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DOI 10.1016/j.jcv.2018.08.001

Медицинская библиотека · Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2018

Diagnostic performance of multiplex PCR on pulmonary samples versus nasopharyngeal aspirates in community-acquired severe lower respiratory tract infections.

Robert Sylvie, Lhommet Claire, Le Brun Cécile, Garot Denis, Legras Annick, Mankikian Julie, Goudeau Alain

Сравнительное исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND

PCR-based techniques for the diagnosis of community- acquired severe lower respiratory tract infections are becoming the standard of care. However, their relative ability to identify either atypical bacteria or viruses that cause LRTI from clinical samples from various sources is yet to be determined.

OBJECTIVES AND STUDY

DESIGN

The aim of our study was to compare the diagnostic yield of nasopharyngeal aspirates with that of pulmonary samples for the etiological diagnosis of severe acute lower respiratory tract infections by multiplex PCR. Patients were adults with community-acquired pneumonia or acute exacerbation of chronic obstructive pulmonary disease.

RESULTS

We obtained concordant results for 81 (79%) of the 103 pairs of samples. In 14 of the 22 discordant results, more pathogens were evidenced in the lower respiratory tract samples.

CONCLUSIONS

Pulmonary samples had a similar diagnostic sensitivity for virus detection by multiplex PCR as nasopharyngeal aspirates. In contrast, in our study, the diagnostic efficacy of pulmonary samples for Legionella pneumophila over simple aspirates was clearly superior.

Для цитирования: Robert Sylvie, Lhommet Claire, Le Brun Cécile, Garot Denis, Legras Annick, Mankikian Julie, Goudeau Alain. Diagnostic performance of multiplex PCR on pulmonary samples versus nasopharyngeal aspirates in community-acquired severe lower respiratory tract infections.. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 2018. DOI: 10.1016/j.jcv.2018.08.001.

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