Background MRI protocols typically involve many imaging sequences and often require too much time. Purpose To simulate artificial intelligence (AI)-directed stratified scanning for screening breast MRI with various triage thresholds and evaluate its diagnostic performance against that of the full breast MRI protocol. Materials and Methods This retrospective reader study included consecutive contrast-enhanced screening breast MRI examinations performed between January 2013 and January 2019 at three regional cancer sites. In this simulation study, an in-house AI tool generated a suspicion score for subtraction maximum intensity projection images during a given MRI examination, and the score was used to determine whether to proceed with the full MRI protocol or end the examination early (abbreviated breast MRI [AB-MRI] protocol). Examinations with suspicion scores under the 50th percentile were read using both the AB-MRI protocol (ie, dynamic contrast-enhanced MRI scans only) and the full MRI protocol. Diagnostic performance metrics for screening with various AI triage thresholds were compared with those for screening without AI triage. Results Of 863 women (mean age, 52 years ± 10 [SD]; 1423 MRI examinations), 51 received a cancer diagnosis within 12 months of screening. The diagnostic performance metrics for AI-directed stratified scanning that triaged 50% of examinations to AB-MRI versus full MRI protocol scanning were as follows: sensitivity, 88.2% (45 of 51; 95% CI: 79.4, 97.1) versus 86.3% (44 of 51; 95% CI: 76.8, 95.7); specificity, 80.8% (1108 of 1372; 95% CI: 78.7, 82.8) versus 81.4% (1117 of 1372; 95% CI: 79.4, 83.5); positive predictive value 3 (ie, percent of biopsies yielding cancer), 23.6% (43 of 182; 95% CI: 17.5, 29.8) versus 24.7% (42 of 170; 95% CI: 18.2, 31.2); cancer detection rate (per 1000 examinations), 31.6 (95% CI: 22.5, 40.7) versus 30.9 (95% CI: 21.9, 39.9); and interval cancer rate (per 1000 examinations), 4.2 (95% CI: 0.9, 7.6) versus 4.9 (95% CI: 1.3, 8.6). Specificity decreased by no more than 2.7 percentage points with AI triage. There were no AI-triaged examinations for which conducting the full MRI protocol would have resulted in additional cancer detection. Conclusion AI-directed stratified MRI decreased simulated scan times while maintaining diagnostic performance. © RSNA, 2025 <i>Supplemental material is available for this article.</i> See also the editorial by Strand in this issue.

We present the first multimodal deep learning framework combining ultrasound (US) and electrocardiography (ECG) data to predict cardiac quiescent periods (QPs) for optimized computed tomography angiography gating (CTA). The framework integrates a 3D convolutional neural network (CNN) for US data and an artificial neural network (ANN) for ECG data. A dynamic heart motion phantom, replicating diverse cardiac conditions, including arrhythmias, was used to validate the framework. Performance was assessed across varying QP lengths, cardiac segments, and motions to simulate real-world conditions. The multimodal US-ECG 3D CNN-ANN framework demonstrated improved QP prediction accuracy compared to single-modality ECG-only gating, achieving 96.87% accuracy compared to 85.56%, including scenarios involving arrhythmic conditions. Notably, the framework shows higher accuracy for longer QP durations (100 ms - 200 ms) compared to shorter durations (<100ms), while still outperforming single-modality methods, which often fail to detect shorter quiescent phases, especially in arrhythmic cases. Consistently outperforming single-modality approaches, it achieves reliable QP prediction across cardiac regions, including the whole phantom, interventricular septum, and cardiac wall regions. Analysis of QP prediction accuracy across cardiac segments demonstrated an average accuracy of 92% in clinically relevant echocardiographic views, highlighting the framework's robustness. Combining US and ECG data using a multimodal framework improves QP prediction accuracy under variable cardiac motion, particularly in arrhythmic conditions. Since even small errors in cardiac CTA can result in non-diagnostic scans, the potential benefits of multimodal gating may improve diagnostic scan rates in patients with high and variable heart rates and arrhythmias.

