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The recommendations address treatment of both adult and pediatric SCD. The systematic review of evidence was led by the Mayo Clinic Evidence-Based Practice Center. Learn more about the development process behind the SCD guidelines.
19 Ιουν 2020 · Individualized care plans, developed with acute care and SCD care providers, are treatment recommendations that include medications and doses that are effective for a given patient. These plans can be embedded in the electronic medical record and used to guide opioid dosing.
16 Απρ 2020 · Stroke, silent cerebral infarcts (silent strokes), and cognitive morbidity are the most common permanent sequelae of sickle cell disease (SCD) in children and adults.
• Evidence-based treatment guidelines for sickle cell disease complications that affect the heart, lungs, and kidneys. • SCD affects multiple organs that require patients to seek care from doctors that
28 Σεπ 2021 · Abstract. Background: Sickle cell disease (SCD) is a life-limiting inherited hemoglobinopathy that results in significant complications and affects quality of life. Hematopoietic stem cell transplantation (HSCT) is currently the only curative intervention for SCD; however, guidelines are needed to inform how to apply HSCT in clinical practice.
Central nervous system (CNS) complications are among the most common, devastating sequelae of sickle cell disease (SCD) occurring throughout the lifespan. These evidence-based guidelines of the American Society of Hematology are intended to support ...
28 Απρ 2020 · American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults - ScienceDirect. Blood Advances. Volume 4, Issue 8, 28 April 2020, Pages 1554-1588. CLINICAL GUIDELINES.
