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National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand Reducing risk in heart disease An expert guide to clinical practice for secondary prevention of coronary heart disease – summary Updated 2012 This summary guide is based on the full guide document: Reducing risk in heart disease: an expert guide to clinical practice for secondary prevention of coronary heart disease (updated 2012). Call the Health Information Service on 1300 36 27 87 or visit www.heartfoundation.org.au for a copy. Endorsed by: Reducing risk in heart disease An expert guide to clinical practice for secondary prevention of coronary heart disease – summary Lifestyle/behavioural risk factors and management Smoking Goal: Complete cessation of smoking and avoidance of second-hand smoke. Nutrition Goals: Establishment and maintenance of healthy eating patterns including: • saturated fatty acid < 7% and trans fatty acid < 1% of total energy intake1 • consumption of 1 g eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA) and > 2 g alpha linolenic acid (ALA) daily • limiting salt intake to ≤ 4 g/day (1550 mg sodium). Alcohol Goal: Consumption of a low-risk amount of alcohol by patients who drink. Physical activity Goal: Progress, over time, to at least 30 minutes of moderate-intensity* physical activity on most, if not all, days of the week (150 minutes/week minimum). Healthy weight Goals:† • Waist measurement < 94 cm (men) and < 80 cm (women) • Body mass index (BMI) = 18.5–24.9 kg/m2 Biomedical risk factors/medical management Lipids Goals: • Low-density lipoprotein cholesterol (LDL-C) < 1.8 mmol/L‡ • High-density lipoprotein cholesterol (HDL-C) > 1.0 mmol/L • Triglyceride (TG) < 2.0 mmol/L • Non–high-density lipoprotein cholesterol (NHDL-C) < 2.5 mmol/L§ Blood pressure Goal: Patients with coronary heart disease (CHD) achieve and maintain a blood pressure (BP) of < 130/80 mmHg.2,** Diabetes Goal: maintain optimal blood sugar level (BSL) (HbA1c ≤ 7%).3 * Moderate-intensity physical activity causes a moderate, noticeable increase in depth and rate of breathing, while still leaving you able to talk comfortably. Examples include † Goals are based mainly on evidence of increased risk of death in European populations. They may not be appropriate for all age groups and ethnic groups. ‡ This target is for high-risk patients who have had a coronary event. § NHDL-C is calculated by subtracting HDL-C from total cholesterol (TC). It combines LDL-C, very low density lipoprotein cholesterol (VLDL-C), intermediate density lipoprotein (IDL-C) and lipoprotein (a) (LP(a)). The NHDL-C does not assume normal lipoprotein composition, does not require a fasting specimen, and may be a better indicator than LDL-C in patients with high TG (such as patients with diabetes).4 **This includes patients with or without diabetes and/or stroke/transient ischaemic attack (TIA) and/or microalubuminuria (men > 2.5 mg/mmol, women > 3.5 mg/mmol). Pharmacological management Antiplatelet agents5 • All patients should take 75–150 mg/day of aspirin unless contraindicated. • Addition of clopidogrel may be relevant in patients with recurrent ischaemic events, post-stent implantation. • Prasugrel and ticagrelor are alternatives to clopidogrel in patients with acute coronary syndromes (ACS). Anticoagulants • Use warfarin in patients at high risk of thromboembolism post–myocardial infarction (MI). • Monitor closely for signs of bleeding, particularly when combined with antiplatelets. ACE inhibitors (ACEIs)/Angiotensin II receptor antagonists (ARAs) 6 • We recommend ACEIs in all patients, especially those at high risk, unless contraindicated. Start early post-MI. • Consider ARAs for patients who develop unacceptable side effects on ACEIs. Beta-blockers6 • We recommend beta-blockers in all patients post-MI, especially in high-risk patients, unless contraindicated. Statins7 • We recommend statins in all patients with CHD, unless contraindicated. • For hospitalised patients, therapy should start during admission. Aldosterone antagonists6,8 • Eplerenone may be used early post-MI in patients with left ventricular systolic dysfunction and symptoms of heart failure. Short-acting nitrates5 • All patients should be prescribed a short-acting nitrate, unless contraindicated, and provided with a written action plan for chest pain. Initiating and sustaining behaviour change Secondary prevention/cardiac rehabilitation (SP/CR) programs Goal: Warning signs of heart attack: action plan9,10 Goal: Everyone with CHD is prescribed a short-acting nitrate, unless contraindicated, and given an action plan to follow if they experience warning signs of heart attack. Psychosocial factors and assessment Psychological