Literature DB >> 2403231

Sweat sodium and chloride concentrations--essential criteria for the diagnosis of cystic fibrosis in adults.

S K Hall1, D E Stableforth, A Green.   

Abstract

Criteria for a positive sweat test in children (sweat sodium greater than 60 mmol/L and sweat chloride greater than 70 mmol/L) were investigated in a series of adults aged between 18 and 40 years using the standard Gibson and Cooke technique of pilocarpine iontophoresis. A significant number of non-cystic fibrosis adults had sweat sodium values greater than 60 mmol/L whereas a concentration of chloride greater than 70 mmol/L always discriminated adults with cystic fibrosis from normal adults and those with chest disease not due to cystic fibrosis. In all cases of adult cystic fibrosis the sweat sodium concentration was greater than 80 mmol/L. The Na:Cl ratio and sum of Na and Cl provided additional helpful criteria in distinguishing between adults with and without cystic fibrosis.

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Year:  1990        PMID: 2403231     DOI: 10.1177/000456329002700406

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  9 in total

1.  The limitations of sweat electrolyte reference intervals for the diagnosis of cystic fibrosis: a systematic review.

Authors:  Avantika Mishra; Ronda Greaves; John Massie
Journal:  Clin Biochem Rev       Date:  2007-05

2.  Indirect measurements of sweat electrolyte concentration in the laboratory diagnosis of cystic fibrosis.

Authors:  M E Heeley; D A Woolf; A F Heeley
Journal:  Arch Dis Child       Date:  2000-05       Impact factor: 3.791

Review 3.  Atypical cystic fibrosis: identification in the primary care setting.

Authors:  Carrie A Schram
Journal:  Can Fam Physician       Date:  2012-12       Impact factor: 3.275

4.  Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype.

Authors:  V Dumur; R Gervais; J M Rigot; E Delomel-Vinner; B Decaestecker; J J Lafitte; P Roussel
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

5.  Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report.

Authors:  Philip M Farrell; Beryl J Rosenstein; Terry B White; Frank J Accurso; Carlo Castellani; Garry R Cutting; Peter R Durie; Vicky A Legrys; John Massie; Richard B Parad; Michael J Rock; Preston W Campbell
Journal:  J Pediatr       Date:  2008-08       Impact factor: 4.406

6.  Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?

Authors:  Alethéa Guimarães Faria; Fernando Augusto Lima Marson; Carla Cristina de Souza Gomez; Maria Ângela Gonçalves de Oliveira Ribeiro; Lucas Brioschi Morais; Maria de Fátima Servidoni; Carmen Sílvia Bertuzzo; Eulália Sakano; Maura Goto; Ilma Aparecida Paschoal; Mônica Corso Pereira; Gabriel Hessel; Carlos Emílio Levy; Adyléia Aparecida Dalbo Contrera Toro; Andressa Oliveira Peixoto; Maria Cristina Ribeiro Simões; Elizete Aparecida Lomazi; Roberto José Negrão Nogueira; Antônio Fernando Ribeiro; José Dirceu Ribeiro
Journal:  Diagn Pathol       Date:  2016-10-26       Impact factor: 2.644

Review 7.  When and how ruling out cystic fibrosis in adult patients with bronchiectasis.

Authors:  Andrea Gramegna; Stefano Aliberti; Manuela Seia; Luigi Porcaro; Vera Bianchi; Carlo Castellani; Paola Melotti; Claudio Sorio; Enza Consalvo; Elisa Franceschi; Francesco Amati; Martina Contarini; Michele Gaffuri; Luca Roncoroni; Barbara Vigone; Angela Bellofiore; Cesare Del Monaco; Martina Oriano; Leonardo Terranova; Maria Francesca Patria; Paola Marchisio; Baroukh M Assael; Francesco Blasi
Journal:  Multidiscip Respir Med       Date:  2018-08-09

Review 8.  A Comprehensive Review of the Recent Developments in Wearable Sweat-Sensing Devices.

Authors:  Nur Fatin Adini Ibrahim; Norhayati Sabani; Shazlina Johari; Asrulnizam Abd Manaf; Asnida Abdul Wahab; Zulkarnay Zakaria; Anas Mohd Noor
Journal:  Sensors (Basel)       Date:  2022-10-10       Impact factor: 3.847

9.  Is sweat testing for cystic fibrosis feasible in patients with down syndrome?

Authors:  Katharina Ruf; Antonia Demerath; Helge Hebestreit; Steffen Kunzmann
Journal:  BMC Pulm Med       Date:  2018-01-16       Impact factor: 3.317

  9 in total

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