Chest computed tomography scans should be considered as a routine investigation in cystic fibrosis
Tài liệu tham khảo
Armstrong, 1997, Lower airway inflammation in infants and young children with cystic fibrosis, Am J Resp Crit Care Med, 156, 1197, 10.1164/ajrccm.156.4.96-11058
Nixon, 2002, Early airway infection, inflammation, and lung function in cystic fibrosis, Arch Dis Child, 87, 306, 10.1136/adc.87.4.306
Young, 1991, high resolution CT and bronchography in the asssessment of bronchiectasis, Acta Radiologica, 32, 439, 10.3109/02841859109177603
Hansell, 1998, Bronchiectasis, Radiologic Clinics of North America, 36, 107, 10.1016/S0033-8389(05)70009-9
Munro, 1990, Comparison of thin section computed tomography with bronchography for identifying bronchiectatic segments in patients with chronic sputum production, Thorax, 45, 135, 10.1136/thx.45.2.135
Bhalla, 1991, Cystic fibrosis: scoring system with thin-section CT, Radiology, 179, 783, 10.1148/radiology.179.3.2027992
Maffessanti, 1996, Cystic fibrosis in children: HRCT findings and distribution of disease, J Thorac Imaging, 11, 27, 10.1097/00005382-199601110-00002
Nathanson, 1991, Ultrafast computerized tomography of the chest in cystic fibrosis: a new scoring system, Pediatr Pulmonol, 11, 81, 10.1002/ppul.1950110112
Santamaria, 1998, Cystic fibrosis: when should high-resolution computed tomography of the chest Be obtained?, Pediatrics, 101, 908, 10.1542/peds.101.5.908
Shale, 1994, Chest radiology in cystic fibrosis: is scoring useful, Thorax, 847, 10.1136/thx.49.9.847
Armstrong, 2000, Lower airway inflammation in cystic fibrosis infants, Pediatr Pulmonol, S5.3
Burns, 2001, Longitudinal assessment of Pseudomonas aeruginosa in young children with cystic fibrosis, J Infect Dis, 183, 444, 10.1086/318075
Li, 2005, Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis, JAMA, 293, 581, 10.1001/jama.293.5.581
Meyer, 1997, Regional variability of lung inflammation in cystic fibrosis, Am J Respir Crit Care Med, 156, 1536, 10.1164/ajrccm.156.5.9701098
Tiddens, 1995, Cartilaginous airway dimensions and airflow obstruction in human lungs, Am J Resp Crit Care Med, 152, 260, 10.1164/ajrccm.152.1.7599833
Tiddens, 2000, Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs, Eur Resp J, 15, 735, 10.1034/j.1399-3003.2000.15d18.x
de Jong, 2004, Pulmonary disease assessment in cystic fibrosis: Comparison of CT scoring systems and value of bronchial and arterial dimension measurements, Radiology, 231, 434, 10.1148/radiol.2312021393
Kuwano, 1993, Small airways dimensions in asthma and chronic obstructive pulmonary disease, Am Rev Resp Dis, 148, 1220, 10.1164/ajrccm/148.5.1220
Hogg, 1968, Site and nature of airway obstruction in chronic obstructive lung disease, New England Journal of Medicine, 278, 1355, 10.1056/NEJM196806202782501
Macklem PT. 1978. The site of airways obstruction in asthma. In M.A. de Kock and N. Lewis, editors. Mechanics of airways obstruction. 209–220.
