Question

In: Nursing

A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential...

A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential complications from transfusion therapy and the nurse’s role in prevention.

Solutions

Expert Solution

Blood transfusion remains an important therapeutic intervention in patients with sickle cell disease.

Complications from transfusion therapy-

Iron overload, delayed hemolytic transfusion reaction, multisystem organ failure, and hyperviscosity along with usual transfusion risks. Repeated transfusions create alloimmunization in SCA patients

Iron overload is the build-up of iron in the body due to the excess presence of iron in the blood. Transfusional iron overload is commonly seen in patients who take multiple transfusions. Delayed hemolytic transfusion reaction presents with red blood cell hemolysis from 2 days to several months after a transfusion. This leads to the absence of expected results. Multisystem organ failure is a condition in which multiple systems of the body fails to perform their function. Hyperviscosity prevents blood from flowing freely through the arteries. Here it is caused due to the excess amount of blood in the system.

Nurses role-

The nurse should thoroughly check the previous records of the client to be aware of the potential complications. The nurse should continuously evaluate the vital signs of the patient. The nurse should be aware of complications while transfusing blood to a child with SDA, Nurse should be capable to assess splenomegaly, hyperviscosity, shock, chest pain, and so on. Nurses should be ready to manage any situation. The nurse should continuously monitor the drop factor and ensure the rate of flow to prevent complications and overload. If any abnormality is observed the nurse should immediately stop the transfusion and keep the line open with normal saline. Notify the physician at the earliest The nurse should monitor symptoms of complications like iron overload, delayed hemolytic transfusion reaction, multisystem organ failure, and hyperviscosity.


Related Solutions

A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential...
A 13-year-old adolescent with sickle cell disease is being admitted for RBC transfusion therapy. Explain potential complications from transfusion therapy and the nurse’s role in prevention.
J.P. is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years...
J.P. is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years ago. J.P. presents to the emergency department with pain related to a sickle cell crisis. Subjective Data Pain level is an 8/10 location = bilateral legs, described as deep muscle pain A student in 10th grade, honor roll student On the track team Lives with mother and father Objective Data Vital signs: T 37 P 80 R 18 BP 140/68 Weight: 140 HT: 5...
J.P is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years...
J.P is a 15-year-old African American adolescent who was diagnosed with sickle cell disease 3 years ago. J.P. 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 37 P 80 R 18 BP 140/68 Weight: 140 HT: 5 feet, 6...
Explain how the sickle cell mutation results in the symptoms of the disease?
Explain how the sickle cell mutation results in the symptoms of the disease?
In humans, the inheritance of ..........is best explained as being polygenic. a. sickle-cell disease b. cystic...
In humans, the inheritance of ..........is best explained as being polygenic. a. sickle-cell disease b. cystic fibrosis c. height d. blood type
Ralp is a 13-year-old boy Black- American with sickle cell anemia. He has been attending a...
Ralp is a 13-year-old boy Black- American with sickle cell anemia. He has been attending a day camp this summer. He was playing flag footbal in 90 dgree wheather. All of a sudden he complain of severe knee pain bilateraly. His Mom took him to his Dr., who had him directly admitted to the hospital for a sickle cell crisis. Ralph was diagnosed with sickle cell anemia as a newborn with a routine screening. His vaccination are up to date...
P.R., a 66-year-old woman who has no history of respiratory disease, is being admitted to your...
P.R., a 66-year-old woman who has no history of respiratory disease, is being admitted to your intensive care unit (ICU) from the emergency department (ED) with a diagnosis of pneumonia and acute respiratory failure (ARF). The ED nurse tells you that P.R. was stuporous and cyanotic on her arrival to the ED. Her initial vital signs were 90/68, 134, 38, 101° F (38.3° C) with an Spo2 of 53%. She was endotracheally intubated orally and placed on mechanical ventilation and...
Chapter 17( Immunohematology and Transfusion Medicine) A 17-year-old man is admitted with multiple injuries after his...
Chapter 17( Immunohematology and Transfusion Medicine) A 17-year-old man is admitted with multiple injuries after his motorcycle crashes. The emergency department physician draws a blood sample for a STAT type and crossmatch. The motorcyclist's passenger also has blood drawn for a STAT type and screen. An immediate-spin crossmatch is compatible between the group A patient and group A donor. The unit of blood is issued from the blood bank as an emergency release. After receiving 50 mL of the first...
A 13-year-old adolescent wants to initiate a vegetarian diet. a) Discuss the emotional, cognitive, and social...
A 13-year-old adolescent wants to initiate a vegetarian diet. a) Discuss the emotional, cognitive, and social development levels at this age and how they would impact her understanding of nutrition and health messages. b) Identify important adults that would help this teen develop her personal identity and feelings of self-worth. c) Select one food group and develop a behavioral-specific nutrition message for this teenager to follow.
Client Profile Nisha is a 14 year old with sickle cell anemia. She lives with her...
Client Profile Nisha is a 14 year old with sickle cell anemia. She lives with her mother and grandmother in a rural neighborhood. Nisha has experienced several “sickle cell crises”, however, they seem to have become more frequent since she became an adolescent. Nisha is enjoying her summer break from school. She is active in softball and enjoys shopping with her girlfriends. Case Study Nisha’s mother brings her to the hematology clinic at the hospital with complaints of severe generalized...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT