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Brief Summary

GUIDELINE TITLE

Guidelines for the prevention, detection and management of chronic heart failure in Australia, 2006.

BIBLIOGRAPHIC SOURCE(S)

  • National Heart Foundation of Australia, Cardiac Society of Australia and New Zealand, Chronic Heart Failure Guidelines Expert Writing Panel. Guidelines for the prevention, detection and management of chronic heart failure in Australia, 2006. Sydney (Australia): National Heart Foundation of Australia; 2006 Nov. 79 p. [335 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: National Heart Foundation of Australia, Cardiac Society of Australia and New Zealand. Guidelines on contemporary management of the patient with chronic heart failure in Australia. Sydney (Australia): National Heart Foundation of Australia; 2002.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s) for which important revised regulatory and/or warning information has been released.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Throughout the original guideline document, boxed "practice points" highlight key issues, while summaries of graded recommendations are provided for most sections.

The grades of recommendations (A-D) are defined at the end of the "Major Recommendations" field.

Diagnosis

Symptoms of Chronic Heart Failure (CHF)

Practice Point

Clinical diagnosis of CHF is often unreliable, especially in obese patients, those with pulmonary disease and the elderly. Therefore, it is important to perform investigations to confirm the diagnosis.

Diagnostic Investigations

Practice Point

The classic symptom of CHF is exertional dyspnoea or fatigue. Orthopnoea, paroxysmal nocturnal dyspnoea (PND) and ankle oedema may appear at a later stage.

Physical signs are often normal in the early stages. Examination should include assessment of vital signs, cardiac auscultation (murmurs, S3 gallop) and checking for signs of fluid retention (e.g., raised jugular venous pressure, peripheral oedema, basal inspiratory crepitations).

All patients with suspected CHF should undergo an electrocardiogram (ECG), chest x-ray, and echocardiogram, even if the physical signs are normal.

Full blood count, plasma urea, creatinine, and electrolytes should be measured during the initial workup, and if there are any changes in the patient's clinical status. Urea, creatinine, and electrolytes should also be checked regularly in stable patients, and when changes are made to medical therapy.

The role of plasma B-type natriuretic peptide (BNP) measurements is evolving, but it has been shown to improve diagnostic accuracy in patients presenting with unexplained dyspnoea. In patients with new symptoms, where the diagnosis is not clear following the initial clinical assessment and an echocardiogram cannot be organised in a timely fashion, then measurement of BNP or N-terminal proBNP may be helpful. In this setting, a normal level makes the diagnosis of heart failure unlikely (especially if the patient is not taking cardioactive medication). If the level is raised, further investigation—including echocardiography — is warranted.

Underlying aggravating or precipitating factors (e.g., arrhythmias, ischaemia, non-adherence to diet or medications, infections, anaemia, thyroid disease, addition of exacerbating medications) should be considered and managed appropriately.

Recommendations for Diagnostic Investigation of CHF

  • All patients with suspected CHF should undergo an echocardiogram to improve diagnostic accuracy and determine the mechanism of heart failure. (Grade of recommendation = D)
  • Coronary angiography should be considered in patients with a history of exertional angina or suspected ischaemic left ventricular (LV) dysfunction. (Grade of recommendation = D)
  • Plasma BNP measurement may be helpful in patients presenting with recent-onset dyspnoea; it has been shown to improve diagnostic accuracy with a high negative predictive value. (Berger et al., 2002) (Grade of recommendation = B)
  • Haemodynamic measurements may be particularly helpful in patients with refractory CHF, recurrent heart failure with preserved systolic function (HFPSF) (diastolic CHF), or in whom the diagnosis of CHF is in doubt (Stevenson et al., 1990) (Grade of recommendation = D)
  • Endomyocardial biopsy may be indicated in patients with cardiomyopathy with recent onset of symptoms, where coronary heart disease (CHD) has been excluded by angiography, or where an inflammatory or infiltrative process is suspected (McCarthy et al., 2000) (Grade of recommendation = D)
  • Nuclear cardiology, stress echocardiography and positron emission tomography (PET) can be used to assess reversibility of ischaemia and viability of myocardium in patients with CHF who have myocardial dysfunction and CHD. Protocols have been developed using magnetic resonance imaging (MRI) to assess ischaemia and myocardial viability, and to diagnose infiltrative disorders. However, MRI is not widely available. (Grade of recommendation = D)
  • Thyroid function tests should be considered, especially in older patients without pre-existing CHD who develop atrial fibrillation, or in whom no other cause of CHF is evident. (Grade of recommendation = D)

