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Journal of Clinical Microbiology, November 1999, p. 3644-3646, Vol. 37, No. 11
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Comparison of the OptiMAL Test with PCR for Diagnosis of Malaria in Immigrants

Jamshaid Iqbal,1,* Ali Sher,1 Parsotam R. Hira,1 and Rashed Al-Owaish2

Department of Microbiology, Faculty of Medicine, Kuwait University,1 and Malaria Laboratory, Department of Community Health, Ministry of Health,2 Safat, Kuwait

Received 19 March 1999/Returned for modification 26 April 1999/Accepted 7 July 1999

The OptiMAL test (Flow Inc., Portland, Oreg.), which detects a malaria parasite lactate dehydrogenase (pLDH) antigen, has not been evaluated for its sensitivity in the diagnosis of malaria infection in various epidemiological settings. Using microscopy and a PCR as reference standards, we performed a comparison of these assays with the OptiMAL test for the detection of Plasmodium falciparum and Plasmodium vivax infection in 550 immigrants who had come from areas where malaria is endemic to reside in Kuwait, where malaria is not endemic. As determined by microscopy, 125 (23%) patients had malaria, and of these, 84 (67%) were infected with P. vivax and 36 were infected with P. falciparum; in 5 cases the parasite species could not be determined due to a paucity of the parasites. The PCR detected malaria infection in 145 (26%) patients; 102 (70%) of the patients had P. vivax infection and 43 had P. falciparum infection. Of the five cases undetermined by microscopy, the PCR detected P. falciparum infection in two cases, P. vivax infection in two cases, and mixed (P. falciparum plus P. vivax) infection in one case. Correspondingly, the OptiMAL test detected malaria infection in 95 patients (17%); of these, 70 (74%) had P. vivax infection and 25 were infected with P. falciparum. In this study, 61 (49%) of the 125 malaria cases, as confirmed by microscopy, had a degree of parasitemia of <100 parasites per µl, and 23 (18%) of the cases had a degree of <50 parasites per µl. Our results show that the sensitivity of the OptiMAL test is high (97%) at a high level of parasitemia (>100 parasites/µl) but drops to 59% when the level is <100 parasites/µl and to 39% when it is <50 parasites/µl. In addition, the OptiMAL test failed to identify four patients whose blood smears contained P. falciparum gametocytes only. We conclude that the sensitivity and specificity of the OptiMAL test are comparable to those of microscopy in detecting malaria infection at a parasitemia level of >100 parasites/µl; however, the test failed to identify more than half of the patients with a parasitemia level of <50 parasites/µl. Thus, the OptiMAL test should be used with great caution, and it should not replace conventional microscopy in the diagnosis of malaria infection.

* Corresponding author. Mailing address: Department of Microbiology, Faculty of Medicine, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. Phone: (965) 531 2300, ext. 6781. Fax: (965) 533 2719. E-mail: iqbal{at}hsc.kuniv.edu.kw.

Journal of Clinical Microbiology, November 1999, p. 3644-3646, Vol. 37, No. 11
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.


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