메뉴 건너뛰기




Volumn 15, Issue 3, 2016, Pages 386-391

Infant lung function tests as endpoints in the ISIS multicenter clinical trial in cystic fibrosis

(23)  Davis, Stephanie D a,d   Ratjen, Felix b   Brumback, Lyndia C c   Johnson, Robin C d   Filbrun, Amy G e   Kerby, Gwendolyn S f   Panitch, Howard B g   Donaldson, Scott H d   Rosenfeld, Margaret h,u   Davis, Stephanie i   Faro, Albert j   Filbrun, Amy k   Hiatt, Peter l   Kerby, Gwendolyn m   McCoy, Karen n   McDowell, Karen o   Acton, James o   Milla, Carlos p   Panitch, Howard q   Prestridge, Adrienne r   more..


Author keywords

FEV; Forced expiratory flow rates; Pulmonary function tests

Indexed keywords

ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; EXPIRATORY RESERVE VOLUME; FEASIBILITY STUDY; FEMALE; FORCED EXPIRATORY FLOW; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; HUMAN; INFANT; INFANT DISEASE; LUNG FIBROSIS; LUNG FUNCTION; LUNG FUNCTION TEST; MALE; MULTICENTER STUDY; QUALITY OF LIFE; RANDOMIZED CONTROLLED TRIAL; SECONDARY ANALYSIS; CLINICAL TRIAL; CYSTIC FIBROSIS; DIMENSIONAL MEASUREMENT ACCURACY; LUNG; PATHOPHYSIOLOGY; PROCEDURES;

EID: 84964992868     PISSN: 15691993     EISSN: 18735010     Source Type: Journal    
DOI: 10.1016/j.jcf.2015.10.007     Document Type: Article
Times cited : (14)

