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A hybrid ML-PBPK digital twin framework for clinically interpretable readmission risk and drug exposure
Nihaal Ahmed K1, Jafar Ali Ibrahim Syed Masood2
1School of Computer Science and Engineering, Vellore Institute of Technology, Vellore, Tamil Nadu, India.
Abstract:
The prediction of whether a diabetic patient will return to the hospital within 30 days is a very difficult clinical situation to navigate. Predicting the chance of a 30- day readmission depends on a wide range of patient-specific risk factors and the variability in how individual patients respond to medication prescribed for them. Traditional machine-learning models are capable of finding patterns in electronic medical records but are typically unable to provide a clear picture of the physiological interactions between the patient and their prescribed drug(s). One way to predict the likelihood of diabetes-related rehospitalization is using a combination of machine-learning risk factors and physiologically based pharmacokinetics (PBPK). An optimized version of the XG Boost machine-learning algorithm was trained on a large in-patient dataset (approximately 100,000 patient encounters) and achieved a predictive model with an area under the receiver operating characteristic curve (AUC) of 0.68 with a recall of 0.60 at clinically meaningful cut-offs. These findings are similar to what has been previously reported in the literature (0.60-0.70) for diabetes-related rehospitalization risk and support the utility of the XG Boost algorithm as a reliable clinical screening tool. Concurrently, multiple PBPK simulations were run to assess the effects chronic renal or hepatic impairments have on PBPK; results show renal impairment results in the highest systemic drug exposures. Predictive risk and simulated exposure will be integrated to yield a patient-specific risk/exposure phenotype and enable clinically meaningful stratification into actionable subgroups. Through this new method, it becomes possible to discern pharmacological vs. non-pharmacological contributors to readmission risk, thus facilitating targeted intervention strategies such as dose modulation, enhanced monitoring, and coordinated care. This work's value lies not in improving prediction accuracy by just a few points, but rather in a new approach to converting static risk prediction into a clinically actionable decision support system based on physiology. The proposed Digital Twin framework offers a scalable path to personalized post-discharge patient management and provides the basis for furthering the implementation of precision medicine in the field of digital health.
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