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Review

Imaging Engineering and Artificial Intelligence in Urinary Stone Disease: Low-Dose Computed Tomography, Spectral Technologies, and Predictive Models

Department of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan
*
Author to whom correspondence should be addressed.
Eng 2026, 7(4), 174; https://doi.org/10.3390/eng7040174
Submission received: 17 January 2026 / Revised: 2 April 2026 / Accepted: 9 April 2026 / Published: 11 April 2026

Abstract

Urinary stone disease is common, recurrent, and increasingly managed through imaging-driven pathways, yet standard-dose CT of the kidneys, ureters, and bladder (CT KUB) raises concerns about cumulative radiation exposure and the limited use of quantitative imaging information for risk stratification. This review synthesizes contemporary evidence on dose-optimized CT, advanced spectral technologies, and artificial intelligence (AI)-enabled analytics that are reshaping diagnosis, treatment selection, and triage. This review summarizes data supporting low-dose and ultra-low-dose CT protocols that preserve diagnostic accuracy while substantially reducing dose, and discusses how dual-energy CT, photon-counting CT, and radiomics facilitate noninvasive stone characterization and extraction of imaging biomarkers beyond size and location. It also reviews AI approaches for automated detection, segmentation, and volumetric quantification across CT, KUB, and ultrasounds, highlighting their potential to standardize stone-burden metrics. It further examines predictive models, including logistic regression, nomograms, and machine learning, for perioperative infectious complications, emergency department admission or intervention, procedure success, and long-term recurrence, and outlines reporting and validation frameworks and implementation considerations, including software as a medical device regulation and human oversight. In contrast to prior reviews that consider imaging and AI separately, this review integrates dose reduction, spectral characterization, and AI-driven analytics within real-world clinical pathways to distinguish established clinical applications from those that remain investigational. Integrating advanced CT and AI outputs into well-validated prediction models embedded in real-world workflows may enable safer imaging, more consistent triage, and more personalized follow-up for urinary stone disease.

1. Introduction

Urinary stone disease is highly prevalent worldwide and is associated with an escalating clinical and economic burden. A recent Global Burden of Disease analysis estimated more than 100 million incident cases, with incident cases, deaths, and disability-adjusted life years all rising substantially between 2000 and 2021 despite modest declines in age-standardized rates [1]. Stone formers are often young or middle-aged and frequently experience recurrence; epidemiologic evidence indicates 10-year recurrence rates of 30–50%, and nephrolithiasis is increasingly associated with obesity, diabetes, and cardiovascular disease [2].
Emergency department (ED) utilization has expanded in parallel. In the United States, ED visits, imaging utilization, and pharmacotherapy related to urolithiasis increased markedly from the early 1990s through the 2010s, with computed tomography (CT) now performed in the majority of ED evaluations for suspected renal colic [3]. This dependence on rapid imaging and timely intervention also exposed the vulnerability of stone-care pathways to system-level shocks [4]. Non-contrast CT of the kidneys, ureters, and bladder (CT KUB) has emerged as the reference standard for the evaluation of acute flank pain because of its high sensitivity and specificity and its ability to delineate alternative diagnoses [5]. Across many health systems, non-contrast CT KUB is widely employed to evaluate non-pregnant adults with suspected renal colic because of its high diagnostic accuracy and capacity to detect alternative diagnoses. Nevertheless, initial imaging recommendations differ across guidelines and practice environments, and an ultrasound (US)-first strategy is often favored for children, pregnant patients, and selected low-risk adults, with CT reserved for equivocal presentations or persistent clinical suspicion [6,7]. However, CT entails exposure to ionizing radiation, and recurrent stone formers may undergo repeated imaging across their lifespan; moreover, many pathways remain centered on binary determinations (“stone present?” “obstructing?”) rather than quantitative risk stratification for sepsis, urgent decompression, or recurrence.
Over the past decade, innovations in CT engineering and image analytics have begun to transform this landscape. Systematic reviews and meta-analyses indicate that low-dose and ultra-low-dose CT (LDCT and ULDCT) preserve excellent diagnostic accuracy while reducing radiation exposure by 40–80% relative to standard renal-protocol CT [8,9]. Photon-counting CT (PCCT) further enhances spatial resolution and contrast-to-noise performance and may enable dose-efficient urolithiasis protocols [10]. Dual-energy CT (DECT) and radiomics approaches now facilitate noninvasive inference of stone composition, potentially informing therapeutic selection such as medical dissolution versus shock-wave lithotripsy or endourologic intervention [11,12,13].
In parallel, artificial intelligence (AI) has rapidly penetrated stone imaging. Deep learning models already demonstrate strong performance for automated stone detection and volumetric segmentation on non-contrast CT [14,15], and analogous methods have been extended to plain radiography of the kidneys, ureters, and bladder (KUB) and US [16,17]. Beyond detection, radiomics and AI-derived imaging features are increasingly integrated with clinical variables in prediction models estimating risks of systemic inflammatory response syndrome (SIRS) or sepsis, need for ED admission or urologic intervention, and long-term recurrence [18,19,20,21,22].
For long-term prognosis, the Recurrence of Kidney Stone (ROKS) nomogram provides individualized estimates of second symptomatic stone episodes using clinical and imaging predictors, and a revised ROKS tool has demonstrated that recurrence risk increases steeply with each successive episode [18,19]. In procedural decision-making, a similar shift toward quantification has occurred in endourology: preoperative scoring systems and nomograms leverage preoperative imaging and patient factors to estimate stone-free outcomes after flexible ureteroscopy and to facilitate individualized counseling and expectation setting [20]. In acute care, nomograms predicting urosepsis among patients with ureteral calculi, including recent external validation and refinement studies, underscore how clinical, laboratory, and CT-derived features can be combined to identify high-risk patients [21]. A broader review of machine learning (ML) applications in kidney stone disease catalogs diverse uses across diagnostics, therapeutics, and prognostication, while highlighting methodological heterogeneity and the imperative for rigorous external validation [22,23,24,25].
This review synthesizes these advances with a clinically oriented perspective, appraising LDCT/ULDCT and advanced CT technologies (DECT, PCCT, radiomics), summarizing AI models across CT, KUB, and US, and discussing predictive modeling and AI-enabled triage strategies. This review uniquely synthesizes: (i) dose-optimized CT acquisition protocols; (ii) spectral CT platforms (DECT/PCCT) and radiomics for robust stone characterization; (iii) AI-enabled detection and segmentation across CT, KUB radiography, and ultrasonography; and (iv) prediction and triage models, with emphasis on reporting standards, validation, and implementation considerations. By structuring these elements around real-world clinical pathways, this review delineates to delineate what is already clinically established versus what remains investigational, and to offer actionable guidance for translation into routine practice.

2. Literature Identification and Selection

A targeted literature search was conducted in PubMed. The search strategy combined terms related to urolithiasis/nephrolithiasis with LDCT, CT KUB, DECT, photon-counting CT, radiomics, deep learning, segmentation, and prediction models/triage. English-language human studies, meta-analyses, and key technical evaluations with clinical relevance were prioritized. The reference lists of included articles were also screened to identify additional relevant publications. The final narrative synthesis focused on publications that collectively represent the current evidence on dose-optimized CT, spectral characterization, AI-based detection/segmentation, and predictive modeling.

3. Current Imaging Workflow and Unmet Needs

In contemporary practice, CT KUB constitutes the mainstay of evaluation for adult patients with suspected renal colic across many health systems. Comprehensive reviews and guideline statements consistently indicate that CT offers the highest sensitivity and specificity for upper-tract stones and has become the de facto standard in the ED for non-pregnant adults [5,6,7,26,27]. CT allows confirmation of ureteral calculi, accurate sizing and localization, assessment of obstruction, and identification of alternative diagnoses within a single encounter.
Guideline statements and expert reviews generally endorse non-contrast CT as the preferred diagnostic modality for many non-pregnant adults with suspected urolithiasis, reflecting its high sensitivity and specificity and its ability to evaluate obstruction and alternative diagnoses. Nevertheless, imaging pathways vary across professional societies and care settings, and US-first strategies are commonly adopted when radiation avoidance is prioritized or when clinical risk is low, with CT applied selectively when ultrasonography is non-diagnostic or symptoms persist [6,7,28,29]. Accordingly, in many EDs, adults with typical renal colic are triaged directly to CT KUB, whereas US or KUB is applied more selectively [5]. By contrast, children, pregnant patients, and selected low-risk adults are often managed with a US-first strategy, with CT reserved for equivocal or negative US findings when clinical suspicion remains high [5,29].
For follow-up, guidelines and expert reviews generally favor US and/or KUB to confirm stone passage or surveil residual fragments, reserving CT for persistent symptoms, complex anatomy, or indeterminate findings [5,6,7]. Nevertheless, real-world evidence demonstrates substantial CT utilization even during follow-up, and recurrent stone formers may accrue meaningful cumulative radiation exposure over years of imaging, particularly when standard-dose CT protocols are employed [3,5].
Several unmet needs emerge from this prevailing care pattern:
  • Radiation stewardship: balancing CT’s diagnostic performance against cumulative dose concerns in often young, recurrent patients.
  • Quantitative triage: progressing beyond binary detection to integrate imaging features (size, number, location, Hounsfield units, obstruction) into structured prediction of sepsis, need for urgent intervention, and recurrence.
  • Workflow efficiency and equity: addressing scanner access, reporting latency, and variability in expertise that can impede rapid, consistent triage.
Collectively, these gaps motivate broader implementation of LDCT/ULDCT, advanced spectral CT, and AI tools capable of extracting greater clinical value from each imaging study while mitigating harm. Figure 1 presents a workflow-oriented framework illustrating where dose-optimized CT, spectral CT/radiomics, and AI tools may add value across ED triage, procedural planning, and follow-up.

