Congestive heart failure acute pharmacotherapy

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Medical Therapy:

Summary
Acute Pharmacotherapy
Chronic Pharmacotherapy in HFpEF
Chronic Pharmacotherapy in HFrEF
Diuretics
ACE Inhibitors
Angiotensin receptor blockers
Aldosterone Antagonists
Beta Blockers
Ca Channel Blockers
Nitrates
Hydralazine
Positive Inotropics
Anticoagulants
Angiotensin Receptor-Neprilysin Inhibitor
Antiarrhythmic Drugs
Nutritional Supplements
Hormonal Therapies
Drugs to Avoid
Drug Interactions
Treatment of underlying causes
Associated conditions

Exercise Training

Surgical Therapy:

Biventricular Pacing or Cardiac Resynchronization Therapy (CRT)
Implantation of Intracardiac Defibrillator
Ultrafiltration
Cardiac Surgery
Left Ventricular Assist Devices (LVADs)
Cardiac Transplantation

ACC/AHA Guideline Recommendations

Initial and Serial Evaluation of the HF Patient
Hospitalized Patient
Patients With a Prior MI
Sudden Cardiac Death Prevention
Surgical/Percutaneous/Transcather Interventional Treatments of HF
Patients at high risk for developing heart failure (Stage A)
Patients with cardiac structural abnormalities or remodeling who have not developed heart failure symptoms (Stage B)
Patients with current or prior symptoms of heart failure (Stage C)
Patients with refractory end-stage heart failure (Stage D)
Coordinating Care for Patients With Chronic HF
Quality Metrics/Performance Measures

Implementation of Practice Guidelines

Congestive heart failure end-of-life considerations

Specific Groups:

Special Populations
Patients who have concomitant disorders
Obstructive Sleep Apnea in the Patient with CHF
NSTEMI with Heart Failure and Cardiogenic Shock

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Acute Pharmacotherapy

The goals of acute pharmacotherapy include:

The following acute therapies are used in the acute management of heart failure and their mechanism of action are as follows

Chronic Pharmacotherapy

Antiarrhythmic Drugs

Antiarrhythmic therapy should be considered as a therapy to prevent sudden cardiac death. Over 50% of heart failure patients will have asymptomatic non-sustained ventricular tachycardia and there is no general indication for treatment of this arrhythmia. T here are multiple causes of the for sudden cardiac death in the patient with congestive heart failure which include not only arrhythmic causes, but also thrombotic and other causes:

Metabolism of Antiarrhythmics in the setting of Congestive Heart Failure

Metabolisms of following anti-arrhythmic drugs are significantly affected in patients with congestive heart failure and care should be taken regarding their administration:

  1. Quinidine
  2. Procainamide
  3. Disopyramide: Contraindicated in patients with heart failure.
  4. Moricizine
  5. Lidocaine
  6. Mexiletine
  7. Tocainide
  8. Flecainide
  9. Propafenone
  10. Amiodarone

Patients with congestive heart failure should not be treated with dronedarone.

Renin-Angiotensin-Aldosterone Axis Inhibitors

Angiotensin converting enzyme inhibitor or ACE Inhibitors

  • ACE Inhibitors (ACEI) should be considered as first-line therapy for the treatment of patients with clinical heart failure due to reduced left ventricular systolic dysfunction (LVSD), patients with asymptomatic LV dysfunction, and for patients who are at high risk for the development of heart failure due to the presence of coronary, cerebrovascular, or peripheral vascular disease.
  • Treatment should not be deferred in patients with few or no symptoms because of the significant mortality benefit derived from ACEI therapy.
  • Initial therapy usually consist of 12.5 mg tid of captopril, 2.5 mg bid of enalapril, or 2.5 mg daily lisinopril. The optimal dose is usually established by optimizing the dose every 4 to 6 weeks.
  • ACE inhibitors are rarely adequate for the treatment of congestion without the use of diuretics.
  • 5-10 % patients cannot tolerate ACE inhibitors because of cough. Cough can be a sign of elevated left-sided filling pressures. Sometimes cough will diminish with the treatment of heart failure. A
  • Renal artery stenosis should be considered if there's a decline in renal function with the initiation of ACE inhibitors.

Angiotensin receptor blockers (ARB)

  • * In the CHARM study candesartan reduced both hospitalization and mortality.

Aldosterone Antagonists

Anticoagulants

The annual incidence of systemic and pulmonary embolism in patients with heart failure is 2-5%. This is not that dissimilar from the risk of severe bleeding among patients to its anticoagulants which is 0.8-2.5% per year.

As a result anticoagulation is not routinely recommended in the current guidelines for the treatment of heart failure. However among those patients with a atrial fibrillation, a history of emboli, or multiple intracardiac thrombi, or akinesis or dyskinesis detected on echo should be anticoagulated.

