Literature DB >> 23506540

Adherence to dornase alfa treatment among commercially insured patients with cystic fibrosis.

Samya Z Nasr1, Will Chou, Kathleen F Villa, Eunice Chang, Michael S Broder.   

Abstract

OBJECTIVE: To investigate adherence to dornase alfa therapy among commercially-insured patients with cystic fibrosis (CF) and to examine the impact of adherence on health and economic outcomes.
METHODS: This retrospective cohort analysis included CF patients with ≥1 dornase alfa (Pulmozyme) pharmacy claim between 1 October 2006 and 30 September 2008 and with continuous enrollment in the health insurance plan at least 1 year before and 1 year after their index dornase alfa claim. Adherence was measured with the medication possession ratio (MPR). Multivariate models were used to estimate the relationship between adherence and exacerbations, utilization, and cost.
RESULTS: Nine hundred and seven patients met the inclusion criteria. The mean age was 19.5 years (SD = 11.5) and 49.1% were female. Overall MPR was 0.59 and by age was 0.66 for patients of 5-12 years, 0.57 for 13-20 years, 0.54 for 21-30 years, and 0.56 for patients ≥31 years. Adherence was better in fall and winter than in spring and summer. There was no statistically significant difference in the proportion of patients with inpatient respiratory exacerbations across groups with low (<0.5), moderate (0.5-0.79), and high (≥0.8) adherence (24.5%, 22.3%, and 19.1%, respectively, p = 0.250). There was a trend toward higher total charges in more-adherent patients (mean $58,612 in the least-adherent group and mean $69,427 in the most adherent group, p = 0.107). In multivariate models, MPR was not significantly associated with the risk of inpatient respiratory exacerbations (hazard ratio = 1.16 for MPR <0.5 vs ≥0.8; 95% CI = 0.83-1.61). LIMITATIONS: Study data were derived from insurance claims; adherence measures were based on prescription fills, not observed medication use.
CONCLUSION: Adherence to dornase alfa was generally low, but varied by age and season. Adherence was not found to be significantly associated with respiratory exacerbations or total charges, but was associated with shorter hospital length of stay.

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Year:  2013        PMID: 23506540     DOI: 10.3111/13696998.2013.787427

Source DB:  PubMed          Journal:  J Med Econ        ISSN: 1369-6998            Impact factor:   2.448


  11 in total

1.  Motivating adherence among adolescents with cystic fibrosis: youth and parent perspectives.

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Journal:  Pediatr Pulmonol       Date:  2014-03-10

2.  Medication beliefs mediate between depressive symptoms and medication adherence in cystic fibrosis.

Authors:  Marisa E Hilliard; Michelle N Eakin; Belinda Borrelli; Angela Green; Kristin A Riekert
Journal:  Health Psychol       Date:  2014-08-11       Impact factor: 4.267

3.  Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftor.

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Review 4.  The impact of medication adherence on lung health outcomes in cystic fibrosis.

Authors:  Michelle N Eakin; Kristin A Riekert
Journal:  Curr Opin Pulm Med       Date:  2013-11       Impact factor: 3.155

5.  Delphi poll to assess consensus on issues influencing long-term adherence to treatments in cystic fibrosis among Italian health care professionals.

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6.  Outcome evaluation of a pharmacy-based therapy management program for patients with cystic fibrosis.

Authors:  Heather S Kirkham; Francis Staskon; Nishita Hira; Darren McLane; Karl M Kilgore; Alexis Parente; Seung Kim; Gregory S Sawicki
Journal:  Pediatr Pulmonol       Date:  2018-03-07

7.  A pragmatic behavior-based habit index for adherence to nebulized treatments among adults with cystic fibrosis.

Authors:  Zhe Hui Hoo; Martin J Wildman; Michael J Campbell; Stephen J Walters; Benjamin Gardner
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8.  Adherence to long-term therapies in cystic fibrosis: a French cross-sectional study linking prescribing, dispensing, and hospitalization data.

Authors:  Héloïse Rouzé; Marie Viprey; Samuel Allemann; Alexandra L Dima; Pascal Caillet; Angélique Denis; Stéphanie Poupon-Bourdy; Boubou Camara; Catherine Llerena; Philippe Reix; Isabelle Durieu; Quitterie Reynaud; Sandrine Touzet
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Review 9.  Cystic Fibrosis Lung Disease Modifiers and Their Relevance in the New Era of Precision Medicine.

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Review 10.  Update on key emerging challenges in cystic fibrosis.

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Journal:  Med Princ Pract       Date:  2014-01-10       Impact factor: 1.927

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