Computed tomography findings in pathological usual interstitial pneumonia: Relationship to survival

Hiromitsu Sumikawa, Takeshi Johkoh, Thomas V. Colby, Kazuya Ichikado, Moritaka Suga, Hiroyuki Taniguchi, Yasuhiro Kondoh, Takashi Ogura, Hiroaki Arakawa, Kiminori Fujimoto, Atsuo Inoue, Naoki Mihara, Osamu Honda, Noriyuki Tomiyama, Hironobu Nakamura, Nestor L. Müller

Research output: Contribution to journalArticlepeer-review

255 Scopus citations


Rationale: Patients with a clinicopathological diagnosis of idiopathic pulmonary fibrosis (IPF) may have typical findings of usual interstitial pneumonia (UIP) on computed tomography (CT) or nonspecific or atypical findings, including those often seen in nonspecific interstitial pneumonia. Objectives: The aims of this study were to revisit the high-resolution CT findings of IPF and to clarify the correlation between the CT findings and mortality. Methods: The study included 98 patients with a histologic diagnosis of UIP and a clinical diagnosis of IPF. Two observers evaluated the CT findings independently and classified each case into one of the following three categories: (1) definite UIP, (2) consistent with UIP, or (3) suggestive of alternative diagnosis. The correlation between the CT categories and mortality was evaluated using the Kaplan-Meier method and the log-rank test, as well as Cox proportional hazards regression models. Measurements and Main Results: Thirty-three of the 98 CT scans were classified as definite UIP, 36 as consistent with UIP, 29 as suggestive of an alternative diagnosis. The mean survival was 45.7, 57.9, and 76.9 months, respectively. There was no significant difference in survival among the three categories (all P > 0.05). Traction bronchiectasis and fibrosis scores were significant predictors of outcome (hazard ratios: 1.30 and 1.10, respectively; 95% confidence intervals: 1.18-14.2 and 1.03-1.19, respectively). Conclusions: In patients with IPF and UIP pattern on the biopsy, the pattern of abnormality on thin-section CT, whether characteristic of UIP or suggestive of alternative diagnosis, does not influence prognosis. Prognosis is influenced by traction bronchiectasis and fibrosis scores.

Original languageEnglish (US)
Pages (from-to)433-439
Number of pages7
JournalAmerican journal of respiratory and critical care medicine
Issue number4
StatePublished - Feb 15 2008


  • High-resolution computed tomography
  • Idiopathic pulmonary fibrosis
  • Interstitial pneumonia
  • Lung

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine


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