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Sickle cell disease in Grenada: Quality of life and barriers to care
Alyssa Grygiel
, Felicia Ikolo
, Raphielle Stephen
, Dawnell Bleasdille
, Patricia Robbins-Furman
, Beverly Nelson
,
Andrew K. Sobering
, Sarah H. Elsea
Research output
:
Contribution to journal
›
Article
›
peer-review
9
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Scopus citations
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Keyphrases
Sickle Cell Disease
100%
Quality of Life
100%
Barriers to Care
100%
Grenada
100%
Caregiver-child Interaction
27%
Caregivers
18%
Living with
18%
Barriers to Health Care
18%
Caregiver Burden Scale
18%
Demographic Variables
9%
Further Analysis
9%
Health Care Delivery
9%
High Incidence
9%
Physical Functioning
9%
Recurrence Risk
9%
West Indies
9%
Well-being
9%
Limited Resources
9%
Access to Care
9%
Genetic Condition
9%
Additional Education
9%
Knowledge Questionnaire
9%
Quality of Life Measurement
9%
Measurement Information
9%
Loneliness
9%
Cultural Expectations
9%
Genetic Knowledge
9%
High-income Countries
9%
Specific Barriers
9%
Pediatric Quality of Life Inventory
9%
Cell Quality
9%
Caribbean Countries
9%
Caribbean Community (CARICOM)
9%
Zarit Burden Interview
9%
Validated Survey Measures
9%
Medicine and Dentistry
Sickle-Cell Disease
100%
Quality of Life
100%
Caregiver Burden
20%
Sickle Cell
10%
Recurrence Risk
10%
Wellbeing
10%
Pediatric Quality of Life Inventory
10%
Loneliness
10%
Nursing and Health Professions
Quality of Life
100%
Sickle Cell Anemia
100%
Health Care Delivery
10%
Recurrence Risk
10%
Information System
10%
Loneliness
10%
Pediatric Quality of Life Inventory
10%