A reference interval for sweat chloride in infants aged between five and six weeks of age

Author:

Jayaraj Rajamanickam1,Barton Paul V2,Newland Paul2,Mountford Roger3,Shaw Nigel J4,Mccarthy Emma3,Isherwood David M2,Southern Kevin W1

Affiliation:

1. Institute of Child Health, University of Liverpool

2. Department of Clinical Biochemistry, Royal Liverpool Children's Hospital

3. Department of Clinical Genetics

4. Department of Neonatal Medicine, Liverpool Women's Hospital, Liverpool, UK

Abstract

Background This study was designed to establish a reference interval for sweat chloride for infants without evidence of cystic fibrosis (CF), aged between 5 wk and 6 wk, a time when sweat testing is an integral part of newborn screening for CF. In addition, we compared the gold standard method of sweat testing (quantitative pilocarpine iontophoresis [QPIT, coulometry]) with an emerging methodology (Macroduct™ [ISE]). Methods This was a prospective study on healthy infants at 5–6 wk of age. Sweat collection was undertaken at home on both outer thigh areas using two methods (QPIT and Macroduct™). The order of testing was randomly assigned. Filter paper samples (QPIT) were analysed using flame photometry and coulometry. Macroduct™ samples were analysed using ion-selective electrodes (ISE, Abbott Architect c8000, UK). Results Insufficient sweat was collected on 28 occasions with the QPIT (coulometry) method and on 31 with the Macroduct™ (ISE) capillary system. We achieved a 92% success rate in undertaking two sweat collections consecutively (n = 177). Sweat chloride concentrations were normally distributed with excellent limits of agreement between the two methods of sweat collection and analysis (n = 150). Median (IQR) sweat chloride was 11.2 mmol/L (8–13) with QPIT (coulometry) method with a 99.5th centile (n = 165) of 24 mmol/L. Conclusion The Macroduct™ (ISE) capillary sweat collection system is valid in this age group. Sweat chloride concentrations above 30 mmol/L should prompt assessment in a specialist CF centre.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cystic Fibrosis;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2020

2. A multicenter evaluation of sweat chloride concentration and variation in infants with cystic fibrosis;Journal of Cystic Fibrosis;2019-03

3. Real life practice of sweat testing in Europe;Journal of Cystic Fibrosis;2018-05

4. Feasibility and normal values of an integrated conductivity (Nanoduct™) sweat test system in healthy newborns;Journal of Cystic Fibrosis;2017-07

5. Functional Evaluation of Cystic Fibrosis Transmembrane Conductance Regulator;Diagnostic Tests in Pediatric Pulmonology;2014-09-27

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