V.V. is a 40 year old African American male who was diagnosed with sickle cell disease at the age of 8. His anemia has been managed with multiple transfusions and recently he has shown signs of chronic renal failure. He is receiving two units of packed RBCs this morning as an outpatient. He has A- Blood type What blood type can he receive? What are your key nursing considerations for the procedural transfusion of blood? What are three potential current complications with s/s and interventions that you need to monitor for? What are three potential delayed complications with s/s and intervention that you need to teach V.V. to monitor for at home?
1.He can recieve A+,AB+,O+,O-
2 Nursing considerations are
3 Current complications of blood transfusion are
Transfusion reactions,Circulatory overload and Hyperkalemia.
Signs of Transfusion reactions are
Nursing intervention
Circulatory overload-it is caused by the infusion of blood at a rate too rapid for the client to tolerate.
Interventions
Hyperkalemia
4 Delayed complications of blood transfusion are Iron overload,Disease transmission, Septicaemia
Iron overload- A delayed transfusion complication that occurs in clients who recieve multiple blood transfusions,such as clients with anaemia or thrombocytopenia..
Assessment
Interventions
Disease transmission
Septicaemia-It occurs with the transfusion of blood that is contaminated with microrganisms.
Assessment
Interventions
V.V. is a 40 year old African American male who was diagnosed with sickle cell disease...
a 39-year-old black man who has sickle cell disease (SCD) marked by frequent episodes of severe pain. His anemia has been managed with multiple transfusions, and he shows signs of chronic renal failure. He is a nonsmoker, nondrinker, and is on Social Security disability. His regular medications are pentoxifylline (Trental), oxycodone/acetaminophen (Roxicet), and folic acid (Folvite). In hematology clinic this AM, V.M.’s Hgb measured 6.7 g/dl. He received 2 units PRC (packed rerd cells) over 3 hours and then went...
Melissa, a 15 year old African American, is diagnosed with sickle cell anemia. She comes to the hematology clinic with a complaint of intense pain in the lower extremities and joints. Melissa recently attended an ice-skating party This case study has 3 questions 1. What type of conditions can trigger the onset of a sickling event? experiencing? sickling events? 2. What would be the cause of the pain that Melissa is Ith teaching can the nurse provide to help prevent
Sickle Cell Case Study Read the following case study and answer the questions below. Provide evidence with correct citations to support your answers. V.M. is a 29 year old African American married man who has sickle cell disease (SCD) marked by frequent episodes of severe pain. His anemia has been managed with multiple transfusions. Six months ago he started showing signs of chronic renal failure. His regular medications are pentoxifylline (Trental), oxycodone-acetaminophen (Percocet), hydroxyurea (Droxia), and folic acid. In the...
CHAPTER 3 CASE STUDY was an African American gentleman who had sickle cell anemia. He had Mr. McGibbins, age 31, just moved to the area, and sought out a local doctor to see what recommendations the doctor could make for handling the sickle cell crises, which Mr. McGibbins had been having at intervals for as long as he could remember. It seemed to him that the pain of the crises had been more intense in the last few months. Just...
Case Study #7 H.M. is a 15-year-old African American adolescent who was diagnosed with sickle cell disease three years ago. H.M. presents to the emergency department with pain related to sickle cell crisis. Subjective Data Pain level is an 8/10 location = bilateral legs, described as deep muscle pain Student in 10th grade, honor roll student On the track team Lives with mother and father Objective Data Vital signs: T= 99.3 P= 80 R= 18 BP= 140/68 Weight: 140 lbs...
Case Study #7 H.M. is a 15-year-old African American adolescent who was diagnosed with sickle cell disease three years ago. H.M. presents to the emergency department with pain related to sickle cell crisis. Subjective Data Pain level is an 8/10 location = bilateral legs, described as deep muscle pain Student in 10th grade, honor roll student On the track team Lives with mother and father Objective Data Vital signs: T= 99.3 P= 80 R= 18 BP= 140/68 Weight: 140 lbs...
My Study on Sickle Cell Anemia Research In 500 words, answer the following questions 1.Select your study sample 2. How have you selected your sample? 3. How will you select your sample population and give the rationale behind your decision Please type the solution on the keyboard so that I can copy and paste Q. No 1. Answer : Sickle cell disease : It is defined as it is a chronic heriditory form of Anemia, in which the red blood...
Mrs. Follex is a 51-year-old African American female who works as a bookkeeper for an insurance company. Her father and brother have type 2 diabetes mellitus, and have had severe complications because of poor control of blood glucose. She is 5' 4" tall and weighs 174 pounds with a medium frame. She has a history of obesity, hypertension, hypothyroidism, and frequent urinary tract infections, and is currently taking propranolol and levothyroxine. Mrs. Follex complains of constant fatigue over the past...
The 56 year old African-American woman is admitted for treatment of newly diagnosed renal cell carcinoma. You find her daughter in the hallway crying. She has heard that her mother has undergone genetic testing related to her cancer diagnosis and wonders if she is at increased risk for the same condition. She was with her mother during the renal scan before admission and is also worried that this exposure to a radioactive isotope will cause cancer in her. Is renal...
Ethics and Values You are caring for a 17-year-old female patient with sickle cell disease who has been admitted for treatment of sickle cell crisis. Sickle cell disease is a genetic abnormality that affects hemoglobin in the red blood cells. In a sickle cell crisis weakened red blood cells clump together and impede blood flow, causing extreme pain. To prevent stroke and manage the pain of the crisis, your patient needs aggressive fluid and comfort management. At the change-of-shift report,...