Severe or progressive glomerular disease eventually leads to oliguria. Which of the following is a correct "definition" of oliguria?
Urine output <30mL/hour
Absence of urine output
Increased urine output
Urine output>100mL/hour
The Correct Answer is A
A. Urine output <30mL/hour: Oliguria is defined as a markedly reduced urine output, typically less than 400 mL per day or less than 30 mL per hour. It indicates decreased kidney function or perfusion and is common in progressive renal conditions.
B. Absence of urine output: This describes anuria, not oliguria. Anuria is defined as urine output less than 100 mL per day and signifies severe kidney failure or complete urinary tract obstruction.
C. Increased urine output: This describes polyuria, often associated with conditions like uncontrolled diabetes mellitus or diabetes insipidus, not oliguria.
D. Urine output >100mL/hour: This is well above the threshold for oliguria and may suggest diuresis or overhydration. It does not meet the criteria for decreased kidney output.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
A. Nausea: Nausea can occur with peptic ulcers, particularly if gastric emptying is delayed or if inflammation affects the stomach lining. However, it is not the most common or defining symptom.
B. Pain in the epigastric region: Epigastric pain is the hallmark symptom of peptic ulcers. It is typically described as burning or gnawing and may occur between meals or at night, often relieved by eating or antacids.
C. Melena: Melena, or black tarry stools, can occur if the ulcer bleeds, but this is more of a complication than a routine symptom. It indicates gastrointestinal bleeding and requires urgent evaluation.
D. Decreased appetite: Appetite changes may occur, especially if eating exacerbates pain in gastric ulcers. However, decreased appetite is not as frequent or specific a symptom as epigastric pain.
Correct Answer is C
Explanation
A. Bruton's disorder: Also known as X-linked agammaglobulinemia, this is a primary immunodeficiency that results in absent or reduced B cells and recurrent bacterial infections. It does not involve distinct facial features or limb defects as described in the question.
B. SCID: Severe Combined Immunodeficiency involves profound defects in both B and T lymphocyte function, leading to severe infections early in life. It is not associated with the described craniofacial abnormalities or limb deformities.
C. Potter syndrome: This condition is caused by severe oligohydramnios, often due to bilateral renal agenesis, and leads to characteristic physical features including widely spaced eyes with epicanthic folds, low-set ears, a broad or beaked nose, a receding chin, and limb deformities.
D. Down Syndrome: While individuals with Down Syndrome often have characteristic facial features such as upslanting palpebral fissures, flat nasal bridges, and low-set ears, they typically do not have beak-like noses, receding chins, or limb defects in the way described.
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