NPS Prescribing Practice Review 41: Improving outcomes in chronic heart failure
Published in MedicineWise News
Date published: About this date
Clinical content may change after this date. This information is not intended as a substitute for medical advice from a qualified health professional. Health professionals should rely on their own expertise and enquiries when providing medical advice or treatment.
- Identify high-risk heart failure patients for frequent review and management of risk factors
- Order an echocardiogram in suspected heart failure due to symptoms, signs or risk factors
- Titrate ACE inhibitors using heart failure dosing regimens; optimal doses may be higher than those used in hypertension
- Use heart-failure-specific beta blockers for all patients with systolic heart failure after stabilisation, and up-titrate slowly to the maximally tolerated or target dose
- Identify and avoid drugs that exacerbate heart failure
- Use the heart failure action plan to discuss fluid balance, medication adherence and lifestyle changes
Heart failure is a clinical syndrome of limited cardiac output and/or fluid congestion. It results from the inability of the heart to meet the body's demands at normal filling pressure. Chronic heart failure is usually progressive, but with appropriate diagnosis and treatment the symptoms and prognosis are markedly improved.
High-risk heart failure patients need frequent review and individualised management
Review patients with heart failure more often if they are at high risk
Frequently review patients with established heart failure when they are at high risk of premature mortality, morbidity or hospital re-admission. Risk factors include:
- age ≥ 65 years
- NYHA Class III or IV symptoms
- left ventricular ejection fraction (LVEF) ≤ 30%
- living alone or remote from specialist medical services
- language barrier (e.g. non-English speaking)
- lower socio-economic status
- significant renal dysfunction (estimated glomerular filtration rate < 60 mL/min/1.73m2).1
High-risk patients, especially the elderly, more frequently develop decompensation of heart failure. More frequent clinical review permits early detection of impending deterioration and adjustments in therapy.
Assess high-risk patients, especially the elderly, for preventable causes of worsening heart failure
More than half of all hospital admissions for worsening heart failure are preventable.2 Addressing these causes with tailored patient education and support, and close follow-up, can reduce the need for hospital admission.3,4
Preventable causes include:
- inadequate or inappropriate medical treatment
- adverse effects of prescribed therapy
- poor understanding of the underlying diagnosis or therapy
- unrecognised decompensation of symptoms or volume overload
- non-adherence with drug and non-drug therapies
- poor social support.1,2
Ensure optimal drug doses are being taken that improve survival
Effective drugs exist for all stages of systolic heart failure. Check for optimal doses by reviewing medication lists at routine visits. Regularly review adherence with medications and identify and address the barriers for individual patients.
Data extraction tools that conduct a practice wide search of electronic records can help to identify patients who may benefit from a medication review. NPS is currently incorporating heart failure indicators into two available tools that extract data from prescribing software.
Suspect heart failure in people with risk factors, symptoms or clinical signs — order an echocardiogram
Be alert to signs and symptoms of heart failure
Symptoms of heart failure can be non-specific and the clinical findings subtle. Heart failure may be virtually asymptomatic in the early stages and many at-risk patients remain undiagnosed.5
Suspect heart failure in patients with unexplained breathlessness, fatigue, exercise limitation, weight gain or fluid retention, especially in the elderly.1
Consider patients at high risk of developing heart failure for further investigation
Also suspect heart failure in people with established risk factors, such as advanced age, existing hypertension, obesity, diabetes, and coronary heart disease. Careful history and physical examination may help to identify heart failure in these patients early.
If heart failure is suspected, further investigations are required including an electrocardiogram (ECG), chest X-ray, echocardiography and, where indicated, specialist assessment.1
Confirm the diagnosis with an echocardiogram
Refer all patients with suspected heart failure for an echocardiogram. This confirms the diagnosis and provides important information about underlying abnormalities in ventricular and valvular cardiac structure and function.
An echocardiogram distinguishes whether the diagnosis is systolic heart failure(left ventricular systolic dysfunction), diastolic heart failure (heart failure with preserved systolic function) or both, which has important treatment implications.1,6
Use target doses of ACE inhibitors in all patients with systolic heart failure
Titrate the ACE inhibitor dose to the recommended target dose or that which is maximally tolerated
ACE inhibitor doses that improve survival in heart failure may be higher than those used to control hypertension. Start an ACE inhibitor at a low dose and increase the dose at regular intervals (no less than 2 weekly intervals).6–8 Refer to NPS News 57 for target doses of ACE inhibitors that are recommended in heart failure.
