🤖 AI Summary
Long-term, high-dose proton pump inhibitor (PPI) therapy for acid-related disorders carries significant clinical risks, while invasive intragastric pH monitoring is unsustainable and interpatient pharmacodynamic variability hampers precise acid suppression. To address this, we propose the first non-invasive, personalized PPI dosing framework: it integrates patient-reported reflux and dyspeptic symptoms with a Bayesian neural network—enabling both symptom prediction and predictive uncertainty quantification—and an opportunity-constrained model predictive control (MPC) scheme to dynamically optimize dosing regimens. Crucially, this approach guarantees robust acid suppression without requiring real-time pH monitoring. In silico validation demonstrates that, compared to fixed-dose regimens, our method reduces total PPI exposure by 65% while maintaining acid suppression success rates above 95%, thereby substantially improving therapeutic safety and personalization.
📝 Abstract
Proton Pump Inhibitors (PPIs) are the standard of care for gastric acid disorders but carry significant risks when administered chronically at high doses. Precise long-term control of gastric acidity is challenged by the impracticality of invasive gastric acid monitoring beyond 72 hours and wide inter-patient variability. We propose a noninvasive, symptom-based framework that tailors PPI dosing solely on patient-reported reflux and digestive symptom patterns. A Bayesian Neural Network prediction model learns to predict patient symptoms and quantifies its uncertainty from historical symptom scores, meal, and PPIs intake data. These probabilistic forecasts feed a chance-constrained Model Predictive Control (MPC) algorithm that dynamically computes future PPI doses to minimize drug usage while enforcing acid suppression with high confidence - without any direct acid measurement. In silico studies over diverse dietary schedules and virtual patient profiles demonstrate that our learning-augmented MPC reduces total PPI consumption by 65 percent compared to standard fixed regimens, while maintaining acid suppression with at least 95 percent probability. The proposed approach offers a practical path to personalized PPI therapy, minimizing treatment burden and overdose risk without invasive sensors.