Inhaled corticosteroids and systemic inflammatory response in community-acquired pneumonia: a prospective clinical study

Respirology. 2014 Aug;19(6):929-35. doi: 10.1111/resp.12324. Epub 2014 Jun 9.

Abstract

Background and objective: The previous use of inhaled corticosteroids (ICS) may reduce the inflammatory response and mortality in patients with community-acquired pneumonia (CAP).

Methods: We measured serum levels of several inflammatory biomarkers, as well as mortality at various time-points, in 663 consecutive patients hospitalized for CAP; 128 (19%) were receiving chronic outpatient treatment with ICS. Patients on previous oral corticosteroids were excluded from the analysis.

Results: On admission, patients treated with ICS were older; had been diagnosed with chronic obstructive pulmonary disease (COPD), asthma and pneumonia in the previous year more often; and had higher CAP severity risk classes and lower tumour necrosis factor (TNF)-alpha (P < 0.001) and interleukin (IL)-6 (P = 0.015) serum levels. After adjusting for potential confounders, this association persisted for TNF-alpha (P < 0.001), but not for IL-6. Mortality at 30 and 90 days tended to be lower in patients treated with ICS (P = 0.062 and 0.050, respectively), but mortality was similar after 1 year in both groups (16, 13% vs 81, 15% for patients treated and not treated with ICS, respectively). Hospital readmission rate after 1 year was higher in patients treated with ICS (49, 38% vs 109, 20%, P < 0.001). The association of ICS treatment with a previous diagnosis of pneumonia, lower levels of TNF-alpha and IL-6 on admission and higher readmission rates during follow up persisted in the subpopulation of 210 patients with COPD.

Conclusions: Previous use of ICS in patients hospitalized for CAP is associated with a reduced systemic inflammatory response without any impact on long-term mortality.

Keywords: community-acquired pneumonia; inflammatory biomarker; inhaled corticosteroid; systemic inflammatory response; tumour necrosis factor-alpha.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Inhalation
  • Adrenal Cortex Hormones / administration & dosage*
  • Adrenal Cortex Hormones / therapeutic use*
  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • Bronchitis / blood
  • Bronchitis / etiology
  • Bronchitis / prevention & control*
  • Community-Acquired Infections / complications
  • Community-Acquired Infections / drug therapy*
  • Community-Acquired Infections / mortality
  • Comorbidity
  • Female
  • Humans
  • Interleukin-6 / blood
  • Male
  • Middle Aged
  • Pneumonia / complications
  • Pneumonia / drug therapy*
  • Pneumonia / mortality
  • Prospective Studies
  • Pulmonary Disease, Chronic Obstructive / complications
  • Retrospective Studies
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Adrenal Cortex Hormones
  • Biomarkers
  • Interleukin-6
  • Tumor Necrosis Factor-alpha