arXiv subjects

Daniel Rueckert

Publications and source records attributed to Daniel Rueckert.

At least 19 recordsLinked to original sources

arXiv2026

MIMIC-Note-Extract: A Large-Scale Structured Dataset Extracted from MIMIC-IV-Note Discharge Summaries

MIMIC is one of the most widely used public hospital datasets for machine learning on electronic health records, yet clinically important information, such as past medical history, allergies, and diagnostic findings, remains confined to free-text discharge summaries. Studies requiring this information must therefore build their own extraction pipelines, duplicating substantial effort across projects. We release MIMIC-Note-Extract (MNE), a large-scale dataset that uses a hybrid extraction pipeline combining deterministic parsing with schema-guided large language model generation to transform 16 sections from 300,720 discharge summaries into structured tables. MNE adds information that has no structured MIMIC counterpart and enriches related tables with broader coverage and greater clinical detail, including 10 times more patient-history entries and medication histories for more than twice as many admissions. Validation by medical doctors confirms extraction accuracy above 92% across sections. Using MNE, we construct a clinical decision-making benchmark for LLM agents, demonstrating how reusable structured representations of clinical narratives reduce data curation effort.

cs.CL↗

arXiv2026

VERIDAH: Solving Enumeration Anomaly Aware Vertebra Labeling across Imaging Sequences

The human spine commonly consists of seven cervical, twelve thoracic, and five lumbar vertebrae. However, enumeration anomalies may result in individuals having eleven or thirteen thoracic vertebrae and four or six lumbar vertebrae. Although the identification of enumeration anomalies has potential clinical implications for chronic back pain and operation planning, the thoracolumbar junction is often poorly assessed and rarely described in clinical reports. Additionally, even though multiple deep-learning-based vertebra labeling algorithms exist, there is a lack of methods to automatically label enumeration anomalies. Our work closes that gap by introducing "Vertebra Identification with Anomaly Handling" (VERIDAH), a novel vertebra labeling algorithm based on multiple classification heads combined with a weighted vertebra sequence prediction algorithm. We show that our approach surpasses existing models on T2w TSE sagittal (98.30% vs. 94.24% of subjects with all vertebrae correctly labeled, p < 0.001) and CT imaging (99.18% vs. 77.26% of subjects with all vertebrae correctly labeled, p < 0.001) and works in arbitrary field-of-view images. VERIDAH correctly labeled the presence 2 Möller et al. of thoracic enumeration anomalies in 87.80% and 96.30% of T2w and CT images, respectively, and lumbar enumeration anomalies in 94.48% and 97.22% for T2w and CT, respectively. Our code and models are available at: https://github.com/Hendrik-code/spineps.

cs.CV↗

arXiv2026

How Much Is One Recurrence Worth? Iso-Depth Scaling Laws for Looped Language Models

We measure how much one recurrence is worth to a looped transformer in equivalent unique parameters. From an iso-depth pretraining sweep across recurrence counts $r \in \{1, 2, 4, 8\}$ spanning ${\sim}50\times$ in training compute, we fit a joint scaling law $L = E + A\,(N_\text{once} + r^φ N_\text{rec})^{-α} + B\,D^{-β}$ and measure a recurrence-equivalence exponent $φ= 0.46$. Intuitively, $φ$ tells us whether looping a block $r$ times is equivalent in validation loss to $r$ unique blocks of a non-looped model (full equivalence, $φ{=}1$) or to a single block run repeatedly with no capacity gain ($φ{=}0$). Our $φ= 0.46$ sits in between, so replacing unique blocks with shared recurrences increases validation loss at matched training compute. For example, at $r{=}4$ a 410M looped model performs on par with a 580M non-looped model, but incurs the training cost of a 1B non-looped one. We demonstrate the utility of $φ$ as a diagnostic tool on two case studies: commonly used truncated backpropagation lowers $φ$ to $0.38$, indicating that the loop mechanism is poorly trained under truncation, even though validation loss decreases. Conversely, hyperconnections raise $φ$ to $0.65$, a genuine capacity gain. Our method separates true loop improvements from training-side gains, a distinction raw validation loss cannot make. Code is available at https://github.com/kschwethelm/looped-lm-scaling.

