Literature DB >> 15995048

Clinical effectiveness and cost-effectiveness of the use of the thyroxine/thyroxine-binding globulin ratio to detect congenital hypothyroidism of thyroidal and central origin in a neonatal screening program.

Caren I Lanting1, David A van Tijn, J Gerard Loeber, Thomas Vulsma, Jan J M de Vijlder, Paul H Verkerk.   

Abstract

CONTEXT: Since the introduction of screening for congenital hypothyroidism (CH) in 1974, the optimal laboratory strategy has been the subject of debate.
OBJECTIVE: To assess the clinical effectiveness and cost-effectiveness of various types of thyroxine (T(4))-based strategies to screen for CH. DESIGN, SETTING, AND PARTICIPANTS: In the Netherlands, since January 1, 1995, a primary T(4) determination with supplemental thyroid-stimulating hormone (TSH) and T(4)-binding globulin (TBG) measurements has been used. Results were calculated from cumulative findings for 1181079 children screened between January 1, 1995, and December 31, 2000. MAIN OUTCOME MEASURES: Rates of detection of patients with CH of thyroidal origin (CH-T) or CH of central origin (CH-C), false-positive rates, laboratory costs, and costs of initial diagnostic evaluations.
RESULTS: All known infants (n = 393) with CH-T and 92% (n = 66) of infants with CH-C were detected on the basis of low T(4) levels, TSH elevation, and/or low T(4)/TBG ratios. If the decision to refer had been based solely on TSH elevation, then 94% of patients with CH-T and none of the patients with CH-C would have been detected. If low T(4) levels (<or=-3.0 SD) and TSH elevation had been used as the criteria for referral, then the rates of detection would have been 96% for CH-T and 31% for CH-C. The false-positive rates for the 3 approaches were 0.5, 3.3, and 4.7 cases per case detected, respectively. The introduction of the T(4)/TBG ratio into a program using a primary T(4) with supplemental TSH approach generates an extra cost of 11206 dollars per additional case detected. The average costs to detect 1 patient are comparable for the 3 approaches. In addition, our data revealed a substantially greater prevalence of CH-C than reported previously (1 case per 16404 children, compared with earlier estimates of 1 case per 26000 infants to 1 case per 29000 infants).
CONCLUSIONS: The T(4) plus TSH plus TBG approach is a recommendable strategy for neonatal CH screening. It offers outstanding detection of patients with CH-C, in addition to those with CH-T, with acceptable costs.

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Year:  2005        PMID: 15995048     DOI: 10.1542/peds.2004-2162

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  26 in total

1.  Introducing new screens: why are we all doing different things?

Authors:  R J Pollitt
Journal:  J Inherit Metab Dis       Date:  2007-07-06       Impact factor: 4.982

2.  Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencing.

Authors:  Ari J Wassner; Laurie E Cohen; Eliana Hechter; Andrew Dauber
Journal:  Horm Res Paediatr       Date:  2013-05-03       Impact factor: 2.852

3.  Central congenital hypothyroidism caused by maternal thyrotoxicosis.

Authors:  Daphne Peeters; Sandra van Gijlswijk; Ralph W Leunissen; Danielle C M van der Kaay
Journal:  BMJ Case Rep       Date:  2018-03-22

Review 4.  Pediatric Hypothyroidism: Diagnosis and Treatment.

Authors:  Ari J Wassner
Journal:  Paediatr Drugs       Date:  2017-08       Impact factor: 3.022

Review 5.  Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted?

Authors:  Samantha Lain; Caroline Trumpff; Scott D Grosse; Antonella Olivieri; Guy Van Vliet
Journal:  Eur J Endocrinol       Date:  2017-07-10       Impact factor: 6.664

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

Review 7.  Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.

Authors:  M C Vigone; M Di Frenna; G Weber
Journal:  J Endocrinol Invest       Date:  2015-04-28       Impact factor: 4.256

8.  [Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia: Benefits and costs of a successful public health program].

Authors:  Guy Van Vliet; Scott D Grosse
Journal:  Med Sci (Paris)       Date:  2021-05-18       Impact factor: 0.716

9.  Improving the Dutch Newborn Screening for Central Congenital Hypothyroidism by Using 95% Reference Intervals for Thyroxine-Binding Globulin.

Authors:  Kevin Stroek; Annemieke C Heijboer; Marja van Veen-Sijne; Annet M Bosch; Catharina P B van der Ploeg; Nitash Zwaveling-Soonawala; Robert de Jonge; A S Paul van Trotsenburg; Anita Boelen
Journal:  Eur Thyroid J       Date:  2021-03-05

Review 10.  Optimising outcome in congenital hypothyroidism; current opinions on best practice in initial assessment and subsequent management.

Authors:  Malcolm Donaldson; Jeremy Jones
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-11-15
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