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Idiopathic Pulmonary Fibrosis: The Importance of Qualitative and Quantitative Phenotyping

التفاصيل البيبلوغرافية
العنوان: Idiopathic Pulmonary Fibrosis: The Importance of Qualitative and Quantitative Phenotyping
المؤلفون: Flaherty, Kevin R.
بيانات النشر: Blackwell Publishing Ltd
سنة النشر: 2009
المجموعة: University of Michigan: Deep Blue
مصطلحات موضوعية: Pulmonary Fibrosis, Imaging, High Resolution Computed Tomography, Computer Science, Medicine (General), Engineering, Health Sciences
الوصف: Peer Reviewed ; http://deepblue.lib.umich.edu/bitstream/2027.42/71750/1/j.1617-0830.2009.01127.x.pdfTest
نوع الوثيقة: article in journal/newspaper
وصف الملف: 577478 bytes; 3109 bytes; application/pdf; text/plain
اللغة: unknown
تدمد: 1433-3317
1617-0830
العلاقة: Flaherty, K. R. (2009). "Idiopathic Pulmonary Fibrosis: The Importance of Qualitative and Quantitative Phenotyping." Imaging Decisions MRI 13(1): 18-23.; https://hdl.handle.net/2027.42/71750Test; Imaging Decisions MRI; American Thoracic Society, European Respiratory Society. American thoracic society/European respiratory society international multidisciplinary consensus classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 2002; 165: 277 – 304.; Bjoraker J, Ryu J, Edwin M et al. Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998; 157: 199 – 203.; Daniil Z, Gilchrist F, Nicholson A et al. A histologic pattern of nonspecific interstitial pneumonia is associated with a better prognosis than usual interstitial pneumonia in patients with cryptogenic fibrosing alveolitis. Am J Respir Crit Care Med 1999; 160: 899 – 905.; Flaherty K, Toews G, Travis W et al. Clinical significance of histological classification of idiopathic interstitial pneumonia. Eur Respir J 2002; 19: 275 – 283.; Katzenstein A, Fiorelli R. Nonspecific interstitial pneumonia/fibrosis. Histologic features and clinical significance. Am J Surg Pathol 1994; 18: 136 – 147.; Katzenstein A, Myers J. Idiopathic pulmonary fibrosis. Clinical relevance of pathologic classification. Am J Respir Crit Care Med 1998; 157: 1301 – 1315.; Travis W, Matsui K, Moss J, Ferrans V. Idiopathic nonspecific interstitial pneumonia: prognostic significance of cellular and fibrosing patterns. Am J Surg Path 2000; 24: 19 – 33.; Flaherty K, Martinez F, Travis W, Lynch J III. Nonspecific interstitial pneumonia (nsip). Sem Respir Crit Care Med 2001; 22: 423 – 433.; Flaherty K, Martinez F. Diagnosing interstitial lung disease: a practical approach to a difficult problem. Cleve Clin J Med 2001; 68: 33 – 49.; Martinez FJ, Flaherty K. Pulmonary function testing in idiopathic interstitial pneumonias. Proc Am Thorac Soc 2006; 3: 315 – 321.; Raghu G, Weycker D, Edelsberg J, Bradford WZ, Oster G. Incidence and prevalence of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2006; 174: 810 – 816.; Hunninghake G, Lynch D, Galvin J et al. Radiologic findings are strongly associated with a pathologic diagnosis of usual interstitial pneumonia. Chest 2003; 124: 1215 – 1223.; Raghu G, Mageto Y, Lockhart D, Schmidt R, Wood D, Godwin J. The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: a prospective study. Chest 1999; 116: 1168 – 1174.; Travis WD, Hunninghake G, King TE Jr et al. Idiopathic nonspecific interstitial pneumonia: report of an american thoracic society project. Am J Respir Crit Care Med 2008; 177: 1338 – 1347.; Flaherty K, Thwaite E, Kazerooni E et al. Radiological versus histological diagnosis in UIP and NSIP: survival implications. Thorax 2003; 58: 143 – 148.; Sumikawa H, Johkoh T, Colby TV et al. Computed tomography findings in pathological usual interstitial pneumonia: relationship to survival. Am J Respir Crit Care Med 2008; 177: 433 – 439.; Gay S, Kazerooni E, Toews G et al. Idiopathic pulmonary fibrosis. Predicting response to therapy and survival. Am J Respir Crit Care Med 1998; 157: 1063 – 1072.; Wells A, Hansell D, Rubens M, Cullinan P, Black C, DuBois R. The predictive value of appearances on thin-section computed tomography in fibrosing alveolitis. Am Rev Respir Dis 1993; 148: 1076 – 1082.; King TE Jr, Behr J, Brown KK et al. A randomized placebo-controlled trial of bosentan in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2009; 374: 222 – 228.; King TE Jr, Albera C, Bradford WZ et al. Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (inspire): a multicentre, randomised, placebo-controlled trial. Lancet 2008; 77: 75 – 81.; Flaherty K, Mumford J, Murray S et al. Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 2003; 168: 543 – 548.; Collard H, King T, Bartelson B, Vourlekis J, Schwarz M, Brown K. Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2003; 168: 538 – 542.; Latsi PI, du Bois RM, Nicholson AG et al. Fibrotic idiopathic interstitial pneumonia: the prognostic value of longitudinal functional trends. Am J Respir Crit Care Med 2003; 168: 531 – 537.; Flaherty KR, Andrei AC, Murray S et al. Idiopathic pulmonary fibrosis: prognostic value of changes in physiology and six-minute-walk test. Am J Respir Crit Care Med 2006; 174: 803 – 809.; Martinez FJ, Safrin S, Weycker D et al. The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med 2005; 142: 963 – 967.; King TE Jr, Safrin S, Starko KM et al. Analyses of efficacy end points in a controlled trial of interferon-gamma1b for idiopathic pulmonary fibrosis. Chest 2005; 127: 171 – 177.; Hartman T, Primack S, Kang E et al. Disease progression in usual interstitial pneumonia compared with desquamative interstitial pneumonia. Chest 1996; 110: 378 – 382.; Xaubet A, Agusti C, Luburich P et al. Pulmonary function tests and ct scan in the management of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998; 158: 431 – 436.; Nagao T, Nagai S, Hiramoto Y et al. Serial evaluation of high-resolution computed tomography findings in patients with idiopathic pulmonary fibrosis in usual interstitial pneumonia. Respiration 2002; 69: 413 – 419.; Azuma A, Nukiwa T, Tsuboi E et al. Double-blind, placebo-controlled trial of pirfenidone in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2005; 171: 1040 – 1047.; Camiciottoli G, Orlandi I, Bartolucci M et al. Lung ct densitometry in systemic sclerosis: correlation with lung function, exercise testing, and quality of life. Chest 2007; 131: 672 – 681.; Best AC, Lynch AM, Bozic CM, Miller D, Grunwald GK, Lynch DA. Quantitative ct indexes in idiopathic pulmonary fibrosis: relationship with physiologic impairment. Radiology 2003; 228: 407 – 414.; Uppaluri R, Hoffman E, Sonka M, Hartley P, Hunninghake G, McLennan G. Computer recognition of regional lung disease patterns. Am J Respir Crit Care Med 1999; 160: 648 – 654.; Uppaluri R, Hoffman E, Sonka M, Hunninghake G, McLennan G. Interstitial lung disease: a quantitative study using the adaptive multiple feature method. Am J Respir Crit Care Med 1999; 159: 519 – 525.; Uppaluri R, Mitsa T, Sonka M, Hoffman E, McLennan G. Quantification of pulmonary emphysema with lung CT images using texture analysis. Am J Respir Crit Care Med 1997; 156: 248 – 254.; Xu Y, vanBeek E, Hwanjo Y, Guo J, McLennan G, Hoffman E. Computer-aided classification of interstitial lung diseases via MDCT: 3D adaptive multiple feature method (3D AMFM). Acad radiol 2006; 13: 969 – 978.
DOI: 10.1111/j.1617-0830.2009.01127.x
الإتاحة: https://doi.org/10.1111/j.1617-0830.2009.01127.xTest
https://hdl.handle.net/2027.42/71750Test
حقوق: © 2009 Blackwell Publishing Ltd
رقم الانضمام: edsbas.AFEBA065
قاعدة البيانات: BASE
الوصف
تدمد:14333317
16170830
DOI:10.1111/j.1617-0830.2009.01127.x