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Updated: Sep 14, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
High acceptability of newborn screening for sickle cell disease among post-natal mothers in Western Kenya
John Orimbo1, Shehu Shagari Awandu1, Faith Muhonja2
1Department of Biomedical and Nursing Sciences, School of Health Sciences, Jaramogi Oginga Odinga University of Science and Technology, Bondo, Kenya.
Insights
Newborn screening for sickle cell disease is highly accepted by mothers in Kenya. Implementing routine screening can improve early identification and care for affected infants.
Area of Science:
- Genetics and Hematology
- Public Health
- Pediatrics
Background:
- Sickle cell disease (SCD) is a prevalent inherited blood disorder in sub-Saharan Africa, necessitating early detection.
- Newborn screening (NBS) for SCD is recommended but underutilized in the region.
- Kenya's 2020 policy promotes NBS for SCD, yet evidence on its acceptability is limited.
Purpose of the Study:
- To assess the acceptability of NBS for SCD among mothers in western Kenya.
- To identify factors influencing mothers' acceptance of NBS for SCD.
Main Methods:
- A cross-sectional study involving 399 postnatal mothers at Homa Bay County Teaching and Referral Hospital.
- Data collected via semi-structured questionnaires on sociodemographics, knowledge, and perceptions.
- Sickle cell disease screening performed using the Sickle SCAN point-of-care test.
Main Results:
- Ninety-four percent of mothers accepted NBS for SCD.
- Maternal age (25-34 years) and formal employment were associated with lower acceptance rates.
- Mothers in formal employment were significantly less likely to accept NBS compared to students.
Conclusions:
- High acceptability of NBS for SCD exists among mothers in Homa Bay County.
- The findings support the implementation of routine NBS for SCD in Kenyan healthcare facilities.
- Targeted strategies may be needed to address lower acceptance among specific maternal demographics.
Abstract:
Sickle cell disease is a genetically inherited blood disorder that manifests early in life with resultant significant health complications. Globally, nearly three quarters of all affected babies are in sub-Saharan Africa. Early identification of babies with sickle cell disease through newborn screening followed by early linkage to care is recommended. However, the program has not been widely adopted in the sub-Saharan Africa. The Kenyan ministry of health, in 2020, published a policy on newborn screening for sickle cell disease from levels 2-6 healthcare facilities. However, evidence on acceptability of newborn screening to scale up newborn screening program is scarce. Few studies have been conducted across the sub-Saharan Africa to assess the acceptability of newborn screening for sickle cell disease with conflicting results. This study assessed factors associated with acceptability of newborn screening among mothers of newborns delivered at Homa bay county teaching and referral hospital, western Kenya. This study employed a cross-sectional design among postnatal mothers at Homa bay county teaching and referral hospital with 399 postnatal mothers enrolled into the study. After obtaining informed consent from the postnatal mothers, a semi-structured questionnaire was used for data collection. Maternal sociodemographic characteristics, knowledge, and perception were assessed. Babies were also screened for sickle cell disease using Sickle SCAN point-of-care test. The acceptability was calculated as percentage of mothers accepting to have their babies screened. Data were analyzed using logistic regression to explore factors associated with acceptability of newborn screening for sickle cell disease. Ninety-four percent of mothers accepted newborn screening for sickle cell disease. Only maternal age and occupation were significantly associated with acceptability of newborn screening for sickle cell disease. Mothers aged 25-34 years were 3 times less likely to accept newborn screening for sickle cell disease than those younger mothers than 25 years (OR=0.33;95%CI = 0.13-0.86; p = 0.024).Similarly, mothers in the formal employment were 6 times less likely to accept newborn screening for sickle cell disease than those who were students (OR= 0.16; 95%CI = 0.03-0.84; p = 0.031).Mothers who were in formal employment were 25 times less likely to accept newborn screening for sickle cell disease than those who were students in the multivariate logistic analysis model (aOR= 0.04; 95% CI = 0.00-0.78; p = 0.034). The acceptability of newborn screening for sickle cell disease is high in the county. The Homabay county ministry of health should implement routine newborn screening for sickle cell disease in all healthcare facilities conducting deliveries of newborns.

