Literature DB >> 21071339

Bilateral sweat tests with two different methods as a part of cystic fibrosis newborn screening (CF NBS) protocol and additional quality control.

Dorota Sands1, Mariusz Ołtarzewski, Anna Nowakowska, Katarzyna Zybert.   

Abstract

Infants with positive CF newborn screening (NBS) results are called to a CF Centre for verification. Those, in whom the sweat test is elevated, undergo further medical procedures. The aim of our study was to evaluate the applicability of Nanoduct - a new system measuring sweat conductivity and giving immediate results in a CF NBS protocol. Measurements with Nanoduct were compared with the classic pilocarpine method. During 3 years 487 infants from CF NBS had both sweat tests performed on the same day, at the same CF centre. CF infants had a mean conductivity of 99.8 ± 1 8.8 mmol/L and a mean chloride concentration of 74.0 ± 18.4 mmol/L. Non-CF infants values were 29.8 ± 7.7 mmol/L and 19.2 ± 6.6 mmol/L respectively. A good correlation between both tests was found (95% confidence level (CI); r=0.87). The optimal cut off, based on follow up experience of screened children, for conductivity tests was 50 mmol/L and for chloride concentration was 34 mmol/L (no lost CF, 11 false positive) with 100% sensitivity and 97.5 % specificity. In conclusion Nanoduct is a very useful and reliable tool in CF NBS protocol, allowing more time efficient organization of the diagnostic and training procedures. Simultaneous bilateral sweat testing with two different methods (concentration and conductivity) provides an extra quality control system.

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Year:  2010        PMID: 21071339     DOI: 10.2478/v10042-010-0044-9

Source DB:  PubMed          Journal:  Folia Histochem Cytobiol        ISSN: 0239-8508            Impact factor:   1.698


  5 in total

1.  Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategy.

Authors:  Agnieszka Sobczyńska-Tomaszewska; Mariusz Ołtarzewski; Kamila Czerska; Katarzyna Wertheim-Tysarowska; Dorota Sands; Jarosław Walkowiak; Jerzy Bal; Tadeusz Mazurczak
Journal:  Eur J Hum Genet       Date:  2012-08-15       Impact factor: 4.246

2.  Clinical evaluation of the Nanoduct sweat test system in the diagnosis of cystic fibrosis after newborn screening.

Authors:  Annette Vernooij-van Langen; Edward Dompeling; Jan-Bart Yntema; Bert Arets; Harm Tiddens; Gerard Loeber; Jeannette Dankert-Roelse
Journal:  Eur J Pediatr       Date:  2015-02-13       Impact factor: 3.183

3.  Comparison of classic sweat test and crystallization test in diagnosis of cystic fibrosis.

Authors:  Fatemeh Farahmand; Nooshin Sadjadei; Mohammad-Taghi Haghi-Ashtiani; Vajiheh Modaresi; Nima Rezaei; Bahar Pakseresht
Journal:  Iran J Pediatr       Date:  2012-03       Impact factor: 0.364

Review 4.  Processing Newborn Bloodspot Screening Results for CF.

Authors:  Jürg Barben; Jane Chudleigh
Journal:  Int J Neonatal Screen       Date:  2020-03-25

5.  Nanoduct sweat conductivity measurements in 2664 patients: relationship to age, arterial blood gas, serum electrolyte profiles and clinical diagnosis.

Authors:  Rabia Gonul Sezer; Gokhan Aydemir; Abdullah Baris Akcan; Cem Paketci; Abdulbaki Karaoglu; Secil Aydinoz; Abdulkadir Bozaykut
Journal:  J Clin Med Res       Date:  2013-01-11
  5 in total

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