Community-acquired pneumonia in Chile: the clinical relevance in the detection of viruses and atypical bacteria
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Luchsinger Farías, Vivian
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Community-acquired pneumonia in Chile: the clinical relevance in the detection of viruses and atypical bacteria
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Abstract
Background Adult community-acquired pneumonia
(CAP) is a relevant worldwide cause of morbidity and
mortality, however the aetiology often remains uncertain
and the therapy is empirical. We applied conventional
and molecular diagnostics to identify viruses and atypical
bacteria associated with CAP in Chile.
Methods We used sputum and blood cultures,
IgG/IgM serology and molecular diagnostic techniques
(PCR, reverse transcriptase PCR) for detection of
classical and atypical bacteria (Mycoplasma pneumoniae,
Chlamydia pneumoniae, Legionella pneumoniae) and
respiratory viruses (adenovirus, respiratory syncytial virus
(RSV), human metapneumovirus, influenza virus,
parainfluenzavirus, rhinovirus, coronavirus) in adults
>18 years old presenting with CAP in Santiago from
February 2005 to September 2007. Severity was
qualified at admission by Fine’s pneumonia severity
index.
Results Overall detection in 356 enrolled adults were
92 (26%) cases of a single bacterial pathogen, 80
(22%) cases of a single viral pathogen, 60 (17%) cases
with mixed bacterial and viral infection and 124 (35%)
cases with no identified pathogen. Streptococcus
pneumoniae and RSV were the most common bacterial
and viral pathogens identified. Infectious agent detection
by PCR provided greater sensitivity than conventional
techniques. To our surprise, no relationship was
observed between clinical severity and sole or
coinfections.
Conclusions The use of molecular diagnostics
expanded the detection of viruses and atypical bacteria
in adults with CAP, as unique or coinfections. Clinical
severity and outcome were independent of the
aetiological agents detected.
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Artículo de publicación ISI
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URI: https://repositorio.uchile.cl/handle/2250/129104
DOI: doi: 10.1136/thoraxjnl-2013-203551
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Thorax 2013;68: 1000–1006
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