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syndromes (ACS)
This presentation reflects the recommendations in the National Heart Foundation of Australia/Cardiac
Society of Australia and New Zealand’s Guidelines for the Management of Acute Coronary Syndromes
(ACS) (2006), updated in the 2007 and 2011 addenda. The presentation is designed for use in health
professional development and training on acute ACS care.
Outline
• Cardiovascular disease (CVD) – the facts and risk factors
• Acute coronary syndromes (ACS)
• Presentation of ACS
ACS management: summary of updates in the 2011 addendum1
1. Systems of care
2. Investigations
3. Management of patients with ST-segment elevation myocardial
infarction (STEMI)
4. Management of patients with non-ST-segment elevation ACS (NSTEACS)
5. Long-term management
Reference
1. 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.
CVD – the facts
• Heart disease is the single leading
cause of death.
References
1. National Heart Foundation of Australia. Heart Attack Facts. Available from: http://www.heartattackfacts.org.au. Accessed 19 June 2012.
2. National Heart Foundation of Australia. The shifting burden of cardiovascular disease, report prepared by Access Economics. Melbourne: National Heart Foundation of Australia, 2005.
Risk factors for CVD
Modifiable risk factors(Those Non-modifiable risk
which can be altered to reduce factors(those which cannot be
CV risk): altered)
• smoking • gender
• poor diet • age
• high cholesterol • family history of CVD
• physical inactivity • diabetes
• high blood pressure • human immunodeficiency virus
• being overweight (HIV).
• depression, social isolation and
lack of social support.
Acute coronary syndromes (ACS)
Reference
1. Chew DP, Allan RM, Aroney CN, et al. National data elements for the clinical management of acute coronary syndromes. Med J Aust 2005; 182 (9 Suppl):S1–S14.
Thrombus formation in the arterial lumen
Acute presentation of ACS
• Critical factors to timely Heart attack
treatment:
recognition
time
The pain may spread to other parts of the upper body, including:
• back, neck, jaw, arm(s), shoulder(s) or epigastric pain.
Reference
1. 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.
1. Systems of care to support delivery of
ACS services
Formal systems of care:
• defined continuum of care – from presentation to long-term management
• system-based approaches to deliver timely reperfusion at a local level (Grade B)
• routine audit integrated into all clinical ACS services (Grade B)
• training GPs/health workers to initiate fibrinolysis (if primary percutaneous coronary
intervention [PCI] services are not readily accessible)
• practitioners are supported by ready access to expert cardiology consultation (Consensus)
• cardiac clinical networks established with appropriate protocols (Grade B).
For example: iCCnet CHSA network links > 70 hospitals, health centres and general
practitioner [GP] surgeries across SA, aligned to the Health Reform Agenda principles.
2. Early response: Timely treatment is critical
Time from symptom onset and likely outcome
< 1 hour
Aborted heart attack or only little heart muscle damage
1–2 hours
Minor heart muscle damage only
2–4 hours
Some heart muscle damage with moderate heart muscle salvage
4–6 hours
Significant heart muscle damage with only minor heart muscle salvage
6–12 hours
No heart muscle salvage (permanent loss) with potential infarct
healing benefit
> 12 hours
Reperfusion is not routinely recommended if the patient is
asymptomatic and haemodynamically stable
Reference
1. Acute Coronary Syndrome Guidelines Working Group. Guidelines for the management of acute coronary syndromes 2006. Med J Aust 2006; 184(8 Suppl):S9–29.
PCI cardiac catheter
The catheter can be inserted via the radial or femoral artery (insertion via the femoral artery
illustrated below).
PCI – how it works
Primary PCI – technique and antithrombotic therapy
• Among patients with STEMI undergoing primary PCI the use of bivalirudin can be
considered as an alternative to heparin and GP IIb/IIIa inhibitors (Grade B).1
• Among patients undergoing primary PCI for reperfusion, consider antiplatelet therapy
with either:
high-dose clopidogrel (600 mg oral bolus + 150 mg daily for 7 days, then 75
mg/day for at least 12 months) (Grade B)
prasugrel (60 mg oral bolus + 10 mg daily) (Grade B)
ticagrelor (180 mg oral bolus + 90 mg twice daily) (Grade B).1
• Careful assessment of bleeding risk should be undertaken before using
antithrombotic agents (Grade B).1
• Consider use of mechanical thrombectomy techniques to reduce thrombus burden
during primary PCI (Grade A).1
Reference
1. 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.
