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Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients: C-Reactive Protein, Procalcitonin, and Leukocytes
- Source :
- Hertz, F B, Ahlström, M G, Bestle, M H, Hein, L, Mohr, T, Lundgren, J D, Galle, T, Andersen, M H, Murray, D, Lindhardt, A, Itenov, T S & Jensen, J U S 2022, ' Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients : C-Reactive Protein, Procalcitonin, and Leukocytes ', Open Forum Infectious Diseases, vol. 9, no. 10, ofac467 . https://doi.org/10.1093/ofid/ofac467
- Publication Year :
- 2022
- Publisher :
- Oxford University Press (OUP), 2022.
-
Abstract
- Background Bloodstream infections (BSIs) often lead to critical illness and death. The primary aim of this study was to determine the diagnostic accuracy of the biomarkers C-reactive protein (CRP), procalcitonin (PCT), and leukocyte count for the diagnosis of BSI in critically ill patients. Methods This was a nested case–control study based on the Procalcitonin And Survival Study (PASS) trial (n = 1200). Patients who were admitted to the intensive care unit (ICU) Results In total, there were 525 patients (n = 175 cases, 350 controls). The fixed low threshold for all 3 biomarkers (CRP = 20 mg/L; leucocytes = 10 × 109/L; PCT = 0.4 ng/mL) resulted in negative predictive values on day 1: CRP = 0.91; 95% CI, 0.75–1.00; leukocyte = 0.75; 95% CI, 0.68–0.81; PCT = 0.91; 95% CI, 0.84–0.96). Combining the 3 biomarkers yielded similar results as PCT alone (P = .5). Conclusions CRP and PCT could in most cases rule out BSI in critically ill patients. As almost no patients had low CRP and ∼20% had low PCT, a low PCT could be used, along with other information, to guide clinical decisions.
- Subjects :
- Infectious Diseases
Oncology
bloodstream infection
BSI
CRP
PCT
leukocyte
Subjects
Details
- ISSN :
- 23288957
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Open Forum Infectious Diseases
- Accession number :
- edsair.doi.dedup.....959479b3411025a67d794197c5ad6ea3
- Full Text :
- https://doi.org/10.1093/ofid/ofac467