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Volumn 70, Issue 4, 2015, Pages 305-306

Wavering in the breeze: Is multiple breath washout useful in primary ciliary dyskinesia?

Author keywords

[No Author keywords available]

Indexed keywords

AIRWAY; ANALYZER; BRONCHIECTASIS; CILIARY DYSKINESIA; CYSTIC FIBROSIS; EDITORIAL; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; HIGH RESOLUTION COMPUTER TOMOGRAPHY; HUMAN; LUNG CLEARANCE; LUNG CLEARANCE INDEX; LUNG FUNCTION TEST; MULTIPLE BREATH WASHOUT; NITROGEN WASHOUT; PLETHYSMOGRAPHY; PRIORITY JOURNAL; RESPIRATORY TRACT PARAMETERS; SCORING SYSTEM; SENSITIVITY ANALYSIS; SPIROMETRY; TIDAL VOLUME; FEMALE; LUNG; MALE; PATHOPHYSIOLOGY;

EID: 84925613937     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2015-206822     Document Type: Editorial
Times cited : (10)

References (20)
  • 1
    • 0347766074 scopus 로고    scopus 로고
    • Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis
    • de Jong PA, Nakano Y, Lequin MH, et al. Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis. Eur Respir J 2004; 23: 93-7.
    • (2004) Eur Respir J , vol.23 , pp. 93-97
    • De Jong, P.A.1    Nakano, Y.2    Lequin, M.H.3
  • 2
    • 9644259076 scopus 로고    scopus 로고
    • Multiple inert gas washout as a measure of ventilation distribution in children with cystic fibrosis
    • Aurora P, Gustafsson P, Bush A, et al. Multiple inert gas washout as a measure of ventilation distribution in children with cystic fibrosis. Thorax 2004; 59: 1068-73.
    • (2004) Thorax , vol.59 , pp. 1068-1073
    • Aurora, P.1    Gustafsson, P.2    Bush, A.3
  • 3
    • 12744277962 scopus 로고    scopus 로고
    • Multiple breath washout as a marker of lung disease in preschool children with cystic fibrosis
    • Aurora P, Bush A, Gustafsson P, et al. Multiple breath washout as a marker of lung disease in preschool children with cystic fibrosis. Am J Respir Crit Care Med 2005; 171: 249-56.
    • (2005) Am J Respir Crit Care Med , vol.171 , pp. 249-256
    • Aurora, P.1    Bush, A.2    Gustafsson, P.3
  • 4
    • 13544250572 scopus 로고    scopus 로고
    • Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis
    • Kraemer R, Blum A, Schibler A, et al. Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis. Am J Respir Crit Care Med 2005; 171: 371-8.
    • (2005) Am J Respir Crit Care Med , vol.171 , pp. 371-378
    • Kraemer, R.1    Blum, A.2    Schibler, A.3
  • 5
    • 79952504576 scopus 로고    scopus 로고
    • Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis
    • Aurora P, Stanojevic S, Wade A, et al; on behalf of the London CF Collaboration. Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis. Am J Respir Crit Care Med 2011; 183: 752-8.
    • (2011) Am J Respir Crit Care Med , vol.183 , pp. 752-758
    • Aurora, P.1    Stanojevic, S.2    Wade, A.3
  • 6
    • 84890309789 scopus 로고    scopus 로고
    • Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis
    • Vermeulen F, Proesmans M, Boon M, et al. Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis. Thorax 2014; 69: 39-45.
    • (2014) Thorax , vol.69 , pp. 39-45
    • Vermeulen, F.1    Proesmans, M.2    Boon, M.3
  • 7
    • 84877593162 scopus 로고    scopus 로고
    • Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation
    • Horsley AR, Davies JC, Gray RD, et al. Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation. Thorax 2013; 68: 532-9.
    • (2013) Thorax , vol.68 , pp. 532-539
    • Horsley, A.R.1    Davies, J.C.2    Gray, R.D.3
  • 8
    • 77951988740 scopus 로고    scopus 로고
    • Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function
    • Amin R, Subbarao P, Jabar A, et al. Hypertonic saline improves the LCI in paediatric patients with CF with normal lung function. Thorax 2010; 65: 379-83.
    • (2010) Thorax , vol.65 , pp. 379-383
    • Amin, R.1    Subbarao, P.2    Jabar, A.3
  • 9
    • 79953287790 scopus 로고    scopus 로고
    • The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis
    • Amin R, Subbarao P, Lou W, et al. The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis. Eur Respir J 2011; 37: 806-12.
    • (2011) Eur Respir J , vol.37 , pp. 806-812
    • Amin, R.1    Subbarao, P.2    Lou, W.3
  • 10
    • 84882662774 scopus 로고    scopus 로고
    • Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline
