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Suda, Takafumi

0000-0001-5300-0504

Mayo Clinic

Hamamatsu University

Citations 2

Prognostic and Clinical Value of Cluster Analysis in Idiopathic Pleuroparenchymal Fibroelastosis Phenotypes
Nakamura, Yutaro , Mori, Kazutaka , Enomoto, Yasunori , Kono, Masato , Sumikawa, Hiromitsu , Johkoh, Takeshi , Colby, Thomas V. , Hozumi, Hironao , Fujisawa, Tomoyuki , Enomoto, Noriyuki , Inui, Naoki , Kaida, Yusuke , Yokomura, Koshi, Koshimizu, Naoki, Toyoshima, Mikio , Imokawa, Shiro , Shirai, Toshihiro , Hayakawa, Hiroshi , Suda, Takafumi , Hozumi, Hironao , Suzuki, Yuzo , Fujisawa, Tomoyuki , Yasui, Hideki , Karayama, Masato , Furuhashi, Kazuki , Yamada, Takashi , Nakamura, Hidenori

Journal of Clinical Medicine | April 5, 2021 | Volume: 10 | Issue: 7 | Pages: 1498

10.3390/jcm10071498 Get It

Idiopathic pleuroparenchymal fibroelastosis (PPFE) is a distinctive interstitial pneumonia with upper lobe predominance that shows unique morphological features among idiopathic interstitial pneumonias (IIPs). Affected patients have a variety of clinical presentations with heterogeneous clinical courses. Cluster analysis is a valuable tool for identifying distinct clinical phenotypes under heterogeneous conditions. This study aimed to identify the phenotypes of patients with idiopathic PPFE. Using cluster analysis, novel PPFE phenotypes were identified among subjects from our multicenter cohort, and outcomes were stratified according to phenotypic clusters. Among the subjects with baseline data (N = 84), four clusters were identified. Cluster 1 included younger male subjects with coexisting non-UIP-like patterns. Cluster 2 included elderly female nonsmokers with low body mass index (BMI). Cluster 3 included elderly male smokers with a coexisting IP-like pattern. Cluster 4 included younger male smokers without lower lobe lesions. Patients in cluster 3 had significantly worse survival outcomes than those in clusters 1, 2, and 4 (p < 0.001, p = 0.0041, and p = 0.0155, respectively). Among idiopathic PPFE patients, cluster analysis using baseline characteristics identified four distinct clinical phenotypes that might predict survival outcomes.
The prognostic significance of pneumothorax in patients with idiopathic pulmonary fibrosis
Nishimoto, Koji , Yoshimura, Katsuhiro , Enomoto, Yasunori , Enomoto, Noriyuki , Nakamura, Yutaro , Inui, Naoki , Sumikawa, Hiromitsu , Johkoh, Takeshi , Colby, Thomas V. , Suda, Takafumi , Fujisawa, Tomoyuki , Enomoto, Noriyuki , Fujisawa, Tomoyuki

Respirology | November 12, 2017 | Volume: 23 | Issue: 5 | Pages: 519-525

10.1111/resp.13219 Get It

ABSTRACTBackground and objectivePneumothorax is a co‐morbidity in patients with idiopathic pulmonary fibrosis (IPF). However, its incidence, risk factors and prognostic significance in IPF remain unclear. The aim of this study was to clarify the incidence and prognostic significance of pneumothorax in patients with IPF, and to further investigate the risk factors for its onset.MethodsEighty‐four consecutive patients with IPF based on the consensus guideline were included in this study. We retrospectively reviewed the medical records, pulmonary function tests and chest high‐resolution computed tomography images, and determined the incidence of pneumothorax. The prognostic significance of pneumothorax was evaluated using the Cox proportional hazards model analysis with time‐dependent covariates. We also assessed the cumulative incidence and the risk factors for pneumothorax.ResultsOf the 84 patients, 17 (20.2%) developed pneumothorax. The cumulative incidence of pneumothorax was 8.5%, 12.5% and 17.7% at 1, 2 and 3 years, respectively. Univariate analysis demonstrated that pneumothorax was significantly related to poor prognosis (hazards ratio, 2.99; P = 0.002). Multivariate analysis, adjusting for sex, age and forced vital capacity (% predicted), revealed that pneumothorax was an independent predictor of poor outcome in IPF (hazards ratio, 2.85; P = 0.006). Lower BMI and the presence of extensive reticular abnormalities were significantly associated with developing pneumothorax.ConclusionThese results confirm that patients with IPF often develop pneumothorax during their clinical course and that the onset of pneumothorax predicts a poor outcome.