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. 2007 Dec;37(3):1017-30.

Antigen capture immuno-chromatographic strip format in detecting parasite-specific lactate dehydrogenase to diagnose malaria in nonimmune patients

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  • PMID: 18383801

Antigen capture immuno-chromatographic strip format in detecting parasite-specific lactate dehydrogenase to diagnose malaria in nonimmune patients

Amal M Abdul-Rasheed El-Moamly. J Egypt Soc Parasitol. 2007 Dec.

Abstract

Several rapid diagnostic test devices (RDT) based on detection of malaria antigen in the whole blood were developed. OptiMal test the presence of parasite-specific lactate dehydrogenase (LDH) enzyme using three monoclonal antibodies was used. Two monoclonal antibodies were pan-specific and recognized all malaria species. The third one was specific only for Plasmodium falciparum. The parasite antigens were detected using an antigen-capture immunochromatographic strip format. One hundred-nine malaria positive and 730 malaria negative cases diagnosed by microscopy were included. 75/109 were P. falciparum 26 as P. vivax, 3 P. malariae and 5 mixed infection of P. falciparum & P. vivax. The RDT showed a low sensitivity (85%, 95% Confidence Interval [CI], 79-92%) with a much lower sensitivity in detecting species other than P. falciparum as well as in mixed infections. The sensitivity was 50% for less than 200 parasites/micro. The sensitivity of OptiMal for P. falciparum was 87% (95% CI, 79-94), 81% (95% CI, 66-96) for P. vivax, and failed with P. malariae. Mixed infections were misdiagnosed as Pfalciparum. The sensitivity of OptiMal was quite good in detecting both P. falciparum & P. vivax (98%; 95% CI, 97-99 & 100%; 95% CI, 100-100 respectively) and 99% (95% CI, 98-99) for all species. The positive and negative ratio for all malaria species was: (+LR = 62.3, -LR = 0.01); for P. falciparum (+LR = 38.9, -LR = 0.01) and for P. vivax (+LR = 0.8077/0, -LR = 0.2). The test value to assess drug resistance in post treatment days was discussed.

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