Abstract

BackgroundMalaria rapid diagnostic tests (RDTs) are nowadays widely used in malaria endemic countries as an alternative to microscopy for the diagnosis of malaria. However, quality control of test performance and execution in the field are important in order to ensure proper use and adequate diagnosis of malaria. The current study compared the performance of a histidine-rich protein 2-based RDT used at peripheral health facilities level in real life conditions with that performed at central reference laboratory level with strict adherence to manufacturer instructions.MethodsFebrile children attending rural health clinics were tested for malaria with a RDT provided by the Ministry of Health of Burkina Faso as recommended by the National Malaria Control Programme. In addition, a blood sample was collected in an EDTA tube from all study cases for retesting with the same brand of RDT following the manufacturer’s instructions with expert malaria microscopy as gold standard at the central reference laboratory. Fisher exact test was used to compare the proportions by estimating the p-value (p ≤ 0.05) as statistically significant.ResultsIn total, 407 febrile children were included in the study and malaria was diagnosed in 59.9% (244/407) of the cases with expert malaria microscopy. The sensitivity of malaria RDT testing performed at health facilities was 97.5% and comparable to that achieved at the laboratory (98.8%). The number of malaria false negatives was not statistically significant between the two groups (p = 0.5209). However, the malaria RDT testing performed at health facilities had a specificity issue (52.8%) and was much lower compared to RDT testing performed at laboratory (74.2%). The number of malaria false positives was statistically significantly different between the two groups (p = 0.0005).ConclusionMalaria RDT testing performed at the participating rural health facilities resulted in more malaria false positives compared to those performed at central laboratory. Several factors, including storage and transportation conditions but also training of health workers, are most likely to influence test performance. Therefore, it is very important to have appropriate quality control and training programmes in place to ensure correct performance of RDT testing.

Highlights

  • Malaria rapid diagnostic tests (RDTs) are nowadays widely used in malaria endemic countries as an alternative to microscopy for the diagnosis of malaria

  • The decision of many countries of sub-Saharan Africa (SSA), including Burkina Faso, to select malaria rapid diagnostic test detecting Plasmodium falciparum-specific histidine-rich protein 2 (PfHRP2) for diagnosis malaria is based on the high sensitivity and specificity reported by the World Health Organization (WHO) and Foundation for Innovative New Diagnostics (FIND) malaria RDT evaluation programme [6]

  • Results of RDT testing and expert microscopy The number of positive cases of malaria determined by performing a PfHRP2 RDT at the health facilities level by nurses (HF-PfHRP2) was 77.4% (315/407)

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Summary

Introduction

Malaria rapid diagnostic tests (RDTs) are nowadays widely used in malaria endemic countries as an alternative to microscopy for the diagnosis of malaria. The current study compared the performance of a histidine-rich protein 2-based RDT used at peripheral health facilities level in real life conditions with that performed at central reference laboratory level with strict adherence to manufacturer instructions. The decision of many countries of sub-Saharan Africa (SSA), including Burkina Faso, to select malaria rapid diagnostic test detecting Plasmodium falciparum-specific histidine-rich protein 2 (PfHRP2) for diagnosis malaria is based on the high sensitivity and specificity reported by the World Health Organization (WHO) and Foundation for Innovative New Diagnostics (FIND) malaria RDT evaluation programme [6]. HRP2-based RDTs are reported to have a good thermal and humid stability compared to tests targeting Plasmodium-specific parasite lactate dehydrogenase (pLDH) [7]. There is increasing concern with respect to reported false positive diagnosis by PfHRP2 RDT in particular in low malaria transmission settings [20]

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