Insurance status as a sociodemographic risk factor for functional outcomes and health-related quality of life among youth with sickle cell disease

Journal of Pediatric Hematology/Oncology

Volumn 36, Issue 1, 2014, Pages 51-56

  Robinson, M Renee ^a   Daniel, Lauren C ^b   O'Hara, Emily A ^c   Szabo, Margo M ^d   Barakat, Lamia P ^e  

^a ST CHRISTOPHER'S HOSPITAL FOR CHILDREN   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF HARTFORD   (United States)

^d WEST VIRGINIA UNIVERSITY   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Chronic health conditions; Health disparities; Insurance coverage; Sickle cell disease; Sociodemographic factors

Indexed keywords

ADULT; ARTICLE; CHILD; CLINICAL EFFECTIVENESS; CONTROLLED STUDY; DATA ANALYSIS; DISEASE ASSOCIATION; ENVIRONMENTAL FACTOR; FEMALE; FUNCTIONAL ASSESSMENT; HEALTH CARE UTILIZATION; HEALTH INSURANCE; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDICAL SERVICE; NEIGHBORHOOD; OUTCOME ASSESSMENT; PATIENT INFORMATION; PREDICTION; PRIORITY JOURNAL; PRIVATE HEALTH INSURANCE; PUBLIC HEALTH INSURANCE; QUALITY OF LIFE; RISK ASSESSMENT; RISK FACTOR; SCHOOL CHILD; SICKLE CELL ANEMIA; SOCIAL STATUS; SOCIAL STRESS; SOCIOECONOMICS; YOUNG ADULT;

EID: 84891828530     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0000000000000013     Document Type: Article

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