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Diagnostic and prognostic evaluation of soluble CD14 subtype for sepsis in critically ill patients: a preliminary study
© Foca et al.; licensee BioMed Central Ltd. 2014
Published: 3 December 2014
Sepsis, a leading cause of death in critical care patients, is the result of complex interactions between the infecting microorganisms and the host responses that influence clinical outcomes . Reliable biochemical markers that enable early diagnosis are still needed. A new marker, presepsin (soluble CD14 subtype, sCD14-ST) is a circulating fragment of 13 kDa of soluble CD14 that originates from the cleavage of the CD14 expressed on the surface membranes of monocytes/macrophages. sCD14-ST has been shown to increase significantly in patients with sepsis . In our study we compare diagnostic performance of presepsin, C-reactive protein (CRP) and procalcitonin (PCT).
Critical patients with suspected sepsis admitted to the Unit of Intensive Care of the University Hospital of Catanzaro (Italy) were recruited into this study; healthy volunteers were also included as controls. Plasma samples in EDTA from each patient were collected at multiple time points; samples were tested for CRP, PCT and presepsin. Blood cultures were also evaluated and processed by a BacT/Alert 3D system (bioMérieux, Italy); CRP was measured by immunonephelometry (Siemens Healthcare Diagnostic, Italy) and PCT was assayed by an enzyme-linked fluorescent assay (VIDAS BRAHMS PCT, bioMérieux, Italy); presepsin levels were measured by rapid automated PATHFAST immunoanalyzer (kindly provided by GEPA SRL, Italy), based on chemiluminescent enzyme immunoassay. A statistical analysis was carried out by Mann-Whitney test.
Presepsin and PCT levels were significantly higher in culture-positive subjects versus negative controls; such difference was found even at the admission time. The presepsin values in worsening/dead patients exhibited a significantly higher level at admission time. On the contrary, in the same group of patients, PCT exhibited a decrease of its level. In poor prognosis patients CRP showed a quite irregular kinetic, although in such a group the admission value was higher than the same marker in live subjects.
In this preliminary study, presepsin and PCT levels exhibited substantial higher values in culture-positive patients. The kinetic curves of presepsin, obtained from both survival and worsening/dead subjects, revealed the optimal performance of this biomarker, particularly in severely ill patients, as also shown in other studies. During sepsis, increase of presepsin levels may be a more reliable marker, indicating an unfavorable outcome [3, 4]. Furthermore, high presepsin levels could alert clinicians not to suspend antibiotic treatments even after clinical symptoms have improved and PCT levels have returned to normal.
- Masson S, Caironi P, Spanuth E, Thomae R, Panigada M, Sangiorgi G, Fumagalli R, Mauri T, Isgrò S, Fanizza C, et al.: Presepsin (soluble CD14 subtype) and procalcitonin levels for mortality prediction in sepsis: data from the Albumin Italian Outcome Sepsis trial. Crit Care 2014, 18: R6. 10.1186/cc13183View ArticlePubMedPubMed CentralGoogle Scholar
- Yaegashi Y, Shirakawa K, Sato N, Suzuki Y, Kojika M, Imai S, Takahashi G, Miyata M, Furusako S, Endo S: Evaluation of a newly identified soluble CD14 subtype as a marker for sepsis. J Infect Chemother 2005, 11: 234-238. 10.1007/s10156-005-0400-4View ArticlePubMedGoogle Scholar
- Ulla M, Pizzolato E, Lucchiari M, Loiacono M, Soardo F, Forno D, Morello F, Lupia E, Moiraghi C, Mengozzi G, et al.: Diagnostic and prognostic value of presepsin in the management of sepsis in the emergency department: a multicenter prospective study. Crit Care 2013, 17: R168. 10.1186/cc12847View ArticlePubMedPubMed CentralGoogle Scholar
- Endo S, Suzuki Y, Takahashi G, Shozushima T, Ishikura H, Murai A, Nishida T, Irie Y, Miura M, Iguchi H, et al.: Presepsin as a powerful monitoring tool for the prognosis and treatment of sepsis: a multicenter prospective study. J Infect Chemother 2014, 20: 30-34. 10.1016/j.jiac.2013.07.005View ArticlePubMedGoogle Scholar
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