4.4 Article

A Risk Prediction Model for Long-term Prescription Opioid Use

期刊

MEDICAL CARE
卷 59, 期 12, 页码 1051-1058

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MLR.0000000000001651

关键词

Prescription Drug Monitoring Program; opioid-naive; long-term opioid use; risk prediction; dose trajectory; opioid analgesic

资金

  1. NIDA NIH HHS [R01 DA044282] Funding Source: Medline

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This study developed and validated a model to predict the risk of previously opioid-naive patients transitioning to long-term opioid use, showing high discrimination and calibration. The model has potential for integration into Prescription Drug Monitoring Programs to assist clinicians in opioid prescribing decisions.
Background: Tools are needed to aid clinicians in estimating their patients' risk of transitioning to long-term opioid use and to inform prescribing decisions. Objective: The objective of this study was to develop and validate a model that predicts previously opioid-naive patients' risk of transitioning to long-term use. Research Design: This was a statewide population-based prognostic study. Subjects: Opioid-naive (no prescriptions in previous 2 y) patients aged 12 years old and above who received a pill-form opioid analgesic in 2016-2018 and whose prescriptions were registered in the California Prescription Drug Monitoring Program (PDMP). Measures: A multiple logistic regression approach was used to construct a prediction model with long-term (ie, >90 d) opioid use as the outcome. Models were developed using 2016-2017 data and validated using 2018 data. Discrimination (c-statistic), calibration (calibration slope, intercept, and visual inspection of calibration plots), and clinical utility (decision curve analysis) were evaluated to assess performance. Results: Development and validation cohorts included 7,175,885 and 2,788,837 opioid-naive patients with outcome rates of 5.0% and 4.7%, respectively. The model showed high discrimination (c-statistic: 0.904 for development, 0.913 for validation), was well-calibrated after intercept adjustment (intercept, -0.006; 95% confidence interval, -0.016 to 0.004; slope, 1.049; 95% confidence interval, 1.045-1.053), and had a net benefit over a wide range of probability thresholds. Conclusions: A model for the transition from opioid-naive status to long-term use had high discrimination and was well-calibrated. Given its high predictive performance, this model shows promise for future integration into PDMPs to aid clinicians in formulating opioid prescribing decisions at the point of care.

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