2014
DOI: 10.1186/s13613-014-0035-7
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Multiplex PCR performed of bronchoalveolar lavage fluid increases pathogen identification rate in critically ill patients with pneumonia: a pilot study

Abstract: BackgroundIn critically ill patients with pneumonia, accurate microorganism identification allows appropriate antibiotic treatment. In patients undergoing bronchoalveolar lavage (BAL), direct examination of the fluid using Gram staining provides prompt information but pathogen identification accuracy is low. Culture of BAL fluid is actually the reference, but it is not available before 24 to 48 h. In addition, pathogen identification rate observed with direct examination and culture is decreased when antibioti… Show more

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Cited by 34 publications
(30 citation statements)
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“…sensitivity by also detecting genotypic markers of resistance. Multiple studies have demonstrated the superior diagnostic accuracy of PCR based platforms for detecting bacterial pathogens in the sputum compared with standard culture [16][17][18][19] . This review will discuss the commercially available syndromic molecular panels for pneumonia, their potential clinical impact and the challenges to implementing them as a 'front line' diagnostic test.…”
Section: Introductionmentioning
confidence: 99%
“…sensitivity by also detecting genotypic markers of resistance. Multiple studies have demonstrated the superior diagnostic accuracy of PCR based platforms for detecting bacterial pathogens in the sputum compared with standard culture [16][17][18][19] . This review will discuss the commercially available syndromic molecular panels for pneumonia, their potential clinical impact and the challenges to implementing them as a 'front line' diagnostic test.…”
Section: Introductionmentioning
confidence: 99%
“…Recent years' development in molecular diagnostic methods has led to a markedly increased availability of both commercial and in-house developed diagnostic panels targeting viruses and atypical bacterial pathogens [3]. However, examples of panels targeting typical respiratory bacteria are few [4][5][6], and molecular panels intended for LRTI diagnostics are even more scarce [7][8][9][10]. Methods combining targets for typical bacterial pathogens, atypical bacteria and viruses have so far been limited to qPCR-based panels, requiring a separate sample extraction step [8][9][10], which limit their use to larger clinical microbiology laboratories during working hours.…”
Section: Introductionmentioning
confidence: 99%
“…Diagnostic PCR-kits designed for sepsis diagnosis, e.g. LightCycler SeptiFast from Roche Diagnostics [11] have broader coverage but lack important respiratory pathogens. Similarly, poor performance and insufficient coverage has been reported for the Unyvero multiplex PCR device (Curetis AG) for direct point-of-care detection of respiratory pathogens [12, 13].…”
Section: Introductionmentioning
confidence: 99%