Schubach Edvar Y P, Figueiredo Fabiano B, Romero Gustavo A S
Núcleo de Medicina Tropical, Universidade de Brasília, Distrito Federal, Brazil.
Instituto de Pesquisas Evandro Chagas, Fundação Instituto Oswaldo Cruz, Rio de Janeiro, Brazil.
Trans R Soc Trop Med Hyg. 2014 Sep;108(9):568-74. doi: 10.1093/trstmh/tru109. Epub 2014 Jul 11.
Visceral leishmaniasis is a major public health concern in Brazil and the domestic dog is the main source of infection. In this study, we aimed to evaluate the accuracy and reliability of a rapid chromatographic immunoassay based on a dual-path platform for the diagnosis of canine visceral leishmaniasis (CVL).
Sampling consisted of 428 domestic dogs selected from two neighborhoods in the municipality of Fortaleza, Ceara state, Brazil. The reference standard was composed of three parasitological tests and was applied samples from 333 dogs. The rapid test was used to analyse whole blood and serum samples.
Accuracy of the rapid test in whole blood samples through visual reading (n=305), serum samples through electronic reading (n=333) and serum samples through visual reading (n=333), yielded sensitivities of 87.5% (21/24; 95% CI: 66.5 to 96.7), 88% (22/25; 95% CI: 67.5 to 96.8) and 88% (22/25; 95% CI: 67.5 to 96.8), and specificities of 73.3% (206/281; 95% CI: 67.7 to 78.4), 68.2% (210/308; 95% CI: 62.2 to 74.3) and 69.2% (213/308; 95% CI: 63.7 to 74.3), respectively. Agreement between the visual and electronic readings in 428 serum samples were classified as almost perfect (Kappa Index=0.88; 95% CI: 0.83 to 0.93). The positive predictive value of the test using whole blood samples was 21.9% for the 7.9% prevalence detected by the reference standard in the study sample. A sensitivity analysis of the positive predictive value revealed that it remained below 50% in scenarios with a prevalence of up to 20%.
The similarity of the accuracy values of the rapid test using whole blood or serum samples, together with its reliable performance in sera through visual and electronic reading, suggests that it may contribute as a screening test for routine use under field-conditions. However, future studies need to improve the accuracy of the test so that it can be successfully implemented in public health programs.
内脏利什曼病是巴西主要的公共卫生问题,家犬是主要感染源。在本研究中,我们旨在评估基于双路径平台的快速色谱免疫分析法诊断犬内脏利什曼病(CVL)的准确性和可靠性。
从巴西塞阿拉州福塔雷萨市的两个社区选取428只家犬进行采样。参考标准由三项寄生虫学检测组成,并应用于333只犬的样本。快速检测用于分析全血和血清样本。
通过视觉读数分析全血样本(n = 305)、通过电子读数分析血清样本(n = 333)以及通过视觉读数分析血清样本(n = 333)时,快速检测的敏感性分别为87.5%(21/24;95%可信区间:66.5至96.7)、88%(22/25;95%可信区间:67.5至96.8)和88%(22/25;95%可信区间:67.5至96.8),特异性分别为73.3%(206/281;95%可信区间:67.7至78.4)、68.2%(210/308;95%可信区间:62.2至74.3)和69.2%(213/308;95%可信区间:63.7至74.3)。428份血清样本的视觉读数和电子读数之间的一致性被分类为几乎完美(Kappa指数 = 0.88;95%可信区间:0.83至0.93)。对于研究样本中参考标准检测出的7.9%的患病率,使用全血样本检测的阳性预测值为21.9%。阳性预测值的敏感性分析表明,在患病率高达20%的情况下,其仍低于50%。
使用全血或血清样本进行快速检测的准确性值相似,以及其在血清中通过视觉和电子读数的可靠性能,表明它可能有助于作为现场条件下常规使用的筛查检测方法。然而,未来的研究需要提高检测的准确性,以便能够在公共卫生项目中成功实施。