Neonatal Screening Program at the University Hospital of the Ribeirao Preto School of Medicine, São Paulo University, Brazil;Programa de Triagem Neonatal do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brasil

Cadernos de Saude Publica

Volumn 25, Issue 2, 2009, Pages 445-454

  Magalhães, Patrícia Künzle Ribeiro ^a   De Fátima Turcato, Marlene ^a   De Lucena Angulo, Ivan ^a   Maciel, Léa Maria Zanini ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Congenital hypothyroidism; Haernoglobinopathies; Health programs and plans; Neonatal screening; Phenylketonuria

Indexed keywords

EID: 63349108203     PISSN: 0102311X     EISSN: 16784464     Source Type: Journal    
DOI: 10.1590/s0102-311x2009000200023     Document Type: Article

References (33)

1. Guthrie R, Susi A. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics 1963; 32:338-43.
2. Carvalho TM, Santos HP, Santos IC, Vargas PR, Pedrosa J. Newborn screening: a national public health programme in Brazil. J Inherit Metab Dis 2007; 30:615.
3. Ministério da Saúde. Portaria no. 822, de 06 de junho de 2001. http://dtr2001.saude.gov.br/sas/ PORTARIAS/Port2001/GM/GM-822.htm (acessado em 19/NOV/2008).
4. Pharoah PO, Madden MP. Audit of screening for congenital hypothyroidism. Arch Dis Child 1992; 67:1073-6.
5. Pollitt RJ, Green A, McCabe CJ, Booth A, Cooper NJ, Leonard JV, et al. Neonatal screening for inborn errors of metabolism: cost, yield and outcome. Health Technol Assess 1997; 1:i-iv, 1-202.
6. LaFranchi S. Detecção neonatal de hipotireoidismo congênito: uma história de sucesso? Arq Bras Endocrinol Metab 1995; 39:80-8.
7. Loeber JG. Neonatal screening in Europe; the situation in 2004. J Inherit Metab Dis 2007; 30:430-8.
8. American Academy of Pediatrics AAP Section on Endocrinology and Committee on Genetics, American Thyroid Association Committee on Public Health. Newborn screening for congenital hypothyroidism: recommended guidelines. Pediatrics. 1993; 91:1203-9.
9. American Academy of Pediatrics, Rose SR; Section on Endocrinology and Committee on Genetics, American Thyroid Association, Brown RS; Public Health Committee, Lawson Wilkins Pediatric Endocrine Society, et al. Update of newborn screening and therapy for congenital hypothyroidism. Pediatrics 2006; 117:2290-303.
10. Bongers-Schokking JJ, Koot HM, Wiersma D, Verkerk PH, Muinck Keizer-Schrama SM. Influence of timing and dose of thyroid hormone replacement on development in infants with congenital hypothyroidism. J Pediatr 2000; 136:292-7.
11. Fisher DA. Clinical review 19: management of congenital hypothyroidism. J Clin Endocrinol Metab 1991;72:523-9.
12. Fisher DA. Physiological variations in thyroid hormones: physiological and pathophysiological considerations. ClinChem 1996; 42:135-9.
13. Grüters A, Delange F, Giovannelli G, Klett M, Rochiccioli P, Torresani T, et al. Guidelines for neonatal screening programs for congenital hypothyroidism. European Society for Pediatric Endocrinology Working Group on Congenital Hypothyroidism. Horm Res 1994; 41:1-2.
14. Simpson N, Randall R, Lenton S, Walker S. Audit of neonatal screening programme for phenylketonuria and congenital hypothyroidism. Arch Dis Child Fetal Neonatal Ed 1997; 77:F228-34.
15. Pass KA, Lane PA, Fernhoff PM, Hlnton CF, Panny SR, Parks JS, et al. US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN). J Pediatr 2000; 137(4 Suppl):S1-46.