Supporting Patients

Recommendations for Discussion with Patients with CHF

  • Lifestyle: Adopt a healthier lifestyle to address risk factors/conditions contributing to the development and progression of CHF (see Section 6, Non-pharmacological management, in the original guideline document).
  • Personal issues: Understand the effect of CHF on personal energy levels, mood, depression, sleep disturbance and sexual function, and develop strategies to cope with changes and emotions related to family, work and social roles.
  • Medical issues: Consider practical issues related to pregnancy, contraception, genetic predisposition and practical items, such as an alert bracelet and a diary for daily weights/medications.
  • Support: Access to support services, such as Heart Support Australia, Cardiomyopathy Association of Australia, home help and financial assistance.

Practice Point

Information for people with CHF can be obtained through the Heart Foundation's telephone information service, Heartline 1300 36 27 87 (local call cost) and the Heart Foundation website: www.heartfoundation.com.au.

Patients should also consult their local phone directories for contact details for Heart Support Australia and the Cardiomyopathy Association of Australia in each state.

Non-pharmacological Management

Physical Activity and Rehabilitation

Practice Point

Non-pharmacological management may be as important as prescribing appropriate medications. Patients with CHF may develop physical deconditioning. Therefore, regular physical activity is recommended using a rehabilitation program tailored to suit the individual. Other measures are listed in the recommendations below.

Sleep Apnoea

Practice Point

If sleep apnoea is suspected, referral to a sleep physician is indicated.

Recommendations for Non-pharmacological Management of CHF*

  • Regular physical activity is recommended (Mancini et al., 1992). All patients should be referred to a specially designed physical activity program, if available (Chati et al., 1996; Meyer et al., 1997; Sinoway, 1998) (Grade of recommendation = B)
  • Patient support by a doctor and pre-discharge review and/or home visit by a nurse is recommended to prevent clinical deterioration (Rich et al., 1995; Stewart et al., 1999) (Grade of recommendation = A)
  • Patients frequently have coexisting sleep apnoea and, if suspected, patients should be referred to a sleep clinician as they may benefit from nasal continuous positive airway pressure (CPAP) (Naughton, 1998) (Grade of recommendation = D)
  • Patients who have an acute exacerbation, or are clinically unstable, should undergo a period of bed rest until their condition improves (McDonald, Burch, & Walsh, 1972) (Grade of recommendation = D)
  • Dietary sodium should be limited to below 2 g/day (Stewart et al., 1999) (Grade of recommendation = C)
  • Fluid intake should generally be limited to 1.5 L/day with mild to moderate symptoms, and 1 L/day in severe cases, especially if there is coexistent hyponatraemia (Fonarow et al., 1997) (Grade of recommendation = C)
  • Alcohol intake should preferably be nil, but should not exceed 10 to 20 g a day (one to two standard drinks) (Fonarow et al., 1997) (Grade of recommendation = D)
  • Smoking should be strongly discouraged. (Grade of recommendation = D)
  • Patients should be advised to weigh themselves daily and to consult their doctor if weight increases by more than 2 kg in a two-day period, or if they experience dyspnoea, oedema, or abdominal bloating. (Grade of recommendation = D)
  • Patients should be vaccinated against influenza and pneumococcal disease. (Grade of recommendation = B)
  • High-altitude destinations should be avoided. Travel to very humid or hot climates should be undertaken with caution, and fluid status should be carefully monitored. (Grade of recommendation = C)
  • Sildenafil and other phosphodiesterase V inhibitors are generally safe in patients with heart failure. However, these medications are contraindicated in patients receiving nitrate therapy, or those who have hypotension, arrhythmias, or angina pectoris (Zusman et al., 1999) (Grade of recommendation = C)
  • Obese patients should be advised to lose weight. (Grade of recommendation = D)
  • A diet with reduced saturated fat intake and a high fibre intake is encouraged in patients with CHF. (Grade of recommendation = D)
  • No more than two cups of caffeinated beverages per day recommended. (Grade of recommendation = D)
  • Pregnancy should be avoided in patients with CHF. (Grade of recommendation = D)

