Accuracy of a Plasmodium falciparum specific histidine-rich protein 2 rapid diagnostic test in the context of the presence of non-malaria fevers, prior anti-malarial use and seasonal malaria transmission

被引:32
作者
Kiemde, Francois [1 ]
Bonko, Massa Dit Achille [1 ]
Tahita, Marc Christian [1 ]
Lompo, Palpouguini [1 ]
Rouamba, Toussaint [1 ]
Tinto, Halidou [1 ]
van Hensbroek, Michael Boele [2 ]
Mens, Petra F. [3 ]
Schallig, Henk D. F. H. [3 ]
机构
[1] Inst Rech Sci Sante, Unite Rech Clin Nanoro, Nanoro, Burkina Faso
[2] Univ Amsterdam, Acad Med Ctr, Global Child Hlth Grp, Amsterdam, Netherlands
[3] Acad Med Ctr, Dept Med Microbiol, Parasitol Unit, Amsterdam, Netherlands
关键词
RDT-PfHRP2; Diagnosis; Malaria; Fever; Sensitivity; Specificity; Accuracy; BURKINA-FASO; CASE-MANAGEMENT; HEALTH-CENTER; PERFORMANCE; CHILDREN; SETTINGS; TANZANIA; UGANDA; CARE; INFECTION;
D O I
10.1186/s12936-017-1941-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: It remains challenging to distinguish malaria from other fever causing infections, as a positive rapid diagnostic test does not always signify a true active malaria infection. This study was designed to determine the influence of other causes of fever, prior anti-malarial treatment, and a possible seasonality of the performance of a PfHRP2 RDT for the diagnosis of malaria in children under-5 years of age living in a malaria endemic area. Methods: A prospective etiology study was conducted in 2015 among febrile children under 5 years of age in Burkina Faso. In order to assess the influence of other febrile illnesses, prior treatment and seasonality on the performance of a PfHRP2 RDT in diagnosing malaria, the RDT results were compared with the gold standard (expert microscopic diagnosis of Plasmodium falciparum) and test results were analysed by assuming that prior anti-malarial use and bacterial/viral infection status would have been known prior to testing. To assess bacterial and viral infection status blood, urine and stool samples were analysed. Results: In total 683 blood samples were analysed with microscopy and RDT-PfHRP2. Plasmodium falciparum malaria was diagnosed in 49.8% (340/683) by microscopy compared to 69.5% (475/683) by RDT-PfHRP2. The RDT-PfHRP2 reported 29.7% (141/475) false positive results and 1.8% (6/340) false negative cases. The RDT-PfHRP2 had a high sensitivity (98.2%) and negative predictive value (97.1%), but a low specificity (58.9%) and positive predictive value (70.3%). Almost 50% of the alternative cause of fever were diagnosed by laboratory testing in the RDT false positive malaria group. Conclusions: The use of a malaria RDT-PfHRP2 in a malaria endemic area may cause misdiagnosis of the actual cause of fever due to false positive test results. The development of a practical diagnostic tool to screen for other causes of fever in malaria endemic areas is required to save lives.
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页数:11
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