ATI RN
Pediatric GU Disorders Test Bank Questions Questions
Question 1 of 5
Complications of chronic kidney disease (CKD) MOSTLY do not manifest until at least stage of
Correct Answer: D
Rationale: In pediatric pharmacology, understanding the progression and complications of chronic kidney disease (CKD) is crucial for safe and effective patient care. The correct answer, option D, 4 CKD, is the most appropriate choice because complications of CKD typically do not manifest until the advanced stages of the disease. By stage 4 CKD, the kidneys have significantly reduced function, leading to a buildup of waste products and fluid imbalance in the body, which can result in severe complications such as anemia, bone disease, and cardiovascular issues. Option A, 1 CKD, is incorrect because in stage 1 CKD, kidney damage is present but with normal or high glomerular filtration rate (GFR) and generally no symptoms or complications. Option B, 2 CKD, is also incorrect as symptoms and complications in CKD are usually not prominent at this stage either, although there may be mild abnormalities in kidney function. Option C, 3 CKD, is closer to the correct answer, but complications typically become more pronounced and severe in stage 4 CKD. For educators, it is important to emphasize the progressive nature of CKD in pediatric patients, highlighting the need for early detection and management to prevent or delay complications. Teaching students to recognize the stages of CKD and understand the associated clinical implications will better prepare them to provide comprehensive care for pediatric patients with renal disorders.
Question 2 of 5
Potter syndrome may have all the following EXCEPT
Correct Answer: D
Rationale: Potter syndrome, also known as Potter sequence or oligohydramnios sequence, is a rare condition characterized by a group of physical features present at birth. The correct answer is D) pulmonary hypoplasia because this is a typical feature of Potter syndrome. Pulmonary hypoplasia refers to underdevelopment of the lungs, which is a key component of the syndrome due to the lack of amniotic fluid in utero, leading to inadequate lung development. Option A) flat face is a common characteristic of Potter syndrome due to the abnormal positioning of the fetus in the uterus as a result of the lack of amniotic fluid. Option B) clubfeet can also be seen in Potter syndrome as part of the physical abnormalities present at birth. Option C) cardiac abnormalities are often associated with Potter syndrome due to the impact of renal agenesis or dysplasia on fetal development, leading to cardiac defects. Educationally, understanding the features of Potter syndrome is crucial for healthcare professionals working in pediatrics, obstetrics, and neonatology. Recognizing these characteristic physical features can aid in early diagnosis and management of the condition, leading to better outcomes for affected infants. It also highlights the importance of prenatal care and monitoring to detect such conditions early in pregnancy.
Question 3 of 5
Approximately 75% of filtered bicarbonate is reabsorbed in the
Correct Answer: B
Rationale: In the context of pediatric GU disorders, understanding the renal handling of bicarbonate is crucial for managing acid-base balance. The correct answer is B) proximal tubule. In the proximal tubule, approximately 75% of filtered bicarbonate is reabsorbed through multiple mechanisms, including the action of carbonic anhydrase which converts bicarbonate to carbon dioxide and water, allowing for reabsorption. This process helps maintain acid-base balance in the body. Now, let's analyze why the other options are incorrect: A) Juxtaglomerular apparatus: This structure is primarily involved in regulating blood pressure and kidney function through the release of renin. It is not directly involved in bicarbonate reabsorption. C) Loop of Henle: The loop of Henle is responsible for concentrating urine and reabsorption of water and electrolytes, but not specifically for bicarbonate reabsorption. D) Distal tubule: The distal tubule is involved in fine-tuning electrolyte balance, particularly sodium and potassium, but it is not a major site for bicarbonate reabsorption. Understanding the site and mechanisms of bicarbonate reabsorption in the pediatric population is essential for diagnosing and managing acid-base disorders, electrolyte imbalances, and renal pathologies. It also provides a foundation for understanding the pharmacological interventions that may be necessary to correct imbalances in pediatric patients with GU disorders.
Question 4 of 5
Polyuria seen in diabetes mellitus
Correct Answer: B
Rationale: In this question, the correct answer is option B) renal obstruction. Polyuria is excessive urination, a common symptom in diabetes mellitus due to the high blood sugar levels. In diabetes mellitus, polyuria occurs as a result of the osmotic diuresis caused by the presence of glucose in the urine, leading to increased urine output. Option A) central and nephrogenic diabetes insipidus is incorrect because these conditions are not typically associated with diabetes mellitus. Diabetes insipidus is a separate disorder characterized by the inability to concentrate urine, leading to excessive dilute urine output. Option C) renal dysplasia is also incorrect as it is a congenital condition affecting the development of the kidneys and is not directly related to polyuria seen in diabetes mellitus. Option D) hyperkalemia is incorrect because while electrolyte disturbances can occur in diabetes mellitus, hyperkalemia is not the primary electrolyte disorder associated with polyuria in this condition. Educationally, understanding the pathophysiology of polyuria in diabetes mellitus is crucial for healthcare professionals managing pediatric patients with this condition. Recognizing the underlying mechanisms of polyuria helps in appropriate diagnosis and management to prevent complications associated with fluid and electrolyte imbalances.
Question 5 of 5
On routine checkup of three years old boy
Correct Answer: D
Rationale: In this scenario, the correct answer is D) urinary tract obstruction. A positive nitrite test in the general urine examination of a three-year-old boy could indicate a urinary tract infection (UTI). UTIs are common in children and can be associated with urinary tract obstructions. Option A is incorrect because a positive nitrite test in a routine checkup should not be dismissed as a false positive without further investigation, especially in a pediatric patient where UTIs can have serious implications. Option C, frequent voiding, is less likely to cause a positive nitrite test compared to a urinary tract obstruction. Frequent voiding may be indicative of other issues like bladder dysfunction but is not directly related to a positive nitrite test. Educationally, this question highlights the importance of recognizing red flags in routine check-ups that may indicate underlying health issues in pediatric patients. Understanding the significance of specific test results in different clinical contexts is crucial for healthcare providers working with children.