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. 2009 Jul 8;2009(3):CD001096. doi: 10.1002/14651858.CD001096.pub2

Judge 2006.

Study characteristics
Methods Cluster RCT
Participants Academically‐affiliated long‐term care facility, Canada
3843 episodes of care, 7 wards
Interventions CDSS intended to improve medication safety at the time of order entry by flagging potential severe drug interactions, recent abnormal lab test results, requirement of special monitoring, dose reduction in elderly patients, or requirement of prophylactic measures
Outcomes Process adherence (prescribing)
Co‐Interventions Educational: None
Beyond Clinician Education: None
CDSS Features ‐ Acknowledgement of CDSS Required Yes ‐ required acknowledgement of the CDSS but not documentation of action taken
CDSS Features ‐ Other Conveyed patient‐specific information, developed by study investigators, included supporting information on‐screen, interruptive, makes care recommendation, 'push' mode of delivery, targeted overuse, user workflow considered in design
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment (selection bias) Low risk N/A
Incomplete outcome data (attrition bias)
All outcomes Unclear risk N/A
Baseline characteristics similar? Unclear risk N/A
Unit of analysis error High risk