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Evaluation of a real time PCR assay for detection and quantification of bacterial DNA directly in blood of preterm neonates with suspected late onset sepsis

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Academic year: 2020

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Figure

Fig. 1 Sample processing method and multiplex PCR assay. EDTA Ethylenediaminetetraacetic acid
Table 2 Performance of the multiplex PCR assay compared withblood culture (polymicrobial infections excluded)
Table 3 Details of episodes of suspected sepsis with discordant results for blood culture and PCR
Fig. 2 Distribution of the bacterial DNA load at onset of sepsis,stratified by pathogen

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