Changes in non-opioid substitution treatment episodes for pharmaceutical opioids and heroin from 2002 to 2011
Introduction
Pharmaceutical opioid (PO) use and associated harms are an important international issue (Fischer et al., 2013c, Maxwell, 2011). Increases in mortality have been described as an ‘epidemic’ (Calcaterra et al., 2013, ONCDP, 2011). Over the past 10–15 years, substantial increases in prescribing and non-medical use of a range of opioids have been reported globally (Atluri et al., 2014, Degenhardt et al., 2007, Leong et al., 2009). In Australia, clear patterns of increased opioid prescribing (Leong et al., 2009) and increased non-medical use of analgesics and ‘other opiates’ (including morphine and oxycodone) have been seen in the general population (Australian Institute of Health and Welfare, 2014a). Likewise, increases in morphine and oxycodone use amongst sentinel samples of people who inject drugs have been reported (Stafford and Burns, 2012).
One important indicator of harm associated with PO use is seeking treatment for drug dependence. In the US, the proportion of all treatment admissions related to prescription opioid abuse increased from 2.2% to 9.8% between 1998 and 2008, with 26.5% of admissions for medication-assisted treatment being for the treatment of prescription opioid dependence (Substance Abuse and Mental Health Services Administration, 2010). Increased treatment admissions for codeine have been reported in South Africa (Myers et al., 2003). Australia has recorded an increase in hospital presentations for PO poisoning (Roxburgh and Burns, 2013), and increases in oxycodone- and fentanyl-related deaths have also been documented (Rintoul et al., 2010, Roxburgh et al., 2011, Roxburgh et al., 2013).
Studies of PO users indicate that some non-treatment seeking populations of pharmaceutical opioid dependent people, such as codeine users, may differ from heroin users in important ways such as employment and education (Nielsen et al., 2011). Further, a recent case series of drug treatment entrants identified differences between codeine and strong opioid users in terms of presenting characteristics and types of treatment received (Nielsen et al., 2014). To date, limited information is available to give a broader picture of PO treatment at a jurisdictional or national level, or to examine the patterns of drug and alcohol service utilization over the time period during which increased pharmaceutical opioid use has been observed. Recent indicators from opioid substitution pharmacotherapy treatment (OST) suggest a significant minority (around one in three) of people on OST report pharmaceutical opioids as the principal drug of concern at treatment entry (Australian Institute of Health and Welfare, 2014c).
Oxycodone has been the subject of much research interest, with new formulations of oxycodone being developed to counter concerns with misuse (Coplan et al., 2013, Sees et al., 2005). Less is known about opioids such as fentanyl and codeine. Fentanyl is a potent opioid with higher efficacy at the mu opioid receptor. Increased fentanyl prescribing has been reported in Australia and the US, with associated increases in mortality, and intentional misuse and injection described in the majority of deaths (Kuhlman et al., 2003, Roxburgh et al., 2013). Recent US studies have identified that between 9 and 20% of patients prescribed fentanyl display signs of non-adherent medication use (Layton et al., 2014, Passik et al., 2014). Reports are emerging of misuse and harms associated with codeine (Dutch, 2008, Frei et al., 2010, McDonough, 2011, Myers et al., 2003, Pilgrim et al., 2013, Sproule et al., 1999), particularly in those countries where access to codeine is less restricted. Estimates on rates of misuse and harms are less readily available.
The aim of this study was to use national drug treatment statistics to examine patterns of pharmaceutical opioid related presentations to services other than opioid substitution therapy (OST), including withdrawal, counselling, case management and support, information and education, and residential rehabilitation services. The two key areas we sought to examine were: (1) numbers of drug treatment episodes where a pharmaceutical opioid was reported as the principal drug of concern compared with episodes where heroin was reported as the principal drug of concern; and (2) to examine if there were differences in demographic and substance use characteristics reported with treatment episodes for ‘weaker’, less restricted opioids such as codeine and strong opioids such as morphine, oxycodone and fentanyl.
Section snippets
Design and participants
All closed treatment episodes from the Alcohol and Other Drug Treatment Services National Minimum Data Set (AODTS-NMDS) were examined for the financial years 2002–2003 to 2010–2011. Data for the AODTS-NMDS are collected to provide national information about drug treatment, to inform policy and strategy decisions, as well as to provide individual service providers information about drug problems and treatment responses in their area. A closed treatment episode refers to a period of contact
Changes in opioid-related presentations over time
In 2002–2003, there were 123,032 closed treatment episodes for all drugs, with heroin (as the principal drug of concern) accounting for 18.4% (n = 22,642) and PO as the principal drug of concern accounting for 1.5% (n = 1799) of all treatment episodes. PO presentations represented 7% of all opioid-related presentations in 2002–2003. In 2010–2011, there were 144,022 closed treatment episodes for all drugs, with heroin accounting for 9.3% (n = 13,354) and PO accounting for 2.4% (n = 3386). PO
Discussion
This study represents the first detailed analysis of Australian treatment episodes for heroin and pharmaceutical opioids. This study has confirmed that there are increasing numbers of non-OST treatment episodes where pharmaceutical opioids are the principal drug of concern, in contrast to fewer heroin treatment episodes over time, though heroin remains the most common opioid reported. Important differences were identified between different pharmaceutical opioids, and between pharmaceutical
Role of funding source
The author SN and LD are supported by a NHMRC Research Fellowship (#1013803 and #1041472). The National Drug and Alcohol Research Centre at the University of New South Wales is supported by funding from the Australian Government under the Substance Misuse Prevention and Service Improvements Grant Fund. The funding sources had no role in the study design, interpretation or manuscript preparation.
Contributors
The study was conceptualized by S.N. and L.D. All authors had input proposed analysis, S.N. and R.B. completed the analysis. All authors were involved in the interpretation of the results and writing of the manuscript.
Conflict of interest
None of the authors have any connections with the tobacco, alcohol, or gaming industry. Authors SN, NL and LD have been investigators on untied educational grants from Reckitt-Benckiser, and NL has received honoraria from Reckitt-Benckiser to present at professional development courses. LD, RB and NL have received an untied educational grant from Mundipharma for post-marketing surveillance studies of Reformulated OxyContin® (the National Opioid Medication Abuse Deterrence, or NOMAD, study). All
Acknowledgements
None.
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