A Cost-Benefit Analysis of Neonatal Screening Tests for Maple Syrup Urine Disease, Homocystinuria, Galactosemia, and Congenital Adrenal Hyperplasia
Journal of Genetic Medicine
;
: 111-118, 2008.
Artigo
em Coreano
| WPRIM
| ID: wpr-124733
ABSTRACT
PURPOSE:
Neonatal screening tests are increasingly being used forearly diagnosis of inborn errors of metabolism (IEM) in the hope of avoiding the severe developmental delay, acute illness, and death that may result from these diseases. In this study, a cost-benefit analysis was performed on the neonatal screening of maple syrup urine disease, homocystinuria, galactosemia, and congenital adrenal hyperplasia in Korea. MATERIALS ANDMETHODS:
This study included 1,259,220 Korean newborns born between January 2005 to December 2007, who were screened for maple syrup urine disease, homocystinuria, galactosemia, and congenital adrenal hyperplasia. We calculated and compared the total costs in cases where these four screening tests were implemented, and those where they were not.RESULTS:
There were no benefits to screening for maple syrup urine disease or homocystinuria due to their low prevalence for these two tests, the costs exceeded the benefits at benefitcost ratios of 0.51 and 0.61, respectively. In contrast, benefits far exceed costs at a ratio of 4.11 for galactosemia and 2.91 for congenital adrenal hyperplasia. The average benefitcost ratio for all four tests was 2.01.CONCLUSION:
Neonatal screening tests for maple syrup urine disease, homocystinuria, galactosemia, and congenital adrenal hyperplasia are financially viable.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Programas de Rastreamento
/
Prevalência
/
Triagem Neonatal
/
Análise Custo-Benefício
/
Hiperplasia Suprarrenal Congênita
/
Acer
/
Galactosemias
/
Homocistinúria
/
Coreia (Geográfico)
/
Doença da Urina de Xarope de Bordo
Tipo de estudo:
Estudo diagnóstico
/
Avaliação Econômica em Saúde
/
Estudo de prevalência
/
Estudo de rastreamento
Limite:
Humanos
/
Recém-Nascido
País/Região como assunto:
Ásia
Idioma:
Coreano
Revista:
Journal of Genetic Medicine
Ano de publicação:
2008
Tipo de documento:
Artigo
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