Patients at risk of sickle cell anemia; Assessment findings; Genetic screening and counseling as primary forms of prevention; Treatment in acute cases; Pathological effect of the disease; Patient teaching points.MitchellRonaldAmerican Journal of Nursing...
Use of non-conventional coverage in ischemic wound treatment in patients with sickle cell anemia: case study Online Brazilian Journal of NursingSilva MSMOliveira SHSSoares MJGPaulo MQRocha PS
SICKLE cell anemiaPATIENT-controlled analgesiaOPIOIDSPATIENTSLooks at sickle cell disease (SCD) patients' perceptions of self-administering parenteral opioids. Overview of SCD; Relationship between pain and SCD; Patient-identified advantages of self-administering analgesia in the hospi...
Sickle cell anemia, the first molecular disease: Overview of molecular etiology, pathophysiology, and therapeutic approaches 2008, TheScientificWorldJournal Hospital readmission for adult acute sickle cell painful episodes: Frequency, etiology, and prognostic significance 2005, American Journal of Hematology ...
Voxelotor (Oxbryta), a treatment for sickle cell anemia, has been removed from the market after research showed that the risks of treatment outweigh any potential benefit.#NPs and other clinicians should stop prescribing voxelotor and present patients with other treatment options.Wolters Kluwer Health...
The most common and most severe form of SCD is the homozygous state known as Sickle Cell Anemia (SCA) due to inheritance of hemoglobin S (HbS) from each parent [1]. The inheritance of HbS in heterozygous state with a normal Hb is known as sickle cell trait which is not part of SCD ...
A case report: psychosis associated with sickle-cell trait. 1 MG Gowardman - 《New Zealand Nursing Journal Kai Tiaki》 被引量: 0发表: 1969年 Complications associated with sickle cell trait: a brief narrative review. Sickle cell trait occurs in approximately 300 million people worldwide, with ...
sickle cell trait (redirected fromSickle-cell trait) Medical Acronyms sickle cell trait n. A hereditary condition, usually harmless and without symptoms, in which an individual carries only one mutated hemoglobin gene for sickle cell anemia. The sickle cell trait confers resistance to some forms of...
This cross-sectional, quantitative and descriptive study assessed the level of informa-tion about sickle cell disease among educators in the public schools of Montes in which there are students with the SS homozygous subtype (sickle cell anemia). There were 136 educators in the research, 94.9% of...
Olatokun WM (2010) Indigenous Knowledge of Traditional Medical practitioners in the treatment of sickle cell anemia. Indian J Traditional Knowledge 9(1):119–125 Google Scholar Oyebode O, Kandala NB, Chilton PJ, Lilford RJ (2016) Use of traditional medicine in middle-income countries: a WHO...