Transparent methodology built on NCQA standards, published trial data, and validated ML models.
We measure adherence using Proportion of Days Covered (PDC), the NCQA-endorsed standard for medication adherence measurement.
A patient is considered adherent when PDC ≥ 80%, consistent with CMS quality measures. For GLP-1 specifically, we account for:
Our dropout risk model uses a gradient-boosted classifier (XGBoost) trained on patient features to predict 90-day discontinuation probability.
Validated via 5-fold cross-validation on historical data:
| Metric | Value |
|---|---|
| AUC-ROC | 0.92-0.99 |
| F1 Score | 0.88-0.96 |
| Precision | 0.85-0.95 |
| Recall | 0.80-0.94 |
| Category | Score Range | Recommended Action |
|---|---|---|
| Low | 0-30 | Standard monitoring |
| Medium | 31-60 | Automated refill reminder, flag for review |
| High | 61-100 | Outreach call within 48 hours, care coordinator referral |
Per-patient weight forecasting uses exponential smoothing with trend damping, calibrated against clinical trial trajectories.
Population-level forecasting aggregates individual trajectories with confidence intervals. Key adjustments:
Financial impact estimates are derived from published health economics literature:
| Component | Per-Patient Estimate | Source |
|---|---|---|
| Healthcare cost reduction | $280 per 1% body weight loss | Cawley et al., J Health Econ 2015 |
| Absenteeism reduction | $1,200/year per 10% loss | CDC Worksite Health ScoreCard |
| Disability claims | $2,400/year per 10% loss | Finkelstein et al., JOEM 2010 |
| Drug cost (GLP-1) | $12,000/year avg | GoodRx market data 2025 |
K-Means clustering identifies distinct patient response patterns across the population:
| Segment | Characteristics |
|---|---|
| Strong Responder | >15% weight loss, high adherence, consistent engagement |
| Moderate Responder | 5-15% weight loss, regular refills |
| Plateau | Initial weight loss followed by stagnation |
| At Risk | Declining engagement, widening refill gaps |
| Disengaged | Minimal observations, low adherence |
Segmentation enables targeted intervention strategies rather than one-size-fits-all approaches.
All clinical data undergoes validation before entering the analytics pipeline:
Program retention is modeled using Kaplan-Meier survival analysis with optional Cox Proportional Hazards for covariate adjustment.
This produces the retention curve shown on the dashboard, answering: "What percentage of patients remain active at day X?"
This methodology is reviewed by our clinical advisory board and updated quarterly. For questions or feedback, contact clinical@pathriva.com