Evidence map›Paper›PMID 41509890›Full record

ArticleOpen research Europe2025

Awareness and Acceptability of Prenatal Diagnosis of Sickle Cell Disease among Mothers of Affected Children in a Northern Nigerian Teaching Hospital.

Aliyu Rm, Sada Si, Adebiyi Nm, Randawa Aj, Abdulkadir I, Ahmad Hr

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Article in Open research Europe, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Aliyu RmDepartment of Obstetrics and Gynaecology, Ahmadu Bello University Faculty of Medicine, Zaria, Kaduna, Nigeria.
Sada SiDepartment of Obstetrics and Gynaecology, Ahmadu Bello University Faculty of Medicine, Zaria, Kaduna, Nigeria.ORCID https://orcid.org/0000-0002-0510-9924
Adebiyi NmDepartment of Paediatrics, Ahmadu Bello University Teaching Hospital, Zaria, Kaduna, Nigeria.ORCID https://orcid.org/0009-0008-8368-6592
Randawa AjDepartment of Obstetrics and Gynaecology, Ahmadu Bello University Faculty of Medicine, Zaria, Kaduna, Nigeria.
Abdulkadir IDepartment of Paediatrics, Ahmadu Bello University Teaching Hospital, Zaria, Kaduna, Nigeria.
Ahmad HrDepartment of Paediatrics, Ahmadu Bello University Teaching Hospital, Zaria, Kaduna, Nigeria.ORCID https://orcid.org/0000-0002-8330-5840

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nigeria has the highest global prevalence of sickle cell disease (SCD), necessitating effective preventive measures to control the disease. Prenatal diagnosis (PND) is a key early intervention for SCD, yet there is a shortage of studies in Northern Nigeria focusing on mothers of children with SCD. These mothers not only carry the burden of the disease but also face the risk of having more affected children, making them vital stakeholders in managing and controlling SCD. This study assessed the awareness and acceptability of prenatal diagnosis PND for SCD among mothers of children with the disease. Methods: A cross-sectional study was conducted involving 297 mothers of children with SCD attending the Paediatric Haematology clinic at Ahmadu Bello University Teaching Hospital, Zaria, Nigeria. Data were collected via an interviewer-administered questionnaire addressing the characteristics of the children and mothers, as well as their awareness, attitudes, and acceptability of PND. SPSS version 23 was used for data analysis, with a p-value < 0.05 considered statistically significant. Results: Most participants (90.9%) were of Hausa ethnicity and 97.0% were of Islamic faith. A majority (77.8%) had less than tertiary education, and 57.9% lacked personal income. Nearly 41% had more than one child affected by SCD, and about one-fifth had lost a child to SCD complications. Only 22.2% of mothers had heard of PND, mostly from healthcare workers, and just 0.3% had undergone the procedure. After receiving information about PND, 93.3% were willing to accept it, though 45% of those who declined cited religious beliefs. Factors associated with PND acceptance included the mother's education and the child's SCD severity. Conclusion: Awareness of PND among at-risk mothers is low, yet most expressed willingness to accept it. Educational level and disease severity were associated with PND acceptability.

Indexed as

acceptabilityawarenessmothersprenatal diagnosissickle cell disease.

Identifiers

PMID41509890
PMCPMC12775652

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