A client diagnosed with sickle cell disease reports having pain in the chest and difficulty breathing.
The client states, "I have sharp chest pain, and it hurts more when I take a deep breath.”.
Which complication of sickle cell disease is the client likely experiencing?
Acute Chest Syndrome.
Renal Failure.
Cholelithiasis.
Functional Asplenia.
Monitor for signs and symptoms of anemia
Correct Answer : A,B,C,E
Choice D rationale:
Evaluation of psychosocial well-being and coping mechanisms Monitoring psychosocial well-being and coping mechanisms is essential for holistic care but may not directly relate to monitoring signs and symptoms of sickle cell disease.
The primary focus should be on physical assessments and symptoms related to the disease itself.
Now, let's provide rationales for The correct answers:
Choice A rationale:
Assessment of vital signs, including temperature, heart rate, blood pressure, and respiratory rate Monitoring vital signs is crucial for assessing a patient's overall health and detecting any signs of deterioration.
Patients with sickle cell disease can experience vaso-occlusive crises, which may result in changes in vital signs, such as an elevated heart rate and respiratory rate.
Elevated temperature may indicate an infection, which is another concern in sickle cell disease.
Choice B rationale:
Evaluation of pain intensity and location Sickle cell disease is associated with recurrent painful vaso-occlusive crises, where sickled red blood cells block blood vessels, leading to pain.
Assessing the intensity and location of pain is essential to determine the severity of the crisis and to provide appropriate pain management.
Choice C rationale:
Assessment of neurologic status, including cognitive function and sensory perception Sickle cell disease can lead to complications such as strokes, which may result in neurological deficits.
Monitoring cognitive function and sensory perception is crucial to detect any neurological complications early and provide timely interventions.
Choice E rationale:
Monitoring for signs and symptoms of anemia, such as fatigue, pallor, and shortness of breath Anemia is a common complication in sickle cell disease, and monitoring for signs and symptoms of anemia is vital.
Fatigue, pallor, and shortness of breath are typical manifestations of anemia, and early detection allows for appropriate management and intervention.
These assessments help in ensuring the comprehensive care of patients with sickle cell disease, addressing both acute and chronic complications.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
Choice A rationale:
Pulmonary Hypertension Sickle cell disease is primarily characterized by the presence of abnormal hemoglobin (HbS), leading to the formation of sickle-shaped red blood cells.
While pulmonary hypertension can occur in patients with sickle cell disease, it is not the most likely complication based on the presented symptoms.
The patient's paleness and easy fatigue are more indicative of anemia, which is a common complication in sickle cell disease.
Anemia results from a reduced number of functional red blood cells, leading to reduced oxygen-carrying capacity and fatigue.
Choice C rationale:
Hematuria Hematuria, the presence of blood in the urine, can occur in sickle cell disease, but it is not the most likely complication based on the child's reported symptoms of paleness and easy fatigue.
Hematuria may be associated with other complications such as kidney damage, but it is not the primary concern in this case.
Choice D rationale:
Functional Asplenia Functional asplenia refers to the impaired function of the spleen, which is a common complication in sickle cell disease.
However, the symptoms described by the child's parent, including paleness and easy fatigue, are more indicative of anemia, which is a consequence of sickle cell disease.
Correct Answer is ["B","C","D"]
Explanation
Choice A rationale:
Administering blood transfusions to increase the number of healthy red blood cells.
This choice is not appropriate for the management of sickle cell disease because blood transfusions are typically reserved for specific situations, such as severe anemia, acute complications, or in patients with frequent vaso-occlusive crises.
It is not a routine intervention for all patients with sickle cell disease.
Choice B rationale:
Providing genetic counseling and education for individuals and families affected by sickle cell disease.
Genetic counseling and education are essential for patients and families affected by sickle cell disease.
This helps individuals understand the inheritance pattern, make informed family planning decisions, and manage the emotional and psychological aspects of living with a genetic disorder.
Education can also include information on preventive measures.
Choice C rationale:
Educating patients about the importance of regular follow-up appointments and adherence to prescribed treatment regimens.
Regular follow-up appointments and adherence to prescribed treatment regimens are crucial in managing sickle cell disease.
Patients need ongoing monitoring and support to detect complications early, manage pain, and optimize their overall health.
Non-adherence can lead to exacerbations and complications.
Choice D rationale:
Offering oxygen therapy for patients with acute chest syndrome or respiratory distress.
Oxygen therapy is vital for patients with sickle cell disease, especially when they experience acute chest syndrome or respiratory distress.
This intervention helps improve oxygenation, alleviate respiratory distress, and prevent further complications.
Adequate oxygenation is essential to minimize tissue damage and support the body during these acute events.
Choice E rationale:
Encouraging patients to engage in high-intensity physical activities to improve overall health.
Encouraging high-intensity physical activities is not appropriate for patients with sickle cell disease, as it can trigger vaso-occlusive crises and increase the risk of complications.
Patients with sickle cell disease are typically advised to engage in moderate, low-impact physical activities to maintain their health without exacerbating their condition.
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