cs.LG↗

arXiv2026

The Predictability Bias of Joint-Embedding Predictive Learning in Medical Imaging

Joint-embedding predictive architectures (JEPAs) learn by predicting teacher representations of masked regions from visible context. Point prediction summarizes the conditional target distribution and cannot reproduce variation that the context does not resolve. We call this constraint predictability bias. In computed tomography (CT), recurrent anatomy is predictable from context, whereas the sporadic, localized pathology that determines clinical interpretation often is not. We introduce TAP-JEPA, a ViT-B/3D trained on 113,611 CT volumes that is competitive with state-of-the-art encoders (COLIPRI, Merlin, VoxelFM) in scan-level classification. We then audit the learned predictive pathway by replaying the exact masking, teacher, and predictor computations used during training. Prediction lowers the mean Skill (prevalence-normalized average precision) from 0.388 to 0.271 for pathology, but only from 0.921 to 0.873 for anatomy. Along the teacher direction, separating pathology from matched control regions in the same organ, prediction moves pathology 34.7% toward the controls and controls 13.6% toward pathology, with larger shifts farther from visible context. Replacing visible matched-control representations increases surrounding-target prediction loss more than fully replacing pathology representations across four pathology categories. Downstream, removing all final-layer pathology tokens reduces the decision margin by at most 0.45% in four of seven scan-level probes. Together, these results show that contextual predictability is not a sufficient proxy for clinical relevance in medical representation learning. Training objectives should therefore retain diagnostic features regardless of their predictability from surrounding anatomy.

eess.IV↗

arXiv2026

EchoTab: Learning Measurement-Grounded Representations for Echocardiographic Diagnosis through Tabular Reconstruction

Diagnostic information in multi-view medical imaging studies, like echocardiography, is distributed across views, each capturing different aspects of cardiac structure and function. In clinical practice, these views are first interpreted through quantitative measurements, which then support specific diagnoses. However, existing echo representation learning methods do not explicitly model measurements as an intermediate representation between views and diagnosis. As a result, individual measurements are not explicitly represented in a form that downstream diagnostic tasks can selectively use, hindering accurate diagnosis. Inspired by this hierarchical clinical workflow, we introduce EchoTab, a measurement-grounded representation learning framework that represents multi-view echocardiography studies using measurement-specific tokens as an intermediate representation between echo views and diagnosis. Each measurement token selectively attends to the views relevant to its estimation and is trained through tabular reconstruction to predict the corresponding measurement value. The resulting tokens form a factorized echo representation, which encode clinically meaningful structural and functional properties and can be selectively used for downstream diagnosis. Unlike the commonly used contrastive approaches, EchoTab does not require negative samples or large batch sizes. Experiments on two datasets demonstrate that EchoTab learns effective measurement-grounded representations that improve diagnosis classification in multi-view echocardiography and its learned attention aligns with established measurement-view relationships used by cardiologists. Our code is accessible at https://github.com/michelleespranita/EchoTab.

cs.LG↗

arXiv2026

Stochastic Siamese MAE Pretraining for Longitudinal Medical Images

Temporally aware image representations are crucial for capturing disease progression in 3D volumes of longitudinal medical datasets. However, recent state-of-the-art self-supervised learning approaches like Masked Autoencoding (MAE), despite their strong representation learning capabilities, lack temporal awareness. In this paper, we propose STAMP (Stochastic Temporal Autoencoder with Masked Pretraining), a Siamese MAE framework that encodes temporal information through a stochastic process by conditioning on the time difference between the 2 input volumes. Unlike deterministic Siamese approaches, which compare scans from different time points but fail to account for the inherent uncertainty in disease evolution, STAMP learns temporal dynamics stochastically by reframing the MAE reconstruction loss as a conditional variational inference objective. We evaluated STAMP on two OCT and one MRI datasets with multiple visits per patient. STAMP pretrained ViT models outperformed both existing temporal MAE methods and foundation models on different late stage Age-Related Macular Degeneration and Alzheimer's Disease progression prediction which require models to learn the underlying non-deterministic temporal dynamics of the diseases.

cs.LG↗

arXiv2026

Sparse cubical complexes for efficient topology-preservation in image data

Persistent homology (PH) is a frequently used tool for extracting and preserving topological information from image data, particularly in image segmentation, where preservation of topological structures is important. However, despite its general applicability across dimensionality, domains, and target structures, the runtime cost of PH-based methods often makes their practical use infeasible. In this work, we argue that this runtime cost is largely driven by processing information that is unimportant for downstream application (e.g. as optimization objective). We propose sparse cubical filtrations as an alternative foundation for PH computation, reducing subsequent computational costs by factors of up to 100 on real datasets. We show close agreement with the optimization signal of the dense counterpart and empirically evaluate our solution's effectiveness as an optimization objective in realistic training regimes where other PH-based objectives can practically not operate (i.e., 3D data with large patch sizes). We show how our solution improves topological accuracy by up to 80\% across six diverse datasets while maintaining pixel- and region-based accuracy.

cs.CV↗

arXiv2026

Depth-adaptive Inference of Looped Language Models via Continuous Depth Batching

A main promise of looped language models is depth-adaptive inference. By looping a block of shared layers a variable number of times, the model can use less compute for "easy" tokens and more for "hard" ones. However, tokens with different numbers of loops cannot share a uniform forward pass and therefore cannot be handled by standard batching systems such as vLLM. The practical value of depth-adaptive inference thus hinges on whether batching can be made efficient. We introduce the first efficient method for depth-adaptive looped LMs via continuous depth batching (CDB), which forms new batches between loop steps. Our method dynamically schedules looped and non-looped parts of the architecture, manages looped KV-caching, and predicts which tokens will exit the loop in advance so it can prepare batches asynchronously. Experiments on Ouro 1.4B and Huginn 3.5B show that fully looped architectures are best suited to depth-adaptive inference, as large non-looped layers outside the recurrent core (e.g., token embedding, LM head, and unshared transformer blocks) slow down and complicate scheduling. Overall, CDB realizes up to 99% of the estimated maximum speedup available, leaving further gains primarily dependent on model architecture and exit behavior.

cs.LG↗

arXiv2026

What Makes a Good Medical Image Tokenizer? Rethinking Reconstruction and Generation in Medical Image Tokenization

Latent diffusion models now dominate medical image generation, and every such pipeline rests on a \emph{tokenizer} that compresses images into the latent codes for image generation to operate on. Thereby, the tokenizer choice bounds every downstream task from reconstruction fidelity and generation quality to the representations available for downstream analysis. Yet, medical imaging pipelines routinely utilize tokenizers from natural imaging on the hypothesis that their behavior carries over. However, this is an assumption never tested in the medical imaging regime, where datasets are orders of magnitude smaller and images exhibit far lower inter-sample variance. We present a systematic evaluation of medical image tokenizers evaluating thirty configurations across ten model families on twelve datasets at three compression factors, spanning reconstruction, generation, latent geometry, downstream classification, and memorization. We find that (1) performance on image reconstruction and generation strongly correlate, unlike prior reports on natural images; (2) modern tokenizers use nearly all of their codebook entries, but still leave most of the latent space unused; (3) training-set memorization is mild and is further suppressed by stronger latent space compression; and (4) discrete quantization can largely preserve downstream classification, with lookup-free schemes being the main exception.

cs.CV↗

arXiv2026

Interpretable Retinal Disease Prediction Using Biology-Informed Heterogeneous Graph Representations

Interpretability is crucial for utilizing machine learning models as clinical decision support tools for medical diagnostics. However, most state-of-the-art image classifiers based on neural networks are not interpretable. As a result, clinicians often resort to known biomarkers to guide diagnosis, although biomarker-based classification often suffers from drastic information loss compared to raw medical images. This work proposes a method that preserves the rich imaging information while simultaneously enhancing the interpretability of predictions for diabetic retinopathy staging from optical coherence tomography angiography (OCTA) images. The core contribution of our method is a novel biology-informed heterogeneous graph representation that models retinal vessel segments, intercapillary areas, and the foveal avascular zone (FAZ) in a human-interpretable way. This graph representation allows us to frame diabetic retinopathy staging as a graph-level classification task, which we solve using an established, efficient graph neural network architecture. We compare our method against established methods, including classical biomarker-based classifiers, convolutional neural networks (CNNs), and vision transformers in predicting the clinically assigned DR stage based on color fundus photography images. We find stage agreement rates of our method and alternative vision model based classifiers saturating at AUC-ROC values of 84%. Crucially, we use our biology-informed graph to provide explanations of great detail. Our approach surpasses existing methods in precisely localizing and identifying abnormal vessels and non-perfusion areas. Our approach sets the stage for the interpretable identification of patients who require special attention due to their traceable microvascular changes, only observable using the details of OCTA images.

cs.CV↗

arXiv2026

Temporally Consistent Graph Extraction and Matching for Longitudinal Angiographic Images

Recent advances in angiographic imaging have enabled longitudinal visualization of the microvasculature. Image processing pipelines based on vessel graphs are able to resolve subtle temporal changes at the level of individual blood vessels. However, current strategies for graph extraction, refinement, and matching are highly sensitive, with even minuscule differences in the underlying segmentation map resulting in substantially different vessel graphs. These artifacts severely inhibit the ability to accurately match sequential vessel graphs of the same subject over time. To address this problem, we propose a strategy that matches graphs before jointly refining them. Specifically, we perform an early matching after basic graph extraction before removing spurious bulges and merging junctions in both graphs using joint information. In experiments with complex retinal vessel graphs, we demonstrate that this strategy results in a higher matched area without graph fragmentation compared to separate or no refinement, respectively.

cs.CV↗

arXiv2026

Memorisation bias in medical AI

Medical AI models hold immense potential to improve patient outcomes, but they are also known to unintentionally memorise individual records from their training datasets. While such memorisation has been linked to targeted privacy attacks, its consequences for clinical deployment, where patients may be assessed by a model that saw their historical data during training, remain poorly understood. Here we show that predictions on a patient's unseen future data can change significantly if a model observed that same patient's anonymised historical data during training, a phenomenon we term "memorisation bias". We demonstrate that this bias exists across diverse data modalities and model architectures, and over prolonged time spans: in some cases, memorisation bias persists on future records acquired decades after the historical records used for training. Moreover, in simulated prospective deployment, memorisation bias has asymmetric effects on the diagnostic accuracy of returning data contributors. When a patient returned with a de novo condition absent from their historical records in the training dataset, diagnostic sensitivity decreased significantly compared to an otherwise identical model not trained on their historical data. Conversely, when their health state was unchanged, both sensitivity and specificity were significantly inflated. Our findings reveal a previously uncharacterised risk in medical AI that arises when a model is deployed on patients who contributed to its training data. This exposes a shortcoming of current model development practice: the de-identification measures designed to protect patients' privacy make it difficult to identify returning contributors and exclude them from the AI-assisted interpretation of their own future data. Mitigating memorisation risks may thus require changes to current model training and deployment protocols.

cs.LG↗

arXiv2026

PRIME-SVR: Physics-infoRmed Implicit Multi-Echo Slice-to-Volume Reconstruction for Fetal T2 mapping

Slice-to-volume reconstruction (SVR) is the standard method for obtaining high-resolution (HR) 3D fetal brain volumes from motion-corrupted 2D MRI slice stacks acquired in multiple orientations. Existing SVR methods are optimized and validated only for clinical-range echo times (TEs), limiting their use at non-clinical TEs and making them incompatible with quantitative T2 mapping, a protocol- and center-independent biomarker of fetal brain maturation requiring HR reconstructions across multiple TEs. We present PRIME-SVR, the first implicit neural representation (INR) framework for joint HR reconstruction from multi-echo MRI. A single fully connected network models a continuous function from spatial coordinates to signal intensities across TEs, while a second network estimates slice-specific acquisition degradations. Cross-TE coherence is enforced via a Bloch equation-derived regularization penalizing deviations from expected T2 decay, with adaptive weighting that strengthens coupling for degraded stacks. The method is fully self-supervised. We validate PRIME-SVR on 39 in vivo fetal acquisitions (13 subjects x 3 TEs) from two centers, two vendors, and two field strengths (1.5 T and 0.55 T). Compared to state-of-the-art SVR, PRIME-SVR improves reconstruction sharpness by 47%, anatomical accuracy by 30%, and cross-TE structural consistency by 14%. It enables reconstruction at late TEs previously inaccessible to SVR, yielding the first 0.8 mm isotropic T2 maps at 0.55 T and the first T2 maps derived from INR-based SVR. PRIME-SVR also accelerates quantitative imaging by reducing the data needed for multi-TE reconstruction, cutting acquisition from 15 to 10 minutes while keeping T2 accuracy within 1.7% in white and deep gray matter, or to 5 minutes with a mean T2 error of 2.3% for high-quality acquisitions.

