Clinical course and changes in high-resolution computed tomography findings in patients with idiopathic pulmonary fibrosis without honeycombing

PLoS ONE

Volumn 11, Issue 11, 2016, Pages

  Yamauchi, Hiroyoshi ^a   Bando, Masashi ^a   Baba, Tomohisa ^b   Kataoka, Kensuke ^c   Yamada, Yoshihito ^d   Yamamoto, Hiroshi ^e   Miyamoto, Atsushi ^f   Ikushima, Soichiro ^g   Johkoh, Takeshi ^h   Sakai, Fumikazu ⁱ   Terasaki, Yasuhiro ^j   Hebisawa, Akira ^k   Kawabata, Yoshinori ^l   Sugiyama, Yukihiko ^a   Ogura, Takashi ^b  

^a JICHI MEDICAL UNIVERSITY   (Japan)

^b Kanagawa Prefectural Cardiovascular and Respiratory Diseases Center Hospital   (Japan)

^c TOSEI GENERAL HOSPITAL   (Japan)

^d EAST JAPAN RAILWAY COMPANY   (Japan)

^e SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f TORANOMON HOSPITAL   (Japan)

^g JAPANESE RED CROSS MEDICAL CENTER   (Japan)

^h Kinki Central Hospital of Mutual Association of Public School Teachers   (Japan)

ⁱ SAITAMA MEDICAL UNIVERSITY INTERNATIONAL MEDICAL CENTER   (Japan)

^j NIPPON MEDICAL SCHOOL   (Japan)

^k NATIONAL HOSPITAL ORGANIZATION   (Japan)

^l Saitama Prefectural Cardiovascular and Respiratory Centre   (Japan)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BRONCHIECTASIS; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; FEMALE; FIBROSING ALVEOLITIS; HIGH RESOLUTION COMPUTER TOMOGRAPHY; HUMAN; IMAGE ANALYSIS; IMAGE RECONSTRUCTION; INTERSTITIAL PNEUMONIA; LUNG BIOPSY; MALE; SURVIVAL TIME; DIAGNOSTIC IMAGING; LUNG; MIDDLE AGED; PATHOLOGY; X-RAY COMPUTED TOMOGRAPHY;

AGED; DISEASE PROGRESSION; FEMALE; HUMANS; IDIOPATHIC PULMONARY FIBROSIS; LUNG; MALE; MIDDLE AGED; TOMOGRAPHY, X-RAY COMPUTED;

EID: 84994430961     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0166168     Document Type: Article

References (22)

