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Volumn 67, Issue 10, 2012, Pages 860-866

Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: A longitudinal study

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; CORRELATION ANALYSIS; CYSTIC FIBROSIS; DANISH; DISEASE REGISTRY; ETHNIC GROUP; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; LONGITUDINAL STUDY; LUNG FUNCTION TEST; MAJOR CLINICAL STUDY; MALE; MEASUREMENT ERROR; POPULATION RESEARCH; PRIORITY JOURNAL; PSEUDOMONAS INFECTION; REFERENCE VALUE;

EID: 84866120215     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2011-200953     Document Type: Article
Times cited : (145)

References (34)
  • 1
    • 33846229616 scopus 로고    scopus 로고
    • Priorities for respiratory research in the UK
    • DOI 10.1136/thx.2006.073882
    • Holgate ST. Priorities for respiratory research in the UK. Thorax 2007;62:5-7. (Pubitemid 46101759)
    • (2007) Thorax , vol.62 , Issue.1 , pp. 5-7
    • Holgate, S.T.1
  • 2
    • 66849138757 scopus 로고    scopus 로고
    • Monitoring respiratory disease severity in cystic fibrosis
    • Davies JC, Alton EW. Monitoring respiratory disease severity in cystic fibrosis. Respir Care 2009;54 :606-17.
    • (2009) Respir Care , vol.54 , pp. 606-617
    • Davies, J.C.1    Alton, E.W.2
  • 4
    • 34447530328 scopus 로고    scopus 로고
    • Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
    • Konstan MW, Morgan WJ, Butler SM, et al. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr 2007;151:134 e9, 139.e1.
    • (2007) J Pediatr , vol.151
    • Konstan, M.W.1    Morgan, W.J.2    Butler, S.M.3
  • 7
    • 0026520359 scopus 로고
    • Prediction of mortality in patients with cystic fibrosis
    • Kerem E, Reisman J, Corey M, et al. Prediction of mortality in patients with cystic fibrosis. N Engl J Med 1992;326:1187-91.
    • (1992) N Engl J Med , vol.326 , pp. 1187-1191
    • Kerem, E.1    Reisman, J.2    Corey, M.3
  • 8
    • 79952522208 scopus 로고    scopus 로고
    • Improved survival at low lung function in cystic fibrosis: Cohort study from 1990 to 2007
    • George PM, Banya W, Pareek N, et al. Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007. BMJ 2011; 342:d1008.
    • (2011) BMJ , vol.342
    • George, P.M.1    Banya, W.2    Pareek, N.3
  • 9
    • 34548278908 scopus 로고    scopus 로고
    • Power considerations for studies of lung function in cystic fibrosis
    • DOI 10.1513/pats.200611-176HT
    • Corey M. Power considerations for studies of lung function in cystic fibrosis. Proc Am Thorac Soc 2007; 4:334-7. (Pubitemid 47330866)
    • (2007) Proceedings of the American Thoracic Society , vol.4 , Issue.4 , pp. 334-337
    • Corey, M.1
  • 11
    • 34548262715 scopus 로고    scopus 로고
    • Poor airway function in early infancy and lung function by age 22 years: A non-selective longitudinal cohort study
    • DOI 10.1016/S0140-6736(07)61379-8, PII S0140673607613798
    • Stern DA, Morgan WJ, Wright AL, et al. Poor airway function in early infancy and lung function by age 22 years: a non-selective longitudinal cohort study. Lancet 2007;370:758-64. (Pubitemid 47320800)
    • (2007) Lancet , vol.370 , Issue.9589 , pp. 758-764
    • Stern, D.A.1    Morgan, W.J.2    Wright, A.L.3    Guerra, S.4    Martinez, F.D.5
  • 12
    • 79955148832 scopus 로고    scopus 로고
    • Genetic variation in TIMP1 but not MMPs predict excess FEV1 decline in two general population-based cohorts
    • van Diemen C, Postma D, Siedlinski M, et al. Genetic variation in TIMP1 but not MMPs predict excess FEV1 decline in two general population-based cohorts. Respir Res 2011;12:57.
