Sickle ce - Study guides, Class notes & Summaries

Anthony Perkins Sickle Cell Anemia Case Study-latest-2023

Anthony Perkins is a 15-year-old African American male who was at a medically monitored summer camp and participated in several sports activities when the outside temperature was greater than 90 degrees. He began having pain in his knees and was evaluated by the camp nurse. After evaluation, he was transported to his primary care provider and evaluated. Anthony was transferred as a direct admit to the pediatric floor of the community hospital where you are the primary nurse responsible for h...

Case Study Sickle Cell Disease Difficulty: Advanced Setting: Emergency department Index Words: sickle cell disease (SCD), anemia, pain management, oxygenation, blood transfusion therapy, fluid volume overload Giddens Concepts: Fluid and Electrolyte Balance, Gas Exchange, Pain, Perfusion, Safety HESI Concepts: Assessment, Fluids & Electrolytes, Gas Exchange, Oxygenation, Pain, Perfusion, Safety . u Scenario V.M. is a 29-year-old African American married man who has sickle cell disease ...

HEMATOLOGY NURSING III SICKLE CELL ANEMIA, ANEMIA, THROMBOCYTOPENIA, IVS QUESTIONS AND CORRECT ANSWERS

A patient is admitted to the nurse's unit with sickle cell crisis. What are the priority medical interventions that the nurse would expect to be ordered by the healthcare provider? Select all that apply. Place the patient on ordered oxygen. Initiate oral and parenteral fluids per order. Medicate the patient for pain. Order an electrocardiogram. Order ultrasound of the abdomen. - A teenage female patient with sickle cell disease has been admitted to the nursing unit with a diagnosis of s...

PLTW Biomedical Science - Unit 3 Sickle Cell Disease Questions With 100% Correct And Verified Answers, Latest update 2024 solutions

Sickle Cell Anemia - ATI: Nursing Care of Children Exam Questions and Answers Sickle Cell Disease - Answer- a group of diseases (autosomal recessive genetic disorder) in which abnormal sickle hemoglobin S (HbS) replaces normal adult hemoglobin (Hgb A). Sickle Cell Anemia - Answer- the homozygous and most common form of SCD. Increased destruction of RBCs occurs. manifestations of SCA (resultl of RBC sickling) - Answer- increased blood viscosity, obstruction of blood flow, and tissue hypox...

Haemoglobinopathies (Sickle Cell, Thalassemia) Questions with solutions 2023 Sickle cell hemoglobins- single amino acid substitution or deletion in globin polypeptide chain results in HbS variants rather than HbA ( normal adult heme) Haemoglobin S •Point mutation of 6th codon substituting valine for glutamic acid- most common Haemoglobin C •Point mutation of 6th codon lysine for glutamic acid Haemoglobin E •Point mutation on 26th codon lysine for glutamic acid What is sic...

The patient who has sickle cell anemia developed the condition of hand-foot syndrome because of what physiological process? Repeat 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 - Answer-C A patient is admitted to the nurse's unit with sickle cell crisis. ...

NURS 325 Sickle Cell Case Study 100% Correct