A nurse is monitoring a client who is receiving warfarin and has an INR of 4 (0.8 to 1.1). Which of the following medications should the nurse plan to administer?
Vitamin K.
Protamine.
Calcium gluconate.
Epinephrine.
The Correct Answer is A
Choice A rationale
An INR (International Normalized Ratio) of 4.0 indicates that the client's blood is much thinner than the therapeutic range for most conditions (usually 2.0-3.0 for warfarin). This significantly increases the risk of bleeding. Vitamin K is the antidote for warfarin because it is essential for the synthesis of clotting factors (II, VII, IX, X) in the liver. Administering vitamin K reverses the anticoagulant effect of warfarin, reducing the risk of hemorrhage by promoting the production of functional clotting proteins.
Choice B rationale
Protamine sulfate is the antidote for heparin. It works by forming a stable ion pair with heparin, neutralizing its anticoagulant effects. It has no effect on the anticoagulant properties of warfarin, which acts by inhibiting vitamin K epoxide reductase, an enzyme crucial for the regeneration of active vitamin K necessary for clotting factor synthesis. Therefore, protamine is not indicated for warfarin overdose.
Choice C rationale
Calcium gluconate is used to treat hypocalcemia and magnesium toxicity. Calcium plays a vital role in numerous physiological processes, including bone health and muscle function, and is essential for blood coagulation. However, it does not directly counteract the effects of warfarin, which targets vitamin K-dependent clotting factors, and is not the appropriate antidote for an elevated INR.
Choice D rationale
Epinephrine is a potent vasoconstrictor and bronchodilator used in anaphylaxis, cardiac arrest, and severe asthma. It acts on alpha and beta-adrenergic receptors, leading to increased heart rate, blood pressure, and bronchodilation. It has no role in reversing the anticoagulant effects of warfarin and is not indicated for managing an elevated INR.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
Choice A rationale
Ipratropium is an anticholinergic bronchodilator that blocks muscarinic receptors in the bronchial smooth muscle, leading to bronchodilation. A common adverse effect of anticholinergic medications is reduced salivary gland secretion, resulting in xerostomia, or dry mouth, due to inhibition of parasympathetic stimulation.
Choice B rationale
Periorbital edema is not a typical adverse effect of ipratropium. This medication primarily targets muscarinic receptors in the respiratory tract. Edema, particularly around the eyes, is more commonly associated with allergic reactions or fluid retention from other medications.
Choice C rationale
Ipratropium, being an anticholinergic, primarily acts on M3 receptors in the lungs and has minimal systemic absorption, thus rarely causing bradycardia. In fact, anticholinergics can sometimes cause a mild increase in heart rate due to blockade of M2 receptors in the heart, but clinically significant changes are uncommon.
Choice D rationale
While xerostomia can contribute to dental issues over time due to reduced saliva's protective effects, dental caries is not a direct, acute adverse effect of ipratropium itself. It is a potential long-term complication of prolonged dry mouth, rather than a direct drug-induced effect to monitor immediately.
Correct Answer is ["C","D"]
Explanation
Choice A rationale
An elevated troponin level indicates myocardial injury or infarction. While severe acetaminophen toxicity can rarely lead to cardiac dysfunction, it is not a primary or common finding. The main organ affected is the liver due to the formation of toxic metabolites.
Choice B rationale
Hyperglycemia is not a typical finding in acetaminophen toxicity. Liver damage can impair glucose regulation, but the immediate and common metabolic derangements are usually related to liver enzyme elevation and acid-base imbalances, not primary glucose elevation.
Choice C rationale
Increased alanine aminotransferase (ALT) level is a critical indicator of hepatotoxicity, the primary concern in acetaminophen overdose. N-acetyl-p-benzoquinone imine (NAPQI), a toxic metabolite, depletes glutathione, leading to hepatocellular necrosis and leakage of intracellular enzymes like ALT (normal range 7–55 U/L).
Choice D rationale
Abdominal discomfort is a common finding in acetaminophen toxicity, particularly as liver damage progresses. This discomfort, often described as right upper quadrant pain, results from hepatocellular injury and inflammation, potentially accompanied by hepatic swelling.
Choice E rationale
Diaphoresis, or excessive sweating, is an early and non-specific symptom of acute acetaminophen overdose. It often accompanies other initial gastrointestinal symptoms like nausea and vomiting, occurring as the body attempts to excrete the drug and in response to initial metabolic stress.
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