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Diagnostic Performance of Two Point-of-Care Tests for Anti-HCV Detection
BACKGROUND: Besides the great importance of the issue in terms of public health, there is a lack of studies evaluating the performance of several of the currently used point of care tests (POCTs) for the detection of anti-HCV. OBJECTIVES: To investigate the performance of two POCTs for anti-HCV dete...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830521/ https://www.ncbi.nlm.nih.gov/pubmed/24282422 http://dx.doi.org/10.5812/hepatmon.12274 |
Sumario: | BACKGROUND: Besides the great importance of the issue in terms of public health, there is a lack of studies evaluating the performance of several of the currently used point of care tests (POCTs) for the detection of anti-HCV. OBJECTIVES: To investigate the performance of two POCTs for anti-HCV detection and to assess the impact of the reading time on diagnostic performance. PATIENTS AND METHODS: A total of 307 subjects were divided into three groups (1- HCV infected; 2- other chronic liver diseases; and 3- controls). The POCTs HCV Rapid Test Bioeasy® and Imuno-Rapido HCV® were read at 3, 5, 10, 15, 20 and 30 minutes. The sensitivity and specificity of the POCTs were calculated in relation to anti-HCV detection by chemiluminescence. RESULTS: Valid results were obtained for all tests. When compared to the chemiluminescence, both tests showed sensitivity of 97.1% and specificity of 100%. No changes in the sensitivity or specificity of the tests were observed at different reading times and when patients with other chronic liver diseases were evaluated as a control group. CONCLUSIONS: The POCTs evaluated in this study showed high sensitivity and specificity, with no change in the performance after the third minute of reading. |
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