Related Experiment Video
Updated: Aug 21, 2026

Augmenting Large Language Models via Vector Embeddings to Improve Domain-Specific Responsiveness
Published on: December 6, 2024
Sequential vancomycin trough and dosing interval prediction in ICU patients using general purpose large language
Azfar Athar Ishaqui1, Tauqeer Hussain Malhi2, Emad Ali Alsaleh3
1Department of Clinical Pharmacy, College of Pharmacy, King Khalid University, Abha, Saudi Arabia.
Background And Objectives:
Vancomycin monitoring remains challenging due to fluctuating renal function and ICU physiology. This study compares ChatGPT and Grok for predicting sequential vancomycin trough levels and dosing intervals across varying renal function.
Research Design And Methods:
This retrospective study used deidentified MIMIC-IV ICU data. Admissions with three sequential vancomycin troughs and complete dosing history were included (239 admissions, 717 predictions: T1-T3). Structured clinical snapshots were submitted to both models to predict trough concentrations (mg/L) and dosing intervals (hours). Performance was assessed using MAE, RMSE, bias, ±2 mg/L and ±2-hour accuracy, sequence success, and generalized estimating equations.
Results:
ChatGPT outperformed Grok in trough prediction (MAE 4.07 vs 5.08 mg/L; RMSE 5.55 vs 7.53 mg/L; ±2 mg/L accuracy 37.0% vs 29.0%), with greater advantage at T1/T2 and in renal dysfunction. Grok was superior for interval prediction (MAE 1.36 vs 1.61 hours; RMSE 2.09 vs 2.98 hours). ChatGPT achieved more successful trough sequences (≥2/3 within ±2 mg/L: 35.1% vs 23.0%), while Grok had more accurate interval sequences (all 3 within ±2 hours: 67.8% vs 59.8%).
Conclusions:
These findings represent comparative model benchmarking and require validation against pharmacist-led therapeutic drug monitoring and Bayesian AUC-guided dosing platforms before clinical use.
Related Concept Videos
One-Compartment Open Model for IV Bolus Administration: Estimation of Clearance
In the one-compartment open model for intravenous (IV) bolus administration, clearance is estimated by dividing the elimination rate by the plasma drug concentration. This equation leverages the elimination rate constant and the apparent...
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations