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Biomarker for infection in children with decompensated chronic liver disease: Neutrophilic CD64 or procalcitonin? - 07/08/24

Doi : 10.1016/j.clinre.2024.102432 
Vignesh Vinayagamoorthy a, Anshu Srivastava a, , Anamika Kumari Anuja b, Vikas Agarwal b, Rungmei Marak c, Moinak Sen Sarma a, Ujjal Poddar a, Surender Kumar Yachha a
a Department of Paediatric Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India 
b Department of Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India 
c Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India 

Corresponding author at: Department of Paediatric Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, Uttar Pradesh, India.Department of Paediatric GastroenterologySanjay Gandhi Postgraduate Institute of Medical SciencesRaebareli RoadLucknowUttar Pradesh226014India

Highlights

nCD64 a novel biomarker which identifies bacterial infection within few hours.
nCD64 identifies infection accurately in pediatric chronic liver disease.
nCD64 correlates with infection severity and resolution.
nCD64 performs better than procalcitonin and leucocyte count.

Il testo completo di questo articolo è disponibile in PDF.

Abstract

Objective

Biomarkers with high accuracy for identification of infection in decompensated chronic liver disease (DCLD) are urgently needed. We compared the accuracy of neutrophilic cluster of differentiation 64 (nCD64) with procalcitonin for diagnosis of bacterial infection in children with DCLD.

Methods

Consecutive children admitted with DCLD were enrolled prospectively. nCD64 was assessed by flow cytometry and expressed in percentage. nCD64, procalcitonin and hemogram were measured at admission and 7-14 days after treatment in those with infection. Complete work-up for infection was done. Presence, site and severity of infection was classified as per guidelines.

Results

107 children [64 boys, age 97(18-168) months] were enrolled. 78(72.9%) had infection, 26(24%) had severe sepsis and 60(56%) had systemic inflammatory response syndrome. The commonest site of infection was ascitic fluid (n=37), followed by pneumonia (n=24), urinary tract (n=15), bacteraemia (n=10), cholangitis (n=8) and cellulitis (n=3). nCD64 (cut-off-51%, AUC-0.82) had a higher sensitivity (79.5%) and specificity (82.8%) than procalcitonin (cut-off ≥0.58ng/mL, AUC-0.74, sensitivity-76.9% and specificity-62.1%) for diagnosis of infection. nCD64 and procalcitonin correlated with infection severity, being highest in children with severe sepsis [88(71-97) %and 1.98(0.83-10.36) ng/mL], than in infection alone [72(45-84) % and 1.09(0.45-2.07) ng/mL], and no-infection [36(20.2-48) % and 0.42(0.19-1.08) ng/mL]. There was no difference in diagnostic utility of procalcitonin or nCD64 with different sites of infection. Elevation of all 3 parameters (nCD64, PCT and total leukocyte count) was uncommon but highly specific for presence of infection.

Conclusion

nCD64 identifies infection better than procalcitonin and correlates well with infection severity in children with DCLD.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Neutrophilic CD64, Infection, Decompensated chronic liver disease, Procalcitonin, Children

Abbreviations : AFI, AIH, ALF, AUC, AVH, BSI, CLD, CRP, CTP, DCLD, EDTA, IS, LR, MELD, MFI, nCD64, NLR, NPV, PCLIF SOFA, PCT, PPV, ROC, SIRS, TLC, UTI


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© 2024  Pubblicato da Elsevier Masson SAS.
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Vol 48 - N° 8

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