Batool Asia, Khan Misbahul Islam, Bano Khatoon Akhtar
PMRC Research Centre, Fatima Jinnah Medical College, Lahore, Pakistan.
J Ayub Med Coll Abbottabad. 2009 Jul-Sep;21(3):38-9.
To asses the efficacy of commercially available tests device method for anti HCV detection.
Total 2000 blood samples for detection of anti HCV were screened initially by immunochromatographic method. Those found positive on initial screening were re-tested by ELISA method at the Biochemistry Laboratory of the Pakistan Medical Research Council, Fatima Jinnah Medical College, Lahore.
Out of a total of 2,000 blood samples, 177 were found to be initially reactive/positive for anti-HCV with immunochromatographic method. When these reactive/positive samples were retested for confirmation with ELISA, 47 blood samples were found to have tested falsely positive for anti-HCV. Overall 2.35% of blood samples were found to be tested false positive for anti-HCV by immunochromatographic device method.
Immunochromatographic device method test is rapid and simple, which can be used in setting with limited facility when rapid testing is required. However it should not be used as sole criteria for diagnosis but should serve the purpose of initial screening only. Further research is required to establish the reliability of such devices for their specificity and sensitivity.
评估市售检测设备方法检测抗丙型肝炎病毒(抗HCV)的效能。
最初采用免疫层析法对总共2000份用于检测抗HCV的血样进行筛查。那些在初次筛查中呈阳性的样本在拉合尔法蒂玛·真纳医学院巴基斯坦医学研究委员会的生物化学实验室通过酶联免疫吸附测定(ELISA)法进行重新检测。
在总共2000份血样中,有177份通过免疫层析法最初检测为抗HCV反应性/阳性。当用ELISA法对这些反应性/阳性样本进行重新检测以确认时,发现有47份血样抗HCV检测为假阳性。总体而言,通过免疫层析设备法发现2.35%的血样抗HCV检测为假阳性。
免疫层析设备法检测快速且简单,在需要快速检测且设施有限的情况下可以使用。然而,它不应作为诊断的唯一标准,而仅应用于初步筛查目的。需要进一步研究以确定此类设备在特异性和敏感性方面的可靠性。