Exploration of eosinopenia as a diagnostic parameter to differentiate sepsis from systemic inflammatory response syndrome: Results from an observational study

JOURNAL TITLE: Indian Journal of Critical Care Medicine

Author
1. Debashish Dhar
2. Ashish Garg
3. Dimple Anand
4. Rahul Singh
5. Lalit M. Srivastava
6. Seema Bhargava
7. Imran Gafoor
ISSN
0972-5229
DOI
10.4103/0972-5229.182199
Volume
20
Issue
5
Publishing Year
2016
Pages
6
Author Affiliations
    1. Sir Ganga Ram Hospital, New Delhi, India
    1. BLK Superspeciality Hospital, New Delhi, India
    1. Neurological Institute of New Jersey, New Jersey Medical School, 90 Bergen Street, Suite 8100, Newark, New Jersey, USA
    1. Department of Biochemistry, Sir Ganga Ram Hospital, New Delhi, India
    1. Department of Biochemistry, Sir Ganga Ram Hospital, New Delhi, India
    1. Department of Biochemistry, Sir Ganga Ram Hospital, New Delhi, India
    1. Department of Critical Care and Emergency Medicine, Sir Ganga Ram Hospital, New Delhi, India
  • Article keywords
    Absolute eosinophil count, negative predictive value, procalcitonin, sepsis, systemic inflammatory response syndrome

    Abstract

    Aim of the Study: Initial differentiation of sepsis from systemic inflammatory response syndrome (SIRS) is of prime importance for early institution of appropriate treatment. This study aimed to compare the differential diagnostic efficacy of absolute eosinophil count (AEC - a routinely available economic marker) with total leukocyte count (TLC) and procalcitonin (PCT - a costly marker available only in specialized settings). Materials and Methods: In this prospective observational study, 170 patients of sepsis (severe sepsis = 125; SIRS = 45) were enrolled. AEC, TLC, and PCT were measured in the blood of all patients at the time of admission and data analyzed statistically. Results: Median AEC was 0 cells/mm3 in both SIRS and sepsis. TLC and PCT levels were significantly higher (P < 0.001) in culture negative, culture positive, and overall sepsis groups in comparison to SIRS group. At a cutoff of < 50 cells/mm3, AEC demonstrated a sensitivity and specificity of 23% and 68%, respectively. The sensitivity, specificity, positive predictive value, and negative predictive value of TLC were 57%, 71%, 85%, 37% and of PCT were 82.4%, 82.2%, 93%, and 63%, respectively with area under curve of 0.455 for AEC, 0.640 for TLC, 0.908 for PCT. Conclusions: This study suggests that eosinopenia is not a reliable diagnostic tool to differentiate sepsis from SIRS. PCT and TLC are better differential diagnostic biomarkers.

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