4. LD and ULD CT for Urolithiasis

From a pragmatic perspective, CT strategies for urolithiasis lie on a dose–information continuum: dose-optimized protocols preserve diagnostic detectability, whereas spectral techniques add characterization that may influence management. Table 1 provides a concise synthesis of this comparison, and Figure 2 illustrates how these CT approaches relate to the broader clinical workflow of urinary stone disease.
Standard renal-protocol CT often delivers effective doses in the 8–16 millisievert (mSv) range, raising concerns about cumulative exposure, especially in young, recurrent stone formers [5]. Early dose-reduction studies showed that substantial reductions in tube current and voltage were feasible, but meta-analytic data were needed to support widespread adoption [30]. Nevertheless, real-world adoption of reduced-dose CT protocols remains variable across institutions and practice settings [31].
Niemann et al. performed one of the first meta-analyses focused on LDCT for urolithiasis, pooling seven studies (1061 patients) that used protocols with effective dose < 3 mSv. They reported pooled sensitivity of 0.966 and specificity of 0.949 versus standard-dose CT and concluded that LDCT could reliably serve as an initial imaging technique for suspected renal colic, with some limitations in obese patients [32]. Xiang et al. later conducted a systematic review and meta-analysis of LDCT KUB and similarly found that LDCT provided excellent diagnostic accuracy for clinically significant stones, with pooled sensitivity and specificity of 93.1% and 96.6%, respectively [8].
Reported diagnostic performance of LDCT varies across studies for several reasons. Differences in patient body habitus and image noise, stone size and anatomic location, particularly small distal ureteral calculi, and the prevalence of mimics such as phleboliths can influence sensitivity and specificity. In addition, heterogeneity in acquisition parameters (kVp/mAs and dose targets), reconstruction approaches, reference standards, and outcome definitions limits direct cross-study comparability.
Rodger et al. [9] extended this work by differentiating LDCT (<3.5 mSv) and ULDCT (<1.9 mSv) protocols in 1529 patients. They found diagnostic accuracies of 94.3% and 95.5% for LDCT and ULDCT, respectively, when standard-dose CT was the reference, with sensitivities of up to 98% and specificities up to 100% in individual series [9]. Single-center studies support these findings. Klüner et al. showed that multislice ULDCT at doses comparable to abdominal KUB (male/female: 0.5/0.7 mSv) reliably detected renal and ureteral calculi [33]. Moore et al. reported that reduced-dose CT in ED patients maintained high sensitivity and specificity for ureteral stones and detected nearly all stones requiring intervention within 90 days [34].
More recently, ULDCT has been evaluated in the follow-up setting. Cheng et al. demonstrated that sub-millisievert ULDCT is highly effective for follow-up of ureterolithiasis, detecting small and distal ureteric stones often missed by KUB or US while maintaining a very low effective dose [35]. Kandasamy et al. prospectively compared sub-mSv ultra-low-dose computed tomography of the kidneys, ureters, and bladder with X-ray KUB in patients with known urolithiasis and found that ULDCT had higher sensitivity for both intrarenal and ureteric stones at similar or lower dose, supporting ULDCT as a superior alternative to KUB for follow-up when CT is available [36].
Dose reductions from low to ultra-low CT have been enabled by advances in reconstruction. Iterative reconstruction techniques reduce noise and allow 40–60% dose reductions without compromising stone detection or assessment of extra-urinary pathology [37]. Deep learning reconstruction further improves noise–texture characteristics and can restore image quality at sub-mSv doses. Zhang et al. compared low-dose CT with hybrid iterative reconstruction to ULDCT reconstructed with deep learning reconstruction in patients with suspected renal calculi; ULDCT with deep learning reconstruction achieved similar detection rates at approximately 25% of the LDCT dose [38].
In practice, LDCT/ULDCT perform best in patients with moderate-to-high pretest probability and without extreme obesity, and are particularly useful in follow-up where stone presence and location are known [37,38,39]. Overall, these data support LDCT/ULDCT as central tools in a radiation-conscious imaging strategy for urinary stone disease (Table 2).

5. Advanced CT Technologies: Spectral, Photon-Counting CT, and Radiomics

Stone composition is a key determinant of management: uric acid stones may be amenable to medical dissolution, whereas calcium oxalate, brushite, and cystine stones more commonly require endourologic intervention and show differential responsiveness to shock-wave lithotripsy.
DECT was the first major CT innovation designed for noninvasive compositional assessment. In a seminal in vivo study, Hidas et al. demonstrated that DECT could differentiate uric acid, cystine, and calcified stones using attenuation-ratio thresholds, achieving approximately 82% overall accuracy compared with X-ray diffraction [11]. Eliahou et al. reviewed DECT applications in urinary stone disease and concluded that DECT reliably discriminates uric-acid from non-uric acid stones and often identifies cystine, thereby informing decisions regarding medical dissolution versus surgical management [40]. Leng et al. extended DECT to mixed stones in a phantom study, showing that DECT can quantify uric-acid and non-uric acid fractions with low error across simulated body sizes, supporting more granular characterization than binary classification [41]. Interpretation benefits from awareness of technique-specific pitfalls and stone mimics when applying DECT in routine practice [42].
PCCT represents a newer detector technology that captures energy-resolved information at the photon level and provides improved spatial resolution and contrast-to-noise performance at equal or lower dose compared with conventional energy-integrating CT. General PCCT evaluations underscore its potential to deliver sharper images and reduce radiation dose in abdominal imaging [43,44]. Niehoff et al. assessed low-dose abdominal PCCT for urolithiasis in 98 examinations and reported that stepwise reductions in image-quality level yielded substantial dose savings without compromising quantitative metrics or radiologist confidence in stone detection [10]. Collectively, these data suggest that PCCT may synergize with LD/ULDCT strategies by improving conspicuity for small stones and enabling richer spectral characterization without degrading diagnostic quality.
Radiomics adds an analytic layer to these imaging datasets [45]. Kaviani et al. applied threshold-based segmentation and radiomics to single-energy non-contrast CT to classify uric-acid versus non-uric acid stones, achieving an area under the receiver operating characteristic curve (AUC) of 0.78 and demonstrating that composition-relevant signatures can be extracted from standard CT without dedicated DECT protocols [12]. Huang et al. developed a radiomics model using conventional CT in 195 patients and reported an AUC of 0.81–0.89 for identifying uric acid stones, outperforming simple Hounsfield unit (HU)-threshold approaches [13]. Hertel et al. leveraged PCCT-based spectral radiomics to classify six stone types in an ex vivo dataset, achieving robust multi-class discrimination and illustrating how PCCT combined with radiomics could enable fine-grained stone typing [46].
Beyond composition, radiomics has also been explored for risk stratification. Lu et al. integrated CT radiomics with clinical variables to distinguish kidney stone-associated urinary tract infection from non-infected stones, achieving excellent discrimination and supporting the potential utility of radiomics-derived biomarkers for early identification of infected stones [47]. Overall, DECT is sufficiently mature for routine composition typing in centers with access to the technology [11,41,48], whereas PCCT and radiomics remain promising avenues for dose-efficient, information-rich imaging that can inform both treatment selection and risk stratification [10,12,13,46,47].

