Volume 47, Issue 2 pp. 221-227
ORIGINAL ARTICLE

CBC With Differential and Cell Population Data in Prediction of Fever With Thrombocytopenia Syndrome

Lixia Zhang

Lixia Zhang

The First Affiliated Hospital With Nanjing Medical University, Nanjing, People's Republic of China

Branch of National Clinical Research Center for Laboratory Medicine, Nanjing, People's Republic of China

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Shuxian Yang

Shuxian Yang

The First Affiliated Hospital With Nanjing Medical University, Nanjing, People's Republic of China

Branch of National Clinical Research Center for Laboratory Medicine, Nanjing, People's Republic of China

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Chen Cheng

Chen Cheng

The First Affiliated Hospital With Nanjing Medical University, Nanjing, People's Republic of China

Branch of National Clinical Research Center for Laboratory Medicine, Nanjing, People's Republic of China

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Yuan Mu

Yuan Mu

The First Affiliated Hospital With Nanjing Medical University, Nanjing, People's Republic of China

Branch of National Clinical Research Center for Laboratory Medicine, Nanjing, People's Republic of China

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Shiyang Pan

Corresponding Author

Shiyang Pan

The First Affiliated Hospital With Nanjing Medical University, Nanjing, People's Republic of China

Branch of National Clinical Research Center for Laboratory Medicine, Nanjing, People's Republic of China

Correspondence:

Shiyang Pan ([email protected])

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First published: 18 December 2024

Funding: This work was supported by National Natural Science Foundation of China (Grant/award number: 82272401), Jiangsu Province Capability Improvement Project through Science and Technology and Education (Grant/award number: ZDXK202239).

Lixia Zhang and Shuxian Yang contributed equally to this work.

ABSTRACT

Introduction

We aimed to identify additional predictors of severe fever with thrombocytopenia syndrome (SFTS), which has a significantly increasing global incidence.

Methods

This retrospective study included 95 patients with SFTS and 30 healthy individuals. Complete blood count with differential was performed using Sysmex XN 9000 and Mindray BC-6800 Plus analyzers. Extended leukocyte cell population data (CPD) parameters were acquired using a Mindray BC-6800 Plus analyzer. Peripheral smears were identified, and SFTS virus (SFTSV) RNA was detected using real-time reverse transcription polymerase chain reaction.

Results

Of 95 patients with SFTS at admission, 75.8% (72/95) presented leukopenia and 96.8% (92/95) thrombocytopenia with SFTS. Neutrophil left shift and smudge cells (32.4/WBC ± 28.2/WBC) were observed 100% (57/57) on the blood smear. Only 21.1% (21/57) of the reactive lymphocytes were > 5% (3.24% ± 3.35%). Moreover, 33.3% (19/57) of apoptotic lymphocytes and 8.8% (5/57) of nucleated red blood cells were present. Furthermore, 78.9% (45/57) of reactive plasmacytoid lymphocytes increased 3–5 days after admission and 61.1% (11/18) of the patients who died presented with dust blue inclusions in the neutrophils. Compared to the control group, Neu-Y and all lymphocyte and monocyte CPD parameters were significantly higher in all SFTS groups. Compared to the surviving patients with SFTS, Lym-Y in Group 2 (p < 0.05) was significantly lower, but Neu-Y and Mon-Z in Group 3 were higher (p < 0.001) in the death group.

Conclusions

The cell count, peripheral blood morphology, and CPD parameters described in this study had a strong prompting effect on SFTSV infection.

Conflicts of Interest

The authors declare no conflicts of interest.

Data Availability Statement

The data in this study are not publicly available The data that support the findings of this study are available from the corresponding author upon reasonable request.

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