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Aug 3, 2023 · People with sickle cell disease have a reduced life expectancy. New treatments for SCD are improving life expectancy and quality of life. People with sickle cell disease can survive beyond their 50s with optimal management of the disease.
Jan 3, 2024 · Sickle cell disease (SCD) affects about 100,000 people in the United States; more than 90% are non-Hispanic Black or African American, and an estimated 3%–9% are Hispanic or Latino. The estimated life expectancy of those with SCD in the United States is more than 20 years shorter than the average expected. Many people with SCD do not receive ...
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Mar 16, 2023 · Researchers found that the average life expectancy for publicly insured individuals with SCD was 52.6 years, with male life expectancy at birth (49.3 years) being significantly lower than that of females at birth (55 years).
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Apr 22, 2024 · Last updated on April 22, 2024. Back to top. Sickle cell disease is an inherited blood disorder that affects hemoglobin, the protein that carries oxygen through the body. Misshapen red blood cells can block blood flow causing lifelong health problems.
Apr 20, 2017 · Despite these remarkable achievements, life expectancy for patients with sickle cell disease is reduced by about 30 years, even with the best medical care, and the quality of life is often poor.
Dec 22, 2022 · Diagnosis. A blood test can check for the form of hemoglobin that underlies sickle cell anemia. In the United States, this blood test is part of routine newborn screening. But older children and adults can get the test too. In adults, a blood sample is taken from a vein in the arm.
Today, studies show people with SCD can expect to live to around 61 years old. To put that number into context, the life expectancy of most people in the United States is about 77 years old. 1,2. New sickle cell disease therapies. Many medical treatments aim to help people to live longer, healthier lives.
