MCQs-Cardiovascular Drugs part 4 I Pharmacology KD Tripathi mcqs part 37

 37.1 The following drug is used to reduce the frequency of

angina pectoris as well as to terminate an acute attack:

A. Isosorbide dinitrate

B. Pentaerythritol tetranitrate

C. Diltiazem

D. Dipyridamole


37.2 Antianginal drugs afford the following benefit/benefits:

A. Terminate anginal attacks

B. Decrease the frequency of anginal attacks

C. Retard the progression of coronary artery disease

D. Both ‘A’ and ‘B’ are correct 


37.3 Choose the correct statement about the action of

nitrates on coronary vessels:

A. They mitigate angina pectoris by increasing total coronary flow

B. They preferentially dilate conducting arteries

without affecting resistance arterioles

C. They preferentially dilate autoregulatory

arterioles without affecting the larger arteries

D. They increase subepicardial blood flow without

affecting subendocardial blood flow


37.4 Organic nitrates have predominantly venodilator action because:

A. They are selectively concentrated in veins

B. Veins express larger quantities of enzymes

that generate nitric oxide from nitrates

C. Venous smooth muscle has greater capacity to relax

D. All of the above are correct 


37.5 Organic nitrates relax vascular smooth muscle by:

A. Increasing intracellular cyclic GMP

B. Increasing intracellular cyclic AMP

C. Decreasing intracellular cyclic AMP

D. Both ‘A’ and ‘C’ are correct 


37.6 Blood flow in the following vascular bed generally

decreases under the influence of glyceryl trinitrate:

A. Coronary

B. Cutaneous

C. Renal

D. Cranial


37.7 Select the organic nitrate which undergoes minimal

first-pass metabolism in the liver:

A. Glyceryl trinitrate

B. Isosorbide dinitrate

C. Isosorbide mononitrate

D. Erythrityl tetranitrate 


37.8 The primary mechanism of beneficial effect of glyceryl

trinitrate in classical angina pectoris is:

A. Increase in total coronary blood flow

B. Redistribution of coronary blood flow

C. Reduction of cardiac preload

D. Reduction of cardiac afterload 


37.9 Nitrate tolerance is least likely to develop with the use of:

A. Sustained release oral glyceryl trinitrate

B. Sublingual glyceryl trinitrate

C. Transdermal glyceryl trinitrate

D. Oral pentaerythritol tetranitrate 


37.10 Glyceryl trinitrate is administered by the following routes except:

A. Oral

B. Sublingual

C. Intramuscular

D. Intravenous 


37.11 Select the drug which can markedly potentiate the

vasodilator action of organic nitrates:

A. Propranolol

B. Fluoxetine

C. Hydrochlorothiazide

D. Sildenafil 


37.12 A patient of acute myocardial infarction being treated

in intensive care unit developed left ventricular failure

with raised central venous pressure. It was decided to

use glyceryl trinitrate. Which route/method of administration

would be most suitable:

A. Sublingual

B. Oral

C. Intravenous bolus injection

D. Slow intravenous infusion 


37.13 A patient suffers from episodic pain diffusely localized

over the chest and upper abdomen, which is relieved

by sublingual glyceryl trinitrate. He could be suffering

from:

A. Angina pectoris

B. Biliary colic

C. Esophageal spasm

D. Any of the above 


37.14 Started within 4-6 hours of acute myocardial infarction,

which of the following drug(s) can reduce the

area of necrosis and the attendant mortality:

A. Propranolol

B. Glyceryl trinitrate

C. Lignocaine

D. Both ‘A’ and ‘B’ are correct


37.15 The dihydropyridines block the following type of

calcium channels:

A. L-type voltage sensitive channels

B. T-type voltage sensitive channels

C. N-type voltage sensitive channels

D. Receptor operated calcium channels


37.16 The antidotal effect of sodium nitrite in cyanide

poisoning is dependent upon:

A. Chemical combination of sodium nitrite with

cyanide

B. Vasodilatation caused by sodium nitrite

C. Conversion of haemoglobin to methaemoglobin

by sodium nitrite

D. Facilitation of cyanocobalamine formation

by sodium nitrite 


37.17 Which of the following drugs is most likely to accentuate

varient (Prinzmetal) angina:

A. Propranolol

B. Atenolol

C. Verapamil

D. Dipyridamole 


37.18 The characteristic feature(s) of dihydropyridine calcium

channel blockers is/are:

A. They have minimal negative inotropic action

on the heart

B. They have no effect on A-V conduction

C. They do not affect the activation-inactivation

kinetics of the calcium channels

D. All of the above 


37.19 Frequency dependent cardiac calcium channel

blockade is exhibited by:

