Abstract

BackgroundTo identify the factors that account for differences in clinical outcomes of malaria as well as its relationship with ethnicity, transmission intensity and parasite density.MethodsA prospective study was conducted in nine health facilities in the Centre, Littoral and South West regions of Cameroon, and in three ethnic groups; the Bantu, Semi-Bantu and Foulbe. Children aged one month to 13 years, with diagnosis suggestive of malaria, were recruited and characterized using the WHO definition for severe and uncomplicated malaria. Malaria parasitaemia was determined by light microscopy, haematological analysis using an automated haematology analyser and glucose level by colorimetric technique.ResultsOf the febrile children screened, 971 of the febrile children screened fulfilled the inclusion criteria for specific malaria clinical phenotypes. Forty-nine (9.2%) children had cerebral malaria, a feature that was similar across age groups, ethnicity and gender but lower (P < 0.004) in proportion in the Centre (3.1%, 5/163) compared to the Littoral (11.3%, 32/284) and South West (13.6%, 12/88) regions. Severe anaemia was the most frequent severe disease manifestation, 28.0% (248/885), which was similar in proportion across the three ethnic groups but was more prevalent in females, less than 60 months old, and the Centre region. About 20% (53/267) of the participants presented with respiratory distress, a clinical phenotype independent of age, gender and ethnicity, but highest (P < 0.001) in the Centre (55%, 11/20) compared to the Littoral (27.3%, 3/11) and South West (16.5%, 39/236) regions. Uncomplicated malaria constituted 27.7% (255/920) of hospital admissions and was similar in proportion with gender and across the three ethnic groups but more prevalent in older children (≥ 60 months) as well as in the South West region. The density of malaria parasitaemia was generally similar across clinical groups, gender and ethnicity. However, younger children and residents of the Centre region carried significantly higher parasite loads, with the burden heavier in the Semi-Bantu compared to their Bantu (P = 0.009) and Foulbe (P = 0.026) counterparts in the Centre region. The overall study case fatality was 4.8 (47/755), with cerebral malaria being the only significant risk factor associated with death. Severe anaemia, though a common and major clinical presentation, was not significantly associated with risk of death.ConclusionAbout half of the acutely febrile children presented with severe malaria, the majority being cases of severe malaria anaemia, followed by respiratory distress and cerebral malaria. The latter two were less prevalent in the Centre region compared to the other regions. Cerebral malaria and hyperpyrexia were the only significant risk factors associated with death.

Highlights

  • To identify the factors that account for differences in clinical outcomes of malaria as well as its relationship with ethnicity, transmission intensity and parasite density

  • Baseline characteristics A total of 971 children satisfied the criteria for specific malaria clinical phenotypes and were enrolled into the study

  • These participants were admitted in the Centre (164, 16.9%), Littoral (292, 30.1%) and South West (515, 53%) regions, from the Bantu (385, 39.6%), Semi-Bantu (416, 42.8%), Foulbe (31, 3.2%) and other (139, 14.3%) ethnic groups

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Summary

Introduction

To identify the factors that account for differences in clinical outcomes of malaria as well as its relationship with ethnicity, transmission intensity and parasite density. Plasmodium falciparum, the deadliest of the malaria parasite species, kills a child every 30 seconds in Africa [2] and wreaks significant economic havoc in highly endemic areas, substantially decreasing Gross Domestic Product (GDP) of affected countries relative to malaria-free regions [3]. The clinical spectrum of paediatric P. falciparum infections range from asymptomatic parasite carriage to a febrile disease that may develop into severe, life-threatening illness [5]. Mortality from malaria is associated largely with the parasite’s ability to induce severe complications, presenting as severe anaemia, cerebral malaria and metabolic acidosis, manifested clinically as respiratory distress. Other severe malaria manifestations at enrolment include multiple or prolonged convulsions, hyperlactataemia, hyperparasitaemia, hypoglycaemia, hyperpyrexia and intravascular haemolysis [6,7]

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