Revisiting the washout period in the incident user study design: why 6-12 months may not be sufficient

J Comp Eff Res. 2015 Jan;4(1):27-35. doi: 10.2217/cer.14.53.

Abstract

Aims: The purpose of this study was to describe how washout period duration affects the size and accuracy of retrospective incident user cohorts.

Materials & methods: MarketScan commercial claims data from 2007 to 2010 were used and included adults with an antihyperlipidemic, antidiabetic or antidepressant claim in 2010. Incident user cohorts using 3-, 6-, 12-, 24- and 36-month washouts were created and changes in sample size and incident user misclassification were described.

Results & conclusion: The 6- and 12-month washouts excluded 75 and 85% of the samples, respectively. Half of subjects in the 6-month washout cohorts were actually prevalent users, and the 12-month washout period resulted in 30% misclassified. Using common washout periods of 6-12 months may insufficiently address prevalent user bias in large commercial claims databases.

Keywords: comparative effectiveness research; incident user design; methods; pharmacoepidemiology; research design; secondary databases; selection bias.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Antidepressive Agents / administration & dosage
  • Comparative Effectiveness Research*
  • Databases, Factual
  • Female
  • Humans
  • Hypoglycemic Agents / administration & dosage
  • Hypolipidemic Agents / administration & dosage
  • Insurance Claim Review*
  • Male
  • Middle Aged
  • Pharmacoepidemiology / methods*
  • Research Design*
  • Time Factors

Substances

  • Antidepressive Agents
  • Hypoglycemic Agents
  • Hypolipidemic Agents