General Planning Guide for Comprehensive Sickle Cell Programs PDF Download
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Author: National Association for Sickle Cell Disease (U.S.)
Publisher:
ISBN:
Category : Sickle cell anemia
Languages : en
Pages : 28
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Book Description
Author: National Association for Sickle Cell Disease (U.S.)
Publisher:
ISBN:
Category : Sickle cell anemia
Languages : en
Pages : 28
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Book Description
Author: National Association for Sickle Cell Disease (U.S.)
Publisher:
ISBN:
Category : Sickle cell anemia
Languages : en
Pages : 64
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Book Description
Author: National Heart, Lung, and Blood Institute. Sickle Cell Disease Branch
Publisher:
ISBN:
Category : Community health services
Languages : en
Pages : 50
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Book Description
Sickle cell facilities in the United States, the Bahamas, and Puerto Rico. Entries arranged under sections titled Comprehensive sickle cell centers, Sickle cell screening and education clinics, National centers for family planning services, Veterans administration hospitals, Job Corps regions, and Public and private organizations. Each entry gives name, address, and telephone number.
Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309669634
Category : Medical
Languages : en
Pages : 523
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Book Description
Sickle cell disease (SCD) is a genetic condition that affects approximately 100,000 people in the United States and millions more globally. Individuals with SCD endure the psychological and physiological toll of repetitive pain as well as side effects from the pain treatments they undergo. Some adults with SCD report reluctance to use health care services, unless as a last resort, due to the racism and discrimination they face in the health care system. Additionally, many aspects of SCD are inadequately studied, understood, and addressed. Addressing Sickle Cell Disease examines the epidemiology, health outcomes, genetic implications, and societal factors associated with SCD and sickle cell trait (SCT). This report explores the current guidelines and best practices for the care of patients with SCD and recommends priorities for programs, policies, and research. It also discusses limitations and opportunities for developing national SCD patient registries and surveillance systems, barriers in the healthcare sector associated with SCD and SCT, and the role of patient advocacy and community engagement groups.
Author:
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 418
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Author:
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 832
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Author: Pennsylvania. Irvis Committee on Sickle Cell Anemia
Publisher:
ISBN:
Category : African Americans
Languages : en
Pages : 116
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Author:
Publisher:
ISBN:
Category : Associations, institutions, etc
Languages : en
Pages : 912
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Book Description
1981- in 2 v.: v.1, Subject index; v.2, Title index, Publisher/title index, Association name index, Acronym index, Key to publishers' and distributors' abbreviations.
Author:
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 1436
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Book Description
Author: United States. Department of Health and Human Services
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 516
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Book Description
