SAF 99-144
Patient Profiling and Provider Feedback to Reduce Adverse Drug Events
Peter A Glassman, MBBS MSc VA Greater Los Angeles Healthcare System, West Los Angeles, CA West Los Angeles, CA Funding Period: January 2000 - December 2003 Portfolio Assignment: Health Care Organization and Implementation |
BACKGROUND/RATIONALE:
Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems. OBJECTIVE(S): The purpose of the study was to evaluate whether adding medication profiling (by using a retrospective drug utilization review program) to computerized provider order entry with embedded order checks (drug alerts) reduces the incidence of adverse drug events. METHODS: Medication profiles mainly focused on possible drug-drug and drug-disease interactions, with some drug duplications. To do the medication profiles we licensed a proprietary computerized retrospective drug utilization review system. We randomly assigned over 900 patients to Usual Care or Provider Feedback. For patients in the latter group, selected providers were contacted by letter with pertinent information; electronic mail was used for follow-up contact. Clinical and other relevant data was retrospectively abstracted from the medical records for up to one year from the last medication profile for all patients. This was done by a pharmacist reviewer, using a study-derived instrument, and blinded to patient assignment. ADE incidence is the primary outcome of interest, with other outcomes such as ADE severity and preventability also assessed. We also developed and implemented provider surveys in pre- and post-profiling periods. FINDINGS/RESULTS: Currently, we are in the process of analyzing and submitting substantive findings from the profiling aspect of the study. In the surveys we noted, among other issues, that recognition of common selected drug interactions was not always comprehensive and that knowledge of those selected interacting drug pairs did not substantially change over time with exposure to order checks within provider order entry. Providers appeared to value order checks (alerts) but signal to noise ratio (e.g., non-relevant warnings) was considered a substantive barrier to utilization of order checks (alerts) in both time periods. IMPACT: We are assessing whether combining computerized provider order entry with medication profiling (by retrospective drug utilization review) impacts medication safety in terms of reducing incidence, preventability and severity of adverse drug events. External Links for this ProjectDimensions for VADimensions for VA is a web-based tool available to VA staff that enables detailed searches of published research and research projects.Learn more about Dimensions for VA. VA staff not currently on the VA network can access Dimensions by registering for an account using their VA email address. Search Dimensions for this project PUBLICATIONS:Journal Articles
DRA:
Health Systems Science
DRE: Prevention Keywords: Adverse events, Education (provider), Safety MeSH Terms: Decision Support Techniques, Delivery of Health Care, Integrated, Drug Therapy, Behavior and Behavior Mechanisms, Controlled Clinical Trials, Safety, Ambulatory Care, Databases, Behavior, Health Care Costs |