6. AI for Automated Detection, Segmentation, and Quantification

Across published AI studies in urinary stone disease, publicly accessible imaging datasets remain limited, and most models have been developed using single-center retrospective cohorts. Dataset composition, including patient selection, the prevalence of mimicking conditions, scanner vendors, and dose and reconstruction settings, as well as annotation strategy and the presence or absence of external testing, materially influences reported performance and clinical generalizability. Table 3 summarizes dataset characteristics and key elements of evaluation design, including training, validation, and testing splits, as well as external validation, as reported in representative studies.
CT-based AI has progressed rapidly in urinary stone disease. Parakh et al. developed a cascading convolutional neural network (CNN) for urinary stone detection on unenhanced CT and reported an AUC of 0.95, with high sensitivity for clinically significant stones across internal and external datasets [14]. Elton et al. developed a deep learning system for automated kidney stone detection and volumetric segmentation on non-contrast CT; in their cohort, lesion-level sensitivity was 0.86, and automated volume estimates demonstrated strong agreement with manual reference standards [15]. Together, these studies suggest that AI can approach radiologist-level detection performance while providing objective, reproducible stone-burden metrics for procedural planning and longitudinal follow-up.
Cui et al. integrated three-dimensional deep learning with thresholding to automate stone detection and compute the S.T.O.N.E. nephrolithometry score from CT, thereby linking AI-derived outputs to a validated percutaneous nephrolithotomy (PCNL) complexity grading framework [49]. Kim et al. trained a deep-learning segmentation network on non-contrast CT and reported Dice coefficients of approximately 0.80 for stone masks, alongside high concordance in stone counts, supporting the feasibility of fully automated segmentation even in patients with multiple stones [50].
AI has also been extended to lower-cost modalities. Kobayashi et al. developed a CNN-based computer-aided diagnosis system for upper-tract stones on KUB in 1017 patients; the model achieved high sensitivity and improved reader performance, particularly for proximal ureteral stones, compared with unaided interpretation [16]. Preedanan et al. proposed a cascaded U-shaped network pipeline for urinary stone segmentation on abdominal KUB images, incorporating organ localization, stone-embedding data augmentation, and lesion-size reweighting to enhance recall for small stones [51].
Liu et al. developed a deep learning-based computer-aided diagnosis system for urolithiasis detection on KUB images using 355 images from 104 patients, with additional preprocessing and augmentation for model development [52]. Their work supports the feasibility of AI-assisted KUB interpretation in acute-care settings and highlights the potential of such systems to assist emergency physicians when rapid image review is required. Ahmed et al. applied a Visual Geometry Group 16-layer network-based classifier with gradient-weighted class activation mapping to identify stones on KUB radiographs, achieving approximately 95% accuracy while generating heatmaps that localize image regions driving model predictions [53]. Obaid et al. developed an ensemble deep learning system to classify noisy kidney ultrasound images as normal versus stone-containing, demonstrating robust performance across noise conditions and underscoring the potential of AI to augment challenging US examinations [17].
Collectively, these studies indicate that AI can automate detection, segmentation, volumetry, and scoring across CT, KUB, and US, and may reduce radiologist workload while delivering standardized quantitative outputs. These outputs include stone presence, number, size, volume, and composition surrogates that can be integrated into risk prediction models. However, most published models remain single-center and retrospective, are constrained by modest training datasets, and lack comprehensive external validation, highlighting the need for rigorous prospective evaluation and multi-center testing [22].
Despite rapid progress, many stone-detection/segmentation studies remain retrospective and single-center, often with modest sample sizes and limited external validation. Reported performance can be sensitive to spectrum effects and to annotation conventions that vary across institutions. Moreover, metrics are often reported on curated test sets and may not reflect real-world prevalence of mimics or operational constraints. Accordingly, much of the current literature may be regarded as proof-of-concept and emphasize the need for multi-site external validation, calibration assessment where relevant, and prospective impact studies that quantify clinical utility and workflow integration. To improve reproducibility and clinical interpretability, reporting of dataset composition, reference standards, and evaluation design should follow established checklists such as the Checklist for Artificial Intelligence in Medical Imaging [54].

7. Predictive Models and AI Triage in Urinary Stone Disease

Logistic regression models the probability of an outcome as p = 1/(1 + e−(β0 + βTx)), yielding an interpretable, odds-based estimate of risk derived from clinical and imaging features. Support vector machine (SVM) models define a decision boundary that maximizes the margin between classes and can accommodate non-linear relationships through kernel functions. Ensemble methods, such as gradient boosting, combine multiple weak learners to enhance discrimination and may be particularly useful when complex interactions exist among predictors. Regardless of the model family, calibration and clinically meaningful decision thresholds remain essential for safe implementation.
Prediction models in urinary stone disease span perioperative infection, ED disposition and intervention, and long-term outcomes. An overview of representative models, key inputs, and target endpoints is provided in Table 4.

7.1. Perioperative Infectious Complications

SIRS and urosepsis after PCNL and ureteroscopy are key targets for risk prediction. Tang et al. developed a logistic-regression nomogram in 785 PCNL patients that used neutrophil-to-lymphocyte ratio, S.T.O.N.E. score, female sex, and positive urine culture to predict postoperative systemic infection (SIRS and urosepsis), achieving C-indices around 0.8 with good calibration [55]. Zhang et al. compared logistic regression and multiple ML algorithms in 337 PCNL cases and found that an SVM model predicted SIRS with an AUC of 0.94, outperforming logistic regression; key predictors included inflammatory indices, stone characteristics, and operative factors [56].
For patients with ureteral calculi, nomograms have also been developed to predict urosepsis risk. A recent Diagnostics study externally validated Hu’s nomogram in a Japanese cohort and identified novel CT-based risk factors such as lower CT attenuation of calculi and higher hydronephrosis grade, yielding a refined model for early urosepsis prediction in ureteral stone patients [21]. These models illustrate how clinical, laboratory, and CT features can be combined to identify high-risk patients who may benefit from early decompression, prolonged antibiotics, or intensive care unit-level monitoring.

7.2. ED Triage, Admission, and Intervention

In the ED, the immediate triage question is not only stone or no stone, but who needs admission or urgent urologic intervention. Daniels et al. analyzed 475 adults with CT-confirmed ureteral stones in a prospective ED cohort and found that only 20% were admitted and 17% underwent urologic intervention within 90 days [57]. Predictors of admission and intervention included markers of symptom burden and clinical severity, as well as stone-related factors such as larger stone size and proximal ureteral location. These findings underscore variation in outcomes and the potential role of prediction tools to standardize decisions.
Haifler et al. applied ML to patients with ureteral stones ≤ 5 mm and showed that a combination of clinical and imaging features could predict justified surgical intervention with good discrimination [58]. Influential variables included stone size, stone location, and selected clinical parameters reflecting acute presentation severity. Their work suggests that ML-enhanced triage could help avoid unnecessary admissions and unsafe discharges by identifying small-stone patients who are less likely to pass stones spontaneously under conservative management.

7.3. Long-Term Recurrence and Procedure Success

At longer time horizons, prediction models have focused on recurrence and procedure success. The original ROKS nomogram by Rule et al. used a population-based cohort of first-time stone formers in Olmsted County to estimate the risk of a second symptomatic episode, with 5-year recurrence risk ranging from <1% to nearly 50% depending on age, sex, body mass index (BMI), family history, stone type, and baseline factors [18]. Vaughan et al. later created a revised ROKS tool using more than 3000 incident stone formers and multiple episodes, showing that recurrence risk escalates sharply with each successive episode and is further influenced by imaging features such as lower-pole location, number of stones, and largest diameter [19]. These tools inform the intensity of preventive strategies and could be integrated with imaging-AI outputs in future follow-up algorithms.
In the surgical domain, nomograms and scoring systems for predicting stone-free rate (SFR) after endourological procedures have proliferated. A recent Japanese Urological Association-affiliated review outlines a step-by-step framework for developing, validating, and implementing nomograms for urological tumors, emphasizing principles that are equally applicable to stone-related prediction tools [25]. More recently, Lee et al. developed and externally validated a machine learning model for SFR after retrograde intrarenal surgery in patients with lower pole renal stones; the Light Gradient Boosting Machine model achieved the highest predictive performance, and stone burden, HU, pelvic stone angle, and renal infundibular length emerged as the most influential features [59]. These findings suggest that non-linear algorithms may better capture the interplay among stone burden, density, and pelvicalyceal anatomy, although prospective validation and broader generalizability remain to be established.

7.4. From Prediction Models to AI-Enabled Triage

Across these domains, several methodological themes are apparent. First, many models are derived from single-center cohorts with limited size and remain vulnerable to overfitting; independent external validation remains relatively uncommon [22,55,56,57,58,59]. Second, relatively few urolithiasis models incorporate image-derived features beyond size and location, despite evidence that CT attenuation, stone volume, and radiomics signatures carry prognostic information [12,13,19,21]. Third, clinical utility has rarely been tested prospectively using decision-curve analysis, workflow simulations, or impact studies [60]. Risk of bias and applicability can be systematically appraised using the Prediction model Risk of Bias Assessment Tool and its recent artificial intelligence extension, complementing transparent reporting and facilitating safer translation [61,62].
Across the literature, no single ML model is uniformly superior, as performance depends on the specific task and underlying data structure. For imaging-centric tasks, such as stone detection and segmentation, deep learning approaches generally demonstrate the most consistent performance gains by learning hierarchical features directly from CT, KUB, or ultrasound images. For tabular prediction tasks, such as SIRS/sepsis or ED intervention, non-linear models such as SVM and gradient boosting may improve discrimination when complex interactions exist among clinical, laboratory, and imaging-derived predictors; however, direct comparisons remain limited by heterogeneity in endpoints, cohort composition, and external validation.
Conceptually, the path toward AI-enabled triage is clear. Automated imaging pipelines can output standardized descriptors, such as stone presence, number, largest diameter, total volume, HU distribution, and obstruction grade, that feed into prediction models for perioperative SIRS/sepsis, ED admission/intervention, and long-term recurrence. Logistic regression and ML models can then translate these features, together with clinical and laboratory data, into individualized risk estimates displayed at the point of care. TRIPOD and TRIPOD + AI provide frameworks to ensure such models are developed and reported transparently [23,24,25]. Figure 3 illustrates a conceptual pipeline linking imaging inputs with AI-based detection, segmentation, and quantification, as well as calibrated prediction models, to point-of-care triage decisions and longitudinal management.
Among prediction and triage models in urolithiasis, direct comparison of performance metrics is limited by heterogeneity in outcome definitions and time horizons. Infection outcomes may range from SIRS to urosepsis, and ED endpoints vary from admission to intervention. Predictor definitions also differ, and calibration reporting remains inconsistent, with many studies focusing on discrimination alone. Consistent adoption of transparent reporting frameworks, explicit outcome definitions, and routine calibration assessment would improve interpretability, facilitate external validation, and support safer clinical translation.

