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Newborn screening for sickle cell disease: an innovative pilot program to improve child survival in Dar es Salaam,
Siana Nkya1,2,3, Lillian Mtei2,3, Deogratias Soka2,3
1Dar es Salaam University College of Education, Dar es Salaam, Tanzania.
Insights
Newborn screening for sickle cell disease (SCD) in Tanzania identified a significant birth prevalence of 8 per 1000 births. Early detection and comprehensive care are crucial for reducing childhood mortality from SCD.
Area of Science:
- Public Health
- Genetics
- Pediatrics
Background:
- Sickle cell disease (SCD) is a major cause of childhood mortality globally.
- Tanzania faces a high incidence of SCD, with an estimated 11,000 annual births.
- No African nation has a sustained national newborn screening (NBS) program for SCD.
Purpose of the Study:
- To establish and evaluate NBS for SCD as a health intervention in Tanzania.
- To determine the birth prevalence of SCD in the Tanzanian population.
- To assess the feasibility of integrating NBS-SCD into a national health program.
Main Methods:
- Muhimbili University of Health and Allied Sciences conducted NBS for SCD between January 2015 and November 2016.
- Dried blood spot samples were collected from newborns.
- Isoelectric focusing was used to test samples for SCD and other hemoglobinopathies.
Main Results:
- A total of 3981 newborns were screened.
- The birth prevalence of SCD was found to be 0.8% (31 infants).
- Sickle cell trait was present in 12.6% (505 infants), and other hemoglobinopathies in 0.7% (26 infants).
- 90.3% (28 infants) of those with SCD were enrolled in comprehensive healthcare.
Conclusions:
- This study reports the first NBS program for SCD in Tanzania.
- The identified SCD birth prevalence of 8 per 1000 births is a significant public health concern.
- Implementing NBS for SCD coupled with comprehensive care is vital for improving child survival rates.
Background:
Sickle cell disease (SCD) is a recognized cause of childhood mortality. Tanzania has the fifth highest incidence of SCD (with an estimated 11 000 SCD annual births) worldwide. Although newborn screening (NBS) for SCD and comprehensive healthcare have been shown to reduce under-5 mortality by up to 94% in high-income countries such as the USA, no country in Africa has maintained NBS for SCD as a national health program. The aims of this program were to establish and evaluate NBS-SCD as a health intervention in Tanzania and to determine the birth prevalence of SCD.
Methods:
Muhimbili University of Health and Allied Sciences conducted NBS for SCD from January 2015 to November 2016. Dried blood spot samples were collected and tested for SCD using isoelectric focusing.
Results:
Screening was conducted on 3981 newborns. Thirty-one (0.8%) babies had SCD, 505 (12.6%) had sickle cell trait and 26 (0.7%) had other hemoglobinopathies. Twenty-eight (90.3%) of the 31 newborns with SCD were enrolled for comprehensive healthcare.
Conclusions:
This is the first report on NBS as a health program for SCD in Tanzania. The SCD birth prevalence of 8 per 1000 births is of public health significance. It is therefore important to conduct NBS for SCD with enrollment into a comprehensive care program.
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