Key uses
• Arrhythmias
• Ischaemia and infarction
• Electrolyte disorders
• Conduction abnormalities
Ischaemia and infarction
• ST elevation → transmural infarction (STEMI)
• ST depression and/or T wave inversion → subendocardial ischaemia, NSTEMI, unstable angina
• New LBBB + chest pain → treat as STEMI equivalent
QT interval
• Prolonged QTc (>450 ms in men, >470 ms in women) → risk of torsades de pointes
• Causes: hypocalcaemia, hypokalaemia, hypomagnesaemia, drugs (antiarrhythmics, antipsychotics)
• Continuous 24–72 h monitoring
• Indications:
o Paroxysmal arrhythmias (e.g., AF, SVT, bradycardia)
o Correlation with palpitations or syncope
• First-line for most cardiac structural assessments
• Assess:
o Valve disease (stenosis/regurgitation)
o LV function (EF)
o Regional wall motion abnormalities (ischaemia)
o Pericardial effusion and tamponade
• Better resolution of posterior structures
• Indications:
o Infective endocarditis (especially prosthetic valves)
o Left atrial thrombus (pre-cardioversion)
o Aortic dissection assessment (ascending aorta)
Exercise ECG
• Detects inducible ischaemia in stable angina
• Positive: typical chest pain + ST depression ≥1 mm
Pharmacological stress
• Agents: dobutamine (increases contractility), adenosine (vasodilation)
• Indicated in patients unable to exercise
• Gold standard for coronary artery disease (CAD) assessment
• Indications:
o ACS
o High-risk angina
o Positive non-invasive stress test
Complications
• Vascular access bleeding/haematoma
• MI, arrhythmias
• Stroke
• Contrast-induced nephropathy (more common with CKD)
• Non-invasive anatomical assessment
• Indicated in low-intermediate risk stable chest pain
• Soft tissue detail
• Indications:
o Cardiomyopathy (e.g., hypertrophic, dilated, infiltrative)
o Myocarditis (late gadolinium enhancement)
o Cardiac masses
• Marker of ventricular wall stress
• Raised in heart failure
• Can be elevated in:
o Ageing
o Renal failure
o AF
• Low levels (<125 pg/mL in non-acute, <300 pg/mL in acute) → HF unlikely
Troponin I/T
• High sensitivity; rise within 3–12 h; peak ~24 h
• Causes of elevation:
o MI (type 1 = atherothrombotic; type 2 = supply-demand imbalance)
o Myocarditis
o PE (RV strain)
o Severe sepsis
o CKD (chronic mild elevation)
Extra Revision Pearls
• Persistent ST elevation weeks after MI → ventricular aneurysm (not re-infarction)
• New T wave inversion post-MI → reperfusion marker
• QT prolongation clue → low Mg²⁺, K⁺, Ca²⁺ or drugs
• BNP/NT-proBNP not reliable if on ARNI (e.g., sacubitril) — prefer NT-proBNP
• Cardiac MRI is gold standard for myocarditis diagnosis
• TOE preferred for left atrial thrombus before DC cardioversion
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Author & Educational Disclaimer
Author:
Dr Phillip Cockrell BM FRCP DipClinEd
Dr Phillip Cockrell is a UK Consultant Physician in Internal Medicine, currently working at Queen Alexandra Hospital, Portsmouth University Hospitals NHS Trust. He has previously worked as a registrar across Intensive Care Medicine, Gastroenterology, Cardiology, Stroke Medicine, Acute Medicine, and Respiratory Medicine.
He has held senior leadership roles including Associate Clinical Director of the Acute Medical Unit, Clinical Director of Internal Medicine, and Chief of Medicine. Dr Cockrell has over 15 years’ experience in postgraduate medical education, having lectured extensively across the MRCP syllabus and contributed to MRCP revision teaching and course development.
Dr Cockrell holds a Bachelor of Medicine (BM), Fellowship of the Royal College of Physicians (FRCP), and a Diploma in Clinical Education (DipClinEd). His teaching approach is based on structured consolidation of complex medical topics to support efficient and effective revision for postgraduate examinations.
Purpose of this content:
The material on this page is intended solely for educational purposes to support revision for the MRCP (UK) Part 1 examination. It reflects examination-relevant principles of internal medicine and is designed to aid learning and pattern recognition.
Medical disclaimer:
This content is designed for postgraduate medical examination revision and does not constitute medical advice, diagnosis, or treatment guidance and must not be used as a substitute for professional clinical judgement, local guidelines, or specialist consultation. Clinical decisions should always be made in the context of individual patient circumstances and current national guidance.