Literature DB >> 21331666

Newborn screening for congenital hypothyroidism in very-low-birth-weight babies: the need for a second test.

Sunita Bijarnia1, Bridget Wilcken, Veronica C Wiley.   

Abstract

BACKGROUND: Very-low-birth-weight babies (VLBW) with hypothyroidism may show a delayed postnatal rise in thyroid stimulating hormone (TSH), mainly due to immaturity of the hypothalamic-pituitary-thyroid axis. Transient hypothyroidism is prevalent in VLBW babies and some affected babies are considered to need treatment. There is disagreement about whether a second screening test is needed in VLBW babies to detect all cases that need treatment.
METHODS: We included in the study all babies with a birth weight ≤ 1,500 g born in New South Wales and the Australian Capital Territory between January 2006 and December 2008. Newborn screening samples for TSH measurement were taken in the first days of life and again at 1 month. During week 1, a blood-spot TSH level of  ≥20 mIU/L was considered positive, and at 1 month a positive level was  ≥7 mIU/L, and triggered full investigation.
RESULTS: In the cohort of 301,000 babies, 2,313 VLBW babies survived for testing, and 2,117 repeat screening samples were received. Forty-three babies had transient hypothyroidism, with thyroid function normalising before 2 months of age, usually without treatment. Eighteen babies required treatment beyond 2 months of age (1:128 of surviving babies), 16 having had normal TSH results on initial testing, and 12 having levels below 6 mIU/L.
CONCLUSION: Significant hypothyroidism, transient or permanent, but persisting beyond 2 months of age is common in VLBW babies. There is a delayed rise in TSH in some, and secondary screening at 1 month of age detects babies deemed by local paediatric endocrinologists as needing treatment.

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Year:  2011        PMID: 21331666     DOI: 10.1007/s10545-011-9286-8

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  22 in total

1.  Screening for congenital hypothyroidism in extreme premature and/or very low birth weight newborns: the importance of a specific protocol.

Authors:  S A B Silva; A J Chagas; E M A Goulart; G A B Silva; L V Marçal; M N A Gomes; V M D Alves
Journal:  J Pediatr Endocrinol Metab       Date:  2010 Jan-Feb       Impact factor: 1.634

2.  Treating patients not numbers: the benefit and burden of lowering TSH newborn screening cut-offs.

Authors:  Heiko Krude; Oliver Blankenstein
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4.  Screening for congenital hypothyroidism: the value of retesting after four weeks in neonates with low and very low birth weight.

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5.  Efficacy of congenital hypothyroidism neonatal screening in preterms less than 32 weeks of gestational age: more evidence.

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3.  Nomogram-based evaluation of thyroid function in appropriate-for-gestational-age neonates in intensive care unit.

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4.  Higher frequency of Congenital Hypothyroidism among Newborns, District Dera Ghazi Khan-Punjab, Pakistan: A case control study.

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6.  How can the occurrence of delayed elevation of thyroid stimulating hormone in preterm infants born between 35 and 36 weeks gestation be predicted?

Authors:  You Jung Heo; Young Ah Lee; Bora Lee; Yun Jeong Lee; Youn Hee Lim; Hye Rim Chung; Seung Han Shin; Choong Ho Shin; Sei Won Yang
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7.  Neonatal screening for congenital hypothyroidism in an Italian Centre: a 5-years real-life retrospective study.

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9.  Trend of Congenital Hypothyroidism Incidence and Its Affecting Factors in Shahr-e-Kord, Western Iran.

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10.  Targeted Secondary Screening for Congenital Hypothyroidism in High-Risk Neonates: A 9 Year Review in a Large California Health Care System.

Authors:  Alan B Cortez; Bryan Lin; Joshua A May
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