Dergiler / Turkish Journal of Pediatrics / 2016 / Cilt: 58 - Sayı: 1

Diagnosis of cystic fibrosis with chloride meter (Sherwood M926S chloride analyzer®) and sweat test analysis system (CFΔ collection system®) compared to the Gibson Cooke method

Sayfa
27–33
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We think that the other sweat test equipments can be used as reliably as the classic GC method to diagnose or exclude CF

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Emiralioğlu N, Özçelik U, Yalçın E, Doğru D, Kiper N.
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Temel Bulgular & Veri:Diagnosis of cystic fibrosis with chloride meter (Sherwood M926S chloride analyzer®) and sweat test analysis system (CFΔ collection system®) compared to the Gibson Cooke method.
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Sonuç & Katkı:We think that the other sweat test equipments can be used as reliably as the classic GC method to diagnose or exclude CF
🔬Tür:Araştırma Makalesi
📍Kapsam:2016 Verileri
⚙️Değişkenler:Alan Parametreleri

Özet

Emiralioğlu N, Özçelik U, Yalçın E, Doğru D, Kiper N. Diagnosis of cystic fibrosis with chloride meter (Sherwood M926S chloride analyzer®) and sweat test analysis system (CFΔ collection system®) compared to the Gibson Cooke method. Turk J Pediatr 2016; 58: 27-33.Sweat test with Gibson Cooke (GC) method is the diagnostic gold standard for cystic fibrosis (CF). Recently, alternative methods have been introduced to simplify both the collection and analysis of sweat samples. Our aim was to compare sweat chloride values obtained by GC method with other sweat test methods in patients diagnosed with CF and whose CF diagnosis had been ruled out. We wanted to determine if the other sweat test methods could reliably identify patients with CF and differentiate them from healthy subjects.Chloride concentration was measured with GC method, chloride meter and sweat test analysis system; also conductivity was determined with sweat test analysis system. Forty eight patients with CF and 82 patients without CF underwent the sweat test, showing median sweat chloride values 98.9 mEq/L with GC method, 101 mmol/L with chloride meter, 87.8 mmol/L with sweat test analysis system. In non-CF group, median sweat chloride values were 16.8 mEq/L with GC method, 10.5 mmol/L with chloride meter, and 15.6 mmol/L with sweat test analysis system. Median conductivity value was 107.3 mmol/L in CF group and 32.1 mmol/L in non CF group. There was a strong positive correlation between GC method and the other sweat test methods with a statistical significance (r=0.85) in all subjects. Sweat chloride concentration and conductivity by other sweat test methods highly correlate with the GC method. We think that the other sweat test equipments can be used as reliably as the classic GC method to diagnose or exclude CF

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Bu Makaleye Atıf Yap

EMİRALİOĞLU, N., ÖZÇELİK, H. U., YALÇIN, E. H. Y., ERSÖZ, D. D., KİPER, E. N. (2016). Diagnosis of cystic fibrosis with chloride meter (Sherwood M926S chloride analyzer®) and sweat test analysis system (CFΔ collection system®) compared to the Gibson Cooke method. Turkish Journal of Pediatrics, Cilt: 58 - Sayı: 1, 27–33. https://ajindex.com/articles/412254

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Kaynakça (16)

  1. Lobo J, Rojas-Balcazar JM, Noone PG. Recent advances in cystic fibrosis. Clin Chest Med 2012; 33: 307-328
  2. Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr 1998; 132: 589-595
  3. De Boeck K, Wilschanski M, Castellani C, et al. Cystic fibrosis: terminology and diagnostic algorithms. Thorax 2006; 61: 627-635
  4. Farrell PM, Rosenstein BJ, White TB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr 2008; 153: S4–S14
  5. O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet 2009; 373: 1891-1904
  6. LeGrys VA, Yankaskas JR, Quittell LM, et al. Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelines. J Pediatr 2007; 151: 85-89
  7. Gibson LE, Cooke RE. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. Pediatrics 1959; 23: 545-549
  8. CLSI. Sweat testing: sample collection and quantitative chloride analysis; approved guideline-third edition. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2009
  9. Guidelines for the performance of the sweat test for the investigation of Cystic Fibrosis in the UK 2nd version. http://www.acb.org.uk ( 2003, Accessed March 2014
  10. Collie JT, Massie RJ, Jones OA, LeGrys VA, Greaves RF. Sixty-five years since the New York heat wave: advances in sweat testing for cystic fibrosis. Pediatr Pulmonol 2014; 49: 106-117
  11. Lezana JL, Vargas MH, Karam-Bechara J, Aldana RS, Furuya ME. Sweat conductivity and chloride titration for cystic fibrosis diagnosis in 3834 subjects. J Cyst Fibros 2003; 2: 1-7
  12. Barben J, Ammann RA, Metlagel A, Schoeni MH. Conductivity determined by a new sweat analyzer compared with chloride concentrations for the diagnosis of cystic fibrosis. J Pediatr 2005; 146: 183-188
  13. Carter EP, Barrett AD, Kuzemko JA. Improved sweat test method for the diagnosis of cystic fibrosis. Arch Dis Child 1984; 59: 919-922
  14. Nguyen-Khoa T, Borgard JP, Miled R, Rota M. [Sweat chloride measurement using direct potentiometry: Spotchem(®) (Elitech-Arkray) evaluation and comparison with coulometry and conductivity]. Ann Biol Clin (Paris) 2013; 71: 443-448
  15. Hammond KB, Turcios NL, Gibson LE. Clinical evaluation of the macroduct sweat collection system and conductivity analyzer in the diagnosis of cystic fibrosis. J Pediatr 1994; 124: 255-260
  16. Matta