Transcript Chapter 20
Chapter 20
Drugs Affecting Circulation:
Antihypertensives, Antianginals,
Antithrombotics
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Epidemiology and Etiology of
Hypertension
Primary: Unknown etiology
Secondary: Due to known disease process
Adversely affects numerous organs
Diagnosis:
Termed cardiovascular disease (CVD)
Two or more seated BP taken on different days
Increased risk of:
Left ventricular (LV) hypertrophy, angina, myocardial
infarction (MI), heart failure, stroke, peripheral arterial
disease (PAD), retinopathy, and renal failure
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Pathophysiology of Hypertension
Arterial blood pressure
Preload is major factor in systolic blood
pressure (SBP)
Product of cardiac output (CO) and total
resistance
Affects venous capacitance
Afterload is major factor in diastolic blood
pressure (DBP)
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Hypertensive Crisis
Patient with BP > 180/120 mmHg
Hypertensive urgency
No signs/symptoms of organ complication
Hypertensive emergency
Acute, chronic, or progressive organ injury
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Hypertension Pharmacotherapy
First-line agents:
Angiotensin-converting enzyme inhibitors (ACEIs)
Angiotensin II receptor blockers (ARBs)
Calcium channel blockers (CCBs)
β Blockers
Thiazide-type diuretics
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Hypertension Pharmacotherapy
(cont’d)
Second-line agents
Vasodilators
α Blockers
α2 Agonists
Antiadrenergics
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Hypertension Pharmacotherapy
(cont’d)
Angiotensin-converting enzyme inhibitors
Suppress renin-angiotensin-aldosterone system
• Block conversion of angiotensin I to angiotensin II
Hemodynamic effect
• Reduce peripheral arterial resistance (PAR)
• Increase CO
• Increase renal blood flow
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Hypertension Pharmacotherapy
(cont’d)
Indicated for:
• Hypertension (HTN), heart failure, systolic dysfunction,
MI prevention, LV dysfunction, and diabetic neuropathy
Generally decrease SBP and DBP 15-25%
Most common side effect is dry cough
Significant interaction with nonsteroidal
antiinflammatory drugs (NSAIDs)
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Hypertension Pharmacotherapy
(cont’d)
Angiotensin II receptor blockers
Angiotensin II type 1 receptor agonists
• Receptors found in vascular smooth muscle, myocardium,
brain, kidney, liver, uterus, adrenal glands
Indicated for HTN and treatment of heart failure
Slightly “weaker” than ACEIs
Side effects: Orthostatic hypotension, hyperkalemia,
neutropenia, nephrotoxicity, and fetotoxicity
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Hypertension Pharmacotherapy
(cont’d)
Calcium channel blockers
Cause coronary and peripheral vasodilation via Lchannel blockade
Verapamil and diltiazem
• Negative chronotropic and inotropic effects
• Long-acting formulations (target circadian rhythm)
• High incidence of constipation
• Side effects
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Hypertension Pharmacotherapy
(cont’d)
β Blockers
Method of action
Indications
• Essential HTN, angina, dysrhythmias, MI prevention,
chronic heart failure
• Also: Migraine prophylaxis and alcohol withdrawal
May induce bronchospasm and render β-agonist
ineffective
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Hypertension Pharmacotherapy
(cont’d)
Diuretics
Five classes
• Thiazide and thiazide-like agents
• Loop diuretics
• K-sparing agents
Used for HTN
• Carbonic anhydrase inhibitors (CAIs)
• Osmotics
Interact with NSAIDs
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Hypertension Pharmacotherapy
(cont’d)
Potassium-sparing diuretics
• Weak if used alone
• Additive effect with thiazides
• Amiloride (Midamor) and triamterene (Dyrenium)
• Side effects
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Hypertension Pharmacotherapy
(cont’d)
Thiazide and thiazide-like diuretics
• Increase Na and Cl excretion
• Dose-ceiling effect
• 2 to 4 weeks to elicit full effect
• Side effects
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Hypertension Pharmacotherapy
(cont’d)
Loop diuretics