Beta Blockers

  • Metoprolol, Carvedilol and Bisoprolol have FDA approved labeling for use in congestive heart failure.
  • Blockade of compensatory sympathetic stimulation is associated with arrhythmic, ischemic, remodeling, and apoptotic benefits.
  • Used as monotherapy or combined with conventional heart failure management, beta-blockers reduce the combined risk of morbidity and mortality.
  • Initiate low starting dosing and titrate up to tolerated target doses.
  • Lopressor should be used instead of atenolol in the patient with CHF

Diuretics

  • Provide symptomatic relief.
  • Slows the progression of ventricular remodeling by reducing ventricular filling pressure and wall stress.
  • No survival benefit and may cause azotemia, hypokalemia, metabolic alkalosis and elevation of neurohormones.
  • Although thiazide diuretics are effective in mild heart failure they are usually inadequate for the treatment of severe heart failure.
  • Thiazide diuretics have also been associative with hyponatremia.
  • Fluid retention usually responds best to furosemide (Lasix) and at doses of 10 to 20 mg per day. The patient should be told to return to their position in the next three to seven days for further assessment including assessment of their potassium concentration. Weight loss should not exceed 1 to 2 pounds/day.
  • If there is no response to the initial dose then it can be increased by at least 50%. The maintenance dose of the diuretics lower than that required to initiate diuresis.
  • If the patient gains more than two pounds and they are instructed to double the dose of their loop diuretic.
  • Once the baseline weight has been re-established than they can resume their previous status.
  • Intermittent use of metolazone into dose of 2.5 or 5 mg can be given if the patient is refractory to furosemide Lasix. Metolazone should be given in the inpatient setting.
  • The role of potassium sparing diuretics such as spironolactone (Aldactone), amiloride, or triamterene remains the subject of controversy.
  • Extreme caution is necessary when adding a potassium sparing agent to the regiment that includes ACE inhibitors particularly when diabetes or renal disease is present because the patient can become hyperkalemic.
  • Electrolyte replacement:

ACE inhibitors reduce potassium excretion, but most patients with good renal function require potassium supplementation during daily therapy with the diuretics such as furosemide (Lasix) despite of ACE inhibitors therapy.

  • Dietary supplementation is rarely adequate.
  • Hypokalemia can aggravate arrhythmia is precipitate muscle cramps.
  • Potassium levels >6 (particularly when occurs rapidly) can be associated with reduction in myocardial contractility.
  • Patients are actually at higher risk of hyperkalemia and hypokalemia. The goal is to maintain a potassium between 3.8 and 4.5 mEq.
  • Unless the hypokalemia is very severe and at life-threatening level, potassium should be replaced by oral administration.
  • For IV route, It should not be administered more than 10 mEq per hour.
  • Patients who use diuretics usually require approximately 20-60 mEq/day of oral potassium.
  • Extra potassium should be given after the patient has noted diuresis or weight change. If patient lost more than two pounds, the electrolyte's level should be checked every three days.
Loop Diuretics
  • Furosemide, bumetanide, ethacrynic acid and torsemide.
  • Inhibit the Na+/K+/2Cl- symporter.
  • Furosemide IV has direct vasodilatory effect.
  • Providing additional blood pressure reduction.
  • Relaxes pre-contracted pulmonary venules: beneficial for treatment of Pulmonary Edema.
Thiazide Diuretics
  • Inhibit the Na+/Cl- co transporter in the distal convoluted tube.
  • Recommended for management of chronic heart failure.
Potassium Sparing Diuretics

Nitrates

  • Nitrates can be added to ACE inhibitors to relieve symptoms of congestion.
  • The addition of a nitrate and ACE inhibitor may improve exercised tolerance.
  • The combination of hydralazine and nitrates is useful when ACE inhibitors are not well tolerated.
  • Hydralazine by itself is only an arterial vasodilator and does not reduced ventricular filling pressures to the same extent that nitrates and ACE inhibitors do. In fact when used alone it can stimulate sympathetic tone reflexively. The combination of hydralazine and nitrates has been shown to decrease mortality as well as improve the left ventricular ejection fraction and exercise capacity in patients with heart failure. However the combination of hydralazine and nitrates has been found to be less effective than ACE inhibitors.
  • The major uses this combination is in those patients who are intolerant of ACE inhibitors.

