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Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians

OBJECTIVE: The United States is in the fourth wave of the opioid epidemic marked by the increase in fentanyl and co‐occurring stimulant use related overdose deaths. Measures are needed to quickly diagnose opioid and stimulant use disorders, yet current traditional diagnostic assessments pose barrier...

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Autores principales: Di Paola, Angela, Farabee, David, Springer, Sandra A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499189/
https://www.ncbi.nlm.nih.gov/pubmed/37711754
http://dx.doi.org/10.1176/appi.prcp.20230022
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author Di Paola, Angela
Farabee, David
Springer, Sandra A.
author_facet Di Paola, Angela
Farabee, David
Springer, Sandra A.
author_sort Di Paola, Angela
collection PubMed
description OBJECTIVE: The United States is in the fourth wave of the opioid epidemic marked by the increase in fentanyl and co‐occurring stimulant use related overdose deaths. Measures are needed to quickly diagnose opioid and stimulant use disorders, yet current traditional diagnostic assessments pose barriers to providing rapid diagnoses. METHODS: This study aimed to (1) validate an updated version of the Rapid Opioid Dependence Screen (RODS) from DSM‐IV criteria for opioid dependence to the now DSM‐5 moderate‐to‐severe opioid use disorder, the Rapid Opioid Use Disorder Assessment (ROUDA); and (2) create and validate the Rapid Stimulant Use Disorder Assessment to DSM‐5 stimulant use disorder (RSUDA) when compared to the substance use disorder module from the DSM‐5 version of the Mini International Neuropsychiatric Interview. RESULTS: One‐hundred and fifty adults completed study assessments, 122 reported opioid misuse and 140 reported stimulant misuse within their lifetime. The ROUDA had a sensitivity of 82.5% (95% confidence interval [CI] 75.7, 89.2), specificity of 100.0% (95% CI: 100, 100), and strong internal consistency α = 0.94. The RSUDA had similarly high sensitivity (83.8%, 95% CI: 77.7, 89.9), specificity (91.4%, 95% CI: 86.8, 96.1), and internal consistency α = 0.87. The ROUDA and RSUDA are efficient and valid measures that can be administered in various settings by non‐clinical staff to rapidly diagnose opioid and stimulant use disorders and allow for immediate treatment and harm reduction interventions. CONCLUSIONS: The ROUDA and RSUDA are efficient and valid measures that can be administered by non‐clinicians to rapidly diagnose opioid and stimulant use disorders.
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spelling pubmed-104991892023-09-14 Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians Di Paola, Angela Farabee, David Springer, Sandra A. Psychiatr Res Clin Pract Articles OBJECTIVE: The United States is in the fourth wave of the opioid epidemic marked by the increase in fentanyl and co‐occurring stimulant use related overdose deaths. Measures are needed to quickly diagnose opioid and stimulant use disorders, yet current traditional diagnostic assessments pose barriers to providing rapid diagnoses. METHODS: This study aimed to (1) validate an updated version of the Rapid Opioid Dependence Screen (RODS) from DSM‐IV criteria for opioid dependence to the now DSM‐5 moderate‐to‐severe opioid use disorder, the Rapid Opioid Use Disorder Assessment (ROUDA); and (2) create and validate the Rapid Stimulant Use Disorder Assessment to DSM‐5 stimulant use disorder (RSUDA) when compared to the substance use disorder module from the DSM‐5 version of the Mini International Neuropsychiatric Interview. RESULTS: One‐hundred and fifty adults completed study assessments, 122 reported opioid misuse and 140 reported stimulant misuse within their lifetime. The ROUDA had a sensitivity of 82.5% (95% confidence interval [CI] 75.7, 89.2), specificity of 100.0% (95% CI: 100, 100), and strong internal consistency α = 0.94. The RSUDA had similarly high sensitivity (83.8%, 95% CI: 77.7, 89.9), specificity (91.4%, 95% CI: 86.8, 96.1), and internal consistency α = 0.87. The ROUDA and RSUDA are efficient and valid measures that can be administered in various settings by non‐clinical staff to rapidly diagnose opioid and stimulant use disorders and allow for immediate treatment and harm reduction interventions. CONCLUSIONS: The ROUDA and RSUDA are efficient and valid measures that can be administered by non‐clinicians to rapidly diagnose opioid and stimulant use disorders. John Wiley and Sons Inc. 2023-08-15 /pmc/articles/PMC10499189/ /pubmed/37711754 http://dx.doi.org/10.1176/appi.prcp.20230022 Text en © 2023 The Authors. Psychiatric Research and Clinical Practice published by Wiley Periodicals LLC on behalf of American Psychiatric Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Di Paola, Angela
Farabee, David
Springer, Sandra A.
Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians
title Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians
title_full Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians
title_fullStr Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians
title_full_unstemmed Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians
title_short Validation of Two Diagnostic Assessments for Opioid and Stimulant Use Disorder for Use by Non‐Clinicians
title_sort validation of two diagnostic assessments for opioid and stimulant use disorder for use by non‐clinicians
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499189/
https://www.ncbi.nlm.nih.gov/pubmed/37711754
http://dx.doi.org/10.1176/appi.prcp.20230022
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