Bleeding risk
The following risk factors should be considered when assessing bleeding risk and choosing
antithrombotic therapies in patients with ACS (Grade B):
• age > 75 years
• female
• history of bleeding
• history of stroke or transient ischaemic attack (TIA)
• creatinine clearance rate < 60 mL/min
• diabetes
• heart failure
• tachycardia
• blood pressure < 120 mmHg or ≥ 180 mmHg
• peripheral vascular disease (PVD)
• anaemia
• concomitant use of GP IIb/IIIa inhibitor
• enoxaparin 48 hours prior
• switching between unfractionated heparin and enoxaparin
• procedural factors (femoral access, prolonged, intra-aortic balloon pump, right heart catheterisation).
Fibrinolysis
Fibrinolysis is the administration of a pharmacologic agent to break down blood clots in the
coronary vessels to restore blood flow to the heart muscle.1
• Consider early routine revascularisation of patients receiving fibrinolysis, regardless of success of
pharmacologic reperfusion (Grade A).
Absolute contraindications
• Active bleeding or bleeding diathesis (excluding menses).
• Significant closed head or facial trauma within 3 months.
• Suspected aortic dissection.
• Any prior intracranial haemorrhage.
• Ischaemic stroke within 3 months.
• Known structural cerebral vascular lesion.
• Known malignant intracranial neoplasm.
Reference
1. Dugdale DC , Chen Y-B, Zieve D, et al. Fibrinolysis – primary or secondary fibrinolysis. Available from: http://www.nlm.nih.gov/medlineplus/ency/article/000577.htm.
Accessed 7 August 2011.
Fibrinolysis
Relative contraindications
• Current use of anticoagulants.
• Non-compressible vascular punctures.
• Recent major surgery (< 3 weeks).
• Traumatic or prolonged (> 10 mins) CPR.
• Recent internal bleeding (within 4 weeks).
• Active peptic ulcer.
• History of chronic, severe, poorly controlled hypertension.
• Severe uncontrolled hypertension on presentation (systolic ≥ 180 mmHg or
diastolic ≥ 110 mmHg).
• Ischaemic stroke > 3 months ago, dementia or known intracranial abnormality.
• Pregnancy.
NSTEACS – what is it?
YES NO
• admit to CCU or high dependency unit: • undertake stress test (e.g. exercise ECG):
estimate ischaemic risk, estimate →positive – refer for angiography to
bleeding risk, choose augmented determine surgery/PCI, or medical
antithrombotic therapy therapy
→refer for angiography to determine →negative – proceed to discharge patient
surgery/PCI, or medical therapy. with urgent cardiac follow-up (on
upgraded medical therapy) according
to long-term management after control
of myocardial ischaemia.
Evolving risk stratification
Appropriate period of
observation. Consider if
stress test (e.g. exercise
ECG) needed?
YES NO
Stress test (e.g. exercise ECG) Proceed to discharge patient with urgent
using treadmill. cardiac follow-up (on upgraded medical
therapy) according to long-term
management after control of myocardial
ischaemia.
Antithrombotic therapy for NSTEACS
• When additional agents are needed, substitute rather than add (Grade B).
• Continued antiplatelet therapies for 12 months for all patients with stents (Grade A).
In addition:
• aspirin
• beta-blockers
• ACE inhibitors
• statins
• warfarin
• nitrates
• insulin/oral hypoglycaemics
• aldosterone antagonists.
Concluding remarks
• This presentation is designed to ensure consistency of information regarding
best practice ACS management, based upon the 2011 addendum to the
National Heart Foundation of Australia/Cardiac Society of Australia and New
Zealand Guidelines for the management of acute coronary syndromes 2006.
• Understandings of the pathophysiology of ACS have improved, together with
increasingly accurate diagnostic tools, better risk stratification and improved
medical and invasive treatments. However, these advances have led to an
increase in the complexity of possible treatment strategies. This is evolving.
• For more information please visit www.heartfoundation.org.au.
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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
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