Literature DB >> 30666534

Cost Effectiveness of Inhaled Mannitol (Bronchitol®) in Patients with Cystic Fibrosis.

Emma Warren1, Kristen Morgan2, Toby J Toward2,3, Matthias Schwenkglenks4, Joanna Leadbetter2.   

Abstract

BACKGROUND: Inhaled mannitol (Bronchitol®) is licensed in Australia as a safe and efficacious addition to best supportive care in patients with cystic fibrosis.
OBJECTIVE: The objective of this study was to assess the cost effectiveness of inhaled mannitol (in addition to best supportive care) in the Australian setting from the perspective of a government-funded national healthcare system.
METHODS: A probabilistic patient-level simulation Markov model estimated life-time costs and outcomes of mannitol when added to best supportive care, compared with best supportive care alone in patients aged 6 years and older. We estimated treatment-related inputs (initial change in percentage of predicted forced expiratory volume, relative reduction in severe pulmonary exacerbations, and treatment discontinuations) from two phase III trials. Longer term natural history rates of predicted forced expiratory volume decline over time and severe pulmonary exacerbation rates for best supportive care were taken from Australian CF registries. The utility value for the cystic fibrosis health state was as measured in the trials using the Health Utility Index, whereas the impact of pulmonary exacerbations and lung transplantation on utility was ascertained from the published literature. The underlying cost of managing cystic fibrosis, and the cost associated with pulmonary exacerbations and transplantations was taken from published Australian sources.
RESULTS: The addition of inhaled mannitol to best supportive care resulted in a discounted cost per quality-adjusted life-year of AU$39,165. The result was robust with 77% of probabilistic sensitivity analysis samples below a willingness-to-pay threshold of AU$45,000/quality-adjusted life-year.
CONCLUSION: Benchmarked against an implicit Australian willingness-to-pay threshold for life-threatening diseases, our model suggests inhaled mannitol provides a cost-effective addition to best supportive care in patients with cystic fibrosis, irrespective of concomitant dornase alfa use.

Entities:  

Year:  2019        PMID: 30666534     DOI: 10.1007/s40273-019-00767-8

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  29 in total

1.  Assessment of quality of life in lung transplantation using a simple generic tool.

Authors:  A C Anyanwu; A McGuire; C A Rogers; A J Murday
Journal:  Thorax       Date:  2001-03       Impact factor: 9.139

2.  rhDNase therapy for the treatment of cystic fibrosis patients with mild to moderate lung disease.

Authors:  F Christopher; D Chase; K Stein; R Milne
Journal:  J Clin Pharm Ther       Date:  1999-12       Impact factor: 2.512

3.  Use of a preference-based measure of health (EQ-5D) in COPD and asthma.

Authors:  A Simon Pickard; Caitlyn Wilke; Eunmi Jung; Sneh Patel; Knut Stavem; Todd A Lee
Journal:  Respir Med       Date:  2008-01-03       Impact factor: 3.415

4.  Clinical Characteristics and Predictors of Reduced Survival for Adult-diagnosed Cystic Fibrosis. Analysis of the Canadian CF Registry.

Authors:  Sameer Desai; Hubert Wong; Jenna Sykes; Anne L Stephenson; Joel Singer; Bradley S Quon
Journal:  Ann Am Thorac Soc       Date:  2018-10

5.  Estimating the Reference Incremental Cost-Effectiveness Ratio for the Australian Health System.

Authors:  Laura Catherine Edney; Hossein Haji Ali Afzali; Terence Chai Cheng; Jonathan Karnon
Journal:  Pharmacoeconomics       Date:  2018-02       Impact factor: 4.981

6.  Pooled analysis of two large randomised phase III inhaled mannitol studies in cystic fibrosis.

Authors:  Diana Bilton; Gabriel Bellon; Brett Charlton; Peter Cooper; Kris De Boeck; Patrick A Flume; Howard G Fox; Charles G Gallagher; David E Geller; Eric G Haarman; Helge U Hebestreit; John Kolbe; Allen Lapey; Phil Robinson; Jian Wu; Jonathan B Zuckerman; Moira L Aitken
Journal:  J Cyst Fibros       Date:  2012-12-09       Impact factor: 5.482

7.  The cost-effectiveness of palivizumab in infants with cystic fibrosis in the Canadian setting: A decision analysis model.

Authors:  Ashleigh A McGirr; Kevin L Schwartz; Upton Allen; Melinda Solomon; Beate Sander
Journal:  Hum Vaccin Immunother       Date:  2016-10-21       Impact factor: 3.452

Review 8.  Ivacaftor for the treatment of patients with cystic fibrosis and the G551D mutation: a systematic review and cost-effectiveness analysis.

Authors:  Penny Whiting; Maiwenn Al; Laura Burgers; Marie Westwood; Steve Ryder; Martine Hoogendoorn; Nigel Armstrong; Alex Allen; Hans Severens; Jos Kleijnen
Journal:  Health Technol Assess       Date:  2014-03       Impact factor: 4.014

Review 9.  Colistimethate sodium powder and tobramycin powder for inhalation for the treatment of chronic Pseudomonas aeruginosa lung infection in cystic fibrosis: systematic review and economic model.

Authors:  P Tappenden; S Harnan; L Uttley; M Mildred; C Carroll; A Cantrell
Journal:  Health Technol Assess       Date:  2013-12       Impact factor: 4.014

10.  Inspiratory flows and volumes in subjects with cystic fibrosis using a new dry powder inhaler device.

Authors:  Mark R Elkins; Philip Robinson; Sandra D Anderson; Clare P Perry; Evangelia Daviskas; Brett Charlton
Journal:  Open Respir Med J       Date:  2014-01-24
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