Evidence map›Paper›PMID 42773426›Full record

ArticleBMC nephrology2026

Renal care readiness and gaps in early detection of sickle cell nephropathy in children in North Kivu Province, Democratic Republic of the Congo: an exploratory cross-sectional study.

Mupenzi Mumbere, Kahindo Kangitsi Charles, Kambale Malengera Victor, Lwanzo Sindikubyo Zaccharie, Katsuva Mbahweka François, Tsongo Kibendelelwa Zaccharie

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Article in BMC nephrology, 2026. 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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5 · Who and what money

Authors and funding

6 authors.

Mupenzi MumbereDepartment of Pediatrics, Université Catholique du Graben (UCG), Butembo, Democratic Republic of the Congo. mupenzimumbere@gmail.com.ORCID https://orcid.org/0000-0003-2035-7165
Kahindo Kangitsi CharlesDepartment of Internal Medicine, Université de Goma (UNIGOM), Goma, Democratic Republic of the Congo.
Kambale Malengera VictorDepartment of Pediatrics, Université Catholique du Graben (UCG), Butembo, Democratic Republic of the Congo.
Lwanzo Sindikubyo ZaccharieCentre de Diagnostic et de Recherche Biomédicale du Nord-Kivu (CDRB/NK), Butembo, Democratic Republic of the Congo.
Katsuva Mbahweka FrançoisDepartment of Pediatrics, Université Catholique du Graben (UCG), Butembo, Democratic Republic of the Congo.
Tsongo Kibendelelwa ZaccharieDepartment of Pediatrics, Université Catholique du Graben (UCG), Butembo, Democratic Republic of the Congo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell nephropathy is a common and progressive complication of sickle cell disease in children and a major contributor to early morbidity and long-term chronic kidney disease. Although early renal screening is essential to prevent irreversible damage, its implementation remains limited in resource-constrained settings. This study assessed healthcare provider readiness for the early detection and management of sickle cell nephropathy in North Kivu Province, Democratic Republic of the Congo.

methodsWe conducted an exploratory cross-sectional study among medical and paramedical healthcare providers involved in the care of children with sickle cell disease. Data were collected using a structured electronic questionnaire evaluating knowledge, attitudes, practices, and diagnostic availability related to renal screening. Composite scores were constructed for these domains, and factors associated with adequate renal care readiness were examined using multivariable logistic regression.

resultsTwo hundred providers were included. Adequate knowledge was observed in 50.5% of participants, while only 21.0% demonstrated favorable attitudes. Reported practices were poor, with good practice identified in only 4.1% of respondents. Diagnostic availability was limited (mean score 39.8 ± 23.5), particularly in primary and secondary facilities. Overall renal care readiness was suboptimal, and adequate diagnostic availability emerged as the main independent determinant. Key barriers included recurrent shortages of diagnostic supplies, financial constraints, and high workload, whereas standardized protocols and institutional support were reported as facilitators.

conclusionsDespite moderate knowledge levels, early renal screening for children with sickle cell disease is insufficiently implemented in North Kivu. Health system capacity, especially access to essential diagnostic tools, is central to effective renal care readiness. Strengthening diagnostic availability, standardizing care pathways, and reinforcing targeted training may substantially improve early detection and prevention of kidney disease in resource-limited settings.

Indexed as

Anemia, Sickle CellHealth Knowledge, Attitudes, PracticeHealth PersonnelKidney DiseasesAttitude of Health PersonnelChildCross-Sectional StudiesDemocratic Republic of the CongoEarly DiagnosisFemaleHumansMaleDemocratic Republic of the CongoDiagnostic availabilityEarly renal screeningHealthcare provider readinessNorth-KivuSickle cell nephropathy

Identifiers

PMID42773426
PMCPMC13595512

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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.