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Posts tagged fentanyl use
Trends in Novel Opioid Use and Detections in Exposures and Police Drug Seizures in New South Wales

By Janette L. Smith, Jared Brown, David Atefi, Thanjira Jiranantakan, Vanessa Shaw, Christopher Ewers, Lorraine du Toit-Prinsloo, Darren M. Roberts

Novel opioids, including non-medical and non-opium-based opioids such as fentanyl analogues and nitazenes, pose a significant risk of harm due to their high potency. There is little published data on novel opioid detections and harms in Australia, yet they are implicated in multiple deaths. This study describes the detections and harms of novel opioids in New South Wales.

Methods

A retrospective analysis was conducted using four statewide datasets: Coronial Toxicology, the Illicit Drug Analysis Unit, the Prescription, Recreational and Illicit Substance Evaluation Program (PRISE), and the NSW Poisons Information Centre. These datasets were interrogated for available data (cases or substances seized by police) on novel opioid detections between 1 January 2019 and 31 May 2024.

Results

Overall, there were 106 novel opioid detections in 103 cases. PRISE identified 91% of clinical cases, reflecting the program's reach. Fentanyl analogues predominated until 2021, whereas nitazenes predominated from 2022. Most detections were acetylfentanyl (n = 54), followed by isotonitazene detections (n = 13). Positive detections were more frequent in urine compared to blood, supporting testing on both samples. Overall numbers were low, but they were often associated with harm, including deaths.

Discussion and Conclusions

We anticipate that these data underestimate the harms from novel opioids; for example, these drugs are not being tested routinely in laboratory testing of biological samples, and not all police seizures are analysed. A change in the predominant novel opioid was observed during the study period. Enhancing systems for readiness to detect and respond to novel opioids is vital, including resourcing laboratories.

Drug Alcohol Rev. 2025;1–11

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Illicit Fentanyl Use and Hepatitis C Virus Seroconversion Among People Who Inject Drugs in Tijuana and San Diego: Results From a Binational Cohort Study

By Joseph R Friedman, Daniela Abramovitz, Britt Skaathun, Gudelia Rangel, Alicia Harvey-Vera, Carlos F Vera, Irina Artamonova, Sheryl Muñoz, Natasha K Martin, William H Eger ...

Background

Illicitly manufactured fentanyl (IMF) increases overdose mortality, but its role in infectious disease transmission is unknown. We examined whether IMF use predicts hepatitis C virus (HCV) and human immunodeficiency virus (HIV) incidence among a cohort of people who inject drugs (PWID) in San Diego, California and Tijuana, Mexico.

Methods

PWID were recruited during 2020–2022, undergoing semi-annual interviewer-administered surveys and HIV and HCV serological rapid tests through 2024. Cox regression was conducted to examine predictors of seroconversion considering self-reported IMF use as a 6-month lagged, time-dependent covariate.

Results

Of 398 PWID at baseline, 67% resided in San Diego, 70% were male, median age was 43 years, 42% reported receptive needle sharing, and 25% reported using IMF. HCV incidence was 14.26 per 100 person-years (95% confidence interval [CI]: 11.49–17.02), and HIV incidence was 1.29 (95% CI: .49–2.10). IMF was associated with HCV seroconversion, with a univariable hazard ratio (HR) of 1.64 (95% CI: 1.09–2.40), and multivariable HR of 1.57 (95% CI: 1.03–2.40). The direction of the relationship with HIV was similar, albeit not significant (HR 2.39; 95% CI: .66–8.64).

Conclusions

We document a novel association between IMF and HCV seroconversion among PWID in Tijuana–San Diego. Few HIV seroconversions (n = 10) precluded our ability to assess if a similar relationship held for HIV. IMF's short half-life may destabilize PWID—increasing the need for repeat dosing and sharing smoking materials and syringes. New preventive care approaches may reduce HCV transmission in the fentanyl era.

Clinical Infectious Diseases, cia e372, 2024.

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