Community-acquired pneumonia related to intracellular pathogens

Catia Cillóniz, Antoni Torres (Lead / Corresponding author), Michael Niederman, Menno van der Eerden, James Chalmers, Tobias Welte, Francesco Blasi

    Research output: Contribution to journalArticlepeer-review

    92 Citations (Scopus)
    897 Downloads (Pure)

    Abstract

    Community-acquired pneumonia (CAP) is associated with high rates of morbidity and mortality worldwide; the annual incidence of CAP among adults in Europe has ranged from 1.5 to 1.7 per 1000 population. Intracellular bacteria are common causes of CAP. However, there is considerable variation in the reported incidence between countries and change over time. The intracellular pathogens that are well established as causes of pneumonia are Legionella pneumophila, Mycoplasma pneumoniae, Chlamydophila pneumoniae, Chlamydophila psittaci, and Coxiella burnetii. Since it is known that antibiotic treatment for severe CAP is empiric and includes coverage of typical and atypical pathogens, microbiological diagnosis bears an important relationship to prognosis of pneumonia. Factors such as adequacy of initial antibiotic or early de-escalation of therapy are important variables associated with outcomes, especially in severe cases. Intracellular pathogens sometimes appear to cause more severe disease with respiratory failure and multisystem dysfunction associated with fatal outcomes. The clinical relevance of intracellular pathogens in severe CAP has not been specifically investigated. We review the prevalence, general characteristics, and outcomes of severe CAP cases caused by intracellular pathogens.

    Original languageEnglish
    Pages (from-to)1374-1386
    Number of pages13
    JournalIntensive Care Medicine
    Volume42
    Issue number9
    Early online date8 Jun 2016
    DOIs
    Publication statusPublished - Sept 2016

    Fingerprint

    Dive into the research topics of 'Community-acquired pneumonia related to intracellular pathogens'. Together they form a unique fingerprint.

    Cite this