Sickle Cell Anemia in Cuba: Prevention and Management, 1982-2018

MEDICC Review
|April 27, 2020
PubMed

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.

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