Positive Inotropics

  1. Agents that increase intracellular cAMP
  2. Agents that affect sarcolemmal ion pumps/channels
  3. Agents that modulate intracellular calcium mechanisms by either:
  4. Drugs having multiple mechanisms of action
    • Pimobendan
    • Vesnarinone
Digoxin
  • Inhibits Na,K+-ATPase resulting in an increase in intracellular Na+, extracellular Ca2+ exchange increasing the velocity and extent of sarcomere shortening.
  • ACC/AHA recommend digoxin for symptomatic patients with left ventricular systolic dysfunction.
  • Commonly used in patients with heart failure and atrial fibrillation to reduce the ventricular response rate.
  • Mortality has not been shown to be improved with use of digoxin, but the use of digoxin has been associated with a reduction in hospitalization.
  • There is no need to load a patient with digoxin for most patients with normal renal function 0.25 mg of digoxin daily is usually adequate. In the only patient or in those patients with renal impairment a dose of 0.125 mg per day may be adequate.
  • Drugs increase the same concentration of digoxin include antibiotics and anticholinergic agents as well as amiodarone, quinidine and verapamil.
Dobutamine
  • Activates beta-1 receptors resulting in enhanced cardiac contractility.
  • Long-term dobutamine infusions are arrhythmogenic and increase mortality.
Dopamine
  • Unique dose dependent mechanism of action.
  • At low doses: (≤2 µg/kg/min), selective dilation of splanchnic and renal arterial beds. assists in increasing renal perfusion.
  • At intermediate doses: (2 to 10 µg/kg/min), increased norepinephrine secretion results in increased cardiac contractility, heart rate and peripheral vascular resistance.
  • At higher doses: (5 to 20 µg/kg/min), direct alpha-adrenergic receptor stimulation increases systemic vascular resistance.
Milrinone
  • Phosphodiesterase-III inhibitor that enhances contractility by increasing intracellular cyclic adenosine monophosphate (cAMP).
  • Potent pulmonary vasodilatation that benefits pts with pulmonary hypertension.
  • Unlike dobutamine: milrinone is beneficial to decompensated heart failure patients on beta-blocker therapy.
  • Long term milrinone infusions are arrhythmogenic, and increase mortality.

Ca Channel Blockers

Although calcium channel blockers cause vasodilation their overall benefit is minimized by the fact that they have a negative inotropic effect and by the reflex activation of the sympathetic nervous system.

These agents are not recommended as vasodilators in patients with congestive heart failure, however they may be useful as antihypertensive agents in patients with diastolic dysfunction.

Biventricular Pacing or Cardiac Resynchronization Therapy (CRT)

  • Cardiac resynchronization therapy should only be undertaken if the blood pressure is low and if the heart failure medicines have been optimized
  • CRT is indicated for symptomatic patients with NYHA III-IV heart failure and wide QRS complex (>120ms) who are him normal sinus rhythm.
  • 70% of patients receiving synchronous ventricular contraction report significant symptomatic improvements.

Implantation of Intracardiac Defibrillator

  • 50% of heart failure patients die of sudden cardiac death.
  • ICDs are indicated for patients with previous myocardial infarction and LVEF <30%, sustained ventricular tachycardia, inducible ventricular tachycardia.
  • Morbidity/mortality benefit of ICD placement vs. anti-arrhythmic drug therapy is controversial.

Ultrafiltration

The process of ultrafiltration consists of the production of plasma water from whole blood across a semipermeable membrane (hemofilter) in response to a transmembrane pressure gradient. Possible benefits of ultrafiltration as follow;

  1. Provides fluid regulation
    • Relieve pulmonary edema
    • Reduce ascites and/or peripheral edema
    • Hemodynamic stabilization
    • Improve oxygenation
    • Facilitate blood product replacement without excess volume
    • Enable parenteral nutritional support without excess volume
  2. Improves solute regulation
    • Correct acid-base balance
    • Correct serum sodium content
    • Eliminate myocardial depressant factors or known toxins
    • Correct uremia
    • Correct hyperkalemia
    • Correct other electrolyte disturbances
  3. Helps to establish homeostasis
    • Reset water omostat
    • Restore diuretic responsiveness
    • Reduce neurohormonal activation

Cardiac Surgery

  • Resection of non-viable myocardium
  • Revascularization without resection of non-viable myocardium
  • Dor procedure: Surgical resection of infarcted myocardium and left ventricular reconstruction.
  • Placement of a passive containment device to prevent progressive cardiac dilation (Under investigation)

Left Ventricular Assist Devices

  • LVADs are temporary devices to bridge end stage patients to cardiac transplantation.
  • Current clinical research in implementing permanent portable LVADs is underway, and first studies have promising results.

Cardiac Transplantation

  • For patients with end-stage congestive heart failure despite all interventions.
  • 80% 1 year survival and 60% 5 year survival.
  • Lifelong immunosuppressive therapy to prevent (or postpone) rejection, increased risk for opportunistic infections and malignancies.

AHA/ACC Guidelines: Indications for heart transplantation

  • Any hemodynamic compromise due to heart failure.
  • Requiring IV inotropic support to maintain adequate organ perfusion.
  • Peak Vo2 <10 ml/kg/min.
  • NYHA Class IV symptoms not amenable to any other intervention.
  • Recurrence of symptomatic ventricular arrhythmias refractory to all therapeutic intervention.

Exercise and Daily Activities

  • Patient should have uninterrupted exercise at least four days a week including a walking program.
  • Rowing machines usually are too vigorous of exercise.
  • Patients with heart failure should avoid weightlifting.
  • The patient should not routinely lift more than 20 pounds.
  • Patients can continue their sexual activity. Some patients take 2.5 or 5.0 mg of sublingual nitroglycerin before sexual activity.

References


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