Which laboratory test is crucial for the diagnosis of sickle cell anemia?
Serum ferritin level
Hemoglobin A1C
Complete blood count (CBC)
Hemoglobin electrophoresis
The Correct Answer is D
A. Serum ferritin reflects the total iron stores within the body and is a critical marker for diagnosing iron deficiency or hereditary hemochromatosis. While patients with sickle cell disease may develop high ferritin levels due to chronic hemolysis or blood transfusions, it is not diagnostic. Ferritin cannot detect the qualitative defects in the hemoglobin molecule that define the sickle cell genotype and phenotype.
B. Hemoglobin A1C measures the percentage of hemoglobin that is chemically linked to sugar, providing an average blood glucose level over 3 months. This test is utilized exclusively for the diagnosis and management of diabetes mellitus and has no utility in identifying hemoglobinopathies. It does not provide information regarding the structure or percentage of fetal or sickle hemoglobin present in the patient's blood.
C. A complete blood count provides quantitative data on red blood cells, white blood cells, and platelets, identifying the presence of anemia. While a CBC may show decreased hemoglobin and hematocrit in a sickle cell patient, it cannot distinguish sickle cell from other forms of anemia. Without further specialized testing, a clinician cannot confirm the presence of hemoglobin S based on a standard hematology profile alone.
D. Hemoglobin electrophoresis is the definitive diagnostic procedure for identifying abnormal hemoglobin variants by separating them based on their unique electrical charges. This laboratory technique allows for the precise identification of hemoglobin S and can distinguish between sickle cell trait and sickle cell disease. It is the essential test for confirming the diagnosis of this genetic disorder by visualizing the migration patterns of different globins.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
A. Interstitial lung disease is the prototypical restrictive lung disorder characterized by inflammation and progressive fibrosis of the alveolar structures. This pathological scarring increases the elastic recoil of the lungs, resulting in significantly decreased lung compliance and reduced total lung capacity. The physiological hallmark is an inability of the lungs to fully expand during the inspiratory phase of the respiratory cycle.
B. A prolonged cough with sputum production in a farmer often suggests an obstructive pathology such as asthma or chronic bronchitis from organic dust exposure. Obstructive disorders are defined by increased airway resistance and air trapping rather than a reduction in the total volume the lungs can hold. These patients typically demonstrate a decreased FEV1 to FVC ratio, which is not characteristic of pure restrictive disease.
C. Chronic obstructive pulmonary disease is a clinical diagnosis encompassing emphysema and chronic bronchitis, both of which are strictly categorized as obstructive lung diseases. These conditions involve permanent enlargement of air spaces and airway narrowing that prevents efficient exhalation of air from the distal units. Consequently, the lungs become hyperinflated over time, which is the functional opposite of the volume restriction seen in fibrosis.
D. Chronic bronchitis is an obstructive pulmonary condition defined by chronic inflammation of the bronchial mucosa and hypertrophy of mucus-secreting glands. This leads to productive coughing and narrowing of the conducting airways, which increases resistance to expiratory airflow. Unlike restrictive disorders, it does not involve the parenchymal stiffening or the reduction in lung volumes associated with interstitial or extra-pulmonary restrictive pathologies.
Correct Answer is D
Explanation
A. Allergic reactions and hypersensitivity represent an overactive or inappropriate immune response to non-pathogenic environmental antigens. These are characteristic of atopic disorders and autoimmune conditions rather than a lack of immune function. Immunodeficiency involves a deficit in the defense mechanisms, which is the functional opposite of the hyper-responsiveness seen in allergies.
B. An increased sensitivity to infections is a general symptom of a weakened immune system, but it lacks the clinical specificity of the disorder's true hallmark. While these patients do get sick more often, this term does not describe the severity or the atypical nature of the pathogens involved. It is a simplified description of the complex immune failure.
C. Remission of autoimmune diseases is not a characteristic of immunodeficiency; in fact, many primary immunodeficiencies are paradoxically associated with a higher risk of autoimmunity. The lack of proper immune regulation can lead to a loss of self-tolerance. Therefore, an immunodeficient state does not typically lead to the resolution of existing autoimmune pathologies.
D. A tendency to develop unusual, recurrent, or unusually severe infections is the definitive clinical hallmark of immunodeficiency disorders. These individuals often suffer from opportunistic infections caused by organisms that do not typically affect healthy people. The frequency, duration, and poor response to standard antibiotic therapy signal a profound defect in the host's immune surveillance.
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