Sickle Cell TraitIntraoperative ComplicationsHemoglobin, SickleBlood TransfusionPreoperative CareAnesthesia, GeneralSurgical Procedures, OperativeNo abstract is available for this article.doi:10.1002/bjs.1800780503A. K. BanerjeeDepartment of Surgery, King's College School of Medicine and Dentistry, Denmark Hill...
Surgery and anesthesia in sickle cell disease. Cooperative Study of Sickle Cell Diseases From 1978 to 1988, The Cooperative Study of Sickle Disease observed 3,765 patients with a mean follow-up of 5.3 +/- 2.0 years. One thousand seventy-nine su... M Koshy,SJ Weiner,ST Miller,... - 《...
Sickle Cell Disease (Clinical) Sickle cell disease (SCD) is a group of genetic disorders in which an abnormal Hb molecule (Hb S) transforms RBCs into sickle-shaped cells, resulting in chronic anemia, vasoocclusive episodes, pain, and organ damage. Sickle cell trait, which is the heterozygous...
Management strategies include prevention and diagnosis of oral lesions related to sickle cell disease and its treatment, as well as methods of preparation and execution of oral surgery procedures. We suggest guidelines for the management of these complications and implementation of preoperative, ...
In subject area: Immunology and Microbiology Sickle cell disease refers to a group of disorders resulting from mutations in the hemoglobin gene that can lead to deformation of the red blood cell (RBC) into a crescent, or sickle, shape. ...
The life expectancy for individuals with sickle cell disease (SCD) has greatly increased over the last 50 years. Adults with SCD experience multiple complications such as cardiopulmonary disease, strokes, and avascular necrosis that lead to limitations that geriatric populations often experience. There ...
Hemoglobinopathies such as sickle cell disease (SCD) are traditionally considered a relative contraindication to free tissue transfer, due to concerns that... A Huang,RA Patel,LJ Gottlieb - 《Archives of Plastic Surgery》 被引量: 0发表: 2023年 加载更多来源...
This study is to (1) assess implicit racial bias among pediatric providers and (2) use virtual patient (VP) vignettes to determine the impact of implicit racial bias on clinical decision-making in pediatric sickle cell disease (SCD) pain care. Design/Methods This cross-sectional study was cond...
Sickle cell disease (SCD) is the most common hereditary blood disorder in the United States. SCD is frequently associated with osteonecrosis, osteoporosis, osteopenia, and other bone-related complications such as vaso-occlusive pain, ischemic damage, osteomyelitis, and bone marrow hyperplasia known as...
Both these pathologies are very complex and although they adversely affect the haemoglobin, they do so in very different ways. In patients with sickle cell disease (SCD) and β-thalassemia, the gene that encodes for the production of adult haemoglobin is mutated. In SCD, red blood cells take...