# Family Functioning and Psychosocial Burden in Caregivers of Children with Sickle Cell Disease in a Tertiary Centre in North-Central Nigeria

**Authors:** Mohammed Abdulkadir, M Alabi Kola, A Oyeleke Oyeronke, N Alabi Anthonia, O Ademola Christy, R Yusuf Adebayo, A Obalowu Ismaila

PMC · DOI: 10.4314/ejhs.v34i6.13 · Ethiopian Journal of Health Sciences · 2024-11-01

## TL;DR

This study examines how caregivers of children with sickle cell disease in Nigeria manage family life and cope with the psychosocial challenges of caregiving.

## Contribution

The study provides insights into family functioning and psychosocial burden specific to caregivers of children with SCD in Nigeria.

## Key findings

- Most caregivers reported high levels of family functioning.
- Significant psychosocial burden was observed in financial and routine disruption areas.
- Negative impact on family interactions was minimal despite the caregiving challenges.

## Abstract

Sickle cell disease (SCD) is a chronic genetic disorder that has significant psychosocial consequences for both patients and their families. This study aimed to investigate family functioning and the psychosocial burden experienced by caregivers of children with SCD.

This descriptive, cross-sectional study involved 170 caregivers of children with SCD, selected through systematic random sampling. Data were collected using both structured and semi-structured questionnaires. Family functioning was assessed using the Family APGAR (Adaptation, Partnership, Growth, Affectation, Resolve) while the psychosocial burden was evaluated using the Sickle Cell Disease Burden Instrument (SCDBI). Statistical analysis was performed using the Statistical Package for Social Sciences (SPSS) version 24.

The mean age of the participants was 34.7 years, and 83% were female. The majority of caregivers reported a high level of family functioning. However, significant psychosocial burden was observed in areas such as finances, disruption of routine family activities, and the caregivers' coping abilities. The impact on family interactions was minimal.

Most caregivers in this study demonstrated good family functioning. Although caring for a child with sickle cell disease imposed a significant psychosocial burden, the negative impact on family interactions was minimal.

## Linked entities

- **Diseases:** sickle cell disease (MONDO:0011382)

## Full-text entities

- **Diseases:** SCD (MESH:D000755), genetic disorder (MESH:D030342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12110272/full.md

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Source: https://tomesphere.com/paper/PMC12110272