Run-in periods and clinical outcomes of antipsychotics in dementia: A meta-epidemiological study of placebo-controlled trials
- PMID: 31730266
- PMCID: PMC7027584
- DOI: 10.1002/pds.4903
Run-in periods and clinical outcomes of antipsychotics in dementia: A meta-epidemiological study of placebo-controlled trials
Abstract
Purpose: Run-in periods are used to identify placebo-responders and washout. Our aim was to assess the association of run-in periods with clinical outcomes of antipsychotics in dementia.
Methods: We searched randomized placebo-controlled trials of conventional and atypical antipsychotics for neuropsychiatric symptoms (NPS) in dementia in electronic sources and references of selected articles. We extracted (a) the presence of a run-in period, use of placebo/investigated drug during run-in (versus washout only), and run-in duration (1 week or more) and (b) the reduction in NPS, number of participants with somnolence, extrapyramidal symptoms (EPS), and deaths per treatment group. We pooled clinical outcomes comparing antipsychotic and placebo groups in trials with and without run-in.
Results: We identified 35 trials. Twenty-nine trials used run-in. The pooled standardized mean difference in the reduction of NPS was -0.170 (95% CI, -0.227 to -0.112) in trials with run-in and -0.142 (95% CI, -0.331 to 0.047) in trials without run-in. The pooled odds ratio for somnolence was 2.8 (95% CI, 2.3-3.5) in trials with run-in and 3.5 (95% CI, 1.2-10.7) in trials without run-in; for EPS, these ORs were 1.8 (95% CI, 1.4-2.2) and 2.0 (95% CI, 1.3-3.1) respectively, and for mortality 1.4 (95% CI, 1.0-2.0) and 1.6 (95% CI, 0.7-3.4). The use of placebo/investigated drug during run-in and run-in duration did not affect the estimates in a consistent way.
Conclusions: The use of run-in in trials might have led to overestimated efficacy and especially underestimated risks of side effects of antipsychotics compared with placebo for NPS in dementia.
Keywords: antipsychotics; dementia; efficacy; meta-analysis; pharmacoepidemiology; run-in; side effects.
© 2019 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd.
Figures
Similar articles
-
Subjective Versus Objective Outcomes of Antipsychotics for the Treatment of Neuropsychiatric Symptoms Associated with Dementia.CNS Drugs. 2019 Sep;33(9):933-942. doi: 10.1007/s40263-019-00654-y. CNS Drugs. 2019. PMID: 31473979 Free PMC article.
-
Baseline imbalances and clinical outcomes of atypical antipsychotics in dementia: A meta-epidemiological study of randomized trials.Int J Methods Psychiatr Res. 2019 Mar;28(1):e1757. doi: 10.1002/mpr.1757. Epub 2018 Dec 4. Int J Methods Psychiatr Res. 2019. PMID: 30515916 Free PMC article.
-
The efficacy and safety of atypical antipsychotics for the treatment of dementia: a meta-analysis of randomized placebo-controlled trials.J Alzheimers Dis. 2014;42(3):915-37. doi: 10.3233/JAD-140579. J Alzheimers Dis. 2014. PMID: 25024323
-
Second-generation antipsychotic drugs and short-term mortality: a systematic review and meta-analysis of placebo-controlled randomised controlled trials.Lancet Psychiatry. 2018 Aug;5(8):653-663. doi: 10.1016/S2215-0366(18)30177-9. Epub 2018 Jul 2. Lancet Psychiatry. 2018. PMID: 30042077
-
Atypical antipsychotics for neuropsychiatric symptoms of dementia: malignant or maligned?Drug Saf. 2006;29(10):833-43. doi: 10.2165/00002018-200629100-00002. Drug Saf. 2006. PMID: 16970508 Review.
Cited by
-
Potential Side Effects and Adverse Events of Antipsychotic Use for Residents With Dementia in Assisted Living: Implications for Prescribers, Staff, and Families.J Appl Gerontol. 2022 Mar;41(3):798-805. doi: 10.1177/07334648211023678. Epub 2021 Jun 23. J Appl Gerontol. 2022. PMID: 34160299 Free PMC article.
-
Interventions from pregnancy to two years after birth for parents experiencing complex post-traumatic stress disorder and/or with childhood experience of maltreatment.Cochrane Database Syst Rev. 2023 May 4;5(5):CD014874. doi: 10.1002/14651858.CD014874.pub2. Cochrane Database Syst Rev. 2023. PMID: 37146219 Free PMC article.
-
Protocol for DEprescribing and Care to reduce Antipsychotics in Dementia (DECADE)-A hybrid effectiveness-implementation pilot study.PLoS One. 2023 Nov 9;18(11):e0294024. doi: 10.1371/journal.pone.0294024. eCollection 2023. PLoS One. 2023. PMID: 37943780 Free PMC article.
-
Treatments of unscheduled vaginal bleeding due to progestin-only contraception.Cochrane Database Syst Rev. 2024 Sep 2;9(9):CD015441. doi: 10.1002/14651858.CD015441. Cochrane Database Syst Rev. 2024. PMID: 39221618 Free PMC article.
-
Using Artificial Intelligence-based Methods to Address the Placebo Response in Clinical Trials.Innov Clin Neurosci. 2022 Jan-Mar;19(1-3):60-70. Innov Clin Neurosci. 2022. PMID: 35382067 Free PMC article. Review.
References
-
- Rothwell P. External validity of randomised controlled trials: to whom do the results of this trial apply? Lancet. 2005;365(1):82‐93. - PubMed
-
- Leber P, Davis C. Threats to the validity of clinical trials sample selection. Control Clin Trials. 1998;19(2):178‐187. - PubMed
-
- Pablos‐Méndez A, Barr R, Shea S. Run‐in periods in randomized trials: implications for the application of results in clinical practice. JAMA. 1998;279(3):222‐225. - PubMed
-
- Cipriani A, Gedds J. What is a run‐in phase? Epidemiol Psichiatr Soc. 2010;19(1):21‐22. - PubMed
-
- Ulmer M, Robinaugh D, Friedberg J, Lipsitz S, Natarajan S. Usefulness of a run‐in period to reduce drop‐outs in a randomized controlled trial of a behavioral intervention. Contemp Clin Trials. 2008;29(5):705‐710. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical