I reduce insulin resistance and may also decrease glucose production. I am used as an adjunct to diet and exercise to improve glycemic control. I am usually well tolerated and most common side effects are upper respiratory tract infection, headache, sinusitis and myalgia. I go by the name of pioglitazone (Actos). What class of oral hypoglycemic am I ?
Bile-acid sequestrant
Thiazolidinedione
Alpha-Glucosidase Inhibitor
Non-insulin injectable drug
The Correct Answer is B
A. Bile-acid sequestrants, such as colesevelam, primarily lower serum cholesterol levels. While they may have a modest effect on glucose levels, they do not directly improve insulin sensitivity or significantly reduce hepatic glucose production, which are the main mechanisms of pioglitazone.
B. Thiazolidinediones (TZDs), including pioglitazone (Actos) and rosiglitazone, are oral hypoglycemic agents used for type 2 diabetes mellitus. They work by activating peroxisome proliferator-activated receptor gamma (PPAR-γ) receptors in adipose, muscle, and liver tissue. This leads to enhanced insulin sensitivity, improved glucose uptake in peripheral tissues, and modest reduction in hepatic glucose production. TZDs are used as adjuncts to diet and exercise to improve glycemic control. They are usually well tolerated, with common side effects including upper respiratory tract infection, headache, sinusitis, and myalgia. However, nurses should monitor for weight gain, fluid retention, edema, and signs of heart failure, which are rare but serious adverse effects.
C. Alpha-glucosidase inhibitors (e.g., acarbose, miglitol) work by slowing carbohydrate absorption in the small intestine to reduce postprandial hyperglycemia. They do not improve insulin sensitivity or reduce hepatic glucose production, so they are mechanistically different from TZDs.
D. Non-insulin injectable drugs, such as GLP-1 receptor agonists (e.g., liraglutide, dulaglutide), are injectable agents that enhance glucose-dependent insulin secretion, slow gastric emptying, and promote satiety. Pioglitazone is an oral agent, not an injectable.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is D
Explanation
A. Levothyroxine dosing is based on thyroid hormone levelsand patient response. The interaction with warfarin does not require reducing levothyroxine; in fact, reducing it unnecessarily could lead to hypothyroidism.
B. Levothyroxine increases the metabolism of vitamin K-dependent clotting factors, which can enhance the anticoagulant effect of warfarin. Reducing warfarin preemptively is not recommended without monitoring, as dose adjustments should be guided by INR results.
C. There is no interaction that necessitates increasing levothyroxine when warfarin is used. Thyroid dosing is independent of warfarin therapy.
D. Starting levothyroxine in a patient taking warfarin can enhance warfarin’s anticoagulant effect, increasing the risk of bleeding. In practice, the provider may need to adjust warfarin dosingbased on INR monitoring, especially during the initial weeks after starting or changing levothyroxine. The nurse should notify the provider so INR can be closely monitoredand warfarin dosage adjusted accordingly.
Correct Answer is D
Explanation
A. A low BUN is not indicative of diabetic nephropathy. In fact, elevated BUN and creatinineare late signs of kidney dysfunction. Early diabetic nephropathy is usually detected before BUN rises.
B. Ketonuria is more indicative of diabetic ketoacidosis (DKA), which is an acute complication of uncontrolled diabetes, not a chronic kidney complication like nephropathy.
C. This value likely refers to 6.6%, which indicates blood glucose control over the last 2–3 months. Poor glycemic control increases the risk for nephropathy, but HbA1c alone does not confirm kidney damage.
D. Microalbuminuria refers to small amounts of albumin in the urineand is one of the earliest detectable signs of diabetic nephropathy. It indicates kidney damage caused by chronic hyperglycemia. Early detection allows interventions, such as strict glucose control and ACE inhibitors, to slow progression to chronic kidney disease.
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