Evidence map›Paper›PMID 33579294›Full record

ArticleInternational journal of health geographics2021

Estimating the local spatio-temporal distribution of malaria from routine health information systems in areas of low health care access and reporting.

Elizabeth Hyde, Matthew H Bonds, Felana A Ihantamalala, Ann C Miller, Laura F Cordier, Benedicte Razafinjato, Herinjaka Andriambolamanana, Marius Randriamanambintsoa, Michele Barry, Jean Claude Andrianirinarison and 2 more

Abstract read
In one paragraph

Article in International journal of health geographics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–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

17 citing papers in PubMed.

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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

12 authors.

Elizabeth HydeStanford University School of Medicine, Stanford, CA, USA.
Matthew H BondsDepartment of Global Health and Social Medicine, Harvard Medical School, Boston, USA.
Felana A IhantamalalaDepartment of Global Health and Social Medicine, Harvard Medical School, Boston, USA.
Ann C MillerDepartment of Global Health and Social Medicine, Harvard Medical School, Boston, USA.
Laura F CordierNGO PIVOT, Ranomafana, Madagascar.
Benedicte RazafinjatoNGO PIVOT, Ranomafana, Madagascar.
Herinjaka AndriambolamananaNGO PIVOT, Ranomafana, Madagascar.
Marius RandriamanambintsoaDirection de La Démographie et des Statistiques Sociales, Institut National de La Statistique, Antananarivo, Madagascar.
Michele BarryStanford University School of Medicine, Stanford, CA, USA.
Jean Claude AndrianirinarisonMinistry of Public Health, Antananarivo, Madagascar.
Mauricette N AndriamananjaraMinistry of Public Health, Antananarivo, Madagascar.
Andres GarchitorenaNGO PIVOT, Ranomafana, Madagascar. andres.garchitorena@gmail.com.ORCID 0000-0001-6225-5226

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReliable surveillance systems are essential for identifying disease outbreaks and allocating resources to ensure universal access to diagnostics and treatment for endemic diseases. Yet, most countries with high disease burdens rely entirely on facility-based passive surveillance systems, which miss the vast majority of cases in rural settings with low access to health care. This is especially true for malaria, for which the World Health Organization estimates that routine surveillance detects only 14% of global cases. The goal of this study was to develop a novel method to obtain accurate estimates of disease spatio-temporal incidence at very local scales from routine passive surveillance, less biased by populations' financial and geographic access to care.

methodsWe use a geographically explicit dataset with residences of the 73,022 malaria cases confirmed at health centers in the Ifanadiana District in Madagascar from 2014 to 2017. Malaria incidence was adjusted to account for underreporting due to stock-outs of rapid diagnostic tests and variable access to healthcare. A benchmark multiplier was combined with a health care utilization index obtained from statistical models of non-malaria patients. Variations to the multiplier and several strategies for pooling neighboring communities together were explored to allow for fine-tuning of the final estimates. Separate analyses were carried out for individuals of all ages and for children under five. Cross-validation criteria were developed based on overall incidence, trends in financial and geographical access to health care, and consistency with geographic distribution in a district-representative cohort. The most plausible sets of estimates were then identified based on these criteria.

resultsPassive surveillance was estimated to have missed about 4 in every 5 malaria cases among all individuals and 2 out of every 3 cases among children under five. Adjusted malaria estimates were less biased by differences in populations' financial and geographic access to care. Average adjusted monthly malaria incidence was nearly four times higher during the high transmission season than during the low transmission season. By gathering patient-level data and removing systematic biases in the dataset, the spatial resolution of passive malaria surveillance was improved over ten-fold. Geographic distribution in the adjusted dataset revealed high transmission clusters in low elevation areas in the northeast and southeast of the district that were stable across seasons and transmission years.

conclusionsUnderstanding local disease dynamics from routine passive surveillance data can be a key step towards achieving universal access to diagnostics and treatment. Methods presented here could be scaled-up thanks to the increasing availability of e-health disease surveillance platforms for malaria and other diseases across the developing world.

Indexed as

Health Information SystemsMalariaChildHealth Services AccessibilityHumansIncidenceSeasons

Identifiers

PMID33579294
PMCPMC7879399

What Socratic 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 Socratic graph.