8. Implementation, Regulation, and Future Directions

To facilitate practical interpretation, the reviewed technologies are categorized according to translational readiness, thereby helping clinicians and engineers align their expectations with real-world deployability. Box 1 summarizes the translational readiness of the imaging and artificial intelligence approaches discussed in this review.
Box 1. Translation readiness map for imaging and AI in urolithiasis.
Clinically established
• LDCT protocols for suspected stones in appropriately selected adults, with attention to body habitus and protocol standardization.
• DECT-based differentiation of uric-acid-containing from calcium-containing stones in centers with appropriate acquisition and post-processing capability.
Emerging but promising
• PCCT applications for stone imaging and dose-efficient spectral characterization.
• CT-based radiomics for stone composition or fragility characterization, although external validation remains limited.
Experimental/proof-of-concept
• AI-enabled ED triage tools and automated detection/segmentation models without robust multi-site external validation.
• ML-based prediction models for complications or intervention that lack consistent outcome definitions, calibration reporting, or prospective impact evaluation.
Clinically, this framework may be used to align the clinical question of whether ED triage, procedural planning, or follow-up, with the lowest-dose and best-validated option, most likely to influence management. It may also help institutions separate near-term protocol standardization from technologies that still require prospective validation, workflow testing, or regulatory maturation before routine deployment.
AI-enabled imaging and prediction tools for urinary stone disease fall within the broader category of software as a medical device (SaMD). The U.S. Food and Drug Administration (FDA) AI/ML SaMD Action Plan and related guidance outline an oversight framework for AI/ML-enabled devices, emphasizing rigorous pre-market evaluation, post-market performance monitoring and model-update management, and mitigation of bias across demographic subgroups [63]. The FDA also maintains a public registry of authorized AI/ML-enabled medical devices, many of which are radiology-focused.
In Europe, the combination of the Medical Device Regulation and the European Union Artificial Intelligence Act is expected to classify many medical AI systems as high-risk, necessitating risk-management systems, high-quality training data, transparency, and human oversight [64]. Ethical guidance for AI in radiology emphasizes that systems should promote well-being, minimize harm, distribute benefits equitably, respect privacy and autonomy, remain transparent and reliable, and preserve human accountability [65,66]. In urinary stone disease, these principles translate into requirements for representative datasets (including diverse patient populations and scanner platforms), robust external validation, transparent reporting (TRIPOD+AI), and human-in-the-loop workflows in which clinicians retain ultimate responsibility for decisions.
Beyond experimental prototypes, commercially available post-processing platforms can already support key components of stone characterization in routine clinical practice. For example, dedicated applications may enable standardized quantification of stone burden (e.g., maximal diameter, volumetry, and attenuation-derived metrics) and generate visualization outputs (e.g., overlays) that enhance communication between radiology and urology. Moreover, spectral CT post-processing, particularly in DECT, can facilitate composition-relevant assessment, including discrimination of uric-acid from non-uric-acid calculi, provided that appropriate acquisition and processing pipelines are available. Collectively, these examples highlight a pragmatic pathway toward clinical translation; however, real-world impact hinges on harmonized imaging protocols, explicit intended-use definitions, interoperability with clinical information systems, and ongoing performance surveillance.
Implementation experience from other radiology AI tools suggests that seamless integration into picture archiving and communication systems and radiology information systems, automated background processing, and the delivery of concise, actionable outputs (e.g., stone overlays, standardized metrics, risk scores) are critical for adoption. Prospective silent-mode deployments, in which AI operates without influencing care while performance and failure modes are systematically monitored, are recommended before activating clinical decision support [63,65,67].
Future priorities in urinary stone disease include:
  • Multimodal models integrating advanced imaging outputs (DECT/PCCT features, radiomics, AI segmentation) with clinical and laboratory data.
  • Rigorous, transparent evaluation of prediction models, including calibration, decision-curve analysis, and external validation, in accordance with TRIPOD+AI guidance [23,24].
  • Prospective impact studies to determine whether AI-assisted triage shortens time to decompression for obstructive infected stones, optimizes admission decisions, or reduces unnecessary imaging without increasing adverse events.
  • When AI-enabled tools are evaluated as clinical interventions, trial protocols and reports should follow the Standard Protocol Items: Recommendations for Interventional Trials–Artificial Intelligence (SPIRIT-AI) and Consolidated Standards of Reporting Trials–Artificial Intelligence (CONSORT-AI) extensions to ensure completeness and transparency [68,69].
  • Fairness and robustness assessments across sex, age, ethnicity, BMI, comorbidity, scanner type, and dose level.
  • Human–AI collaboration paradigms that prioritize augmentation of clinician performance and patient communication rather than automation alone [22,65,66].
If these technical, regulatory, and ethical challenges are addressed, urinary stone disease is well positioned to become a model use-case for clinically meaningful integration of imaging engineering and AI.

9. Limitations

This review has several limitations. First, as a narrative review, study identification and selection were targeted rather than exhaustive, and relevant publications may have been overlooked. Second, heterogeneity in imaging protocols, reference standards, and outcome definitions limits direct cross-study comparisons and may constrain generalizability. Third, much of the AI literature remains based on single-center retrospective studies with modest sample sizes and incomplete external validation, which may overstate reported performance relative to real-world settings. Finally, regulatory and implementation considerations vary across jurisdictions and continue to evolve; accordingly, the present discussion should be interpreted within that context.

10. Conclusions

Urinary stone disease is highly prevalent, frequently recurrent, and intrinsically reliant on imaging for diagnosis and management. Standard-dose CT KUB has long served as the diagnostic workhorse, yet it raises concerns regarding cumulative radiation exposure and the underutilization of the abundant quantitative information embedded within imaging data. Accumulating evidence indicates that LDCT and ULDCT can maintain diagnostic performance while substantially reducing dose; spectral and photon-counting CT, in concert with radiomics, enable robust composition assessment and the derivation of novel imaging biomarkers; and AI models can automate detection, segmentation, and stone-burden quantification across CT, KUB, and ultrasound.
In parallel, prediction models can stratify risks of SIRS/sepsis, ED admission and intervention, and long-term recurrence. Nomogram development frameworks and TRIPOD/TRIPOD+AI guidance provide methodological scaffolding for constructing robust, clinically meaningful tools. The next logical step is to integrate these components: to channel standardized imaging outputs from advanced CT and AI pipelines into rigorously validated prediction models, and to deploy them within real-world ED and perioperative workflows under appropriate regulatory and ethical governance. If implemented thoughtfully, this integrated paradigm offers the prospect of safer imaging, more consistent triage, and more personalized longitudinal care for patients with urinary stone disease.

Author Contributions

Conceptualization, S.I. and T.U.; methodology, T.U.; software, T.S.; validation, T.N., Y.S. (Yuka Sugizaki), R.O. and T.E.; formal analysis, Y.S. (Yuta Suzuki); investigation, S.I. and T.U.; resources, R.I., N.I., Y.S. (Yuta Suzuki) and S.I.; data curation, R.I., N.I., Y.S. (Yuka Sugizaki), T.S. and T.E.; writing—original draft preparation, S.I.; writing—review and editing, T.U.; visualization, T.U.; supervision, N.K. and H.S.; project administration, N.K. and H.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The original contributions presented in this study are included in the article. Further inquiries can be directed to the corresponding author.

