Christine Allomba , Leonie Busack , Niklas Ziegahn , Charlotte O. Pioch , Alexandra N. Schnorr , Bent R. Fuhlrott , Eva Steinke , Marcus A. Mall , Mirjam Stahl
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引用次数: 0
Abstract
Background
Pulmonary function tests play an important role in diagnosis, management and treatment of people with cystic fibrosis (pwCF). Multiple-breath washout (MBW) is a sensitive method to detect ventilation inhomogeneities and is established in children with CF. Despite promising data in adults with pulmonary diseases, its feasibility remains questioned in adults due to longer examination times and limited added value over spirometry. We aimed to analyse feasibility of MBW in pwCF and healthy controls (HC) and evaluate factors influencing test duration.
Methods
We analysed 1,395 MBW measurements from pwCF (n = 1,158) and HC (n = 237). PwCF were divided according to percent predicted forced expiratory volume in one second (ppFEV1; high, >90 %; mid, 40-90 %; low, <40 %) and age groups. Test feasibility was defined as two acceptable trials. The impact of constitutional and disease severity factors was analysed.
Results
Test feasibility was 100.0 % in HC and 94.3 % in pwCF, with higher feasibility in children than adults (96.0 % vs. 92.5 %, p = 0.01), and in those pwCF with higher ppFEV1 (high, 96.6 %; mid, 94.9 %; low, 82.6 %; p < 0.001). The higher the ppFEV1, the larger is the influence of constitutional factors over the impact of disease severity on trial time. Mean single trial time was 2.0 min, 2.7 min respectively 5.2 min in high, mid and low ppFEV1.
Conclusion
This study suggests extending MBW to adults with CF. Despite concerns about time efficiency, this study shows a good feasibility of MBW (92.5 %) in adults. Based on correlating factors, this study provides a decision-making tool for clinicians forecasting trial time.
期刊介绍:
The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.