* These grades of recommendation apply only to patients with CHF

Pharmacological Therapy

Recommendations for Preventing CHF and Treating Asymptomatic LV Dysfunction

  • All patients with asymptomatic systolic LV dysfunction should be treated with an angiotensin-converting enzyme inhibitor (ACEI) indefinitely, unless intolerant (Pfeffer et al., 1992; "Effect of enalapril," 1992) (Grade of recommendation = A)
  • Anti-hypertensive therapy should be used to prevent subsequent CHF in patients with elevated blood pressure (Kostis et al., 1997; Dahlof et al., 1991; "Medical Research Council trial of treatment," 1992; Hansson et al., 1999; Hansson et al., 2000; Brown et al., 2000) (Grade of recommendation = A)
  • Preventive treatment with an ACEI may be considered in individual patients at high risk of ventricular dysfunction (Yusuf et al., 2000) (Grade of recommendation = B)
  • Beta-blockers should be commenced early after a myocardial infarction (MI), whether or not the patient has systolic ventricular dysfunction (Dahlof et al., 1991; "Medical Research Council trial of treatment," 1992) (Grade of recommendation = B)
  • Statin therapy should be used as part of a risk management strategy to prevent ischaemic events and subsequent CHF in patients who fulfill criteria for lipid-lowering (Kjekshus et al., 1997) (Grade of recommendation = B)

Treatment of Symptomatic Systolic Heart Failure

Practice Point

All patients with systolic LV dysfunction, whether symptomatic or asymptomatic, should be commenced on ACE inhibitors with every effort made to up-titrate to the dose shown to be of benefit in major trials. Other recommended medications are listed in the recommendations below.

Practice Point

Drugs to avoid in CHF:

  • Anti-arrhythmic agents (apart from beta-blockers and amiodarone)
  • Non-dihydropyridine calcium-channel blockers (verapamil, diltiazem)
  • Tricyclic antidepressants
  • Non-steroidal anti-inflammatory drugs and COX-2 inhibitors
  • Clozapine
  • Metformin and thiazolidinediones (pioglitazone, rosiglitazone)
  • Corticosteroids (glucocorticoids and mineralocorticoids)
  • Tumour necrosis factor antagonist biologicals

