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Biomarker for infection in children with decompensated chronic liver disease: Neutrophilic CD64 or procalcitonin?
被引:0
作者:
Vinayagamoorthy, Vignesh
[1
]
Srivastava, Anshu
[1
]
Anuja, Anamika Kumari
[2
]
Agarwal, Vikas
[2
]
Marak, Rungmei
[3
]
Sen Sarma, Moinak
[1
]
Poddar, Ujjal
[1
]
Yachha, Surender Kumar
[1
]
机构:
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Paediat Gastroenterol, Lucknow 226014, Uttar Pradesh, India
[2] Sanjay Gandhi Postgrad Inst Med Sci, Dept Clin Immunol, Lucknow 226014, Uttar Pradesh, India
[3] Sanjay Gandhi Postgrad Inst Med Sci, Dept Microbiol, Lucknow 226014, Uttar Pradesh, India
关键词:
Neutrophilic CD64;
Infection;
Decompensated chronic liver disease;
Procalcitonin;
Children;
INFLAMMATORY RESPONSE SYNDROME;
C-REACTIVE PROTEIN;
BACTERIAL-INFECTION;
EXPRESSION;
DIAGNOSIS;
SEPSIS;
CIRRHOSIS;
PREVALENCE;
MORTALITY;
MARKERS;
D O I:
10.1016/j.clinre.2024.102432
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
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 714 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(0.452.07) 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.
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