Evidence map›Paper›PMID 25930101›Full record

Observational studyBMC infectious diseases2015

Patterns of mixed Plasmodium species infections among children six years and under in selected malaria hyper-endemic communities of Zambia: population-based survey observations.

Lungowe Sitali, James Chipeta, John M Miller, Hawela B Moonga, Nirbhay Kumar, William J Moss, Charles Michelo

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. UndetectedMalariaWorld journal · 2025
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  11. Arthropod-borne diseases among travellers arriving in Europe from Africa, 2015 to 2019.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2023
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  20. Diagnostic tools in childhood malaria.Parasites & vectors · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Lungowe SitaliDepartment of Biomedical Science, University of Zambia, School of Medicine, Lusaka, Zambia. lungowesitali@gmail.com.
James ChipetaDepartment of Paediatrics and Child Health, School of Medicine, Malaria Research Unit (SMUTH-MRU), Lusaka, Zambia. jameschipeta@smuth-mru.org.zm.
John M MillerPATH-Malaria Control and Elimination Partnership in Africa (MACEPA), National Malaria Control Centre, Lusaka, Zambia. jmiller@path.org.
Hawela B MoongaMinistry of Health, National Malaria Control Centre, Lusaka, Zambia. mhawela@yahoo.co.uk.
Nirbhay KumarDepartment of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, USA. nkumar@tulane.edu.
William J MossJohn Hopkins Malaria Research Institute, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA. wmoss1@jhu.edu.
Charles MicheloDepartment of Paediatrics and Child Health, School of Medicine, Malaria Research Unit (SMUTH-MRU), Lusaka, Zambia. ccmichelo@yahoo.com.
Ministry of Health · ZMJohns Hopkins University · USMalaria Consortium · GBTulane University · US

Funding

TransmissionU19AI089680 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WILLIAM J MOSS · 2010 to 2026
$25.6M
Malaria Training and Research Capacity Building in Southern AfricaD43TW001587 · FIC · TULANE UNIVERSITY OF LOUISIANA · PI KUMAR, NIRBHAY · 2000 to 2012
$1.4M
FIC NIH HHS 2D43TW001587-06A2FIC NIH HHS D43 TW001587NIAID NIH HHS U19 AI089680
6 · The paper itself

Abstract

backgroundAlthough malaria is preventable and treatable, it still claims 660,000 lives every year globally with children under five years of age having the highest burden. In Zambia, malaria rapid diagnostic tests (RDTs) that only detect Plasmodium falciparum are the main confirmatory means for malaria diagnosis in most health facilities without microscopy services. As a consequence of this P. falciparum species diagnostic approach, non-falciparum malaria is not only under-diagnosed but entirely missed, thereby making the exact disease burden unknown. We thus investigated the prevalence of various Plasmodium spp. and associated burden of infection in selected communities in Zambia.

methodsData from two malaria hyper-endemic provinces (Eastern and Luapula) of the 2012 National Malaria Indicator Survey (MIS), conducted between April and May 2012, were used. The MIS is a nationally representative, two-stage cluster survey conducted to coincide with the end of the malaria transmission season. Social, behavioural and background information were collected from households as part of the survey. Thick blood smears, RDTs and dried blood spots (DBS) were collected from children below six years of age. Slides were stained using Giemsa and examined by microscopy while polymerase chain reaction (PCR) was used to analyse the DBS for malaria Plasmodium spp. Multivariate logistic regression was employed to examine the association between background factors and malaria.

resultsOverall, 873 children younger than six years of age were surveyed. The overall prevalence of Plasmodium spp. by PCR was 54.3% (95% CI 51-57.6%). Of the total Plasmodium isolates, 88% were P. falciparum, 10.6% were mixed infections and 1.4% were non-falciparum mono infections. Among the mixed infections, the majority were a combination of P. falciparum and P. malariae (6.5% of all mixed infections). Children two years and older (2-5 years) had three-fold higher risk of mixed malaria infections (aOR 2.8 CI 1.31-5.69) than children younger than two years of age.

conclusionThe high prevalence of mixed Plasmodium spp. infections in this population stresses review of the current malaria RDT diagnostic approaches. The observed less incidence of mixed infections in children under two years of age compared to their older two-to-five-year-old counterparts is probably due to the protective maternal passive immunity, among other factors, in that age group.

Indexed as

ChildChild Health ServicesChild, PreschoolDiagnostic Tests, RoutineEndemic DiseasesFemaleHumansInfantInfant, NewbornMalariaMalaria, FalciparumMalePlasmodiumPlasmodium falciparumPolymerase Chain ReactionPrevalence

Identifiers

PMID25930101
PMCPMC4424549
OpenAlexW2057800009

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.