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. 2019 Jan;28(1):97-105.
doi: 10.1002/pds.4683. Epub 2018 Nov 13.

Increases in controlled-release oxycodone utilisation following the subsidy of oxycodone with naloxone formulations: An Australian population-based study

Affiliations

Increases in controlled-release oxycodone utilisation following the subsidy of oxycodone with naloxone formulations: An Australian population-based study

Andrea L Schaffer et al. Pharmacoepidemiol Drug Saf. 2019 Jan.

Abstract

Purpose: Despite increasing use of oxycodone/naloxone controlled-release (CR) in Australia, little is known about how it has affected the overall oxycodone CR market since its subsidy in 2011.

Methods: We used Pharmaceutical Benefits Scheme dispensing claims (2006-2016) and interrupted time series analysis to examine changes in the quarterly rates of dispensing of oral oxycodone CR formulations (oxycodone/naloxone CR and single-ingredient oxycodone CR) and new oxycodone CR treatment episodes. We also performed a retrospective cohort study in a sample of people initiating a new oxycodone CR treatment episode in 2009, 2012/2013, and 2016 to compare opioid utilisation patterns over time.

Results: The subsidy of oxycodone/naloxone CR was associated with a 1.6-fold increase in the growth rate of oxycodone CR dispensing, resulting from rapid uptake of low strength (≤5 mg) oxycodone/naloxone CR. In our cohort of initiators, the number of new oxycodone CR treatment episodes increased 2.1-fold between 2009 and 2016; in 2016, 91.4% of new treatment episodes involved oxycodone/naloxone CR. Comparing 2016 with 2009, we observed an increase in people initiating with a tablet strength less than or equal to 5-mg (risk difference [RD] = 21.1%, 95% CI, 19.9%-22.4%) in people initiating with no other opioid dispensing 90 days prior to initiation (RD = 5.2%, 3.8%-6.6%) and with no further opioid dispensing 90 days after initiation (RD = 8.8%, 7.4%-10.2%).

Conclusions: After its subsidy, the uptake of low-dose oxycodone/naloxone CR was greater than expected if it were substituting the single-ingredient oxycodone CR, resulting in an expansion of the oxycodone CR market.

Keywords: Australia; drug utilisation; opioids; oxycodone; pharmacoepidemiology.

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Conflict of interest statement

Conflict of interest: BL and LD have received investigator-initiated untied educational grants from Reckitt Benckiser/Indivior for studies of buprenorphine-naloxone, buprenorphine depot, naloxone (LD), the development of an opioid-related behaviour scale, and a study of opioid substitution therapy uptake among chronic non-cancer pain patients. BL and LD have received an untied educational grant from Mundipharma Australia to examine the impacts of a tamper-resistant formulation of oxycodone.

Figures

Figure 1.
Figure 1.
Oxycodone CR tablets dispensed per 1,000 population per quarter, by strength and formulation Legend: Date of oxycodone/naloxone CR subsidy: December 1, 2011 (Q4 2011); date of introduction of tamper-resistant formulation and withdrawal of 5 mg single-ingredient oxycodone CR: April 1, 2014 (Q2 2014)
Figure 2.
Figure 2.
New treatment episodes with oxycodone CR, by strength and formulation among concessional beneficiaries Legend: Date of oxycodone/naloxone CR subsidy: December 1, 2011 (Q4 2011); date of introduction of tamper-resistant formulation and withdrawal of 5 mg single-ingredient oxycodone CR: April 1, 2014 (Q2 2014). 2.5 mg/1.25 mg, 15 mg/7.5 mg and 30 mg/15 mg oxycodone/naloxone CR tablets were introduced in May 2016.

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References

    1. US Food and Drug Administration. Drug@FDA: FDA Approved Drug Products. https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.... 2017. Accessed Oct 10, 2017.
    1. European Medicines Agency. Oxynal-Targin and associated names. http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/referr.... 2017. Accessed Oct 10, 2017.
    1. Health Canada. Drug Details - Drug and Health Product Register. https://hpr-rps.hres.ca/details.php?drugproductid=2247&query=targin. 2017. Accessed Oct 11, 2017.
    1. Poelaert J, Koopmans-Klein G, Dioh A, et al. Treatment with prolonged-release oxycodone/naloxone improves pain relief and opioid-induced constipation compared with prolonged-release oxycodone in patients with chronic severe pain and laxative-refractory constipation. Clin Ther. 2015;37(4):784–792. - PubMed
    1. DePriest AZ, Miller K. Oxycodone/Naloxone: role in chronic pain management, opioid-induced constipation, and abuse deterrence. Pain Ther. 2014;3(1):1–15. - PMC - PubMed

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