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Anthony Perkins – Sickle Cell Anemia Case Study (2023) | Detailed Nursing Analysis and Patient Care Plan
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    Anthony Perkins – Sickle Cell Anemia Case Study (2023) | Detailed Nursing Analysis and Patient Care Plan

  • This document presents an in-depth case study of Anthony Perkins, focusing on the diagnosis, symptoms, and treatment of sickle cell anemia. It includes patient assessment details, laboratory findings, pathophysiology, and comprehensive nursing interventions aligned with current clinical guidelines (2023). The content is ideal for nursing and medical students seeking to understand the management of chronic hematologic disorders and evidence-based care strategies.
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Sickle Cell Anemia Test Questions and Answers Graded A
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    Sickle Cell Anemia Test Questions and Answers Graded A

  • The client who has sickle cell anemia developed the condition of hand-foot syndrome because of what physiological process? Repeated crisis and infarction of the bones leading to uneven development of fingers and toes Damage to the liver related to repeat sickle cell crisis Repeat crisis and infarction involving the circulatory system of the arms and legs Damage to the kidneys related to repeat sickle cell crisis - A
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Sickle Cell Anemia Hesi Test Questions with Correct Answers Already Passed
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    Sickle Cell Anemia Hesi Test Questions with Correct Answers Already Passed

  • Sickle Cell Anemia Hesi Test Questions with Correct Answers Already Passed What is the best response by the nurse to Gladys' stmt? - Answers RBCs become "C" shaped, stiff, and sticky, which blocks the blood vessels How should the nurse respond? - Answers "Brianna has the disease because she inherited the gene from both of her parents, who were carriers" Which stmt by Brianna's grandmother supports a common cultural communication expectation in the African American heritage?...
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Sickle Cell Anemia Hesi Case Study Questions & Correct Answers/ Graded A+
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    Sickle Cell Anemia Hesi Case Study Questions & Correct Answers/ Graded A+

  • Which is the best initial response by the nurse to explain SCD to the child's caregiver? : "Red blood cells become 'C' shaped, stiff, and sticky, which blocks the blood vessels." How should the nurse respond? : "This disease is an inherited autosomal recessive disease and your daughter inherited the gene responsible for causing the disease." Which intervention should the nurse implement? : Request the child be allowed to go to the bathroom whenever she asks. Which recommendation a...
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Sickle Cell Anemia - ATI: Nursing Care of  Children Questions & 100% Verified  Answers | Latest Update | Already Graded  A+
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    Sickle Cell Anemia - ATI: Nursing Care of Children Questions & 100% Verified Answers | Latest Update | Already Graded A+

  • Sickle Cell Disease ☑: a group of diseases (autosomal recessive genetic disorder) in which abnormal sickle hemoglobin S (HbS) replaces normal adult hemoglobin (Hgb A). Sickle Cell Anemia ☑: the homozygous and most common form of SCD. Increased destruction of RBCs occurs. manifestations of SCA (resultl of RBC sickling) ☑: increased blood viscosity, obstruction of blood flow, and tissue hypoxia (causes tissue ischemia, resulting in pain) when manifestations begin to appear ☑: late...
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Sickle Cell Anemia (SCD) questions with correct answers
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    Sickle Cell Anemia (SCD) questions with correct answers

  • Adult Hb - Answer HbA (alpha 2, beta 2) Fetal Hb - Answer HbF (alpha 2, gamma 2) Alpha chains made on chromosome ___. - Answer 16 Beta and gamma chains made on chromosome ___. - Answer 11 HbS has a substitution of ___ for glutamic acid at ___ in beta chain. - Answer *valine*, 6th amino acid HbC has a substitution of ___ for glutamic acid at ___ in beta chain. - Answer lysine, 6th amino acid Difference between adult (HbA / HbS) and fetal (HbF) RBC. - Answer Fetal R...
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Sickle Cell Anemia questions with correct answers
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    Sickle Cell Anemia questions with correct answers

  • What is sickle cell anemia? - Answer An autosomal recessive disorder resulting in a mutated form of hemoglobin (HbS) What causes sickle cell TRAIT? - Answer ONE allele on the beta globin gene carries the sickle mutation, one normal allele for HbA (heterozygous) What causes sickle cell DISEASE? - Answer TWO alleles on the beta globin gene carries mutation for sickle mutation (homozygous) What does the sickle cell mutation cause resistance to? - Answer Plasmodium falciparum (malar...
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