Design characteristics that influence attrition in geriatric antidepressant trials: meta-analysis. Review uri icon

Overview

abstract

  • OBJECTIVE: To identify study-level and treatment group-level characteristics that are associated with attrition in antidepressant trials for the depressed elderly. METHODS: This meta-analysis used 68 published antidepressant randomized trials for the elderly depressed. Study-level and treatment group-level variables were extracted. The former consisted of: use of placebo arm, number of arms, unbalanced treatment allocation, year conducted, study duration, study location, number of centers, and patient pool. The latter consisted of: assigned treatments, baseline mean Hamilton Depression Rating Scale (HDRS), baseline mean age, gender ratio, attrition size, and sample size. Univariate logistic regressions with attrition as the dependent variable were applied, followed by application of a forward stepwise selection method for identification of independent attrition correlates. RESULTS: The 68 studies had a total of 153 treatment groups and 8,385 subjects. Among them, 2,287 subjects were terminated early, resulting in an overall 27.3% attrition rate. The stepwise results showed that higher attrition was significantly associated with active antidepressant groups as opposed to placebo groups, higher baseline HDRS, smaller sample size, unbalanced allocation of treatments, longer duration, and studies conducted in USA. CONCLUSIONS: The attrition in geriatric antidepressant trials can be affected by study and group-level design characteristics that include severity of depression symptoms and active treatments among others.

publication date

  • September 1, 2009

Research

keywords

  • Antidepressive Agents
  • Depressive Disorder
  • Patient Dropouts

Identity

Scopus Document Identifier

  • 70350757993

Digital Object Identifier (DOI)

  • 10.1002/gps.2211

PubMed ID

  • 19263464

Additional Document Info

volume

  • 24

issue

  • 9