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Volumn 69, Issue 1, 2014, Pages 39-45

Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BIOMETRY; CF QUESTIONNAIRE REVISED; CHILD; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE EXACERBATION; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; LUNG CLEARANCE; LUNG CLEARANCE INDEX; MAJOR CLINICAL STUDY; MALE; OUTCOME ASSESSMENT; PREDICTION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSPECTIVE STUDY; QUESTIONNAIRE; RESPIRATORY TRACT PARAMETERS; SPIROMETRY; SYMPTOM; YOUNG ADULT;

EID: 84890309789     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2013-203807     Document Type: Article
Times cited : (76)

References (35)
  • 1
    • 34548278908 scopus 로고    scopus 로고
    • Power considerations for studies of lung function in cystic fibrosis
    • Corey M. Power considerations for studies of lung function in cystic fibrosis. Proc Am Thorac Soc 2007;4:334-7.
    • (2007) Proc Am Thorac Soc , vol.4 , pp. 334-337
    • Corey, M.1
  • 2
    • 84862184652 scopus 로고    scopus 로고
    • Feasibility and variability of measuring the Lung Clearance Index in a multi-center setting
    • Fuchs SI, Ellemunter H, Eder J, et al. Feasibility and variability of measuring the Lung Clearance Index in a multi-center setting. Pediatr Pulmonol 2012;47:649-57.
    • (2012) Pediatr Pulmonol , vol.47 , pp. 649-657
    • Fuchs, S.I.1    Ellemunter, H.2    Eder, J.3
  • 3
    • 84881381613 scopus 로고    scopus 로고
    • Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting
    • Singer F, Kieninger E, Abbas C, et al. Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting. Pediatr Pulmonol 2013;48:739-46.
    • (2013) Pediatr Pulmonol , vol.48 , pp. 739-746
    • Singer, F.1    Kieninger, E.2    Abbas, C.3
  • 4
    • 84875266201 scopus 로고    scopus 로고
    • Consensus statement for inert gas washout measurement using multiple- and single- breath tests
    • Robinson PD, Latzin P, Verbanck S, et al . Consensus statement for inert gas washout measurement using multiple- and single- breath tests. Eur Respir J 2013;41:507-22.
    • (2013) Eur Respir J , vol.41 , pp. 507-522
    • Robinson, P.D.1    Latzin, P.2    Verbanck, S.3    Al, E.4
  • 5
    • 84860477440 scopus 로고    scopus 로고
    • A realistic validation study of a new nitrogen multiple-breath washout system
    • Singer F, Houltz B, Latzin P, et al. A realistic validation study of a new nitrogen multiple-breath washout system. PLoS One 2012;7:e36083.
    • (2012) PLoS One , vol.7
    • Singer, F.1    Houltz, B.2    Latzin, P.3
  • 6
    • 49649099229 scopus 로고    scopus 로고
    • A novel sidestream ultrasonic flow sensor for multiple breath washout in children
    • Fuchs SI, Sturz J, Junge S, et al. A novel sidestream ultrasonic flow sensor for multiple breath washout in children. Pediatr Pulmonol 2008;43:731-8.
    • (2008) Pediatr Pulmonol , vol.43 , pp. 731-738
    • Fuchs, S.I.1    Sturz, J.2    Junge, S.3
  • 7
    • 73449102215 scopus 로고    scopus 로고
    • Lung clearance index: Normal values, repeatability, and reproducibility in healthy children and adolescents
    • Fuchs SI, Eder J, Ellemunter H, et al. Lung clearance index: normal values, repeatability, and reproducibility in healthy children and adolescents. Pediatr Pulmonol 2009;44:1180-5.
    • (2009) Pediatr Pulmonol , vol.44 , pp. 1180-1185
    • Fuchs, S.I.1    Eder, J.2    Ellemunter, H.3
  • 8
    • 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
  • 9
    • 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. 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
  • 10
    • 68049093796 scopus 로고    scopus 로고
    • Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis
    • Robinson PD, Cooper P, Van Asperen P, et al. Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis. Pediatr Pulmonol 2009;44:733-42.
    • (2009) Pediatr Pulmonol , vol.44 , pp. 733-742
    • Robinson, P.D.1    Cooper, P.2    Van Asperen, P.3
  • 11
    • 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
  • 12
    • 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
  • 13
    • 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
  • 14
    • 84872215342 scopus 로고    scopus 로고
    • Effect of ivacaftor on lung function in subjects with cystic fibrosis who have the G551D-CFTR mutation and mild lung disease: A comparison of lung clearance index (LCI) vs. Spirometry
    • abstract
    • Davies JC, Sheridan H, Lee P-S, et al. Effect of ivacaftor on lung function in subjects with cystic fibrosis who have the G551D-CFTR mutation and mild lung disease: a comparison of lung clearance index (LCI) vs. spirometry [abstract]. J Cyst Fibros 2012;11(Suppl 1):S15.
