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1.
An Pediatr (Engl Ed) ; 90(4): 250.e1-250.e8, 2019 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-30686624

RESUMO

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.


Assuntos
Hipotireoidismo Congênito/diagnóstico , Triagem Neonatal/métodos , Hormônios Tireóideos/análise , Assistência ao Convalescente/métodos , Pré-Escolar , Hipotireoidismo Congênito/complicações , Hipotireoidismo Congênito/terapia , Diagnóstico Diferencial , Humanos , Lactente , Recém-Nascido
2.
An Pediatr (Engl Ed) ; 89(4): 254.e1-254.e7, 2018 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-30177500

RESUMO

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.


Assuntos
Doenças Autoimunes , Doenças Fetais/diagnóstico , Doenças Fetais/terapia , Doenças do Recém-Nascido/diagnóstico , Doenças do Recém-Nascido/terapia , Complicações na Gravidez , Doenças da Glândula Tireoide , Feminino , Seguimentos , Humanos , Recém-Nascido , Gravidez
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