Safety and feasibility of intranasal heroin-assisted treatment: 4-week preliminary findings from a Swiss multicentre observational study

Harm Reduction Journal - Tập 20 - Trang 1-8 - 2023
Marc Vogel1, Maximilian Meyer1, Jean N. Westenberg1,2, Adrian Kormann3, Olivier Simon4, Roba Salim Hassan Fadlelseed5, Markus Kurmann6, Rebecca Bröer7, Nathalie Devaud8, Ulrike Sanwald9, Sophie Baumgartner10, Hannes Binder11, Johannes Strasser1, R. Michael Krausz2, Thilo Beck12, Kenneth M. Dürsteler1,13, Luis Falcato12
1University of Basel Psychiatric Clinics, Basel, Switzerland
2Department of Psychiatry, Faculty of Medicine, University of British Columbia, Vancouver, Canada
3ZOPA Zuger Opiat-Abgabe, Baar, Switzerland
4Service of Addiction Medicine, Lausanne University Hospital (CHUV), University of Lausanne, Lausanne, Switzerland
5Clinic for Psychiatry and Psychotherapy, Schaffhausen, Switzerland
6HeGeBe HEROL, Psychiatric Services, Olten, Switzerland
7SuGeBe Gourrama, Psychiatric Services, Solothurn, Switzerland
8Crossline Clinic, Zurich, Switzerland
9Integrierte Suchthilfe Winterthur ISW, Integrated Psychiatry Winterthur, Winterthur, Switzerland
10Heroingestützte Behandlung KODA, Bern, Switzerland
11Outpatient Clinic for Substance Use Disorders, Psychiatric Clinic Baselland, Reinach, Switzerland
12Arud Zentrum Für Suchtmedizin, Zurich, Switzerland
13Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zurich, Zurich, Switzerland

Tóm tắt

Heroin-assisted treatment (HAT) is effective for individuals with severe opioid use disorder (OUD) who do not respond sufficiently to other opioid agonist treatments. It is mostly offered with injectable diacetylmorphine (DAM) or DAM tablets creating a barrier for individuals who need the rapid onset of action but are either unable or unwilling to inject, or primarily snort opioids. To explore another route of administration, we evaluated the safety and feasibility of intranasal (IN) DAM. This is a multicentre observational cohort study among patients in Swiss HAT. All patients planning to receive IN DAM within the treatment centres were eligible to participate. Participants were either completely switched to IN DAM or received IN DAM in addition to other DAM formulations or opioid agonists. Patients were followed up for four weeks. Sociodemographic characteristics, current HAT regimen, reasons for starting IN DAM, IN DAM doses, number of injection events in the sample, IN DAM continuation rate, and appearance of adverse events and nose-related problems were evaluated. Participants (n = 52) reported vein damage, preference for nasal route of administration, and desire of a stronger effect or for a less harmful route of administration as primary reasons for switching to IN DAM. After four weeks, 90.4% of participants (n = 47) still received IN DAM. Weekly average realised injection events decreased by 44.4% from the month before IN DAM initiation to the month following. No severe adverse events were reported. After four weeks, IN DAM was a feasible and safe alternative to other routes of administration for patients with severe OUD in HAT. It addressed the needs of individuals with OUD and reduced injection behaviour. More long-term research efforts are needed to systematically assess efficacy of and patient satisfaction with IN DAM.

Tài liệu tham khảo

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