Improving ambulatory prescribing safety with a handheld decision support system: a randomized controlled trial
AuthorsBerner, Eta S.
Houston, Thomas K.
Ray, Midge N.
Allison, Jeroan J.
Heudebert, Gustavo R.
Chatham, W. Winn
Kennedy, John I. Jr.
Glandon, Gerald L.
Norton, Patricia A.
Crawford, Myra A.
Maisiak, Richard S.
UMass Chan AffiliationsDepartment of Quantitative Health Sciences
Document TypeJournal Article
KeywordsAmbulatory Care Information Systems
Anti-Inflammatory Agents, Non-Steroidal
*Decision Support Systems, Clinical
*Drug Therapy, Computer-Assisted
Outpatient Clinics, Hospital
Health Services Research
MetadataShow full item record
AbstractOBJECTIVE: To evaluate the effectiveness of a personal digital assistant (PDA)-based clinical decision support system (CDSS) on nonsteroidal anti-inflammatory drug (NSAID) prescribing safety in the outpatient setting. DESIGN: The design was a randomized, controlled trial conducted in a university-based resident clinic. Internal medicine residents received a PDA-based CDSS suite. For intervention residents, the CDSS included a prediction rule for NSAID-related gastrointestinal risk assessment and treatment recommendations. Unannounced standardized patients (SPs) trained to portray musculoskeletal symptoms presented to study physicians. Safety outcomes were assessed from the prescriptions given to the SPs. Each prescription was reviewed by a committee of clinicians blinded to participant, intervention group assignment, and baseline or follow-up status. MEASUREMENTS: Prescriptions were judged as safe or unsafe. The main outcome measure was the differential change in unsafe prescribing of NSAIDs for the intervention versus the control group. RESULTS: At baseline, the mean proportion of cases per physician with unsafe prescriptions for the two groups was similar (0.27 vs. 0.29, p > 0.05). Controlling for baseline performance, intervention participants prescribed more safely than controls after receiving the CDSS (0.23 vs. 0.45 [F = 4.24, p < 0.05]). With the CDSS, intervention participants documented more complete assessment of patient gastrointestinal risk from NSAIDs. CONCLUSION: PARTICIPANTS provided with a PDA-based CDSS for NSAID prescribing made fewer unsafe treatment decisions than participants without the CDSS.
SourceJ Am Med Inform Assoc. 2006 Mar-Apr;13(2):171-9. Epub 2005 Dec 15. Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/47670
Related ResourcesLink to Article in PubMed