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OPINIONI - Opinions

Volume:

Biochimica Clinica 2020; 44(1) 068-072

Pubblicato on-line:

Febbraio 1, 2020

DOI:

10.19186/BC_2020.026

Scarica in PDF:
Autenticazione richiesta

Determinazione della presepsina: non solo diagnosi di sepsi
Presepsin measurement: beyond sepsis diagnosis

AUTORI

Giada Bragato1, Monica Maria Mion1, Andrea Padoan1,2, Martina Zaninotto1, Mario Plebani1,2
1UOC Medicina di Laboratorio, Azienda Ospedaliera-Università, Padova
2Dipartimento di Medicina, Università degli Studi, Padova

ABSTRACT

Presepsin measurement: beyond sepsis diagnosis

As sepsis is the leading cause of death among critically ill patients, early diagnosis is essential for the subsequent treatment to improve the outcome. Several diagnostic pathways have been proposed considering multiparametric approaches that combine clinical and biochemical evaluations. Among the several biomarkers proposed, procalcitonin measurement has been obtained significant consensus particularly in the evaluation of the efficacy of the therapeutic treatment. However, the need to define the prognosis and the outcome and to identify the patients at major risk of events during the hospitalization or at a short time later, seems to be an additional clinical value. The soluble cluster of differentiation 14 (S-CD14-ST or presepsin) is a free fragment of a glycoprotein expressed on monocytes and macrophages; several studies have demonstrated the significative prognostic value of the biomarker blood concentrations (at admission in particular) while the diagnostic performance of presepsin remains unclear. In a study carried out in a population of old patients (67-102 years) suffering from suspected pneumonia (n=50) the results of presepsin at admission in association with a Muldimensional Prognostic Index (MPI) score allow to identify the patients at major risk of adverse events (mortality) within 30 days. The prognostic efficiency of presepsin has been evaluated in different studies confirming, in different patient populations, the additional clinical value of this biomarker. Therefore, presepsin and prolacitonin measurements may provide complementary information that, in addition to clinical score and blood culture or molecular biology, can improve the management of patients with suspected sepsis.

BIBLIOGRAFIA

1. Rhodes A, Evans LE, Alhazzani W, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock: 2016. Crit Care Med 2017;45:486-552.
2. Galliera E, Massacesi L, de Vecchi E, et al. Clinical application of presepsin as diagnostic biomarker of infection: overview and updates. Clin Chem Lab Med 2020;58:11-7.
3. Clerico A, Plebani M. Biomarkers for sepsis: an unfinished journey. Clin Chem Lab Med 2013;51:1135-8.
4. Singer M, Deutschman CS, Seymour CW et al. The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA 2016;315:801–10.
5. Galliera E, Massacesi L, de Vecchi E et al. Applicazioni cliniche della presepsina come biomarcatore diagnostico d’infezione: rassegna e aggiornamenti Biochim Clin 2020;44:21-7.
6. Song J, Park DE, Moon S, et al. Diagnostic and prognostic value of interleukin-6, pentraxin 3, and procalcitonin levels among sepsis and septic shock patients: a prospective controlled study according to the Sepsis-3 definitions. BMC Infectious Diseases 2019;19:968-79.
7. Nguyen HB, Jaehne AK, Jayaprakash N et al. Early goal-directed therapy in severe sepsis and septic shock: insights and comparisons to ProCESS, ProMISe, and ARISE. Crit Care 2016:20:160-76.
8. Bouadma L, Luyt CE, Tubach F. et al Use of procalcitonin to reduce patients’ exposure to antibiotics in intensive care units (PRORATA trial): a multicentre randomised controlled trial. Lancet 2010;375:463-74.
9. Chenevier-Gobeaux C, Borderie D, Weiss N et al. Presepsin (sCD14-ST), an innate immune response marker in sepsis. Clin Chim Acta 2015;450: 97-103.
10. Arai Y, Mizugishi K, Nonomura K et al. Phagocytosis by human monocytes is required for the secretion of presepsin. J Infect Chemother 2015;2:564-69.
11. Carpio R, Zapata J, Spanuth E, et al. Utility of presepsin (sCD14-ST) as a diagnostic and prognostic marker of sepsis in the emergency department. Clin Chim Acta 2015;450:169-75.
12. Charles PE, Gibot S. Predicting outcome in patients with sepsis: new biomarkers for old expectations. Crit Care 2014;18:108-9.
13. Brodska H, Valenta J, Pelinkova K, et al. Diagnostic and prognostic value of presepsin vs. established biomarkers in critically ill patients with sepsis or systemic inflammatory response syndrome. Clin Chem Lab Med 2018;56:658-68.
14. Ugajin M, Matsuura Y, Matsuura K et al. Impact of initial plasma presepsin level for clinical outcome in hospitalized patients with pneumonia. J Thorac Dis 2019;11:1387-96.
15. Ali FT, Ali MA, Elnakeeb MM, et al. Presepsin is an early monitoring biomarker for predicting clinical outcome in patients with sepsis. Clin Chim Acta 2016;490:93-101.
16. Masson S, Caironi P, Spanuth E, 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.
17. Pilotto A, Dini S, Daragjati J, et al. Combined Use of the Multidimensional Prognostic Index (MPI) and Procalcitonin Serum Levels in Predicting 1-month Mortality Risk in Older Patients Hospitalized With Community-Acquired Pneumonia (CAP): A Prospective Study. Aging Clin Exp Res 2018;30:193-7.
18. Pilotto A, Rengo F, Marchionni N, et al. Comparing the prognostic accuracy for all-cause mortality of frailty instruments: a multicentre 1-year follow-up in hospitalized older patients. PLoS ONE 2012; 7:e29090.
19. Klouche K, Cristol JP, Devin J, et al. Diagnostic and prognostic value of soluble CD14 subtype (Presepsin) for sepsis and community-acquired pneumonia in ICU patients. Ann Intensive Care 2016 6:59-70.
20. Bomberg H, Klingele M, Wagenpfeil S, et al. Presepsin (sCD14-ST) is a novel marker for risk stratification in cardiac surgery patients. Anesthesiology 2017;126:631-42.
21. Elefsiniotis I, Tsakiris AS, Barla G et al. Presepsin levels in cirrhotic patients with bacterial infections and/or portal hypertension-related bleeding, presenting with or without acute kidney injury. Ann Gastroenterol 2018;31:604-12.
22. Mussap M, Puxeddu E, Puddu M, et al. Soluble CD14 subtype (sCD14-ST) presepsin in premature and full term critically ill newborns with sepsis and SIRS. Clin Chim Acta 2015;451:65-70.
23. Takahashi G, Shibata S, Fukui Y, et al. Diagnostic accuracy of procalcitonin and presepsin for infectious disease in patients with acute kidney injury. Diagn Microbiol Infect Dis 2016;86:205-10.
24. Yu H, Qi Z, Hang C, et al. Evaluating the value of dynamic procalcitonin and presepsin measurements for patients with severe sepsis. Am J Emerg Med 2017;35:835-41.
25. Cervellin G, Schuetz P, Lippi G. Toward a holistic approach for diagnosing sepsis in the emergency department. Adv Clin Chem 2019;92:201-16.

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