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Newborn screening for sickle cell disease in Caluquembe, southwestern Angola, 2024-2025
Jasmine J Su1, Vasco S Kupua1, Daniel Cummings1
1Hospital Evangélico de Caluquembe, Caluquembe, Angola.
Insights
Newborn screening in Angola found sickle cell trait in 6.0% of infants, with no sickle cell disease (SCD) cases detected. This study highlights the feasibility of point-of-care SCD testing in rural areas, indicating a disease burden beyond major cities.
Area of Science:
- Public Health
- Genetics
- Epidemiology
Background:
- Angola faces a high prevalence of sickle cell disease (SCD).
- Neonatal SCD screening is recommended but not widely implemented.
- Previous SCD research in Angola has focused on urban populations.
Purpose of the Study:
- To implement a neonatal SCD screening program in a rural hospital in Huíla province.
- To investigate the epidemiology of SCD in an Umbundu-speaking population.
- To assess the feasibility of point-of-care (POC) SCD testing in a rural setting.
Main Methods:
- Screened 353 infants (<1 month old) for the hemoglobin S (HbS) gene using HemoTypeSC POC tests.
- Reviewed pediatric outpatient records from 2024 to identify incident SCD cases.
- Conducted screening between October 2024 and February 2025 at Hospital Evangélico de Caluquembe.
Main Results:
- Sickle cell trait (HbAS) was detected in 21 (6.0%) of 353 neonates.
- No neonates were diagnosed with sickle cell disease (HbSS).
- 26 incident cases of SCD were identified through outpatient record reviews.
Conclusions:
- While HbS prevalence is lower in Caluquembe compared to other Angolan cities, SCD poses a significant disease burden in the region.
- Accessible sickle cell screening and treatment programs are crucial for all high-burden areas, including rural settings.
- POC tests offer a cost-effective method for immediate SCD screening results, demonstrating potential for wider implementation despite cost concerns for universal screening.
Objectives:
Angola is one of the countries with the highest prevalence of sickle cell disease (SCD). Neonatal SCD testing is recommended by the Angolan government, but it is not routinely performed. Nearly all previous studies of SCD have been conducted in cities. We implemented a neonatal SCD screening program in a referral hospital in Huíla province to examine the epidemiology of SCD in this Umbundu-speaking population and to demonstrate the feasibility of using point-of-care (POC) tests for SCD in a rural setting.
Methods:
Between October 2024 and February 2025, we screened 353 infants less than one month old at Hospital Evangélico de Caluquembe for the hemoglobin S (HbS) gene using HemoTypeSC rapid diagnostic tests. We also reviewed all pediatric outpatient visits from 2024 to identify newly-diagnosed SCD cases.
Results:
Twenty-one (6.0%) of the 353 neonates had sickle cell trait (HbAS); none had SCD (HbSS). The outpatient register review identified 26 incident cases of SCD.
Conclusions:
The prevalence of HbS is lower in Caluquembe than in Luanda and Cabinda, but the combined results of our newborn screening and pediatric records provide evidence that there is a burden of disease from SCD in Caluquembe and the surrounding areas. Sickle cell screening and treatment programs should be available in all high-burden areas, not just large cities. The per-test costs may still be too expensive for universal newborn screening to be scaled up nationwide, but our pilot study demonstrates that POC tests can be a cost-effective method that yields immediate results.
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