Goris, 2003, An automated approach to quantitative air trapping measurements in mild cystic fibrosis, Chest, 123, 1655, 10.1378/chest.123.5.1655
Robinson, 2001, Spirometer-triggered high-resolution computed tomography and pulmonary function measurements during an acute exacerbation in patients with cystic fibrosis, J Pediatr, 138, 553, 10.1067/mpd.2001.111820
Long, 2004, Structural airway abnormalities in infants and young children with cystic fibrosis, J Pediatr, 144, 154, 10.1016/j.jpeds.2003.09.026
Martinez, 2005, High Resolution Computed Tomography Imaging of Airway Disease in Infants with Cystic Fibrosis, Am J Respir Crit Care Med, 10.1164/rccm.200412-1665OC
de Jong, 2004, Progressive damage on high-resolution computed tomography despite stable lung function in CF, Eur Respir J, 23, 93, 10.1183/09031936.03.00006603
Garcia, 2005, Internal consistency and validity of the spanish version of the St. George Respiratory questionnaire for use in patients with clinically stable bronchiectasis, Archivos de Bronchoneumologia, 41, 110, 10.1016/S1579-2129(06)60410-2
Scheinberg, 2005, A pilot study of the safety and efficacy of tobramycin s olution for inhalation in patients with severe bronchiectasis, Chest, 127, 1420, 10.1378/chest.127.4.1420
Marom, 1999, Cystic fibrosis: usefulness of thoracic CT in the examination of patients before lung transplantation, Radiology, 213, 283, 10.1148/radiology.213.1.r99oc12283
Paul, 2004, Effect of treatment with dornase alpha on airway inflammation in patients with cystic fibrosis, Am J Respir Crit Care Med, 169, 719, 10.1164/rccm.200307-959OC
Gappa, 2001, Lung function testing in infants with cystic fibrosis: lessons from the past and future directions, Pediatr Pulmonol, 32, 228, 10.1002/ppul.1113
Tepper, 1998, Assessment of the respiratory status of infants and toddlers with cystic ibrosis [editorial; comment], J Pediatr, 132, 380, 10.1016/S0022-3476(98)70002-2
Ranganathan, 2004, The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis, Am J Respir Crit Care Med, 169, 928, 10.1164/rccm.200309-1344OC
Aurora, 2005, Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis, Am J Respir Crit Care Med, 171, 249, 10.1164/rccm.200407-895OC
Gustafsson, 2003, Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis, Eur Respir J, 22, 972, 10.1183/09031936.03.00049502
Quan, 2001, A two-year randomized, placebo controlled trial of dornase alfa in young cystic fibrosis patients with mild lung function abnormalities, Journal of Pediatrics, 139, 813, 10.1067/mpd.2001.118570
Tiddens, 2002, Detecting early structural lung damage in cystic fibrosis, Pediatr Pulmonol Suppl, 34, 228, 10.1002/ppul.10134
Corey, 1997, Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis [see comments], J Pediatr, 131, 809, 10.1016/S0022-3476(97)70025-8
Goa, 1997, Dornase alfa. A review of pharmacoeconomic and quality-of-life aspects of its use in cystic fibrosis, Pharmacoeconomics, 12, 409, 10.2165/00019053-199712030-00011
Nasr, 2001, se of computerized tomography and chest x-rays in evaluating efficacy of aerosolized recombinant human DNase in cystic fibrosis patients younger than age 5 years: a preliminary study, Pediatr Pulmonol, 31, 377, 10.1002/ppul.1061
Robinson, 2003, Composite Spirometric-Ct Outcome Measure in Early Cystic Fibrosis (Cf) Lung Disease, Am J Respir Crit Care Med, 10.1164/rccm.200209-1093OC
Brody, 2005, Computed tomography correlates with pulmonary exacerbations in children with cystic fibrosis, Am J Respir Crit Care Med, 172, 1246, 10.1164/rccm.200503-401PP
Shah, 1997, High-resolution CT in the acute exacerbation of cystic fibrosis: evaluation of acute findings, reversibility of those findings, and clinical correlation, AJR Am J Roentgenol, 169, 375, 10.2214/ajr.169.2.9242738
Brody, 1999, High-resolution computed tomography of the chest in children with cystic fibrosis: support for use as an outcome surrogate, Pediatr Radiol, 29, 731, 10.1007/s002470050684
Joseph, 2001, Aerosol and lobar administration of a recombinant adenovirus to individuals with cystic fibrosis. I. Methods, safety, and clinical implications, Hum Gene Ther, 12, 1369, 10.1089/104303401750298535
de Jong, 2006, Estimation of cancer mortality associated with repetitive computed tomography scanning, Am J Respir Crit Care Med, 173, 199, 10.1164/rccm.200505-810OC
