Only 3% of US sickle cell patients receive red blood cell exchange for disease, researchers find

Researchers work at the National Heart, Lung, and Blood Institute on 8 February 2024 in Bethesda, Maryland./Getty Images Researchers work at the National Heart, Lung, and Blood Institute on 8 February 2024 in Bethesda, Maryland./Getty Images Sickle cell disease Only 3% of US sickle cell patients receive red blood cell exchange for disease, researchers find Various factors block sufferers of disease from receiving treatment that is effective and has widespread availability
Prefer the Guardian on Google Sickle cell patients are missing out on an effective treatment despite widespread US hospital access to the technology, new research has found.
That treatment is called a red blood cell exchange, a procedure that discards a patient’s damaged red blood cells while simultaneously mixing the patient’s remaining plasma, platelets and white blood cells with red blood cells from a donor before returning them to the body.
Get smarter about the news
Sign up free for a feed built around what you actually care about, Dive Deeper research on any story, and the full text of every article.
Create free accountAlready have an account? Sign in