Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros












Base de datos
Intervalo de año de publicación
1.
Endocrinol Diabetes Nutr (Engl Ed) ; 67(1): 61-69, 2020 Jan.
Artículo en Inglés, Español | MEDLINE | ID: mdl-30962160

RESUMEN

Although iodine nutrition in Spain has improved in recent years, the problem is not completely resolved. It is necessary that health institutions establish measures to ensure an adequate iodine nutrition of the population, especially among the highest risk groups (children and adolescents, women of childbearing age, pregnant women and nursing mothers). A low salt intake should be advised, but it should be iodized. It is also imperative that food control agencies establish effective control over adequate iodization of salt. Indicators on iodine nutrition should be included in future health surveys. The EUthyroid study and the Krakow Declaration on iodine nutrition provide an opportunity to set up a pan-European plan for the prevention of iodine deficiency that should be considered and used by health authorities.


Asunto(s)
Yodo/administración & dosificación , Yodo/deficiencia , Cloruro de Sodio Dietético/administración & dosificación , Adolescente , Factores de Edad , Animales , Niño , Preescolar , Europa (Continente) , Femenino , Humanos , Lactante , Recién Nacido , Lactancia , Leche/química , Embarazo , Ingesta Diaria Recomendada/legislación & jurisprudencia , España/epidemiología
2.
An Pediatr (Engl Ed) ; 90(4): 250.e1-250.e8, 2019 Apr.
Artículo en Español | MEDLINE | ID: mdl-30686624

RESUMEN

The screening program of congenital hypothyroidism (CH) is probably one of the best achievements in paediatrics. Thyroid hormones are essential for brain development and brain maturation that continue through the neonatal period. Hypothyroidism that begins in the first months of life causes irreversible damage to the central nervous system, and is one of the most frequent and preventable causes of mental retardation. As children with congenital hypothyroidism are born with a normal appearance, analytical studies are required to immediately start the appropriate therapy. This article analyses the aims, diagnostic procedures, tests required, aetiology, and differential diagnosis in this disorder. Especially relevant is to perform frequent monitoring to ensure dose adjustments of L-Thyroxine therapy, avoiding infra- or supra-dosing that negatively affects neurosensory functions. Re-evaluation of the aetiology permanent vs transient hypothyroidism is always recommended after 3years of chronological age. The relevance of this screening program should be widely discussed in paediatrics. The main objective is to avoid cerebral damage in these patients, and has been highly successful and economically beneficial. Other aspects are required to optimise patient outcomes, to perform all the controls according to the recommendations and to include, in the near future, the diagnosis of central hypothyroidism. Implementation of this program is necessary to progress in accordance with current scientific knowledge.


Asunto(s)
Hipotiroidismo Congénito/diagnóstico , Tamizaje Neonatal/métodos , Hormonas Tiroideas/análisis , Cuidados Posteriores/métodos , Preescolar , Hipotiroidismo Congénito/complicaciones , Hipotiroidismo Congénito/terapia , Diagnóstico Diferencial , Humanos , Lactante , Recién Nacido
3.
An Pediatr (Engl Ed) ; 89(4): 254.e1-254.e7, 2018 Oct.
Artículo en Español | MEDLINE | ID: mdl-30177500

RESUMEN

The objective of this document is to review the current recommendations in the management of the foetus and the newborn child born to mothers with autoimmune thyroid disease. In 2017, the American Thyroid Association published guidelines for the diagnosis and management of thyroid disease during pregnancy and post-partum. In this guide, 97 recommendations were made, and an algorithm for the diagnosis and treatment of gestational hypothyroidism was proposed. Also, in this last year, a wide review was been published on the foetal and neonatal approach of the child of a mother with Graves' disease. The importance of the determination of maternal antibodies against thyrotropin receptor in the second half of pregnancy is stressed, in order to adequately stratify the risk in the neonate.


Asunto(s)
Enfermedades Autoinmunes , Enfermedades Fetales/diagnóstico , Enfermedades Fetales/terapia , Enfermedades del Recién Nacido/diagnóstico , Enfermedades del Recién Nacido/terapia , Complicaciones del Embarazo , Enfermedades de la Tiroides , Femenino , Estudios de Seguimiento , Humanos , Recién Nacido , Embarazo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...