Ischaemic heart disease Flashcards

1
Q

Define ischaemic heart disease

A

Characterised by decreased blood supply to the heart muscle resulting in chest pain (angina pectoris)

May present as stable angina or acute coronary
syndrome.

ACS can be further subdivided into:
Unstable angina- chest pain at rest due to ischaemia but
without cardiac injury
NSTEMI
STEMI -ST elevation with transmural infarction

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2
Q

Summarise the epidemiology of ischaemic heart disease

A

COMMON
Prevalence: > 2 %
More common in males
Annual incidence of MI in the UK ~ 5/1000

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3
Q

Explain the aetiology of ischaemic heart disease

A

Angina pectoris = myocardial oxygen demand > oxygen supply (usually due to atherosclerosis)

Rarer causes of angina pectoris include coronary artery spasm (e.g. induced bycocaine), arteritis and emboli

Atherosclerosis pathophysiology - Endothelial injury -> migration of monocytes into the subendothelial space.
Monocytes become macrophages. Macrophages become foam cells from LDL. Foam cells release GFs that stimulate smooth muscle proliferation, production of collagen and proteoglycans -> atherosclerotic plaque

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4
Q

Explain the risk factors of ischaemic heart disease

A
Male
Diabetes mellitus
Family history
Hypertension
Hyperlipidaemia
Smoking
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5
Q

Recognise the presenting symptoms of ischaemic heart

disease

A

ACS
Acute-onset chest pain
Central, heavy, tight, crushing pain
Radiates to the arms, neck, jaw or epigastrium
Occurs at rest
More severe and frequent pain that previously occurring stable angina

Associated symptoms:
Breathlessness
Sweating
Nausea and vomiting
SILENT INFARCTS - occur in the elderly and diabetics

Stable Angina - Chest pain brought on by exertion and relieved by rest

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6
Q

Recognise the signs of ischaemic heart disease on physical examination

A

Stable Angina - Check for signs of risk factors

ACS
May be NO CLINICAL SIGNS
Pale
Sweating
Restless
Low - grade pyrexia
Check both radial pulses to rule out aortic dissection
Arrhythmias
Disturbances of BP
New heart murmurs

Signs of complications (e.g. acute heart failure, cardiogenic shock)

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7
Q

Identify appropriate investigations for ischaemic heart disease

A
FBC
U&Es
CRP
Glucose
Lipid profile
Cardiac enzymes (troponins and CK-MB)
Amylase (pancreatitis could mimic MI)
TFTs
AST and LDH (raised 24 and 48 hours post-MI, respectively)

ECG -
Unstable Angina or NSTEMI: possible ST depression or T wave inversion
STEMI: Hyperacute T waves, ST elevation (> 1 mm in limb leads, > 2 mm in chest leads)
New-onset LBBB
Later changes:
T wave inversion
Pathological Q waves

CXR - Check for signs of heart failure

Exercise ECG

Radionuclide Myocardial Perfusion Imaging (rMPI)

Echocardiogram

Pharmacological Stress Testing - Dipyridamole, Adenosine, Dobutamine

Cardiac Catheterisation/Angiography

Coronary Calcium Scoring

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8
Q

Generate a management plan for Stable Angina

A

Minimise cardiac risk factors
(e.g. blood pressure, hyperlipidaemia, diabetes)

All patients should receive aspirin 75 mg/day
unless contraindicated

Immediate symptom relief (e.g. GTN spray)

Long-term management

Beta-blockers Contraindicated in:
Acute heart failure
Cardiogenic shock
Bradycardia
Heart block
Asthma

Calcium channel blockers
Nitrates

Percutaneous coronary intervention (PCI) - Performed in patients with stable angina despite maximal tolerable medical therapy

Coronary artery bypass graft (CABG) = Occurs in more severe cases (e.g. three-vessel disease)

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9
Q

Generate a management plan for Unstable Angina

A

Admit to coronary care unit
Oxygen, IV access, monitor vital signs and serial ECG

GTN
Morphine + Metoclopramide (to counteract the nausea caused by morphine)

Aspirin (300 mg initially, followed by 75 mg indefinitely)
Clopidogrel (300 mg initially, followed by 75 mg for at least 1 year if troponin positive or high risk)

LMWH (e.g. enoxaparin)

Beta-blocker (e.g. metoprolol)

Glucose- insulin infusion if blood glucose > 11 mmol/L

GlpIIb/IIIa inhibitors may also be considered (e.g. tirofiban) in patients: Undergoing PCI, At high risk of further cardiac events

If little improvement, consider urgent angiography with/without revascularisation

NOTE: the acute management of ACS can be remembered using the mnemonic
MONABASH

Morphine
Oxygen
Nitrates
Anticoagulants (aspirin + clopidogrel)
Beta-blockers
ACE inhibitors
Statins
Heparin
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10
Q

STEMI Management?

A

Same as UAP/NSTEMI management except:

Clopidogrel - 600 mg if patient is going to PCI
300 mg if undergoing thrombolysis and < 75 yrs
75 mg if undergoing thrombolysis and > 75 yrs
MAINTENANCE: 75 mg daily for at least 1 year

If undergoing primary PCI: IV heparin (plus GlpIIb/IIIa inhibitor), Bivalirudin (antithrombin)

Primary PCI - Goal <90 min if available

Thrombolysis - Uses fibrinolytics such as streptokinase and tissue plasminogen activator (e.g. alteplase)

Only considered if within 12 hours of chest pain with ECG changes and not contraindicated
Rescue PCI - may be performed if continued chest pain or ST elevation after thrombolysis

Secondary Prevention - Dual antiplatelet therapy (aspirin + clopidogrel)

Beta-blockers
ACE inhibitors
Statins
Control risk factors
Advice - No driving for 1 month following MI

CABG
Considered in patients with left main stem or three-vessel disease

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11
Q

Identify the possible complications of ischaemic heart disease

A

Increased risk of MI and other vascular disease (e.g. stroke, PVD). Cardiac injury from an MI can lead to heart failure and arrhythmias

Early Complications (within 24-72 hrs)
Death
Cardiogenic shock
Heart failure
Ventricular arrythmias
Heart block
Pericarditis
Myocardial rupture
Thromboembolism
Late Complications
Ventricular wall rupture
Valvular regurgitation
Ventricular aneurysms
Tamponade
Dressler's syndrome
Thromboembolism
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12
Q

MNEMONIC for Complications of MI

A

Darth Vader

Death
Arrhythmias
Rupture
Tamponade
Heart failure
Ventricular disease
Aneurysm
Dressler's syndrome
Embolism
Regurgitation
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13
Q

Summarise the prognosis for patients with ischaemic heart disease

A
TIMI score (0-7) can be used for risk stratification
NOTE: TIMI = thrombolysis in myocardial infarction

High scores are associated with high risk of cardiac events within 30 days of MI

Killip Classification of acute MI can also be used:
Class I: no evidence of heart failure
Class II: mild to moderate heart failure
Class III: over pulmonary oedema
Class IV: cardiogenic shock
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