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Encyclopedia of Health and Medicine

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82 The Cardiovascular System<br />

Fibrates The fibrates work by blocking the<br />

liver’s production <strong>of</strong> LDL <strong>and</strong> VLDL (very lowdensity<br />

lipoprotein), the carriers for triglycerides.<br />

However, fibrates do not lower LDL-C or VLDL-C<br />

in the blood. Rather, they primarily reduce triglycerides<br />

though also raise high-density lipoprotein<br />

cholesterol (HDL-C), the “good” cholesterol. The<br />

most common side effect <strong>of</strong> fibrates is gastrointestinal<br />

distress, which usually disappears after<br />

taking the medication for a few weeks.<br />

COMMON FIBRATES<br />

cl<strong>of</strong>ibrate (Atromid-S)<br />

fen<strong>of</strong>ibrate (Tricor)<br />

gemfibrozil (Lopid)<br />

Statins Statins—or 3-hydroxy-3-methylglutaryl<br />

coenzyme A (HMG-CoA) reductase inhibitors—are<br />

the most commonly prescribed lipid-lowering medications.<br />

They work by blocking the action <strong>of</strong> HMG-<br />

CoA reductase, an enzyme necessary for the liver to<br />

synthesize cholesterol. Statins can lower blood LDL<br />

cholesterol by as much as 35 percent in just three to<br />

six weeks, making them very effective at quickly<br />

lowering the risk for atherosclerosis-related cardiovascular<br />

events. Statins reduce the risk for the progression<br />

<strong>of</strong> CAD, which could improve heart<br />

function after heart attack <strong>and</strong> are part <strong>of</strong> the st<strong>and</strong>ard<br />

medication regimen after heart attack <strong>and</strong><br />

HEART TRANSPLANTATION. Common side effects <strong>of</strong><br />

statins include gastrointestinal distress, fatigue,<br />

headache, <strong>and</strong> sleep disturbances.<br />

COMMON STATINS<br />

atorvastatin (Lipitor)<br />

fluvastatin (Lescol)<br />

lovastatin (Mevacor)<br />

pravastatin (Pravachol)<br />

simvastatin (Zocor)<br />

Selective cholesterol absorption inhibitors The<br />

selective cholesterol absorption inhibitors block<br />

the gastrointestinal tract from absorbing dietary<br />

cholesterol, limiting the cholesterol that enters the<br />

bloodstream. Ezetimibe (Zetia) is currently the<br />

only drug in this classification that is available in<br />

the United States. Doctors <strong>of</strong>ten prescribe ezetimibe<br />

in combination with statin medications for the<br />

most effective lipid-lowering effect.<br />

Potassium Channel Blockers<br />

Potassium channel blockers, also called potassium<br />

channel antagonists or class III antiarrhythmics,<br />

limit the amount <strong>of</strong> potassium, a key electrolyte<br />

(chemical that can carry an electrical impulse), that<br />

can enter myocardial cells. This limitation restricts<br />

the flow <strong>and</strong> pattern <strong>of</strong> electrical impulses through<br />

the heart in very specific ways. Cardiologists prescribe<br />

potassium channel blockers to treat atrial fibrillation<br />

that does not respond to other medications<br />

<strong>and</strong> to treat atrial tachycardia. These drugs interact<br />

with numerous medications, including those prescribed<br />

to treat cardiovascular conditions (notably<br />

digoxin <strong>and</strong> warfarin) <strong>and</strong> to treat other health<br />

conditions such as DIABETES. Amiodarone increases<br />

sensitivity to ultraviolet light, which can result in<br />

severe SUNBURN even through clothing. Potassium<br />

channel blockers have numerous serious side<br />

effects including life-threatening or fatal arrhythmias<br />

<strong>and</strong> TORSADE DE POINTES, a highly unstable form<br />

<strong>of</strong> ventricular tachycardia.<br />

COMMON POTASSIUM CHANNEL BLOCKERS<br />

amiodarone (Cordarone)<br />

d<strong>of</strong>etilide (Tikosyn)<br />

ibutilide (Corvert)<br />

Sodium Channel Blockers<br />

Sodium channel blockers, also called sodium<br />

channel antagonists or class I antiarrhythmics,<br />

limit the amount <strong>of</strong> sodium that enters myocardial<br />

cells. This limitation restricts the flow <strong>and</strong> pattern<br />

<strong>of</strong> electrical impulses through the heart in very<br />

specific ways that differ from the actions <strong>of</strong> potassium<br />

channel blockers. Because sodium is critical<br />

for myocardial contraction, restricting it requires a<br />

delicate therapeutic balance. Cardiologists reserve<br />

sodium channel blockers to treat potentially lifethreatening<br />

ventricular tachycardia that does not<br />

respond to other treatment. The risks <strong>and</strong> complications<br />

<strong>of</strong> these medications are numerous <strong>and</strong><br />

serious; they can cause fatal arrhythmias.<br />

COMMON SODIUM CHANNEL BLOCKERS<br />

disopyramide (Norpace)<br />

flecainide (Tambocor)<br />

mexiletine (Mexitil)<br />

moricizine (Ethmozine)<br />

procainamide (Pronestyl)<br />

propafenone (Rythmol)<br />

quinidine (Cardioquin, Quinidex)<br />

Thrombolytic Agents<br />

Thrombolytic agents, commonly called “clot<br />

busters,” dissolve blood clots that have already<br />

formed. Given early enough, they can prevent the

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