Pretreatment attrition in a comparative treatment outcome study on panic disorder

Am J Psychiatry. 1998 Jan;155(1):43-7. doi: 10.1176/ajp.155.1.43.

Abstract

Objective: Whereas the fact of attrition during the course of treatment is well documented, little is known about the factors that affect sample selection before the beginning of a study ("pretreatment attrition"). The present study reports on the degree and sources of pretreatment attrition at two sites of a multicenter study on panic disorder that compared treatment outcomes for imipramine and cognitive behavior therapy.

Method: Data were collected at two clinical research sites, one with a pharmacological treatment orientation (N = 420) and one with a psychosocial treatment orientation (N = 208).

Results: The main source of pretreatment attrition was participant refusal. At both research sites, eligible patients most often refused participation because they were either unwilling to start treatment with imipramine (30.6% and 47.4%, respectively) or discontinue their current medication (22.6% and 35.1%, respectively).

Conclusions: Results from comparative treatment outcome studies are limited not only to people who meet the study criteria but also to those who are willing to begin a medication treatment and discontinue their current medication.

Publication types

  • Clinical Trial
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Clinical Protocols
  • Cognitive Behavioral Therapy
  • Combined Modality Therapy
  • Female
  • Humans
  • Imipramine / therapeutic use
  • Male
  • Middle Aged
  • Panic Disorder / drug therapy
  • Panic Disorder / therapy*
  • Patient Compliance
  • Patient Dropouts*
  • Patient Selection*
  • Treatment Outcome
  • Treatment Refusal

Substances

  • Imipramine