While research has long established disparities in health outcomes among individuals living with sickle cell disease (SCD), few studies have quantified these gaps. A new study finds that the average life expectancy of publicly insured patients living with SCD is roughly 52.6 years. In contrast, the CDC reports that the average life expectancy in the United States is 73.5 years for men and 79.3 years for women, demonstrating the considerable burden SCD can have on affected populations.
Click here for original story, Quantifying the life expectancy gap for people living with sickle cell disease
Source: ScienceDaily