Spirk 2017.
Study characteristics | ||
Methods | RCT | |
Participants | General internal medicine wards, academic health center, Switzerland (University Hospital Bern) 1593 patients |
|
Interventions | Prompted clinicians to evaluate pulmonary embolism risk using risk calculator and recommended thromboprophylaxis for patients at high‐risk | |
Outcomes | Process adherence (other), Clinical endpoint (mortality, venous thromboembolism, bleeding) | |
Co‐Interventions | Educational: None Beyond Clinician Education: None |
|
CDSS Features ‐ Acknowledgement of CDSS Required | Yes ‐ required acknowledgement of the CDSS and documentation of action taken | |
CDSS Features ‐ Other | Ambush, considered alert fatigue in design, developed by study investigators, interruptive, makes care recommendation, 'push' mode of delivery, targeted overuse and underuse | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment (selection bias) | Low risk | |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | N/A |
Baseline characteristics similar? | Low risk |