A week-long outpatient induction onto XR-naltrexone in patients with opioid use disorder.


Journal

The American journal of drug and alcohol abuse
ISSN: 1097-9891
Titre abrégé: Am J Drug Alcohol Abuse
Pays: England
ID NLM: 7502510

Informations de publication

Date de publication:
03 05 2020
Historique:
pubmed: 21 12 2019
medline: 12 1 2021
entrez: 21 12 2019
Statut: ppublish

Résumé

Extended-release (XR) naltrexone can prevent relapse to opioid use disorder following detoxification. However, one of the barriers to initiating XR-naltrexone is the recommendation for a 7-10-day period of abstinence from opioids prior to the first dose. The current study evaluated the feasibility of an XR-naltrexone induction protocol that can be implemented over 1 week in the outpatient clinic. Participants (N = 44) were seen in the clinic daily. On Day 1, after abstaining from opioids for at least 12 h, they received buprenorphine 6-8 mg. Adjunctive medications (clonidine, clonazepam, zolpidem, trazodone, and prochlorperazine) were dispensed on Days 2-5, while ascending oral doses of naltrexone were given on Days 3-5 starting with 1 mg dose. An injection of XR-naltrexone was given on Day 5, 1 h after receiving and tolerating naltrexone 24 mg. Of the 44 participants (38 males), 35 (80%) were heroin users and 9 (20%) used prescription opioids. A total of 26 participants (59%) completed the induction and received their first injection of XR-naltrexone. XR-naltrexone was initiated in 54% (19/35) of heroin users and 78% (7/9) of prescription opioid users. The results support the feasibility of a week-long outpatient induction onto XR-naltrexone with ascending doses of naltrexone and standing doses of adjunctive medications. By circumventing the need for a protracted period of abstinence and mitigating the severity of withdrawal symptoms experienced during naltrexone titration, this strategy has the potential to increase patient acceptability and access to relapse prevention treatment with XR-naltrexone.

Sections du résumé

BACKGROUND
Extended-release (XR) naltrexone can prevent relapse to opioid use disorder following detoxification. However, one of the barriers to initiating XR-naltrexone is the recommendation for a 7-10-day period of abstinence from opioids prior to the first dose.
OBJECTIVES
The current study evaluated the feasibility of an XR-naltrexone induction protocol that can be implemented over 1 week in the outpatient clinic.
METHODS
Participants (N = 44) were seen in the clinic daily. On Day 1, after abstaining from opioids for at least 12 h, they received buprenorphine 6-8 mg. Adjunctive medications (clonidine, clonazepam, zolpidem, trazodone, and prochlorperazine) were dispensed on Days 2-5, while ascending oral doses of naltrexone were given on Days 3-5 starting with 1 mg dose. An injection of XR-naltrexone was given on Day 5, 1 h after receiving and tolerating naltrexone 24 mg.
RESULTS
Of the 44 participants (38 males), 35 (80%) were heroin users and 9 (20%) used prescription opioids. A total of 26 participants (59%) completed the induction and received their first injection of XR-naltrexone. XR-naltrexone was initiated in 54% (19/35) of heroin users and 78% (7/9) of prescription opioid users.
CONCLUSION
The results support the feasibility of a week-long outpatient induction onto XR-naltrexone with ascending doses of naltrexone and standing doses of adjunctive medications. By circumventing the need for a protracted period of abstinence and mitigating the severity of withdrawal symptoms experienced during naltrexone titration, this strategy has the potential to increase patient acceptability and access to relapse prevention treatment with XR-naltrexone.

Identifiants

pubmed: 31860366
doi: 10.1080/00952990.2019.1700265
pmc: PMC7260104
mid: NIHMS1564524
doi:

Substances chimiques

Delayed-Action Preparations 0
Narcotic Antagonists 0
Buprenorphine 40D3SCR4GZ
Naltrexone 5S6W795CQM

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

289-296

Subventions

Organisme : NIDA NIH HHS
ID : K24 DA029647
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030484
Pays : United States

Références

Drug Alcohol Depend. 1999 Oct 1;56(3):181-90
pubmed: 10529020
Am J Psychiatry. 2017 May 1;174(5):459-467
pubmed: 28068780
Lancet. 2018 Jan 27;391(10118):309-318
pubmed: 29150198
Am J Psychiatry. 2017 Aug 1;174(8):738-747
pubmed: 27978771
Lancet. 2011 Apr 30;377(9776):1506-13
pubmed: 21529928
Am J Psychiatry. 2019 Feb 1;176(2):129-137
pubmed: 30336703
Addiction. 2019 May;114(5):782-783
pubmed: 30661265
Drug Alcohol Depend. 2014 May 1;138:83-8
pubmed: 24602363
JAMA Psychiatry. 2017 Dec 1;74(12):1197-1205
pubmed: 29049469
J Psychoactive Drugs. 2003 Apr-Jun;35(2):253-9
pubmed: 12924748
Am J Drug Alcohol Abuse. 2006;32(4):503-17
pubmed: 17127538
J Subst Abuse Treat. 2011 Jan;40(1):56-66
pubmed: 21036514
Drug Alcohol Depend. 2018 Jun 1;187:171-178
pubmed: 29674251
Addiction. 2005 Aug;100(8):1090-100
pubmed: 16042639
Am J Drug Alcohol Abuse. 1987;13(3):293-308
pubmed: 3687892

Auteurs

Mohammad Sibai (M)

Department of Psychology, University of Detroit Mercy , Detroit, MI, USA.

Kaitlyn Mishlen (K)

Division on Substance Use Disorders New York State Psychiatric Institute , New York, NY, USA.

Edward V Nunes (EV)

Division on Substance Use Disorders New York State Psychiatric Institute , New York, NY, USA.
Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons , New York, NY, USA.

Frances R Levin (FR)

Division on Substance Use Disorders New York State Psychiatric Institute , New York, NY, USA.
Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons , New York, NY, USA.

John J Mariani (JJ)

Division on Substance Use Disorders New York State Psychiatric Institute , New York, NY, USA.
Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons , New York, NY, USA.

Adam Bisaga (A)

Division on Substance Use Disorders New York State Psychiatric Institute , New York, NY, USA.
Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons , New York, NY, USA.

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Classifications MeSH