Evidence map›Paper›PMID 38292384›Full record

ArticleFrontiers in public health2023

The prevalence of gestational syphilis in Malawi between 2014 and 2022: spatiotemporal modeling of population-level factors.

James Chirombo, Annielisa Majamanda, Vester Gunsaru, Simeon Yosefe, Washington Ozituosauka, Christina Mchoma, Chelsea Morroni, Effie Chipeta, Peter MacPherson, Bridget Freyne

Open access · goldAbstract read
In one paragraph

Article in Frontiers in public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 4 citations in OpenAlex.

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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

10 authors at 9 institutions in 4 countries.

James ChiromboStatistical Support Unit, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Annielisa MajamandaDepartment of Quality, Blantyre District Health Office, Blantyre, Malawi.
Vester GunsaruStatistical Support Unit, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Simeon YosefeDigital Health Department, Ministry of Health, Lilongwe, Malawi.
Washington OzituosaukaSTI/HIV Program, Ministry of Health, Lilongwe, Malawi.
Christina MchomaReproductive Health Department, Ministry of Health of Malawi, Lilongwe, Malawi.
Chelsea MorroniBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Effie ChipetaKamuzu University of Health Sciences, Blantyre, Malawi.
Peter MacPhersonSchool of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
Bridget FreyneDepartment of Paediatric Infectious Diseases, Children's Health Ireland, Dublin, Ireland.
Ministry of Health · MWBlantyre Institute for Community Ophthalmology · MWKamuzu Central Hospital · MWLiverpool School of Tropical Medicine · GBMalawi-Liverpool-Wellcome Trust Clinical Research Programme · MWPublic Health Institute of Malawi · MWUniversity College Dublin · IEUniversity of Edinburgh · GBUniversity of Glasgow · GB

Funding

Wellcome Trust 206575/Z/17/Z
6 · The paper itself

Abstract

Background: Mother-to-child transmission of syphilis remains high especially in the WHO AFRO region with a prevalence of 1.62%, resulting in a congenital syphilis rate of 1,119 per 100,000 live births. Elimination efforts can be supported by an understanding of the spatial and temporal changes in disease over time, which can identify priority areas for targeted interventions aimed at reducing transmission. Methods: We collated routine surveillance data from health facilities and covariate data from demographic and health surveys conducted in Malawi between 2014 and 2022. We fitted a Bayesian hierarchical mixed model with spatial and temporally structured random effects to model the district-level monthly counts of maternal syphilis notifications as a function of individual- and district-level predictors. We then generated district-level spatiotemporally explicit risk profiles to estimate the effect of individual- and district-level covariates on maternal syphilis notifications and to identify hotspot areas. Results: Overall, the national prevalence of maternal syphilis increased from 0.28% (95% CI: 0.27-0.29%) in 2014 to peaking in 2021 at 1.92% (95% CI: 1.89-1.96%). Between 2020 and 2022, there was a decline in prevalence, with the most significant decline seen in Zomba District (1.40, 95% CI: 1.12-1.66%). In regression models, a one percentage point increase in district-level antenatal HIV prevalence was associated with increased maternal syphilis (prevalence ratio [PR]: 1.15, 95% credible interval [CrI]: 1.10-1.21). There was also an increased prevalence of maternal syphilis associated with an increased district-level mean number of sex partners (PR: 1.05, 95% CrI: 0.80-1.37). The number of districts with a high prevalence of maternal syphilis also increased between 2014 and 2022, especially in the southern region, where most had a high probability (approaching 100%) of having high maternal syphilis (defined as relative risk >1 compared to the standard population of women aged 15-49 years) in 2022. Conclusion: Maternal syphilis prevalence in Malawi shows an increasing upward trend, with an estimated six times relative increase between 2014 and 2022 (0.28% to 1.73%) and strong associations with higher district-level HIV prevalence. Controlling syphilis depends on reaching vulnerable populations at the sub-national level, which may be disproportionately affected. Our findings support the move to integrate the elimination of mother-to-child transmission (EMTCT) of syphilis programs with existing prevention of mother-to-child transmission (PMTCT) of HIV programs.

Indexed as

HIV InfectionsPregnancy Complications, InfectiousSyphilisBayes TheoremFemaleHumansInfectious Disease Transmission, VerticalMalawiPregnancyPrevalenceeMTCTHIVmaternal syphilisspatio-temporal modelsyphilis prevalence

Identifiers

PMID38292384
PMCPMC10825961
OpenAlexW4390743357

What OpenQuestion holds

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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.