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Validation and threshold identification of a prescription drug monitoring program clinical opioid risk metric with the WHO alcohol, smoking, and substance involvement screening test.
Cochran, Gerald; Brown, Jennifer; Yu, Ziji; Frede, Stacey; Bryan, M Aryana; Ferguson, Andrew; Bayyari, Nadia; Taylor, Brooke; Snyder, Margie E; Charron, Elizabeth; Adeoye-Olatunde, Omolola A; Ghitza, Udi E; Winhusen, T.
Affiliation
  • Cochran G; University of Utah, Department of Internal Medicine, 295 Chipeta Way Salt Lake City, UT 84132, USA. Electronic address: jerry.cochran@hsc.utah.edu.
  • Brown J; University of Cincinnati, Department of Psychiatry and Behavioral Neuroscience, 260 Stetson Street Cincinnati, OH 45267-0559, USA; Center for Addiction Research, University of Cincinnati College of Medicine, 3230 Eden Avenue, Cincinnati, OH 45267, USA. Electronic address: brown5j8@ucmail.uc.edu.
  • Yu Z; University of Utah, Department of Internal Medicine, 295 Chipeta Way Salt Lake City, UT 84132, USA. Electronic address: ziji.yu@hsc.utah.edu.
  • Frede S; Kroger Pharmacy, 1014 Vine Street, Cincinnati, OH 45202, USA. Electronic address: stacey.frede@kroger.com.
  • Bryan MA; University of Utah, Department of Internal Medicine, 295 Chipeta Way Salt Lake City, UT 84132, USA. Electronic address: aryana.bryan@utah.edu.
  • Ferguson A; University of Cincinnati, Department of Psychiatry and Behavioral Neuroscience, 260 Stetson Street Cincinnati, OH 45267-0559, USA. Electronic address: fergusam@ucmail.uc.edu.
  • Bayyari N; University of Cincinnati, Department of Psychiatry and Behavioral Neuroscience, 260 Stetson Street Cincinnati, OH 45267-0559, USA. Electronic address: bayyarnm@ucmail.uc.edu.
  • Taylor B; Kroger Pharmacy, 1014 Vine Street, Cincinnati, OH 45202, USA. Electronic address: b-taylor.2@onu.edu.
  • Snyder ME; Purdue University, College of Pharmacy, 575 Stadium Mall Drive West Lafayette, IN 47907, USA. Electronic address: snyderme@purdue.edu.
  • Charron E; University of Utah, Department of Internal Medicine, 295 Chipeta Way Salt Lake City, UT 84132, USA. Electronic address: betsy.charron@utah.edu.
  • Adeoye-Olatunde OA; Purdue University, College of Pharmacy, 575 Stadium Mall Drive West Lafayette, IN 47907, USA. Electronic address: adeoyeo@purdue.edu.
  • Ghitza UE; National Institute on Drug Abuse, Center for Clinical Trials Network, 3 White Flint North MSC 6022, 301 North Stonestreet Avenue, North Bethesda, MD 20852, USA. Electronic address: ghitzau@nida.nih.gov.
  • Winhusen T; University of Cincinnati, Department of Psychiatry and Behavioral Neuroscience, 260 Stetson Street Cincinnati, OH 45267-0559, USA; Center for Addiction Research, University of Cincinnati College of Medicine, 3230 Eden Avenue, Cincinnati, OH 45267, USA. Electronic address: winhust@ucmail.uc.edu.
Drug Alcohol Depend ; 228: 109067, 2021 11 01.
Article in En | MEDLINE | ID: mdl-34610516
ABSTRACT

BACKGROUND:

Prescription drug monitoring programs (PDMPs) are critical for pharmacists to identify risky opioid medication use. We performed an independent evaluation of the PDMP-based Narcotic Score (NS) metric.

METHODS:

This study was a one-time, cross-sectional health assessment within 19 pharmacies from a national chain among adults picking-up opioid medications. The NS metric is a 3-digit composite indicator. The WHO Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST) was the gold-standard to which the NS metric was compared. Machine learning determined optimal risk thresholds; Receiver Operating Characteristic curves and Spearman (P) and Kappa (K) coefficients analyzed concurrent validity. Regression analyses evaluated participant characteristics associated with misclassification.

RESULTS:

The NS metric showed fair concurrent validity (area under the curve≥0.70; K=0.35; P = 0.37, p < 0.001). The ASSIST and NS metric categorized 37% of participants as low-risk (i.e., not needing screening/intervention) and 32.3% as moderate/high-risk (i.e., needing screening/intervention). Further, 17.2% were categorized as low ASSIST risk but moderate/high NS metric risk, termed false positives. These reported disability (OR=3.12), poor general health (OR=0.66), and/or greater pain severity/interference (OR=1.12/1.09; all p < 0.05; i.e., needing unmanaged-pain screening/intervention). A total of 13.4% were categorized as moderate/high ASSIST risk but low NS metric risk, termed false negatives. These reported greater overdose history (OR=1.24) and/or substance use (OR=1.81-12.66; all p < 0.05).

CONCLUSIONS:

The NS metric could serve as a useful initial universal prescription opioid-risk screener given its 1) low-burden (i.e., no direct assessment); 2) high accuracy (86.5%) of actionable data identifying low-risk patients and those needing opioid use/unmanaged pain screening/intervention; and 3) broad availability.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prescription Drug Monitoring Programs / Opioid-Related Disorders Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Adult / Humans Language: En Journal: Drug Alcohol Depend Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prescription Drug Monitoring Programs / Opioid-Related Disorders Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Adult / Humans Language: En Journal: Drug Alcohol Depend Year: 2021 Document type: Article