Literature DB >> 6510425

Finnish national screening for hypothyroidism. Few false positives, early therapy.

M Virtanen, J Perheentupa, J Mäenpää, L Pitkänen, J Pikkarainen.   

Abstract

National cord blood screening for congenital hypothyroidism has operated in Finland with complete coverage since 1980. A low frequency of false positives, 0.08%, was achieved by supplementing the TSH screen with a T4 determination in borderline samples. Among 175188 infants the incidence of (unconfirmed) hypothyroidism was 1/2637. The median age at start of therapy was 6 days. The programme imposed a 2-3 week therapy on the false positive cases. This did not appear to cause any adverse effects. A mechanism for masking congenital hypothyroidism was observed: two athyroid infants were euthyroid at birth because of feto-fetal transfusion.

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Year:  1984        PMID: 6510425     DOI: 10.1007/bf00442737

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  14 in total

1.  The incidence of Pku in Finland.

Authors:  J K Visakorpi; J Palo; O V Renkonen
Journal:  Acta Paediatr Scand       Date:  1971-11

2.  Recovery of pituitary thyrotropic function after withdrawal of prolonged thyroid-suppression therapy.

Authors:  A G Vagenakis; L E Braverman; F Azizi; G I Portinay; S H Ingbar
Journal:  N Engl J Med       Date:  1975-10-02       Impact factor: 91.245

3.  American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism.

Authors: 
Journal:  Pediatrics       Date:  1982-01       Impact factor: 7.124

4.  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

5.  Screening for congenital hypothyroidism. I. Laboratory results of a pilot study based on dried blood samples collected for PKU screening.

Authors:  A Larsson; J G Ljunggren; K Ekman; A Nilsson; P Olin
Journal:  Acta Paediatr Scand       Date:  1981-03

6.  Psychological reactions in 102 families with a newborn who has a falsely positive screening test for congenital hypothyroidism.

Authors:  G Bodegård; K Fyrö; A Larsson
Journal:  Acta Paediatr Scand Suppl       Date:  1983

7.  Neuropsychological study in treated thyroid dysgenesis.

Authors:  R Wolter; P Noël; P De Cock; M Craen; C Ernould; P Malvaux; F Verstaeten; J Simons; S Mertens; N Van Broeck; M Vanderschueren-Lodeweyckx
Journal:  Acta Paediatr Scand Suppl       Date:  1979

8.  Congenital hypothyroidism in Sweden. Psychomotor development in patients detected by clinical signs and symptoms.

Authors:  J Alm; A Larsson; R Zetterström
Journal:  Acta Paediatr Scand       Date:  1981-11

9.  Screening for congenital hypothyroidism: results of screening one million North American infants.

Authors:  D A Fisher; J H Dussault; T P Foley; A H Klein; S LaFranchi; P R Larsen; M L Mitchell; W H Murphey; P G Walfish
Journal:  J Pediatr       Date:  1979-05       Impact factor: 4.406

10.  Neurological abnormalities in patients treated for hypothyroidism from early life.

Authors:  R Macfaul; S Dorner; E M Brett; D B Grant
Journal:  Arch Dis Child       Date:  1978-08       Impact factor: 3.791

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  6 in total

1.  The high incidence of neonatal hypothyroidism: artificial or real?

Authors:  M Portolés; A Jordá
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

2.  Screening for congenital hypothyroidism in Turkey.

Authors:  N Yordam; A S Calikoğlu; S Hatun; N Kandemir; H Oğuz; T Teziç; I Ozalp
Journal:  Eur J Pediatr       Date:  1995-08       Impact factor: 3.183

3.  Prevalence of hypothyroidism in Finland--a nationwide prescription study.

Authors:  Lauri J Virta; Seija I Eskelinen
Journal:  Eur J Clin Pharmacol       Date:  2010-08-31       Impact factor: 2.953

4.  Manifestations of congenital hypothyroidism during the 1st week of life.

Authors:  M Virtanen
Journal:  Eur J Pediatr       Date:  1988-04       Impact factor: 3.183

5.  Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort.

Authors:  Christoffer Löf; Konrad Patyra; Teemu Kuulasmaa; Jagadish Vangipurapu; Henriette Undeutsch; Holger Jaeschke; Tuulia Pajunen; Andreina Kero; Heiko Krude; Heike Biebermann; Gunnar Kleinau; Peter Kühnen; Krista Rantakari; Päivi Miettinen; Turkka Kirjavainen; Juha-Pekka Pursiheimo; Taina Mustila; Jarmo Jääskeläinen; Marja Ojaniemi; Jorma Toppari; Jaakko Ignatius; Markku Laakso; Jukka Kero
Journal:  Thyroid       Date:  2016-08-02       Impact factor: 6.568

6.  Screening for Mutations in Isolated Central Hypothyroidism Reveals a Novel Mutation in Insulin Receptor Substrate 4.

Authors:  Konrad Patyra; Kristiina Makkonen; Maria Haanpää; Sinikka Karppinen; Liisa Viikari; Jorma Toppari; Mary Pat Reeve; Jukka Kero
Journal:  Front Endocrinol (Lausanne)       Date:  2021-05-21       Impact factor: 5.555

  6 in total

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