Signal Fidelity Index-aware calibration for addressing distributional shift in predictive modeling across heterogeneous real-world data
Year: 2025
Type: article
Abstract: Machine learning models trained on real-world data (RWD) often experience performance degradation when deployed across different settings due to distributional shift. However, a fundamental but under-explored factor contributing to this degradation is the decay of diagnostic signals: systematic variability in diagnostic quality and consistency across institutional contexts, which affects the reliability of clinical codes used for model training and prediction. To develop and evaluate a Signal Fidelity Index (SFI) that quantifies diagnostic signal decay at the patient level across diverse clinical conditions, and to assess the effectiveness of SFI-aware calibration in improving model performance compared to established calibration methods, without requiring outcome labels in target domains after initial method development. We developed a comprehensive simulation framework using synthetic patient datasets across six clinically diverse phenotypes: dementia, geriatric bipolar disorder, fibromyalgia, adult ADHD, type 2 diabetes, and hypertension. Each phenotype included independent simulation batches with varying demographic compositions and data quality characteristics. The SFI was constructed from six components: diagnostic specificity, temporal consistency, entropy, contextual concordance, medication alignment, and trajectory stability. We implemented SFI-aware calibration using a multiplicative adjustment formula with phenotype-specific calibration parameters optimized through supervised parameter development, then evaluated performance in label-free deployment across heterogeneous testing datasets. We compared SFI-aware calibration against established baseline calibration methods. SFI-aware calibration significantly improved predictive performance against both uncalibrated predictions and all baseline methods across nearly all six phenotypes (Cohen's d = 0.603-5.002, [Formula: see text]). Performance improvements varied by phenotype complexity, with F1-score gains ranging from +4.2% for fibromyalgia to +34.9% for dementia, and AUC gains ranging from +4.7% to +40.1%. Traditional calibration methods often led to degraded performance, with isotonic regression exhibiting universal failure (AUC values degraded to 0.51-0.56 across all phenotypes) and Platt scaling demonstrating inconsistent, phenotype-dependent effects. Brier score decomposition revealed that SFI-aware calibration improved performance through a dual mechanism: reliability reductions ranging from 11% to 29% and resolution increases ranging from +35% to +238%. Notably, even well-diagnosed conditions with standardized diagnostic criteria (type 2 diabetes, hypertension) showed substantial benefits (+8.0% to +13.3% F1-score, +25.1% to +40.1% AUC), suggesting that diagnostic signal variability affects all EHR-based phenotyping. These findings demonstrate that diagnostic signal decay is a tractable problem that can be systematically addressed through patient-level fidelity-aware calibration strategies. SFI-aware calibration offers a practical approach for enhancing the performance of clinical prediction models across diverse healthcare contexts, requiring supervised parameter development once per phenotype, followed by label-free deployment to unlimited target populations. The method consistently outperforms established calibration techniques while avoiding their tendency to degrade performance, making it particularly suitable for large-scale administrative datasets where outcome labels are unavailable. Multi-phenotype validation confirms generalizability across clinical conditions ranging from complex, under-diagnosed phenotypes to well-diagnosed conditions with standardized criteria.
Source: Scientific Reports
Language: English
Subfield: Artificial Intelligence
Field: Computer Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $2,690
Awards: Susceptibility and adverse health outcomes related to climate-sensitive events among older Medicare beneficiaries with Alzheimer and Dementia, G625211643, The confluence of extreme heat and cold on aging and longevity, National Cohort Studies of Alzheimer's Disease, Related Dementias and Air Pollution, Temporal Phenotypes and Risk Models for the Post-COVID Syndrome and its sub-types
OpenAlex ID: W4417524264
