# Prediction of adherence to treatment with statins and anti-platelet drugs in first-year post-stroke patients: Validation of beta-regression models

**Authors:** Elias Edward Tannous, Shlomo Vinker, David Stepensky, Eyal Schwarzberg, Yee Gary Ang, Yee Gary Ang, Yee Gary Ang, Yee Gary Ang, Yee Gary Ang

PMC · DOI: 10.1371/journal.pone.0345936 · PLOS One · 2026-03-26

## TL;DR

This study validates models that predict long-term medication adherence in post-stroke patients using early adherence data.

## Contribution

The novelty lies in validating beta-regression models for predicting statin and antiplatelet adherence using 90-day data in post-stroke patients.

## Key findings

- The statin model had an R² of 0.67 and a calibration slope of 1.06.
- The antiplatelet model had an R² of 0.56 and a calibration slope of 0.96.
- The models can identify high-risk patients early for targeted interventions.

## Abstract

Stroke is the third most common cause of disability and the second most common cause of death worldwide. Greater levels of medication adherence after stroke or transient ischemic attack are associated with improved survival. Very few medication adherence prediction models are available and have not been validated using external data. The current study aimed to evaluate the predictive performance of previously published beta regression models for statin and antiplatelet adherence at 1 year in patients’ post-stroke or transient ischemic attack. The models use the first 90-day adherence data as a single predictor for 1-year adherence. Adherence was measured using the Proportion of Days Covered (PDC), which utilized prescription-filling data. Model performance was assessed using the following metrics: R² (proportion of variance explained), the difference between the mean observed and the mean predicted PDC, and the calibration slope, which ideally should be one. 2369 were included in the statin cohort, and 2147 patients were included in the antiplatelet cohort. R2 was 0.67 and 0.56 for statin and antiplatelet models, respectively. The difference between the mean observed and the mean predicted PDC was −3.7% and −2.5% for statin and antiplatelet models, respectively. The calibration slopes were 1.06 and 0.96 for the statin and antiplatelet models, respectively. The model performed well on a new patient population comprised of post-stroke patients and may be used for early identification of patients at high risk for low 1-year adherence within 90 days post-stroke, enabling timely, targeted adherence-support interventions.

## Linked entities

- **Diseases:** stroke (MONDO:0005098), transient ischemic attack (MONDO:0005264)

## Full-text entities

- **Genes:** PDC (phosducin) [NCBI Gene 5132] {aka MEKA, PHD, PhLOP, PhLP}
- **Diseases:** post-MI (MESH:D006342), intracerebral hemorrhage (MESH:D002543), depression (MESH:D003866), ACADEMIC EDITOR (MESH:D007859), death (MESH:D003643), Stroke (MESH:D020521), bleeding (MESH:D006470), post (MESH:D000094025), ischemic stroke (MESH:D002544), TIA (MESH:D002546), Atrial Fibrillation (MESH:D001281), MI (MESH:D009203)
- **Chemicals:** atorvastatin (MESH:D000069059), MPH (MESH:C041626), P2Y12 (-), -D (MESH:D003903), rosuvastatin (MESH:D000068718), lipid (MESH:D008055), Aspirin (MESH:D001241), clopidogrel (MESH:D000077144)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13020832/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC13020832/full.md

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Source: https://tomesphere.com/paper/PMC13020832