    • Subbarao P, Stanojevic S, Brown M, et al. Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline. Am J Respir Crit Care Med 2013; 188: 456-60.
    • (2013) Am J Respir Crit Care Med , vol.188 , pp. 456-460
    • Subbarao, P.1    Stanojevic, S.2    Brown, M.3
  • 11
    • 84885071273 scopus 로고    scopus 로고
    • Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: A randomised controlled trial
    • Davies J, Sheridan H, Bell N, et al. Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: A randomised controlled trial. Lancet Respir Med 2013; 1: 630-8.
    • (2013) Lancet Respir Med , vol.1 , pp. 630-638
    • Davies, J.1    Sheridan, H.2    Bell, N.3
  • 12
    • 39049084491 scopus 로고    scopus 로고
    • Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis
    • Gustafsson PM, De Jong PA, Tiddens HA, et al. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis. Thorax 2008; 63: 129-34.
    • (2008) Thorax , vol.63 , pp. 129-134
    • Gustafsson, P.M.1    De Jong, P.A.2    Tiddens, H.A.3
  • 13
    • 79956360940 scopus 로고    scopus 로고
    • Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF
    • Owens CM, Aurora P, Stanojevic S, et al; London Cystic Fibrosis Collaboration. Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF. Thorax 2011; 66: 481-8.
    • (2011) Thorax , vol.66 , pp. 481-488
    • Owens, C.M.1    Aurora, P.2    Stanojevic, S.3
  • 14
    • 84878792913 scopus 로고    scopus 로고
    • Age and height dependence of lung clearance index and functional residual capacity
    • Lum S, Stocks J, Stanojevic S, et al. Age and height dependence of lung clearance index and functional residual capacity. Eur Respir J 2013; 41: 1371-7.
    • (2013) Eur Respir J , vol.41 , pp. 1371-1377
    • Lum, S.1    Stocks, J.2    Stanojevic, S.3
  • 15
    • 84865289066 scopus 로고    scopus 로고
    • Ventilation heterogeneity in the acinar and conductive zones of the normal ageing lung
    • Verbanck S, Thompson BR, Schuermans D, et al. Ventilation heterogeneity in the acinar and conductive zones of the normal ageing lung. Thorax 2012; 67(Suppl 9): 789-95.
    • (2012) Thorax , vol.67 , pp. 789-795
    • Verbanck, S.1    Thompson, B.R.2    Schuermans, D.3
  • 16
    • 84855203126 scopus 로고    scopus 로고
    • Ventilation inhomogeneity in children with primary ciliary dyskinesia
    • Green K, Buchvald FF, Marthin JK, et al. Ventilation inhomogeneity in children with primary ciliary dyskinesia. Thorax 2012; 67: 49-53.
    • (2012) Thorax , vol.67 , pp. 49-53
    • Green, K.1    Buchvald, F.F.2    Marthin, J.K.3
  • 17
    • 84883527776 scopus 로고    scopus 로고
    • Lung clearance index and high-resolution computed tomography scores in primary ciliary dyskinesia
    • Irving SJ, Ives A, Davies G, et al. Lung clearance index and high-resolution computed tomography scores in primary ciliary dyskinesia. Am J Respir Crit Care Med 2013; 188: 545-9.
    • (2013) Am J Respir Crit Care Med , vol.188 , pp. 545-549
    • Irving, S.J.1    Ives, A.2    Davies, G.3
  • 18
    • 84895535623 scopus 로고    scopus 로고
    • Lung clearance index is a repeatable and sensitive indicator of radiological changes in bronchiectasis
    • Rowan SA, Bradley JM, Bradbury I, et al. Lung clearance index is a repeatable and sensitive indicator of radiological changes in bronchiectasis. Am J Respir Crit Care Med 2014; 189: 586-92.
    • (2014) Am J Respir Crit Care Med , vol.189 , pp. 586-592
    • Rowan, S.A.1    Bradley, J.M.2    Bradbury, I.3
  • 19
    • 84899848113 scopus 로고    scopus 로고
    • Lung clearance index in primary ciliary dyskinesia and bronchiectasis
    • Irving SJ, Davies JC, Alton EW, et al. Lung clearance index in primary ciliary dyskinesia and bronchiectasis. Am J Respir Crit Care Med 2014; 189: 1147-8.
    • (2014) Am J Respir Crit Care Med , vol.189 , pp. 1147-1148
    • Irving, S.J.1    Davies, J.C.2    Alton, E.W.3
  • 20
    • 84925667139 scopus 로고    scopus 로고
    • Lung structure-function correlation in patients with primary ciliary dyskinesia
    • Boon M, Vermeulen F, Gysemans M, et al. Lung structure-function correlation in patients with primary ciliary dyskinesia. Thorax 2015; 70: 339-45.
    • (2015) Thorax , vol.70 , pp. 339-345
    • Boon, M.1    Vermeulen, F.2    Gysemans, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.