• Decrease Na reabsorption at ascending limb of loop of
Henle
• Indicated for chronic heart failure, ascites, renal failure,
pulmonary edema, hypercalcemia, hypermagnesemia,
syndrome of inappropriate antidiuretic hormone
• Second-line treatment for management of HTN
• Cause frequent urination
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Hypertension Pharmacotherapy
(cont’d)
Aldosterone antagonists
Spironolactone (Aldactone) and Eplerenone (Inspra)
Spironolactone is weak, often used with other
antihypertensives
• Adverse effects: Impotence, gynecomastia, deep voice,
menstrual irregularities, hirsutism, gastrointestinal upset, rash,
drowsiness
Eplerenone
• Indicated for HTN and post-MI heart failure
• Minimal adverse sexual side effects
• Higher risk of hyperkalemia
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Hypertension Pharmacotherapy
(cont’d)
Centrally acting adrenergic agents
Affect CO and peripheral resistance
Negative inotrope/negative chronotrope
α2 Agonists are effective, but riddled with side
effects
• Clonidine transdermal is most effective and least toxic
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Hypertension Pharmacotherapy
(cont’d)
α1-Adrenergic antagonists
Cause arterial and venous dilation
• Decrease preload and afterload
First-dose phenomenon
• Initial doses low and at bedtime
Indicated for HTN, benign prostatic hyperplasia,
heart failure, and Raynaud’s vasospasm
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Hypertension Pharmacotherapy
(cont’d)
Antiadrenergic agents
Second-line drugs
Reserpine
• Depletes postganglionic norepinephrine
• May cause: Sedation, depression, psychosis, peptic ulcers,
nasal stuffiness
Guanethidine (Ismelin) and Guanadrel (Hylorel)
• Substitute neurotransmitters
• May cause orthostatic hypotension, sexual dysfunction,
explosive diarrhea
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Hypertension Pharmacotherapy
(cont’d)
Vasodilators
Hydralazine (Apresoline) and minoxidil (Rogaine,
Loniten)
Second-line treatment for HTN because of side
effects
Act on vascular smooth muscle to decrease total
peripheral resistance
• May cause reflex tachycardia, renin release, increased
CO
• Often given with β blocker and loop diuretic
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Epidemiology, Etiology, and
Pathophysiology of Angina
“Chest pain”
Symptom of myocardial ischemia
Imbalance of myocardial O2 supply and
demand
May present as:
Heavy weight or pressure on chest
Burning sensation
Shortness of breath (SOB)
Pain over sternum, left shoulder, or lower jaw
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Pharmacotherapy for Angina
Nitrates
Nitroglycerin dilates coronary arteries and
collaterals (mostly venous effect)
Indications: Angina, acute MI, HTN
Formulations: Oral, IV, ointment, transdermal,
translingual, sublingual
• Sublingual: Q 5 minutes x 3, then seek care
Adverse effects: Tachycardia, palpitations,
hypotension, dizziness, flushing, headache
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Pharmacotherapy for Angina (cont’d)
Ranolazine (Ranexa)
Indicated for chronic angina not responding to
other medications
Shifts energy production from fatty acid oxidation
to glucose oxidation (uses less O2)
500 mg BID (maximum, 1 g BID)
Contraindicated in hepatic dysfunction
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Antithrombotic Agents
Formation and elimination of acute coronary
thrombus
Formation initiated by injury to endothelium
Platelets adhere to site of injury, release chemicals
that cause further aggregation, forming unstable
thrombus
Eventually forms insoluble fibrin clot
• Must be removed by fibrinolytic system for homeostasis
to be maintained
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Antithrombotic Agents (cont’d)
Anticoagulant agents
Heparins: Unfractionated heparin and low
molecular weight heparin
• Indicated for venous thromboembolism, pulmonary
embolism, atrial fibrillation (AF), disseminated
intravascular coagulation (DIC), and peripheral arterial
embolism
• Extracted from porcine intestinal mucosa
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Antithrombotic Agents (cont’d)
Anticoagulant agents (cont’d)
Heparins: Unfractionated heparin and low
