The diagnostic value of (1,3)-β-D-glucan alone or combined with traditional inflammatory markers in neonatal invasive candidiasis
Open Access
- 14 August 2019
- journal article
- research article
- Published by Springer Nature in BMC Infectious Diseases
- Vol. 19 (1) , 1-8
Abstract
Asymptom of invasive candidiasis (IC) and low positive rate of blood culture lead to delay diagnose of neonatal infection. Serum (1,3)-β-D-glucan (BDG) performs well in adult IC, but its use in neonatal IC is unclear. We evaluated the use of BDG, procalcitonin (PCT), high-sensitive C-reactive protein (hsCRP) or platelet count (PC) in neonatal IC. We collected the data of neonates admitted to our institute. Eighty neonates were enrolled, and divided into IC group, bacterial infection (BI) group and control (CTRL) group. We analyzed the difference of these indicators between groups, and generated Receiver operator characteristic (ROC) curve. The value of BDG in antifungal therapy efficacy assessment was also investigated. The BDG level was higher in IC group compared with BI and CTRL group. C. albicans lead to significant increase of BDG compared with C. parapsilosis. IC group had highest hsCRP level and lowest PC. PCT level was similar between groups. ROC showed that BDG or hsCRP performs well in neonatal IC, the optimal cut-off for BDG was 13.69 mg/ml. Combined BDG with hsCRP, PCT and PC increased diagnostic value. Serum BDG level was decreased during antifungal treatment. Serum BDG performs well in identification of neonatal IC and in monitoring the antifungal therapy efficacy.Keywords
Funding Information
- Guangzhou Science, Technology and Innovation Commission (201804010120)
- Guangdong Natural Science Foundation (2018A030310056)
This publication has 28 references indexed in Scilit:
- Substantially elevated C-reactive protein (CRP), together with low levels of procalcitonin (PCT), contributes to diagnosis of fungal infection in immunocompromised patientsSupportive Care in Cancer, 2013
- (1–3)-β-D-glucan levels in candidiasis infections in the critically ill neonateThe Journal of Maternal-Fetal & Neonatal Medicine, 2012
- Early and late onset sepsis in very-low-birth-weight infants from a large group of neonatal intensive care unitsEarly Human Development, 2012
- -Glucan Antigenemia Assay for the Diagnosis of Invasive Fungal Infections in Patients With Hematological Malignancies: A Systematic Review and Meta-Analysis of Cohort Studies From the Third European Conference on Infections in Leukemia (ECIL-3)Clinical Infectious Diseases, 2011
- Clinical Performance of the (1,3)-β- d -Glucan Assay in Early Diagnosis of Nosocomial Candida Bloodstream InfectionsClinical and Vaccine Immunology, 2011
- Early diagnosis of candidemia in intensive care unit patients with sepsis: a prospective comparison of (1→3)-β-D-glucan assay, Candida score, and colonization indexCritical Care, 2011
- Diagnostic Performance of 1→3-β-D-Glucan in Neonatal and Pediatric Patients with CandidemiaInternational Journal of Molecular Sciences, 2011
- Reactivity of (1 → 3)-β-d-glucan assay in bacterial bloodstream infectionsEuropean Journal of Clinical Microbiology & Infectious Diseases, 2011
- Prospective Survey of (1→3)-β- d -Glucan and Its Relationship to Invasive Candidiasis in the Surgical Intensive Care Unit SettingJournal of Clinical Microbiology, 2011
- Pseudomonas aeruginosaas a Cause of 1,3‐β‐d‐Glucan Assay ReactivityClinical Infectious Diseases, 2008