Differentials

ST-elevation myocardial infarction

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Clinical presentation may not differentiate.

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ECG will show ST-segment elevation.

Cardiac biomarkers are elevated in both NSTEMI and STEMI.

Unstable angina

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Clinical presentation may not differentiate.

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ECG may show non-specific ST-segment and T-wave changes.

Cardiac biomarkers are normal.

Aortic dissection

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Pain is described as a 'tearing' back pain. There may be blood pressure differential between upper and lower extremities.

Aortic dissection often occurs in patients who have collagen vascular disease (i.e., Marfan syndrome).

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Chest CT angiography with contrast or MR angiography may show the dissection or an intimal flap. CXR may reveal widened mediastinum.

Transoesophageal echocardiography may show a dissection depending on the location.

Pulmonary embolism

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Patients often present with dyspnoea, pleuritic chest pain, cough, or haemoptysis. Hypoxia may be present. Lower limbs should be examined for deep vein thrombosis (enlarged, tender, erythematous calves).

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For patients with a high probability of pulmonary embolism (PE) on clinical scoring (i.e., PE likely) or an abnormal D-dimer, imaging is required. The multiple-detector computed tomographic pulmonary angiography (CTPA) scanning of the chest is the imaging study of choice for acute pulmonary embolism.

For patients with renal insufficiency or iodinated contrast allergies, ventilation-perfusion scan ± peripheral venous doppler exam are recommended.

Chest CT scan may show central filling defects within the vascular lumen, sharp cut-off of the artery, or a 'tram track' appearance of the artery in non-occlusive embolism.

Peptic ulcer disease

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Pain is described as burning epigastric pain that occurs hours after meals or with hunger. It often wakes the patient at night and is relieved by food and antacids.

There may be a previous history of reflux or medicines that can cause peptic ulcer (i.e., recent use of steroid or non-steroidal anti-inflammatory drugs).

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Endoscopy may show ulcers, erosion, or gastropathy.

Acute pericarditis

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Pain is relieved by sitting forwards. Friction rub or distant heart sounds may be heard on auscultation.

A history of a recent cardiac procedure (Dressler syndrome), renal failure, or preceding illness (fever or diarrhoea) may be present.

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ECG may show diffuse ST elevations (although PR elevation in aVR is most specific finding).

Echocardiogram and chest CT scan may show pericardial effusion or thickening of the pericardium. Cardiac MRI is useful and has high sensitivity for detection of pericardial effusion, loculations, and pericardial thickening.

Blood tests may indicate systemic inflammation (e.g., elevated white blood cell count, elevated erythrocyte sedimentation rate or C-reactive protein). Renal failure can cause uraemic pericarditis.

Oesophageal spasm

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Usually diagnosed after ruling out other causes of chest pain. A past history of oesophageal spasm is typical and there may be a precipitating event.

Pain due to oesophageal spasm is often relieved by glyceryl trinitrate, making it difficult to differentiate from cardiac pain.

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The oesophagus may have a corkscrew appearance on barium swallow. This represents simultaneous rings of contraction in the distal oesophagus.[92]

Costochondritis

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Diagnosis is made on the history or exclusion of other causes. There may be a history of recent or repeated trauma. The pain is typically localised with point tenderness, sharp in nature, and relieved by non-steroidal anti-inflammatory drugs.

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There are no specific studies or imaging to diagnose costochondritis.

Panic attack

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Most often diagnosed after exclusion of other causes. Patients often have other psychiatric illness. Women are affected more than men. Panic attacks may be situational.

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No tests or procedures can diagnose anxiety disorders.

Stable ischaemic heart disease

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Angina pain is recurrent and reproducible with exertion, and is relieved by rest or glyceryl trinitrate.

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Diagnosis is most often made on history alone. Coronary artery catheterisation may show the typical fixed coronary artery luminal wall narrowing.

Intravascular ultrasound during cardiac catheterisation may reveal the typical stable plaque of stable angina (calcified, thick fibrous caps) rather than the unstable plaques (lipid-laden, thin caps) that cause acute coronary syndrome.

Myocarditis

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There is a wide spectrum of presentation from asymptomatic to cardiogenic shock. Patients may present with a history of recent influenza-like illness associated with arthralgias and malaise. The symptoms of heart failure may be present.

Myocarditis may be idiopathic or caused by infections (viral, bacterial, or fungal), drugs (e.g., chemotherapy agents, anti-hypertensives, and anti-epileptics), and autoimmune disorders (e.g., systemic lupus erythematosus, sarcoidosis, and rheumatoid arthritis).

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The definitive test is endomyocardial biopsy, which shows lymphocyte infiltration and myocyte necrosis.

Cardiac enzymes or brain natriuretic protein may be raised.

Leukocytosis, eosinophilia, elevated erythrocyte sedimentation rate and C-reactive protein, and a rise in serum viral titres are common.

Acute cholecystitis

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On physical examination there is constant right upper quadrant pain with or without Murphy's sign (inhibition of inspiration due to pain on palpation). There may be a history of gallstones or previous episodes of biliary colic.

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Ultrasound may show a distended gallbladder and gallstones.[93] If ECG changes accompany cholecystitis, these would most likely include ST elevation.

Boerhaave syndrome

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Caused by oesophageal rupture with mediastinitis. It typically follows retching or vomiting, aggravated by swallowing. Patients may have subcutaneous emphysema and a hoarse voice.

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Chest x-ray shows pneumomediastinum >90% of the time. Oesophagram and CT scan can confirm diagnosis or reveal the condition. CT may show pneumomediastinum and peri-oesophageal air tracks. Oesophagram may show an oesophageal tear.[94] Endoscopy is not recommended for Boerhaave syndrome.

Brugada syndrome

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More common in Asian people and men aged 30 to 50 years. Patients typically present after an episode of polymorphic ventricular tachycardia or a cardiac arrest.

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ECG shows saddle-shaped ST elevation in leads V1 to V3. These changes are associated with complete or incomplete right bundle-branch block and T-wave inversions.

Acute stress cardiomyopathy

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Clinical features are similar to NSTEMI and may include chest pain, shortness of breath, and left ventricular wall motion abnormalities. A characteristic feature is that often the clinical state is triggered by a severe extracardiac stressor (e.g., intracranial haemorrhage, phaeochromocytoma, exogenous catecholamine administration, severe emotional stress, takotsubo cardiomyopathy, apical ballooning syndrome).

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Often these patients present with ECG changes, cardiac biomarker elevations, and left ventricular dysfunction on cardiac imaging that are indistinguishable from NSTEMI but on coronary angiography will have no obstructive lesion. Coronary angiography remains the definitive test for diagnosis of this condition.

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