A Short extension to multiple breath washout provides additional signal of distal airway disease in people with CF: A pilot study
A Short extension to multiple breath washout provides additional signal of distal airway disease in people with CF: A pilot study
复制标题
多次呼吸冲洗的短期延长为 CF 患者提供了远端气道疾病的额外信号:一项试点研究
DOI:
10.1016/j.jcf.2021.06.013
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发表时间:
2022
影响因子:
5.2
通讯作者:
Short C
中科院分区:
文献类型:
--
作者:
Short C
BackgroundAdding a slow vital capacity (SVC) to multiple breath washout (MBW) allows quantification of otherwise overlooked signal from under/un-ventilated lung units (UVLU) and may provide a more comprehensive assessment of airway disease than conventional lung clearance index (LCI2.5).MethodsWe conducted a pilot study on people undergoing MBW tests: 10 healthy controls (HC) and 43 cystic fibrosis (CF) subjects performed an SVC after the standard end of test. We term the new outcome LCI with Short extension (LCIShX). We assessed (i) CF/ HC differences, (ii) variability (iii) effect of pulmonary exacerbation (PEx)/treatment and (iv) relationship with CF computed tomography (CFCT) scores.ResultsHC/ CF group differences were larger with LCIShXthan LCI2.5(P<0.001). Within the CF group UVLU was highly variable and when abnormal it did not correlate with corresponding LCI2.5. Signal showed little variability during clinical stability (n= 11 CF; 2 visits; median inter-test variability 2.6% LCIShX,2.5% LCI2.5). PEx signal was significantly greater for LCIShXboth for onset and resolution. Both MBW parameters correlated significantly with total lung CT scores and hyperinflation but only LCIShXcorrelated with mucus plugging.ConclusionsUVLU captured within the LCIShXvaries between individuals; the lack of relationship with LCI2.5demonstrates that new, additional information is being captured. LCIShXrepeatability during clinical stability combined with its larger signal around episodes of PEx may lend it superior sensitivity as an outcome measure. Further studies will build on this pilot data to fully establish its utility in monitoring disease status.