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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Patients typically present with tearing chest pain, notably between the shoulder blades.

They can be in considerable distress and haemodynamically unstable.

Peripheral pulses may be unequal or absent distally.

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CXR may show a widened mediastinum.

ECG may be unremarkable, show sinus tachycardia, or show ST-segment changes if the dissection extends proximally and involves the coronary ostium.

A CT of chest and abdomen with intravenous contrast showing the presence of a dissection flap and a true lumen and false lumen is diagnostic for aortic dissection.

A transoesophageal echocardiogram may also show the dissection flap with the true and false lumens.

Pulmonary embolism

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Patients classically present with acute onset of sharp, stabbing chest pain that is pleuritic in nature and associated with shortness of breath.

A background of increased clotting tendency, such as known hereditary thrombophilia or connective tissue disease; known deep venous thrombosis; or previous pulmonary embolism (PE) increases the likelihood of the diagnosis.

Other risk factors include recent prolonged immobilisation and limb trauma.

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Patients are hypoxic with an increased arterial-alveolar gradient on the arterial blood gas.

ECG may show sinus tachycardia or right ventricular strain with prominent S wave in lead I, prominent Q in lead III, and flipped T in lead III (S1Q3T3), or can be unremarkable.

D-dimer is useful for risk stratifications. In a patient with a low probability of PE on clinical scoring, with a non-elevated d-dimer, a PE can be excluded; if elevated, further work-up is required to confirm PE.

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

Pneumothorax

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Patients present with sudden onset of pleuritic chest discomfort and shortness of breath.

Tachycardia, hypotension, and cyanosis suggest a tension pneumothorax.

Known underlying medical conditions that predispose to pneumothorax, such as COPD, connective tissue disease, or recent chest trauma, may support this diagnosis.

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CXR shows a visceral pleural line.

Pneumonia

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Patients usually have an insidious onset of fevers, cough (that may be productive of sputum), and shortness of breath.

Chest discomfort may be pleuritic in nature.

Examination will usually confirm pneumonic consolidation with decreased resonance, decreased air entry, and rales over the affected lung.

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WBC count is usually raised with neutrophilia.

CXR has increased alveolar markings.

Blood and sputum cultures may be positive for an infective organism.

Acute pericarditis

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Patients can present with chest pain of varying quality that is typically better on sitting up and leaning forward and worse with lying down.

There may be a history of recent viral syndrome and a pericardial friction rub on clinical examination.

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ECG may have diffuse ST-segment elevation that is concave up ('saddle-shaped') with PR segment depression.[107]

Cardiac biomarkers can be elevated if inflammation extends into the myocardium.

Inflammatory markers such as CRP and ESR may be raised.

CXR demonstrating a globular cardiac shadow is suggestive.

Echocardiogram may show a pericardial effusion or may be unremarkable.

Myocarditis

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Patients often have a recent history of influenza-like illness or underlying autoimmune condition such as systemic lupus erythematosus.

They are likely to be young and often do not have risk factors for coronary artery disease.

Myocarditis is more likely to present with symptoms of cardiac failure than with chest pain.

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ECG changes and cardiac biomarkers can mimic myocardial infarction.

Inflammatory markers (ESR and CRP) and autoimmune assays may be raised.

Test of choice is cardiac MRI, with delayed enhancement imaging showing an epicardial or midmyocardial involvement.

Gastro-oesophageal reflux disease

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Patients present with burning retrosternal discomfort that is relieved by antacids.

Discomfort/pain is usually non-exertional.

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Diagnosis is usually clinical.

Cardiac biomarkers, ECG, and CXR are normal.

Oesophagogastroduodenoscopy is indicated for patients with persistent or atypical symptoms and may show oesophagitis (erosions, ulcerations, strictures) or Barrett oesophagus.

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.

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.[108]

Costochondritis

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Musculoskeletal chest wall discomfort that is worse with certain movement and deep breaths.

Focal tenderness over the costochondral joints may be present.

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Cardiac biomarkers, ECG, and CXR are normal.

Anxiety/Panic attack

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Normal exam; however, evidence of hyperventilation is sometimes present.

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Cardiac biomarkers, ECG, and CXR are all normal.

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.

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.[109] If ECG changes accompany cholecystitis, these would most likely include ST elevation.

Oesophageal rupture (Boerhaave syndrome)

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Clinical presentation may not differentiate.

There may be a history of vomiting.

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CXR shows pneumomediastinum >90% of the time. Non-specific ECG changes, including ST-elevation, but without rise in cardiac biomarkers.[110][111]

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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