Diagnostic Performance of Loop-Mediated Isothermal Amplification and Ultrasensitive Rapid Diagnostic Tests for Malaria Screening Among Pregnant Women in Kenya

Author:

Samuels Aaron M123ORCID,Towett Oliver4,Seda Brian4,Wiegand Ryan E2,Otieno Kephas4,Chomba Miriam4,Lucchi Naomi2,Ljolje Dragan2,Schneider Kammerle5,Walker Patrick G T6,Kwambai Titus K134,Slutsker Laurence5,ter Kuile Feiko O34,Kariuki Simon K4

Affiliation:

1. Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention , Kisumu , Kenya

2. Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention , Atlanta, Georgia , USA

3. Department of Clinical Sciences, Liverpool School of Tropical Medicine , Liverpool , United Kingdom

4. Centre for Global Health Research, Kenya Medical Research Institute , Kisumu , Kenya

5. Center for Malaria Control and Elimination, PATH , Seattle, Washington , USA

6. Department of Infectious Disease Epidemiology, Imperial College London , London , United Kingdom

Abstract

Abstract Background Screen-and-treat strategies with sensitive diagnostic tests may reduce malaria-associated adverse pregnancy outcomes. We conducted a diagnostic accuracy study to evaluate new point-of-care tests to screen pregnant women for malaria at their first antenatal visit in western Kenya. Methods Consecutively women were tested for Plasmodium infection by expert microscopy, conventional rapid diagnostic test (cRDT), ultra sensitive RDT (usRDT), and loop-mediated isothermal amplification (LAMP). Photoinduced electron-transfer polymerase chain reaction (PET-PCR) served as the reference standard. Diagnostic performance was calculated and modelled at low parasite densities. Results Between May and September 2018, 172 of 482 screened participants (35.7%) were PET-PCR positive. Relative to PET-PCR, expert microscopy was least sensitive (40.1%; 95% confidence interval [CI], 32.7%–47.9%), followed by cRDT (49.4%; 95% CI, 41.7%–57.1), usRDT (54.7%; 95% CI, 46.9%–62.2%), and LAMP (68.6%; 95% CI, 61.1%–75.5%). Test sensitivities were comparable in febrile women (n = 90). Among afebrile women (n = 392), the geometric-mean parasite density was 29 parasites/µL and LAMP (sensitivity = 61.9%) and usRDT (43.2%) detected 1.74 (95% CI, 1.31–2.30) and 1.21 (95% CI, 88–2.21) more infections than cRDT (35.6%). Per our model, tests performed similarly at densities >200 parasites/µL. At 50 parasites/µL, the sensitivities were 45%, 56%, 62%, and 74% with expert microscopy, cRDT, usRDT, and LAMP, respectively. Conclusions This first-generation usRDT provided moderate improvement in detecting low-density infections in afebrile pregnant women compared to cRDTs.

Funder

PATH MACEPA

Bill and Melinda Gates Foundation

PATH

US Centers for Diseases Control and Prevention

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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