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Recent increase in detection of alprazolam in Victorian heroin-related deaths

Angela C Rintoul, Malcolm D H Dobbin, Suzanne Nielsen, Louisa Degenhardt and Olaf H Drummer
Med J Aust 2013; 198 (4): 206-209. || doi: 10.5694/mja12.10986
Published online: 4 March 2013

The use of benzodiazepines by opioid-dependent people is widespread.1-4 The 2011 Victorian Illicit Drug Reporting System (IDRS), a sentinel survey of people who inject drugs (PWID), reported 92% lifetime and 71% recent (in the past 6 months) use among PWID.5 PWID use benzodiazepines for a number of reasons: to enhance the intoxicating effects of heroin or other opioids, manage anxiety, or manage withdrawal symptoms.3

The contribution of benzodiazepines to heroin overdose is well established.6,7 Alprazolam is a benzodiazepine registered in Australia for short-term treatment of anxiety and panic disorder. It is not recommended as first-line treatment because of concerns about risks of dependence and its potential for misuse.4,8

Alprazolam, like other commonly misused drugs, has a rapid onset and offset of action and high potency.8 Alprazolam may also be more toxic in overdose than other benzodiazepines.9 Laboratory-based studies have found that in combination with methadone, alprazolam has significant effects on respiration.10 A review of the interaction concluded that most evidence suggests the interaction is pharmacodynamic in nature.11

Victorian IDRS reports showed recent alprazolam use increased from 8% in 200512 to 69% in 2011.5 Alprazolam is now the most commonly injected benzodiazepine,5 with a reported street price of three tablets for $10.13 Alprazolam use is associated with disproportionate levels of harm, including amnesia, violent outbursts of rage in otherwise non-violent individuals, and theft.1,13-15 In Victoria, most alprazolam (81%) used by PWID in 2011 was obtained from illicit sources.5

Given the increased number of episodes of serious harm associated with alprazolam use, we aimed to examine its public health impact, to inform prescribing and to guide appropriate policy responses. We investigated trends in alprazolam prescribing and its detection in heroin-related deaths (HRDs) in Victoria. Our hypothesis was that increased mean consumption of alprazolam is likely to have significant effects on heroin users,16 a population already vulnerable to drug toxicity.

Methods
Results
Alprazolam prescribing

Alprazolam supply increased by 1426% from 0.42 DDD/1000/day in 1990 to 6.41 DDD/1000/day in 2010 (Box 1). The estimated number of Victorian prescriptions for alprazolam increased by 611%, from 609/100 000 population in 1990 to 4327/100 000 population in 2010 (Box 1). The most remarkable change was in prescriptions for the 2 mg formulation, which increased from 4.1% to 27.9% of the population-adjusted rate for alprazolam prescriptions between 1998 and 2010. Box 2 shows trends in total DDD/1000/day for the four alprazolam dose formulations. A large proportion of alprazolam prescriptions were private; in 2009, private prescriptions accounted for 37.2% of all prescriptions.

Discussion

Our study over the 21 years from 1990 to 2010 showed a number of interesting trends in alprazolam prescribing and supply and its relationship to HRDs in Victoria. First, the supply of alprazolam increased despite its status as a second-line treatment for its approved indications; second, the increase in the supply of the high-dose formulation was disproportionate to the increase in other formulations; and third, the rate of detection of alprazolam in HRDs increased more rapidly after 2005, concurrently with other reports of increasing harm among PWID.13 The association between the detection of alprazolam in HRDs and alprazolam supply was strong and significant. While alprazolam may be more toxic in overdose than other benzodiazepines,9 the accelerated rate of detection in this population since 2005 could reflect an increased preference for and use of alprazolam,1 particularly the high-dose formulation, among heroin users.