1. American Thoracic Society/European Respiratory Society: Idiopathic pulmonary fibrosis: diagnosis and treatment. International Consensus Statement. Am J Respir Crit Care Med 2000; 161: 646-664. doi: 10.1164/ajrccm.161.2.ats3-00 PMID: 10673212
2. Travis WD, Costabel U, Hansell DM, King TE Jr, Lynch DA, Nicholson AG, et al. An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 2013; 188: 733-748. doi: 10.1164/rccm.201308-1483ST PMID: 24032382
3. Bjoraker JA, Ryu JH, Edwin MK, Myers JL, Tazelaar HD, Schroeder DR, et al. Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998; 157: 199-203. doi: 10.1164/ajrccm.157.1.9704130 PMID: 9445300
4. Flaherty KR, Toews GB, Travis WD, Colby TV, Kazerooni EA, Gross BH, et al. Clinical significance of histological classification of idiopathic interstitial pneumonia. Eur Respir J 2002; 19: 275-283. PMID: 11866008
5. Lay B, Collard HR, King TE Jr. Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2011; 183: 431-440. doi: 10.1164/rccm.201006-0894CI PMID: 20935110
6. Tristan JH, Kevin KB. Definition of disease: Should possible and probable idiopathic pulmonary fibrosis be enrolled in treatment trials? Respiratory Investig 2015; 53: 88-92.
7. Vancheri C, Failla M, Crimi N, Raghu G. Idiopathic pulmonary fibrosis: a disease with similarities and links to cancer biology. Eur Respir J 2010; 35: 496-504. doi: 10.1183/09031936.00077309 PMID: 20190329
8. Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 2011; 183: 788-824. doi: 10.1164/rccm.2009-040GL PMID: 21471066
9. Raghu G. Idiopathic pulmonary fibrosis: a rational clinical approach. Chest 1987; 92: 148-154. PMID: 3297516
10. Selman M, Carrillo G, Estrada A, Mejia M, Becerril C, Cisneros J, et al. Accelerated variant of idiopathic pulmonary fibrosis: clinical behavior and gene expression pattern. PLoS One 2007; 2: e482. doi: 10.1371/journal.pone.0000482 PMID: 17534432
11. Raghu G, Lynch D, Godwin JD, Webb R, Colby TV, Leslie KO, et al. Diagnosis of idiopathic pulmonary fibrosis with high-resolution CT in patients with little or no radiological evidence of honeycombing: secondary analysis of a randomised, controlled trial. Lancet Respir Med 2014; 2: 277-284. doi: 10.1016/S2213-2600(14)70011-6 PMID: 24717624
12. Hansell DM, Bankier AA, MacMahon H, McLoud TC, Müller NL, Remy J, et al. Fleischner Society: glossary of terms for thoracic imaging. Radiology 2008; 246: 697-722. doi: 10.1148/radiol.2462070712 PMID: 18195376
13. Schettino IA, Ab'Saber AM, Vollmer R, Saldiva PH, Carvalho CR, Kairalla RA, et al. Accuracy of high resolution CT in assessing idiopathic pulmonary fibrosis histology by objective morphometric index. Pathol Res Pract 2002; 198: 347-354. doi: 10.1078/0344-0338-00265 PMID: 12092771
14. Kazerooni EA, Martinez FJ, Flint A, Jamadar DA, Gross BH, Spizarny DL, et al. Thin-section CT obtained at 10-mm increments versus limited three-level thin-section CT for idiopathic pulmonary fibrosis: correlation with pathologic scoring. AJR Am J Roentgenol 1997; 169: 977-983. doi: 10.2214/ajr.169.4.9308447 PMID: 9308447
15. Akira M, Inoue Y, Arai T, Okuma T, Kawata Y. Long-term follow-up high-resolution CT findings in non-specific interstitial pneumonia. Thorax 2011; 66: 61-65. doi: 10.1136/thx.2010.140574 PMID: 21071764
16. Silva CI, Müller NL, Hansell DM, Lee KS, Nicholson AG, Wells AU. Nonspecific interstitial pneumonia and idiopathic pulmonary fibrosis: changes in pattern and distribution of disease over time. Radiology 2008; 247: 251-259. doi: 10.1148/radiol.2471070369 PMID: 18270375
17. Sumikawa H, Johkoh T, Fujimoto K, Arakawa H, Colby TV, Fukuoka J, et al. Pathologically proved nonspecific interstitial pneumonia: CT pattern analysis as compared with usual interstitial pneumonia CT pattern. Radiology 2014; 272: 549-556. doi: 10.1148/radiol.14130853 PMID: 24661246
18. Lee HY, Lee KS, Jeong YJ, Hwang JH, Kim HJ, Chung MP, et al. High-resolution CT findings in fibrotic idiopathic interstitial pneumonias with little honeycombing: serial changes and prognostic implications. AJR Am J Roentgenol 2012; 199: 982-989. doi: 10.2214/AJR.11.8192 PMID: 23096169
19. Battista G, Zompatori M, Fasano L, Pacilli A, Basile B. Progressive worsening of idiopathic pulmonary fibrosis. High resolution computed tomography (HRCT) study with functional correlations. Radiol Med 2003; 105: 2-11. PMID: 12700539
20. Raghu G, Chen SY, Yeh WS, Maroni B, Li Q, Lee YC, et al. Idiopathic pulmonary fibrosis in US Medicare beneficiaries aged 65 years and older: incidence, prevalence, and survival, 2001-11. Lancet Respir Med. 2014; 2: 566-572. doi: 10.1016/S2213-2600(14)70101-8 PMID: 24875841
21. Bando M, Sugiyama Y, Azuma A, Ebina M, Taniguchi H, Taguchi Y, et al. A prospective survey of idiopathic interstitial pneumonias in a web registry in Japan. Respir Investig. 2015; 53: 51-59. doi: 10.1016/j.resinv.2014.11.001 PMID: 25745849
22. Richeldi L, du Bois RM, Raghu G, Azuma A, Brown KK, Costabel U, et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med 2014; 370: 2071-2082. doi: 10.1056/NEJMoa1402584 PMID: 24836310