| Literature DB >> 31744807 |
Anthony Brown1, Laura Jenkins2, Alastair Reid2, Anne Leavy2, Glen McDowell3, Claire McIlroy4, Andrew Thompson5, Ben McNaughten6.
Abstract
Cystic fibrosis (CF) is the most common life-threatening autosomal-recessive disease affecting Caucasians in the western world. The sweat test is the main diagnostic test for CF. It is indicated as part of the clinical assessment for infants that have picked up on the national neonatal screening programme. It may also be requested where clinical suspicion of a diagnosis of CF exists despite normal screening results. This article outlines the physiological basis behind sweat testing and the technical aspects of performing the test. Indications for performing the test are also considered. The article aims to provide clinicians with a guide to interpretation of results. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: cystic fibrosis; paediatric practice; sweat test
Mesh:
Year: 2019 PMID: 31744807 DOI: 10.1136/archdischild-2018-316615
Source DB: PubMed Journal: Arch Dis Child Educ Pract Ed ISSN: 1743-0585 Impact factor: 1.309