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Diagnostic and prognostic value of procalcitonin among febrile critically ill patients with prolonged ICU stay

Authors :
Stylianos E. Orfanos
Apostolos Armaganidis
Iraklis Tsangaris
Ioanna Dimopoulou
Evangelos J. Giamarellos-Bourboulis
Petros Kopterides
Dimitra Kavatha
George Michael Gourgoulis
Helen Giamarellou
Diamantis Plachouras
George Tsaknis
Argirios E. Tsantes
Source :
BMC Infectious Diseases, BMC Infectious Diseases, Vol 9, Iss 1, p 213 (2009)
Publication Year :
2009
Publisher :
BioMed Central, 2009.

Abstract

Background Procalcitonin (PCT) has been proposed as a diagnostic and prognostic sepsis marker, but has never been validated in febrile patients with prolonged ICU stay. Methods Patients were included in the study provided they were hospitalised in the ICU for > 10 days, were free of infection and presented a new episode of SIRS, with fever >38°C being obligatory. Fifty patients fulfilled the above criteria. PCT was measured daily during the ICU stay. The primary outcome was proven infection. Results Twenty-seven out of 50 patients were diagnosed with infection. Median PCT on the day of fever was 1.18 and 0.17 ng/ml for patients with and without proven infections (p < 0.001). The area under the curve for PCT was 0.85 (95% CI; 0.71-0.93), for CRP 0.65 (0.46-0.78) and for WBC 0.68 (0.49-0.81). A PCT level of 1 ng/mL yielded a negative predictive value of 72% for the presence of infection, while a PCT of 1.16 had a specificity of 100%. A two-fold increase of PCT between fever onset and the previous day was associated with proven infection (p 0.001) (OR = 8.55; 2.4-31.1), whereas a four-fold increase of PCT of any of the 6 preceding days was associated with a positive predictive value exceeding 69.65%. A PCT value less than 0.5 ng/ml on the third day after the advent of fever was associated with favorable survival (p 0.01). Conclusion The reported data support that serial serum PCT may be a valuable diagnostic and prognostic marker in febrile chronic critically ill patients.

Details

Language :
English
ISSN :
14712334
Volume :
9
Database :
OpenAIRE
Journal :
BMC Infectious Diseases
Accession number :
edsair.doi.dedup.....89b60d98be8fae1d3db854e04e19f3f4