017 Dec 07;8:275. (PMID: 29270136)
BMC Med Res Methodol. 2017 Dec 04;17(1):159. (PMID: 29202708)
Lancet. 2018 Apr 7;391(10128):1357-1366. (PMID: 29477251)
Cochrane Database Syst Rev. 2017 Feb 16;2:MR000033. (PMID: 28207928)
Lancet Healthy Longev. 2022 Oct;3(10):e674-e689. (PMID: 36150402)
Psychopharmacol Bull. 2021 Jun 1;51(3):79-108. (PMID: 34421147)
Psychiatr Clin North Am. 2006 Jun;29(2):553-84, xi. (PMID: 16650723)
Neuropsychopharmacology. 2021 Mar;46(4):844-850. (PMID: 33244149)
Mol Psychiatry. 2020 Sep;25(9):1967-1974. (PMID: 31988433)
BMJ Open. 2019 Jun 27;9(6):e024886. (PMID: 31248914)
N Engl J Med. 2004 Sep 16;351(12):1250-1. (PMID: 15356289)
Clin Psychol Rev. 2004 Dec;24(8):1011-30. (PMID: 15533282)
Arch Gen Psychiatry. 1991 Aug;48(8):730-8. (PMID: 1883256)
Int J Neuropsychopharmacol. 2005 Mar;8(1):107-29. (PMID: 15450126)
Syst Rev. 2016 Dec 5;5(1):210. (PMID: 27919275)
J Epidemiol Community Health. 2000 May;54(5):326-7. (PMID: 10814650)
J Psychiatr Pract. 2013 May;19(3):227-33. (PMID: 23653079)
Evid Based Ment Health. 2018 Feb;21(1):4-6. (PMID: 28710065)
BMC Psychiatry. 2017 Feb 8;17(1):58. (PMID: 28178949)
فهرسة مساهمة: Keywords: Adult psychiatry; Anxiety disorders; Data Interpretation, Statistical
المشرفين على المادة: 0 (Selective Serotonin Reuptake Inhibitors)
NUV44L116D (Clomipramine)
تواريخ الأحداث: Date Created: 20240213 Date Completed: 20240807 Latest Revision: 20240812
رمز التحديث: 20240813
مُعرف محوري في PubMed: PMC10862307
DOI: 10.1136/bmjment-2023-300951
PMID: 38350669
قاعدة البيانات: MEDLINE
الوصف
تدمد:2755-9734
DOI:10.1136/bmjment-2023-300951