Objective:
To assess the efficacy of buprenorphine for short-term maintenance/detoxification.
Design:
A randomized, double-blind, parallel group study comparing buprenorphine, 8 mg/d, methadone, 60 mg/d, and methadone, 20 mg/d, in a 17-week maintenance phase followed by an 8-week detoxification phase.
Setting:
Outpatient facilities at the Addiction Research Center, Baltimore, Md.
Patients:
One hundred sixty-two volunteers seeking treatment for opioid dependence.
Intervention:
In addition to the medication, counseling using a relapse prevention model was offered but not required.
Primary Outcome Measures:
Retention time in treatment, urine samples negative for opioids, and failure to maintain abstinence.
Results:
Throughout the maintenance phase, retention rates were significantly greater for buprenorphine (42%) than for methadone, 20 mg/d (20%, P less than .04); the percentage of urine samples negative for opioids was significantly greater for buprenorphine (53%, P less than .001) and methadone, 60 mg/d (44%, P less than .04), than for methadone, 20 mg/d (29%). Failure to maintain abstinence during the maintenance phase was significantly greater for methadone, 20 mg/d, than for buprenorphine (P less than .03). During the detoxification phase, no differences were observed between groups with respect to urine samples negative for opioids. For the entire 25 weeks, retention rates for buprenorphine (30%, P less than .01) and methadone, 60 mg/d (20%, P less than .05), were significantly greater than for methadone, 20 mg/d (6%). All treatments were well tolerated, with similar profiles of self-reported adverse effects. The percentages of patients who received counseling did not differ between groups.
Conclusions:
Buprenorphine was as effective as methadone, 60 mg/d, and both were superior to methadone, 20 mg/d, in reducing illicit opioid use and maintaining patients in treatment for 25 weeks.
Citing Articles
Critical access medication for opioid use disorder (MOUD) treatment facilities in the continental United States.
Pollack H, Lee F, Paykin S, Aguilera J
Drug Alcohol Depend Rep. 2023; 6:100130.
PMID: 36994373
PMC: 10040320.
DOI: 10.1016/j.dadr.2022.100130.
History of the discovery, development, and FDA-approval of buprenorphine medications for the treatment of opioid use disorder.
Heidbreder C, Fudala P, Greenwald M
Drug Alcohol Depend Rep. 2023; 6:100133.
PMID: 36994370
PMC: 10040330.
DOI: 10.1016/j.dadr.2023.100133.
Opioid agonist treatment for people who are dependent on pharmaceutical opioids.
Nielsen S, Tse W, Larance B
Cochrane Database Syst Rev. 2022; 9:CD011117.
PMID: 36063082
PMC: 9443668.
DOI: 10.1002/14651858.CD011117.pub3.
Duration of medication treatment for opioid-use disorder and risk of overdose among Medicaid enrollees in 11 states: a retrospective cohort study.
Burns M, Tang L, Chang C, Kim J, Ahrens K, Allen L
Addiction. 2022; 117(12):3079-3088.
PMID: 35652681
PMC: 10683938.
DOI: 10.1111/add.15959.
The Feasibility and Utility of Harnessing Digital Health to Understand Clinical Trajectories in Medication Treatment for Opioid Use Disorder: D-TECT Study Design and Methodological Considerations.
Marsch L, Chen C, Adams S, Asyyed A, Does M, Hassanpour S
Front Psychiatry. 2022; 13:871916.
PMID: 35573377
PMC: 9098973.
DOI: 10.3389/fpsyt.2022.871916.
Effects of Buprenorphine Dose and Therapeutic Engagement on Illicit Opiate Use in Opioid Use Disorder Treatment Trials.
Bergen A, Baurley J, Ervin C, McMahan C, Bible J, Stafford R
Int J Environ Res Public Health. 2022; 19(7).
PMID: 35409790
PMC: 8998781.
DOI: 10.3390/ijerph19074106.
Relative effectiveness of medications for opioid-related disorders: A systematic review and network meta-analysis of randomized controlled trials.
Lim J, Farhat I, Douros A, Panagiotoglou D
PLoS One. 2022; 17(3):e0266142.
PMID: 35358261
PMC: 8970369.
DOI: 10.1371/journal.pone.0266142.
Advancing Pharmacological Treatments for Opioid Use Disorder (ADaPT-OUD): an Implementation Trial in Eight Veterans Health Administration Facilities.
Hagedorn H, Gustavson A, Ackland P, Bangerter A, Bounthavong M, Clothier B
J Gen Intern Med. 2022; 37(14):3594-3602.