A. Verapamil

B. Nifedipine

C. Felodipine

D. Amlodipine


37.20 The following calcium channel blocker is specifically

indicated to counteract cerebral vasospasm and

neurological sequelae following subarachnoid

haemorrhage:

A. Lacidipine

B. Nimodipine

C. Nicardipine

D. Nitrendipine 


37.21 The following calcium channel blocker should not be

used in patients with ischaemic heart disease:

A. Verapamil sustained release tablet

B. Amlodipine tablet

C. Nifedipine soft geletin capsule

D. Nifedipine extended release tablet


37.22 The following antianginal drug is most likely to produce

tachycardia as a side effect:

A. Amlodipine

B. Nifedipine

C. Diltiazem

D. Verapamil


37.23 The cardiac response to verapamil and nifedipine in

human subjects is:

A. Verapamil causes tachycardia while nifedipine

causes bradycardia

B. Both cause bradycardia

C. Verapamil causes bradycardia while nifedipine

causes tachycardia

D. Both cause tachycardia


37.24 The following is true of nifedipine except:

A. It can aggravate urine voiding difficulty in elderly males with prostatic hypertrophy

B. It promotes Na+ retention by a renal tubular action to cause ankle oedema as side effect

C. It can inhibit insulin release from pancreas

D. At high doses it can paradoxically increase the frequency of angina pectoris


37.25 Which of the following is not an attribute of amlodipine:

A. Generation of an active metabolite

B. Large volume of distribution

C. High and consistent oral bioavailability

D. Long elimination half life


37.26 Propranolol should not be prescribed for a patient of

angina pectoris who is already receiving:

A. Nifedipine

B. Felodipine

C. Verapamil

D. Isosorbide mononitrate


37.27 The short acting dihydropyridine preparations can

aggravate myocardial ischaemia by invoking:

A. Coronary vasospasm

B. Thrombus formation

C. Vagal activation

D. Reflex sympathetic discharge to the heart


37.28 Which of the following drugs is a potassium channel opener:

A. Nicorandil

B. Hydralazine

C. Glibenclamide

D. Amiloride


37.29 Though nitrates and calcium channel blockers are

both vasodilators, they are used concurrently in angina

pectoris, because:

A. They antagonise each other’s side effects

B. Nitrates primarily reduce preload while calcium channel blockers primarily reduce

after-load

C. Nitrates increase coronary flow while calcium

channel blockers reduce cardiac work

D. Both ‘B’ and ‘C’ are correct


37.30 Select the drug which is a potassium channel opener

as well as nitric oxide donor:

A. Diazoxide

B. Sodium nitroprusside

C. Minoxidil

D. Nicorandil


37.31 Select the drug that may improve myocardial

tolerance to ischaemia and reduce anginal attacks

without altering heart rate, blood pressure or

myocardial O2 consumption:

A. Trimetazidine

B. Nicorandil

C. Dipyridamole

D. Nicotinic acid


37.32 Choose the correct statement about trimetazidine:

A. It is a novel calcium channel blocker

B. It improves tissue perfusion by modifying rheological property of blood

C. It is an antianginal drug which acts by nonhaemodynamic mechanisms

D. Both 'A' and 'B' are correct


37.33 A drug which preferentially dilates autoregulatory

coronary arterioles with little effect on large conducting

vessels is likely to:

A. Evoke coronary steal phenomenon

B. Mitigate classical angina but not variant angina

C. Decrease total coronary blood flow in healthy subjects

D. Avert ECG changes of ischaemia


37.34 ‘Coronary steal phenomenon’ has been noted most

frequently with:

A. Glyceryl trinitrate

B. Dipyridamole

C. Propranolol

D. Diltiazem


37.35 The following drug is believed to improve

microcirculation in peripheral vascular diseases by

promoting RBC flexibility:

A. Cyclandelate

B. Theophylline

C. Pentoxiphylline

D. Nicotinic acid


Ans:

37.1 A 37.2 D 37.3 B 37.4 B 37.5 A 37.6 C 37.7 C 37.8 C 37.9 B 37.10 C 37.11 D 37.12 D 37.13 D 37.14 D 37.15 A 37.16 C 37.17 A 37.18 D 37.19 A 37.20 B 37.21 C 37.22 B 37.23 C 37.24 B 37.25 A 37.26 C 37.27 D 37.28 A 37.29 B 37.30 D 37.31 A 37.32 C 37.33 A 37.34 B 37.35 C 

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