Evidence map›Paper›PMID 40509968›Full record

ArticleTropical medicine & international health : TM & IH2025

Lymphopenia: An early indicator of Crimean-Congo haemorrhagic fever.

Hatice Bozkurt Yavuz, Hüseyin Haydar Kutlu

Abstract read
In one paragraph

Article in Tropical medicine & international health : TM & IH, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Lymphopenia: An early indicator of Crimean-Congo haemorrhagic fever.Tropical medicine & international health : TM & IH · 2025
    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

2 authors.

Hatice Bozkurt YavuzDepartment of Clinical Biochemistry, Uşak University Faculty of Medicine, Usak, Turkey.ORCID https://orcid.org/0000-0003-0468-2486
Hüseyin Haydar KutluDepartment of Medical Microbiology, Uşak University Faculty of Medicine, Usak, Turkey.ORCID https://orcid.org/0000-0001-6616-046X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCrimean-Congo haemorrhagic fever is a lethal tick-borne disease characterised by initially nonspecific symptoms. While thrombocytopenia and leucopenia are established diagnostic markers, there is a need for earlier indicators. This study evaluates lymphopenia as a marker for Crimean-Congo haemorrhagic fever.

methodsThis retrospective study analysed patients admitted with arthropod bites from 2018 to 2021. Patients were classified based on initial leucocyte and platelet counts into Group 1 (normal values) and Group 2 (low values). Within Group 1, patients were classified as Group 1B if they developed thrombocytopenia and leucopenia during follow-up, whereas those with stable counts were designated as Group 1A. Variance and ROC curve analysis were used to evaluate blood counts.

resultsOf 914 evaluated patients, 870 with normal CBCs were categorised into Group 1, and 44 with low counts into Group 2. Within Group 1, 16 patients subsequently developed thrombocytopenia and leucopenia (Group 1B), while the rest remained stable (Group 1A). All patients in Groups 1B and 2 were later confirmed to have Crimean-Congo haemorrhagic fever via RT-PCR. Initial lymphocyte counts varied significantly, with 2.7 × 10

conclusionsLymphocyte depletion precedes changes in leucocyte and platelet counts, affirming its potential as an early diagnostic marker for Crimean-Congo haemorrhagic fever. Early detection through lymphocyte monitoring could improve patient management and reduce transmission in endemic areas.

Indexed as

Hemorrhagic Fever, CrimeanLymphopeniaAdultAgedBiomarkersFemaleHumansLeukocyte CountLeukopeniaMaleMiddle AgedPlatelet CountRetrospective StudiesROC CurveThrombocytopeniaBiomarkersCrimean‐Congo haemorrhagic feverleucopenialymphopeniathrombocytopeniatick bites

Identifiers

PMID40509968
PMCPMC12318437

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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.