To train and evaluate the performance of a machine learning triaging tool that identifies MRI negative for clinically significant prostate cancer and to compare this against non-MRI models. 2895 MRIs were collected from two sources (1630 internal, 1265 public) in this retrospective study. Risk models compared were: Prostate Cancer Prevention Trial Risk Calculator 2.0, Prostate Biopsy Collaborative Group Calculator, PSA density, U-Net segmentation, and U-Net combined with clinical parameters. The reference standard was histopathology or negative follow-up. Performance metrics were calculated by simulating a triaging workflow compared to radiologist interpreting all exams on a test set of 465 patients. Sensitivity and specificity differences were assessed using the McNemar test. Differences in PPV and NPV were assessed using the Leisenring, Alonzo and Pepe generalized score statistic. Equivalence test p-values were adjusted within each measure using Benjamini-Hochberg correction. Triaging using U-Net with clinical parameters reduced radiologist workload by 12.5% with sensitivity decrease from 93 to 90% (p = 0.023) and specificity increase from 39 to 47% (p < 0.001). This simulated workload reduction was greater than triaging with risk calculators (3.2% and 1.3%, p < 0.001), and comparable to PSA density (8.4%, p = 0.071) and U-Net alone (11.6%, p = 0.762). Both U-Net triaging strategies increased PPV (+ 2.8% p = 0.005 clinical, + 2.2% p = 0.020 nonclinical), unlike non-U-Net strategies (p > 0.05). NPV remained equivalent for all scenarios (p > 0.05). Clinically-informed U-Net triaging correctly ruled out 20 (13.4%) radiologist false positives (12 PI-RADS = 3, 8 PI-RADS = 4). Of the eight (3.6%) false negatives, two were misclassified by the radiologist. No misclassified case was interpreted as PI-RADS 5. Prostate MRI triaging using machine learning could reduce radiologist workload by 12.5% with a 3% sensitivity decrease and 8% specificity increase, outperforming triaging using non-imaging-based risk models. Further prospective validation is required.

Invasive coronary angiography (ICA) is the gold standard in the diagnosis of coronary artery disease (CAD). Being invasive, it carries rare but serious risks including myocardial infarction, stroke, major bleeding, and death. A large proportion of elective outpatients undergoing ICA have nonobstructive CAD, highlighting the suboptimal use of this test. Coronary computed tomographic angiography (CCTA) is a noninvasive option that provides similar information with less risk and is recommended as a first-line test for patients with low-to-intermediate risk of CAD. Leveraging artificial intelligence (AI) to appropriately direct patients to ICA or CCTA based on the predicted probability of disease may improve the efficiency and safety of diagnostic pathways. he CarDIA-AI (Coronary computed tomographic angiography to optimize the Diagnostic yield of Invasive Angiography for low-risk patients screened with Artificial Intelligence) study aims to evaluate whether AI-based risk assessment for obstructive CAD implemented within a centralized triage process can optimize the use of ICA in outpatients referred for nonurgent ICA. CarDIA-AI is a pragmatic, open-label, superior randomized controlled trial involving 2 Canadian cardiac centers. A total of 252 adults referred for elective outpatient ICA will be randomized 1:1 to usual care (directly proceeding to ICA) or to triage using an AI-based decision support tool. The AI-based decision support tool was developed using referral information from over 37,000 patients and uses a light gradient boosting machine model to predict the probability of obstructive CAD based on 42 clinically relevant predictors, including patient referral information, demographic characteristics, risk factors, and medical history. Participants in the intervention arm will have their ICA referral forms and medical charts reviewed, and select details entered into the decision support tool, which recommends CCTA or ICA based on the patient's predicted probability of obstructive CAD. All patients will receive the selected imaging modality within 6 weeks of referral and will be subsequently followed for 90 days. The primary outcome is the proportion of normal or nonobstructive CAD diagnosed via ICA and will be assessed using a 2-sided z test to compare the patients referred for cardiac investigation with normal or nonobstructive CAD diagnosed through ICA between the intervention and control groups. Secondary outcomes include the number of angiograms avoided and the diagnostic yield of ICA. Recruitment began on January 9, 2025, and is expected to conclude in mid to late 2025. As of April 14, 2025, we have enrolled 81 participants. Data analysis will begin once data collection is completed. We expect to submit the results for publication in 2026. CarDIA-AI will be the first randomized controlled trial using AI to optimize patient selection for CCTA versus ICA, potentially improving diagnostic efficiency, avoiding unnecessary complications of ICA, and improving health care resource usage. ClinicalTrials.gov NCT06648239; https://clinicaltrials.gov/study/NCT06648239/. DERR1-10.2196/71726.

