On the same note, women who had IDA history in their family tree would also give insight on the results obtained. VAT Registration No: 842417633.

Abstract Sickle Cell Anemia is a hereditary disease that changes the smallest and most important components of the body. Normal red blood cells are flexible and can easily pass through capillaries to bring oxygen to different parts of the body.

There is no cure, therefore nurses should understand the actions that can prevent or relieve symptoms in order to meet the challenges of caring for patients with sickle cell disease and helping them to minimize its effect on their lives. Normally a person has flexible and round blood cells. However, sickle cells are fragile, and can easily die, leading to anemia (red blood cell deficiency). Outline Churchill Livingstone. Understanding Nursing Research. Guideline CG62, published March 2008, revised February 2014. https://www.nice.org.uk/guidance/cg62, NICE quality standard 58: Sickle cell acute painful episode, Guidelines CG143, publication date June 2012, reviewed May 2014. https://www.nice.org.uk/guidance/cg143, Odame, I.

Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. “The first effective drug treatment for adults with severe sickle cell anemia was reported in early 1995, when a study conducted by the National Heart, Lung, and Blood Institute showed that daily doses of the anticancer drug hydroxyurea reduced the frequency of painful crises and acute chest syndrome”. 2011). Sickle cell anemia occurs when a person inherits two abnormal genes, Sickle Cell Anemia These include; iron deficiency anemia and major common risks factors for development of iron deficiency anemia, women education, family status, ethnicity and social economic status. All work is written to order.

The authors of the article did come up with a number of independent variables.

SC patients experience periods of acute illness termed “crises” resulting from the two different effects of SCD; vaso-occlusion (pain, stroke and acute chest syndrome) and those from hemolysis (for example, anemia from RBC destruction and inefficient oxygen carrying capacity) (Glassberg 2011). Despite the fact that the authors did not in a succinct manner states the research questions and hypotheses, a close examination of the research make the reader easily come up with two major research questions; these revolves around how prevalent is iron deficiency anemia in pregnant women and infant from a low-income background and what are the major/common factors for development of iron deficiency anemia in pregnant women (Leblanc, et al.

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