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August Sigle

Publications and source records attributed to August Sigle.

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Typical Healthcare Pathways as a Basis for Admixture Modeling of Patient Trajectories

Background: Understanding whether patients follow similar or distinct patterns of care is important for characterizing clinical practice, identifying patient subgroups, and supporting quality improvement. However, routine healthcare trajectories are difficult to compare directly because patients may differ in their diagnostic workup, treatment sequencing, timing of clinical events, and documentation practices. Despite this variation, trajectories often contain recurring patterns at the cohort level. Methods: To address this challenge, we present a framework that explicitly separates cohort-level typical pathway identification from patient-level inference. At the cohort level, we derive an interpretable representation of care processes using a rule-based algorithm to identify typical healthcare pathways, resulting in a compact pathway graph. These pathways are then modeled as Markov chains and used as structured components in an admixture model, allowing each patient to be represented as a probabilistic mixture of typical pathways rather than being assigned to a single pathway component. The resulting admixture weights provide a compact representation of patient trajectories for subgroup characterization. We further assess the stability of the identified pathways and inferred admixture representations across multiple train-test splits. Results: Across train-test splits, the framework demonstrated consistent pathway structures and patient-level mixture patterns. Applied to routine care data from prostate cancer patients undergoing radical prostatectomy, the framework identified interpretable care patterns and supported the identification of patient subgroups with similar clinical event patterns. Conclusion: Overall, the proposed framework provides an interpretable and stable approach for summarizing treatment pathways and characterizing patient subgroups in real-world practice.

stat.ME

Similarity of competing risks models with constant intensities in an application to clinical healthcare pathways involving prostate cancer surgery

The recent availability of routine medical data, especially in a university-clinical context, may enable the discovery of typical healthcare pathways, i.e., typical temporal sequences of clinical interventions or hospital readmissions. However, such pathways are heterogeneous in a large provider such as a university hospital, and it is important to identify similar care pathways that can still be considered typical pathways. We understand the pathway as a temporal process with possible transitions from a single initial treatment state to hospital readmission of different types, which constitutes a competing risk setting. In this paper, we propose a multi-state model-based approach to uncover pathway similarity between two groups of individuals. We describe a new bootstrap procedure for testing the similarity of transition intensities from two competing risk models with constant transition intensities. In a large simulation study, we investigate the performance of our similarity approach with respect to different sample sizes and different similarity thresholds. The studies are motivated by an application from urological clinical routine and we show how the results can be transferred to the application example.

stat.ME

Convolutional neural network based deep-learning architecture for intraprostatic tumour contouring on PSMA PET images in patients with primary prostate cancer

Accurate delineation of the intraprostatic gross tumour volume (GTV) is a prerequisite for treatment approaches in patients with primary prostate cancer (PCa). Prostate-specific membrane antigen positron emission tomography (PSMA-PET) may outperform MRI in GTV detection. However, visual GTV delineation underlies interobserver heterogeneity and is time consuming. The aim of this study was to develop a convolutional neural network (CNN) for automated segmentation of intraprostatic tumour (GTV-CNN) in PSMA-PET. Methods: The CNN (3D U-Net) was trained on [68Ga]PSMA-PET images of 152 patients from two different institutions and the training labels were generated manually using a validated technique. The CNN was tested on two independent internal (cohort 1: [68Ga]PSMA-PET, n=18 and cohort 2: [18F]PSMA-PET, n=19) and one external (cohort 3: [68Ga]PSMA-PET, n=20) test-datasets. Accordance between manual contours and GTV-CNN was assessed with Dice-Sørensen coefficient (DSC). Sensitivity and specificity were calculated for the two internal test-datasets by using whole-mount histology. Results: Median DSCs for cohorts 1-3 were 0.84 (range: 0.32-0.95), 0.81 (range: 0.28-0.93) and 0.83 (range: 0.32-0.93), respectively. Sensitivities and specificities for GTV-CNN were comparable with manual expert contours: 0.98 and 0.76 (cohort 1) and 1 and 0.57 (cohort 2), respectively. Computation time was around 6 seconds for a standard dataset. Conclusion: The application of a CNN for automated contouring of intraprostatic GTV in [68Ga]PSMA- and [18F]PSMA-PET images resulted in a high concordance with expert contours and in high sensitivities and specificities in comparison with histology reference. This robust, accurate and fast technique may be implemented for treatment concepts in primary PCa. The trained model and the study's source code are available in an open source repository.

cs.CV