Evidence map›Paper›PMID 28126001›Full record

ArticleMalaria journal2017

Serology reveals heterogeneity of Plasmodium falciparum transmission in northeastern South Africa: implications for malaria elimination.

Joseph Biggs, Jaishree Raman, Jackie Cook, Khumbulani Hlongwana, Chris Drakeley, Natashia Morris, Ishen Serocharan, Eunice Agubuzo, Philip Kruger, Aaron Mabuza and 4 more

Abstract read
In one paragraph

Article in Malaria journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  3. The American journal of tropical medicine and hygiene · 2018
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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

14 authors.

Joseph BiggsFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0001-7273-874X
Jaishree RamanCentre for Opportunistic Tropical and Hospital Infections, National Institute for Communicable Diseases, Johannesburg, South Africa. jaishreer@nicd.ac.za.
Jackie CookTropical Epidemiology Group, Department of Infectious Diseases Epidemiology, London School of Hygiene and Tropical Medicine, London, UK.
Khumbulani HlongwanaSchool of Nursing and Public Health, University of KwaZulu-Natal, Durban, South Africa.
Chris DrakeleyFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Natashia MorrisHealth GIS Centre, South Africa Medical Research Council, Durban, South Africa.
Ishen SerocharanHealth GIS Centre, South Africa Medical Research Council, Durban, South Africa.
Eunice AgubuzoCentre for Opportunistic Tropical and Hospital Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.
Philip KrugerLimpopo Provincial Malaria Control Programme, Polokwane, South Africa.
Aaron MabuzaMpumalanga Provincial Malaria Control Programme, Nelspruit, South Africa.
Alpheus ZithaMpumalanga Provincial Malaria Control Programme, Nelspruit, South Africa.
Elliot MachabaLimpopo Provincial Malaria Control Programme, Polokwane, South Africa.
Maureen CoetzeeCentre for Opportunistic Tropical and Hospital Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.
Immo KleinschmidtWits Research Institute for Malaria, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Funding

Medical Research Council MR/L00433X/1Wellcome Trust
6 · The paper itself

Abstract

backgroundIt is widely acknowledged that modifications to existing control interventions are required if South Africa is to achieve malaria elimination. Targeting indoor residual spraying (IRS) to areas where cases have been detected is one strategy currently under investigation in northeastern South Africa. This seroprevalence baseline study, nested within a targeted IRS trial, was undertaken to provide insights into malaria transmission dynamics in South Africa and evaluate whether sero-epidemiological practices have the potential to be routinely incorporated into elimination programmes.

methodsFilter-paper blood spots, demographic and household survey data were collected from 2710 randomly selected households in 56 study wards located in the municipalities of Ba-Phalaborwa and Bushbuckridge. Blood spots were assayed for Plasmodium falciparum apical membrane antigen-1 and merozoite surface protein-1

resultsThe overall SCR across the entire study site was 0.012 (95% CI 0.008-0.017) per year. Contrasting SCRs, corresponding to distinct geographical regions across the study site, ranging from <0.001 (95% CI <0.001-0.005) to 0.022 (95% CI 0.008-0.062) per annum revealed prominent transmission heterogeneity. Geospatial cluster analysis of household seroprevalence and age-adjusted antibody responses detected statistically significant (p < 0.05) spatial clusters of P. falciparum exposure. Formal secondary education was associated with lower malaria exposure in the sampled population (AOR 0.72, 95% CI 0.56-0.95, p = 0.018).

conclusionsAlthough overall transmission intensity and exposure to malaria was low across both study sites, malaria transmission intensity was highly heterogeneous and associated with low socio-economic status in the region. Findings suggest focal targeting of interventions has the potential to be an appropriate strategy to deploy in South Africa. Furthermore, routinely incorporating sero-epidemiological practices into elimination programmes may prove useful in monitoring malaria transmission intensity in South Africa, and other countries striving for malaria elimination.

Indexed as

AdolescentAdultAge FactorsChildChild, PreschoolCluster AnalysisCross-Sectional StudiesFemaleHumansIncidenceMalaria, FalciparumMaleMiddle AgedPlasmodium falciparumPrevalenceRisk FactorsEliminationHeterogeneityHotspotMalariaPfAMA-1PfMSP-119SerologySouth AfricaTransmission

Identifiers

PMID28126001
PMCPMC5270351

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.