Perceptions of extended-release naltrexone, methadone, and buprenorphine treatments following release from jail.


Journal

Addiction science & clinical practice
ISSN: 1940-0640
Titre abrégé: Addict Sci Clin Pract
Pays: England
ID NLM: 101316917

Informations de publication

Date de publication:
01 10 2019
Historique:
received: 15 02 2019
accepted: 11 09 2019
entrez: 2 10 2019
pubmed: 2 10 2019
medline: 19 5 2020
Statut: epublish

Résumé

Few studies have documented patient attitudes and experiences with extended-release naltrexone (XR-NTX) opioid relapse prevention in criminal justice settings. This study assessed barriers and facilitators of jail-to-community reentry among adults with opioid use disorder (OUD) treated with XR-NTX, buprenorphine, methadone, and no medications. This qualitative study conducted individual interviews with a purposeful and convenience sample of adults with OUD who were recently released from NYC jails. XR-NTX, no medication, and methadone participants were concurrently enrolled in a large randomized controlled trial evaluating XR-NTX vs. a no medication Enhanced Treatment As Usual (ETAU) condition, or enrolled in a non-randomized quasi-experimental methadone maintenance cohort. Buprenorphine participants were referred from NYC jails to a public hospital office-based buprenorphine program and not enrolled in the parent trial. Interviews were audio recorded, transcribed, independently coded by two researchers, and analyzed per a grounded theory approach adapted to the Social Cognitive Theory framework. The research team reviewed transcripts and coding to reach consensus on emergent themes. N = 33 adults with OUD (28 male, 5 female) completed a single individual interview. Purposeful sampling recruited persons leaving jail on XR-NTX (n = 11), no active medication treatment (n = 9), methadone (n = 9), and buprenorphine (n = 4). Emergent themes were: (1) general satisfaction with XR-NTX's long-acting antagonist effects and control of cravings; (2) "testing" XR-NTX's blockade with heroin upon reentry was common; (3) early discontinuation of XR-NTX treatment was most common among persons with high self-efficacy and/or heavy exposure to drug use environments and peers; (4) similar satisfaction regarding effects of methadone and buprenorphine maintenance among retained-in-treatment individuals, alongside general dissatisfaction with daily observed dosing requirements and misinformation and stigmas regarding methadone adverse effects; (5) unstable housing, economic insecurity, and exposure to actively using peers were attributed to early termination of treatment and relapse; (6) individual motivation and willpower as central to long-term opioid abstinence and reentry success. In the context of more familiar agonist maintenance treatments, XR-NTX relapse prevention during jail-to-community reentry was viewed as a helpful and unique intervention though with important limitations. Commonly described barriers to treatment retention and heroin abstinence included homelessness, economic insecurity, and drug-using peers. Trial registration ClinicalTrials.gov, NCT01999946 (XOR), Registered 03 December 2013, https://clinicaltrials.gov/ct2/show/NCT01999946 .

Sections du résumé

BACKGROUND
Few studies have documented patient attitudes and experiences with extended-release naltrexone (XR-NTX) opioid relapse prevention in criminal justice settings. This study assessed barriers and facilitators of jail-to-community reentry among adults with opioid use disorder (OUD) treated with XR-NTX, buprenorphine, methadone, and no medications.
METHODS
This qualitative study conducted individual interviews with a purposeful and convenience sample of adults with OUD who were recently released from NYC jails. XR-NTX, no medication, and methadone participants were concurrently enrolled in a large randomized controlled trial evaluating XR-NTX vs. a no medication Enhanced Treatment As Usual (ETAU) condition, or enrolled in a non-randomized quasi-experimental methadone maintenance cohort. Buprenorphine participants were referred from NYC jails to a public hospital office-based buprenorphine program and not enrolled in the parent trial. Interviews were audio recorded, transcribed, independently coded by two researchers, and analyzed per a grounded theory approach adapted to the Social Cognitive Theory framework. The research team reviewed transcripts and coding to reach consensus on emergent themes.
RESULTS
N = 33 adults with OUD (28 male, 5 female) completed a single individual interview. Purposeful sampling recruited persons leaving jail on XR-NTX (n = 11), no active medication treatment (n = 9), methadone (n = 9), and buprenorphine (n = 4). Emergent themes were: (1) general satisfaction with XR-NTX's long-acting antagonist effects and control of cravings; (2) "testing" XR-NTX's blockade with heroin upon reentry was common; (3) early discontinuation of XR-NTX treatment was most common among persons with high self-efficacy and/or heavy exposure to drug use environments and peers; (4) similar satisfaction regarding effects of methadone and buprenorphine maintenance among retained-in-treatment individuals, alongside general dissatisfaction with daily observed dosing requirements and misinformation and stigmas regarding methadone adverse effects; (5) unstable housing, economic insecurity, and exposure to actively using peers were attributed to early termination of treatment and relapse; (6) individual motivation and willpower as central to long-term opioid abstinence and reentry success.
CONCLUSIONS
In the context of more familiar agonist maintenance treatments, XR-NTX relapse prevention during jail-to-community reentry was viewed as a helpful and unique intervention though with important limitations. Commonly described barriers to treatment retention and heroin abstinence included homelessness, economic insecurity, and drug-using peers. Trial registration ClinicalTrials.gov, NCT01999946 (XOR), Registered 03 December 2013, https://clinicaltrials.gov/ct2/show/NCT01999946 .

Identifiants

pubmed: 31570100
doi: 10.1186/s13722-019-0166-0
pii: 10.1186/s13722-019-0166-0
pmc: PMC6771097
doi:

Substances chimiques

Analgesics, Opioid 0
Delayed-Action Preparations 0
Buprenorphine 40D3SCR4GZ
Naltrexone 5S6W795CQM
Methadone UC6VBE7V1Z

Banques de données

ClinicalTrials.gov
['NCT01999946']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

37

Subventions

Organisme : NIDA NIH HHS
ID : 5U01DA033336
Pays : United States

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Auteurs

Melissa Velasquez (M)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Mara Flannery (M)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Ryan Badolato (R)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Alexandria Vittitow (A)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Ryan D McDonald (RD)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Babak Tofighi (B)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.
Department of Medicine, Division of General Internal Medicine and Clinical Innovation, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Ann R Garment (AR)

Department of Medicine, Division of General Internal Medicine and Clinical Innovation, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA.

Jonathan Giftos (J)

Correctional Health Services, New York City Health + Hospitals Corporation, 55 Water Street, New York, NY, 10041, USA.

Joshua D Lee (JD)

Department of Population Health, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA. Joshua.lee@nyulangone.org.
Department of Medicine, Division of General Internal Medicine and Clinical Innovation, New York University School of Medicine, 550 First Avenue, New York, NY, 10016, USA. Joshua.lee@nyulangone.org.
New York University School of Medicine, 180 Madison Avenue, 17th Floor, 1714, New York, NY, 10016, USA. Joshua.lee@nyulangone.org.

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Classifications MeSH