    • (2012) J Cyst Fibros , vol.11 , Issue.SUPPL. 1
    • Davies, J.C.1    Sheridan, H.2    Lee, P.-S.3
  • 15
    • 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 . 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    Al, E.4
  • 16
    • 84890309625 scopus 로고    scopus 로고
    • Does lung clearance index predict time to pulmonary excerbation?
    • Vermeulen F, Ophoff J, Proesmans M, et al. Does lung clearance index predict time to pulmonary excerbation? J Cyst Fibros 2012;11(Suppl 1):S14.
    • (2012) J Cyst Fibros , vol.11 , Issue.SUPPL. 1
    • Vermeulen, F.1    Ophoff, J.2    Proesmans, M.3
  • 17
    • 84863437624 scopus 로고    scopus 로고
    • Multi-ethnic reference values for spirometry for the 3-95-yr age range: The global lung function 2012 equations
    • Quanjer PH, Stanojevic S, Cole TJ, et al. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations. Eur Respir J 2012;40:1324-43.
    • (2012) Eur Respir J , vol.40 , pp. 1324-1343
    • Quanjer, P.H.1    Stanojevic, S.2    Cole, T.J.3
  • 18
    • 70450239749 scopus 로고    scopus 로고
    • References for growth and pubertal development from birth to 21 years in Flanders, Belgium
    • Roelants M, Hauspie R, Hoppenbrouwers K. References for growth and pubertal development from birth to 21 years in Flanders, Belgium. Ann Hum Biol 2009;36:680-94.
    • (2009) Ann Hum Biol , vol.36 , pp. 680-694
    • Roelants, M.1    Hauspie, R.2    Hoppenbrouwers, K.3
  • 19
    • 39049142717 scopus 로고    scopus 로고
    • Exacerbations in cystic fibrosis: 3 - Management
    • Smyth A, Elborn JS. Exacerbations in cystic fibrosis: 3 - Management. Thorax 2008;63:180-4.
    • (2008) Thorax , vol.63 , pp. 180-184
    • Smyth, A.1    Elborn, J.S.2
  • 20
    • 84867065315 scopus 로고    scopus 로고
    • Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national sample
    • Quittner AL, Sawicki GS, McMullen A, et al . Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national sample. Qual Life Res 2012;21:1267-78.
    • (2012) Qual Life Res , vol.21 , pp. 1267-1278
    • Quittner, A.L.1    Sawicki, G.S.2    McMullen, A.3    Al, E.4
  • 21
    • 1642402055 scopus 로고    scopus 로고
    • Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults
    • Klijn PH, van Stel HF, Quittner AL, et al. Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults. J Cyst Fibros 2004;3:29-36.
    • (2004) J Cyst Fibros , vol.3 , pp. 29-36
    • Klijn, P.H.1    Van Stel, H.F.2    Quittner, A.L.3
  • 22
    • 0032870518 scopus 로고    scopus 로고
    • Cystic fibrosis clinical score: A new scoring system to evaluate acute pulmonary exacerbation
    • Kanga J, Kuhn R, Craigmyle L, et al. Cystic fibrosis clinical score: a new scoring system to evaluate acute pulmonary exacerbation. Clin Ther 1999;21:1343-56.
    • (1999) Clin Ther , vol.21 , pp. 1343-1356
    • Kanga, J.1    Kuhn, R.2    Craigmyle, L.3
  • 23
    • 0038102859 scopus 로고    scopus 로고
    • Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients
    • Lee TW, Brownlee KG, Conway SP, et al. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros 2003;2:29-34.
    • (2003) J Cyst Fibros , vol.2 , pp. 29-34
    • Lee, T.W.1    Brownlee, K.G.2    Conway, S.P.3
  • 24
    • 34147215995 scopus 로고    scopus 로고
    • Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis
    • Goss CH, Burns JL. Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis. Thorax 2007;62:360-7.
    • (2007) Thorax , vol.62 , pp. 360-367
    • Goss, C.H.1    Burns, J.L.2
  • 25
    • 79958077769 scopus 로고    scopus 로고
    • Pulmonary exacerbation: Towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials
    • Bilton D, Canny G, Conway S, et al. Pulmonary exacerbation: towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials. J Cyst Fibros 2011;10(Suppl 2):S79-81.
