Abstract

Many patients with idiopathic pulmonary fibrosis (IPF) undergo hospitalizations due to pulmonary infections. We retrospectively investigated the characteristics of hospitalizations due to pulmonary infection in patients with IPF to elucidate causative pathogens and mortality. We reviewed patients with IPF who were admitted between January 2008 and December 2014 for pulmonary infections including pneumonia and bronchitis. The causative pathogen, the relationship between the site of pneumonia and existing IPF radiological patterns on high-resolution chest CT, and predictors of mortality were evaluated. Forty-eight IPF patients were hospitalized a totally of 81 times due to pulmonary infection during the study period. In the 48 first-time admissions after IPF diagnosis, causative pathogens were detected in 20 patients (41.6%). The most common pathogen was Haemophilus influenzae (14.5%) followed by Pseudomonas aeruginosa (4.1%), Staphylococcus aureus (4.1%), Branhamella catarrhalis (4.1%), and Klebsiella pneumoniae (4.1%). Among all 81 admissions, the most common pathogen was P. aeruginosa (12.3%), followed by H. influenzae (8.6%), S. aureus (6.1%) and Escherichia coli (4.9%). No relationship was observed between the detected pathogen and the site of pneumonia. The 30-day and hospital mortality rates were 14.5% and 18.7%, respectively. Pneumonia severity index on admission was significantly associated with both 30-day and hospital mortality. In conclusion, IPF patients hospitalized for pulmonary infections had high 30-day and hospital mortality. In contrast to community-acquired pneumonia, the causative pathogens mainly consisted of gram-negative bacteria. The PSI score may be a significant predictor of mortality. These results provide information for empiric antibiotic selection when treating IPF patients with pulmonary infections.

Highlights

  • Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease that is characterized by the histopathologic pattern of usual interstitial pneumonia [1]

  • We retrospectively examined the medical charts of all patients with IPF who were admitted to the Kindai University Hospital between January 2008 and December 2014 for pulmonary infections, including pneumonia and bronchitis

  • Over the 7-year study period, 48 patients with IPF were admitted a total of 81 times for pulmonary infections

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Summary

Introduction

Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease that is characterized by the histopathologic pattern of usual interstitial pneumonia [1]. Pulmonary Infection in IPF poor and the median survival after diagnosis is 2 to 3 years, the natural history is variable [1,2]. Many patients with IPF undergo acute respiratory events [3]. Acute respiratory events occur most frequently due to acute exacerbations, followed by pulmonary infections such as pneumonia and bronchitis [3]. Patients with IPF are usually hospitalized when an acute respiratory event occurs, this depends on regional medical resources. Respiratory-related hospitalizations have recently been recognized as an important factor in IPF outcomes, because mortality during respiratory hospitalization is high and because hospitalization influences subsequent survival [4]

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