PMID: 34981352
PMC: 8722660.
DOI: 10.1007/s11606-021-07274-7.
Assessing the determinants of completing OAT induction and long-term retention: A population-based study in British Columbia, Canada.
Kurz M, Min J, Dale L, Nosyk B
J Subst Abuse Treat. 2021; 133:108647.
PMID: 34740484
PMC: 9833672.
DOI: 10.1016/j.jsat.2021.108647.
Retention in opioid agonist treatment: a rapid review and meta-analysis comparing observational studies and randomized controlled trials.
Klimas J, Hamilton M, Gorfinkel L, Adam A, Cullen W, Wood E
Syst Rev. 2021; 10(1):216.
PMID: 34362464
PMC: 8348786.
DOI: 10.1186/s13643-021-01764-9.
Diversity inclusion in United States opioid pharmacological treatment trials: A systematic review.
Nalven T, Spillane N, Schick M, Weyandt L
Exp Clin Psychopharmacol. 2021; 29(5):524-538.
PMID: 34242040
PMC: 8511246.
DOI: 10.1037/pha0000510.
Early impacts of a multi-faceted implementation strategy to increase use of medication treatments for opioid use disorder in the Veterans Health Administration.
Gustavson A, Wisdom J, Kenny M, Salameh H, Ackland P, Clothier B
Implement Sci Commun. 2021; 2(1):20.
PMID: 33588952
PMC: 7885503.
DOI: 10.1186/s43058-021-00119-8.
Comparative effectiveness of buprenorphine-naloxone versus methadone for treatment of opioid use disorder: a population-based observational study protocol in British Columbia, Canada.
Piske M, Thomson T, Krebs E, Hongdilokkul N, Bruneau J, Greenland S
BMJ Open. 2020; 10(9):e036102.
PMID: 32912944
PMC: 7482450.
DOI: 10.1136/bmjopen-2019-036102.
How Motivations for Using Buprenorphine Products Differ From Using Opioid Analgesics: Evidence from an Observational Study of Internet Discussions Among Recreational Users.
Butler S, Oyedele N, Govoni T, Green J
JMIR Public Health Surveill. 2020; 6(1):e16038.
PMID: 32209533
PMC: 7142742.
DOI: 10.2196/16038.
Rapid effect of a single-dose buprenorphine on reduction of opioid craving and suicidal ideation: A randomized, double blind, placebo-controlled study.
Ahmadi J, Sarani E, Jahromi M
Tzu Chi Med J. 2020; 32(1):58-64.
PMID: 32110522
PMC: 7015018.
DOI: 10.4103/tcmj.tcmj_220_18.
Effects of lorcaserin on oxycodone self-administration and subjective responses in participants with opioid use disorder.
Brandt L, Jones J, Martinez S, Manubay J, Mogali S, Ramey T
Drug Alcohol Depend. 2020; 208:107859.
PMID: 31980285
PMC: 7063580.
DOI: 10.1016/j.drugalcdep.2020.107859.
A call for consensus in defining efficacy in clinical trials for opioid addiction: combined results from a systematic review and qualitative study in patients receiving pharmacological assisted therapy for opioid use disorder.
Dennis B, Sanger N, Bawor M, Naji L, Plater C, Worster A
Trials. 2020; 21(1):30.
PMID: 31907000
PMC: 6945391.
DOI: 10.1186/s13063-019-3995-y.
The Opioid Epidemic: Impact on Inflammation and Cardiovascular Disease Risk in HIV.
Hileman C, McComsey G
Curr HIV/AIDS Rep. 2019; 16(5):381-388.
PMID: 31473903
PMC: 6814576.
DOI: 10.1007/s11904-019-00463-4.
[New slow-release buprenorphine formulations for optimization of opioid substitution].
Soyka M, Pogarell O
Nervenarzt. 2019; 90(9):932-937.
PMID: 31399813
DOI: 10.1007/s00115-019-0783-6.
Advancing pharmacological treatments for opioid use disorder (ADaPT-OUD): protocol for testing a novel strategy to improve implementation of medication-assisted treatment for veterans with opioid use disorders in low-performing facilities.
Hagedorn H, Kenny M, Gordon A, Ackland P, Noorbaloochi S, Yu W
Addict Sci Clin Pract. 2018; 13(1):25.
PMID: 30545409
PMC: 6293521.
DOI: 10.1186/s13722-018-0127-z.