Evidence map›Paper›PMID 41901712›Full record

ArticlePathogens (Basel, Switzerland)2026

Assessment of Systemic Inflammation as a Tool for Estimating the Risk of Death by Visceral Leishmaniasis.

Ingridi de Souza Sene, Vladimir Costa Silva, Débora Cavalcante Brás, Dorcas Lamounier Costa, Gabriel Reis Ferreira, Carlos Henrique Nery Costa

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Ingridi de Souza SeneLAPAC-Patologia Cirúrgica e Molecular and Mestrado em Ciências e Saúde, Centro de Ciências das Saúde, Universidade Federal do Piauí, Teresina 64049-550, Brazil.
Vladimir Costa SilvaLaboratory of Genomic Surveillance and Molecular Biology (LVGBM)-Oswaldo Cruz Foundation-Piauí, Teresina 64049-550, Brazil.ORCID 0000-0003-3109-7899
Débora Cavalcante BrásLaboratory of Genomic Surveillance and Molecular Biology (LVGBM)-Oswaldo Cruz Foundation-Piauí, Teresina 64049-550, Brazil.ORCID 0000-0001-5978-1241
Dorcas Lamounier CostaLAPAC-Patologia Cirúrgica e Molecular and Mestrado em Ciências e Saúde, Centro de Ciências das Saúde, Universidade Federal do Piauí, Teresina 64049-550, Brazil.ORCID 0000-0001-7115-7978
Gabriel Reis FerreiraCentro de Inteligência em Agravos Tropicais Emergentes e Negligenciados (CIATEN) and Tropical Diseases Department of Microbiology, Infectious Disease and Immunology, Faculty of Medicine, University of Laval, Québec, QC G1V 0A6, Canada.ORCID 0000-0002-4584-8588
Carlos Henrique Nery CostaLAPAC-Patologia Cirúrgica e Molecular and Mestrado em Ciências e Saúde, Centro de Ciências das Saúde, Universidade Federal do Piauí, Teresina 64049-550, Brazil.ORCID 0000-0001-7302-2006

Funding

National Council for Scientific and Technological Development 302571/2015-9
6 · The paper itself

Abstract

backgroundVisceral leishmaniasis (VL) is a life-threatening protozoan disease prevalent in tropical and subtropical regions and a frequent coinfection among people living with HIV. Early identification of patients at high risk of death may reduce case-fatality. This study evaluated the post-test prognostic value of C-reactive protein (CRP) and interleukin-6 (IL-6) as biomarkers of mortality in VL.

methodsA retrospective hospital-based cohort of 101 VL patients was analyzed. CRP and IL-6 concentrations at admission were correlated with clinical findings, the Kala-Cal

resultsEight patients died, most presenting with hemorrhagic manifestations. At admission, 87.1% of patients had both biomarkers above the predefined cut-offs. CRP and IL-6 levels were markedly elevated in patients with hemorrhage or fatal outcomes. The AUC was 0.85 for CRP and 0.87 for IL-6, with no significant difference between markers. Optimal prognostic cut-offs were 150 mg/L for CRP and 90 pg/mL for IL-6.

conclusionsIn this sample, CRP and IL-6 showed good prognostic performance in VL. In patients with low initial clinical risk, positive biomarker results substantially increased the probability of death. When combined with Kala-Cal

Indexed as

InflammationLeishmaniasis, VisceralAdultBiomarkersC-Reactive ProteinFemaleHumansInterleukin-6MaleMiddle AgedPrognosisRetrospective StudiesBiomarkersC-Reactive ProteinInterleukin-6biomarkersC-reactive proteinIL-6mortalityprognosisseverity of illness indexvisceral leishmaniasis

Identifiers

PMID41901712
PMCPMC13028813

What Socratic 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 Socratic graph.