Cost-Effectiveness/Cost-Benefit Analysis of Newborn Screening for Severe Combined Immune Deficiency in Washington State
- PMID: 26876279
- PMCID: PMC4846488
- DOI: 10.1016/j.jpeds.2016.01.029
Cost-Effectiveness/Cost-Benefit Analysis of Newborn Screening for Severe Combined Immune Deficiency in Washington State
Abstract
Objective: To evaluate the expected cost-effectiveness and net benefit of the recent implementation of newborn screening (NBS) for severe combined immunodeficiency (SCID) in Washington State.
Study design: We constructed a decision analysis model to estimate the costs and benefits of NBS in an annual birth cohort of 86 600 infants based on projections of avoided infant deaths. Point estimates and ranges for input variables, including the birth prevalence of SCID, proportion detected asymptomatically without screening through family history, screening test characteristics, survival rates, and costs of screening, diagnosis, and treatment were derived from published estimates, expert opinion, and the Washington NBS program. We estimated treatment costs stratified by age of identification and SCID type (with or without adenosine deaminase deficiency). Economic benefit was estimated using values of $4.2 and $9.0 million per death averted. We performed sensitivity analyses to evaluate the influence of key variables on the incremental cost-effectiveness ratio (ICER) of net direct cost per life-year saved.
Results: Our model predicts an additional 1.19 newborn infants with SCID detected preclinically through screening, in addition to those who would have been detected early through family history, and 0.40 deaths averted annually. Our base-case model suggests an ICER of $35 311 per life-year saved, and a benefit-cost ratio of either 5.31 or 2.71. Sensitivity analyses found ICER values <$100 000 and positive net benefit for plausible assumptions on all variables.
Conclusions: Our model suggests that NBS for SCID in Washington is likely to be cost-effective and to show positive net economic benefit.
Published by Elsevier Inc.
Figures


Similar articles
-
The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience.Milbank Q. 2016 Jun;94(2):366-91. doi: 10.1111/1468-0009.12196. Milbank Q. 2016. PMID: 27265561 Free PMC article.
-
A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID).Mol Genet Metab. 2011 Nov;104(3):383-9. doi: 10.1016/j.ymgme.2011.07.007. Epub 2011 Jul 12. Mol Genet Metab. 2011. PMID: 21810544 Free PMC article.
-
Cost-effectiveness of newborn screening for severe combined immunodeficiency.Eur J Pediatr. 2019 May;178(5):721-729. doi: 10.1007/s00431-019-03346-3. Epub 2019 Feb 25. Eur J Pediatr. 2019. PMID: 30805731
-
Newborn screening for severe combined immune deficiency (technical and political aspects).Curr Opin Allergy Clin Immunol. 2015 Dec;15(6):539-46. doi: 10.1097/ACI.0000000000000221. Curr Opin Allergy Clin Immunol. 2015. PMID: 26485096 Review.
-
Neonatal screening for inborn errors of metabolism: cost, yield and outcome.Health Technol Assess. 1997;1(7):i-iv, 1-202. Health Technol Assess. 1997. PMID: 9483160 Review.
Cited by
-
Genomic-Based Newborn Screening for Inborn Errors of Immunity: Practical and Ethical Considerations.Int J Neonatal Screen. 2023 Apr 11;9(2):22. doi: 10.3390/ijns9020022. Int J Neonatal Screen. 2023. PMID: 37092516 Free PMC article.
-
Using Decision Analysis to Support Newborn Screening Policy Decisions: A Case Study for Pompe Disease.MDM Policy Pract. 2018 Jan-Jun;3(1):2381468318763814. doi: 10.1177/2381468318763814. Epub 2018 Apr 18. MDM Policy Pract. 2018. PMID: 30123835 Free PMC article.
-
The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience.Milbank Q. 2016 Jun;94(2):366-91. doi: 10.1111/1468-0009.12196. Milbank Q. 2016. PMID: 27265561 Free PMC article.
-
A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency-An Ontario Single-Centre Experience Spanning 2013-2023.Genes (Basel). 2024 Jul 15;15(7):920. doi: 10.3390/genes15070920. Genes (Basel). 2024. PMID: 39062699 Free PMC article.
-
Rare Disease, Advocacy and Justice: Intersecting Disparities in Research and Clinical Care.Am J Bioeth. 2023 Jul;23(7):17-26. doi: 10.1080/15265161.2023.2207500. Epub 2023 May 19. Am J Bioeth. 2023. PMID: 37204146 Free PMC article.
References
-
- Puck JM. Population-based newborn screening for severe combined immunodeficiency: steps toward implementation. J Allergy Clin Immunol. 2007;120:760–8. - PubMed
-
- Adeli MM, Buckley RH. Why newborn screening for severe combined immunodeficiency is essential: a case report. Pediatrics. 2010;126:e465–9. - PubMed
-
- Brown L, Xu-Bayford J, Allwood Z, Slatter M, Cant A, Davies EG, et al. Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening. Blood. 2011;117:3243–6. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous