Literature DB >> 30923288

Discontinuing Psychotropic Drugs from Participants in Randomized Controlled Trials: A Systematic Review.

David Cohen1, Alexander Recalt2,3.   

Abstract

BACKGROUND AND
OBJECTIVE: Methods and justifications for discontinuing psychotropic drugs in randomized controlled trials (RCTs), and RCTs' acknowledgement of possible withdrawal symptoms following discontinuation, have not been examined systematically, which this review aims to do. Study Eligibility, Data Extraction, and Synthesis: Publications in MEDLINE, EMBASE, and PsycINFO (2000-2017) randomly assigning participants diagnosed with mental disorders to discontinue antipsychotic, antidepressant, anticonvulsant, antimanic, mood-stabilizing, benzodiazepine, or stimulant drugs. Authors independently extracted data, devised a typology of trials, and assessed trials' recognition of with-drawal symptoms.
RESULTS: Eighty RCTs (70% with industry participation) discontinued drugs from 5,757 participants to investigate relapse prevention (44%), successful dis-continuation (26%), architecture of withdrawal (14%), and practicality of discontinuation (10%). RCTs of stimulants, antidepressants, and antipsychotics mostly aimed to reach conclusions about relapse prevention by testing abrupt or rapid discontinuations; RCTs of benzodiazepines mostly aimed to reduce drug use by testing longer-lasting, supportive discontinuations. In 67% of RCTs, no justification was given for the specific discontinuation strategy, which lasted under 2 weeks in 60% of RCTs. Possible withdrawal confounding of trial outcomes was addressed in 14% of eligible RCTs. LIMITATIONS: Only the published literature was searched. CONCLUSIONS AND IMPLICATIONS: RCTs use drug discontinuation to study several key issues in psychopharmacology but infrequently justify how they implement it or acknowledge that possible withdrawal symptoms may threaten internal validity. Reappraising the use of drug discontinuation and the recognition of withdrawal symptoms in RCTs is required.
© 2019 S. Karger AG, Basel.

Entities:  

Keywords:  Confounding; Discontinuation; Psychotropic drugs; Randomized controlled trials; Research participants; Withdrawal

Mesh:

Substances:

Year:  2019        PMID: 30923288     DOI: 10.1159/000496733

Source DB:  PubMed          Journal:  Psychother Psychosom        ISSN: 0033-3190            Impact factor:   17.659


  5 in total

1.  Approaches for discontinuation versus continuation of long-term antidepressant use for depressive and anxiety disorders in adults.

Authors:  Ellen Van Leeuwen; Mieke L van Driel; Mark A Horowitz; Tony Kendrick; Maria Donald; An Im De Sutter; Lindsay Robertson; Thierry Christiaens
Journal:  Cochrane Database Syst Rev       Date:  2021-04-15

2.  Long-term outcomes of trials in the National Institute for Health and Care Excellence depression guideline.

Authors:  Susan McPherson; Michael P Hengartner
Journal:  BJPsych Open       Date:  2019-09-09

3.  Prophylactic effects or withdrawal reactions? An analysis of time-to-event data from antidepressant relapse prevention trials submitted to the FDA.

Authors:  Michael P Hengartner; Martin Plöderl
Journal:  Ther Adv Psychopharmacol       Date:  2021-08-10

4.  Later is not necessarily better: limitations of survival analysis in studies of long-term drug treatment of psychiatric conditions.

Authors:  Joanna Moncrieff; Janus Christian Jakobsen; Max Bachmann
Journal:  BMJ Evid Based Med       Date:  2021-09-23

5.  Effects of lithium on suicide and suicidal behaviour: a systematic review and meta-analysis of randomised trials.

Authors:  Zainab Nabi; Jacki Stansfeld; Martin Plöderl; Lisa Wood; Joanna Moncrieff
Journal:  Epidemiol Psychiatr Sci       Date:  2022-09-16       Impact factor: 7.818

  5 in total

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