Providing the Tools to Facilitate Quality Care for Children with Sickle Cell Disease

Meeting best-practice guidelines can significantly enhance quality of life and longevity for those with sickle cell disease (SCD). However, many clinical settings lack the necessary resources for optimal care. We present an integrated suite of tools and collaborative actions designed to enhance SCD...

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Bibliographic Details
Published inJournal of health care for the poor and underserved Vol. 35; no. 3; pp. 143 - 150
Main Authors Albert, Marcy Stein, Alphonso, Candace, Patel, Urvi, Balaoura, Kathrin, DeLuna, Neal, Mack, Jason, Castano, Francisco, Muhyedeen, Salma, Bernstein, Bruce, Poulard, Jean-Bernard, Rivlin, Kenneth
Format Journal Article
LanguageEnglish
Published United States Johns Hopkins University Press 01.08.2024
Subjects
Anemia, Sickle Cell - therapy
Best practice
Child
Chronic illnesses
Collaboration
Community health care
Community organizations
Community support
Education
Electronic health records
Emergency medical care
Health care policy
Hematology
Hemoglobin
Hospital systems
Humans
Initiatives
Medicaid
Pain management
Pediatrics
Practice Guidelines as Topic
Primary care
Quality of care
Quality of Health Care - organization & administration
Quality of Health Care - standards
Quality of life
Sickle cell disease
New York
United States > US
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Summary:Meeting best-practice guidelines can significantly enhance quality of life and longevity for those with sickle cell disease (SCD). However, many clinical settings lack the necessary resources for optimal care. We present an integrated suite of tools and collaborative actions designed to enhance SCD care.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:1049-2089
1548-6869
1548-6869
DOI:10.1353/hpu.2024.a933288