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...
Clinical practice guidelines on sickle cell disease stem cell transplantation by the American Society of Hematology (ASH) were published in September 2021 in Blood Advances.[1] For patients with sickle cell disease who have had an overt stroke or who have abnormal transcranial Doppler ultrasound ...
Clinical Guideline Highlights for the Hospitalist: Management of Acute and Chronic Pain in Sickle Cell DiseaseGuideline title: American Society of Hematology 2020 Guidelines for Sickle Cell Disease: Management of Acute and Chronic Pain RELEASE DATE: June 19, 2020 PRIOR VERSION: Not applicable ...
The interdisciplinary healthcare team developed a clinical guideline based on National Heart Lung Blood Institute and The American Pain Society Guidelines on the care of sickle cell patients. Outcomes were identified. Data was compared with other medical surgical hospitals as well as other ca...
Sickle Cell Disease is the most common genetic disease world wide and in the UK. It has marked geographical variation in its distribution in the UK, with a concentration in London and other major conurbations (Birmingham and Manchester). In these areas, specialist centres have become established...
Anemia-Clinical: Sickle cell anemiaRED CELLSBackground Central nervous system (CNS) complications are among the most common, devastating sequelae of sickle cell disease (SCD) occurring throughout the lifespan. Objective These evidence-based guidelines of the American Society of Hematology are intended ...
Sickle-cell anemia in pregnancy ☆ : A review of the literature and report of six cases Sickle cell anemia in pregnancy: a review of the literature and report of six cases. Am J Obstet Gynecol. 1941;41:811.Kobak, A.J. , Stein, P.J. & Daro, A.F. ( 1941 ) Sickle-cell anemia ...
The sickle cell diseases are disorders in which ‘sickling’ of erythrocytes produces clinical manifestations. In 1910, James Herrick was the first to observe sickled cells and, in 1923, it was demonstrated that the sickling phenomenon was inherited as an autosomal dominant trait. Subsequently, the...
The establishment of treatment guidelines and protocols standardized treatment across the country. The centres gradually shifted towards basic and clinical research, and the NIH Comprehensive Sickle Cell Center programme was disassembled in 2008. as 4 weeks of gestation. Some couples who test positive...
- 《Journal of Clinical Sleep Medicine Jcsm Official Publication of the American Academy of Sleep Medicine》 被引量: 44发表: 2014年 Adherence to National Comprehensive Cancer Network guidelines for time to initiation of postoperative radiation therapy for patients with head and neck cancer Adherence ...