Evidence map›Paper›PMID 40121016›Full record

ArticleBMJ paediatrics open2025

Mortality in children and adolescents in Western Democratic Republic of Congo: retrospective analysis of verbal autopsy and demographic data from the Kimpese Health and Demographic Surveillance System.

Joël Kiniati Fumwakwau, Mattias Schedwin, Mireille Amba Ngale, Helena Hildenwall, Tobias Alfven, Mala Ali Mapatano, Carina King, Delphin Mavinga Phanzu

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Article in BMJ paediatrics open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Joël Kiniati FumwakwauKimpese Health Research Center, Kimpese, Congo (the Democratic Republic of the).
Mattias SchedwinDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden mattias.schedwin@ki.se.ORCID http://orcid.org/0000-0002-3777-2034
Mireille Amba NgaleKimpese Health Research Center, Kimpese, Congo (the Democratic Republic of the).
Helena HildenwallDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
Tobias AlfvenDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-2328-3512
Mala Ali MapatanoDepartment of Nutrition, Kinshasa School of Public Health, Kinshasa, Congo (the Democratic Republic of the).
Carina KingDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-6885-6716
Delphin Mavinga PhanzuKimpese Health Research Center, Kimpese, Congo (the Democratic Republic of the).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is a paucity of data on causes of death in children and adolescents that can be used for public health prioritisation in settings with the highest mortality burden. We aimed to estimate the causes and circumstances around deaths for the age group 1 month to 19 years in the Western Democratic Republic of Congo.

methodsAnalysis of verbal autopsy and demographic data from the Kimpese Health and Demographic Surveillance System (rural setting 200 km west of Kinshasa) was collected between September 2018 and September 2021. About 66 000 individuals were surveyed yearly using structured questionnaires. Vital events were registered and identified deaths followed up with the World Health Organization 2012 or 2016 verbal autopsy questionnaire. Verbal autopsies were analysed using the InterVA-5 algorithm to generate cause of death and circumstances of mortality categories at the population level. Individual and household characteristics relevant to child survival were compared between deceased and surviving individuals using Fisher's exact test.

resultsOverall, 166/273 (61%) of identified deaths had a complete verbal autopsy. 74% of deaths occurred in children 1-59 months of age, and 70% of all deaths were classified as due to infectious diseases. The top three causes were malaria (35%), lower respiratory infection (12%) and diarrhoeal disease (9%). 78% of deaths occurred at home, and <5% were considered inevitable. However, 70% of individuals sought healthcare in the days preceding death. Recognition (39%), emergencies (27%) and accessing care (20%) were the main contributing categories to fatal outcomes. Characteristics had low coverage (32-72% for the first dose of vaccinations and <10% for water, sanitation and hygiene).

conclusionsResults suggest a need to sensitise caregivers about care-seeking, home treatment and danger signs and improve access to health facilities, combined with improving the quality of care in facilities. Improvements in access to safe water, sanitation and vaccination coverage are also needed.

Indexed as

Child MortalityAdolescentAutopsyCause of DeathChildChild, PreschoolDemocratic Republic of the CongoFemaleHumansInfantMalePopulation SurveillanceRetrospective StudiesRural PopulationYoung AdultAdolescent HealthChild HealthEpidemiologyInfantMortality

Identifiers

PMID40121016
PMCPMC11931915

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