Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Jun 20;14(12):1311.
doi: 10.3390/diagnostics14121311.

Presepsin in Critical Illness: Current Knowledge and Future Perspectives

Affiliations
Review

Presepsin in Critical Illness: Current Knowledge and Future Perspectives

Paolo Formenti et al. Diagnostics (Basel). .

Abstract

The accurate identification of infections is critical for effective treatment in intensive care units (ICUs), yet current diagnostic methods face limitations in sensitivity and specificity, alongside cost and accessibility issues. Consequently, there is a pressing need for a marker that is economically feasible, rapid, and reliable. Presepsin (PSP), also known as soluble CD14 subtype (sCD14-ST), has emerged as a promising biomarker for early sepsis diagnosis. PSP, derived from soluble CD14, reflects the activation of monocytes/macrophages in response to bacterial infections. It has shown potential as a marker of cellular immune response activation against pathogens, with plasma concentrations increasing during bacterial infections and decreasing post-antibiotic treatment. Unlike traditional markers such as procalcitonin (PCT) and C-reactive protein (CRP), PSP specifically indicates monocyte/macrophage activation. Limited studies in critical illness have explored PSP's role in sepsis, and its diagnostic accuracy varies with threshold values, impacting sensitivity and specificity. Recent meta-analyses suggest PSP's diagnostic potential for sepsis, yet its standalone effectiveness in ICU infection management remains uncertain. This review provides a comprehensive overview of PSP's utility in ICU settings, including its diagnostic accuracy, prognostic value, therapeutic implications, challenges, and future directions.

Keywords: critical care patients; presepsin; sepsis.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 2
Figure 2
The mechanism of presepsin production.
Figure 1
Figure 1
Flowchart of search strategy.

References

    1. Wang H., Zhang W., Tang Y.-W. Clinical Microbiology in Detection and Identification of Emerging Microbial Pathogens: Past, Present and Future. Emerg. Microbes Infect. 2022;11:2579–2589. doi: 10.1080/22221751.2022.2125345. - DOI - PMC - PubMed
    1. Dellinger R.P., Rhodes A., Evans L., Alhazzani W., Beale R., Jaeschke R., Machado F.R., Masur H., Osborn T., Parker M.M., et al. Surviving Sepsis Campaign. Crit. Care Med. 2023;51:431–444. doi: 10.1097/CCM.0000000000005804. - DOI - PubMed
    1. Peri A.M., Stewart A., Hume A., Irwin A., Harris P.N.A. New Microbiological Techniques for the Diagnosis of Bacterial Infections and Sepsis in ICU Including Point of Care. Curr. Infect. Dis. Rep. 2021;23:12. doi: 10.1007/s11908-021-00755-0. - DOI - PMC - PubMed
    1. Burillo A., Bouza E. Use of Rapid Diagnostic Techniques in ICU Patients with Infections. BMC Infect. Dis. 2014;14:593. doi: 10.1186/s12879-014-0593-1. - DOI - PMC - PubMed
    1. Heilmann E., Gregoriano C., Schuetz P. Biomarkers of Infection: Are They Useful in the ICU? Semin. Respir. Crit. Care Med. 2019;40:465–475. doi: 10.1055/s-0039-1696689. - DOI - PMC - PubMed