Recommendations for Pharmacological Treatment of Symptomatic CHF

First-line Agents

  • ACEIs, unless not tolerated or contraindicated, are recommended for all patients with systolic heart failure (left ventricular ejection fraction [LVEF] <40%), whether symptoms are mild, moderate, or severe (The SOLVD Investigators, 1991; The CONSENSUS Trial Study Group, 1987) (Grade of recommendation = A)
  • Every effort should be made to increase doses of ACEIs to those shown to be of benefit in major trials ("Clinical outcome," 1998; Packer et al., 1999). If this is not possible, a lower dose of ACEI is preferable to none at all. (Grade of recommendation = B)
  • Diuretics should be used, if necessary, to achieve euvolaemia in fluid-overloaded patients. In patients with systolic LV dysfunction, diuretics should never be used as monotherapy, but should always be combined with an ACEI to maintain euvolaemia. (Grade of recommendation = D)
  • Beta-blockers are recommended, unless not tolerated or contraindicated, for all patients with systolic CHF who remain mildly to moderately symptomatic despite appropriate doses of an ACEI (Packer et al., "The effect of carvedilol," 1996; "Effect of metoprolol CR/XL," 1999; "The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II)," 1999; Packer et al., 2001) (Grade of recommendation = A)
  • Beta-blockers are also indicated for patients with symptoms of advanced CHF (Packer et al.,  2001) (Grade of recommendation = B)
  • Aldosterone receptor blockade with spironolactone is recommended for patients who remain severely symptomatic, despite appropriate doses of ACEIs and diuretics (Pitt et al., 1999) (Grade of recommendation = B)
  • Eplerenone is recommended in the early post-MI period for patients with LV systolic dysfunction and symptoms of heart failure. (Grade of recommendation = B)
  • Angiotensin II receptor antagonists may be used as an alternative in patients who do not tolerate ACEIs due to kinin-mediated adverse effects (e.g., cough) (Pitt et al., 1997). They should also be considered for reducing morbidity and mortality in patients with systolic CHF who remain symptomatic despite receiving ACEIs. (Grade of recommendation = A)

Second-line Agents

  • Digoxin may be considered for symptom relief and to reduce hospitalisation in patients with advanced CHF (Digitalis Investigation Group, 1997). It remains a valuable therapy in CHF patients with atrial fibrillation. (Grade of recommendation = B)
  • Hydralazine-isosorbide dinitrate combination should be reserved for patients who are truly intolerant of ACEIs and angiotensin II receptor antagonists, or for whom these agents are contraindicated and no other therapeutic option exists (Cohn et al., 1986) (Grade of recommendation = B)

Other Agents

  • Amlodipine and felodipine can be used to treat comorbidities such as hypertension and CHD in patients with systolic CHF. They have been shown to neither increase nor decrease mortality (Packer et al., "Effect of amlodipine," 1996; Cohn et al., 1997; Packer, 2000) (Grade of recommendation = B)

Devices

Pacing

Practice Point

Bradycardia is common in elderly patients with advanced heart disease treated with beta-blocker therapy.

Implantable Cardioverter Defibrillators

Practice Point

Prophylactic implantable cardioverter defibrillator (ICD) implantation may be considered in patients with an LVEF <35%; however, this is currently constrained by funding and other logistical issues. Until these issues are resolved, this therapy may not be universally available.

Decisions about pacing, cardiac resynchronisation therapy, defibrillators, and choice of device are complex and generally require specialist review.

Recommendations for Device-Based Treatment of Symptomatic CHF

  • Biventricular pacing (cardiac resynchronisation therapy, with or without ICD) should be considered in patients with CHF who fulfill each of the following criteria (Cazeau et al., 2001) (Grade of recommendation = A):
    • New York Heart Association [NYHA] symptoms Class III–IV on treatment
    • Dilated heart failure with left ventricular ejection fraction <35%
    • QRS duration >120 ms
    • Sinus rhythm
  • ICD implantation should be considered in patients with CHF who fulfill any of the following criteria (Bristow et al., 2004) (Grade of recommendation = A):
    • Survived cardiac arrest resulting from ventricular fibrillation or ventricular tachycardia not due to a transient or reversible cause
    • Spontaneous sustained ventricular tachycardia in association with structural CHD
    • LVEF <30% measured at least 1 month after acute MI, or 3 months after coronary artery revascularisation surgery
    • Symptomatic CHF (i.e., NYHA functional class II–III) and left ventricular ejection fraction <35%

Surgery

Indications for Cardiac Transplantation

Definite
  • Persistent NYHA Class IV symptoms
  • VO2 max <10 mL/kg/min
  • Severe ischaemia not amenable to revascularisation
  • Recurrent uncontrollable ventricular arrhythmias
Probable
  • NYHA Class III
  • VO2 max <14 mL/kg/min + major limitation
  • Recurrent unstable angina with poor LV function
Inadequate
  • LVEF <20% without significant symptoms
  • Past history of NYHA Class III or IV symptoms
  • VO2 max >14 mL/kg/min without other indication

Acute Exacerbations of CHF

Practice Point

Acute pulmonary oedema (APO) is a life-threatening disorder. However, appropriate therapy will often result in a marked improvement in the patient's clinical status within a few hours.

