2013
DOI: 10.1016/j.mimet.2012.11.005
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A rapid flow cytometric method for distinguishing between febrile bacterial and viral infections

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Cited by 33 publications
(31 citation statements)
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“…11 Also, the role of WBC in the prediction of a bacterial or viral origin is limited. 12,13 Absolute neutrophil count (ANC) performs better, but is still moderate. 12,13 Circulating immature granulocytes ('left shift') either as band count or _ENREF_8metamyelocyte, myelocyte and promyelocyte count (immature granulocytes count) as single diagnostic marker for an infection in the ICU is not (yet) supported by the few studies on this topic.…”
Section: Cellular Diagnostic Biomarkersmentioning
confidence: 99%
See 3 more Smart Citations
“…11 Also, the role of WBC in the prediction of a bacterial or viral origin is limited. 12,13 Absolute neutrophil count (ANC) performs better, but is still moderate. 12,13 Circulating immature granulocytes ('left shift') either as band count or _ENREF_8metamyelocyte, myelocyte and promyelocyte count (immature granulocytes count) as single diagnostic marker for an infection in the ICU is not (yet) supported by the few studies on this topic.…”
Section: Cellular Diagnostic Biomarkersmentioning
confidence: 99%
“…12,13 Absolute neutrophil count (ANC) performs better, but is still moderate. 12,13 Circulating immature granulocytes ('left shift') either as band count or _ENREF_8metamyelocyte, myelocyte and promyelocyte count (immature granulocytes count) as single diagnostic marker for an infection in the ICU is not (yet) supported by the few studies on this topic. 9,10,14 Contradictory results have been obtained for eosinopenia (with cutoffs of 25e50 cells/mm 3 …”
Section: Cellular Diagnostic Biomarkersmentioning
confidence: 99%
See 2 more Smart Citations
“…In the clinical laboratory, counterinsurgency intelligence gathering would require new technology, a new electronic health record, and a new mindset. Various technologies for community characterization are already available -particularly high-throughput sequencing (Xu et al 2012), but also multiplexed PCR Hartley 2003, Lindsay et al 2013), hybridization arrays (Gardner et al 2010), microfluidic culture (Ho et al 2012), flow cytometry (Jolkkonen et al 2010, Nuutila et al 2012, and novel approaches to microscopy (Foreman et al 2010, Harris et al 2013. Each has limitations and none of them provide quite what would be desired to understand the function of a microbial community de novo.…”
Section: Intelligencementioning
confidence: 99%