Lung clearance index in adults with non-cystic fibrosis bronchiectasis

被引:39
作者
Gonem, Sherif [1 ,5 ]
Scadding, Alys [1 ]
Soares, Marcia [1 ]
Singapuri, Amisha [1 ]
Gustafsson, Per [2 ]
Ohri, Chandra [1 ]
Range, Simon [1 ]
Brightling, Christopher E. [1 ]
Pavord, Ian [1 ]
Horsley, Alex [3 ,4 ]
Siddiqui, Salman [1 ]
机构
[1] Univ Leicester, Inst Lung Hlth, Leicester, Leics, England
[2] Cent Hosp Skovde, Dept Paediat, S-54185 Skovde, Sweden
[3] Manchester Adult Cyst Fibrosis Ctr, Manchester, Lancs, England
[4] Univ Manchester, Inst Inflammat & Repair, Manchester, Lancs, England
[5] Glenfield Gen Hosp, Resp BRU, Leicester LE3 9QP, Leics, England
来源
RESPIRATORY RESEARCH | 2014年 / 15卷
关键词
Bronchiectasis; Lung clearance index; Ventilation heterogeneity; VENTILATION HETEROGENEITY; AIRWAYS DISEASE; ACINAR; STANDARDIZATION; ASTHMA; CF;
D O I
10.1186/1465-9921-15-59
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Lung clearance index (LCI) is a measure of abnormal ventilation distribution derived from the multiple breath inert gas washout (MBW) technique. We aimed to determine the clinical utility of LCI in non-CF bronchiectasis, and to assess two novel MBW parameters that distinguish between increases in LCI due to specific ventilation inequality (LCIvent) and increased respiratory dead space (LCIds). Methods: Forty-three patients with non-CF bronchiectasis and 18 healthy control subjects underwent MBW using the sulphur hexafluoride wash-in technique, and data from 40 adults with CF were re-analysed. LCIvent and LCIds were calculated using a theoretical two-compartment lung model, and represent the proportional increase in LCI above its ideal value due to specific ventilation inequality and increased respiratory dead space, respectively. Results: LCI was significantly raised in patients with non-CF bronchiectasis compared to healthy controls (9.99 versus 7.28, p < 0.01), and discriminated well between these two groups (area under receiver operating curve = 0.90, versus 0.83 for forced expiratory volume in one second [% predicted]). LCI, LCIvent and LCIds were repeatable (intraclass correlation coefficient > 0.75), and correlated significantly with measures of spirometric airflow obstruction. Conclusion: LCI is repeatable, discriminatory, and is associated with spirometric airflow obstruction in patients with non-CF bronchiectasis. LCIvent and LCIds are a practical and repeatable alternative to phase III slope analysis and may allow a further level of mechanistic information to be extracted from the MBW test in patients with severe ventilation heterogeneity.
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页数:9
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共 27 条
[1]   The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis [J].
Amin, R. ;
Subbarao, P. ;
Lou, W. ;
Jabar, A. ;
Balkovec, S. ;
Jensen, R. ;
Kerrigan, S. ;
Gustafsson, P. ;
Ratjen, F. .
EUROPEAN RESPIRATORY JOURNAL, 2011, 37 (04) :806-812
[2]   Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function [J].
Amin, Reshma ;
Subbarao, Padmaja ;
Jabar, Alisha ;
Balkovec, Susan ;
Jensen, Renee ;
Kerrigan, Shawn ;
Gustafsson, Per ;
Ratjen, Felix .
THORAX, 2010, 65 (05) :379-383
[3]   Early Cystic Fibrosis Lung Disease Detected by Bronchoalveolar Lavage and Lung Clearance Index [J].
Belessis, Yvonne ;
Dixon, Barbara ;
Hawkins, Glenn ;
Pereira, John ;
Peat, Jenny ;
MacDonald, Rebecca ;
Field, Penny ;
Numa, Andrew ;
Morton, John ;
Lui, Kei ;
Jaffe, Adam .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2012, 185 (08) :862-873
[4]   VOLUNTARY CHANGES IN BREATHING PATTERN AND N2 CLEARANCE FROM LUNGS [J].
BOUHUYS, A ;
LUNDGREN, C ;
LUDIN, G ;
LICHTNECKERT, S .
JOURNAL OF APPLIED PHYSIOLOGY, 1961, 16 (05) :1039-&
[5]   CONVECTION-DEPENDENT AND DIFFUSION-DEPENDENT VENTILATION MALDISTRIBUTION IN NORMAL SUBJECTS [J].
CRAWFORD, ABH ;
MAKOWSKA, M ;
PAIVA, M ;
ENGEL, LA .
JOURNAL OF APPLIED PHYSIOLOGY, 1985, 59 (03) :838-846
[6]   Studies on the intrapulmonary mixture of gases. III. An open circuit method for measuring residual air [J].
Darling, RC ;
Cournand, A ;
Richards, DW .
JOURNAL OF CLINICAL INVESTIGATION, 1940, 19 (04) :609-618
[7]   Research priorities in bronchiectasis [J].
De Soyza, Anthony ;
Brown, Jeremy Stuart ;
Loebinger, Michael R. .
THORAX, 2013, 68 (07) :695-696
[8]   Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis [J].
Horsley, A. R. ;
Gustafsson, P. M. ;
Macleod, K. A. ;
Saunders, C. ;
Greening, A. P. ;
Porteous, D. J. ;
Davies, J. C. ;
Cunningham, S. ;
Alton, E. W. F. W. ;
Innes, J. A. .
THORAX, 2008, 63 (02) :135-140
[9]   Lung clearance index in the assessment of airways disease [J].
Horsley, Alex .
RESPIRATORY MEDICINE, 2009, 103 (06) :793-799
[10]   Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis [J].
Horsley, Alex R. ;
Macleod, Kenneth A. ;
Robson, Andrew G. ;
Lenney, Jill ;
Bell, Nicholas J. ;
Cunningham, Steve ;
Greening, Andrew P. ;
Gustafsson, Per M. ;
Innes, J. Alastair .
RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY, 2008, 162 (03) :197-203