Sexual minority disparities in opioid and benzodiazepine misuse among adults with opioid use disorder.


Journal

The American journal on addictions
ISSN: 1521-0391
Titre abrégé: Am J Addict
Pays: England
ID NLM: 9208821

Informations de publication

Date de publication:
05 2022
Historique:
revised: 17 12 2021
received: 14 09 2021
accepted: 03 01 2022
pubmed: 5 3 2022
medline: 20 5 2022
entrez: 4 3 2022
Statut: ppublish

Résumé

Sexual minority individuals demonstrate disparate rates of substance use. Research suggests that bisexual women are vulnerable to substance use disorders when compared to other sexual minority groups. This study explored differences in prevalence of past-year alcohol use disorder (AUD) with and without concurrent past-year opioid and/or benzodiazepine misuse. The present study utilized responses from the National Survey on Drug Use and Health (NSDUH) public dataset between the years 2015-2019 (N = 16,002) to examine the association between sexual orientation and concurrent misuse of opioids and/or benzodiazepines among individuals with past-year AUD, stratified by sex. Bisexual females demonstrated higher rates of concurrent opioid and benzodiazepine use compared to all other groups. Although there was no association between sexual orientation and concurrent substance use patterns among males, female respondents with past-year AUD endorsing past-year misuse of opioids and benzodiazepines, both alone and in combination, were more likely to be bisexual compared to heterosexual. Lesbians were less likely to endorse concurrent misuse of opioids and benzodiazepines compared to bisexual females. In a national sample, bisexual females demonstrated higher odds of risky concurrent substance use patterns. Identifying sexual minority individuals who exhibit elevated risk of co-occurring alcohol, opioid, and/or benzodiazepine misuse is an important step to targeted prevention efforts and allocation of resources to combat rising overdose deaths. For the first time, this study explored risky concurrent alcohol, opioid, and benzodiazepine misuse patterns among individuals of different sexual orientations.

Sections du résumé

BACKGROUND AND OBJECTIVES
Sexual minority individuals demonstrate disparate rates of substance use. Research suggests that bisexual women are vulnerable to substance use disorders when compared to other sexual minority groups. This study explored differences in prevalence of past-year alcohol use disorder (AUD) with and without concurrent past-year opioid and/or benzodiazepine misuse.
METHODS
The present study utilized responses from the National Survey on Drug Use and Health (NSDUH) public dataset between the years 2015-2019 (N = 16,002) to examine the association between sexual orientation and concurrent misuse of opioids and/or benzodiazepines among individuals with past-year AUD, stratified by sex.
RESULTS
Bisexual females demonstrated higher rates of concurrent opioid and benzodiazepine use compared to all other groups. Although there was no association between sexual orientation and concurrent substance use patterns among males, female respondents with past-year AUD endorsing past-year misuse of opioids and benzodiazepines, both alone and in combination, were more likely to be bisexual compared to heterosexual. Lesbians were less likely to endorse concurrent misuse of opioids and benzodiazepines compared to bisexual females.
DISCUSSION AND CONCLUSIONS
In a national sample, bisexual females demonstrated higher odds of risky concurrent substance use patterns. Identifying sexual minority individuals who exhibit elevated risk of co-occurring alcohol, opioid, and/or benzodiazepine misuse is an important step to targeted prevention efforts and allocation of resources to combat rising overdose deaths.
SCIENTIFIC SIGNIFICANCE
For the first time, this study explored risky concurrent alcohol, opioid, and benzodiazepine misuse patterns among individuals of different sexual orientations.

Identifiants

pubmed: 35243706
doi: 10.1111/ajad.13258
pmc: PMC9117396
mid: NIHMS1769543
doi:

Substances chimiques

Analgesics, Opioid 0
Benzodiazepines 12794-10-4

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

200-209

Subventions

Organisme : NIAAA NIH HHS
ID : P01 AA027473
Pays : United States
Organisme : NIDA NIH HHS
ID : T32 DA037202
Pays : United States
Organisme : NIAAA NIH HHS
ID : U54 AA027989
Pays : United States

Informations de copyright

© 2022 American Academy of Addiction Psychiatry.

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Auteurs

Cara A Struble (CA)

Department of Biomedical Data Science, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, USA.

Kathryn Thomas (K)

Justice Collaboratory, Yale Law School, Yale University, New Haven, Connecticut, USA.
SEICHE Center for Health and Justice, Yale School of Medicine, New Haven, Connecticut, USA.

Madeline R Stenersen (MR)

Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut, USA.

Kelly E Moore (KE)

Department of Psychology, East Tennessee State University, Johnson City, Tennessee, USA.

Catherine Burke (C)

Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut, USA.

Brian Pittman (B)

Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut, USA.

Sherry A McKee (SA)

Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut, USA.

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