A US Retrospective Claims Analysis Comparing Healthcare Costs of Patients Transitioning from Immediate-Release Oxycodone to Two Different Formulations of Extended-Release Oxycodone: Xtampza ER or OxyContin.
abuse-deterrent
chronic pain
cost
long-acting
opioids
short-acting
Journal
ClinicoEconomics and outcomes research : CEOR
ISSN: 1178-6981
Titre abrégé: Clinicoecon Outcomes Res
Pays: New Zealand
ID NLM: 101560564
Informations de publication
Date de publication:
2022
2022
Historique:
received:
01
10
2021
accepted:
23
02
2022
entrez:
10
3
2022
pubmed:
11
3
2022
medline:
11
3
2022
Statut:
epublish
Résumé
Opioid therapy for managing chronic pain remains a challenge, as providers must weigh the medical benefit to the patient with the risk of adverse events. Manipulation of many extended-release (ER) opioid formulations may lead to increased serious medical outcomes or death. The economic burden of opioid use disorders due to opioid misuse and abuse may vary depending on which abuse deterrent opioid formulation is prescribed. The study aimed to compare demographic and clinical characteristics and healthcare costs of chronic pain patients treated with two different abuse-deterrent opioid formulations, Xtampza ER and reformulated OxyContin. The source of data was IBM After applying selection criteria, 464 patients were observed in the Xtampza ER cohort versus 1927 patients in the OxyContin cohort. In unmatched patients, ER opioid costs were lower for Xtampza ER than OxyContin ($2645 vs $3141; This study suggests that Xtampza ER may result in lower healthcare costs than OxyContin for a population of chronic pain patients switching from immediate release oxycodone based on real-world data.
Identifiants
pubmed: 35264862
doi: 10.2147/CEOR.S340290
pii: 340290
pmc: PMC8901186
doi:
Types de publication
Journal Article
Langues
eng
Pagination
119-128Informations de copyright
© 2022 Olatoke et al.
Déclaration de conflit d'intérêts
OO, VZ, FS, DV, and PY are employees of ZRx Outcomes Research. VZ reports grants and/or personal fees from Glympse Bio, HutchMed Pharmaceuticals, Endo Pharmaceuticals, Stealth Biotherapeutics, RedHill Pharmaceuticals, and Collegium Pharmaceuticals, outside the submitted work. FS reports grants from Collegium Pharmaceutical Inc., during the conduct of the study. DV reports grants from Collegium Pharmaceutical, Inc., during the conduct of the study. CT, MKDG, and SP are employees of Collegium Pharmaceutical, Inc. The authors’ competing interests had no influence on study design, interpretation of the results or impose a censoring of the obtained results. The authors declare no other competing interest.
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