Conflicts of Interest

Hiroyoshi Suzuki reports research funding from Astellas, AstraZeneca, Bayer, Chugai, Eli Lilly, Janssen, MSD, Nihon Kayaku, and Sanofi; advisory fees from AstraZeneca, Bayer, Chugai-Roche, Eli Lilly, Ferring, Janssen, MSD, Novartis, Pfizer, and Sanofi; and lecture fees from Astellas, AstraZeneca, Bayer, Janssen, Novartis, Pfizer, and Sanofi. The authors declare no conflict of interest.

Abbreviations

The following abbreviations are used in this manuscript:
AIArtificial intelligence
AUCArea under the receiver operating characteristic curve
BMIBody mass index
CNNConvolutional neural network
CTComputed tomography
CT KUBComputed tomography of the kidneys, ureters, and bladder
DECTDual-energy computed tomography
EDEmergency department
FDAFood and Drug Administration
HUHounsfield unit
KUBKidneys, ureters, and bladder
LDCTLow-dose computed tomography
MLMachine learning
mSvMillisievert
NCCTNon-contrast computed tomography
PCCTPhoton-counting computed tomography
PCNLPercutaneous nephrolithotomy
QCQuality control
ROKSRecurrence of kidney stone
SaMDSoftware as a medical device
SFRStone-free rate
SIRSSystemic inflammatory response syndrome
SVMSupport vector machine
TRIPODTransparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis
TRIPOD+AITransparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis + Artificial Intelligence
ULDCTUltra-low-dose computed tomography
USUltrasound

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Figure 1. Workflow-oriented mapping of imaging and AI in urinary stone disease. AI, artificial intelligence; CT, computed tomography; ED, emergency department; LDCT, low-dose computed tomography; ULDCT, ultra-low-dose computed tomography.
Figure 1. Workflow-oriented mapping of imaging and AI in urinary stone disease. AI, artificial intelligence; CT, computed tomography; ED, emergency department; LDCT, low-dose computed tomography; ULDCT, ultra-low-dose computed tomography.
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Figure 2. Evolution of CT technologies for urinary stone disease: radiation dose versus informational yield. DECT, dual-energy computed tomography; LDCT, low-dose computed tomography; PCCT, photon-counting computed tomography; SECT, single-energy computed tomography; ULDCT, ultra-low-dose computed tomography.
Figure 2. Evolution of CT technologies for urinary stone disease: radiation dose versus informational yield. DECT, dual-energy computed tomography; LDCT, low-dose computed tomography; PCCT, photon-counting computed tomography; SECT, single-energy computed tomography; ULDCT, ultra-low-dose computed tomography.
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Figure 3. Conceptual pipeline from imaging to AI-enabled triage in urolithiasis. AI, artificial intelligence; CT, computed tomography; HU, Hounsfield unit; KUB, kidneys, ureters, and bladder; ML, machine learning; QC, quality control.
Figure 3. Conceptual pipeline from imaging to AI-enabled triage in urolithiasis. AI, artificial intelligence; CT, computed tomography; HU, Hounsfield unit; KUB, kidneys, ureters, and bladder; ML, machine learning; QC, quality control.
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Table 1. Practical summary of CT approaches for urolithiasis.
Table 1. Practical summary of CT approaches for urolithiasis.
ApproachTypical Use-CaseAdded ValueKey Cautions
SECTED evaluation; broad differentialHighest robustness and image quality; alternative diagnosesHigher radiation burden
LDCTFirst-line adult stone evaluationMaintains high diagnostic accuracy at reduced dosePerformance varies with BMI, stone size/location, protocol/reconstruction
ULDCTFollow-up; focused questionDose approaching radiography in optimized protocolsLimited for very small/distal stones; not ideal for broad differential
DECTWhen composition mattersUric-acid vs. non-uric-acid discrimination; added characterizationRequires spectral acquisition/processing; availability varies
PCCTEmerging/early adoptionHigher spatial/spectral resolution; potential dose efficiencyLimited availability; evidence and standardization still evolving
BMI, body mass index; CT, computed tomography; DECT, dual-energy CT; ED, emergency department; LDCT, low-dose CT; PCCT, photon-counting CT; SECT, single-energy CT; ULDCT, ultra-low-dose CT.
Table 2. Clinical evidence for low- and ultra-low-dose CT in urinary stone disease.
Table 2. Clinical evidence for low- and ultra-low-dose CT in urinary stone disease.
StudyEvidence TypeDose MetricComparatorKey Findings
Niemann et al. [32]Meta-analysisLDCT (<3 mSv)Standard-dose CTPooled sensitivity 0.966; specificity 0.949
Xiang et al. [8]Meta-analysisLDCT KUBStandard-dose CTPooled sensitivity 93.1%; specificity 96.6%
Rodger et al. [9]Meta-analysisLDCT (<3.5 mSv), ULDCT (<1.9 mSv)Standard-dose CTDiagnostic accuracy 94.3% (LDCT) and 95.5% (ULDCT); sensitivities up to 98% and specificities up to 100% in individual series
Klüner et al. [33]Single-center validationULDCT (KUB-equivalent (0.5/0.7 mSv))Standard evaluationReliable detection of renal and ureteral calculi at very low dose
Moore et al. [34]ED cohortReduced-dose CTStandard-dose CTHigh sensitivity/specificity for ureteral stones; detected nearly all stones requiring intervention within 90 days
Cheng et al. [35]Follow-up studySub-mSv ULDCTKUB/USDetected small/distal ureteric stones often missed by KUB or US at very low effective dose
Kandasamy et al. [36]Prospective studySub-mSv ULDCT KUBX-ray KUBHigher sensitivity for intrarenal and ureteric stones at similar or lower dose
den Harder et al. [37]Reconstruction-enabled dose reductionLDCT with iterative reconstructionStandard-dose CTComparable detection with improved noise characteristics
Zhang et al. [38]Reconstruction-enabled dose reductionLDCT (hybrid iterative reconstruction) vs. ULDCT (deep learning reconstruction)LDCT as referenceSimilar detection at ~25% of LDCT dose
CT, computed tomography; CT KUB, computed tomography of the kidneys, ureters, and bladder; LDCT, low-dose computed tomography; ULDCT, ultra-low-dose computed tomography; ED, emergency department; KUB, kidneys, ureters, and bladder; US, ultrasound; mSv, millisievert; sub-mSv, sub-millisievert. Note: dose definitions are presented as reported in the original publications. When an explicit effective-dose threshold (mSv) was specified, it is reproduced here. For studies employing protocol-defined descriptors without a single quantitative effective-dose value, the terminology used in the original reports is retained, recognizing that delivered dose may vary by scanner/vendor, patient body habitus, and reconstruction approach. Where available, readers are directed to the original reports for detailed acquisition parameters.
Table 3. Dataset characteristics and evaluation design in representative AI studies for urinary stone disease.
Table 3. Dataset characteristics and evaluation design in representative AI studies for urinary stone disease.
StudyModalityDataset SizeTraining/TestingValidation
Parakh et al. [14]CT535 CT scans (stones present 279; absent 256)Test set n = 100; remaining scans used for developmentCross-scanner evaluation within two scanners
Elton et al. [15]CT91 scans with stones + 89 without stones50% training/50% testingExternal validation: 6185 patients
Cui et al. [49]CTSegmentation dataset n = 167; hydronephrosis Classification dataset n = 282; test dataset n = 117NRNR
Kim et al. [50]CT410 NCCT scans5-fold cross-validation; fold ratio training/validation/testing = 3:1:1NR
Kobayashi et al. [16]KUB1017 patientsTraining n = 827; test n = 190NR
Preedanan et al. [51]KUBStone-contained 1156 images; stone-free 1200 images5-fold cross-validation; stone-contained split 64%/16%/20%NR
Liu et al. [52]KUB355 images from 104 patientsPre-processed/augmented dataset n = 1130; 856 images used for model development (684 for training and 172 for validation), and 274 images used for testingNR
Ahmed et al. [53]KUB500 images (250 stone/250 normal)Augmented dataset n = 14,265; 70% training/30% testing, corresponding to 9986 training and 4279 testing imagesNR
Obaid et al. [17]US4413 images (1821 normal; 2592 stone)NRNR
CT, computed tomography; KUB, kidneys, ureters, and bladder; NCCT, non-contrast computed tomography; NR, not reported; US, ultrasound.
Table 4. Representative prediction and AI-triage models in urinary stone disease.
Table 4. Representative prediction and AI-triage models in urinary stone disease.
StudyDomainOutcomeModel TypeKey Predictors
Tang et al. [55]Perioperative infectionSIRS/urosepsis after PCNLLogistic regression nomogramNLR, S.T.O.N.E. score, female sex, positive urine culture
Zhang et al. [56]Perioperative infectionSIRS after PCNLML (SVM; compared with logistic regression)Inflammatory indices, stone characteristics, operative factors
Daniels et al. [57]ED triage/interventionAdmission and urologic intervention (90 days)Logistic regressionPain control, infection signs, creatinine, stone size, proximal location, outpatient follow-up
Haifler et al. [58]ED triage/intervention“Justified” surgical intervention for ureteral stones ≤ 5 mmML (gradient boosting)Persistent pain, hydronephrosis, stone size/location, WBC, kidney function
Rule et al. [18]Long-term recurrenceSecond symptomatic stone episode (5-year risk)Nomogram (ROKS)Age, sex, BMI, family history, stone type, baseline factors
Vaughan et al. [19]Long-term recurrenceRecurrence across successive episodesPrediction tool (ROKS update)Prior episodes plus imaging features (e.g., lower-pole location, number, diameter)
Lee et al. [59]SFRSFR after RIRS for lower pole renal stonesML (LightGBM)Stone burden, HU, pelvic stone angle, renal infundibular length
BMI, body mass index; ED, emergency department; HU, Hounsfield units; LightGBM, Light Gradient Boosting Machine; ML, machine learning; NLR, neutrophil-to-lymphocyte ratio; PCNL, percutaneous nephrolithotomy; SFR, stone-free rate; SIRS, systemic inflammatory response syndrome; SVM, support-vector machine; WBC, white blood cell count.
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Iijima, S.; Utsumi, T.; Ikeda, R.; Ishitsuka, N.; Noro, T.; Suzuki, Y.; Sugizaki, Y.; Somoto, T.; Oka, R.; Endo, T.; et al. Imaging Engineering and Artificial Intelligence in Urinary Stone Disease: Low-Dose Computed Tomography, Spectral Technologies, and Predictive Models. Eng 2026, 7, 174. https://doi.org/10.3390/eng7040174