References (23)
  • 1
    • 67650712233 scopus 로고    scopus 로고
    • Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening
    • Sly P.D., Brennan S., Gangell C., de Klerk N., Murray C., Mott L., et al. Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening. Am J Respir Crit Care Med 2009, 180:146-152.
    • (2009) Am J Respir Crit Care Med , vol.180 , pp. 146-152
    • Sly, P.D.1    Brennan, S.2    Gangell, C.3    de Klerk, N.4    Murray, C.5    Mott, L.6
  • 3
    • 11144355490 scopus 로고    scopus 로고
    • The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis
    • Ranganathan S.C., Stocks J., Dezateux C., Bush A., Wade A., Carr S., et al. The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis. Am J Respir Crit Care Med 2004, 169:928-933.
    • (2004) Am J Respir Crit Care Med , vol.169 , pp. 928-933
    • Ranganathan, S.C.1    Stocks, J.2    Dezateux, C.3    Bush, A.4    Wade, A.5    Carr, S.6
  • 7
    • 84861892411 scopus 로고    scopus 로고
    • Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial
    • Rosenfeld M., Ratjen F., Brumback L., Daniel S., Rowbotham R., McNamara S., et al. Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial. JAMA 2012, 307:2269-2277.
    • (2012) JAMA , vol.307 , pp. 2269-2277
    • Rosenfeld, M.1    Ratjen, F.2    Brumback, L.3    Daniel, S.4    Rowbotham, R.5    McNamara, S.6
  • 8
    • 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., Oliver C., Wallis C., Price J., et al. Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis. Am J Respir Crit Care Med 2005, 171:249-256.
    • (2005) Am J Respir Crit Care Med , vol.171 , pp. 249-256
    • Aurora, P.1    Bush, A.2    Gustafsson, P.3    Oliver, C.4    Wallis, C.5    Price, J.6
  • 9
    • 9644259076 scopus 로고    scopus 로고
    • Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis
    • Aurora P., Gustafsson P., Bush A., Lindblad A., Oliver C., Wallis C.E., et al. Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis. Thorax 2004, 59:1068-1073.
    • (2004) Thorax , vol.59 , pp. 1068-1073
    • Aurora, P.1    Gustafsson, P.2    Bush, A.3    Lindblad, A.4    Oliver, C.5    Wallis, C.E.6
  • 10
    • 84866070431 scopus 로고    scopus 로고
    • On behalf of the LCFC. Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening
    • Hoo A.F., Thia L.P., Nguyen T.T.D., Bush A., Chudleigh J., Lum S., et al. On behalf of the LCFC. Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening. Thorax 2012, 67:874-881.
    • (2012) Thorax , vol.67 , pp. 874-881
    • Hoo, A.F.1    Thia, L.P.2    Nguyen, T.T.D.3    Bush, A.4    Chudleigh, J.5    Lum, S.6
  • 11
    • 84959576858 scopus 로고    scopus 로고
    • Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?
    • Matecki S., Kent L., de Boeck K., Le Bourgeois M., Zielen S., Braggion C., et al. Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?. J Cyst Fibros 2016, 15:10-20.
    • (2016) J Cyst Fibros , vol.15 , pp. 10-20
    • Matecki, S.1    Kent, L.2    de Boeck, K.3    Le Bourgeois, M.4    Zielen, S.5    Braggion, C.6
  • 12
    • 30944466084 scopus 로고    scopus 로고
    • A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
    • Elkins M.R., Robinson M., Rose B.R., Harbour C., Moriarty C.P., Marks G.B., et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006, 354:229-240.
    • (2006) N Engl J Med , vol.354 , pp. 229-240
    • Elkins, M.R.1    Robinson, M.2    Rose, B.R.3    Harbour, C.4    Moriarty, C.P.5    Marks, G.B.6
  • 13
    • 85011306110 scopus 로고    scopus 로고
    • The ISIS Study Group, Infant PFTs as an Endpoint in the Infant Study of Inhaled Saline Randomized Controlled Trial
    • Davis S.D., Rosenfeld M., Brumback L., Donaldson S., Johnson R., Rowbotham R., et al. The ISIS Study Group, Infant PFTs as an Endpoint in the Infant Study of Inhaled Saline Randomized Controlled Trial. Pediatr Pulmonol Suppl 2012, 12:302.
    • (2012) Pediatr Pulmonol Suppl , vol.12 , pp. 302
    • Davis, S.D.1    Rosenfeld, M.2    Brumback, L.3    Donaldson, S.4    Johnson, R.5    Rowbotham, R.6
  • 14
    • 0034960994 scopus 로고    scopus 로고
    • ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/American Thoracic Society. Plethysmographic measurements of lung volume and airway resistance. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/ American Thoracic Society
    • Stocks J., Godfrey S., Beardsmore C., Bar-Yishay E., Castile R. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/American Thoracic Society. Plethysmographic measurements of lung volume and airway resistance. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/ American Thoracic Society. Eur Respir J 2001, 17:302-312.
    • (2001) Eur Respir J , vol.17 , pp. 302-312
    • Stocks, J.1    Godfrey, S.2    Beardsmore, C.3    Bar-Yishay, E.4    Castile, R.5
  • 15
    • 0033850618 scopus 로고    scopus 로고
    • Adult-type pulmonary function tests in infants without respiratory disease
    • Castile R., Filbrun D., Flucke R., Franklin W., McCoy K. Adult-type pulmonary function tests in infants without respiratory disease. Pediatr Pulmonol 2000, 30:215-227.
    • (2000) Pediatr Pulmonol , vol.30 , pp. 215-227
    • Castile, R.1    Filbrun, D.2    Flucke, R.3    Franklin, W.4    McCoy, K.5
  • 16
    • 30344465311 scopus 로고    scopus 로고
    • ATS/ERS statement: raised volume forced expirations in infants
    • ATS/ERS statement: raised volume forced expirations in infants. Am J Respir Crit Care Med 2005, 172:1463-1471.
    • (2005) Am J Respir Crit Care Med , vol.172 , pp. 1463-1471
  • 19
    • 84923183136 scopus 로고    scopus 로고
    • Pulmonary exacerbations and parent-reported outcomes in children <6 years with cystic fibrosis
    • Brumback L.C., Baines A., Ratjen F., Davis S.D., Daniel S.L., Quittner A.L., et al. Pulmonary exacerbations and parent-reported outcomes in children <6 years with cystic fibrosis. Pediatr Pulmonol 2014, 50(3):236-243.
    • (2014) Pediatr Pulmonol , vol.50 , Issue.3 , pp. 236-243
    • Brumback, L.C.1    Baines, A.2    Ratjen, F.3    Davis, S.D.4    Daniel, S.L.5    Quittner, A.L.6
  • 20
    • 84937435578 scopus 로고    scopus 로고
    • Initial evaluation of the Parent Cystic Fibrosis Questionnaire-Revised (CFQ-R) in infants and young children
    • Alpern A.N., Brumback L.C., Ratjen F., Rosenfeld M., Davis S.D., Quittner A.L. Initial evaluation of the Parent Cystic Fibrosis Questionnaire-Revised (CFQ-R) in infants and young children. J Cyst Fibros 2015, 14(3):403-411.
    • (2015) J Cyst Fibros , vol.14 , Issue.3 , pp. 403-411
    • Alpern, A.N.1    Brumback, L.C.2    Ratjen, F.3    Rosenfeld, M.4    Davis, S.D.5    Quittner, A.L.6
  • 21
    • 84884683771 scopus 로고    scopus 로고
    • Evolution of lung function during the first year of life in newborn screened cystic fibrosis infants
    • Nguyen T.T.D., Thia L.P., Hoo A.F., Bush A., Aurora P., Wade A., et al. Evolution of lung function during the first year of life in newborn screened cystic fibrosis infants. Thorax 2014, 69:910-917.
    • (2014) Thorax , vol.69 , pp. 910-917
    • Nguyen, T.T.D.1    Thia, L.P.2    Hoo, A.F.3    Bush, A.4    Aurora, P.5    Wade, A.6
  • 22
    • 34247167236 scopus 로고    scopus 로고
    • Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests
    • Lum S., Gustafsson P., Ljungberg H., Hulskamp G., Bush A., Carr S.B., et al. Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests. Thorax 2007, 62:341-347.
    • (2007) Thorax , vol.62 , pp. 341-347
    • Lum, S.1    Gustafsson, P.2    Ljungberg, H.3    Hulskamp, G.4    Bush, A.5    Carr, S.B.6
  • 23
    • 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., Jensen R., Rosenfeld M., Davis S., 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, 188:456-460.
    • (2013) Am J Respir Crit Care Med , vol.188 , pp. 456-460
    • Subbarao, P.1    Stanojevic, S.2    Brown, M.3    Jensen, R.4    Rosenfeld, M.5    Davis, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.