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Hypothyroxinemia of prematurity: Cause, diagnosis and management

  • University of Liverpool - School of Reproductive and Developmental Medicine
  • University of Liverpool

Research output: Contribution to journalArticle (journal)peer-review

Abstract

Infants born at extreme prematurity are at a high risk of developmental disability. A major risk factor for disability is having a low level of thyroid hormone, described as hypothyroxinemia, which is recognized to be a frequent phenomenon in these infants. At present, there is uncertainty among clinicians regarding the most appropriate method of managing hypothyroxinemia of prematurity. The literature suggests that some, but not all, forms of thyroid supplementation may reduce the incidence of disability in infants born at extreme prematurity. There is a pressing need to confirm the benefit of treatment and to establish the optimal way to treat transient hypothyroxinemia in these infants.

Original languageEnglish
Pages (from-to)453-462
Number of pages10
JournalExpert Review of Endocrinology and Metabolism
Volume3
Issue number4
DOIs
Publication statusPublished - 31 Jul 2008

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Hypothyroxinemia
  • Prematurity
  • Thyroid hormonies
  • Thyroxine T4

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