Newborn screening for cystic fibrosis in Switzerland - Consequences after analysis of a 4 months pilot study

被引:15
作者
Torresani, Toni [1 ]
Fingerhut, Ralph [1 ]
Rueegg, Corina S. [2 ]
Gallati, Sabina [3 ]
Kuehni, Claudia E. [2 ]
Baumgartner, Matthias R. [4 ]
Barben, Juerg [5 ]
机构
[1] Univ Childrens Hosp, Swiss Newborn Screening Lab, Zurich, Switzerland
[2] Univ Bern, ISPM, Bern, Switzerland
[3] Univ Childrens Hosp, Div Human Genet, Bern, Switzerland
[4] Univ Childrens Hosp, Div Metab & Swiss Newborn Screening, Zurich, Switzerland
[5] Childrens Hosp, Div Paediat Pulmonol, CH-9006 St Gallen, Switzerland
关键词
Newborn screening; Cystic fibrosis; Immunoreactive trypsinogen; Recall rate; IMMUNOREACTIVE TRYPSINOGEN; DIAGNOSIS; GUIDELINES; MUTATIONS; CONSENSUS; PROTOCOL;
D O I
10.1016/j.jcf.2013.04.008
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Switzerland introduced newborn screening (NBS) for CF in 2011, using an IRT/DNA/IRT protocol. This paper describes the results of the first year and compares two versions of the protocol with different IRT cut-offs, particularly effects on recall rate, sensitivity and specificity. Methods: IRT cut-offs were >45 ng/ml (99.0th percentile) in period 1 (months 1-4) and >50 ng/ml (99.2nd percentile) in period 2 (months 5-12). In period 2 we abstained from recalls when none of the 7 most common CF mutations were detected and IRT was <60 ng/ml. Results: hi periods 1 and 2, 26,535 and 56,663 tests were performed. Recall rates were 0.94% and 0.48%, respectively (p <0.001), PPV increased from 23% to 47% (p = 0.024) and sensitivity was 90% and 100%. Conclusions: Raising initial IRT cut-off from the 99.0th to the 99.2nd percentile and abstaining from recalls for children with an IRT < 60 ng/ml and carrying no major CFTR mutation significantly reduced the recall rate without affecting sensitivity. (C) 2013 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:667 / 674
页数:8
相关论文
共 21 条
[1]   Conductivity determined by a new sweat analyzer compared with chloride concentrations for the diagnosis of cystic fibrosis [J].
Barben, J ;
Ammann, RA ;
Metlagel, A ;
Schoeni, MH .
JOURNAL OF PEDIATRICS, 2005, 146 (02) :183-188
[2]  
Barben J, 2011, SCHWEIZ ARZTEZTG, V92, P18
[3]   Retrospective analysis of stored dried blood spots from children with cystic fibrosis and matched controls to assess the,performance of a proposed newborn screening protocol in Switzerland [J].
Barben, Juerg ;
Gallati, Sabina ;
Fingerhut, Ralph ;
Schoeni, Martin H. ;
Baumgartner, Matthias R. ;
Torresani, Toni .
JOURNAL OF CYSTIC FIBROSIS, 2012, 11 (04) :332-336
[4]   A dissociative fluorescence enhancement technique for one-step time-resolved immunoassays [J].
Blomberg, Kaj R. ;
Mukkala, Veli-Matti ;
Hakala, Harri H. O. ;
Makinen, Pauliina H. ;
Suonpaa, Mikko U. ;
Hemmila, Ilkka A. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 399 (04) :1677-1682
[5]   Benchmarks for Cystic Fibrosis carrier screening: A European consensus document [J].
Castellani, Carlo ;
Macek, Milan, Jr. ;
Cassiman, Jean-Jacques ;
Duff, Alistair ;
Massie, John ;
ten Kate, Leo P. ;
Barton, David ;
Cutting, Garry ;
Dallapiccola, Bruno ;
Dequeker, Elisabeth ;
Girodon, Emmanuelle ;
Grody, Wayne ;
Highsmith, Edward W. ;
Kaariainen, Helenal ;
Kruip, Stephan ;
Morris, Michael ;
Pignatti, Pier Franco ;
Pypops, Ulrike ;
Schwarz, Martin ;
Soller, Maria ;
Stuhrman, Manfred ;
Cuppens, Harry .
JOURNAL OF CYSTIC FIBROSIS, 2010, 9 (03) :165-178
[6]  
CLSI, 2009, SWEAT TEST SAMPL COL, pC34
[7]   Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report [J].
Comeau, Anne Marie ;
Accurso, Frank J. ;
White, Terry B. ;
Campbell, Preston W., III ;
Hoffman, Gary ;
Parad, Richard B. ;
Wilfond, Benjamin S. ;
Rosenfeld, Margaret ;
Sontag, Marci K. ;
Massie, John ;
Farrell, Philip M. ;
O'Sullivan, Brian P. .
PEDIATRICS, 2007, 119 (02) :E495-E518
[8]   Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report [J].
Farrell, Philip M. ;
Rosenstein, Beryl J. ;
White, Terry B. ;
Accurso, Frank J. ;
Castellani, Carlo ;
Cutting, Garry R. ;
Durie, Peter R. ;
LeGrys, Vicky A. ;
Massie, John ;
Parad, Richard B. ;
Rock, Michael J. ;
Campbell, Preston W., III .
JOURNAL OF PEDIATRICS, 2008, 153 (02) :S4-S14
[9]  
Heinonen P, 1997, CLIN CHEM, V43, P1142
[10]   Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease [J].
Liechti-Gallati, S ;
Schneider, V ;
Neeser, D ;
Kraemer, R .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (05) :590-598