Translating sickle cell guidelines into practice for primary care providers with Project ECHO

Author:

Shook Lisa M.1,Farrell Christina B.1,Kalinyak Karen A.1,Nelson Stephen C.2,Hardesty Brandon M.3,Rampersad Angeli G.3,Saving Kay L.4,Whitten-Shurney Wanda J.5,Panepinto Julie A.6,Ware Russell E.1,Crosby Lori E.7

Affiliation:

1. Department of PediatricsCincinnati Comprehensive Sickle Cell Center, Division of Hematology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA

2. Children's Hospitals and ClinicsMinneapolis, MN, USA

3. Indiana Hemophilia and Thrombosis Center, Inc., Indianapolis, IN, USA

4. Children's Hospital of Illinois, OSF Saint Francis Medical Center, University of Illinois College of Medicine, Peoria, IL, USA

5. Sickle Cell Disease Association of America, Michigan Chapter, Detroit, MI

6. Children's Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, WI, USA

7. Division of Behavioral MedicineDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA

Publisher

Informa UK Limited

Subject

Education,General Medicine

Reference43 articles.

1. National Heart, Lung and Blood Institute, Disease and Conditions Index. Sickle cell anemia: who is at risk? 2009; Bethesda, MD, USA: US Department of Health and Human Services, National Institutes of Health, National Heart, Lung and Blood Institute.

2. Newborn screening for sickle cell diseases in the United States: A review of data spanning 2 decades

3. Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state

4. Update of Newborn Screening and Therapy for Congenital Hypothyroidism

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