    • (2011) Respir Res , vol.12 , pp. 57
    • Van Diemen, C.1    Postma, D.2    Siedlinski, M.3
  • 14
    • 0031471090 scopus 로고    scopus 로고
    • Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
    • DOI 10.1016/S0022-3476(97)70025-8
    • Corey M, Edwards L, Levison H, et al. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis. J Pediatr 1997;131:809-14. (Pubitemid 28027602)
    • (1997) Journal of Pediatrics , vol.131 , Issue.6 , pp. 809-814
    • Corey, M.1    Edwards, L.2    Levison, H.3    Knowles, M.4
  • 17
    • 0027551290 scopus 로고
    • Pulmonary function between 6 and 18 years of age
    • Wang X, Dockery DW, Wypij D, et al. Pulmonary function between 6 and 18 years of age. Pediatr Pulmonol 1993;15:75-88.
    • (1993) Pediatr Pulmonol , vol.15 , pp. 75-88
    • Wang, X.1    Dockery, D.W.2    Wypij, D.3
  • 20
    • 0020333131 scopus 로고
    • Random-effects models for longitudinal data
    • Laird NM, Ware JH. Random-effects models for longitudinal data. Biometrics 1982;38:963-74.
    • (1982) Biometrics , vol.38 , pp. 963-974
    • Laird, N.M.1    Ware, J.H.2
  • 21
    • 1642534562 scopus 로고    scopus 로고
    • The Repeatability of Forced Expiratory Volume Measurements in Adults with Cystic Fibrosis
    • DOI 10.1378/chest.125.1.150
    • Stanbrook MB, Corey M, Tullis DE. The repeatability of forced expiratory volume measurements in adults with cystic fibrosis. Chest 2004;125:150-5. (Pubitemid 38114577)
    • (2004) Chest , vol.125 , Issue.1 , pp. 150-155
    • Stanbrook, M.B.1    Corey, M.2    Tullis, D.E.3
  • 22
    • 0016811540 scopus 로고
    • Variability of routine pulmonary function tests
    • Hruby J, Butler J. Variability of routine pulmonary function tests. Thorax 1975;30:548-53.
    • (1975) Thorax , vol.30 , pp. 548-553
    • Hruby, J.1    Butler, J.2
  • 23
    • 0019387335 scopus 로고
    • Changes in measured spirometric indices. What is significant?
    • Pennock BE, Rogers RM, McCaffree DR. Changes in measured spirometric indices. What is significant? Chest 1981;80:97-9. (Pubitemid 11002843)
    • (1981) Chest , vol.80 , Issue.1 , pp. 97-99
    • Pennock, B.E.1    Rogers, R.M.2    McCaffree, D.R.3
  • 24
    • 0024985943 scopus 로고
    • Variability of pulmonary function tests in cystic fibrosis
    • Cooper PJ, Robertson CF, Hudson IL, et al. Variability of pulmonary function tests in cystic fibrosis. Pediatr Pulmonol 1990;8:16-22.
    • (1990) Pediatr Pulmonol , vol.8 , pp. 16-22
    • Cooper, P.J.1    Robertson, C.F.2    Hudson, I.L.3
  • 26
    • 55049140569 scopus 로고    scopus 로고
    • Annual assessment spirometry, plethysmography, and gas transfer in cystic fibrosis: Do they predict death or transplantation
    • Rosenthal M. Annual assessment spirometry, plethysmography, and gas transfer in cystic fibrosis: do they predict death or transplantation. Pediatr Pulmonol 2008;43:945-52.
    • (2008) Pediatr Pulmonol , vol.43 , pp. 945-952
    • Rosenthal, M.1
  • 27
    • 0033806235 scopus 로고    scopus 로고
    • Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis
    • Mastella G, Rainisio M, Harms HK, et al . Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis. Eur Respir J 2000;16:464-71.