management11 Goal: Assess all patients for comorbid depression. Initiate psychological and medical management if appropriate. Social support Goal: Assess all patients for their level of social support. Further information Executive writing group Key contributors Professor Patricia Davidson (chair) Professor Nigel Stocks Dr Anu Aggarwal Ms Jill Waddell Ms Rebecca Lee Professor Derek Chew Associate Professor David Sullivan Ms Shanthi Thuraisingham All members of the writing group were asked to declare any conflicts of interest at the commencement of the project and at each teleconference. Professor Nigel Stocks received consultancy fees from AstraZeneca (ACCOUNT study) and Novartis (VIPER-BP study). No other conflicts of interest were declared by members of the writing group. This guide will be reviewed regularly and modified when necessary to take into account new research, new technologies, and the results of evaluation of guideline outcomes. References 1.National Heart Foundation of Australia. Position statement: Dietary fats and dietary sterols for cardiovascular health. Melbourne: National Heart Foundation of Australia, 2009. 2.National Heart Foundation of Australia (National Blood Pressure and Vascular Disease Advisory Committee). Guide to management of hypertension 2008. Updated 2010. Melbourne: National Heart Foundation of Australia, 2010. 3.Colagiuri S, Dickinson S, Girgis S, et al. National evidence based guideline for blood glucose control in type 2 diabetes. Canberra: Diabetes Australia and the National Health and Medical Research Council, 2009. 4.Hirsch GA, Vaid N, Blumenthal RS. The significance of measuring non-HDL-cholesterol. Available from: www.medscape.com/ viewarticle/438773. Accessed 4 January 2012. 5.Chew DP, Aroney CN, Aylward PE, et al. 2011 Addendum to the National Heart Foundation of Australia/Cardiac Society of Australia and New Zealand Guidelines for the management of acute coronary syndromes (ACS) 2006. Heart Lung Circ 2011; 20(8):487–502. 6.National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand. Guidelines for the management of acute coronary syndromes 2006. Med J Aust 2006; 184 (Suppl.):S1–S32. 7.Tonkin A, Barter P, Best J, et al. National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand: position statement on lipid management 2005. Heart Lung Circ 2005; 14(4):275–291. 8.National Heart Foundation of Australia and 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. Updated July 2011. Melbourne: National Heart Foundation of Australia, 2011. 9.National Heart Foundation of Australia. Heart attack warning signs: checklist of important information to discuss with patients. Melbourne: National Heart Foundation of Australia, 2011. 10.National Heart Foundation of Australia. Heart attack warning signs: fact sheet about reducing delays in patient response. Melbourne: National Heart Foundation of Australia, 2011. 11.Lichtman JH, Bigger JT Jr, Blumenthal JA, et al. Depression and coronary heart disease: recommendations for screening, referral, and treatment: a science advisory from the American Heart Association Prevention Committee of the Council on Cardiovascular Nursing, Council on Clinical Cardiology, Council on Epidemiology and Prevention, and Interdisciplinary Council on Quality of Care and Outcomes Research: endorsed by the American Psychiatric Association. Circulation 2008; 118(17):1768–1765. © 2012 National Heart Foundation of Australia ABN 98 008 419 761 This work is copyright. No part of this publication may be reproduced in any form or language without prior written permission from the National Heart Foundation of Australia (national office). Enquiries concerning permissions should be directed to [email protected]. ISBN 978-1-74345-022-2 PRO-139 Disclaimer: This document has been produced by the National Heart Foundation of Australia for the information of health professionals. The statements and recommendations it contains are, unless labelled as ‘expert opinion’, based on independent review of the available evidence. Interpretation of this document by those without appropriate medical and/or clinical training is not recommended, other than at the request of, or in consultation with, a relevant health professional. While care has been taken in preparing the content of this material, the Heart Foundation and its employees cannot accept any liability, including for any loss or damage, resulting from the reliance on the content, or for its accuracy, currency and completeness. The information is obtained and developed from a variety of sources including, but not limited to, collaborations with third parties and information provided by third parties under licence. 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