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arXiv 最近完成扫描:2026-11-15 06:43 · 全站最近入库:2026-11-14 15:09各信源进度 →

统计口径与数据新鲜度

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新论文 · v1arXiv:2611.12385

Clinical predictions using artificial intelligence in neurosurgery and its subspecialties: a systematic review and meta-analysis

Prajwal Ghimire, Aswin Chari, Jonathan Shapey, Keyoumars Ashkan

原文摘要

Artificial intelligence models for clinical prediction are proliferating across neurosurgery, but their aggregate discriminative performance, distribution along the care pathway and methodological quality are unclear. We systematically reviewed and meta-analysed these studies in neurosurgery and its subspecialities along with their risk of bias appraisal. We performed a PRISMA search for peer-reviewed original studies using AI to predict a clinical outcome in neurosurgical populations. Metrics were pooled using random effects modelling. Each study was classified as diagnostic, prognostic or forecasting and was assigned an evidence level. Clinical prediction task sub-stratification analysis was performed. Risk-of-bias was assessed using PROBAST. 1063 studies were included. Across 451 studies reporting AUC, pooled discrimination was 0.86, ranging from 0.84 (spine) to 0.87 (neuro-oncology), with extreme heterogeneity. Performance varied by clinical pathway stage, highest for diagnosis, grading and molecular tasks and lowest for post-operative tasks. Only 51 studies were using prospective data with external validation, whereas 619 rested on internal validation alone or no validation. 89 percent studies were at high risk-of-bias, driven by the analysis domain. AI models report high performance across all the neurosurgical subspecialities, concordant across AUC, accuracy, sensitivity and specificity and robust to risk-of-bias stratification. Performance is highest for imaging-anchored diagnostic tasks and lowest at decision-facing post-operative stage. However, the literature is dominated by optimism-prone, internally-validated and poorly calibrated models with extreme heterogeneity. External validation, calibration analysis and reporting guidelines adherence remain prerequisites for clinical adoption.

q-bio.TO · cs.AI

版本更新 · v4arXiv:2610.05900

Sub-Voxel Displacement and Ipsilateral Territory Decoupling for 3D Bilateral Coronary Artery Tree Reconstruction in Cardiac CT Angiography

Zeyu Jia, Xin Ming

原文摘要

Reconstructing topologically complete, sub-voxel-accurate 3D bilateral coronary artery trees from cardiac CT angiography (CCTA) requires simultaneously recovering continuous centerline trajectories and separating dense left/right coronary territories without cross-ostial collisions. We present a five-stage tubular drift and ipsilateral territory decoupling framework (M1-M5). Stage M1 pairs a 398,843-parameter multi-scale 3D pyramid encoder with a four-head tubular field network predicting vesselness probability, signed tubular boundary distance, unit tangent vectors, and continuous 3D centripetal displacement vectors. Stage M2 introduces recall-preserving multi-task optimization with 7-group AdamW parameter decoupling, L2-SP backbone regularization, and per-step anchor shrinkage. Stage M3 calibrates cylindrical Valsalva-sinotubular-junction wall coordinates and native-resolution orifice contact expectations for robust left and right ostial rooting. Stage M4 constructs a scalar-potential-weighted minimum-cost arborescence followed by normal-plane cross-sectional pullback and centripetal trajectory pruning. Stage M5 enforces coverage-guarded ipsilateral-field-coupled bilateral collision reduction and subtree handover. Across a 14-case held-out development cohort (Dev-14, 17-arm forward incremental build and 9-arm leave-one-out ablation) and an independent 50-case out-of-sample evaluation cohort (OOS-50) benchmarked against seven external architectures (nnU-Net, 3D UX-Net, Swin-UNETR, MedNeXt, CS2-Net, clDice-UNet, and Point-UNet), M1-M5 reduces bilateral chamfer distance on Dev-14 from 3.4381 mm to 2.2759 mm and achieves 2.7671 mm on OOS-50 with 7.11% bilateral collision rate and 79.7% distal branch completeness.

cs.CV · q-bio.TO

版本更新 · v2arXiv:2506.09661

A Cytology Dataset for Early Detection of Oral Squamous Cell Carcinoma

Garima Jain, Sanghamitra Pati, Mona Duggal, Amit Sethi, Abhijeet Patil, Gururaj Malekar, Nilesh Kowe, Jitender Kumar 等 37 位作者

原文摘要

Oral squamous cell carcinoma OSCC is a major global health burden, particularly in several regions across Asia, Africa, and South America, where it accounts for a significant proportion of cancer cases. Early detection dramatically improves outcomes, with stage I cancers achieving up to 90 percent survival. However, traditional diagnosis based on histopathology has limited accessibility in low-resource settings because it is invasive, resource-intensive, and reliant on expert pathologists. On the other hand, oral cytology of brush biopsy offers a minimally invasive and lower cost alternative, provided that the remaining challenges, inter observer variability and unavailability of expert pathologists can be addressed using artificial intelligence. Development and validation of robust AI solutions requires access to large, labeled, and multi-source datasets to train high capacity models that generalize across domain shifts. We introduce the first large and multicenter oral cytology dataset, comprising annotated slides stained with Papanicolaou(PAP) and May-Grunwald-Giemsa(MGG) protocols, collected from ten tertiary medical centers in India. The dataset is labeled and annotated by expert pathologists for cellular anomaly classification and detection, is designed to advance AI driven diagnostic methods. By filling the gap in publicly available oral cytology datasets, this resource aims to enhance automated detection, reduce diagnostic errors, and improve early OSCC diagnosis in resource-constrained settings, ultimately contributing to reduced mortality and better patient outcomes worldwide.

eess.IV · cs.CV · q-bio.TO

新论文 · v1arXiv:2610.34645

Regional prediction of hematoma expansion from non-contrast computed tomography in spontaneous intracerebral hemorrhage patients

Natasha Ironside, Hongyu Kan, Kristofor Pas, Mohammad Shifat-E-Rabbi, Benjamin Newman, Shinjini Kundu, Kareem El Naamani, Tanvir Rizvi 等 20 位作者

原文摘要

Background The combination of hematoma location, expansion and final volume influence neurological outcome. The aim of this study was to derive and validate a quantitative and interpretable region-based NCCT image feature model for predicting hematoma expansion. Methods The Ethnic/Racial Variations of Intracerebral Hemorrhage(ERICH) study was used for derivation and the Virtual International Trials in Stroke Archive(VISTA) was used for validation. NCCT images at presentation and 24+/-6hours were pre-processed, segmented and categorized into lobar, basal ganglia or thalamic regions. Hematoma expansion was defined by region and according to its effect on clinical outcome. Transport-based morphometry (TBM) produced a unique transport-based representation from each NCCT hematoma image. Linear classifiers applied to transport representations were used to derive a predictive model. The regional TBM model's performance was compared to alternate methods using AUROC analyses. Results The derivation dataset included 574 patients, comprising 162 lobar, 257 basal ganglia and 155 thalamic hematomas. The validation dataset included 196 patients, comprising 31 lobar, 119 basal ganglia and 46 thalamic hematomas. A combined regional model predicted hematoma expansion in the validation dataset with an AUROC of 0.787. The principal image features which varied by location were size, heterogeneity, eccentricity and density distribution towards the hematoma periphery. The regional TBM model outperformed alternative clinician based and machine-learning methods. Conclusions TBM discriminated and visualized regional features of hematoma expansion from presentation NCCT scans. This provides preliminary evidence for regional radiographic features of hematoma expansion. It has the potential to improve hematoma expansion prediction and understanding of hematoma expansion pathophysiology.

cs.CV · q-bio.TO