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Performance of point of care assays for hepatitis B and C viruses in chronic kidney disease patients

Authors :
Danielle Malta Lima
Jeová Keny Baima Colares
Juliana Custódio Miguel
Jakeline Ribeiro Barbosa
Livia Melo Villar
Moyra Machado Portilho
Vanessa Alves Marques
Elisabeth Lampe
Cristianne Sousa Bezerra
Natália Vasconcelos de Souza
Lia Laura Lewis-Ximenez
Vanessa Faria Cortes
Source :
Journal of Clinical Pathology. 71:879-884
Publication Year :
2018
Publisher :
BMJ, 2018.

Abstract

AimsPoint of care testing (POCT) has been used for hepatitis B and C diagnosis in general population, but little is known about the influence of clinical conditions in the accuracy of these assays. This study aims to evaluate the performance of POCTs for detection of hepatitis B virus surface antigen (HBsAg) and antibodies to Hepatitis C Virus (anti-HCV) in Chronic Kidney Disease (CKD) patients.MethodsA total of 286 subjects were included in this study. HBsAg and anti-HCV were detected using commercial EIAs and four POCTs: HBsAg (WAMA Imuno-Rápido HBsAg and VIKIA HBsAg) and anti-HCV (DOLES HCV teste rápido and WAMA Imuno-Rápido anti-HCV) in serum and whole blood.ResultsUsing EIA, HBsAg and anti-HCV prevalence was 4.5% and 16.1% in CKD patients. HBsAg and anti-HCV POCTs had sensitivities from 92.3% to 100% and 84.8% to 89.1% while specificities were 99.3% to 100% and 99.2% to 99.6%, respectively. POCT using serum samples performed well compared with whole blood samples and true positive samples of POCTs had high optical density to cut-off (OD/CO) values compared with EIA.ConclusionsThis study demonstrates good performance of HBsAg and anti-HCV POCTs in CKD patients, especially in serum samples indicating low interference of this disease in the performance of these assays. POCTs could be an important tool for HBV and HCV screening in high-risk populations.

Details

ISSN :
14724146 and 00219746
Volume :
71
Database :
OpenAIRE
Journal :
Journal of Clinical Pathology
Accession number :
edsair.doi.dedup.....0b317025226f4442f483e64fea012807
Full Text :
https://doi.org/10.1136/jclinpath-2018-205024