ATI RN
Genitourinary Assessment in Pediatrics Questions
Question 1 of 5
Hemorrhagic cystitis can occur in response to all the following EXCEPT
Correct Answer: D
Rationale: In this case, the correct answer is D) amyloidosis. Hemorrhagic cystitis is a condition characterized by inflammation and bleeding of the bladder, commonly caused by certain medications like cyclophosphamide, infections like adenovirus, and immunosuppressive drugs like cyclosporine. Amyloidosis, on the other hand, is a condition where abnormal protein buildup can affect various organs but does not directly lead to hemorrhagic cystitis. Cyclophosphamide is a known cause of hemorrhagic cystitis as it can irritate the bladder lining. Adenovirus infection can also lead to hemorrhagic cystitis due to the viral impact on the bladder. Cyclosporine, an immunosuppressive medication, can cause bladder irritation and bleeding, contributing to hemorrhagic cystitis. In an educational context, understanding the potential causes of hemorrhagic cystitis in pediatric patients is crucial for healthcare providers involved in their care. It helps in prompt identification of the underlying issue and appropriate management to prevent complications. This knowledge aids in ensuring the well-being of pediatric patients undergoing treatments that may predispose them to such conditions.
Question 2 of 5
When you investigate for first attack of minimal change nephrotic syndrome (MCNS), one of the following is TRUE
Correct Answer: A
Rationale: In investigating the first attack of minimal change nephrotic syndrome (MCNS) in children, the correct answer is A) microscopic hematuria is present in 20% of children. This is true because while hematuria is not a common feature of MCNS, it can be present in a small percentage of cases. Option B) spot urine protein:creatinine ratio should be <2.0 is incorrect because in MCNS, the proteinuria is usually massive and the ratio is typically much higher than 2.0. Option C) serum complement levels are low is incorrect because MCNS is not associated with low complement levels. Option D) renal biopsy is routinely performed is incorrect because MCNS is a clinical diagnosis and renal biopsy is not routinely performed unless there are atypical features present. Educationally, understanding the nuances of MCNS presentation in pediatric patients is crucial for healthcare providers involved in the care of children with renal conditions. Recognizing the atypical features and knowing when to consider further investigations like renal biopsy is essential for accurate diagnosis and appropriate management of MCNS.
Question 3 of 5
Congenital nephrotic syndrome is defined as nephrotic syndrome manifesting at birth or within the first 3 months of life. The etiologies include all the following EXCEPT
Correct Answer: D
Rationale: The correct answer is D) infantile systemic lupus erythematosus. Congenital nephrotic syndrome is a rare condition characterized by the presence of nephrotic syndrome at birth or within the first three months of life. The etiology of congenital nephrotic syndrome can be diverse, but infantile systemic lupus erythematosus is not typically associated with this condition. Option A) syphilis can lead to congenital nephrotic syndrome due to the inflammatory response caused by the infection affecting the kidneys. Option B) herpes infection can also cause nephrotic syndrome in newborns due to direct viral invasion of the kidneys. Option C) mercury exposure can damage the kidneys and result in nephrotic syndrome. Educationally, understanding the etiologies of congenital nephrotic syndrome is crucial for healthcare providers working with pediatric populations. Recognizing the various causes can aid in early diagnosis and appropriate management of this condition, leading to better outcomes for affected infants. It is essential to differentiate between different etiologies to provide targeted and effective treatment.
Question 4 of 5
Urinalysis in patients with Fanconi syndrome may show all the following EXCEPT
Correct Answer: D
Rationale: In patients with Fanconi syndrome, there is a defect in the proximal tubule of the kidney leading to impaired reabsorption of various substances. The correct answer is D) elevated urinary sodium. In Fanconi syndrome, there is increased excretion of substances like glucose, uric acid, amino acids, and bicarbonate, which can result in glycosuria, uricosuria, and alkaline urine pH. Option A) urine pH is alkaline is incorrect because Fanconi syndrome can lead to a decreased ability to reabsorb bicarbonate, resulting in a more acidic urine pH. Option B) glycosuria is correct because the impaired renal tubules in Fanconi syndrome lead to the loss of glucose in the urine. Option C) uricosuria is correct as well because there is increased excretion of uric acid in the urine due to the tubular defect in Fanconi syndrome. Educationally, understanding the characteristic findings in Fanconi syndrome helps healthcare providers diagnose and manage this condition effectively. Recognizing the pattern of electrolyte and solute abnormalities in urinalysis can aid in early identification and intervention in pediatric patients with Fanconi syndrome.
Question 5 of 5
Nephrogenic diabetes insipidus is a disorder of water metabolism characterized by an inability to concentrate urine, even in the presence of antidiuretic hormone. Of the following, the LEAST likely cause is
Correct Answer: D
Rationale: Nephrogenic diabetes insipidus (NDI) is characterized by the kidney's inability to respond to antidiuretic hormone (ADH), leading to the inability to concentrate urine. Chronic hyperglycemia (Option D) is the least likely cause of NDI among the provided options. The correct answer is D because chronic hyperglycemia does not directly interfere with the kidney's response to ADH. The other options, genetic mutations (Option A), lithium toxicity (Option B), and hypercalcemia (Option C), are known causes of NDI as they can disrupt the normal functioning of the renal tubules, affecting water reabsorption. In an educational context, understanding the etiology of NDI is crucial for healthcare professionals, especially when assessing and managing pediatric patients with this condition. Recognizing the different causes of NDI helps in accurate diagnosis and appropriate treatment selection. This knowledge is vital for pharmacology students and healthcare practitioners to provide optimal care for patients with genitourinary disorders.