Sickle Cell Disease
Sickle Cell Disease ( 15 Questions)
A nurse is educating a patient with sickle cell disease (SCD) and their family about the treatment and management of the condition.
Which interventions should the nurse include in the education and counseling plan? (Select three)
Medication adherence is essential in the treatment and management of sickle cell disease (SCD) Patients with SCD often require medications such as hydroxyurea to reduce the frequency of painful crises and other complications. Non-adherence to medications can lead to worsened outcomes and increased morbidity. Educating the patient and their family about the importance of taking medications as prescribed is crucial.
Avoidance of cold and altitude is important for patients with SCD because exposure to cold temperatures and high altitudes can trigger vaso-occlusive crises. Cold can cause red blood cells to sickle more easily, leading to pain and tissue damage. Altitude can result in lower oxygen levels in the blood, exacerbating the risk of sickling. Educating the patient and their family about these environmental factors and strategies to minimize exposure is essential for SCD management.
Blood transfusion is not a first-line treatment for all SCD patients. It is typically reserved for specific indications, such as severe anemia or acute complications like stroke. Stem cell transplantation (
Stem cell transplantation is not recommended as a treatment for all SCD patients. It is considered a high-risk procedure with potential complications, and its suitability depends on factors such as patient age, disease severity, and the availability of a suitable donor. Therefore, it is not included as a standard intervention in the education and counseling plan for all SCD patients.
Providing emotional support and coping strategies is a crucial component of managing SCD. Patients with SCD often experience chronic pain, frequent hospitalizations, and a reduced quality of life. Emotional support can help them cope with the physical and emotional challenges associated with the disease. Teaching patients and their families how to manage stress, anxiety, and depression can improve their overall well-being.
Choice A rationale:
Medication adherence is essential in the treatment and management of sickle cell disease (SCD)
Patients with SCD often require medications such as hydroxyurea to reduce the frequency of painful crises and other complications.
Non-adherence to medications can lead to worsened outcomes and increased morbidity.
Educating the patient and their family about the importance of taking medications as prescribed is crucial.
Choice B rationale:
Avoidance of cold and altitude is important for patients with SCD because exposure to cold temperatures and high altitudes can trigger vaso-occlusive crises.
Cold can cause red blood cells to sickle more easily, leading to pain and tissue damage.
Altitude can result in lower oxygen levels in the blood, exacerbating the risk of sickling.
Educating the patient and their family about these environmental factors and strategies to minimize exposure is essential for SCD management.
Choice E rationale:
Providing emotional support and coping strategies is a crucial component of managing SCD.
Patients with SCD often experience chronic pain, frequent hospitalizations, and a reduced quality of life.
Emotional support can help them cope with the physical and emotional challenges associated with the disease.
Teaching patients and their families how to manage stress, anxiety, and depression can improve their overall well-being.
Choice C rationale:
Blood transfusion is not a first-line treatment for all SCD patients.
It is typically reserved for specific indications, such as severe anemia or acute complications like stroke.
Stem cell transplantation (Choice D) is a potential curative treatment for some individuals with SCD, but it is not applicable to all patients due to factors like donor availability and eligibility.
Therefore, Choices C and D are not universally applicable and may not be included in the education and counseling plan for all SCD patients.
Choice D rationale:
Stem cell transplantation is not recommended as a treatment for all SCD patients.
It is considered a high-risk procedure with potential complications, and its suitability depends on factors such as patient age, disease severity, and the availability of a suitable donor.
Therefore, it is not included as a standard intervention in the education and counseling plan for all SCD patients.