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Evaluation of a rapid immunochromatographic test kit to the gold standard fluorescent antibody test for diagnosis of rabies in animals in Bhutan

机译:评价对金标准荧光抗体试验试验试验试验,以诊断胃丹动物狂犬病

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Rabies kills approximately 59,000 people each year worldwide. Rapid and accurate diagnosis of rabies is important for instituting rapid containment measures and for advising the exposed people for postexposure treatment. The application of a rapid diagnostic tests in the field can greatly enhance disease surveillance and diagnostic activities, especially in resource poor settings. In this study, a total of 179 brain tissue samples collected from different rabies suspect animal species (113 dogs, 50 cattle, 10 cats, 3 goats, 2 horses, and 1 bear) were selected and tested using both rapid immunochromatographic kit and the reference standard fluorescent antibody test (FAT). We evaluated the sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of a rapid antigen detection test kit produced by BioNote, Inc. (Hwaseong-si, Korea) relative to a FAT for its fit-for-purpose for confirmation of clinical cases of rabies for early response and enhancing rabies surveillance. Among 179 samples examined in this study, there was a concordance in results by the rapid test and FAT in 115 positive samples and 54 negative samples. Test results were discordant in 10 samples which were positive by FAT, but negative (false negative) by rapid kit. The rapid test kit showed a sensitivity of 92% (95% CI: 85.9–95.6) and specificity of 100% (95% CI: 93.4–100) using FAT as the reference standard. The positive and negative predictive values were found to be 100% (95% CI:96.7–100) and 84.4% (95% CI: 73.6–91.3), respectively. Overall, there was 94.4% (95% CI: 90–96.9) test agreement between rapid test and FAT (Kappa value?=?0.874) with a positive percent agreement and negative percent agreement of 92 and 100%, respectively. Our finding demonstrated that the rapid test kit (BioNote) can be used for rabies surveillance and confirming clinical case of rabies in animals for making rapid decisions particularly controlling rabies outbreaks in resource poor settings.
机译:狂犬病在全球每年杀死约59,000人。对狂犬病的快速和准确诊断对于机构提供快速遏制措施并为向暴露的人提供露出的曝光措施来说很重要。在现场中的快速诊断测试中的应用可以大大提高疾病监测和诊断活动,特别是在资源差的环境中。在这项研究中,使用快速免疫粒状试剂盒和参考,选择了从不同狂犬病嫌疑动物物种(113只狗,50只牛,10只猫,3只山羊,2马和1只熊)中收集的179个脑组织样本。和测试标准荧光抗体试验(脂肪)。我们评估了Bionote,Inc。(HWASEONG-SI,韩国)产生的快速抗原检测试剂盒的敏感性,特异性,阳性预测值(PPV)和负预测值(NPV),相对于其适合的脂肪 - 用于确认早期反应狂犬病临床病例的目的,提高狂犬病监测。在本研究中检查的179个样本中,通过115个阳性样品和54个阴性样品的快速测试和脂肪产生了一致性。测试结果在10个样品中不全于脂肪阳性,但快速试剂盒的阴性(假阴性)。快速检测试剂盒显示出92%(95%CI:85.9-95.6)的敏感性,使用脂肪作为参考标准的脂肪含量为100%(95%CI:93.4-100)。发现阳性和阴性预测值是100%(95%CI:96.7-100)和84.4%(95%CI:73.6-91.3)。总体而言,94.4%(95%CI:90-96.9)在快速试验和脂肪(Kappa Value?= 0.874)之间的测试协议,分别具有较正百分比和负百分比的百分比和为92和100%。我们的发现表明,快速的测试套件(Bionote)可用于狂犬病监测和确认动物中狂犬病的临床情况,以便在资源差的资源中控制狂犬病爆发的快速决策。

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