1996
DOI: 10.1016/0378-3782(96)01760-4
|View full text |Cite
|
Sign up to set email alerts
|

The need for standardized bloodspot TSH-calibrators in congenital hypothyroidism screening

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
2
0
1

Year Published

1998
1998
2020
2020

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(3 citation statements)
references
References 1 publication
0
2
0
1
Order By: Relevance
“…Infant blood was collected on dried blood spot cards at postnatal days 7, 14, 28 and 34 weeks’ gestational age (had the fetus remained in utero, referred to hereafter as equivalent gestational age), ±1 day. Cards were sent to the Amsterdam Neonatal Screening Laboratory for measurement of TSH, T4 and TBG18 (for details see online supplementary appendix). T4 is expressed as absolute levels and as a SD of the daily mean, which is calculated from the results of approximately 150 cards of term and preterm infants; levels ≤−3.0 SD are considered abnormal (in term infants).…”
Section: Methodsmentioning
confidence: 99%
“…Infant blood was collected on dried blood spot cards at postnatal days 7, 14, 28 and 34 weeks’ gestational age (had the fetus remained in utero, referred to hereafter as equivalent gestational age), ±1 day. Cards were sent to the Amsterdam Neonatal Screening Laboratory for measurement of TSH, T4 and TBG18 (for details see online supplementary appendix). T4 is expressed as absolute levels and as a SD of the daily mean, which is calculated from the results of approximately 150 cards of term and preterm infants; levels ≤−3.0 SD are considered abnormal (in term infants).…”
Section: Methodsmentioning
confidence: 99%
“…Screening parameters such as sensitivity and specificity cannot be compared between programmes without discussion of cut-off values, and this is problematic because of highly variable numeric results given by different test kits, even when pure or international reference material is available for calibrator production (Elvers and Loeber 1996) The use of regional standard materials for phenylalanine measurement has been shown to improve this situation (Dhondt et al 1996(Dhondt et al , 1998 It has been shown that this type of material (for phenylalanine and TSH) can be reliably produced over time and between centres (Adam et al 2000). Standards have been produced for these analytes and 17-hydroxyprogesterone (17-OHP) (Elvers et al 2005(Elvers et al , 2006 Unfortunately adoption of the values on the international materials would necessitate changes by some manufacturers of their kit values and some fear repercussions from their customers were they to do this, so the international screening community has been slow in adopting this particular standardization.…”
Section: Laboratory Qualitymentioning
confidence: 99%
“…La concentración del analito medida en manchas de sangre neonatal depende de la forma en que son preparados los calibradores. Muchas variables están involucradas en este proceso; tales como el tipo y el lote del papel de filtro usado, la matriz de los calibradores, el porcentaje del hematocrito, el tamaño de la mancha de sangre, el uso de células rojas lisadas o intactas, el uso de anticoagulantes y bactericidas, las condiciones de almacenamiento y el secado, la preparación de referencia usada para establecer la concentración de los calibradores y el método de análisis usado (4).…”
Section: Introduccionunclassified