Cited by 89Malaria Research and ControlBiosensors and Analytical DetectionClinical Laboratory Practices and Quality Control

Field and laboratory comparative evaluation of ten rapid malaria diagnostic tests

Craig, M.H., Bredenkamp, B.L., Williams, C.H.Vaughan, Rossouw, E.J., Kelly, V.J., Kleinschmidt, I., Martineau, A., Henry, G.F.J.·2002·Transactions of the Royal Society of Tropical Medicine and Hygiene

Abstract

The paper reports on a comparative evaluation of 10 rapid malaria tests available in South Africa in 1998: AccuCheck (AC, developmental), Cape Biotech (CB), ICT Malaria Pf (ICT1) and Pf/Pv (ICT2), Kat Medical (KAT), MakroMal (MM), OptiMAL (OP), ParaSight-F (PS), Quorum (Q), Determine-Malaria (DM). In a laboratory study, designed to test absolute detection limits, Plasmodium falciparum-infected blood was diluted with uninfected blood to known parasite concentrations ranging from 500 to 0.1 parasites per microlitre (P/microL). The 50% detection limits were: ICT1, 3.28; ICT2, 4.86; KAT, 6.36; MM, 9.37; CB, 11.42; DM, 12.40; Q, 16.98; PS, 20; AC, 31.15 and OP, 91.16 P/microL. A field study was carried out to test post-treatment specificity. Blood samples from malaria patients were tested with all products (except AC and DM) on the day of treatment and 3 and 7 days thereafter, against a gold standard of microscopy and polymerase chain reaction (PCR). OP and PS produced fewer false-positive results on day 7 (18 and 19%, respectively) than the other rapid tests (38-56%). However, microscopy, PCR, OP and PS disagreed largely as to which individuals remained positive. The tests were further compared with regard to general specificity, particularly cross-reactivity with rheumatoid factor, speed, simplicity, their ability to detect other species, storage requirements and general presentation.

Integrity signals

Registry

Crossref · 10.1016/s0035-9203(02)90092-1

Cites

1 of 1 references verified0 citation errors · 0 not checkable

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  • Antigenemia may persist weeks beyond the actual infection, leading to the false diagnosis of malaria parasitemia.

    “In addition, antigenemia may persist weeks beyond the actual infection, leading to the false diagnosis of malaria parasitemia (6, 22).”
  • The persistence of Plasmodium DNA is less than the persistent antigenemia reported with immunochromatographic assays.

    “However, this persistence of Plasmodium DNA is still less than the persistent antigenemia reported with immunochromatographic assays (6, 22).”

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Authors
Craig, M. H., Bredenkamp, B. L., Williams, C. H. V., Rossouw, E. J., Kelly, V. J., Kleinschmidt, I., Martineau, A., & Henry, G. F. J.
Venue
Transactions of the Royal Society of Tropical Medicine and Hygiene
Published
2002-05
Volume
96
Issue
3
Pages
258-265
ISSN
0035-9203 (ISSN-L)
OpenAlex
W1978943655
Cited by
89
References
1
Citations by year
2023: 3 · 2020: 2 · 2019: 2 · 2018: 1 · 2017: 1 · 2015: 2 · 2014: 3 · 2013: 3 · 2012: 7
FWCI
6.62
Type
journal article
Language
en
Open access
closed
Locations
  • Transactions of the Royal Society of Tropical Medicine and Hygiene (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Royal Society
  • Royal Society of Tropical Medicine and Hygiene
  • South African Medical Research Council
  • Abbott Diagnostics
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
  • Physical Sciences › Engineering › Biomedical Engineering › Biosensors and Analytical Detection
  • Health Sciences › Medicine › Physiology › Clinical Laboratory Practices and Quality Control
Keywords
Plasmodium falciparum, Plasmodium vivax, diagnostic accuracy, detection limit, false positives, OptiMAL, South Africa
MeSH terms
Animals, Enzyme-Linked Immunosorbent Assay, Female, Humans, Male, Parasitology, Plasmodium falciparum, Reagent Kits, Diagnostic, Sensitivity and Specificity, South Africa, Malaria, Falciparum

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