Abstract

Background125 million women are pregnant each year in malaria endemic areas and are, therefore, at risk of Malaria in Pregnancy (MiP). MiP is the direct consequence of Plasmodium infection during pregnancy. The sequestration of Plasmodium falciparum parasites in the placenta adversely affects fetal development and impacts newborn birth weight. Importantly, women presenting with MiP commonly develop anaemia. In Ethiopia, the Ministry of Health recommends screening symptomatic women only at antenatal care visits with no formal intermittent preventive therapy. Since MiP can display low-level parasitaemia, current tests which include microscopy and RDT are challenged to detect these cases. Loop mediated isothermal Amplification (LAMP) technology is a highly sensitive technique for DNA detection and is field compatible. This study aims to evaluate the impact of active malaria case detection during pregnancy using LAMP technology in terms of birth outcomes.MethodsA longitudinal study was conducted in two health centres of the Kafa zone, South West Ethiopia. Both symptomatic and asymptomatic pregnant women were enrolled in the first or second trimester and allocated to either Standard of Care (SOC—microscopy and RDT) or LAMP (LAMP, microscopy and RDT). Women completed at least three visits prior to delivery, and the patient was referred for treatment if Plasmodium infection was detected by any of the testing methods. The primary outcome was to measure absolute birth weight, proportion of low birth weight, and maternal/neonatal haemoglobin in each arm. Secondary outcomes were to assess the performance of microscopy and RDT versus LAMP conducted in the field.ResultsOne hundred and ninety-nine women were included and assigned to either LAMP or SOC. Six were lost to follow up. In this cohort, 66.8% of women did not display any clinical symptoms and 70.9% were multi-parous. A reduced proportion of low birth weight newborns was observed in the LAMP group (0%) compared to standard of care (14%) (p <0.001). Improved neonatal haemoglobin was observed in the LAMP (13.1 g/dL) versus the SOC (12.8 g/dL) (p = 0.024) arm. RDT and microscopy had an analytical sensitivity of 66.7% and 55.6% compared to LAMP as a reference standard.ConclusionsThese results support the use of highly sensitive tools for rapid on-site active case detection of MiP which may improve birth outcomes in the absence of IPT. However, further large-scale studies are required to confirm this finding.

Highlights

  • 125 million women are pregnant each year in malaria endemic areas and are, at risk of Malaria in Pregnancy (MiP)

  • Tadesse et al Malar J (2020) 19:305. These results support the use of highly sensitive tools for rapid on-site active case detection of MiP which may improve birth outcomes in the absence of intermitted preventive treatment (IPT)

  • Included women were allocated to the standard of care (SOC) arm (1/4) where women were tested by microscopy and rapid diagnostic tests (RDT), or the Loop mediated isothermal Amplification (LAMP) arm (3/4) where women were tested by LAMP, microscopy and RDT (Fig. 1)

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Summary

Introduction

125 million women are pregnant each year in malaria endemic areas and are, at risk of Malaria in Pregnancy (MiP). Plasmodium infection and subsequent sequestration of infected erythrocytes in the placenta restricts maternal blood supply, oxygen, and nutrients necessary for normal fetal development [1] Maternal anaemia is another complication and results from peripheral destruction of infected erythrocytes during Plasmodium asexual multiplication. It is estimated that 20% of stillbirth and 11% of all newborn deaths are direct consequences of MiP [3]. Both Plasmodium falciparum and Plasmodium vivax induce adverse pregnancy outcomes. Plasmodium falciparum pathogenicity in MiP is well described [4, 5] while the pathophysiology of P. vivax infection during pregnancy needs yet to be elucidated [6, 7]

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