Emergency Management of Suspected Cardiogenic APO

A (airway)
  • Exclude obstruction
B (breathing)
  • Hypoxaemia (→ oxygenation)
  • Respiratory fatigue (→ mechanical ventilation)
C (circulation)
  • Heart rate/rhythm (→ anti-arrthymics/cardioversion)
  • Hypotension (→ inotropes/intra-aortic balloon pump)
D (differential diagnosis)
  • Cardiogenic APO
  • Non-cardiogenic pulmonary oedema
  • Acute exacerbation of airways disease
  • Acute massive pulmonary embolism
  • Pneumothorax
  • Foreign body aspiration
  • Hyperventilation syndrome
E (aetiology)
(cardiogenic APO)
  • Precipitants
  • Ischaemia, tachyarrhythmia, fluid overload, medication
  • Underlying pathology
  • Systolic LV dysfunction—coronary heart disease, dilated cardiomyopathy, mitral regurgitation
  • Diastolic LV dysfunction—hypertensive heart disease, hypertrophic cardiomyopathy, aortic stenosis
  • Normal LV function—mitral stenosis

See Figure 10.1 in the original guideline document for emergency therapy of acute heart failure.

Heart Failure with Preserved Systolic Function (HFPSF)

Epidemiology/Clinical Characteristics

Practice Point

Although the epidemiology of HFPSF or diastolic heart failure has been incompletely described, the main risk factors are advanced age, hypertension, diabetes, LV hypertrophy, and CHD. Diagnosis, investigation, and treatment are summarised in the Table below.

Diagnosis, Investigation, and Treatment of HFPSF

Diagnosis
  • Clinical history of CHF
  • Exclude myocardial ischaemia, valvular disease
  • Objective evidence of CHF (x-ray consistent with CHF)
  • Ejection fraction >45% (echocardiography, gated blood pool scanning, left ventriculography)
  • Echocardiographic or cardiac catheterization evidence of diastolic dysfunction, where possible
  • Use of plasma BNP measurement for diagnosis of diastolic heart failure is not proven.
Investigations

Echocardiography

  • Pseudonormal or restrictive filling pattern demonstrated by mitral inflow (age appropriate)
  • Left atrial enlargement
  • Reduced septal annular velocity (Ea) on tissue Doppler imaging
  • Ratio of E wave to Ea >15

Cardiac catheterisation

  • Elevated LV end diastolic pressure
  • Prolonged Tau
Treatment (empirical at this stage)
  • Aggressive risk factor reduction
  • Hypertension—blood pressure (BP) reduction; consider ACEIs or angiotensin II receptor antagonists to reduce LV hypertrophy
  • Diabetes mellitus—strict glycaemic and BP control; consider ACEIs or angiotensin II receptor antagonists early, using lower BP recommendations for treating hypertension in diabetic patients

Treatment of Associated Disorders

See Chapter 12 in the original guideline document for a discussion of treatment of associated disorders, including cardiac arrhythmia, valvular heart disease, CHD, arthritis, chronic renal failure, anaemia, cancer, diabetes, thromboembolism, and gout.

Post-discharge Management Programs

Practice Point

Multidisciplinary programs of care targeting high-risk CHF patients following acute hospitalisation prolong survival, improve quality of life, and are cost effective in reducing recurrent hospital stays.

Palliative Support

Practice Point

An individualised program of palliative care should be considered for patients facing the strong possibility of death within 12 months and who have advanced symptoms (i.e., NYHA Class IV) and poor quality of life, resistant to optimal pharmacological and non-pharmacological therapies.

Practice Point

Palliative care should only be considered when progressive symptoms prove to be refractory to optimal treatment.

Treating doctors should discuss with their patients the level of intervention appropriate and/or desirable during this phase of their illness, so that unwanted, traumatic interventions are prevented in the last few days of life. Both the patient and their family and carers may need significant emotional support during this process.

Definitions:

Grades of Recommendations

  1. Rich body of high-quality randomized controlled trial (RCT) data
  2. Limited body of RCT data or high-quality non-RCT data
  3. Limited Evidence
  4. No evidence available – panel consensus judgment

CLINICAL ALGORITHM(S)

Clinical algorithms are provided in the original guideline document for the following:

  • Diagnostic algorithm for chronic heart failure (CHF)
  • Advanced diagnostic/treatment algorithm for CHF
  • Pharmacological treatment of asymptomatic left ventricular (LV) dysfunction (left ventricular ejection fraction [LVEF] <40%) (New York Heart Association [NYHA] Class I)
  • Pharmacologic treatment of systolic heart failure (LVEF <40%) (NYHA Class II-III)
  • Pharmacologic treatment of refractory systolic heart failure (LVEF <40%) (NYHA Class IV)
  • Pharmacologic treatment of heart failure after recent or remote myocardial infarction (MI)
  • Management of clinical deterioration in CHF
  • Management of heart failure with preserved systolic function (HFPSF) (diastolic heart failure)

EVIDENCE SUPPORTING THE RECOMMENDATIONS

REFERENCES SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for selected recommendations (see "Major Recommendations" field).

Recommendations based on consensus expert opinion are also included where evidence-based recommendations are not available.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • National Heart Foundation of Australia, Cardiac Society of Australia and New Zealand, Chronic Heart Failure Guidelines Expert Writing Panel. Guidelines for the prevention, detection and management of chronic heart failure in Australia, 2006. Sydney (Australia): National Heart Foundation of Australia; 2006 Nov. 79 p. [335 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2002 (revised 2006 Nov)

GUIDELINE DEVELOPER(S)

Cardiac Society of Australia and New Zealand - Disease Specific Society
National Heart Foundation of Australia - Disease Specific Society

SOURCE(S) OF FUNDING

National Heart Foundation of Australia
Cardiac Society of Australia and New Zealand

GUIDELINE COMMITTEE

Writing Panel

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Panel Members: Prof Henry Krum (Co-chair); A/Prof Michael Jelinek (Co-chair); Prof Simon Stewart; Prof Andrew Sindone; A/Prof John Atherton; Dr Anna Hawkes (Executive Officer)

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Many members of the Writing Panel have received paid honoraria for work performed on behalf of manufacturers of therapies described in these guidelines. However, no members of the Writing Panel stand to gain financially from their involvement in these guidelines and no conflicts of interest exist for Writing Panel members, the National Heart Foundation of Australia or the Cardiac Society of Australia and New Zealand.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: National Heart Foundation of Australia, Cardiac Society of Australia and New Zealand. Guidelines on contemporary management of the patient with chronic heart failure in Australia. Sydney (Australia): National Heart Foundation of Australia; 2002.

GUIDELINE AVAILABILITY

Electronic copies: Available in Portable Document Format (PDF) from the National Heart Foundation of Australia.

Print copies: Available from the National Heart Foundation of Australia's national telephone information service at 1300 36 27 87 or E-mail: heartline@heartfoundation.com.au.

AVAILABILITY OF COMPANION DOCUMENTS

The following is available:

Print copies: Available from the National Heart Foundation of Australia's national telephone information service at 1300 36 27 87 or E-mail: heartline@heartfoundation.com.au.

PATIENT RESOURCES

The following are available:

Print copies of the entire booklet available via e-mail at: heartline@heartfoundation.org.au.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This NGC summary was completed by ECRI on April 12, 2007. The information was verified by the guideline developer on June 27, 2007. This summary was updated by ECRI Institute on September 7, 2007 following the revised U.S. Food and Drug Administration (FDA) advisory on Coumadin (warfarin). This summary was updated by ECRI Institute on November 6, 2007, following the updated U.S. Food and Drug Administration advisory on Viagra, Cialis, Levitra, and Revatio.

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