Metrics details. Sickle cell disease SCD is a chronic condition associated with high mortality and morbidity. It is characterized by acute clinical symptoms such as painful vaso-occlusive crises, which can impair health-related quality of life HRQL. This study was conducted to identify validated patient-reported outcome PRO instruments for use in future trials of potential treatments for SCD. Fifteen of those instruments were developed and validated for adults and 10 for children one instrument was used in both children and young adults aged up to 21 years.
Sickle Cell Anemia Essay Example
Gall Bladder and Liver Disorders in Sickle Cell Disease
It arises from a complication of a disease. Fox was diagnosed with sickle cell anemia as a child and has had multiple cri-ses requiring hospitalization. Learn vocabulary, terms, and more with flashcards, games, and other study tools In-Text Answer 5. Sickle cell disease SCD and its variants are genetic disorders resulting from the presence of a mutated form of hemoglobin, hemoglobin S HbS see the image below.
Sickle cell retinopathy: A literature review
Objective: To report a case of coexisting systemic lupus erythematosus SLE and sickle cell disease SCD with a review of the literature on the topic. Descriptors used: 1. Sickle cell anemia; 2. Sickle cell disease; 3.
Sickle cell disease SCD pain continues to emerge in adolescents. In fact, 1 in Black infants will be affected by SCD. Identifying standards of care for this unique population can improve pain management and treatment. A significant effect of vaso-occlusive crisis is a decrease in the quality of life in children. Therefore, pain management is multidimensional and includes pharmacologic, physical, and psychological strategies.