Clinical decision support to promote safe prescribing to women of reproductive age: a cluster-randomized trial

J Gen Intern Med. 2012 Jul;27(7):831-8. doi: 10.1007/s11606-012-1991-y.

Abstract

Background: Potentially teratogenic medications are frequently prescribed without provision of contraceptive counseling.

Objective: To evaluate whether computerized clinical decision support (CDS) can increase primary care providers' (PCPs') provision of family planning services when prescribing potentially teratogenic medications.

Design: Cluster-randomized trial conducted in one academic and one community-based practice between October of 2008 and April of 2010.

Participants/interventions: Forty-one PCPs were randomized to receive one of two types of CDS which alerted them to risks of medication-induced birth defects when ordering potentially teratogenic medications for women who may become pregnant. The 'simple' CDS provided a cautionary alert; the 'multifaceted' CDS provided tailored information and links to a structured order set designed to facilitate safe prescribing. Both CDS systems alerted PCPs about medication risk only once per encounter.

Main measures: We assessed change in documented provision of family planning services using data from 35,110 encounters and mixed-effects models. PCPs completed surveys before and after the CDS systems were implemented, allowing assessment of change in PCP-reported counseling about the risks of medication-induced birth defects and contraception.

Key results: Both CDS systems were associated with slight increases in provision of family planning services when potential teratogens were prescribed, without a significant difference in improvement by CDS complexity (p = 0.87). Because CDS was not repeated, 13% of the times that PCPs received CDS they substituted another potential teratogen. PCPs reported significant improvements in several counseling and prescribing practices. The multifaceted group reported a greater increase in the number of times per month they discussed the risks of medication use during pregnancy (multifaceted: +4.9 ± 7.0 vs. simple: +0.8 ± 3.2, p = 0.03). The simple CDS system was associated with greater clinician satisfaction.

Conclusions: CDS systems hold promise for increasing provision of family planning services when fertile women are prescribed potentially teratogenic medications, but further refinement of these systems is needed.

Trial registration: ClinicalTrials.gov NCT00766207.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Drug-Induced / etiology
  • Abnormalities, Drug-Induced / prevention & control*
  • Adolescent
  • Adult
  • Counseling / standards
  • Decision Support Systems, Clinical*
  • Drug Prescriptions / standards*
  • Family Planning Services / standards
  • Family Planning Services / supply & distribution
  • Female
  • Humans
  • Middle Aged
  • Outcome Assessment, Health Care
  • Patient Education as Topic / standards
  • Pennsylvania
  • Physician-Patient Relations
  • Preconception Care / standards
  • Primary Health Care / standards
  • Reproductive Behavior / statistics & numerical data*
  • Teratogens
  • Young Adult

Substances

  • Teratogens

Associated data

  • ClinicalTrials.gov/NCT00766207