Using comparative effectiveness design to improve the generalizability of bipolar treatment trials data: contrasting LiTMUS baseline data with pre-existing placebo controlled trials
- PMID: 23845385
- DOI: 10.1016/j.jad.2013.05.052
Using comparative effectiveness design to improve the generalizability of bipolar treatment trials data: contrasting LiTMUS baseline data with pre-existing placebo controlled trials
Abstract
Background: Efficacy-based double-blind placebo controlled trials were conducted to establish efficacy and safety for FDA approval. Such designs allowed and encouraged the use of exclusion criteria to improve assay sensitivity and internal validity. The LiTMUS trial increased the representation of real-world individuals with bipolar disorder despite the acknowledgment that this compromises assay sensitivity.
Method: To maximize generalizability, LiTMUS used broad inclusion and narrow exclusion criteria: participants experiencing mood symptoms of sufficient intensity (at least with a CGI-BP ≥ 3) that would warrant a change in treatment, and that lithium treatment would be a reasonable therapeutic option if they were randomized to it. At baseline demographic, illness, clinical, and treatment characteristics were collected. The LiTMUS study design and baseline sociodemographic data were compared to previous efficacy studies.
Results: As compared to the previous bipolar disorder efficacy studies, LiTMUS participants were of similar age, gender, weight and illness severity; however LiTMUS participants were more racially and ethnically representative of the general population, had a greater number of mood episodes in the past 12 months, more Axis I/II comorbidity, a greater number of prior suicide attempts, and higher functional capacity.
Conclusions: LiTMUS was a comparative effectiveness trial that had broad inclusion and minimal exclusion criteria that produced a more representative sample comprised of real-world participants. This design enables the results of the LiTMUS study to be a more representative of real world pharmacotherapuetic outcomes.
Limitations: Limitations include possible selection bias, paucity of sociodemographic data in efficacy trials, and lack of a placebo.
Keywords: Baseline characteristics; Bipolar; Comparative effectiveness; Generalizability.
Copyright © 2013. Published by Elsevier B.V.
Similar articles
-
Bipolar I and II disorder residual symptoms: oxcarbazepine and carbamazepine as add-on treatment to lithium in a double-blind, randomized trial.Prog Neuropsychopharmacol Biol Psychiatry. 2009 Feb 1;33(1):94-9. doi: 10.1016/j.pnpbp.2008.10.012. Epub 2008 Oct 31. Prog Neuropsychopharmacol Biol Psychiatry. 2009. PMID: 19007842 Clinical Trial.
-
Lithium treatment -- moderate dose use study (LiTMUS) for bipolar disorder: rationale and design.Clin Trials. 2009 Dec;6(6):637-48. doi: 10.1177/1740774509347399. Epub 2009 Nov 23. Clin Trials. 2009. PMID: 19933719 Clinical Trial.
-
Double-blind, randomized, placebo-controlled 6-week study on the efficacy and safety of the tamoxifen adjunctive to lithium in acute bipolar mania.J Affect Disord. 2011 Mar;129(1-3):327-31. doi: 10.1016/j.jad.2010.08.015. Epub 2010 Sep 16. J Affect Disord. 2011. PMID: 20843556 Clinical Trial.
-
ECNP consensus meeting. Bipolar depression. Nice, March 2007.Eur Neuropsychopharmacol. 2008 Jul;18(7):535-49. doi: 10.1016/j.euroneuro.2008.03.003. Epub 2008 May 23. Eur Neuropsychopharmacol. 2008. PMID: 18501566 Review.
-
Lithium: still a cornerstone in the long-term treatment in bipolar disorder?Neuropsychobiology. 2010;62(1):27-35. doi: 10.1159/000314307. Epub 2010 May 7. Neuropsychobiology. 2010. PMID: 20453532 Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous