Chronic Heart Failure

Chapter: Chronic Heart Failure
McMaster Section Editor(s): P.J. Devereaux
Section Editor(s) in Interna Szczeklika: Andrzej Budaj, Wiktoria Leśniak
McMaster Author(s): Harriette G.C. Van Spall, Tahseen Rahman
Author(s) in Interna Szczeklika: Andrzej Surdacki, Jacek Bednarek, Olga Kruszelnicka
Additional Information

DefinitionTop

Definition and classification of heart failure: see Heart Failure.

Epidemiology, Etiology, Pathophysiology Top

Heart failure with reduced ejection fraction (HFrEF) is better understood than heart failure with preserved ejection fraction (HFpEF) and represents approximately half of all heart failure (HF) cases. The most common etiology of HFrEF is coronary artery disease (CAD) and arterial hypertension. Other causes include viral infection, alcohol abuse, valvular heart disease, chemotherapy (eg, doxorubicin or trastuzumab), peripartum cardiomyopathy, “idiopathic” dilated cardiomyopathy, and genetic cardiomyopathies.

In HFrEF, maladaptive changes after myocardial injury lead to pathologic remodeling of the ventricle with dilatation and impaired contractility. This is mediated by:

1) Maladaptive left ventricle (LV) hypertrophy associated with the reexpression of fetal isoforms of contractile proteins and progressive loss of cardiomyocytes via apoptosis or necrosis.

2) Abnormal calcium homeostasis and depressed beta-receptor density in cardiomyocytes.

3) Myocardial fibrosis.

4) Progression of mitral insufficiency and pulmonary hypertension.

5) Neurohormonal activation involving the renin-angiotensin-aldosterone system, the sympathetic nervous system, and enhanced vasopressin secretion accompanied by impaired vasodilatory and renal responses to natriuretic peptides, which increases preload and afterload. These systemic neurohormonal responses are triggered by cardiac output lowering, have detrimental long-term effects on the heart and systemic vasculature, and create a vicious cycle of further myocardial injury and remodeling, which in turn exacerbates neurohormonal activation.

Additionally, the following systemic abnormalities both underlie HF symptoms and contribute to HF progression: depressed sensitivity of baroreceptors, enhanced reactivity of chemoreceptors and muscular ergoreceptors, vascular endothelial dysfunction and impaired vasodilatory reserve, renal dysfunction, skeletal muscle dysfunction, functional or absolute iron deficiency with or without anemia, chronic inflammatory activation, and neuroendocrine dysfunction favoring catabolic pathways.

HFpEF is less understood and is increasing in prevalence. Patients are more likely to be older, female, and obese, and have a better prognosis than those with HFrEF. They are less likely to have coronary heart disease and more likely to have hypertension, atrial fibrillation, and sleep apnea. Pathophysiology involves heterogeneous factors, such as impaired LV relaxation due to excessive afterload (owing to elevated blood pressure, aortic stenosis, increased arterial stiffness, and impaired peripheral vasodilatory reserve), decreased passive LV compliance (mediated by changes in the extracellular matrix associated with concentric LV hypertrophy), chronotropic incompetence, microvascular coronary dysfunction, and accompanying myocardial oxidative stress with consequent stimulation of proinflammatory and profibrotic pathways.

Causes of high-output HF include conditions associated with hyperdynamic circulation: severe anemia, thyrotoxicosis, large systemic arteriovenous fistulas, advanced cirrhosis, polycythemia or secondary erythrocytosis, Paget disease, beriberi, carcinoid syndrome, or pregnancy. HF usually develops in patients with hyperdynamic circulation superimposed on an underlying heart disease, although it can occur in absence of structural heart disease.

Cardiomyopathies (abnormalities in cardiac myocytes that result in impaired function) are a predisposing condition for clinical HF but may not always be associated with clinical HF. The World Health Organization categorizes the etiology of HF based on the type of underlying cardiomyopathy, which is defined as pathologic myocardial processes and dysfunction that are a direct consequence of cardiovascular abnormalities other than valvular heart disease, systemic hypertension, congenital heart disease, and atherosclerotic coronary artery disease. The European Society of Cardiology classification scheme helps with identifying etiology based on cardiac structure:

1) Dilated cardiomyopathy: Dilatation of ventricle(s) with impaired ability to contract leading to eccentric hypertrophy. Etiologies may include toxins (eg, alcohol, cocaine, and chemotherapeutic agents such as anthracyclines, fluorouracil, and trastuzumab), myocarditis, Chagas disease, peripartum cardiomyopathy, and familial cardiomyopathies (eg, Becker or Duchenne muscular dystrophy), among others.

2) Hypertrophic cardiomyopathy: Concentric hypertrophy of the ventricle or its segments, with resulting diastolic dysfunction.

3) Restrictive cardiomyopathy: Impaired ventricular filling with no or minimal dilatation or hypertrophy, although ventricular thickening may occur.

4) Arrhythmogenic right ventricular cardiomyopathy: Fatty and fibrous replacement of the normal myocardium, usually affecting the right ventricular free wall.

5) Unclassified cardiomyopathies: Cardiomyopathies that do not fit the above types. Takotsubo and noncompaction are examples of unclassified cardiomyopathies.

Causes of HF exacerbations: Patients with chronic heart failure may develop exacerbations due to the following reasons:

1) Acute coronary syndrome.

2) Poorly controlled hypertension.

3) Tachyarrhythmia (most commonly atrial fibrillation) or bradyarrhythmia.

4) Pulmonary embolism.

5) Endocarditis, myocarditis.

6) Conditions associated with hyperdynamic circulation.

7) Infections (particularly pneumonia).

8) Renal dysfunction.

9) Dietary indiscretion (high sodium intake).

10) Nonadherence to prescribed medications.

11) Iatrogenic: Intravenous fluids, use of medications with negative chronotropic or inotropic effects (eg, verapamil, diltiazem, or inappropriate doses of beta-blockers), cardiotoxic agents (eg, anthracyclines), drugs causing sodium and/or water retention (eg, glucocorticoids, estrogens, nonsteroidal anti-inflammatory drugs [NSAIDs]).

12) Abnormalities in thyroid function (eg, caused by amiodarone).

13) Alcohol abuse, cocaine use.

14) Untreated sleep apnea.

Clinical FeaturesTop

Symptoms of HF are a combination of pulmonary and/or systemic congestion with or without low output. The New York Heart Association (NYHA) classification of the severity of HF (functional status) is based on the assessment of fatigue, dyspnea, and palpitations, which are caused by physical activity (Table 3.8-3). A validated scale, such as that by the NYHA, is commonly used to document functional capacity.

1. Clinical manifestations of LV failure (pulmonary congestion):

1) Symptoms: Dyspnea (at rest or on exertion); orthopnea (occurs 1-2 minutes after lying down and resolves within a few minutes of sitting or standing up); paroxysmal nocturnal dyspnea, which unlike orthopnea occurs much later after lying down, wakes the patient up, and takes much more time (usually ≥30 minutes) to resolve; cough (an equivalent of exertional dyspnea or orthopnea), generally dry, occasionally producing pink sputum (usually in patients with pulmonary edema); fatigue.

2) Signs: Dilated LV or displaced apex with a third heart sound; crackles over the lung fields (typically audible in the basal regions, although they may extend up to the apical regions), which may be accompanied by wheezing and rhonchi (caused in part by edema of the bronchial mucosa).

2. Clinical manifestations of right ventricular failure (systemic congestion):

1) Symptoms: Peripheral dependent edema (most commonly affecting the feet and ankles, or the sacral area in bedridden patients), abdominal pain or discomfort caused by liver congestion, or nocturia. The symptoms may also include anorexia, nausea, and constipation caused by venous congestion of the gastric and intestinal mucosa and by reduced cardiac output, which in some cases may lead to malabsorption and subsequent malnutrition or even cachexia in patients with advanced HF.

2) Signs: Exudates, including pleural effusions (usually bilateral; when unilateral, they occur more frequently on the right) or ascites; right ventricular heave or a right ventricle that is palpable in the subxiphoid region; an enlarged and tender liver (tenderness is due to stretching of the hepatic capsule and occurs when congestion develops rapidly); a firm and atrophic liver may be observed in a long-standing (several years-long) HF. Other signs include mild jaundice, jugular vein distention with or without sustained elevation, and in some patients Kussmaul sign (increased jugular venous pressure during inspiration, similar to that observed in constrictive pericarditis).

3. Manifestations common to right and left ventricular failure (including manifestations of low cardiac output):

1) Symptoms: Impaired exercise tolerance, oliguria (in advanced HF).

2) Signs: Pale and cool skin of the extremities, diaphoresis, rarely acrocyanosis (features of sympathetic stimulation); tachycardia, third heart sound (often audible in patients with systolic LV dysfunction) or fourth heart sound (more suggestive of isolated diastolic HF), an accentuated pulmonary component of the second heart sound; occasionally murmurs associated with valvular heart disease, which is a cause of HF or is secondary to ventricular dilatation; low pulse pressure, mild elevation of diastolic blood pressure; Cheyne-Stokes respiration; symptoms of abnormal cerebral perfusion, especially in the elderly.

4. Symptoms and signs of HF with an increased cardiac output caused by hyperdynamic circulation: High pulse pressure (reduction in diastolic blood pressure); increased precordial pulsation; pulsus altus et celer, capillary pulsation (Quincke pulse); tachycardia; abnormal features on auscultation (hyperdynamic heart sounds, sometimes a third or fourth heart sound, midsystolic ejection murmur audible along the left sternal border, sometimes midsystolic murmur over the mitral or tricuspid valve and constant venous hum, carotid bruit); warming and erythema of the skin (not present in patients with ischemia; it may be local, eg, in patients with Paget disease or arteriovenous fistulas). In patients with arteriovenous fistulas, applying pressure on a fistula causes a decrease in heart rate.

5. Clinical features of HFpEF are similar to those of HFrEF and include exertional dyspnea and other symptoms of pulmonary congestion, while the features of peripheral hypoperfusion are usually absent.

DiagnosisTop

Diagnostic Tests

A thorough history and physical examination are essential to screen for conditions that cause or precipitate HF.

Basic laboratory investigations are used to establish the cause of HF, detect associated complications, or ascertain prognosis. Chest radiographs and echocardiography play a key role in diagnosing HF.

1. Laboratory investigations:

1) Hyponatremia caused by volume overload may be observed in patients with advanced HF or those who are treated with thiazide diuretics.

2) Hypokalemia or hyperkalemia and increased serum creatinine levels may be caused by diuresis, kidney injury, and/or adverse effects of drugs (see below).

3) Elevated serum aminotransferase, lactate dehydrogenase, and bilirubin levels are observed in patients with hepatic congestion.

4) Anemia (worsening or triggering HF) or high hematocrit values (eg, in chronic obstructive pulmonary disease and congenital heart disease with right-to-left shunt).

5) Serum levels of the natriuretic peptides can be measured to diagnose patients with a clinical suspicion of HF (especially in case of diagnostic uncertainty and unavailability of bedside echocardiography, which is increasingly being used in clinical practice). Due to a high negative but limited positive predictive value, natriuretic peptides are recommended to exclude HF but not to establish HF diagnosis. Exclusionary cut-points for natriuretic peptides are higher in the acute than in the nonacute setting:

a) HF is unlikely in patients with no acute worsening of the symptoms (ie, in the nonacute setting), B-type natriuretic peptide (BNP) levels <35 pg/mL, N-terminal pro–B-type natriuretic peptide (NT-proBNP) levels <125 pg/mL, and normal ECG.

b) In patients with rapidly worsening symptoms (ie, in the acute setting), the cut-points are as follows: BNP <100 pg/mL, NT-proBNP <300 pg/mL, midregional proatrial natriuretic peptide (MR-proANP) <120 pmol/L.

c) BNP/NT-proBNP can be used for prognostic stratification in patients with known HF. In ambulatory patients aged <75 years and with low EF, BNP/NT-proBNP can be used to guide management.Evidence 1Weak recommendation (benefits likely outweigh downsides, but the balance is close or uncertain; an alternative course of action may be better for some patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Quality of Evidence is based on individual patient meta-analysis demonstrating a 38% risk reduction for all-cause mortality and 18% risk reduction in HF rehospitalization. Of note, however, clinicians generally used their discretion in how to optimize therapy in response to BNP/NT-proBNP levels. There is no clear algorithm to guide titration of medications in BNP-guided care. Savarese G, Trimarco B, Dellegrottaglie S, et al. Natriuretic peptide-guided therapy in chronic heart failure: a meta-analysis of 2686 patients in 12 randomized trials. PLoS One. 2013;8(3):e58287. doi: 10.1371/journal.pone.0058287. Erratum in: PLoS One. 2014;9(4):e96706. PubMed PMID: 23472172; PubMed Central PMCID: PMC3589263. Troughton RW, Frampton CM, Brunner-La Rocca HP, et al. Effect of B-type natriuretic peptide-guided treatment of chronic heart failure on total mortality and hospitalization: an individual patient meta-analysis. Eur Heart J. 2014 Jun 14;35(23):1559-67. doi: 10.1093/eurheartj/ehu090. Review. PubMed PMID: 24603309; PubMed Central PMCID: PMC4057643.

It should be noted that (1) because natriuretic peptides tend to be lower in HFpEF than in HFrEF, the BNP/NT-proBNP threshold for diagnosis of HF in HFpEF is lower than in HFrEF; (2) BNP, but not NT-proBNP, is a substrate of neprilysin. Thus, BNP levels cannot be used to assess HF severity or treatment response in patients on angiotensin receptor neprilysin inhibitors (ARNIs); NT-proBNP, however, can be used for these purposes in patients on ARNIs.

2. ECG can reveal clues about the underlying etiology: ischemic heart disease, arrhythmia, conduction disturbances, or ventricular hypertrophy.

3. Chest radiographs usually reveal an enlarged cardiac silhouette (except for the majority of patients with hyperdynamic circulation or HFpEF) and features of pulmonary congestion. They help identify pulmonary edema while excluding other lung diseases that may be contributing.

4. Echocardiography is a key diagnostic study in HF and is usually performed in patients with suspected HF as it allows assessment of:

1) LV systolic function through the analysis of global and segmental LV contractility and measurements of LVEF.

2) LV diastolic function through the analysis of tissue Doppler indices, left atrial volume, estimated pulmonary pressure, and presence of predisposing conditions.

3) Structural heart disease: Ventricular and/or atrial hypertrophy or dilatation, valvular heart disease, congenital heart disease, pericardial effusion.

In some cases (eg, a poor acoustic window in transthoracic echocardiography, significant native or prosthetic valve dysfunction, suspected thrombus in the left atrial appendage in patients with atrial fibrillation, diagnosis of bacterial endocarditis or congenital heart disease), transesophageal echocardiography may be indicated.

Dobutamine stress echocardiography is useful in the diagnosis of coronary artery disease and can be considered in patients with intermediate pretest probability or for assessment of reversible ischemia prior to proceeding to coronary angiography and revascularization.

5. Coronary angiography is indicated in patients with suspected ischemic heart disease, a history of unexplained cardiac arrest, severe ventricular arrhythmias if myocardial ischemia is suspected as a cause, HF that is treatment resistant or of unknown etiology, or prior to an elective cardiac surgery.

6. Exercise stress test may be useful in patients with a discrepancy between the severity of symptoms and signs of the disease, in patients qualified for heart transplantation, and to differentiate between cardiac and pulmonary causes of dyspnea.

7. Multislice CT (MSCT) and cardiac MRI may be used in determining the etiology of HF and in differential diagnosis when other methods (especially echocardiography and coronary angiography) are not sufficient to make a diagnosis. MSCT and MRI are particularly useful when differentiating between various forms of cardiomyopathy, cardiac tumors, pericardial disease, and congenital heart disease.

8. Endomyocardial biopsy has utility in selected patients with HF of unexplained etiology and with a suspected disease requiring specific treatment, including myocarditis (giant cell or eosinophilic), infiltrative or storage diseases (amyloidosis, sarcoidosis, hemochromatosis, or Fabry disease), and in diagnostics of transplant rejection.

Diagnostic Criteria

HF is diagnosed in patients with typical signs and symptoms accompanied by objective features of systolic or significant diastolic LV dysfunction at rest, usually observed in echocardiography. Chest radiography criteria include interstitial or pulmonary edema. Another important indicator of the dysfunction is an increase in serum levels of natriuretic peptides (see above) and clinical improvement in response to standard HF pharmacotherapy. The Boston criteria offer objective scoring to facilitate the diagnosis of heart failure. (See Table 1 in Am Fam Physician. 2000;61(5):1319-28.)

Differential Diagnosis

Differential diagnosis includes other causes of dyspnea, edema, and jugular vein distension.

TreatmentTop

Treatment of HF includes:

1) Definitive treatment of the underlying condition (eg, coronary revascularization, valvular surgery).

2) Long-term treatment of HF (see below).

3) Treatment of exacerbations of HF (see Acute Heart Failure).

Nonpharmacologic Management

1. In patients with symptoms of sodium and fluid retention, sodium restriction to 2 to 3 g/d is usually recommended (<2 g/d if the symptoms persist, especially if they are resistant to diuretic treatment). In patients with hyponatremia and severe symptoms (NYHA classes III-IV), add fluid restriction to 1.5 to 2 L/d.

2. Regular body weight monitoring:

1) Monitor the patient’s body weight; an increase >2 kg in body weight over 3 days may indicate fluid retention caused by HF.

2) Reduce body weight in obese patients, especially those with a body mass index (BMI) >35 kg/m2.

3) Improve nutrition in patients with features of malnutrition (BMI, <22 kg/m2, <90% of ideal body weight).

3. Reduction in alcohol consumption to ≤10 to 12 g/d in women and ≤20 to 25 g/d in men. Abstinence is necessary in patients with suspected alcohol cardiomyopathy.

4. Smoking cessation.

5. In patients with HF who have recently been hospitalized for an acute HF exacerbation, nurse home visits, nurse case management, and outpatient disease management/heart failure clinics should be considered, as they reduce all-cause mortality and readmissions.Evidence 2Weak recommendation (benefits likely outweigh downsides, but the balance is close or uncertain; an alternative course of action may be better for some patients). Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to heterogeneity among control groups in randomized controlled trials and indirectness (differences exist between intervention programs despite belonging to the same transitional care program classification in the meta-analysis). Feltner C, Jones CD, Cené CW, et al. Transitional care interventions to prevent readmissions for persons with heart failure: a systematic review and meta-analysis. Ann Intern Med. 2014 Jun 3;160(11):774-84. doi: 10.7326/M14-0083. Review. PubMed PMID: 24862840. Van Spall H, Rahman T, Mytton O, Ramasundarahettige C, Ibrahim Q, Kabali C, Coppens M, Haynes RB, Connolly S. Comparative effectiveness of transitional care services for patients discharged from the hospital with heart failure: Systematic review and network meta-analysis. 2016. Unpublished data. Currently under review.

6. Avoidance of the following drugs (if possible):

1) NSAIDs, including cyclooxygenase-2 (COX-2) inhibitors (these increase fluid retention; reduce the effectiveness of diuretics, angiotensin-converting enzyme inhibitors [ACEIs], angiotensin receptor blockers [ARBs], and aldosterone antagonists; and increase the risk of adverse effects of these classes of drugs).

2) Glucocorticoids (these increase fluid retention and the risk of hypokalemia).

3) Class I antiarrhythmic drugs (particularly class Ia and Ic agents) and class III sotalol and ibutilide.

4) Tricyclic antidepressants (these have proarrhythmic effects and are associated with a risk of hypotension and HF exacerbation; selective serotonin reuptake inhibitors are relatively safe).

5) Dronedarone is contraindicated in patients with HF, as it increases cardiovascular mortality and risk of HF exacerbation.Evidence 3Strong recommendation (downsides clearly outweigh benefits; right action for all or almost all patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Køber L, Torp-Pedersen C, McMurray JJ, et al; Dronedarone Study Group. Increased mortality after dronedarone therapy for severe heart failure. N Engl J Med. 2008 Jun 19;358(25):2678-87. doi: 10.1056/NEJMoa0800456. Erratum in: N Engl J Med. 2010 Sep 30;363(14):1384. PubMed PMID: 18565860.

6) Verapamil and diltiazem (except in patients with HFpEF; high doses of verapamil are routinely used in patients with hypertrophic cardiomyopathy); dihydropyridine calcium-channel blockers (in patients with coexisting hypertension or angina, only long-acting agents [amlodipine and felodipine] may be used). Nondihydropyridine calcium-channel blockers are usually avoided in patients with HFrEF, given their negative inotropic effect.

7) Alpha1-blockers (these cause fluid retention and increase the risk of hypotension; in the case of voiding problems caused by symptomatic prostatic hyperplasia, switch to 5alpha-reductase inhibitors).

8) Moxonidine (increases the risk of death).

9) Metformin should be avoided in the patients with contraindications (risk of lactic acidosis in patients with acute HF or severe respiratory, liver, or renal failure; it is commonly used and considered the first-line antidiabetic drug in patients with stable HF).

10) Thiazolidinediones (rosiglitazone, pioglitazone; these increase fluid retention and are absolutely contraindicated in NYHA class III or IV).Evidence 4Strong recommendation (downsides clearly outweigh benefits; right action for all or almost all patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Lago RM, Singh PP, Nesto RW. Congestive heart failure and cardiovascular death in patients with prediabetes and type 2 diabetes given thiazolidinediones: a meta-analysis of randomised clinical trials. Lancet. 2007 Sep 29;370(9593):1129-36. Review. PubMed PMID: 17905165. Home PD, Pocock SJ, Beck-Nielsen H, et al; RECORD Study Team. Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial. Lancet. 2009 Jun 20;373(9681):2125-35. doi: 10.1016/S0140-6736(09)60953-3. PubMed PMID: 19501900.

11) Anthracyclines (in the case of life-saving therapy, consider using liposomal doxorubicin or pretreatment with dexrazoxane; closely monitor LV function).

7. Annual influenza and pneumococcal vaccination.

8. Regular moderate physical activity: 30 minutes of aerobic exercise at least 3 times a week (clinically stable HF patients).

9. Caution is advised when traveling to altitudes >1500 meters above sea level or to hot and humid climates. In the case of long-distance journeys, air travel is preferred over land travel to avoid prolonged periods of immobilization.

10. Diagnosis and treatment of clinically significant depression (see Depressive Disorders).

11. In the case of concomitant central sleep apnea, consider continuous positive airway pressure (see Obstructive Sleep Apnea).

Pharmacotherapy

Pharmacotherapy of HFrEF: Figure 3.8-3.

General recommendations: Start with low doses of drugs and titrate them up to a target dose that has been proven effective in clinical trials or up to the maximum tolerated dose.

In hospitalized patients, start treatment with low-dose beta-blockers (after HF is stabilized), ACEIs, ARBs, or aldosterone antagonists before discharge, if possible. The pattern of use of ARBs + ARNIs is evolving rapidly.

1. Diuretics (loop with or without potassium-sparing diuretics) are used in patients with symptoms of volume overload and then continued at the lowest dose that prevents water retention. Agents and dosage: Table 3.8-4.

General recommendations:

1) Loop diuretics are generally the first-line agents in managing volume overload, particularly in symptomatic HF.

2) Adjust doses to the patient’s needs. Closely monitor the clinical status as well as serum levels of potassium, sodium, and creatinine.

3) Increase doses of diuretics until the signs and symptoms of volume overload improve (a recommended rate of body weight reduction is 0.5 to 1 kg/d). Adjust doses of diuretics (particularly when the desired dry body weight has been achieved) to avoid kidney injury and dehydration.

4) Encourage patients or caregivers to self-adjust the doses of diuretics based on the daily measurements of body weight and signs and symptoms of fluid retention.

5) In the case of resistance to diuretics, assess the patient’s adherence to the treatment regimen; make sure that the patient does not use NSAIDs, COX-2 inhibitors, glucocorticoids, cyclosporine (INN ciclosporin), or estrogens; assess the patient’s sodium/fluid intake; and then increase the dose of diuretics. If this is not effective, consider replacing furosemide with another loop diuretic (eg, bumetanide). At this point, administer the loop diuretic bid or when fasting, and finally consider a short-term intravenous infusion of a loop diuretic.

6) Ensure optimal afterload reduction, use of an aldosterone antagonist, and use of other guideline-recommended medical therapy.

Management of adverse effects:

1) In patients with hypokalemia/hypomagnesemia, start potassium or magnesium supplementation. Consider increasing the dose of the ACEI/ARB or aldosterone antagonist for long-term prevention of hypokalemia/hypomagnesemia.

2) Hyperkalemia may occur in patients treated with ACEIs or ARBs in combination with potassium-sparing diuretics, including aldosterone antagonists. Do not use potassium-sparing diuretics other than aldosterone antagonists.

3) In patients with hyponatremia, restrict fluid intake, discontinue the thiazide diuretic and substitute it (if possible) with a loop diuretic, and reduce the dose of or discontinue (if possible) the loop diuretic.

4) In patients with hyperuricemia and gout, avoid NSAIDs.

5) In patients with possible hypovolemia, determine the volume status and consider reducing doses of diuretics.

6) In patients with renal failure, exclude hypovolemia and concomitant use of other nephrotoxic agents (eg, NSAIDs), then discontinue aldosterone antagonists and thiazides (in patients treated with loop diuretics in combination with thiazides) and consider reduction of the dose of the ACEI/ARB.

7) High-dose loop diuretics may be ototoxic.

2. Beta-blockers: Evidence supporting beta-blockers is drug-specific to bisoprolol, carvedilol, and metoprolol. They should be used in patients with NYHA classes II to IV and LVEF ≤40% or in patients with asymptomatic systolic LV dysfunction after myocardial infarction (MI) who have already been receiving an optimal ACEI or ARB dose and are clinically stable.Evidence 5Strong recommendation (benefits clearly outweigh downsides; right action for all or almost all patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Foody JM, Farrell MH, Krumholz HM. beta-Blocker therapy in heart failure: scientific review. JAMA. 2002 Feb 20;287(7):883-9. Review. PubMed PMID: 11851582. Treatment with a beta-blocker may be started with caution in patients with a recent history of HF decompensation as long as their condition has improved as a result of other treatments or the use of ongoing intravenous inotropic agents is not required. Agents and doses: Table 3.8-5.

General recommendations: During dose titration follow-up visits should be scheduled every 2 to 4 weeks and the dose should be doubled at each visit as tolerated. Do not increase the dose in case of symptoms of HF exacerbation, symptomatic hypotension (eg, dizziness), or bradycardia <50 beats/min.

Management of adverse effects:

1) Symptomatic hypotension frequently resolves spontaneously with time. Consider reducing doses of other antihypertensive agents (except for ACEIs and ARBs), for instance, diuretics or nitrates.

2) HF exacerbation: Increase the dose of diuretics (frequently a temporary increase is sufficient) and continue the beta-blocker treatment (frequently at a lower dose), if possible. In case of cardiogenic shock/hypoperfusion, discontinue the beta-blocker and use an intravenous inotropic agent such as milrinone or dobutamine (Table 3.8-2).

3) Excessive bradycardia: Perform ECG (or Holter ECG) to exclude a heart block. Consider discontinuation of digoxin if the patient is treated with this agent. Dose reduction or discontinuation of the beta-blocker may be necessary.

3. ACEIs: ACEIs should be initiated in patients with LVEF ≤40%, regardless of symptoms.Evidence 6Strong recommendation (benefits clearly outweigh downsides; right action for all or almost all patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Flather MD, Yusuf S, Køber L, et al. Long-term ACE-inhibitor therapy in patients with heart failure or left-ventricular dysfunction: a systematic overview of data from individual patients. ACE-Inhibitor Myocardial Infarction Collaborative Group. Lancet. 2000 May 6;355(9215):1575-81. PubMed PMID: 10821360. Once target or maximal tolerated doses are achieved, consideration should be given for persistently symptomatic patients to be switched to the equivalent dose of ARNIs (see below). Doses: Table 3.8-6.

General recommendations:

1) Avoid excessive diuretic treatment before starting ACEIs (you may reduce the doses of diuretics 24 hours before the start of ACEI treatment).

2) Consider increasing the dose after 2 to 4 weeks of ACEI treatment. Do not increase the dose in patients with significant deterioration in renal function or with hyperkalemia. In hospitalized or closely-monitored patients who tolerate the drug, the dose may be uptitrated more rapidly.

3) Monitor renal function and serum electrolyte levels at baseline; within 1 to 2 weeks of starting ACEI treatment; 1 and 4 weeks after the dose increase; 1, 3, and 6 months after reaching the target maintenance dose; and subsequently every 6 months.

Management of adverse effects (suggestions):

1) Kidney function impairment: Serum blood urea nitrogen and creatinine levels may increase after the initiation of ACEI treatment; this is not clinically relevant unless rapid and severe. Exclude hypovolemia, dehydration, other medications (eg, NSAIDs, COX-2 inhibitors, cyclosporine, excessive doses of diuretics). The patient should be closely monitored.

a) An increase in serum creatinine levels ≤50% is acceptable unless it exceeds 265 micromol/L (~3 mg/dL).

b) In patients with a serum creatinine increase of 50% to 100% or >265 micromol/L but ≤310 micromol/L (~3.5 mg/dL), reduce the ACEI dose by half.

c) In patients with a serum creatinine increase >100% or >310 micromol/L, discontinue the ACEI immediately.

2) Hyperkalemia: Check for other agents that may be the cause (eg, potassium supplements, potassium-sparing diuretics) and discontinue them.

a) In patients with serum potassium levels >5.5 mmol/L, reduce the ACEI dose by half.

b) In patients with serum potassium levels >6.0 mmol/L, discontinue the ACEI immediately and admit for cardiac monitoring and treating hyperkalemia.

3) Symptomatic hypotension (eg, dizziness) often resolves spontaneously even if the ACEI dose is not changed. Consider reducing the dose of diuretics and other hypotensive agents (except for ARBs, beta-blockers, and aldosterone antagonists).

4) Cough (in ~10% patients): Independent of the ACEI dose, cough usually appears within 1 week of ACEI treatment but may also occur after up to several months. It generally resolves within 3 to 5 days after discontinuation of ACEIs, but may persist for up to a month or in rare cases even for several months. It usually recurs with the use of a different ACEI. If the cough is persistent and troublesome, switch to an ARB, if needed.

5) Angioedema (<1% patients): Switch to an ARB (although on very rare occasions angioedema may also occur after ARBs).

4. ARNIs: Use these preferentially over ACEIs in patients with HFrEF (LVEF <40%) who remain symptomatic (NYHA classes II-IV) and have elevated levels of BNP or NT-proBNP despite treatment with optimal medical therapy, including maximally tolerated ACEIs (ARBs), beta-blockers, and mineralocorticoid-receptor antagonists.Evidence 7Weak recommendation (benefits likely outweigh downsides, but the balance is close or uncertain; an alternative course of action may be better for some patients). Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to lack of long-term follow up and single-trial data. McMurray JJ, Packer M, Desai AS, et al; PARADIGM-HF Investigators and Committees. Angiotensin-neprilysin inhibition versus enalapril in heart failure. N Engl J Med. 2014 Sep 11;371(11):993-1004. doi: 10.1056/NEJMoa1409077. PubMed PMID: 25176015. Patients on ACEIs should be converted to the equivalent dose of ARNIs after a washout period of 36 hours (see above). Patients who do not tolerate ARNIs may be switched back to ACEIs after a 36-hour washout period. The role of ARNIs is rapidly evolving, and long-term data on this class of medications are unavailable at this time.

ARNIs are contraindicated in patients with hypotension (systolic blood pressure ≤95 mm Hg), significant renal impairment (glomerular filtration rate ≤30 mL/min), hyperkalemia (K+ ≥5.2 mmol/L), or severe hepatic disease (liver enzymes >2 × upper limit of normal).

Closely monitor serum levels of K+ (≤5.2 mmol/L) and creatinine (estimated glomerular filtration rate ≥30 mL/min).

Ensure that patients are not concomitantly on an ACEI (a 36-hour washout period from ACEIs is required to reduce the risk of angioedema).

Agents and dosage: Table 3.8-6. Doses can be uptitrated every 2 to 4 weeks.

5. ARBs: ARBs are used in NYHA classes II to IV patients with LVEF ≤40% who do not tolerate ACEIs or ARNIs because of persistent cough or angioedema.Evidence 8Weak recommendation (benefits likely outweigh downsides, but the balance is close or uncertain; an alternative course of action may be better for some patients). Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to imprecision and heterogeneity. Heran BS, Musini VM, Bassett K, Taylor RS, Wright JM. Angiotensin receptor blockers for heart failure. Cochrane Database Syst Rev. 2012 Apr 18;(4):CD003040. doi: 10.1002/14651858.CD003040.pub2. Review. PubMed PMID: 22513909. Granger CB, McMurray JJ, Yusuf S, et al; CHARM Investigators and Committees. Effects of candesartan in patients with chronic heart failure and reduced left-ventricular systolic function intolerant to angiotensin-converting-enzyme inhibitors: the CHARM-Alternative trial. Lancet. 2003 Sep 6;362(9386):772-6. PubMed PMID: 13678870. Do not use a combination of an ACEI and an ARB due to the risk of adverse events.

General recommendations and management of adverse effects are the same as in ACEIs except for cough. Agents and dosage: Table 3.8-6.

6. Aldosterone antagonists (eplerenone, spironolactone) should be used in patients with:Evidence 9Strong recommendation (benefits clearly outweigh downsides; right action for all or almost all patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Zannad F, McMurray JJ, Krum H, et al; EMPHASIS-HF Study Group. Eplerenone in patients with systolic heart failure and mild symptoms. N Engl J Med. 2011 Jan 6;364(1):11-21. doi: 10.1056/NEJMoa1009492. PubMed PMID: 21073363. Pitt B, Remme W, Zannad F, et al; Eplerenone Post-Acute Myocardial Infarction Heart Failure Efficacy and Survival Study Investigators. Eplerenone, a selective aldosterone blocker, in patients with left ventricular dysfunction after myocardial infarction. N Engl J Med. 2003 Apr 3;348(14):1309-21. Erratum in: N Engl J Med. 2003 May 29;348(22):2271. PubMed PMID: 12668699. Pitt B, Zannad F, Remme WJ, et al. The effect of spironolactone on morbidity and mortality in patients with severe heart failure. Randomized Aldactone Evaluation Study Investigators. N Engl J Med. 1999 Sep 2;341(10):709-17. PubMed PMID: 10471456.

1) LVEF ≤35% and NYHA classes II to IV.

2) LVEF ≤40%, recent MI, and HF symptoms or diabetes mellitus.

In both cases, patients should have been already treated with an ACEI or an ARB (but not both!) and a beta-blocker, all in optimal doses. Agents and dosage: Table 3.8-4.

General recommendations:

1) Consider increasing the dose 4 to 8 weeks after starting the treatment. Do not increase the dose in case of significant deterioration of kidney function or hyperkalemia.

2) Monitor kidney function and serum electrolyte levels 1 and 4 weeks after starting the treatment and after increasing the dose; then at 2, 3, 6, 9, and 12 months; and subsequently every 4 months.

3) Do not use aldosterone antagonists in pregnant patients.

Management of adverse effects:

1) In patients with deterioration of kidney function, close monitoring is necessary (suggestions below):

a) In patients with serum creatinine levels >220 micromol/L (~2.5 mg/dL), reduce the dose by half (eg, 25 mg every other day).

b) In patients with serum creatinine levels >310 micromol/L (~3.5 mg/dL), immediately discontinue aldosterone antagonists.

2) In patients with hyperkalemia, close monitoring is necessary:

a) In patients with serum potassium levels >5.5 mmol/L, reduce the dose by half.

b) In patients with serum potassium levels >6.0 mmol/L, immediately discontinue aldosterone antagonists.

3) In patients with breast tenderness and/or enlargement, switch from spironolactone to eplerenone.

7. Consider ivabradine,Evidence 10Weak recommendation (benefits likely outweigh downsides, but the balance is close or uncertain; an alternative course of action may be better for some patients). Low Quality of Evidence (low confidence that we know true effects of the intervention). Quality of Evidence lowered due to indirectness (patients in the SHIFT trial were not on optimal tolerated dose of beta-blockers and relatively young [60 years; standard deviation, 11.2]; the safety may be different in older patients who are more sensitive to heart-rate reduction therapy) and heterogeneity of results (in post-MI patients with reduced ejection fraction there was no difference vs placebo for their primary composite outcomes). Swedberg K, Komajda M, Böhm M, et al; SHIFT Investigators. Ivabradine and outcomes in chronic heart failure (SHIFT): a randomised placebo-controlled study. Lancet. 2010 Sep 11;376(9744):875-85. doi: 10.1016/S0140-6736(10)61198-1. Erratum in: Lancet. 2010 Dec 11;376(9757):1988. Lajnscak, M [corrected to Lainscak, M]; Rabanedo, I Roldan [corrected to Rabadán, I Roldan]; Leva, M [corrected to Ieva, M]. PubMed PMID: 20801500. Fox K, Ford I, Steg PG, Tendera M, Ferrari R; BEAUTIFUL Investigators. Ivabradine for patients with stable coronary artery disease and left-ventricular systolic dysfunction (BEAUTIFUL): a randomised, double-blind, placebo-controlled trial. Lancet. 2008 Sep 6;372(9641):807-16. doi: 10.1016/S0140-6736(08)61170-8. PubMed PMID: 18757088. which reduces the heart rate by having selective effects on the sinus node, in patients with:

1) LVEF ≤35%, preserved sinus rhythm ≥70 beats/min, and NYHA classes II to IV despite the use of an ACEI (or an ARB), an aldosterone antagonist, and a beta-blocker at optimal doses.

2) Contraindications to or intolerance of beta-blockers.

General recommendations: Start with 5 mg bid and after 2 weeks increase the dose to 7.5 mg bid, provided the patient continues to be in sinus rhythm with a rate of >60 beats/min (treatment with ivabradine cannot be the reason for reducing the dose of a beta-blocker without a strong justification, as the benefit of ivabradine is in reducing readmissions [no effect on mortality]).

Management of adverse effects:

1) Asymptomatic sinus bradycardia <50 beats/min or symptomatic bradycardia: Reduce the dose to 2.5 mg bid. If the symptoms persist, discontinue ivabradine.

2) Bradycardia associated with hemodynamic instability: Discontinue ivabradine. Consider administration of a beta-agonist (eg, isoproterenol [INN isoprenaline]) or temporary pacing, if necessary.

3) Vision disturbances (transient sensation of bright light in a portion of the visual field, which may interfere with the ability to drive) usually occur in the first 2 months of treatment and generally resolve spontaneously. However, discontinuation of treatment must be considered in case of a sudden vision impairment.

Note: Occurrence of atrial fibrillation (AF) or atrial flutter during treatment with ivabradine increases the risk of rapid ventricular rate if the patient does not receive concomitant beta-blockers or low-dose beta-blockers. Ivabradine should be discontinued ≥24 hours before an elective cardioversion.

8. Digoxin reduces hospitalization with no survival benefit. It may be considered in HF patients with LVEF ≤40% who remain symptomatic (NYHA classes II-IV) despite receiving treatment with an ARNI or ACEI (or an ARB in patients intolerant to either ARNIs or ACEIs), a beta-blocker, and an aldosterone antagonist at optimal doses.Evidence 11Weak recommendation (benefits likely outweigh downsides, but the balance is close or uncertain; an alternative course of action may be better for some patients). Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to indirectness (main trial was conducted in an era when beta-blockers and aldosterone antagonists were not the mainstay of HF treatment). Digitalis Investigation Group. The effect of digoxin on mortality and morbidity in patients with heart failure. N Engl J Med. 1997 Feb 20;336(8):525-33. PubMed PMID: 9036306.

Once the clinical status is stabilized, digoxin is preferably used in combination with a beta-blocker. Digoxin may be used in stable patients in whom beta-blockers are not tolerated, ineffective, or contraindicated. If the effects of the combined treatment with digoxin and a beta-blocker are insufficient for rate control in AF, you may switch from digoxin to amiodarone. Avoid combination of digoxin, a beta-blocker, and amiodarone.

Contraindications: Hypertrophic cardiomyopathy with LV outflow tract obstruction, preexcitation syndromes, hypokalemia, hypercalcemia, life-threatening ventricular arrhythmia, cardiac amyloidosis (digoxin binds to amyloid), multifocal atrial tachycardia, patients prior to planned electric cardioversion, bradycardia, second-degree and third-degree atrioventricular blocks, sick sinus syndrome (unless the patient has an implanted pacemaker).

General recommendations:

1) Boluses of 0.25 to 0.5 mg IV (loading dose up to 1 mg over 8-24 hours) may be used to slow down rapid ventricular rate in digoxin-naive patients with HF and AF in an acute setting followed by 0.125 to 0.25 mg/d. Loading doses are not recommended in hemodynamically stable patients with AF and in patients with preserved sinus rhythm. With routine maintenance doses (0.125-0.25 mg orally per day), steady state serum drug levels are achieved within ~7 days.

2) In elderly patients and in patients with impaired renal function, hypothyroidism, or low body weight, the maintenance doses are 0.0625 or 0.125 mg/d orally. Exercise caution with the loading dose in this population.

3) It has not been proven that regular serum digoxin level measurements are associated with improved outcomes (therapeutic range is 0.6-1.2 ng/mL).

4) Serum digoxin levels may be increased by amiodarone, diltiazem, verapamil, certain antibiotics (macrolides, tetracyclines), proton pump inhibitors, H2-blockers, and quinidine.

Management of adverse effects: see Digoxin and Other Cardiac Glycosides.

9. A fixed-dose combination of hydralazine (or dihydralazine) and isosorbide dinitrate: In patients with LVEF ≤35% (or LVEF ≤45% and LV dilation), this may be considered an alternative to the ACEI/ARNI/ARB if none of these agents are tolerated due to renal dysfunction (in such cases, use it in combination with a beta-blocker and an aldosterone antagonist). Adding the combination to treatment may also be considered in patients who have persistent symptoms of HF when receiving treatment with an ACEI/ARNI/ARB, a beta-blocker, and an aldosterone antagonist and is recommended in HF patients self-described as African Americans who remain symptomatic despite treatment with an ACEI, a beta-blocker, and an aldosterone antagonist.

Adverse effects: Symptomatic hypotension, tachycardia, arthralgia, myalgia, drug-induced lupus-like syndrome.

10. Omega-3 polyunsaturated fatty acids: 1 g/d may be considered.

11. Antithrombotic treatment should be used in patients with additional indications, that is, paroxysmal or persistent AF or atrial flutter, intracardiac thrombus, or a history of peripheral embolism.

Treatment of HFpEF

There is no convincing data to date for treatments that reduce morbidity or mortality in patients with HF and preserved EF. Nonetheless, the current standard of practice includes:

1) Optimal treatment of the underlying condition: This may involve rate control in the setting of AF, treatment of sleep apnea with continuous positive airway pressure, strict control of hypertension (preferably using agents that reduce LV remodeling [ACEIs and ARBs]), revascularization in CAD.

2) Restriction of sodium and of fluid intake if the patient is hyponatremic: As in HFrEF.

3) Beta-Blockers are used to improve LV filling by extending diastole (target resting heart rates 60-70 beats/min, or 55-60 beats/min in patients with angina), particularly in patients after MI or with angina, either with sinus rhythm or with AF. Digoxin may be used in patients with AF and rapid ventricular rhythm or in patients with AF not responding to monotherapy with a beta-blocker, verapamil, or diltiazem (digoxin reduces mainly the resting heart rate, while beta-blockers reduce heart rates on exertion). Assess the feasibility of restoring sinus rhythm.

4) Diuretics are used in patients with symptoms of fluid retention. Use these with caution to avoid excessive reduction in cardiac output and subsequent hypotension (measure supine and standing BP) as well as impairment of kidney function.

Invasive Treatment

Consider referral to a specialized center.

1. Cardiac resynchronization therapy (CRT) involves placement of 2 electrodes to stimulate the right and left ventricles, and an additional electrode in the right atrium to synchronize the stimulation of the ventricles with the intrinsic atrial rhythm. CRT improves exercise tolerance, reduces the incidence of hospitalization caused by symptom exacerbation, and in patients with preserved sinus rhythm also reduces the risk of death.

Consider referral to a specialized center in patients who are clinically stable, have a life expectancy >1 year with reasonable functional status, and (1) are symptomatic with EF ≤35%, and QRS ≥130 milliseconds in the case of left bundle branch block (LBBB); or (2) have QRS ≥150 milliseconds in the case of non-LBBB QRS morphology.

Note: Patients with a decreased EF may be candidates for CRT-D (CRT defibrillator; CRT + ICD placement). Therefore, when qualifying patients for CRT, we typically assess LVEF and the NYHA class after ≥3 months of optimal pharmacotherapy; in patients with ischemic heart disease, after >40 days post-MI; and after >3 months post–percutaneous coronary intervention.

2. Implantable cardioverter-defibrillator (ICD): These devices have been shown to reduce sudden cardiac death (SCD) and are typically considered in patients receiving optimal pharmacotherapy for ≥3 months, after revascularization (where indicated), and with >1-year life expectancy of good functional status. Consider referral to a specialized cardiac center for assessment in the following cases:

1) Primary prevention:

a) Post-MI systolic LV dysfunction (LVEF ≤35% measured >40 days after MI and >3 months after coronary revascularization, whenever performed) in patients with NYHA classes II to III.

b) NYHA classes II to III systolic LV dysfunction (LVEF ≤35%) of a nonischemic etiology (primary prevention of SCD).

2) Secondary prevention: History of ventricular fibrillation or ventricular tachycardia causing a loss of consciousness or hemodynamic instability regardless of LVEF, as long these were not due to a transient or reversible condition, for instance, in the first 48 hours of MI.

In patients who meet the above criteria and have concomitant indications for CRT, implantation of a device with both CRT and ICD functions (CRT-D) is preferred.

3. Coronary revascularization is usually done in patients with HF caused by ischemic heart disease, particularly with symptoms of angina. In the absence of angina, establish indications for revascularization on the basis of documented ischemia of a viable myocardium supplied by an artery suitable for revascularization.

4. In patients refractory to medical, invasive, and device treatments, consider referral to a specialized center for heart transplantation assessment. Left ventricular assist devices (LVADs) may be used when waiting for the transplant in patients with HFrEF.

RehabilitationTop

Participation in interval or continuous training programs is recommended in HF regardless of LVEF values as long as the patient is clinically stable and physical activity does not lead to exhaustion or trigger new HF symptoms.Evidence 12Strong recommendation (benefits clearly outweigh downsides; right action for all or almost all patients). Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to low precision of estimates for all-cause mortality and unclear risk of bias. Taylor RS, Sagar VA, Davies EJ, et al. Exercise-based rehabilitation for heart failure. Cochrane Database Syst Rev. 2014 Apr 27;(4):CD003331. doi: 10.1002/14651858.CD003331.pub4. Review. PubMed PMID: 24771460. O'Connor CM, Whellan DJ, Lee KL, et al; HF-ACTION Investigators. Efficacy and safety of exercise training in patients with chronic heart failure: HF-ACTION randomized controlled trial. JAMA. 2009 Apr 8;301(14):1439-50. doi: 10.1001/jama.2009.454. PubMed PMID: 19351941; PubMed Central PMCID: PMC2916661. Isometric exercise is not recommended.

PrognosisTop

SCD accounts for up to 50% of all deaths among patients with HF. An improved prognosis in HF has been documented in:

1) Patients treated with ACEIs or ARBs or ARNIs, beta-blockers, aldosterone antagonists, and hydralazine/isosorbide (the last one in African Americans on contemporary treatments with other drugs). Diuretics in monotherapy have no effect on prognosis.

2) Certain subgroups of patients treated with CRT or ICD as well as patients after coronary revascularization.

Chronic heart failure is marked by periods of stability interspersed with exacerbations requiring hospitalization. Epidemiologic data from Medicare beneficiaries hospitalized for HF suggested a 30-day readmission risk of 25% and a 1-year mortality risk of 37%. Advanced HF is characterized by frequent exacerbations, intolerance of preventive therapies, metabolic perturbations, and overall deterioration that culminates in death.Evidence 13 Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to indirectness to today’s evolving treatment options. Curtis LH, Greiner MA, Hammill BG, et al. Early and long-term outcomes of heart failure in elderly persons, 2001-2005. Arch Intern Med. 2008 Dec 8;168(22):2481-8. doi: 10.1001/archinte.168.22.2481. PubMed PMID: 19064833; PubMed Central PMCID: PMC2629051. Meta-analysis Global Group in Chronic Heart Failure (MAGGIC). The survival of patients with heart failure with preserved or reduced left ventricular ejection fraction: an individual patient data meta-analysis. Eur Heart J. 2012 Jul;33(14):1750-7. doi: 10.1093/eurheartj/ehr254. Review. PubMed PMID: 21821849. In the current era of ICD use, SCD has been replaced by pump failure as a common mechanism of death.

Overall, patients with HFpEF may have a better prognosis than those with HFrEF. A meta-analysis of published trials in HF patients found the 3-year all-cause mortality rate to be 32% in HFrEF (adjusted for prognostic risk factors) versus 24% in HFpEF.

Patients with HFpEF are typically older, more often female, less likely to have ischemic heart disease, and more likely to have a history of hypertension than patients with HFrEF patients.

