1. Short report: Failure of the OptiMAL rapid malaria test as a tool for the detection of asymptomatic malaria in an area of Thailand endemic for Plasmodium falciparum and P. vivax.
- Author
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Coleman RE, Maneechai N, Ponlawat A, Kumpitak C, Rachapaew N, Miller RS, and Sattabongkot J
- Subjects
- Animals, Humans, Malaria, Falciparum diagnosis, Malaria, Falciparum parasitology, Malaria, Vivax diagnosis, Malaria, Vivax parasitology, Microscopy, Parasitemia diagnosis, Parasitemia epidemiology, Parasitemia parasitology, Plasmodium falciparum enzymology, Plasmodium falciparum isolation & purification, Plasmodium vivax enzymology, Plasmodium vivax isolation & purification, Reagent Kits, Diagnostic, Sensitivity and Specificity, Thailand epidemiology, Time Factors, Endemic Diseases, L-Lactate Dehydrogenase analysis, Malaria, Falciparum epidemiology, Malaria, Vivax epidemiology
- Abstract
We evaluated the efficacy of the OptiMAL assay in a cross-sectional malaria survey in western Thailand from April to August 2001. Expert microscopy of Giemsa-stained thick and thin blood films was used as the gold standard. Positive control lines were evident in 99% (1,128 of 1,137) of the assays tested. However, 34% (384 of 1,128) of assays produced an aberrant result (a positive P. falciparum-specific line and a negative panmalarial line). False-positive panmalarial and Plasmodium falciparum-specific lines occurred in 25.9% (270 of 1,042) and 60.3% (628 of 1,042) of microscopy-negative samples, respectively. Due to the preponderance of false-positive test results, it was necessary to develop subjective criteria for test positivity based on line intensity. For determination of assay performance during this study, we therefore considered all test lines that were scored as intermediate or strong as positive and lines that were faint as negative. Using these criteria, we determined that the sensitivity of the OptiMAL assay for P. falciparum was 25% with > 500 parasites/microl and 10.5% with > 100 parasites/microl, while for P. vivax, the sensitivity at the same parasite rates was 100% and 41.7%, respectively. Further studies are required to determine whether the problems we identified are limited to this particular lot of OptiMAL assays.
- Published
- 2002
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