ATI RN
Cardiovascular Drugs Pharmacology Questions
Question 1 of 5
Which of the following drugs was most likely included in the immediate medical treatment of the 63-year-old woman with symptoms of dyspnea?
Correct Answer: D
Rationale: The correct answer is D: Epinephrine. Epinephrine is a vasopressor and bronchodilator used in emergency situations like dyspnea to improve breathing and increase blood pressure. Hydrochlorothiazide and Amiloride are diuretics used to treat hypertension and edema, not acute dyspnea. Mannitol is an osmotic diuretic used to reduce intracranial pressure, not for dyspnea. Epinephrine is the most appropriate choice for immediate relief of dyspnea due to its bronchodilator effects and ability to improve breathing quickly.
Question 2 of 5
Which one of the following drugs increase digoxin plasma concentration by a pharmacokinetic mechanism?
Correct Answer: D
Rationale: The correct answer is D) Quinidine. Quinidine is known to increase digoxin plasma concentration by a pharmacokinetic mechanism. Quinidine competes with digoxin for renal tubular secretion, leading to reduced excretion of digoxin and ultimately higher plasma concentrations of digoxin. Option A) Captopril is an angiotensin-converting enzyme (ACE) inhibitor used to treat hypertension. It does not have a direct impact on digoxin plasma concentration. Option B) Hydrochlorothiazide is a diuretic that acts on the kidneys to increase urine output. It does not interact with digoxin to increase its plasma concentration. Option C) Lidocaine is a local anesthetic that does not affect digoxin plasma concentration through pharmacokinetic mechanisms. Educationally, understanding drug interactions is crucial for healthcare professionals to ensure safe and effective treatment for patients. Knowing how different drugs can affect each other's pharmacokinetics helps in preventing adverse reactions and optimizing therapeutic outcomes. In this case, recognizing that quinidine can increase digoxin levels is important for managing patients who are on both medications to avoid potential toxicity.
Question 3 of 5
The action of digitalis is enhanced by
Correct Answer: B
Rationale: The correct answer is B) Calcium. To understand why, we need to delve into the pharmacology of digitalis. Digitalis, such as digoxin, is a medication commonly used in the management of heart failure and certain arrhythmias. It exerts its therapeutic effects by inhibiting the sodium-potassium ATPase pump in cardiac myocytes, leading to an increase in intracellular sodium and subsequently an increase in intracellular calcium levels. This increase in intracellular calcium enhances the contractility of the heart muscle, improving cardiac output. Calcium plays a crucial role in the mechanism of action of digitalis. Therefore, the action of digitalis is enhanced by an increase in calcium levels. This is why option B is correct. Now, let's discuss why the other options are incorrect: A) Sodium: While digitalis does affect sodium levels intracellularly, it is not the primary mechanism by which digitalis exerts its therapeutic effects. Therefore, sodium does not enhance the action of digitalis. C) Magnesium: Magnesium levels can influence cardiac function, but they do not directly enhance the action of digitalis. Magnesium is more relevant in the context of arrhythmias rather than enhancing digitalis action. D) Potassium: Potassium levels are important in cardiac function, but they do not enhance the action of digitalis. In fact, low potassium levels can increase the risk of digitalis toxicity. In an educational context, understanding the pharmacology of cardiovascular drugs like digitalis is essential for healthcare professionals, especially those involved in managing patients with heart failure or arrhythmias. Understanding how different electrolytes and ions interact with these medications can help in optimizing therapy and preventing potential complications.
Question 4 of 5
The earliest toxic symptom of chronic digitalis administration is
Correct Answer: C
Rationale: In the context of cardiovascular drugs pharmacology, understanding the toxic effects of chronic digitalis administration is crucial. The correct answer is C) Anorexia, nausea, vomiting. This is because the earliest toxic symptoms of digitalis toxicity often involve the gastrointestinal system. Anorexia, nausea, and vomiting are commonly observed due to the drug's effects on the chemoreceptor trigger zone in the brain, leading to disturbances in the gastrointestinal tract. Option A) Altered color vision is a known symptom of digitalis toxicity, but it typically occurs at higher and later stages of toxicity. It is not usually the earliest symptom to manifest. Option B) Psychic symptoms such as confusion, hallucinations, or changes in mood can occur with digitalis toxicity, but they also tend to present at a more advanced stage. Option D) Retrosternal pain is not a typical early symptom of digitalis toxicity. It is more commonly associated with other conditions like angina or myocardial infarction. Educationally, recognizing the early signs of drug toxicity is essential for healthcare providers involved in patient care. Understanding the progression of symptoms can aid in early detection and intervention to prevent serious complications. This knowledge is particularly vital in the management of patients on digitalis therapy to ensure their safety and well-being.
Question 5 of 5
The client is given an alpha agonist. What might it be used for?
Correct Answer: A
Rationale: In this scenario, the correct answer is A) For hemostasis. Alpha agonists, such as drugs like epinephrine or norepinephrine, are commonly used in medicine to promote hemostasis, which refers to the stopping of bleeding. When an alpha agonist is administered, it causes vasoconstriction by stimulating alpha-adrenergic receptors on blood vessels. This vasoconstriction helps to reduce blood flow to the site of injury, thereby aiding in the cessation of bleeding. Now, let's explore why the other options are incorrect: B) To dilate the arteries: This is incorrect because alpha agonists typically cause vasoconstriction, not dilation, of arteries. C) To dilate the veins: This is also incorrect as alpha agonists primarily target alpha-adrenergic receptors causing vasoconstriction, not dilation, of veins. D) To decrease afterload: While alpha agonists can affect vascular tone and impact afterload, their primary effect is not to decrease afterload but rather to promote hemostasis through vasoconstriction. In an educational context, understanding the pharmacology of cardiovascular drugs is crucial for healthcare professionals to make informed decisions regarding drug therapy for their patients. Knowing the specific actions and uses of different drug classes, such as alpha agonists, can help healthcare providers optimize patient care and outcomes in various clinical situations, including managing bleeding episodes.