physics.med-ph↗

arXiv2026

NOAH: Learning the Full Patient Journey. A Longitudinal Multimodal Time-Aware Model for Representation and Forecasting

The digitization of healthcare has generated vast, longitudinal, and multimodal patient records over a lifetime, yet fully exploiting these data to represent and predict patient state trajectories remains a critical challenge. Current AI models often struggle to capture the complex, irregular temporal dynamics and inherent stochasticity of real-world multimodal patient data. Existing AI approaches for modeling longitudinal patient records are predominantly discriminative, limited to a few modalities, constrained by closed categorical vocabularies, treating time as a monotonic inductive bias, or they are limited in forecasting future patient states. We introduce NOAH, a time-aware, task-agnostic, generative transformer model representing and forecasting the full multimodal patient journey. NOAH features a novel bidirectional time integration and a variational latent space to capture the continuous evolution of patient states and the stochasticity of clinical trajectories. Built from over 559 million clinical events from 431,000 hospital visits of 299,000 patients across the MIMIC dataset family, NOAH natively processes medical images, time-series and numeric signals, categorical events, as well as structured and unstructured clinical records. NOAH is the first truly holistic generative model in its field, enabling autoregressive forecasting with optional time control, zero-shot classification, and counterfactual intervention simulation. It generates highly informative and predictive patient state representations that demonstrate strong performance in probing for clinical outcomes, 15 ICD chapters, and 29 comorbidities, as well as in time-to-event prediction. Seamlessly handling diverse modalities and complex temporal dynamics, NOAH provides a versatile, task-agnostic, scalable foundation for intelligent predictive systems in personalized clinical care and digital medicine.

cs.LG↗

arXiv2026

Agentic Large Language Models for Training-Free Neuro-Radiological Image Analysis

State-of-the-art large language models (LLMs) show high performance in general visual question answering. However, a fundamental limitation remains: current architectures lack the native 3D spatial reasoning required to directly analyze volumetric medical imaging, such as CT or MRI. Emerging agentic AI offers a new solution, eliminating the need for intrinsic 3D processing by enabling LLMs to orchestrate and leverage specialized external tools. Yet, the feasibility of such agentic frameworks in complex, multi-step radiological workflows remains underexplored. In this work, we present a training-free agentic pipeline for automated brain MRI analysis. Validating our methodology on several LLMs (GPT-5.4, Gemini 3.1 Pro, Claude Sonnet 4.6) with off-the-shelf domain-specific tools, our system autonomously executes complex end-to-end workflows, including preprocessing (skull stripping, registration), pathology segmentation (glioma, meningioma, metastases), and volumetric reasoning. We evaluate our framework across increasingly complex radiological tasks, from single-scan tumor and anatomy analysis to longitudinal response assessment requiring multi-timepoint comparisons. We analyze the impact of architectural design by comparing single-agent models against multi-agent "domain-expert" collaborations. To support rigorous evaluation of future agentic systems, we release a benchmark dataset of image-prompt-answer tuples derived from public data. Our results demonstrate that agentic AI can solve highly neuro-radiological image analysis tasks through tool use without the need for training or fine-tuning.

