Evidence map›Paper›PMID 41339821›Full record

SynthesisBMC emergency medicine2025

Diagnostic performance of procalcitonin and presepsin in sepsis: a systematic review and meta-analysis.

Tanakon Chairaj, Pajaree Mongkhon, Pit Leewongsakorn, Kritsada Saensongkwae, Sawitree Nangola, Somphot Saoin, Eakkapote Prompunt, Prawat Chantharit, Chiraphat Kloypan

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC emergency medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Tanakon Chairaj *Department of Pathology, School of Medicine, University of Phayao, Phayao, Thailand.
Pajaree Mongkhon *Division of Social and Administrative Pharmacy, Department of Pharmaceutical Care, School of Pharmaceutical Sciences, University of Phayao, Phayao, Thailand.
Pit LeewongsakornDepartment of Pathology, School of Medicine, University of Phayao, Phayao, Thailand.
Kritsada SaensongkwaeDepartment of Pathology, School of Medicine, University of Phayao, Phayao, Thailand.
Sawitree NangolaDepartment of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Thailand.
Somphot SaoinDepartment of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Thailand.
Eakkapote PrompuntDepartment of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Thailand.
Prawat ChantharitDivision of Infectious Diseases, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Chiraphat KloypanDepartment of Pathology, School of Medicine, University of Phayao, Phayao, Thailand. chiraphat.kl@up.ac.th.

Funding

Research Fund of the School of Medicine, University of Phayao MD67-02
6 · The paper itself

Abstract

backgroundSepsis is a critical emergency condition characterized by life-threatening organ dysfunction due to a dysregulated response to infection. In the fast-paced emergency department (ED) setting, rapid identification and prompt initiation of treatment within the initial hours following sepsis onset are critical for reducing mortality and improving patient outcomes. However, a timely and accurate diagnosis remains a significant challenge in emergency medicine. Biomarkers such as procalcitonin (PCT) and presepsin (P-SEP) have been proposed as tools to distinguish sepsis from other non-infectious inflammatory conditions frequently encountered in the ED, though their diagnostic effectiveness remains controversial. This study aimed to evaluate the diagnostic performance of PCT and P-SEP for diagnosis patients with sepsis.

methodsA comprehensive systematic search was conducted across the Cochrane Central Register of Controlled Trials, PubMed, and Scopus databases up to April 1st, 2024 and updated on June 30th, 2025. Studies reporting sensitivity and specificity of PCT and P-SEP for sepsis detection among patients in acute and emergency settings were included. Hierarchical modeling techniques were utilized to pool data for sensitivity, specificity, and area under the receiver operating characteristic curve (AUROC) along with their 95% confidence intervals (CIs).

resultsThirty-eight observational studies met inclusion criteria. The pooled sensitivities and specificities for detecting sepsis using PCT were 0.78 (95% CI: 0.74-0.81) and 0.77 (95% CI: 0.71-0.82), respectively. Similarly, for P-SEP, pooled sensitivity and specificity were 0.82 (95% CI: 0.77-0.86) and 0.78 (95% CI: 0.73-0.83), respectively. No statistically significant differences were identified between PCT and P-SEP regarding sensitivity (p = 0.169) or specificity (p = 0.792). The summary receiver operating characteristic analysis yielded an AUROC of 0.84 (95% CI: 0.81-0.87) for PCT and 0.87 (95% CI: 0.84-0.90) for P-SEP.

conclusionsBoth PCT and P-SEP represent reliable biomarkers for early and accurate sepsis detection in acute and ED settings, demonstrating comparable diagnostic performance. Their integration into routine ED assessment protocols may support timely clinical decision-making and prompt initiation of appropriate treatment strategies.

Indexed as

Lipopolysaccharide ReceptorsPeptide FragmentsProcalcitoninSepsisBiomarkersEmergency Service, HospitalHumansROC CurveSensitivity and SpecificityBiomarkersLipopolysaccharide ReceptorsPeptide Fragmentspresepsin protein, humanProcalcitoninDiagnostic testPresepsinProcalcitoninSensitivitySepsisSpecificity

Identifiers

PMID41339821
PMCPMC12798056

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.