To maximise the survival benefits of ACE inhibitor therapy, review medication lists regularly and increase the dose toward the recommended target. However, treatment must always be individualised depending on patient tolerability, blood pressure and renal function.
Angiotensin II-receptor antagonists are an alternative in ACE inhibitor intolerance
Angiotensin II-receptor antagonists appear to be as effective as ACE inhibitors in reducing mortality and morbidity in symptomatic heart failure (NYHA Class II – IV).9–12 They are an alternative for those who are intolerant of ACE inhibitors.1
Studies evaluating the effects of combined therapy with an ACE inhibitor and an angiotensin II-receptor antagonist have shown mixed results. Such combination therapy should generally only be undertaken under specialist supervision.6
Use diuretics for symptom relief only
Diuretics control fluid retention, they have no clear effect on mortality and thus should be used in combination with standard therapies that improve survival.1 Titrate the dose according to symptoms and volume status to reduce fluid overload but minimise dehydration and intravascular volume depletion. Monitor renal function and potassium levels to avoid electrolyte disturbances.1,6
Add spironolactone and/or digoxin for people who remain symptomatic despite optimal doses of an ACE inhibitor and diuretic
Low-dose spironolactone improves survival in severe symptomatic left ventricular systolic heart failure.13 Eplerenone is used early in addition to standard therapy (ACE inhibitor and beta blocker) for myocardial infarction complicated by heart failure and left ventricular impairment.14
Digoxin can be added to spironolactone if symptoms worsen or for rate control of coexisting atrial fibrillation.1 Digoxin reduces hospitalisation due to worsening heart failure, but has no clear effect on mortality.15
Start a heart-failure-specific beta blocker in stabilised systolic heart failure and titrate toward the target dose
Add a heart-failure-specific beta blocker to an ACE inhibitor to improve survival
Add a heart-failure-specific beta blocker (carvedilol, bisoprolol or metoprolol SR) to an ACE inhibitor for all patients with stable symptomatic heart failure (NYHA Class II – IV), and those with asymptomatic left ventricular systolic dysfunction (NYHA Class I) following myocardial infarction.1
Using a heart-failure-specific beta blocker with an ACE inhibitor provides significant additional mortality and morbidity benefits compared with placebo.16–20 A meta-analysis of 22 trials with over 10 000 patients (mean duration 3 to 23 months), showed that adding a beta blocker to an ACE inhibitor reduced the risk of all-cause mortality and hospital admission for heart failure by about one third compared with placebo (8.4% vs 12.8% and 10.3% vs 15.6% respectively).20
Start very low and go slow
Start heart-failure-specific beta blockers at a very low dose and slowly titrate upwards if tolerated (at not less than 2-weekly intervals). Aim for a target dose that has proven benefits in heart failure, or the maximally tolerated dose.6,8 Refer to NPS News 57 for the recommended target doses of beta blockers in heart failure.
Frequent monitoring is required when initiating and titrating the dose
Initiating beta blocker therapy can temporarily worsen heart failure — it should not be started until patients are stabilised on appropriate doses of an ACE inhibitor and/or other medications.1
Monitor heart rate, blood pressure and clinical status for signs of worsening heart failure when starting a beta blocker and during dose titration. Check serum urea, creatinine and electrolytes at baseline, 1–2 weeks after starting therapy, at each dose titration and regularly thereafter.6,8
Symptomatic hypotension or bradycardia (heart rate less than 50 beats per minute) may necessitate a dose reduction. Manage other possible causes of hypotension or bradycardia and consider resuming beta blocker therapy once the patient is stable.6,8,21
Specialist input may be valuable when initiating a beta blocker in primary care, especially for GPs less familiar with managing heart failure.8
Identify and avoid drugs that exacerbate heart failure
Ask patients what other drugs they take and regularly review medication lists for drugs that worsen heart failure
Identify and avoid where possible drugs known to exacerbate heart failure including:
- anti-arrhythmic drugs (except heart-failure-specific beta blockers and amiodarone)
- non-dihydropyridine calcium channel blockers (e.g. verapamil, diltiazem)
- tricyclic antidepressants (e.g. amitriptyline, doxepin)
- conventional NSAIDs
- COX-2 selective NSAIDs (e.g. celecoxib)
- thiazolidinediones (e.g. rosiglitazone, pioglitazone)
- corticosteroids (e.g. hydrocortisone, prednisone)
- oncology drugs (e.g. anthracyclines, trastuzumab)
- tumour necrosis factor antagonists (e.g. infliximab, etanercept)
- preparations with a high salt content (e.g. urinary alkalinisers).1,14
Consider potential drug interactions that may occur between therapies for heart failure
Monitor adverse effects when adding a drug to existing therapy, especially in elderly patients and patients with renal impairment. Adding an aldosterone antagonist (spironolactone or eplerenone) to an ACE inhibitor or angiotensin II-receptor antagonist may cause hyperkalaemia. Additive hypotensive effects may occur if beta blockers are taken with other drugs that have this effect.14
Enabling patients to play an active role in self-management improves outcomes
Talk about heart failure using the 'Living well with chronic heart failure' information sheet and action plan
Ensure that patients understand their condition and treatment goals by providing the Heart Foundation's 'Living well with chronic heart failure' information sheet and action plan. This outlines important aspects of self-management and answers common questions asked by patients. This resource is available for download at www.heartfoundation.org.au/chf and can be printed from prescribing software.
