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Caregivers’ Perspective on the Psychological Burden of Living with Children Affected by Sickle Cell Disease in Kinshasa, the Democratic Republic of Congo

Bibliographic Data

ID15719217
AuthorsPatricia Lelo (University of Bergen, corresponding author), Patricia V M Lelo (Department of Infectious Diseases, Kalembelembe Pediatric Hospital, Kinshasa 012, Democratic Republic of the Congo), Faustin Kitetele (0000-0002-6963-8825, University of Bergen), Cathy E Akele (Kinshasa General Hospital), David L Sam (0000-0003-4275-0697, University of Bergen), Michael J Boivin (0000-0002-0097-1777, Michigan State University), Espérance Kashala-Abotnes (0000-0002-6441-7003, University of Bergen)
Year2023
Volume10
Issue2
Pages261-261
Publication date2023-01-31
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children10020261
PMID36832390
OpenAlexW4318613333
LanguageEN
Citations received1
References cited22

There is limited information on knowledge, perceptions, and management of sickle cell disease (SCD) in Africa in general and in the Democratic Republic of the Congo (DRC) in particular. This study explored knowledge, perceptions, and burden of 26 parents/caregivers of children with SCD in three selected hospitals in Kinshasa, DRC. We conducted a focus group with in-depth interviews with parents/caregivers of children affected with SCD. Four themes were discussed, including knowledge and perceptions, diagnosis and management, society's perceptions, and the psychosocial burden and the quality of life of the family affected by SCD. The majority of participants/caregivers felt that society, in general, had negative perceptions of, attitudes toward, and knowledge about SCD. They reported that children with sickle cell are often marginalized, ignored, and excluded from society or school. They face a number of challenges related to care, management, financial difficulties, and a lack of psychological support. The results suggest the need to promote measures and strategies to improve knowledge and management of SCD in Kinshasa, DRC

Democracy · Disease · Disease burden · Disease management · Focus group · Pathology · Perception · Perspective (graphical · Political science · Psychiatry · Psychosocial · Quality of life (healthcare · Sociology · Global Maternal and Child Health · Hemoglobinopathies and Related Disorders · Iron Metabolism and Disorders · Medicine · Nursing · Psychology · Gerontology

  • Neurocognitive Profile and Associated Factors Among Children Affected by Sickle Cell Disease in Kinshasa, Democratic Republic of Congo

    Open Access•Patricia Lelo, Faustin Kitetele et al.•Children•2024

  • Psychosocial impact of sickle cell disorder

    Open Access•Kofi A Anie, Feyijimi E Egunjobi et al.•Globalization and Health•2010

  • All her children are born that way’

    Vicki Marsh, Vicki M Marsh et al.•Ethnicity and Health•2011

  • The psychosocial problems of sickle cell disease sufferers and their methods of coping

    Open Access•Jude U Ohaeri, Wuraola A Shokunbi et al.•Social Science & Medicine•1995

Unique citing works1
Citations per year0.5
Citation span2024 - 2024 (1)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 1

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