The urinalysis results for a client diagnosed with chronic kidney disease (CKD) indicate the presence of protein in the urine. The impairment of which structure within the kidney results in proteinuria?
Loop of Henle.
Glomerulus.
Distal convoluted tubule.
Bowman’s capsule.
The Correct Answer is B
Choice A reason: The loop of Henle regulates water and electrolyte reabsorption, not protein filtration. Proteinuria results from glomerular damage, allowing proteins to leak into urine. The loop’s role in concentration does not involve protein handling, making it incorrect for the structure impaired in CKD-related proteinuria.
Choice B reason: The glomerulus filters blood, normally preventing large proteins from entering urine. In CKD, glomerular damage (e.g., from hypertension or diabetes) increases permeability, causing proteinuria. This is a hallmark of glomerular injury, aligning with CKD’s pathophysiology, making the glomerulus the correct structure responsible for proteinuria.
Choice C reason: The distal convoluted tubule regulates electrolytes and acid-base balance, not protein filtration. Proteinuria stems from glomerular dysfunction, not tubular issues. The distal tubule’s role in reabsorption does not involve proteins, making it incorrect for the structure causing proteinuria in chronic kidney disease.
Choice D reason: Bowman’s capsule collects glomerular filtrate but does not filter proteins itself. Proteinuria occurs due to glomerular barrier damage, allowing proteins to pass into the capsule. While adjacent, the capsule is not the primary impaired structure, making the glomerulus the correct choice for CKD-related proteinuria.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
Choice A reason: Macrophages, lymph, and cytokines are part of the innate immune response, acting after pathogens breach initial barriers. First-line defenses are physical and chemical barriers like mucosa and secretions, not immune cells or fluids. This choice represents secondary defenses, making it incorrect for the primary barrier role.
Choice B reason: Lung epithelium, gastric mucosa, and tears are first-line defenses, preventing pathogen entry. Lung cilia trap microbes, gastric acid kills bacteria, and tears’ lysozymes neutralize pathogens. These physical and chemical barriers form the body’s initial protection, aligning with immunology principles for primary defense against infection.
Choice C reason: Interferon, T cells, and neutrophils are part of adaptive and innate immunity, activated after pathogen penetration. First-line defenses involve barriers like mucosa, not immune mediators or cells. This choice describes secondary immune responses, making it incorrect for the initial protective structures in humans.
Choice D reason: Thymus, bone marrow, and pancreas are involved in immune cell production and metabolism, not direct pathogen defense. First-line defenses are external barriers like lung epithelium or tears. These internal organs support immunity but are not primary barriers, making this incorrect for first-line defense structures.
Correct Answer is C
Explanation
Choice A reason: Hypertensive crisis is not a feature of Addison’s disease, which causes hypotension due to cortisol and aldosterone deficiency. Cortisol kits address adrenal insufficiency during stress, not hypertension. This choice is incorrect, as it misaligns with Addison’s pathophysiology and cortisol’s role.
Choice B reason: Cortisol is not used for systemic allergic reactions, which require antihistamines or epinephrine. Addison’s patients need cortisol for adrenal insufficiency during stress, as their bodies cannot produce it. This choice is incorrect, as cortisol kits address hypoadrenalism, not anaphylaxis.
Choice C reason: Addison’s disease involves adrenal insufficiency, impairing cortisol production. Stress increases cortisol demand, which the patient cannot meet, risking adrenal crisis. Carrying a cortisol kit allows rapid administration during stress, preventing life-threatening hypotension or shock, aligning with endocrinology evidence for Addison’s management.
Choice D reason: Hyperglycemia is unrelated to Addison’s disease, which does not typically affect glucose metabolism. Cortisol kits address adrenal insufficiency, not blood glucose. This choice is incorrect, as cortisol replacement is for stress-induced hypoadrenalism, not glycemic control, per Addison’s pathophysiological basis.
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