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1.
Mol Genet Metab ; 113(1-2): 42-5, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25174966

RESUMEN

The aim of our study was to assess the current state of newborn screening (NBS) in the region of southeastern Europe, as an example of a developing region, focusing also on future plans. Responses were obtained from 11 countries. Phenylketonuria screening was not introduced in four of 11 countries, while congenital hypothyroidism screening was not introduced in three of them; extended NBS programs were non-existent. The primary challenges were identified. Implementation of NBS to developing countries worldwide should be considered as a priority.


Asunto(s)
Enfermedades Genéticas Congénitas/diagnóstico , Tamizaje Neonatal , Hipotiroidismo Congénito/diagnóstico , Hipotiroidismo Congénito/epidemiología , Europa (Continente) , Enfermedades Genéticas Congénitas/epidemiología , Humanos , Recién Nacido , Tamizaje Masivo/economía , Tamizaje Masivo/métodos , Tamizaje Neonatal/economía , Tamizaje Neonatal/métodos , Fenilcetonurias/diagnóstico , Fenilcetonurias/epidemiología
2.
Orphanet J Rare Dis ; 10: 68, 2015 May 30.
Artículo en Inglés | MEDLINE | ID: mdl-26025111

RESUMEN

BACKGROUND: We aimed to assess the current state of PKU screening and management in the region of southeastern Europe. METHODS: A survey was performed involving all identified professionals responsible for the PKU management in the 11 countries from South-Eastern region of Europe (Albania, Bulgaria, Bosnia and Herzegovina, Croatia, Kosovo, Macedonia, Moldova, Montenegro, Romania, Serbia, Slovenia). The questionnaire was designed to assess the characteristics regarding PKU management in three main areas: nation-wide characteristics, PKU screening, and characteristics of the PKU management in the responding centre. It consisted of 56 questions. The distribution and collection of the questionnaires (via e-mail) was taking place from December 2013 to March 2014. RESULTS: Responses from participants from 11 countries were included; the countries cumulative population is approx. 52.5 mio. PKU screening was not yet introduced in 4 of 11 countries. Reported PKU incidences ranged from 1/7325 to 1/39338 (and were not known for 5 countries). National PKU guidelines existed in 5 of 11 countries and 7 of 11 countries had PKU registry (registries included 40 to 194 patients). The number of PKU centers in each country varied from 1 to 6. Routine genetic diagnostics was reported in 4 of 11 countries. Most commonly used laboratory method to assess phenylalanine levels was fluorometric. Tetrahydrobiopterine was used in only 2 of 11 countries. Most frequently, pediatricians were caring for the patients. Dietitian was a member of PKU team in only 4 of 11 countries, while regular psychological assessments were performed in 6 of 11 countries. Patient's PKU society existed in 7 of 11 countries. CONCLUSIONS: The region of southeastern Europe was facing certain important challenges of PKU screening and management. Neonatal PKU screening should be introduced throughout the region. Furthermore, PKU management was falling behind internationally established standards-of-care in many aspects.


Asunto(s)
Fenilcetonurias/diagnóstico , Adulto , Anciano , Anciano de 80 o más Años , Manejo de la Enfermedad , Europa (Continente) , Femenino , Humanos , Masculino , Persona de Mediana Edad , Fenilcetonurias/epidemiología , Encuestas y Cuestionarios , Adulto Joven
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