Literature DB >> 25736347

Clinical findings and outcomes in patients with possible usual interstitial pneumonia.

Jin Wook Lee1, Esmeralda Shehu2, Juarda Gjonbrataj3, Young Eun Bahn4, Byung Hak Rho4, Mi-Young Lee5, Won-Il Choi6.   

Abstract

BACKGROUND: Patients with possible usual interstitial pneumonia (UIP) constitute a substantial group, and their clinical characteristics and outcomes are not well defined. We compared the clinical characteristics and survival between patients with possible UIP and the UIP pattern.
METHODS: We evaluated 62 patients with possible UIP and 544 patients with the UIP pattern. Both groups were diagnosed by clinical characteristics and high-resolution computed tomography (HRCT) findings. Two radiologists performed radiological evaluation based on the new idiopathic pulmonary fibrosis (IPF) guidelines. Two risk-stratification methods were used to compare UIP pattern and possible UIP patients.
RESULTS: The groups had similar demographic and clinical characteristics. Pulmonary function tests revealed no significant differences in lung volumes between the 2 groups. However, DLCO was significantly lower with the UIP pattern than with possible UIP (p = 0.004). Multivariate analysis showed age, sex, and carbon monoxide diffusing capacity (DLCO) as important independent variables for survival. The UIP HRCT pattern did not affect survival (hazard ratio, 0.83; 95% confidence interval, 0.51-1.24; p = 0.32). Possible UIP was not associated with prognosis when independent predictors for survival rate and propensity score were considered. In the case-control study, the 3-year survival rate was 44.6% in the UIP pattern group and 56.8% in the possible UIP group (p = 0.16).
CONCLUSIONS: Clinical characteristics and outcomes were similar in possible UIP and UIP patients, except for differences in DLCO. The UIP pattern itself did not affect survival.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  HRCT; Idiopathic pulmonary fibrosis; Prognosis

Mesh:

Substances:

Year:  2015        PMID: 25736347     DOI: 10.1016/j.rmed.2015.02.008

Source DB:  PubMed          Journal:  Respir Med        ISSN: 0954-6111            Impact factor:   3.415


  12 in total

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Authors:  So-My Koo; Soo-Taek Uh; Dong Soon Kim; Young Whan Kim; Man Pyo Chung; Choon Sik Park; Sung Hwan Jeong; Yong Bum Park; Hong Lyeol Lee; Jong Wook Shin; Eun Joo Lee; Jin Hwa Lee; Yangin Jegal; Hyun Kyung Lee; Yong Hyun Kim; Jin Woo Song; Moo Suk Park; Young Hwangbo
Journal:  J Thorac Dis       Date:  2016-11       Impact factor: 2.895

2.  What Is in a Pattern? That Which We Call Idiopathic Pulmonary Fibrosis by Any Other Pattern Would Behave Alike!

Authors:  Joao A de Andrade; Tracy Luckhardt
Journal:  Am J Respir Crit Care Med       Date:  2017-01-01       Impact factor: 21.405

3.  Possible UIP pattern on high-resolution computed tomography is associated with better survival than definite UIP in IPF patients.

Authors:  Margaret L Salisbury; Leslie B Tolle; Meng Xia; Susan Murray; Nabihah Tayob; Anoop M Nambiar; Shelley L Schmidt; Amir Lagstein; Jeffery L Myers; Barry H Gross; Ella A Kazerooni; Baskaran Sundaram; Aamer R Chughtai; Fernando J Martinez; Kevin R Flaherty
Journal:  Respir Med       Date:  2017-09-12       Impact factor: 3.415

Review 4.  "Structure-Function Imaging of Lung Disease Using Ultrashort Echo Time MRI".

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5.  Effect of Nintedanib in Subgroups of Idiopathic Pulmonary Fibrosis by Diagnostic Criteria.

Authors:  Ganesh Raghu; Athol U Wells; Andrew G Nicholson; Luca Richeldi; Kevin R Flaherty; Florence Le Maulf; Susanne Stowasser; Rozsa Schlenker-Herceg; David M Hansell
Journal:  Am J Respir Crit Care Med       Date:  2017-01-01       Impact factor: 21.405

6.  Differences in Clinical Characteristics and Outcomes Between Men and Women With Idiopathic Pulmonary Fibrosis: A Multicenter Retrospective Cohort Study.

Authors:  Tanzira Zaman; Teng Moua; Eric Vittinghoff; Jay H Ryu; Harold R Collard; Joyce S Lee
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Review 7.  Chronic hypersensitivity pneumonitis.

Authors:  Carlos Ac Pereira; Andréa Gimenez; Lilian Kuranishi; Karin Storrer
Journal:  J Asthma Allergy       Date:  2016-09-21

8.  Effect of smoking and comorbidities on survival in idiopathic pulmonary fibrosis.

Authors:  Miia Kärkkäinen; Hannu-Pekka Kettunen; Hanna Nurmi; Tuomas Selander; Minna Purokivi; Riitta Kaarteenaho
Journal:  Respir Res       Date:  2017-08-22

9.  Changes in management of idiopathic pulmonary fibrosis: impact on disease severity and mortality.

Authors:  Charlotte Hyldgaard; Janne Møller; Elisabeth Bendstrup
Journal:  Eur Clin Respir J       Date:  2020-08-12

10.  Usual interstitial pneumonia: typical, possible, and "inconsistent" patterns.

Authors:  Pedro Paulo Teixeira E Silva Torres; Marcelo Fouad Rabahi; Maria Auxiliadora Carmo Moreira; Gustavo de Souza Portes Meirelles; Edson Marchiori
Journal:  J Bras Pneumol       Date:  2017 Sep-Oct       Impact factor: 2.624

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