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Parasight F检测与聚合酶链反应及显微镜检查在旅行者恶性疟原虫疟疾诊断中的比较。

Parasight F test compared with the polymerase chain reaction and microscopy for the diagnosis of Plasmodium falciparum malaria in travelers.

作者信息

Humar A, Ohrt C, Harrington M A, Pillai D, Kain K C

机构信息

Department of Medicine, Toronto Hospital, Ontario, Canada.

出版信息

Am J Trop Med Hyg. 1997 Jan;56(1):44-8. doi: 10.4269/ajtmh.1997.56.44.

Abstract

Imported malaria is an increasing problem worldwide. A rapid and accurate test for Plasmodium falciparum infection would facilitate the diagnosis of malaria in the returned traveler. The ParaSight F antigen capture assay (dipstick test) is a new diagnostic test for P. falciparum based on detection of circulating histidine-rich protein-2 antigen. We performed a blinded evaluation of this assay compared with microscopy and the polymerase chain reaction (PCR) for the detection of P. falciparum infection in 151 febrile travelers. Compared with the PCR, the dipstick test had a sensitivity of 88% and a specificity of 97%. The ability of the dipstick test to detect P. falciparum was similar with that of microscopy (88% versus 83%) since the species of Plasmodium in 14 of 133 malaria-infected patients could not be determined by microscopy due to low parasite numbers. The dipstick test was 40% sensitive for infections with < 50 parasites/microliter, 89% with 50-100 parasites/microliter, and > or = 93% with > 100 parasites/microliter. Circulating antigen was detectable in 68% of the patients seven days after initiation of treatment and in 27% at day 28. The dipstick test represents a simple and accurate test for the diagnosis of P. falciparum infection in the returned traveler.

摘要

输入性疟疾在全球范围内是一个日益严重的问题。一种快速、准确的恶性疟原虫感染检测方法将有助于对归国旅行者的疟疾进行诊断。ParaSight F抗原捕获试验(试纸条检测)是一种基于检测循环富组氨酸蛋白-2抗原的新型恶性疟原虫诊断试验。我们对151名发热旅行者进行了一项盲法评估,将该试验与显微镜检查和聚合酶链反应(PCR)用于检测恶性疟原虫感染进行比较。与PCR相比,试纸条检测的灵敏度为88%,特异性为97%。试纸条检测检测恶性疟原虫的能力与显微镜检查相似(88%对83%),因为在133例疟疾感染患者中有14例由于寄生虫数量少而无法通过显微镜检查确定疟原虫种类。对于每微升寄生虫数<50个的感染,试纸条检测的灵敏度为40%,50 - 100个寄生虫/微升时为89%,>或=100个寄生虫/微升时为>93%。在开始治疗7天后,68%的患者可检测到循环抗原,在第28天时为27%。试纸条检测是一种用于诊断归国旅行者恶性疟原虫感染的简单、准确的检测方法。

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