This raises questions about the increased prescribing of a drug not preferred for treatment of its primary indication,8,18 and for which little evidence exists for effectiveness beyond short-term use.4 This is especially important given that it may be more toxic in overdose.9 We have shown that the proportion of HRDs in which this benzodiazepine was detected increased over time as supply increased. Understanding the reasons for the increasing average population-level consumption of alprazolam may help to decrease its supply and the harmful effects seen among PWID. This would be consistent with a previous study that showed that the average consumption of potentially harmful products such as salt and alcohol predicts the number of people affected in the statistically “deviant” tail end of a population distribution.16,19

The number of HRDs has remained fewer than during the heroin glut in the late 1990s,20 which led to the peak in deaths shown in 1999. The lower numbers are likely to reflect trends in heroin supply and should not be interpreted as evidence that alprazolam is relatively safe.

A relative strength of our study is the reporting of all Victorian HRDs spanning a 21-year period, enabling the identification of long-term trends in alprazolam used shortly before death. These data provide valuable information for the future prevention of deaths among people who use heroin. In addition, the prescription data and DDD calculations are estimates of the total number of prescriptions dispensed, based on data from the ASM and Medicare. Incorporating the ASM data improves the accuracy of total prescription volume through the inclusion of private prescriptions.

The finding of a strong and statistically significant association between detection of alprazolam in cases of HRD and its supply in the community is useful for generating a hypothesis about possible causes of increasing detection of this drug in cases of HRD. However, this does not mean a causal relationship exists between the increasing alprazolam supply and such deaths. The contribution of alprazolam to deaths involving multiple drugs is difficult to determine, and it is therefore not possible to specify the proportion of cases of drug toxicity due to combined drugs where alprazolam contributed directly to death.21 We used detection of alprazolam as an indication of use by PWID, rather than contribution to death per se.

The absolute number and rate of cases of HRD in which alprazolam was detected has increased substantially since 2005. Concern about the misuse of alprazolam in 2010 led to a request to the Australian National Drugs and Poisons Schedule Committee to reschedule it to the more restrictive Schedule 8.22 Among the committee’s stated reasons for not doing so at that time was that there was insufficient evidence of a problem.

This study provides further evidence of the increasing problem, perhaps involving high-dose formulations, of use of diverted medications among PWID.1 Given the growing concerns with alprazolam use among PWID and its increasing involvement in HRDs, supply control measures — such as better monitoring and surveillance (including real-time prescription monitoring), rescheduling to Schedule 8, and education of health professionals — are warranted. Provision of information about the risks of concurrent use of opioids and alprazolam to PWID is also essential.

Received 20 June 2012, accepted 28 October 2012

  • Angela C Rintoul1
  • Malcolm D H Dobbin2
  • Suzanne Nielsen3
  • Louisa Degenhardt4
  • Olaf H Drummer5

  • 1 Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC.
  • 2 Mental Health, Drugs and Regions Division, Department of Health, Victoria, Melbourne, VIC.
  • 3 Discipline of Addiction, University of Sydney, Sydney, NSW.
  • 4 National Drug and Alcohol Research Centre, University of New South Wales, Sydney, NSW.
  • 5 Department of Forensic Medicine, Monash University, Melbourne, VIC.


Correspondence: angela.rintoul@monash.edu

Acknowledgements: 

We are grateful to Damien Jolley and Rory Wolfe of Monash University for providing statistical advice; the PBAC Drug Utilisation Sub-Committee for extracting ASM national prescription volume data; and Katayoon Yazdani for assisting in the compilation of Medicare Australia data.

Angela Rintoul is currently funded through an Australian Postgraduate Award scholarship. Some of this work was completed during her participation in the Victorian Public Health Training Scheme, funded by the State of Victoria through the Department of Health, while on placement with the Drugs Policy Unit at the Victorian Department of Health.

The views and conclusions in this article are ours and do not necessarily represent those of the Department of Health.

Competing interests:

Suzanne Nielsen has worked in an unpaid capacity as an investigator on projects funded by untied educational grants from Reckitt-Benckiser (RB). She has not received any direct funding. Louisa Degenhardt has received untied educational grants from RB to undertake postmarketing surveillance of suboxone tablet and film products in Australia. Malcolm Dobbin has received an honorarium from Pfizer for lectures, which was donated to charity. Neither RB nor Pfizer had knowledge of, or input into, this paper.

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