Increases in controlled-release oxycodone utilisation following the subsidy of oxycodone with naloxone formulations: An Australian population-based study.
Administration, Oral
Adult
Aged
Aged, 80 and over
Analgesics, Opioid
/ administration & dosage
Australia
Chronic Pain
/ diagnosis
Delayed-Action Preparations
/ administration & dosage
Dose-Response Relationship, Drug
Drug Combinations
Drug Utilization
/ statistics & numerical data
Female
Humans
Interrupted Time Series Analysis
Male
Middle Aged
Naloxone
/ administration & dosage
Narcotic Antagonists
/ administration & dosage
Oxycodone
/ administration & dosage
Practice Patterns, Physicians'
/ statistics & numerical data
Retrospective Studies
Severity of Illness Index
Substance-Related Disorders
/ etiology
Australia
drug utilisation
opioids
oxycodone
pharmacoepidemiology
Journal
Pharmacoepidemiology and drug safety
ISSN: 1099-1557
Titre abrégé: Pharmacoepidemiol Drug Saf
Pays: England
ID NLM: 9208369
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
18
06
2018
revised:
21
08
2018
accepted:
03
09
2018
pubmed:
14
11
2018
medline:
25
2
2020
entrez:
14
11
2018
Statut:
ppublish
Résumé
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. 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. 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%). 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.
Identifiants
pubmed: 30421838
doi: 10.1002/pds.4683
pmc: PMC6687879
mid: NIHMS1037302
doi:
Substances chimiques
Analgesics, Opioid
0
Delayed-Action Preparations
0
Drug Combinations
0
Narcotic Antagonists
0
Naloxone
36B82AMQ7N
Oxycodone
CD35PMG570
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
97-105Subventions
Organisme : NIDA NIH HHS
ID : R01 DA044170
Pays : United States
Informations de copyright
© 2018 John Wiley & Sons, Ltd.
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