Sweat testing for cystic fibrosis: standards of performance in Australasia

被引:10
作者
Coakley, John [1 ]
Scott, Sue [2 ]
Mackay, Richard [3 ]
Greaves, Ronda [4 ]
Jolly, Lisa [2 ]
Massie, John [5 ]
Mishra, Avantika [6 ]
Bransden, Anna [7 ]
Doery, James C. G. [8 ,9 ]
Chiriano, Angela [4 ]
Robins, Heather [10 ]
机构
[1] Childrens Hosp Westmead, Dept Biochem, Westmead, NSW 2145, Australia
[2] RCPA Chem Pathol Qual Assurance Programs, Adelaide, SA, Australia
[3] Canterbury Hlth Labs, Clin Biochem Unit, Christchurch, New Zealand
[4] Royal Childrens Hosp, Dept Clin Biochem, Melbourne, Vic, Australia
[5] Royal Childrens Hosp, Dept Resp Med, Melbourne, Vic, Australia
[6] Victorian Clin Genet Serv, Melbourne, Vic, Australia
[7] Royal Brisbane Hosp, Dept Chem Pathol, Brisbane, Qld 4029, Australia
[8] Monash Univ, Dept Biochem, Monash Med Ctr, Melbourne, Vic 3004, Australia
[9] Monash Univ, Dept Med, Melbourne, Vic 3004, Australia
[10] Canberra Hosp, Dept Biochem, Canberra, ACT, Australia
关键词
LABORATORIES; DIAGNOSIS; AGE;
D O I
10.1258/acb.2009.009023
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Accurate measurement of sweat chloride concentration is essential for the diagnosis of cystic fibrosis (CF). We surveyed all laboratories enrolled in the Royal College of Pathologists of Australasia Quality Assurance Program (QAP) for Sweat Electrolytes to determine how closely they comply with the Australian Guidelines for the performance of the sweat test for the diagnosis of CF. Methods: A detailed questionnaire covering most aspects of sweat collection and analysis was sent to all participating laboratories in 2007. Results: Twenty out of 38 laboratories completed the questionnaire. While adherence to accepted guidelines was noted in many areas, the following main variations were recorded: some laboratories were not doing enough sweat tests to maintain expertise; some were not collecting sweat for the recommended collection time; sweat conductivity was the only test available in some laboratories; there was a lack of agreement between the sweat chloride concentration used to indicate CF or define an equivocal result. Conclusions: There is room for improvement in the performance of the sweat test in some laboratories in Australasia. The Sweat Testing Working Party of the Australasian Association of Clinical Biochemists is the appropriate body to address the problems involved in sweat testing and to bring about change.
引用
收藏
页码:332 / 337
页数:6
相关论文
共 11 条
[1]  
[Anonymous], GUIDELINES PERFORMAN
[2]   Sweat-testing in preterm and full-term infants less than 6 weeks of age [J].
Eng, W ;
LeGrys, VA ;
Schechter, MS ;
Laughon, MM ;
Barker, PM .
PEDIATRIC PULMONOLOGY, 2005, 40 (01) :64-67
[3]   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
[4]  
Farrell PM, 1996, PEDIATRICS, V97, P524
[5]  
GIBSON LE, 1959, PEDIATRICS, V23, P545
[6]   SWEAT TESTS IN NEWBORN PERIOD [J].
HARDY, JD ;
DAVISON, SHH ;
HIGGINS, MU ;
POLYCARPOU, PN .
ARCHIVES OF DISEASE IN CHILDHOOD, 1973, 48 (04) :316-318
[7]   Inconsistencies in sweat testing in UK laboratories [J].
Kirk, JM .
ARCHIVES OF DISEASE IN CHILDHOOD, 2000, 82 (05) :425-427
[8]  
LEGRYS VA, 2000, C34A2 NCCLS
[9]   Sweat testing for cystic fibrosis: A review of New Zealand laboratories [J].
Mackay, R ;
George, P ;
Kirk, J .
JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2006, 42 (04) :160-164
[10]   Diagnosis of Cystic Fibrosis by Sweat Testing: Age-Specific Reference Intervals [J].
Mishra, Avantika ;
Greaves, Ronda ;
Smith, Katherine ;
Carlin, John B. ;
Wootton, Andrew ;
Stirling, Rob ;
Massie, John .
JOURNAL OF PEDIATRICS, 2008, 153 (06) :758-763