    • (2011) J Cyst Fibros , vol.10 , Issue.SUPPL. 2
    • Bilton, D.1    Canny, G.2    Conway, S.3
  • 26
    • 84863453860 scopus 로고    scopus 로고
    • Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis
    • Waters V, Stanojevic S, Atenafu EG, et al. Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis. Eur Respir J 2012;40:61-6.
    • (2012) Eur Respir J , vol.40 , pp. 61-66
    • Waters, V.1    Stanojevic, S.2    Atenafu, E.G.3
  • 27
    • 67049100159 scopus 로고    scopus 로고
    • Quality of life in young people with cystic fibrosis: Effects of hospitalization, age and gender, and differences in parent/child perceptions
    • Hegarty M, Macdonald J, Watter P, et al. Quality of life in young people with cystic fibrosis: effects of hospitalization, age and gender, and differences in parent/child perceptions. Child Care Health Dev 2009;35:462-8.
    • (2009) Child Care Health Dev , vol.35 , pp. 462-468
    • Hegarty, M.1    Macdonald, J.2    Watter, P.3
  • 28
    • 77949502126 scopus 로고    scopus 로고
    • Impact of socioeconomic status, race, and ethnicity on quality of life in patients with cystic fibrosis in the United States
    • Quittner AL, Schechter MS, Rasouliyan L, et al. Impact of socioeconomic status, race, and ethnicity on quality of life in patients with cystic fibrosis in the United States. Chest 2010;137:642-50.
    • (2010) Chest , vol.137 , pp. 642-650
    • Quittner, A.L.1    Schechter, M.S.2    Rasouliyan, L.3
  • 29
    • 79960412250 scopus 로고    scopus 로고
    • Bronchiectasis and pulmonary exacerbations in children and young adults with cystic fibrosis
    • Loeve M, Gerbrands K, Hop WC, et al. Bronchiectasis and pulmonary exacerbations in children and young adults with cystic fibrosis. Chest 2011;140:178-85.
    • (2011) Chest , vol.140 , pp. 178-185
    • Loeve, M.1    Gerbrands, K.2    Hop, W.C.3
  • 30
    • 84882730090 scopus 로고    scopus 로고
    • Impact of bronchiectasis and trapped air on quality of life and exacerbations in CF
    • Tepper LA, Utens E, Caudri D, et al. Impact of bronchiectasis and trapped air on quality of life and exacerbations in CF. Eur Respir J 2013;42:371-9.
    • (2013) Eur Respir J , vol.42 , pp. 371-379
    • Tepper, L.A.1    Utens, E.2    Caudri, D.3
  • 31
    • 84860622874 scopus 로고    scopus 로고
    • Determining presence of lung disease in young children with cystic fibrosis: Lung clearance index, oxygen saturation and cough frequency
    • Bakker EM, van der Meijden JC, Nieuwhof EM, et al. Determining presence of lung disease in young children with cystic fibrosis: lung clearance index, oxygen saturation and cough frequency. J Cyst Fibros 2012;11:223-30.
    • (2012) J Cyst Fibros , vol.11 , pp. 223-230
    • Bakker, E.M.1    Van Der Meijden, J.C.2    Nieuwhof, E.M.3
  • 32
    • 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
  • 33
    • 84886379324 scopus 로고    scopus 로고
    • Small airway involvement in cystic fibrosis lung disease: Routine spirometry as an early and sensitive marker
    • Published Online First: 13 Feb doi: 10.1002/ppul.22777
    • Bakker EM, Borsboom GJ, van der Wiel-Kooij EC, et al. Small airway involvement in cystic fibrosis lung disease: routine spirometry as an early and sensitive marker. Pediatr Pulmonol Published Online First: 13 Feb 2013. doi: 10.1002/ppul.22777.
    • (2013) Pediatr Pulmonol
    • Bakker, E.M.1    Borsboom, G.J.2    Van Der Wiel-Kooij, E.C.3
  • 34
    • 39049105720 scopus 로고    scopus 로고
    • Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis
    • Horsley AR, Gustafsson PM, Macleod KA, et al. Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis. Thorax 2008;63:135-40.
    • (2008) Thorax , vol.63 , pp. 135-140
    • Horsley, A.R.1    Gustafsson, P.M.2    Macleod, K.A.3
  • 35
    • 0029924585 scopus 로고    scopus 로고
    • Determinants of mortality from cystic fibrosis in Canada, 1970-1989
    • Corey M, Farewell V. Determinants of mortality from cystic fibrosis in Canada, 1970-1989. Am J Epidemiol 1996;143:1007-17.
    • (1996) Am J Epidemiol , vol.143 , pp. 1007-1017
    • Corey, M.1    Farewell, V.2


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