16. França SN. Análise clínico-laboratorial dos pacientes com hipotireoidismo congênito diagnosticado pelo programa de rastreamento neonatal no Estado do Paraná [Tese de Doutorado]. Curitiba: Universidade Federal do Paraná; 1997.
17. Ramalho RJR, Ramalho ARO, Oliveira CRP, AguiarOliveira MH. Evolução do programa de triagem neonatal para o hipotireoidismo congênito e fenilcetonúria no Estado de Sergipe de 1995 a 2003. Arq Bras Endocrinol Metab 2004; 48:890-6.
18. Ramalho RJR, Valido DP, Aguiar-Oliveira MH. Avaliação do programa de triagem para o hipotireoidismo congénito no estado de Sergipe. Arq Bras Endocrinol Metab, 2000; 44:157-61.
19. Nascimento ML, Pires MMS, Nassar SM, Ruhland L. Avaliação do programa de rastreamento neonatal para hipotireoidismo congénito da Secretaria de Estado da Saúde de Santa Catarina. Arq Bras Endocrinol Metab, 2003; 47:75-81.
20. Ramos AJS, Rocha AM, Costa ADM, Benicio AVL, Ramos ALC, Silva CRA, et al. Avaliação do programa de rastreamento de doenças congênitas em Campina Grande-PB, Brasil. Arq Bras Endocrinol Metab 2003; 47:280-4.
21. Jones JH, Mackenzie J, Croft GA, Beaton S, Young D, Donaldson MD. Improvement in screening performance and diagnosis of congenital hypothyroidism in Scotland 1979-2003. Arch Dis Child 2006; 91:680-5.
22. Franco DB, Maciel RMB, Matsumura LK, Kuni IS, Furuzawa GK, Faria AM, et al. Implantação do programa de rastreamento do hipotireoidismo congénito na Fundação Hospitalar do Distrito Federal: metodologia, resultados, dificuldades e propostas: estudo comparativo com recém-natos de outros estados. Arq Bras Endocrinol Metab 1997; 41:6-13.
23. Sociedade Brasileira de Triagem Neonatal. Dados estatísticos 2002/2003. http://www.sbtn.org.br (acessado em 08/Abr/2008).
24. Dubuls JM, Glorieux J, Richer F, Deal CL, Dussault JH, van Vliet G. Outcome of severe congenital hypothyroidism: closing the developmental gap with early high dose levothyroxine treatment. J Clin Endocrinol Metab 1996; 81:222-7.
25. Fisher DA. The importance of early management in optimizing IQ in infants with congenital hypothyroidism. J Pediatr 2000; 136:273-4.
26. Toublanc JE. Guidelines for neonatal screening programs for congenital hypothyroidism. Working Group for Neonatal Screening in Paediatric Endocrinology of the European Society for Paediatric Endocrinology. Acta Paediatr Suppl 1999; 88:13-4.
27. Revised guidelines for neonatal screening programmes for primary congenital hypothyroidism. Working Group on Neonatal Screening of the European Society for Paediatric Endocrinology. Horm Res 1999; 52:49-52.
28. Olivieri A, Fazzini C, Grandolfo ME, Medda E, Stazi MA, D'Archivio M, et al. La rivalutazione della diagnosi nel'ipotiroidismo congenito. Ann Ist Super Sanita. 1999; 35:273-82.
29. Webster D, Essex C. Neonatal screening in New Zealand. BMJ 1996; 312:312.
30. Kurinczuk JJ, Bower C, Lewis B, Byrne G. Congenital hypothyroidism in Western Australia 1981-1998. J Paediatr Child Health 2002; 38:187-91.
31. Waller DK, Anderson JL, Lorey F. Cunningham GC. Risk factors for congenital hypothyroidism: an investigation of infant's birth weight, ethnicity, and gender in California, 1990-1998. Teratology 2000; 62:36-41.
32. Borrajo GJ. Newborn screening in Latin America at the beginning of the 21st century. J Inherit Metab Dis 2007; 30:466-81.
33. Farriaux JP, Vldailhet M, Briard ML, Belot V, Dhondt JL. Neonatal screening for cystic fibrosis: France rises to the challenge. J Inherit. Metab Dis 2003; 26:729-44.