Anemia ABSTRACT The purpose of this paper is to briefly describe the initial core diagnostic questioning and core set of diagnostic testing related to the patient presenting with anemia. Subjective information and recommended testing are written with consideration of the scope of practice of the family nurse practitioner. In addition‚ three specific case studies are examined. Anemia Core set of subjective questions The healthcare provider should initially obtain a history of any previous
Premium Anemia Red blood cell Hemoglobin
Anemia A blood type is a classification of blood based on the presence or absence of inherited antigenic substances on the surface of red blood cells (RBCs). These antigens may be proteins‚ carbohydrates‚ glycoproteins‚ or glycolipids‚ depending on the blood group system. Some of these antigens are also present on the surface of other types of cells. Some of these red blood cell surface antigens can stem from one allele and collectively form a blood group system. It is called The ABO system and it
Premium Blood Red blood cell Hematology
The core reading for this week included an excerpt that read “…the first cases of sickle cell disease were mostly amongst Africans and African Caribbeans. Racial thinking led to the assumption that sickle cell disease was a ‘Black disease’‚ even though many African people are not at risk for these disease and many carriers are not African” (Russell‚ 2014‚ p. 69). This‚ for me‚ was very insightful and enlightening‚ as it presents a way of thinking that is not common or taught in our society. It brought
Premium Health care Medicine Race
families with a history of the autosomal recessive disease Sickle cell anaemia should have all embryos screened with Pre-Implantation Genetic Diagnosis technology (PGD). If tested positive‚ treatment should be made compulsory for the child at a young age and will be treated with stem cell gene therapy. This disease has no personal relevance to me‚ however‚ there is currently 90K people suffering from Sickle cell anaemia in the United States. Sickle cell anaemia is relevant to society because it greatly reduces
Premium DNA Gene Genetics
Sickle cell disease (SCD) is a group of inherited conditions that affect the red blood cells. People affected with sickle cell disease produce abnormally shaped red blood cells that causes health problems. Sickle cell disease is caused by a defective gene passed on from the parent to the child. Sickle cell disease is condition that is considered serious and lifelong. People of African descent are mainly affected with sickle cell disease in addition to ‚ Caribbean‚ Middle Eastern‚ Eastern Mediterranean
Premium Red blood cell Sickle-cell disease Malaria
offspring. He also discovered that traits pass down through families in different patterns. Sickle cell‚ which is an inherited disease‚ is mainly found in those of African descent. Mendel’s research ultimately helped lead to the discovery and understanding of the HBS allele‚ the connection of malaria to sickle cell now and in future generations‚ and the new technology that helps diagnose and treat sickle cell. In 1910‚ a black man named Walter Clement Noel‚ went to Dr. James B. Herrick‚ complaining
Premium Malaria Sickle-cell disease Red blood cell
Anemia: People with anemia have a low number of red blood cells. Mild anemia often causes no symptoms. More severe anemia can cause fatigue‚ pale skin‚ and shortness of breath with exertion. Polycythemia vera: The body produces too many blood cells‚ from an unknown cause. The excess red blood cells usually create no problems but may cause blood clots in some people. Leukemia: A form of blood cancer in which a white blood cell becomes malignant and multiplies inside bone marrow. Leukemia may be
Premium Red blood cell Bone marrow Blood
The Sickle Cell disease is that affects all people at all ages. There are interventions that address the needs of the people except for those young adults 18-26 years of age. These SCD patients are transitioning from pediatric care into adult care. These young adults are most susceptible to death due to the lack of a structured education system that provides wellness facts and intervention medical services to assist them during this transition period. The mortality rate is the highest among the total
Premium
Aplastic anemia is a condition where bone marrow does not produce sufficient new cells to replenish blood cells.[1] The condition‚ per its name‚ involves both aplasia and anemia. Typically‚ anemia refers to low red blood cell counts‚ but aplastic anemia patients have lower counts of all three blood cell types: red blood cells‚ white blood cells‚ and platelets‚ termed pancytopenia. ------------------------------------------------- [edit]Signs and symptoms * Anemia with malaise‚ pallor and associated
Premium Blood Red blood cell Hematology
Explain in details regarding the sideroblastic anemia. - The sideroblastic anemia is a heterogeneous group of blood disorders. This type of anemia will occur because an impaired ability of the bone marrow to produce normal red blood cells. The person who has these anemia can found sideroblasts (abnormal red blood cells) in the blood. Sideroblastic anemia can be categorized into three groups such as reversible‚ acquired and reversible hereditary. 2. Explain in details regarding the morphology of siderocytes
Premium