Tables and FiguresTop

Table 3.8-3. New York Heart Association (NYHA) classification of heart failure

Class

Functional capacity

I

No limitation of physical activity. Ordinary physical activity does not cause undue fatigue, dyspnea, or palpitation

II

Slight limitation of physical activity. The patient is comfortable at rest, but ordinary physical activity results in fatigue, palpitation, or dyspnea

III

Marked limitation of physical activity. The patient is comfortable at rest, but less than ordinary activity causes fatigue, palpitation, or dyspnea

IV

Any physical activity causes discomfort. Symptoms of heart failure may be present even at rest. Discomfort increases with any physical activity

Based on: The Criteria Committee of the New York Heart Association. Nomenclature and Criteria for Diagnosis of Diseases of the Heart and Great Vessels. 9th ed. Boston, Mass: Little, Brown & Co; 1994:253-256.

Table 3.8-4. Dosage of oral diuretics in patients with chronic heart failure

Agent

Starting dose (mg/d)

Usual dose (mg/d)

Loop diuretics

Furosemidea

20-40

40-240

Torasemide

5-10

10-20

Thiazide and thiazide-like diuretics

Chlorthalidone

12.5-25

25-100

Hydrochlorothiazide

25

12.5-100

Indapamide

2.5 (1.5 mg when using controlled-release formulations)

2.5-5

Potassium-sparing diureticsb

Amiloride (available only in a fixed combination with hydrochlorothiazide)

2.5 (5)

5-10 (10-20)

Eplerenone

25 (50)

50 (100)

Spironolactone

12.5-25 (50)

50 (100-200)

a The diuretic effect starts within 30 to 60 minutes, peaks in 1 to 2 hours, and ends after 6 to 8 hours.

b Doses used in patients who are not treated with an angiotensin-converting enzyme inhibitor or an angiotensin receptor blocker are given in parenthesis.

Table 3.8-5. Dosage of evidence-informed beta-blockers in patients with chronic heart failure

Beta-blocker

Starting dose (mg)a

Subsequent doses up to target dose (mg)

Bisoprolol

1.25

2.5 to 3.75 to 5 to 7.5 to 10

Carvedilol

3.125

6.25 to 12.5 to 25 to 50

Metoprolol succinate controlled-release

12.5 or 25

25 to 50 to 100 to 200

a Carvedilol is administered 2 times a day, while other listed beta-blockers are administered once daily. The table lists single doses of the agents.

Table 3.8-2. Use of intravenous inotropic agents in patients with acute heart failure

Agents

Dosage

Comments

Dopamine

1) <3 microg/kg/min

2) 3-5 microg/kg/min

3) >5 microg/kg/min (max, 30 microg/kg/min)

– Low doses (1) mainly cause vasodilation of the visceral, renal, and coronary vascular beds; intermediate doses (2) increase myocardial contractility and cardiac output via adrenergic stimulation; high doses (3) increase peripheral vascular resistance through alpha-adrenergic stimulation (this may cause clinical deterioration in patients with AHF due to an increase in LV and right ventricular afterloads)

– May be used in patients with AHF and low BP

– Low-dose dopamine is often used in combination with higher doses of dobutamine

– Survival on dopamine may be worse compared to norepinephrine in case of cardiogenic shock (hypotension and hypoperfusion)Evidence 14Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to subgroup analysis of a randomized controlled trial with unclear classification of the type of shock. De Backer D, Biston P, Devriendt J, et al; SOAP II Investigators. Comparison of dopamine and norepinephrine in the treatment of shock. N Engl J Med. 2010 Mar 4;362(9):779-89. doi: 10.1056/NEJMoa0907118. PubMed PMID: 20200382.

Dobutamine

2-20 microg/kg/min

– Used to increase cardiac output

– Stimulates beta1-receptors, increases myocardial contractility, increases heart rate; lower doses cause vasodilation while higher doses cause vasoconstriction

– Infusion over >24 to 48 hours is associated with the development of tolerance and partial loss of hemodynamic effects

– Discontinuation may be difficult because of recurrent low BP, congestion, or kidney failure, which is why the infusion rates should be reduced gradually (by 2 microg/kg/min per day) and used together with optimized vasodilator therapy (eg, PO ACEIs)

– May cause ventricular or supraventricular arrhythmia and chest pain in patients with IHD

Milrinone

Bolus 25-75 microg/kg over 10-20 min followed by infusion of 0.375-0.75 microg/kg/min

– Phosphodiesterase inhibitor (inhibits cAMP degradation); has positive inotropic effects and facilitates myocardial relaxation and vasodilation

– Indicated in patients with peripheral hypoperfusion and normal BP with or without pulmonary congestion in whom diuretic and vasodilator treatment was ineffective

– May be used instead of dopamine in patients treated with beta-blockers in the case of inadequate response to dobutamine

– May have proarrhythmic effects and should be used with caution in patients with IHD

Norepinephrine

0.2-2 microg/kg/min

– Use (with caution!) only in patients with cardiogenic shock and BP <90 mm Hg when organ perfusion is inadequate in spite of other interventions

– May be indicated in shock patients with AHF and sepsis

– May be combined with each of the above inotropic agents (use with caution in combination with dopamine)

Epinephrine

1 mg every 3-5 min (only during CPR); 0.05-0.5 microg/kg/min

Use only during CPR in patients with cardiac arrest or in the case of dobutamine resistance and persistent hypotension

Digoxin

Loading dose 0.5-1 mg, followed by 0.125-0.375 mg/day (monitor serum drug levels)

Effective in patients with AHF caused by tachyarrhythmia (eg, AF); not recommended in patients with AHF after acute MI because of its proarrhythmic effects

ACEI, angiotensin-converting enzyme inhibitor; AF, atrial fibrillation; AHF, acute heart failure; BP, blood pressure; cAMP, cyclic adenosine monophosphate; CPR, cardiopulmonary resuscitation; IHD, ischemic heart disease; LV, left ventricle; MI, myocardial infarction; PO, oral.

Table 3.8-6. Recommended dosage of ACEIs, ARBs, and ARNIs in patients with chronic heart failure

Agent

Dose

Starting

Target

ACEIs

Enalapril

2.5 mg bid

10-20 mg bid

Captopril

6.25 mg tid

50 mg tid

Lisinopril

2.5-5 mg once daily

20-35 mg once daily

Ramipril

2.5 mg once daily

5 mg bid

Trandolapril

0.5 mg once daily

4 mg once daily

ARBs

Candesartan

4 mg or 8 mg once daily

32 mg once daily

Valsartan

40 mg bid

160 mg bid

Losartana

50 mg once daily

150 mg once daily

ARB + ARNI

Valsartan/sacubitrilb

24/26 mg bid

97/103 mg bid

Contraindications: Table 3.9-5.

a Losartan is mentioned in the 2012 European Society of Cardiology guidelines but it has been stressed in the text that the benefits of using the agent may be lower.

b Valsartan component in the valsartan/neprilysin combination pill Entresto is more potent than valsartan monotherapy pills available on the market. Therefore, caution must be exercised not to equate valsartan dosage found in current monotherapy with the dose found in Entresto, as it will lead to prescribing a higher than the intended dose.

ACEI, angiotensin-converting enzyme inhibitors; ARB, angiotensin receptor blockers; ARNI, angiotensin receptor neprilysin inhibitor; bid, 2 times a day; tid, 3 times a day.

Figure 3.8-3. Suggested management of chronic heart failure. Adapted from the 2016 European Society of Cardiology guidelines.

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