Early sepsis markers in patients admitted to intensive care unit with moderate-to-severe diabetic ketoacidosis

Background Bacterial infections are frequent triggers for diabetic ketoacidosis. In this context, delayed antibiotic treatment is associated with increased morbidity and mortality. Unnecessary administration of antimicrobial therapy might however, also negatively impact the prognosis. The usefulness...

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Veröffentlicht in:Annals of Intensive Care 2020-05, Vol.10 (1), p.58-58, Article 58
Hauptverfasser: Blanchard, Florian, Charbit, Judith, Van der Meersch, Guillaume, Popoff, Benjamin, Picod, Adrien, Cohen, Regis, Chemouni, Frank, Gaudry, Stephane, Bihan, Helene, Cohen, Yves
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Sprache:eng
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Zusammenfassung:Background Bacterial infections are frequent triggers for diabetic ketoacidosis. In this context, delayed antibiotic treatment is associated with increased morbidity and mortality. Unnecessary administration of antimicrobial therapy might however, also negatively impact the prognosis. The usefulness of sepsis markers in diabetic ketoacidosis has not been assessed. Thus, we sought to investigate diagnostic performances of clinical and biological sepsis markers during diabetic ketoacidosis. Methods In this monocentric retrospective cohort study, all consecutive episodes of diabetic ketoacidosis (defined as pH ≤ 7.25, glycaemia > 300 mg/dL and presence of ketones) admitted in intensive care unit were included. A proven bacterial infection was defined as bacteriological documentation on any bacterial sample. Clinical (presence of fever: temperature > 38 °C and presence of hypothermia: temperature < 36 °C) and biological markers (whole blood count, neutrophils count, neutrophils-to-lymphocytes count ratio and procalcitonin), recorded at admission, were compared according to the presence or absence of a proven bacterial infection. Results Between 2011 and 2018, among 134 episodes of diabetic ketoacidosis, 102 were included (91 patients). Twenty out of 102 were infected. At admission, procalcitonin (median: 3.58 ng/mL vs 0.52 ng/mL, p  
ISSN:2110-5820
2110-5820
DOI:10.1186/s13613-020-00676-6