BibTex format
@article{Herrmann:2015:10.1039/C5NR01851J,
author = {Herrmann, IK and Bertazzo, S and O'Callaghan, D and Schlegel, AA and Kallepitis, C and Antcliffe, D and Gordon, A and Stevens, MM},
doi = {10.1039/C5NR01851J},
journal = {Nanoscale},
pages = {13511--13520},
title = {Differentiating sepsis from non-infectious systemic inflammation based on microvesicle-bacteria aggregation},
url = {http://dx.doi.org/10.1039/C5NR01851J},
volume = {7},
year = {2015}
}
RIS format (EndNote, RefMan)
TY - JOUR
AB - Sepsis is a severe medical condition and a leading cause of hospital mortality. Prompt diagnosis and early treatment has a significant, positive impact on patient outcome. However, sepsis is not always easy to diagnose, especially in critically ill patients. Here, we present a conceptionally new approach for the rapid diagnostic differentiation of sepsis from non-septic intensive care unit patients. Using advanced microscopy and spectroscopy techniques, we measure infection-specific changes in the activity of nano-sized cell-derived microvesicles to bind bacteria. We report on the use of a point-of-care-compatible microfluidic chip to measure microvesicle-bacteria aggregation and demonstrate rapid (≤1.5 hour) and reliable diagnostic differentiation of bacterial infection from non-infectious inflammation in a double-blind pilot study. Our study demonstrates the potential of microvesicle activities for sepsis diagnosis and introduces microvesicle-bacteria aggregation as a potentially useful parameter for making early clinical management decisions.
AU - Herrmann,IK
AU - Bertazzo,S
AU - O'Callaghan,D
AU - Schlegel,AA
AU - Kallepitis,C
AU - Antcliffe,D
AU - Gordon,A
AU - Stevens,MM
DO - 10.1039/C5NR01851J
EP - 13520
PY - 2015///
SN - 2040-3364
SP - 13511
TI - Differentiating sepsis from non-infectious systemic inflammation based on microvesicle-bacteria aggregation
T2 - Nanoscale
UR - http://dx.doi.org/10.1039/C5NR01851J
UR - http://hdl.handle.net/10044/1/25154
VL - 7
ER -