Literature DB >> 24238947

Cost effectiveness of newborn screening for cystic fibrosis: a simulation study.

L Nshimyumukiza1, A Bois2, P Daigneault3, L Lands4, A-M Laberge5, D Fournier2, J Duplantie1, Y Giguère6, J Gekas3, C Gagné2, F Rousseau6, D Reinharz1.   

Abstract

BACKGROUND: Early detection of cystic fibrosis (CF) by newborn screening (NBS) reduces the rate of avoidable complications. NBS protocols vary by jurisdiction and the cost effectiveness of these different protocols is debated.
OBJECTIVE: To compare the cost effectiveness of various CF NBS options.
METHODS: A Markov model was built to simulate the cost effectiveness of various CF-NBS options for a hypothetical CF-NBS program over a 5-year time horizon assuming its integration into an existing universal NBS program. NBS simulated options were based on a combination of tests between the two commonly used immunoreactive trypsinogen (IRT) cutoffs (96th percentile and 99.5th percentile) as first tier tests, and, as a second tier test, either a second IRT, pancreatic-associated protein (PAP) or CFTR mutation panels. CFTR mutation panels were also considered as an eventual third tier test. Data input parameters used were retrieved from a thorough literature search. Outcomes considered were the direct costs borne by the Quebec public health care system and the number of cases of CF detected through each strategy, including the absence of screening option.
RESULTS: IRT-PAP with an IRT cutoff at the 96th percentile is the most favorable option with a ratio of CAD$28,432 per CF case detected. The next most favorable alternative is the IRT1-IRT2 option with an IRT1 cutoff at the 96th percentile. The no-screening option is dominated by all NBS screening protocols considered. Results were robust in sensitivity analyses.
CONCLUSION: This study suggests that NBS for cystic fibrosis is a cost-effective strategy compared to the absence of NBS. The IRT-PAP newborn screening algorithm with an IRT cutoff at the 96th percentile is the most cost effective NBS approach for Quebec.
© 2013. Published by Elsevier B.V. on behalf of European Cystic Fibrosis Society. All rights reserved.

Entities:  

Keywords:  CFTR; Cost effectiveness; Cystic fibrosis; Immune-reactive trypsinogen (IRT); Newborn screening; Pancreatic-associated protein (PAP); Simulation

Mesh:

Substances:

Year:  2013        PMID: 24238947     DOI: 10.1016/j.jcf.2013.10.012

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  4 in total

1.  The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience.

Authors:  Scott D Grosse; John D Thompson; Yao Ding; Michael Glass
Journal:  Milbank Q       Date:  2016-06       Impact factor: 4.911

2.  Innovative assessment of inpatient and pulmonary drug costs for children with cystic fibrosis.

Authors:  Joseph F Levy; Marjorie A Rosenberg; Philip M Farrell
Journal:  Pediatr Pulmonol       Date:  2016-10-14

Review 3.  Early Diagnosis and Intervention in Cystic Fibrosis: Imagining the Unimaginable.

Authors:  Andrea M Coverstone; Thomas W Ferkol
Journal:  Front Pediatr       Date:  2021-01-11       Impact factor: 3.418

4.  Showing Value in Newborn Screening: Challenges in Quantifying the Effectiveness and Cost-Effectiveness of Early Detection of Phenylketonuria and Cystic Fibrosis.

Authors:  Scott D Grosse
Journal:  Healthcare (Basel)       Date:  2015-11-11
  4 in total

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