Emphasise to patients the importance of:
- taking medicines as prescribed
- monitoring and controlling fluid balance (i.e. fluid and salt restriction, recording weight daily)
- making long-term lifestyle changes.
Reinforce at every visit the benefits of adherence with therapies and health-related behaviours, to prevent worsening heart failure.
Encourage patients to call the Heart Foundation's Heart Health Information Service on 1300 362 787 to obtain a copy of the 'Living well with chronic heart failure' booklet.
Refer patients to a specialised heart failure management program, ideally within their local community
There is increasing evidence to support multidisciplinary management of heart failure, especially in the elderly and those at high risk of re-admission to hospital.22–27 A systematic review found that specialised follow-up by a multidisciplinary team reduced all-cause mortality by 25%, all-cause hospitalisation by 19%, and heart failure hospitalisation by 26% compared with usual care.22
Call the Heart Foundation on 1300 362 787 to find out what programs are available for your patients in their local area.
Provide patients with advice and strategies for making long-term lifestyle changes
Strategies for long-term lifestyle changes include:
- accessing smoking cessation information and support
- restricting alcohol intake to 1–2 standard drinks per day (preferably no intake)
- undertaking regular light to moderate physical activity
- participating in a rehabilitation or exercise program specifically designed for people with heart failure.1
Call the Heart Foundation on 1300 362 787 for information about rehabilitation or exercise programs available in your local area.
Dr Michael McCready MD, FRCPC, Cardiologist and General Physician, Wagga Wagga, NSW, Conjoint Lecturer, University of New South Wales
Professor Henry Krum MBBS, PhD, FRACP, Director, NHMRC Centre of Clinical Research Excellence in Therapeutics, Department of Epidemiology and Preventive Medicine, Monash University/Alfred Hospital
- National Heart Foundation of Australia and the Cardiac Society of Australia and New Zealand. Guidelines for the prevention, detection and management of chronic heart failure in Australia. 2006.
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- Krumholz H, et al. J Am Coll Cardiol 2002;39:83–9.
- Jovicic A, et al. BMC Cardiovasc Disord 2006;6:43.
- Abhayaratna WP, et al. Med J Aust 2006;184:151–4.
- Scottish Intercollegiate Guidelines Network (SIGN). Management of chronic heart failure: a national clinical guideline. 2007.
- National Institute for Clinical Excellence. Management of chronic heart failure in adults in primary and secondary care. 2003.
- Sowerby Centre for Health Informatics at Newcastle (SCHIN) Ltd. Clinical Knowledge Summaries: heart failure. 2006.
- Pitt B, et al. Lancet 2000;355:1582–7.
- Pfeffer M, et al. N Engl J Med 2003;349:1893–906.
- Dickstein K, et al. Lancet 2002;360:752–60.
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- CIBIS-II Investigators and Committees. Lancet 1999;353:9–13.
- MERIT-HF study group. Lancet 1999;353:2001–7.
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- Packer M, et al. N Engl J Med 2001;344:1651–8.
- Brophy J, et al. Ann Intern Med 2001;134:550–60.
- Swedberg K, et al. Eur Heart J 2005;26:1115–40.
- McAlister F, et al. J Am Coll Cardiol 2004;44:810–9.
- Gonseth J, et al. Eur Heart J 2004 25:1570–95.
- Phillips C, et al. JAMA 2004;291:1358–67.
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- Rich M, et al. N Engl J Med 1995;333:1190–5.
- Doughty R, et al. Eur Heart J 2002;23:139–46.