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The relative abuse liability of oral oxycodone, hydrocodone and hydromorphone assessed in prescription opioid abusers

Producción científica: Articlerevisión exhaustiva

148 Citas (Scopus)

Resumen

Abuse of prescription opioids has risen precipitously in the United States. Few controlled comparisons of the abuse liability of the most commonly abused opioids have been conducted. This outpatient study employed a double-blind, randomized, within-subject, placebo-controlled design to examine the relative abuse potential and potency of oral oxycodone (10, 20 and 40 mg), hydrocodone (15, 30 and 45 mg), hydromorphone (10, 17.5 and 25 mg) and placebo. Healthy adult volunteers (n = 9) with sporadic prescription opioid abuse participated in 11 experimental sessions (6.5 h in duration) conducted in a hospital setting. All three opioids produced a typical mu opioid agonist profile of subjective (increased ratings of liking, good effects, high and opiate symptoms), observer-rated, and physiological effects (miosis, modest respiratory depression, exophoria and decrements in visual threshold discrimination) that were generally dose-related. Valid relative potency assays revealed that oxycodone was roughly equipotent to or slightly more potent than hydrocodone. Hydromorphone was only modestly more potent (less than two-fold) than either hydrocodone or oxycodone, which is inconsistent with prior estimates arising from analgesic studies. These data suggest that the abuse liability profile and relative potency of these three commonly used opioids do not differ substantially from one another and suggest that analgesic potencies may not accurately reflect relative differences in abuse liability of prescription opioids.

Idioma originalEnglish
Páginas (desde-hasta)191-202
Número de páginas12
PublicaciónDrug and Alcohol Dependence
Volumen98
N.º3
DOI
EstadoPublished - dic 1 2008

Nota bibliográfica

Funding Information:
Role of funding source : Grants from the National Institute on Drug Abuse (R01 016717 SLW, K12 14040 MRL) and the National Resources Center (M01-RR02602) provided support for this project. These institutes had no role in the study design, collection, analysis or interpretation of the data, writing of the report or in the decision to submit the paper for publication.

Financiación

Role of funding source : Grants from the National Institute on Drug Abuse (R01 016717 SLW, K12 14040 MRL) and the National Resources Center (M01-RR02602) provided support for this project. These institutes had no role in the study design, collection, analysis or interpretation of the data, writing of the report or in the decision to submit the paper for publication.

FinanciadoresNúmero del financiador
National Center for Research ResourcesM01-RR02602
National Institute on Drug AbuseK12 14040 MRL, R01 016717
National Center for Research ResourcesM01RR002602

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Toxicology
    • Pharmacology
    • Psychiatry and Mental health
    • Pharmacology (medical)

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