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Review
. 2017 Jul;55(7):2009-2017.
doi: 10.1128/JCM.02562-16. Epub 2017 Apr 12.

Update on Malaria Diagnostics and Test Utilization

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Review

Update on Malaria Diagnostics and Test Utilization

Blaine A Mathison et al. J Clin Microbiol. 2017 Jul.

Abstract

Malaria is a potentially life-threatening disease requiring rapid diagnosis and treatment. Although microscopic examination of thick and thin blood films remains the gold standard for laboratory diagnosis, rapid antigen tests and nucleic acid amplification methods may also play a useful role in detection of acute infection. This review discusses the advantages and disadvantages of the commonly used diagnostic methods and provides important practice points for optimal malaria test utilization.

Keywords: diagnostics; malaria; utilization.

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Figures

FIG 1
FIG 1
Malaria laboratory testing algorithm. 1Algorithm includes only commonly used/available laboratory methods. Serology should not be used for detection of acute malaria. 2Malaria can be a rapidly fatal disease, particularly when due to P. falciparum, and less commonly P. vivax and P. knowlesi, and testing must be performed on a STAT basis. If testing is not available at the local laboratory, then arrangements must be made with another nearby laboratory that can provide immediate testing. A single negative test does not rule out malaria. Perform testing every 6 to 8 h for up to 3 days if clinically indicated. Other laboratory tests (e.g., complete blood count with differential, electrolyte panel, blood glucose, bilirubin, urinalysis, blood cultures) may be indicated to assess the severity of malaria and evaluate other potential causes of the patient's illness. 3Rapid screening tests such as lateral flow immunochromatographic assays generally provide sensitive detection of high levels of P. falciparum and P. vivax infection (i.e., 2,000 parasites/μl) but lack sufficient sensitivity for detecting low levels of parasitemia (i.e., ≤200 parasites/μl) and other Plasmodium species. 4Confirmatory testing may be performed by microscopic examination of blood films or NAAT. 5Examination of both thick and thin blood films is the gold standard for malaria diagnosis. 6If necessary, refer for confirmation of species identification by blood film microscopy or NAAT at a reference laboratory. 7Percent parasitemia is calculated using microscopic examination of thick or thin blood films. (Used with permission of Mayo Foundation for Medical Education and Research. All rights reserved.)

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References

    1. Centers for Disease Control and Prevention. 2017. Malaria. https://www.cdc.gov/malaria/. Accessed 2 April 2017.
    1. Pritt BS. 2015. Plasmodium and Babesia, p 2338–2356. In Jorgensen JH, Pfaller MA, Carroll KC, Funke G, Landry ML, Richter SS, Warnock DW (ed), Manual of clinical microbiology, 11th ed, vol 2 ASM Press, Washington, DC.
    1. World Health Organization. 2016. World malaria report 2016. World Health Organization, Geneva, Switzerland: http://www.who.int/malaria/publications/world-malaria-report-2016/report... Accessed 2 April 2017.
    1. Coatney GR, Collins WE, Contacos PG. 1971. The primate malarias. U.S. National Institute of Allergy and Infectious Diseases, Bethesda, MD.
    1. Centers for Disease Control and Prevention. 2016. CDC health information for international travel 2016. Oxford University Press, New York, NY.

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