Arase Y, Suzuki F, Suzuki Y, Akuta N, Kobayashi M, Kawamura Y, Yatsuji H, Sezaki H, Hosaka T, Hirakawa M, Saito S, Ikeda K, Kumada H. Hepatitis C virus enhances incidence of idiopathic pulmonary fibrosis. World J Gastroenterol 2008; 14(38): 5880-5886 [PMID: 18855988 DOI: 10.3748/wjg.14.5880]
Corresponding Author of This Article
Yasuji Arase, MD, Department of Hepatology, Toranomon Hospital, 2-2-2, Toranomon, Minato-ku, Tokyo 105-8470, Japan. es9y-ars@asahi-net.or.jp
Article-Type of This Article
Rapid Communication
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World J Gastroenterol. Oct 14, 2008; 14(38): 5880-5886 Published online Oct 14, 2008. doi: 10.3748/wjg.14.5880
Table 1 Diagnostic criteria of IPF
Number
Criteria
Major criteria 1
Exclusion of other known caused of interstitial lung disease, such as certain drug toxicities, environmental exposures, and connective tissue diseases
Major criteria 2
Abnormal pulmonary function studies that include evidence of restriction (reduced breathing vital capacity) and impaired gas exchange (increased AaPO2 with rest or after exercising or decreased diffusion lung capacity)
Major criteria 3
Bibasilar reticular abnormalities with minimal ground glass opacities on conventional chest radiographs or high-resolution computed tomography scans
Major criteria 4
Histological lung examination or bronchoalveolar lavage showing no features to support an alternative diagnosis
Minor criteria 1
Age > 50 yr
Minor criteria 2
Insidious onset of otherwise unexplained dyspnea on exertion
Minor criteria 3
Duration of illness ≥ 3 mo
Minor criteria 4
Bibasilar, inspiratory crackles (dry or “Velcro” type in quality)
Citation: Arase Y, Suzuki F, Suzuki Y, Akuta N, Kobayashi M, Kawamura Y, Yatsuji H, Sezaki H, Hosaka T, Hirakawa M, Saito S, Ikeda K, Kumada H. Hepatitis C virus enhances incidence of idiopathic pulmonary fibrosis. World J Gastroenterol 2008; 14(38): 5880-5886