4.4 Article

Application of regression-discontinuity analysis in pharmaceutical health services research

Journal

HEALTH SERVICES RESEARCH
Volume 41, Issue 2, Pages 550-563

Publisher

BLACKWELL PUBLISHING
DOI: 10.1111/j.1475-6773.2005.00487.x

Keywords

regression discontinuity; drug utilization review; quasi-experimental design

Funding

  1. AHRQ HHS [R24 HS011673, 1R24HS11673] Funding Source: Medline

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Objective. To demonstrate how a relatively underused design, regression-discontinuity (RD), can provide robust estimates of intervention effects when stronger designs are impossible to implement. Data Sources/Study Setting. Administrative claims from a Mid-Atlantic state Medicaid program were used to evaluate the effectiveness of an educational drug utilization review intervention. Study Design. Quasi-experimental design. Data Collection/Extraction Methods. A drug utilization review study was conducted to evaluate a letter intervention to physicians treating Medicaid children with potentially excessive use of short-acting beta(2)-agonist inhalers (SAB). The outcome measure is change in seasonally-adjusted SAB use 5 months pre- and postintervention. To determine if the intervention reduced monthly SAB utilization, results from an RD analysis are compared to findings from a pretest-posttest design using repeated-measure ANOVA. Principal Findings. Both analyses indicated that the intervention significantly reduced SAB use among the high users. Average monthly SAB use declined by 0.9 canisters per month (p <.001) according to the repeated-measure ANOVA and by 0.2 canisters per month (p <.001) from RD analysis. Conclusions. Regression-discontinuity design is a useful quasi-experimental methodology that has significant advantages in internal validity compared to other pre-post designs when assessing interventions in which subjects' assignment is based on cutoff scores for a critical variable.

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