To perform a systematic review on the impact of deep learning (DL)-based triage for reducing diagnostic delays and improving patient outcomes in peer-reviewed and pre-print publications. A search was conducted of primary research studies focused on DL-based worklist optimization for diagnostic imaging triage published on multiple databases from January 2018 until July 2024. Extracted data included study design, dataset characteristics, workflow metrics including report turnaround time and time-to-treatment, and patient outcome differences. Further analysis between clinical settings and integration modality was investigated using nonparametric statistics. Risk of bias was assessed with the risk of bias in non-randomized studies-of interventions (ROBINS-I) checklist. A total of 38 studies from 20 publications, involving 138,423 images, were analyzed. Workflow interventions concerned pulmonary embolism (n = 8), stroke (n = 3), intracranial hemorrhage (n = 12), and chest conditions (n = 15). Patients in the post DL-triage group had shorter median report turnaround times: a mean difference of 12.3 min (IQR: -25.7, -7.6) for pulmonary embolism, 20.5 min (IQR: -32.1, -9.3) for stroke, 4.3 min (IQR: -8.6, 1.3) for intracranial hemorrhage and 29.7 min (IQR: -2947.7, -18.3) for chest diseases. Sub-group analysis revealed that reductions varied per clinical environment and relative prevalence rates but were the highest when algorithms actively stratified and reordered the radiological worklist, with reductions of -43.7% in report turnaround time compared to -7.6% from widget-based systems (p < 0.01). DL-based triage systems had comparable report turnaround time improvements, especially in outpatient and high-prevalence settings, suggesting that AI-based triage holds promise in alleviating radiology workloads. Question Can DL-based triage address lengthening imaging report turnaround times and improve patient outcomes across distinct clinical environments? Findings DL-based triage improved report turnaround time across disease groups, with higher reductions reported in high-prevalence or lower acuity settings. Clinical relevance DL-based workflow prioritization is a reliable tool for reducing diagnostic imaging delay for time-sensitive disease across clinical settings. However, further research and reliable metrics are needed to provide specific recommendations with regards to false-negative examinations and multi-condition prioritization.

Artificial intelligence (AI) shows promise in clinical tasks, yet its integration into workflows remains underexplored. This study proposes an AI-aided same-day diagnostic imaging workup to reduce recall rates following abnormal screening mammograms and alleviate patient anxiety while waiting for the diagnostic examinations. Using discrete simulation, we found minimal disruption to the workflow (a 4% reduction in daily patient volume or a 2% increase in operating time) under specific conditions: operation from 9 am to 12 pm with all radiologists managing all patient types (screenings, diagnostics, and biopsies). Costs specific to the AI-aided same-day diagnostic workup include AI software expenses and potential losses from unused pre-reserved slots for same-day diagnostic workups. These simulation findings can inform the implementation of an AI-aided same-day diagnostic workup, with future research focusing on its potential benefits, including improved patient satisfaction, reduced anxiety, lower recall rates, and shorter time to cancer diagnoses and treatment.