Literature DB >> 617976

Early detection of neonatal hypothyroidism by serial TSH determination in dried blood. Six months experience with a reliable, efficient and inexpensive method.

R Illig, T Torresani, B Sobradillo.   

Abstract

Mass newborn screening for primary hypothyroidism was introduced in Switzerland on January 1st, 1977, using a radioimmunoassay of TSH in dried blood spotted on filter paper. After incubation for 38 h at 20 degrees C, bound and free TSH is separated by double antibody precipitation. The filter paper discs of 6.5 mm diameter remain in the test tubes. At present, one TSH determination costs approx. SFr. 4.40. All reagents used are commercially available and their costs amount to not more than 15% of the total expenses. During the first 8 months of 1977, of 21862 newborns tested routinely on day 5 (together with the Guthrie-test), 7 infants with primary hypothyroidism were discovered owing to blood TSH values of greater than 100 muU/ml. Diagnosis was not recognized clinically although all of the infants showed some symptoms. Thyroxin therapy was started within the second week of life. The incidence of about 1 in 3000 newborns is higher than reported so far. It has to be shown whether this is due to genetic or geographic factors, to the occurrence of transitory forms, or to a higher efficiency of screening by the TSH (versus T4) assay.

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Year:  1977        PMID: 617976

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN: 0018-022X


  8 in total

1.  Audit of screening programme for congenital hypothyroidism in Scotland 1979-93.

Authors:  M Ray; T M Muir; G D Murray; R Kennedy; R W Girdwood; M D Donaldson
Journal:  Arch Dis Child       Date:  1997-05       Impact factor: 3.791

2.  Investigation and management of neonatal jaundice: a problem-orientated case record.

Authors:  P M Mathew; B A Wharton
Journal:  Arch Dis Child       Date:  1981-12       Impact factor: 3.791

3.  Neonatal screening for hypothyroidism in Greece.

Authors:  C Mengreli; K Kassiou; S Tsagaraki; S Pantelakis
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

4.  Congenital hypothyroidism. Clinical and laboratory characteristics in infants detected by neonatal screening.

Authors:  D A Price; R M Ehrlich; P G Walfish
Journal:  Arch Dis Child       Date:  1981-11       Impact factor: 3.791

5.  Population screening for congenital hypothyroidism.

Authors:  J A Hulse; D B Grant; B E Clayton; P Lilly; D Jackson; A Spracklan; R W Edwards; D Nurse
Journal:  Br Med J       Date:  1980-03-08

Review 6.  Newborn screening strategies for congenital hypothyroidism: an update.

Authors:  Stephen H LaFranchi
Journal:  J Inherit Metab Dis       Date:  2010-03-02       Impact factor: 4.982

7.  Pilot study for congenital hypothyroidism, preliminary report.

Authors:  M Carta Sorcini; L Fiore; S Tomarchio; S Carta; C Romagnoli; V Currò; G Segni
Journal:  J Endocrinol Invest       Date:  1980 Apr-Jun       Impact factor: 4.256

8.  Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.

Authors:  I Antonozzi; R Dominici; M Andreoli; F Monaco
Journal:  J Endocrinol Invest       Date:  1980 Oct-Dec       Impact factor: 4.256

  8 in total

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