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Updated: Dec 23, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Sickle Cell Anemia in Cuba: Prevention and Management, 1982-2018
Insights
Cuba
Area of Science:
- Genetics
- Public Health
- Hematology
Background:
- Sickle cell anemia is a prevalent hereditary condition in Cuba.
- The Cuban public health system initiated a prevention program in 1982.
- The program targets carrier identification and antenatal diagnosis.
Observation:
- Over 4.8 million pregnant women were screened between 1982 and 2018.
- 3.5% of screened women were identified as carriers or having sickle cell disease.
- 8180 at-risk couples were identified, with 79.2% undergoing fetal genetic testing.
Findings:
- 20.1% of tested fetuses had the severe SS genotype.
- 76.2% of couples opted for pregnancy termination following a positive fetal diagnosis.
- The program achieved a 3-fold reduction in sickle cell disease prevalence.
Implications:
- Cuba's program led to a 10-fold decrease in annual births of infants with sickle cell disease.
- Life expectancy for sickle cell disease patients increased by an average of 16 years.
- A middle-income country can effectively mitigate genetic disease impact via primary care-based prevention.
Abstract:
Sickle cell anemia is the most common hereditary disease in Cuba. On average, 1 in 33 Cubans is a carrier of this severe hemolytic anemia that can cause early death. In early 1980, its incidence in Cuba was calculated at 1 in 1600 births. In 1982, the Cuban public health system established the Sickle Cell Anemia Prevention Program, which aims to prevent the disease through identification of carrier couples and antenatal diagnosis of fetuses with disease-associated genotypes. In 1982-2018, hemoglobin genotypes were tested in 4,847,239 pregnant women. Of these, 168,865 (3.5%) were found to be carriers or to have sickle cell disease. During the same period, 8180 at-risk couples were identified, of whom 79.2% agreed to an antenatal study for detection of the sickle cell gene in the fetus. Among fetuses diagnosed, 20.1% had the SS genotype, the most clinically severe; 76.2% of the associated couples decided to interrupt the pregnancy. This program has resulted in a 3-fold reduction in prevalence of sickle cell disease in Cuba, a 10-fold reduction in the number of infants born with it each year, and a 16-year average increase in life expectancy of sickle cell disease patients of both sexes. Key contributors to these results have been universal screening of pregnant women in primary care, installation of diagnostic laboratories in every province, genetic counseling for couples, testing of fetal DNA (allowing couples to decide whether to continue the pregnancy if the fetus tests positive for the disease) and guaranteed multidisciplinary clinical care for patients. The Cuban experience shows that a middle-income country can mitigate the impact of a genetic disease through a universal preventive program based in primary care, which also pays particular attention to afflicted patients. KEYWORDS Sickle cell anemia, sickle cell disease, sickle cell disorders, hemolytic anemia, sickle cell trait, sickle cell hemoglobin C disease, HbS disease, prevention, antenatal screening, preventive health services, Cuba.
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