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ABSTRACT: Background
Medication errors, adverse drug events and potential adverse drug events are common and serious in terms of the harms and costs that they impose on the health system and those who use it. Errors resulting in preventable adverse drug events have been shown to occur most often at the stages of ordering and administration. This paper describes the protocol for a pragmatic trial of electronic prescribing to reduce prescription error. The trial was designed to overcome the limitations associated with traditional study design.Design
This study was designed as a 65-week, cluster randomized, parallel study.Methods
The trial was conducted within ambulatory outpatient clinics in an academic tertiary care centre in Ontario, Canada. The electronic prescribing softwar
SUBMITTER: Zwarenstein MF
PROVIDER: S-EPMC2092426 | biostudies-literature | 2007 Oct
REPOSITORIES: biostudies-literature