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Randomized Controlled Trial
. 2025 Apr 8;333(14):1212-1221.
doi: 10.1001/jama.2024.27853.

Evaluation of a Clinical Decision Support System for Imaging Requests: A Cluster Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Evaluation of a Clinical Decision Support System for Imaging Requests: A Cluster Randomized Clinical Trial

Stijntje W Dijk et al. JAMA. .

Abstract

Importance: Given the widespread use of medical imaging, evaluating the effectiveness of interventions to improve appropriateness is crucial for optimizing health care resources and patient outcomes.

Objective: To assess the effects of implementing a clinical decision support system (CDSS), the European Society of Radiology iGuide, on the appropriateness of the medical imaging ordering behavior of physicians.

Design and setting: A cluster randomized clinical trial with 26 departments at 3 German university hospitals acting as clusters, incorporating a before and after discontinued design. All imaging requests originating from physicians in the participating departments over a 2.5-year period were included (between December 2021 and June 2024).

Interventions: All departments started without a CDSS and required structured clinical indication data entry and tracking of requested imaging. After randomization, 13 clusters (departments at hospitals) received the CDSS intervention (intervention clusters) and 13 clusters did not (control clusters). The CDSS intervention provided ordering physicians with information as to whether their imaging requests were appropriate, appropriate under certain conditions, or inappropriate; in addition, alternative diagnostic tests, including the corresponding appropriateness score, were suggested by the CDSS, after which physicians could choose to modify their imaging requests.

Main outcomes and measures: The primary outcome measure was the proportion of inappropriate imaging requests made per department. A difference-in-differences analysis was used to investigate changes in the proportion of inappropriate imaging requests between departments with vs those without the CDSS.

Results: A total of 65 764 imaging requests were scored using the CDSS; 50.1% of imaging requests were for female patients and the mean patient age was 64 years (SD, 17.1 years). Prior to implementation of the CDSS, there were 21 625 imaging requests from the control clusters, 1367 (6.3%) of which were categorized as inappropriate; and there were 13 338 imaging requests from the intervention clusters, 1007 (7.6%) of which were categorized as inappropriate. After implementation of the CDSS, there were 10 055 imaging requests from the control clusters, 518 (5.2%) of which were categorized as inappropriate; and there were 7206 imaging requests from the intervention clusters, 461 (6.4%) of which were categorized as inappropriate. The intervention clusters showed a similar reduction (mean difference, -0.5% [99% CI, -2.4% to 0.4%]) in inappropriate imaging requests compared with the control clusters (mean difference, -1.8% [99% CI, -4.3% to -0.4%]) and there was a difference-in-differences value of 1.3 percentage points (99% CI, -2.0 to 1.8 percentage points; P = .69), which was not statistically significant.

Conclusions and relevance: The CDSS did not reduce the number of inappropriate imaging requests ordered by physicians in academic hospital settings.

Trial registration: ClinicalTrials.gov Identifier: NCT05490290.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Dijk reported receiving research funding from the Gordon and Betty Moore Foundation. Dr Jansen reported receiving research funding from DFG (a German scientific society) and receiving personal fees from Philips Medical, Rapid AI, mRAY, Boehringer Ingelheim, Bayer, TÜV Süd, Radiologie Holding, and Stryker. Dr Hunink reported receiving royalties from Cambridge University Press, receiving reimbursement for travel expenses from the European Society of Radiology, and receiving research funding from the American Diabetes Association, the Gordon and Betty Moore Foundation, and the Netherlands Organization for Health Research and Development. Dr Kroencke reported receiving research funding the Bavarian Centre for Cancer Research, the Network of University Medicine, and Siemens Healthineers, receiving personal fees from SIRTEX Medical, Boston Scientific, Canon Medical Systems, AstraZeneca, Bracco Imaging, and Abbott Medical GmbH, and receiving reimbursement for expenses from the Cardiovascular and Interventional Radiological Society of Europe.

Figures

Figure 1.
Figure 1.. Flow of Hospitals and Departments in the MIDAS Trial of a Clinical Decision Support System for Diagnostic Imaging Requests
MIDAS indicates Medical Imaging Decision And Support. aThis is the total number registered by the hospital information system, including requests originating from nonparticipating departments and interventional radiology requests. bAdditional data by department (cluster) description, department specialty type (medical or surgical), hospital location, and study period (preimplemention of the decision support intervention, early and established implementation, and discontinued implementation) appear in Table 1.
Figure 2.
Figure 2.. Imaging Request Change Matrix
Early and established implementation of the intervention occurred during months 17 to 27; the total number of diagnostic tests during these months was 9532. The right lower boxes represent imaging requests that improved in score; these sessions moved from an initially lower score to a higher final score (eg, from red [inappropriate] to yellow [appropriate under certain conditions] or green [appropriate]; or from yellow to green).

Comment in

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