molecular weight heparin (cont’d)
• Goal: Balance unwanted clotting with risk of hemorrhage
• Side effects: Bleeding, thrombocytopenia, hyperkalemia,
osteoporosis, increased liver enzyme tests (LETs)
• Antidote: Protamine sulfate
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Antithrombotic Agents (cont’d)
Anticoagulant agents (cont’d)
Direct thrombin inhibitors
• Desirudin (Iprivask): Indicated for deep vein thrombosis
(DVT)
• Bivalirudin (Angiomax): Indicated for unstable angina
• Argatroban and lepirudin (Refludan): Used for
anticoagulation of patients with heparin-induced
thrombocytopenia type 2 (HIT-2)
• Common adverse side effect: Hemorrhage
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Antithrombotic Agents (cont’d)
Anticoagulant agents (cont’d)
Warfarin (Coumadin)
• Oral anticoagulant for venous thrombosis, pulmonary
•
•
•
•
embolism (PE), AF, valve replacement, coronary
occlusion
Daily dosing (delayed onset of 3-5 days)
International normalized ratio (INR) is standard for
monitoring therapy
Hemorrhage is common side effect
Many drugs may increase/decrease effects
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Antithrombotic Agents (cont’d)
Antiplatelet agents
Aspirin
• Reduces platelet aggregation by inhibition of
prostaglandin production
• Antithrombotic indications: Reduce risk of thrombosis,
transient ischemic attack (TIA), or stroke
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Antithrombotic Agents (cont’d)
Antiplatelet agents (cont’d)
Aspirin (cont’d)
• Side effects: Peptic ulcer, renal dysfunction, HTN,
tinnitus, pulmonary dysfunction, and bleeding
• Ibuprofen inhibits pharmacological effect; concurrent
NSAID use may cause fatal gastropathy
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Antithrombotic Agents (cont’d)
Antiplatelet agents (cont’d)
Dipyridamole
• Vasodilator and platelet adhesion inhibitor
• Indicated as an adjunct to warfarin in prevention of
postoperative thromboembolic complications of cardiac
valve replacement
• May potentiate effect of adenosine
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Antithrombotic Agents (cont’d)
Antiplatelet agents (cont’d)
Clopidogrel (Plavix)
• Platelet aggregation inhibitor
• Indications: History of MI, stroke, PAD, acute coronary
•
•
•
•
syndrome
Slightly more effective than aspirin (except for stroke
prophylaxis)
Metabolized by liver
Steady state in 3 to 7 days
75 mg QD (plus aspirin)
300-mg loading dose for acute coronary syndrome (ACS)
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Antithrombotic Agents (cont’d)
Antiplatelet agents (cont’d)
Ticlopidine
• Platelet aggregation inhibitor
• Indicated for stroke
• More effective than aspirin
• Steady state in 14 to 21 days
• Metabolized by liver
• Risk of life-threatening blood dyscrasias
Use only if aspirin/clopidogrel are unacceptable
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Antithrombotic Agents (cont’d)
Antiplatelet agents (cont’d)
Cilostazol and pentoxifylline
• Cause vasodilation and inhibition of platelet aggregation
• Indicated for PAD pain
• Clinical benefits may take up to 12 weeks
• Transient adverse effects: Headache, diarrhea,
dizziness, palpitations
• 100 mg BID on an empty stomach
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Antithrombotic Agents (cont’d)
Antiplatelet agents (cont’d)
Glycoprotein IIb/IIIa inhibitors
• Indicated for ACS
• Abciximab (ReoPro) is “drug of choice”
• Not available in oral formulation (ineffective)
• Bleeding is most common adverse side effect
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Antithrombotic Agents (cont’d)
Thrombolytic agents
Indicated for PE, ischemic stroke, and acute ST
segment elevation MI
Agents: Streptokinase (second line), alteplase,
reteplase, and tenecteplase
• Therapy should begin within 12 hours of symptoms
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Antithrombotic Agents (cont’d)
Thrombolytic agents (cont’d)
Contraindications: Internal bleeding, aortic
dissection, head injury or stroke in last 3 months,
HTN, anticoagulant use
Bleeding is most common adverse effect
• Gastrointestinal, genitourinary, respiratory tract,
retroperitoneal, intracranial
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