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Potential utility of the N2 VC SBW test in cystic fibrosis (CF)

Authors :
Marita Gilljam
Sanna Kjellberg
Anders Lindblad
Paul Robinson
Per A. Gustafsson
Source :
Cystic Fibrosis.
Publication Year :
2017
Publisher :
European Respiratory Society, 2017.

Abstract

Introduction: Cystic fibrosis (CF) lung disease is characterized by uneven ventilation distribution, which can be measured by the N 2 multiple breath washout (MBW) and the vital capacity single breath washout (VC SBW) test. A MBW test is more time consuming than a VC SBW test. Aims: To determine the prevalence of abnormal MBW and SBW test results in teenagers and adults with CF. Methods: Spirometry and triplicates of N 2 MBW and N 2 VC SBW were performed in 31 subjects (9 females) with CF, aged 13-45 yrs (median 23 yrs) using the Exhalyzer D washout device. Washout results were related to 400 healthy control subjects for N 2 MBW and 224 for N 2 VC SBW. Results: FEV 1 was abnormal in 7/31 (23%) subjects, VC SBW phase III slope (S III ) was abnormal in 20/31 (65%), LCI 29/31 (94%), S cond 30/31 (97%), S acin 24/31 (77%) and fast-to-slow regions specific ventilation ratio in 30/31 (97%). Among the 11 subjects with normal VC SBW S III , 10 (91%) showed abnormal MBW results. Consclusions: Abnormal N 2 VC SBW S III was seen in the majority of teenagers and adult CF subjects with normal FEV 1 , suggesting additional value of this method, but normal S III does not exclude pathological MBW outcomes.

Details

Database :
OpenAIRE
Journal :
Cystic Fibrosis
Accession number :
edsair.doi...........a14f2a8fb95431e46b0aca42294099d4
Full Text :
https://doi.org/10.1183/1393003.congress-2017.pa1840