Retrospective Analysis of Medication Utilization and Clinical Outcomes in Patients With Idiopathic Pulmonary Fibrosis Treated With Nintedanib or Pirfenidone
Autor: | Melanie Radi, Francis Staskon, Richard T. Miller, Anastasia Y Ipatova, Pamela H. Koerner |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Pulmonary and Respiratory Medicine
medicine.medical_specialty lcsh:Diseases of the circulatory (Cardiovascular) system pulmonary Gastroenterology chemistry.chemical_compound Idiopathic pulmonary fibrosis Interstitial tissue Internal medicine Retrospective analysis nintedanib Medicine In patient Respiratory system Original Research lcsh:RC705-779 business.industry Pirfenidone lcsh:Diseases of the respiratory system medicine.disease respiratory chemistry Lung disease lcsh:RC666-701 idiopathic Nintedanib pirfenidone Cardiology and Cardiovascular Medicine business medicine.drug |
Zdroj: | Clinical Medicine Insights. Circulatory, Respiratory and Pulmonary Medicine Clinical Medicine Insights: Circulatory, Respiratory and Pulmonary Medicine, Vol 13 (2019) |
ISSN: | 1179-5484 |
Popis: | Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease which results in thickening and scarring of the interstitial tissue. As the only 2 Food and Drug Administration (FDA)-approved medications on the market, it is valuable to compare the impact of nintedanib and pirfenidone on clinical outcomes. Records of patients who started nintedanib or pirfenidone between calendar years 2015 and 2016 at a national specialty pharmacy were retrospectively reviewed. Data collection was derived from patient management applications and statistical data analysis was completed in SAS (SAS Institute Inc®). The nintedanib population contained 2605 patients and of the population completing clinical assessment surveys (n = 1343), 46% of respondents (n = 612) reported no adverse events, with the remaining 54% reporting at least 1 adverse event. Average proportion of days covered (PDC) was 84.2% (SD = 17.0). Average final monthly copay for this group was $235. The pirfenidone population had 1322 patients, and of the surveyed population (n = 764), 58% of respondents (n = 445) reported no adverse events, with the remaining 42% reporting at least 1 adverse event. Average PDC was 83.4% (SD = 17.3). Average final monthly copay for this group was $339. Outcomes in the studied IPF population were similar for nintedanib and pirfenidone. |
Databáze: | OpenAIRE |
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