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{{WBRQuestion
{{WBRQuestion
|QuestionAuthor=Gerald Chi
|QuestionAuthor=Gerald Chi (Reviewed by {{YD}})
|ExamType=USMLE Step 1
|ExamType=USMLE Step 1
|MainCategory=Pharmacology
|MainCategory=Pharmacology
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|MainCategory=Pharmacology
|MainCategory=Pharmacology
|SubCategory=Cardiology
|SubCategory=Cardiology
|MainCategory=Pharmacology
|MainCategory=Pharmacology
|MainCategory=Pharmacology
|MainCategory=Pharmacology
|MainCategory=Pharmacology
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|MainCategory=Pharmacology
|MainCategory=Pharmacology
|SubCategory=Cardiology
|SubCategory=Cardiology
|Prompt=A 58-year-old female comes to the clinic for a routine examination. She reports that she has started an antihypertensive drug recently. Physical examination is normal. Her blood pressure is 130/80 and laboratory studies show total cholesterol 220 mg/dl, LDL 100 mg/dl, HDL 50 mg/dl, triglyceride 350 mg/dl. She states that she has never had abnormal lipid profiles. Which of the following medications is most likely to cause her dyslipidemia?
|Prompt=A 58-year-old woman presents to her physician's office for a routine examination. Upon review of systems, the women states that she is asymptomatic and has no complaints. She reports that she was prescribed an antihypertensive drug by another primary care physician 6 months ago and has been taking one tablet each day. In the clinic, she is afebrile with a blood pressure of 130/80 mmHg, heart rate of 58/min, and respiratory rate of 14/min. Physical examination is unremarkable. Laboratory work-up demonstrates a total cholesterol concentration of 220 mg/dl, LDL-C of 100 mg/dl, HDL-C of 50 mg/dl, triglyceride concentration of 350 mg/dl. Upon further questioning, she states that she never had abnormal lipid profiles in the past. Which of the following antihypertensive drugs is the patient most likely receiving?
|Explanation=Adverse effects associated with β2-adrenergic antagonism include bronchospasm, peripheral vasoconstriction, and alteration of glucose and lipid metabolism.  
|Explanation=The patient is most likely receiving a beta blocker. Beta-blockers are antihypertensive, sympatholytic agents that reduce the cardiac output by binding to beta-adrenoreceptors present in the cardiac nodal tissue, thereby decreasing the number of unoccupied receptors available for norepinephrine and epinephrine to bind to. Beta blockers bind to may be either cardioselective (B1 blockade > B2 blockade) or non-selective (both B1 and B2 blockade). Adverse effects associated with the undesired β2-adrenergic antagonism include bradycardia (heart rate < 60/min), bronchospasm, peripheral vasoconstriction, and alteration of glucose and lipid metabolism. These effects are typically observed with administration of non-selective beta blockers or at higher doses of cardioselective beta blockers.
|AnswerA=Prazosin
|AnswerA=Prazosin
|AnswerAExp='''Incorrect'''<BR>Prazosin is an alpha1-adrenergic antagonist and can cause side effects of orthostatic hypotension and nasal congestion.
|AnswerAExp=Prazosin is an alpha-1 adrenergic antagonist (alpha blocker). Prazosin is typically associated with orthostatic hypotension and nasal congestion.
|AnswerB=Lisinopril
|AnswerB=Lisinopril
|AnswerBExp='''Incorrect'''<BR>Lisinopril is an angiotensin-converting enzyme inhibitor and may cause dry cough and hyperkalemia.
|AnswerBExp=Lisinopril is an angiotensin-converting enzyme inhibitor (ACE-I). ACE-I are typically associated with cough and hyperkalemia.
 
|AnswerC=Clonidine
|AnswerC=Clonidine
|AnswerCExp='''Incorrect'''<BR>Clonidine is a centrally acting alpha2-agonist and has the adverse effects of lightheadednes, dry mouth, dizziness, constipation, and hypotension.
|AnswerCExp=Clonidine is a centrally acting alpha-2 agonist. Clonidine is typically associated with lightheadednes, dry mouth, dizziness, constipation, and hypotension.
 
