Background Repetitive inpatient laboratory testing contributes to waste in healthcare. We evaluated an intervention bundle combining education and multilevel social comparison feedback to safely reduce repetitive use of inpatient routine laboratory tests.
Methods This non-randomised controlled pre-intervention post-intervention study was conducted in four adult hospitals from October 2016 to March 2018. In the medical teaching unit (MTU) of the intervention site, learners received education and aggregate social comparison feedback and attending internists received individual comparison feedback on routine laboratory test utilisation. MTUs of the remaining three sites served as control units. Number and cost of routine laboratory tests ordered per patient-day before and after the intervention was compared with the control units, adjusting for patient factors. Safety endpoints included number of critically abnormal laboratory test results, number of stat laboratory test orders, patient length of stay, transfer rate to the ICU, and 30-day readmission and mortality.
Results A total of 14 000 patients were included. Pre-intervention and post-intervention groups were similar in age, sex, Charlson Comorbidity Index and length of stay. From the pre-intervention period to the post-intervention period, significantly fewer routine laboratory tests were ordered at the intervention MTU (incidence rate ratio=0.89; 95% CI 0.79 to 1.00; p=0.048) with associated costs savings of $C68 877 (p=0.020) as compared with the control sites. The variability in the ordering pattern of internists at the intervention site also decreased post-intervention. No worsening was noted in the safety endpoints between the pre-intervention and post-intervention period at the intervention unit compared with the controls.
Conclusions Combination of education and multilevel social comparison feedback significantly and safely led to cost savings through reduced use of routine laboratory tests in hospitalised patients.
- health care waste
- low value testing
- routine laboratory testing
- social comparison
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Presented at Early part of this project including plan was presented at the Canadian Society of Internal Medicine conference in 2017 in Toronto, Ontario, Canada.
Contributors All authors contributed materially to the inception, design, conduct, analysis, and write-up of the manuscript.
Funding This study was funded by Alberta Health Services.
Disclaimer The funding body played no role in the design of the study; collection, analysis and interpretation of the data; and the decision to approve publication of the finished manuscript.
Competing interests None declared.
Patient consent for publication Not required.
Ethics approval This study was approved by the Conjoint Health Research Ethics Board in our institution and University (REB17-1215). As this was a study of a health system QI initiative, the review board waived participant informed consent.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available on reasonable request. All deidentified data from this study are available on request from the corresponding author (firstname.lastname@example.org).
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