Vital Signs: Use of Recommended Health Care Measures to Prevent Selected Complications of Sickle Cell Anemia in Children and Adolescents — Selected U.S. States, 2019

INTRODUCTIONSickle cell disease (SCD), a group of inherited blood cell disorders that primarily affects Black or African American persons, is associated with severe complications and a >20-year reduction in life expectancy. In 2014, an expert panel convened by the National Heart, Lung, and Blood...

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Veröffentlicht in:	MMWR. Morbidity and mortality weekly report 2022-09, Vol.71 (39), p.1241-1246
Hauptverfasser:	Schieve, Laura A, Simmons, Gretchen M, Payne, Amanda B, Abe, Karon, Hsu, Lewis L, Hulihan, Mary, Pope, Shammara, Rhie, Sarah, Dupervil, Brandi, Hooper, W. Craig
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescents African Americans Ambulatory care Analysis Anemia Blood Blood transfusions Children Complications Complications and side effects Disease prevention Doppler effect Genetic aspects Government programs Health aspects Health care Health care industry Health risks Hemoglobin Hispanic Americans Hospitalization Hydroxyurea Life expectancy Life span Malaria Medicaid Medical care Patient compliance Public health Quality management Sickle cell anemia Sickle cell disease Stroke Teenagers Ultrasonic imaging Ultrasound Utilization
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