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用于诊断婴儿利什曼原虫犬类感染的DPP®和SNAP®快速检测法的评估

Evaluation of DPP® and SNAP® Rapid Tests for diagnosis of Leishmania infantum canine infections.

作者信息

Souza Celeste da Silva Freitas de, Silva Valmir Laurentino, Labarthe Norma

机构信息

Laboratório de Imunomodulação e Protozoologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.

Faculdade de Medicina de Campos, Fundação Benedito Pereira Nunes, Campos, RJ, Brasil.

出版信息

Rev Soc Bras Med Trop. 2019 Jul 18;52:e20190154. doi: 10.1590/0037-8682-0154-2019.

Abstract

INTRODUCTION

Visceral leishmaniasis is a disease that affects humans, wildlife, and domestic species. Since dogs play a key role in urban Leishmania spp. transmission, the Brazilian government maintains the Monitoring and Control Program of Visceral Leishmaniasis (VLMCP) in endemic regions, which promotes awareness campaigns aiming to enhance the control of the infection. The VLMCP recommends the Dual Path Platform (DPP®) canine visceral leishmaniasis test (Bio-Manguinhos, Brazil) for screening and enzyme-linked immunosorbent assay to confirm the infection. The DPP® test is produced and distributed by the Health Ministry to the Municipal Health Centers responsible for the local VLMCP. The test is not available to all the clinics, forcing some veterinarians to use other rapid tests for screening and diagnosis of this disease in their daily routine.

METHODS

The present study was conducted to compare the performance of the DPP® and SNAP® tests using sera from the dogs with confirmed infections of L. infantum and from the dogs with no previous testing, residing in areas with a low Leishmania infection.

RESULTS

There was 97.0% agreement between the two tests. Sensitivity and specificity of the SNAP® test were 96.3% and 100%, respectively. Agreement between both the antibody tests and the parasitological detection methods was 96.8%. The DPP® test had 95.8% sensitivity and 100% specificity.

CONCLUSIONS

The SNAP® and the DPP® tests were virtually equivalent in terms of detection of canine antibodies against L. infantum, and both the tests demonstrated high and similar levels of sensitivity and specificity.

摘要

引言

内脏利什曼病是一种影响人类、野生动物和家畜的疾病。由于狗在城市利什曼原虫传播中起关键作用,巴西政府在流行地区维持内脏利什曼病监测与控制项目(VLMCP),该项目开展宣传活动以加强感染控制。VLMCP推荐使用双路径平台(DPP®)犬内脏利什曼病检测试剂盒(巴西Bio-Manguinhos公司生产)进行筛查,并采用酶联免疫吸附测定法确认感染情况。DPP®检测试剂盒由卫生部生产并分发给负责当地VLMCP的市卫生中心。并非所有诊所都能获得该检测试剂盒,这迫使一些兽医在日常工作中使用其他快速检测方法来筛查和诊断这种疾病。

方法

本研究旨在比较DPP®检测试剂盒和SNAP®检测试剂盒对来自确诊感染婴儿利什曼原虫的犬以及之前未进行过检测、生活在利什曼原虫感染率较低地区的犬的血清检测性能。

结果

两种检测方法的一致性为97.0%。SNAP®检测试剂盒的灵敏度和特异性分别为96.3%和100%。两种抗体检测方法与寄生虫学检测方法之间的一致性为96.8%。DPP®检测试剂盒的灵敏度为95.8%,特异性为100%。

结论

在检测犬抗婴儿利什曼原虫抗体方面,SNAP®检测试剂盒和DPP®检测试剂盒实际上是等效的,两种检测方法均显示出较高且相似的灵敏度和特异性水平。

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