Abstract
Background: During a COVID-19 outbreak in the congregate shelter system in Halifax, Nova Scotia, Canada, a healthcare team provided an emergency “safe supply” of medications and alcohol to facilitate isolation in COVID-19 hotel shelters for residents who use drugs and/or alcohol. We aimed to evaluate (a) substances and dosages provided, and (b) outcomes of the program. Methods: We reviewed medical records of all COVID-19 isolation hotel shelter residents during May 2021. The primary outcome was successful completion of 14 days isolation, as directed by public health orders. Adverse events included (a) overdose; (b) intoxication; and (c) diversion, selling, or sharing of medications or alcohol. Results: Seventy-seven isolation hotel residents were assessed (mean age 42 ± 14 years; 24% women). Sixty-two (81%) residents were provided medications, alcohol, or cigarettes. Seventeen residents (22%) received opioid agonist treatment (methadone, buprenorphine, or slow-release oral morphine) and 27 (35%) received hydromorphone. Thirty-one (40%) residents received prescriptions stimulants. Six (8%) residents received benzodiazepines and forty-two (55%) received alcohol. Over 14 days, mean daily dosages increased of hydromorphone (45 ± 32 – 57 ± 42 mg), methylphenidate (51 ± 28 – 77 ± 37 mg), and alcohol (12.3 ± 7.6 – 13.0 ± 6.9 standard drinks). Six residents (8%) left isolation prematurely, but four returned. During 1059 person-days, there were zero overdoses. Documented concerns regarding intoxication occurred six times (0.005 events/person-day) and medication diversion/sharing three times (0.003 events/person-day). Conclusions: COVID-19 isolation hotel residents participating in an emergency safe supply and managed alcohol program experienced high rates of successful completion of 14 days isolation and low rates of adverse events.
Original language | English |
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Article number | 109440 |
Journal | Drug and Alcohol Dependence |
Volume | 235 |
DOIs | |
Publication status | Published - Jun 1 2022 |
Bibliographical note
Funding Information:This project had no dedicated funding. TDB is supported by the Dalhousie University Internal Medicine Research Foundation ,Canada, Fellowship, a Canadian Institutes of Health Research Fellowship ( CIHR-FRN# 171259 ), and through the Research in Addiction Medicine Scholars (RAMS) Program ( U.S. National Institutes of Health/National Institute on Drug Abuse ; R25DA033211 ). Funders had no role in the in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript should be declared.
Publisher Copyright:
© 2022 The Authors
ASJC Scopus Subject Areas
- Toxicology
- Pharmacology
- Psychiatry and Mental health
- Pharmacology (medical)
PubMed: MeSH publication types
- Journal Article