    • (2000) Eur Respir J , vol.16 , pp. 464-471
    • Mastella, G.1    Rainisio, M.2    Harms, H.K.3
  • 28
    • 67949095989 scopus 로고    scopus 로고
    • Characterizing aggressiveness and predicting future progression of CF lung disease
    • Konstan MW, Wagener JS, VanDevanter DR. Characterizing aggressiveness and predicting future progression of CF lung disease. J Cyst Fibros 2009;8(Suppl 1): S15-19.
    • (2009) J Cyst Fibros , vol.8 , Issue.SUPPL. 1
    • Konstan, M.W.1    Wagener, J.S.2    VanDevanter, D.R.3
  • 29
    • 78649662363 scopus 로고    scopus 로고
    • Pulmonary outcome prediction (POP) tools for cystic fibrosis patients
    • Vandevanter DR, Wagener JS, Pasta DJ, et al. Pulmonary outcome prediction (POP) tools for cystic fibrosis patients. Pediatr Pulmonol 2010;45:1156-66.
    • (2010) Pediatr Pulmonol , vol.45 , pp. 1156-1166
    • Vandevanter, D.R.1    Wagener, J.S.2    Pasta, D.J.3
  • 30
    • 0026316543 scopus 로고
    • Cystic fibrosis: Current survival and population estimates to the year 2000
    • Elborn JS, Shale DJ, Britton JR. Cystic fibrosis: current survival and population estimates to the year 2000. Thorax 1991;46:881-5.
    • (1991) Thorax , vol.46 , pp. 881-885
    • Elborn, J.S.1    Shale, D.J.2    Britton, J.R.3
  • 31
    • 0033614639 scopus 로고    scopus 로고
    • Long-term effect of inhaled budesonide in mild and moderate chronic obstructive pulmonary disease: A randomised controlled trial
    • DOI 10.1016/S0140-6736(98)10019-3
    • Vestbo J, Sorensen T, Lange P, et al. Long-term effect of inhaled budesonide in mild and moderate chronic obstructive pulmonary disease: a randomised controlled trial. Lancet 1999;353:1819-23. (Pubitemid 29251012)
    • (1999) Lancet , vol.353 , Issue.9167 , pp. 1819-1823
    • Vestbo, J.1    Sorensen, T.2    Lange, P.3    Brix, A.4    Tone, P.5    Viskum, K.6
  • 32
    • 57349180789 scopus 로고    scopus 로고
    • Longitudinal decline in lung volume in a population of children with sickle cell disease
    • MacLean JE, Atenafu E, Kirby-Allen M, et al. Longitudinal decline in lung volume in a population of children with sickle cell disease. Am J Respir Crit Care Med 2008;178:1055-9.
    • (2008) Am J Respir Crit Care Med , vol.178 , pp. 1055-1059
    • MacLean, J.E.1    Atenafu, E.2    Kirby-Allen, M.3
  • 33
    • 67649777117 scopus 로고    scopus 로고
    • The natural history of chronic airflow obstruction revisited: An analysis of the Framingham offspring cohort
    • Kohansal R, Martinez-Camblor P, Agusti A, et al. The natural history of chronic airflow obstruction revisited: an analysis of the Framingham offspring cohort. Am J Respir Crit Care Med 2009;180:3-10.
    • (2009) Am J Respir Crit Care Med , vol.180 , pp. 3-10
    • Kohansal, R.1    Martinez-Camblor, P.2    Agusti, A.3
  • 34
    • 0029921514 scopus 로고    scopus 로고
    • Improved survival in the Danish center-treated cystic fibrosis patients: Results of aggressive treatment
    • DOI 10.1002/(SICI)1099-0496(199603)21:3<153::AID-PPUL1>3.0.CO;2-R
    • Frederiksen B, Lanng S, Koch C, et al. Improved survival in the Danish center-treated cystic fibrosis patients: results of aggressive treatment. Pediatr Pulmonol 1996;21:153-8. (Pubitemid 26127307)
    • (1996) Pediatric Pulmonology , vol.21 , Issue.3 , pp. 153-158
    • Frederiksen, B.1    Lanng, S.2    Koch, C.3    Hoiby, N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.