cs.CV↗

arXiv2026

CMRVision: A Foundation Model for Cardiac MR Image Analysis

Cardiac magnetic resonance (CMR) imaging provides complementary information on cardiac anatomy, function, and tissue characterization across multiple sequences and views. In this work, we investigate foundation model pretraining for 2D CMR and introduce CMRVision, a CMR-specific foundation model trained using DINOv3-style self-supervised learning on a multi-center, multi-sequence cohort of 36 million CMR images. We systematically evaluate architectural and training design choices for domain-specific pretraining. CMRVision is evaluated on two downstream tasks: multi-task segmentation across cine, late gadolinium enhancement (LGE), and mapping sequences, and cine view classification. Our experiments show that CMR-specific pretraining, smaller patch sizes, and patch-level objectives consistently improve downstream performance. Across a multi-task segmentation benchmark, CMRVision achieved the strongest overall performance, outperforming prior natural-image (NI), medical-image, supervised, and CMR foundation model baselines. Improvements were modest but consistent across structures and sequences, with Dice scores ranging from 0.940-0.967 for LV and 0.855-0.905 for myocardium, and reaching 0.929 for RV, 0.920 for LA, and 0.931 for RA. The largest gains were observed for myocardium segmentation in LGE and mapping images. In a zero-shot segmentation task on unseen LGE long-axis views, the model achieved an average Dice score of 0.692, demonstrating cross-view generalization. For cine view classification, CMRVision achieved the highest average accuracy (0.906), compared to prior methods reported in the literature. These results highlight the potential of CMRVision to support robust and generalizable cardiac MRI analysis across multiple sequences and views.

cs.CV↗

arXiv2026

Are LLMs Ready to Assist Physicians? PhysAssistBench for Interactive Doctor-Patient-EHR Assistance

The most plausible near-term role of medical LLMs is to assist rather than replace physicians, yet current evaluations often test isolated capabilities: clinical knowledge, EHR system interaction, or patient communication. Physician assistance instead requires coordinating these capabilities within the same interaction, where physicians issue underspecified requests, patients describe symptoms ambiguously, and EHR systems demand precise tool use. We introduce PhysAssistBench, a benchmark for interactive doctor-patient-EHR assistance. Built from real MIMIC-IV cases, PhysAssistBench uses a scalable pipeline to construct agentic patients: interactive, record-grounded agents that turn static EHR records into multi-turn clinical scenarios while preserving clinical factuality. PhysAssistBench provides a curated bilingual evaluation set of 1,296 manually reviewed and physician-validated turns. Experiments with leading LLMs show that current models remain unreliable in this setting, which exposes a key bottleneck for clinical LLMs: reliable assistance requires coordination across knowledge, communication, and systems, not isolated gains in any of them.

cs.CL↗

arXiv2026

MR-JEPA: A General Purpose Video Foundation Model for Cardiac MRI

Cardiac magnetic resonance imaging (CMR) produces rich sequential data such as temporal cine videos and spatial LGE/mapping stacks, yet most deep learning approaches process individual 2D slices, discarding this context. We present MR-JEPA, a self-supervised video foundation model for CMR that extends LeJEPA to 3D spatiotemporal inputs through tubelet tokenization, spatiotemporal masking augmentation, and initialization from a 2D CMR foundation model. Unlike prior CMR video models limited to cine data, MR-JEPA is pretrained on multi-sequence data (cine, LGE, mapping) from 10,505 patients across two centers without annotations. We evaluate the frozen encoder on six downstream tasks using a unified multi-view gated attention architecture: LV ejection fraction, RV ejection fraction, three myocardial strains (GLS, GCS, GRS), and four-class disease detection. MR-JEPA outperforms other compared methods on all five regression tasks, including both a domain-specific CMR model pretrained on more data with text supervision and a natural-video foundation model, achieving an LV EF MAE of 4.79% (r =0.764) and a GLS MAE of 1.87 (r=0.805), with 21-27% MAE reductions over baselines on strain tasks. For disease detection, MR-JEPA achieved a macro AUG of 0.868, remaining competitive with the domain-specific baseline despite using a fully self-supervised pretraining objective. These results demonstrate the potential of a unified video encoder for robust, multi-view utilization of diverse CMR sequences in clinical cardiac quantification and diagnosis.

cs.CV↗