Appl Clin Inform 2025; 16(05): 1683-1694
DOI: 10.1055/a-2639-4974
Special Issue on CDS Failures

Learning from Misses: Evaluating a Clinical Decision Support for Chronic Pain Management in Primary Care

Authors

  • Olena Mazurenko

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
    2   Regenstrief Institute, Indianapolis, Indiana, United States
  • Nate C. Apathy

    2   Regenstrief Institute, Indianapolis, Indiana, United States
    3   School of Public Health, The University of Maryland, College Park, Maryland, United States
  • Lindsey M. Sanner

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
  • Emma McCord

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
  • Meredith C.B. Adams

    4   Department of Anesthesiology, Wake Forest University, Winston-Salem, North Carolina, United States
  • Robert W. Hurley

    4   Department of Anesthesiology, Wake Forest University, Winston-Salem, North Carolina, United States
  • Randall W. Grout

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
    2   Regenstrief Institute, Indianapolis, Indiana, United States
    5   Primary Care, Eskenazi Health, Indianapolis, Indiana, United States
  • Burke Mamlin

    2   Regenstrief Institute, Indianapolis, Indiana, United States
    5   Primary Care, Eskenazi Health, Indianapolis, Indiana, United States
  • Saura Fortin

    5   Primary Care, Eskenazi Health, Indianapolis, Indiana, United States
  • Justin Blackburn

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
    2   Regenstrief Institute, Indianapolis, Indiana, United States
  • Nir Menachemi

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
    2   Regenstrief Institute, Indianapolis, Indiana, United States
  • Joshua R. Vest

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
    2   Regenstrief Institute, Indianapolis, Indiana, United States
  • Matthew Gurka

    6   Department of Public Health Sciences, University of Virginia, Charlottesville, Virginia, United States
  • Christopher A. Harle

    1   Department of Health Policy & Management, Richard M. Fairbanks School of Public Health-Indiana University, Indianapolis, Indiana, United States
    2   Regenstrief Institute, Indianapolis, Indiana, United States

Funding Research reported in this publication was entirely funded by the National Institute on Drug Abuse (NIDA) of the National Institutes of Health (NIH) under the award number R33D1046085. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. NIDA was not involved in the study design, data collection, analysis, interpretation of data, and manuscript development. E.M. is part of the Public and Population Health Informatics training program at Indiana University Richard M. Fairbanks School of Public Health and the Regenstrief Institute, supported by the National Library of Medicine of the NIH under award number T15LM012502.

Abstract

Objective

This study aimed to assess the effect of a passive, opt-in electronic health record (EHR)-based clinical decision support (CDS), the Chronic Pain OneSheet, on guideline-recommended chronic pain management in primary care.

Methods

A pragmatic randomized controlled trial with a parallel group design was conducted between October 2020 and May 2022. Participants were 137 primary care clinicians (PCCs) treating qualifying patients with chronic pain at 25 primary care clinics within two academic health systems in the United States. PCCs were randomized in the EHR to have access to OneSheet or usual care. OneSheet aggregates guideline-relevant information in a single view and provides shortcuts to guideline-recommended actions (e.g., ordering urine drug screening [UDS] for patients prescribed opioids). We constructed five visit-level binary outcomes: (1) documenting pain-related goals; (2) documenting pain and function via Pain, Enjoyment of Life and General Activity (PEG) scale; (3) reviewing prescription drug monitoring programs (PDMPs); (4) ordering UDS; and (5) ordering naloxone. Analysis used generalized linear mixed models for each outcome.

Results

OneSheet access minimally increased rates of pain-related goal documentation (0.2 percentage point increase, p = 0.013), PEG scale documentation (0.7 percentage point increase, p < 0.001), and UDS orders (2.2 percentage point increase, p = 0.006). OneSheet access decreased the rate of ordering naloxone (0.5 percentage point decrease, p < 0.001). OneSheet access did not affect PDMP review rates (0.5 percentage point decrease, p = 0.382).

Conclusion

OneSheet access did not result in clinically significant improvements in guideline-recommended management of chronic pain in primary care despite a robust user-centered design incorporating clinician input and EHR integration. Several factors likely limited OneSheet effectiveness, including limited ability to target certain patient visits, workflow limits on data collection and ordering, and evolving COVID-19 and opioid epidemic-related policies and procedures. These findings highlight specific limitations of OneSheet and the broader challenges of implementing effective EHR-based CDS in complex health care environments.

Protection of Human and Animal Subjects

The study complied with the World Medical Association Declaration of Helsinki on Ethical Principles for Medical Research Involving Human Subjects. The Indiana University Institutional Review Board approved the study protocol. Study participants (PCCs) signed an informed consent. A waiver of patient consent was approved because patient data were routinely collected in the EHR and a high volume of patient visits, making obtaining informed consent not feasible.




Publication History

Received: 17 February 2025

Accepted: 18 June 2025

Article published online:
14 November 2025

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