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印度德里地区用于诊断恶性疟原虫疟疾的聚合酶链反应分析评估

Evaluation of the polymerase chain reaction analysis for diagnosis of falciparum malaria in Delhi, India.

作者信息

Nandwani S, Mathur M, Rawat S

机构信息

Department of Microbiology, University College of Medical Sciences and Guru Teg Bahadur Hospital, Shahdara, New Delhi - 110 095, India.

出版信息

Indian J Med Microbiol. 2005 Jul;23(3):176-8. doi: 10.4103/0255-0857.16590.

Abstract

Plasmodium falciparum infections are frequently fatal if untreated and hence need to be diagnosed and treated early. Malaria diagnosis, with conventional Giemsa staining as a gold standard, has had several limitations. New rapid and accurate methods are needed for diagnosis. In this study, polymerase chain reaction (PCR) analysis specific for diagnosis of P. falciparum was evaluated. For the study, blood samples were collected from 310 patients suspected of having malaria. PCR analysis for P. falciparum from venous blood and at the same time Giemsa staining of thick and thin blood smears was done. A total of 160 (51.6 %) samples were positive for malarial parasite of which 63 (39.4 %) were positive for P. falciparum by Giemsa staining while 61 (38.1 %) were positive for P. falciparum by PCR analysis. Giemsa staining was time consuming, laborious and may give poor results in cases with low parasitaemia. The PCR analysis for P. falciparum was able to detect 3 cases of low parasitaemia missed initially on Giemsa staining, was 96.8 % sensitive, 100% specific but was very costly, needed a lot of practice and standardization and was time consuming. PCR analysis can be used to supplement the conventional Giemsa staining for reliable diagnosis of falciparum malaria especially in cases with low parasitaemia.

摘要

恶性疟原虫感染若不治疗往往会致命,因此需要尽早诊断和治疗。以传统吉姆萨染色作为金标准的疟疾诊断存在若干局限性。需要新的快速准确的诊断方法。在本研究中,对用于诊断恶性疟原虫的聚合酶链反应(PCR)分析进行了评估。在该研究中,从310名疑似疟疾患者采集了血样。对静脉血进行恶性疟原虫的PCR分析,同时对厚血膜和薄血膜进行吉姆萨染色。总共160份(51.6%)样本疟原虫呈阳性,其中63份(39.4%)经吉姆萨染色恶性疟原虫呈阳性,而61份(38.1%)经PCR分析恶性疟原虫呈阳性。吉姆萨染色耗时、费力,在疟原虫血症较低的病例中可能结果不佳。恶性疟原虫的PCR分析能够检测出最初吉姆萨染色遗漏的3例低疟原虫血症病例,敏感性为96.8%,特异性为100%,但成本非常高,需要大量实践和标准化,且耗时。PCR分析可用于补充传统吉姆萨染色,以可靠诊断恶性疟,尤其是在低疟原虫血症的病例中。

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