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通过乳胶凝集试验检测内脏利什曼病患者尿液中的利什曼原虫抗原。

Detection of leishmanial antigen in the urine of patients with visceral leishmaniasis by a latex agglutination test.

作者信息

Sundar Shyam, Agrawal Shrinkhla, Pai Kalpana, Chance Michael, Hommel Marcel

机构信息

Kala-Azar Medical Research Center, Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.

出版信息

Am J Trop Med Hyg. 2005 Aug;73(2):269-71.

Abstract

Diagnosis of visceral leishmaniasis (VL) is usually done by demonstration of parasites in tissue smears. However, obtaining these smears may be risky, painful, and difficult. Antibody-based diagnostics are limited by their inability to predict active disease. In this study, a new latex agglutination test (KAtex), which detects parasite antigen in freshly voided and boiled urine, was evaluated in patients with VL before the start (n = 382) and at the end of treatment (n = 273); 185 healthy controls from leishmaniasis-endemic region were also studied. The KAtex result was positive in 87% (95% confidence interval [CI] = 83.3-90.3). However, at the end of treatment only 3% (95% CI = 1.6-6.2) patients were positive. The specificity of the test was 99% and 2 of 185 healthy controls tested positive. Positive and negative predictive values were 0.994 and 0.788, respectively. KAtex is a promising test, and in a simplified and improved format it could be applied meaningfully in the diagnosis of VL.

摘要

内脏利什曼病(VL)的诊断通常通过在组织涂片中发现寄生虫来进行。然而,获取这些涂片可能有风险、会带来疼痛且困难。基于抗体的诊断方法因无法预测活动性疾病而受到限制。在本研究中,一种新的乳胶凝集试验(KAtex)在VL患者治疗开始前(n = 382)和治疗结束时(n = 273)进行了评估,该试验可检测新鲜排出和煮沸尿液中的寄生虫抗原;还对来自利什曼病流行地区的185名健康对照者进行了研究。KAtex结果在87%的患者中呈阳性(95%置信区间[CI] = 83.3 - 90.3)。然而,在治疗结束时,只有3%(95% CI = 1.6 - 6.2)的患者呈阳性。该试验的特异性为99%,185名健康对照者中有2人检测呈阳性。阳性预测值和阴性预测值分别为0.994和0.788。KAtex是一种有前景的试验,以简化和改进的形式,它可在VL诊断中得到有意义的应用。

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