AMA Style

Iijima S, Utsumi T, Ikeda R, Ishitsuka N, Noro T, Suzuki Y, Sugizaki Y, Somoto T, Oka R, Endo T, et al. Imaging Engineering and Artificial Intelligence in Urinary Stone Disease: Low-Dose Computed Tomography, Spectral Technologies, and Predictive Models. Eng. 2026; 7(4):174. https://doi.org/10.3390/eng7040174

Chicago/Turabian Style

Iijima, Shota, Takanobu Utsumi, Rino Ikeda, Naoki Ishitsuka, Takahide Noro, Yuta Suzuki, Yuka Sugizaki, Takatoshi Somoto, Ryo Oka, Takumi Endo, and et al. 2026. "Imaging Engineering and Artificial Intelligence in Urinary Stone Disease: Low-Dose Computed Tomography, Spectral Technologies, and Predictive Models" Eng 7, no. 4: 174. https://doi.org/10.3390/eng7040174

APA Style

Iijima, S., Utsumi, T., Ikeda, R., Ishitsuka, N., Noro, T., Suzuki, Y., Sugizaki, Y., Somoto, T., Oka, R., Endo, T., Kamiya, N., & Suzuki, H. (2026). Imaging Engineering and Artificial Intelligence in Urinary Stone Disease: Low-Dose Computed Tomography, Spectral Technologies, and Predictive Models. Eng, 7(4), 174. https://doi.org/10.3390/eng7040174

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