|AnswerD=Atenolol
|AnswerD=Atenolol
|AnswerDExp='''Correct'''<BR> Atenolol is a non-selective beta blocker and may cause dyslipidemia.
|AnswerDExp=Atenolol is a non-selective beta blocker. Beta blockers are typically associated with bradycardia and dyslipidemia.
|AnswerE=Verapamil
|AnswerE=Verapamil
|AnswerEExp='''Incorrect'''<BR>Verapamil is a non-dihydropyridine calcium channel blocker which has vasodilatory and negative inotropic, chronotropic, and dromotropic effects. Common side effects are dizziness, constipation, gastroesophageal reflux, and peripheral edema.
|AnswerEExp=Verapamil is a non-dihydropyridine calcium channel blocker (CCB). Non-dihydropyridine CCBs are typically associated with constipation and GI distress.
 
|EducationalObjectives=Beta-blockers are antihypertensive, sympatholytic agents that reduce the cardiac output by binding to beta-adrenoreceptors present in the cardiac nodal tissue, thereby decreasing the number of unoccupied receptors available for norepinephrine and epinephrine to bind to. Adverse effects associated with the undesired β2-adrenergic antagonism include bradycardia (heart rate < 60/min), bronchospasm, peripheral vasoconstriction, and alteration of glucose and lipid metabolism.
|RightAnswer=D
|RightAnswer=D
|Approved=No
|Approved=No
}}
}}

Revision as of 21:01, 6 August 2015

 
Author [[PageAuthor::Gerald Chi (Reviewed by Yazan Daaboul, M.D.)]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Pharmacology
Sub Category SubCategory::Cardiology
Prompt [[Prompt::A 58-year-old woman presents to her physician's office for a routine examination. Upon review of systems, the women states that she is asymptomatic and has no complaints. She reports that she was prescribed an antihypertensive drug by another primary care physician 6 months ago and has been taking one tablet each day. In the clinic, she is afebrile with a blood pressure of 130/80 mmHg, heart rate of 58/min, and respiratory rate of 14/min. Physical examination is unremarkable. Laboratory work-up demonstrates a total cholesterol concentration of 220 mg/dl, LDL-C of 100 mg/dl, HDL-C of 50 mg/dl, triglyceride concentration of 350 mg/dl. Upon further questioning, she states that she never had abnormal lipid profiles in the past. Which of the following antihypertensive drugs is the patient most likely receiving?]]
Answer A AnswerA::Prazosin
Answer A Explanation AnswerAExp::Prazosin is an alpha-1 adrenergic antagonist (alpha blocker). Prazosin is typically associated with orthostatic hypotension and nasal congestion.
Answer B AnswerB::Lisinopril
Answer B Explanation AnswerBExp::Lisinopril is an angiotensin-converting enzyme inhibitor (ACE-I). ACE-I are typically associated with cough and hyperkalemia.
Answer C AnswerC::Clonidine
Answer C Explanation AnswerCExp::Clonidine is a centrally acting alpha-2 agonist. Clonidine is typically associated with lightheadednes, dry mouth, dizziness, constipation, and hypotension.
Answer D AnswerD::Atenolol
Answer D Explanation AnswerDExp::Atenolol is a non-selective beta blocker. Beta blockers are typically associated with bradycardia and dyslipidemia.
Answer E AnswerE::Verapamil
Answer E Explanation AnswerEExp::Verapamil is a non-dihydropyridine calcium channel blocker (CCB). Non-dihydropyridine CCBs are typically associated with constipation and GI distress.
Right Answer RightAnswer::D
Explanation [[Explanation::The patient is most likely receiving a beta blocker. Beta-blockers are antihypertensive, sympatholytic agents that reduce the cardiac output by binding to beta-adrenoreceptors present in the cardiac nodal tissue, thereby decreasing the number of unoccupied receptors available for norepinephrine and epinephrine to bind to. Beta blockers bind to may be either cardioselective (B1 blockade > B2 blockade) or non-selective (both B1 and B2 blockade). Adverse effects associated with the undesired β2-adrenergic antagonism include bradycardia (heart rate < 60/min), bronchospasm, peripheral vasoconstriction, and alteration of glucose and lipid metabolism. These effects are typically observed with administration of non-selective beta blockers or at higher doses of cardioselective beta blockers.

Educational Objective: Beta-blockers are antihypertensive, sympatholytic agents that reduce the cardiac output by binding to beta-adrenoreceptors present in the cardiac nodal tissue, thereby decreasing the number of unoccupied receptors available for norepinephrine and epinephrine to bind to. Adverse effects associated with the undesired β2-adrenergic antagonism include bradycardia (heart rate < 60/min), bronchospasm, peripheral vasoconstriction, and alteration of glucose and lipid metabolism.
References: ]]

Approved Approved::No
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