The Italian screening programfor primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance

A. Cassio, C. Corbetta, I. Antonozzi, F. Calaciura, U. Caruso, G. Cesaretti, R. Gastaldi, E. Medda, F. Mosca, E. Pasquini, M. C. Salerno, V. Stoppioni, M. Tonacchera, G. Weber, A. Olivieri

Research output: Contribution to journalArticle

Abstract

ABSTRACT. The Italian screening program for primary congenital hypothyroidism (CH) is an integrated system including neonatal screening, diagnosis, treatment, follow-up, and nationwide surveillance of the disease. The aim of the Italian screening program for CH is to identify not only babies with severe permanent CH (core target), but also babies with mild persistent and transient forms of CH who could have a benefit from an early replacement therapy (secondary target). In the last years, despite the important results obtained in terms of standardization of screening and follow-up procedures, it has become clear the need of optimizing the program in order to harmonize the screening strategy and the screening procedures among Regions, and to improve the diagnostic and therapeutic approach in all affected infants. On the basis of available guidelines, the experience of the Italian screening and clinical reference centers, and the knowledge derived from the nation-wide surveillance activity performed by the Italian National Registry of Infants with CH, the Italian Society for Pediatric Endocrinology and Diabetology together with the Italian Society for the Study of Metabolic Diseases and Neonatal Screening and the Italian National Institute of Health promoted actions aimed at improving diagnosis, treatment, follow-up and surveillance of CH in our country. In this paper the most important actions to improve the Italian screening program for CH are described.

Original languageEnglish
Pages (from-to)195-203
Number of pages9
JournalJournal of Endocrinological Investigation
Volume36
Issue number3
DOIs
Publication statusPublished - Mar 2013

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Keywords

  • Congenital hypothyroidism
  • Diagnosis
  • Follow-up
  • Neonatal screening
  • Surveillance

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Cite this

Cassio, A., Corbetta, C., Antonozzi, I., Calaciura, F., Caruso, U., Cesaretti, G., Gastaldi, R., Medda, E., Mosca, F., Pasquini, E., Salerno, M. C., Stoppioni, V., Tonacchera, M., Weber, G., & Olivieri, A. (2013). The Italian screening programfor primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance. Journal of Endocrinological Investigation, 36(3), 195-203. https://doi.org/10.3275/8849