By Robert Preidt
MONDAY, July 13, 2020 (HealthDay News) -- People with sickle cell disease are at increased risk for severe complications from COVID-19, an expert says.
"Many patients experience a pain crisis, also known as a vaso-occlusive crisis, early in COVID-19 infection before respiratory symptoms develop," said Dr. Jennie Hart, clinical director of pediatric hematology/oncology at Herman and Walter Samuelson Children's Hospital at Sinai in Baltimore.
People with the disease, which most commonly affects Black people, have misshapen red cells that can get stuck and clog blood flow, inhibiting oxygen delivery, damaging blood vessels and causing inflammation.
Some conditions -- including respiratory infections such as COVID-19 -- increase formation of sickle-shaped cells, because infections in the lungs lead to lower oxygen levels and worse inflammation.
"This increase in sickled red blood cells makes patients with sickle cell disease and COVID-19 infection particularly vulnerable to developing acute chest syndrome, a rapid and deadly lung injury," Hart said in a news release.
People with sickle cell disease should stay home unless travel is essential, according to the Sickle Cell Disease Association of America.
"Patients who can work from home are strongly encouraged to do so. Your physician can provide a letter to your employer," Hart said. Social distancing is a must, she added.
Take all your medications as prescribed, especially if you're taking hydroxyurea, which reduces certain complications from sickle cell disease, she added.
Stay well hydrated, wash your hands often and avoid close contact with people who have symptoms of a respiratory infection, Hart said.