Adverse Drug Events
Conditions
Keywords
Adverse drug events, medical errors, computerized physician order entry, clinical decision support
Brief summary
The study will measure the effect of basic clinical decision support on medical errors and adverse drug events in the ambulatory setting.
Interventions
The computerized physician order entry (CPOE) intervention provides physicians with a menu of medications from the formulary, default doses, and a range of potential doses for each medication. Physicians were required to enter dosage, route, and frequency for all orders. Also, CPOE ensured that all orders were legible and included the prescribing physician's signature. For a number of medications, the system displayed relevant laboratory results on the screen at the time of ordering. Other features included consequent orders, which are orders that should follow from other orders, and drug-allergy checking, drug-drug interaction checking, and drug-laboratory checking. This included checking for the most frequent drug allergies, about 80 carefully selected drug-drug interactions, and several drug-laboratory combinations
Routine Care
Sponsors
Study design
Eligibility
Inclusion criteria
* provider practicing at sites implementing order entry with basic clinical decision support using either the longitudinal medical record (LMR) or Medical Gopher
Exclusion criteria
* provider or practice unwilling to participate
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Adverse Drug Events | 6 months | Adverse drug events are measured through use of a computerized surveillance system augmented by focused structured human review |
| Medical Errors | 6 months | Medical Errors are identified through a computerized surveillance system with structured human review |
Countries
United States