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Association of Prior Authorization and Out-of-pocket Costs With Patient Access to PCSK9 Inhibitor Therapy.
Navar, Ann Marie; Taylor, Benjamin; Mulder, Hillary; Fievitz, Eugene; Monda, Keri L; Fievitz, Anna; Maya, Juan F; López, J Antonio G; Peterson, Eric D.
Afiliação
  • Navar AM; Duke Clinical Research Institute, Durham, North Carolina.
  • Taylor B; Amgen Inc, Thousand Oaks, California.
  • Mulder H; Duke Clinical Research Institute, Durham, North Carolina.
  • Fievitz E; Symphony Health, Phoenix, Arizona.
  • Monda KL; Amgen Inc, Thousand Oaks, California.
  • Fievitz A; Symphony Health, Phoenix, Arizona.
  • Maya JF; Amgen Inc, Thousand Oaks, California.
  • López JAG; Amgen Inc, Thousand Oaks, California.
  • Peterson ED; Duke Clinical Research Institute, Durham, North Carolina.
JAMA Cardiol ; 2(11): 1217-1225, 2017 11 01.
Article em En | MEDLINE | ID: mdl-28973087
Importance: Although PCSK9 inhibitors (PCSK9i) were approved in 2015, their high cost has led to strict prior authorization practices and high copays, and use of PSCK9i in clinical practice has been low. Objective: To evaluate patient access to PCSK9i among those prescribed therapy. Design, Setting, and Participants: Using pharmacy transaction data, we evaluated 45 029 patients who were newly prescribed PCSK9i in the United States between August 1, 2015, and July 31, 2016. Main Outcomes and Measures: The proportion of PCSK9i prescriptions approved and abandoned (approved but unfilled); multivariable analyses examined factors associated with approval/abandonment including payor, prescriber specialty, pharmacy benefit manager, out-of-pocket cost (copay), clinical diagnoses, lipid-lowering medication use, and low-density lipoprotein cholesterol levels. Results: Of patients given an incident PCSK9i prescription, 51.2% were women, 56.6% were 65 years or older, and 52.5% had governmental insurance. Of the patients given a prescription, 20.8% received approval on the first day, and 47.2% ever received approval. Of those approved, 65.3% filled the prescription, resulting in 30.9% of those prescribed PCSK9i ever receiving therapy. After adjustment, patients who were older, male, and had atherosclerotic cardiovascular disease were more likely to be approved, but approval rates did not vary by patient low-density lipoprotein cholesterol level nor statin use. Other factors associated with drug approval included having government vs commercial insurance (odds ratio [OR], 3.3; 95% CI, 2.8-3.8), and those filled at a specialty vs retail pharmacy (OR, 1.96; 95% CI, 1.66-2.33). Approval rates varied nearly 3-fold among the top 10 largest pharmacy benefit managers. Prescription abandonment by patients was most associated with copay costs (C statistic, 0.86); with abandonment rates ranging from 7.5% for those with $0 copay to more than 75% for copays greater than $350. Conclusions and Relevance: In the first year of availability, only half of patients prescribed a PCSK9i received approval, and one-third of approved prescriptions were never filled owing to copay.
Assuntos

Texto completo: 1 Temas: ECOS / Aspectos_gerais / Financiamentos_gastos Bases de dados: MEDLINE Assunto principal: Custo Compartilhado de Seguro / Gastos em Saúde / Aterosclerose / Autorização Prévia / Hipercolesterolemia / Anticorpos Monoclonais / Anticolesterolemiantes Tipo de estudo: Etiology_studies / Health_economic_evaluation / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: JAMA Cardiol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Temas: ECOS / Aspectos_gerais / Financiamentos_gastos Bases de dados: MEDLINE Assunto principal: Custo Compartilhado de Seguro / Gastos em Saúde / Aterosclerose / Autorização Prévia / Hipercolesterolemia / Anticorpos Monoclonais / Anticolesterolemiantes Tipo de estudo: Etiology_studies / Health_economic_evaluation / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: JAMA Cardiol Ano de publicação: 2017 Tipo de documento: Article