Cited by 361Opioid Use Disorder TreatmentSubstance Abuse Treatment and OutcomesPain Management and Opioid Use

Extended vs Short-term Buprenorphine-Naloxone for Treatment of Opioid-Addicted Youth: A Randomized Trial

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Woody, George E., Poole, Sabrina A., Subramaniam, Geetha, Dugosh, Karen, Bogenschutz, Michael, Abbott, Patrick, Patkar, Ashwin, Publicker, Mark +8 more·2008·JAMA

Abstract

CONTEXT: The usual treatment for opioid-addicted youth is detoxification and counseling. Extended medication-assisted therapy may be more helpful. OBJECTIVE: To evaluate the efficacy of continuing buprenorphine-naloxone for 12 weeks vs detoxification for opioid-addicted youth. DESIGN, SETTING, AND PATIENTS: Clinical trial at 6 community programs from July 2003 to December 2006 including 152 patients aged 15 to 21 years who were randomized to 12 weeks of buprenorphine-naloxone or a 14-day taper (detox). INTERVENTIONS: Patients in the 12-week buprenorphine-naloxone group were prescribed up to 24 mg per day for 9 weeks and then tapered to week 12; patients in the detox group were prescribed up to 14 mg per day and then tapered to day 14. All were offered weekly individual and group counseling. MAIN OUTCOME MEASURE: Opioid-positive urine test result at weeks 4, 8, and 12. RESULTS: The number of patients younger than 18 years was too small to analyze separately, but overall, patients in the detox group had higher proportions of opioid-positive urine test results at weeks 4 and 8 but not at week 12 (chi(2)(2) = 4.93, P = .09). At week 4, 59 detox patients had positive results (61%; 95% confidence interval [CI] = 47%-75%) vs 58 12-week buprenorphine-naloxone patients (26%; 95% CI = 14%-38%). At week 8, 53 detox patients had positive results (54%; 95% CI = 38%-70%) vs 52 12-week buprenorphine-naloxone patients (23%; 95% CI = 11%-35%). At week 12, 53 detox patients had positive results (51%; 95% CI = 35%-67%) vs 49 12-week buprenorphine-naloxone patients (43%; 95% CI = 29%-57%). By week 12, 16 of 78 detox patients (20.5%) remained in treatment vs 52 of 74 12-week buprenorphine-naloxone patients (70%; chi(2)(1) = 32.90, P < .001). During weeks 1 through 12, patients in the 12-week buprenorphine-naloxone group reported less opioid use (chi(2)(1) = 18.45, P < .001), less injecting (chi(2)(1) = 6.00, P = .01), and less nonstudy addiction treatment (chi(2)(1) = 25.82, P < .001). High levels of opioid use occurred in both groups at follow-up. Four of 83 patients who tested negative for hepatitis C at baseline were positive for hepatitis C at week 12. CONCLUSIONS: Continuing treatment with buprenorphine-naloxone improved outcome compared with short-term detoxification. Further research is necessary to assess the efficacy and safety of longer-term treatment with buprenorphine for young individuals with opioid dependence. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00078130.

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Crossref · 10.1001/jama.2008.574

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  • Buprenorphine is a partial μ-opioid receptor agonist and κ-opioid receptor antagonist with a half-life of 2.33 ± 0.24 hours that might be an alternative to methadone because it is effective in treating opioid addiction or pain.

    “Buprenorphine, a partial μ-opioid receptor agonist and κ-opioid receptor antagonist with a half-life of 2.33 ± 0.24 hours might be an alternative to methadone because it is effective in treating opioid addiction or pain.21–26”

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References 31 · Cited by 361

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  1. [3]Nightingale SL Wurmser L Platt PC Adolescents on methadone: preliminary observations Presented at: Third Annual Conference on Methadone Treatment November 14-16, 1970 New York, New York
  2. [4]Millman RB Nyswander ME Slow detoxification of adolescent heroin addicts in New York City Presented at: Third Annual Conference on Methadone Treatment November 14-16, 1970 New York, New York

Authors
Woody, G. E., Poole, S. A., Subramaniam, G., Dugosh, K., Bogenschutz, M., Abbott, P., Patkar, A., Publicker, M., McCain, K., Potter, J. S., Forman, R., Vetter, V., McNicholas, L., Blaine, J., Lynch, K. G., & Fudala, P.
Affiliations
  • Treatment Research Institute (US)
  • Johns Hopkins University (US)
  • Harvard University (US)
  • National Institutes of Health (US)
Corresponding author
Woody, George E.
Venue
JAMA
Published
2008-11-05
Volume
300
Issue
17
Pages
2003-11
ISSN
  • 0002-9955 (ISSN-L)
  • 0098-7484
OpenAlex
W1992227982
Cited by
361
References
31
Citations by year
2026: 11 · 2025: 7 · 2024: 14 · 2023: 9 · 2022: 13 · 2021: 23 · 2020: 29 · 2019: 22 · 2018: 22 · 2017: 25 · 2016: 24 · 2015: 17 · 2014: 28 · 2013: 17 · 2012: 22
FWCI
24.19
Type
journal article
Language
en
Open access
Locations
  • JAMA (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health (5u10da013034-15, 5u10da013043-15)
  • National Institute on Drug Abuse (U10DA1533, U10-DA-013043, U10DA13043, U10-DA013034, U10DA013711, U10 DA13034, K05DA017009, U10DA015831, U10DA015833, K23DA022297, R01DA001533, K12DA000357, R37DA001533)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Opioid Use Disorder Treatment
  • Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
  • Health Sciences › Medicine › Anesthesiology and Pain Medicine › Pain Management and Opioid Use
Keywords
buprenorphine/naloxone, opioid use disorder, medication-assisted treatment, opioid detoxification, urine drug testing, treatment retention, relapse, counseling, community-based treatment, opioid tapering, cost-effectiveness
MeSH terms
Buprenorphine, Naloxone Drug Combination, Adolescent, Adult, Buprenorphine, Counseling, Female, Humans, Male, Naloxone, Narcotic Antagonists, Opioid-Related Disorders, Substance Abuse Detection

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