HKMLE Part III study materials
HKMLE Part III study resources

HKMLE Part III cheat sheet

HKMLE Part III · Keep the key ideas within reach.

Quick reference

Professional Knowledge and Clinical Practice - Core Reference Points

  • Hong Kong medical registration: full registration requires an acceptable primary qualification plus internship and licensure; limited registration is time- and scope-bound, and the Licensing Examination (Part I professional knowledge, Part II English, Part III clinical) is the route for non-exempt candidates.

  • Resuscitation standard: high-quality CPR at 100–120 compressions/min, depth 5–6 cm in adults, full recoil, minimal interruptions (<10 s), compression:ventilation 30:2 without an advanced airway, and early defibrillation for shockable rhythms (VF/pulseless VT).

  • Sepsis: suspect when infection plus organ dysfunction (qSOFA ≥2 or NEWS escalation); give broad-spectrum antibiotics within 1 hour of recognition in septic shock and measure lactate; fluid resuscitation 30 mL/kg crystalloid for hypotension or lactate ≥4 mmol/L.

  • Acute coronary syndrome: ST-elevation on ECG mandates reperfusion - primary PCI within 90 minutes of first medical contact where achievable, otherwise fibrinolysis within 30 minutes of arrival if no contraindication; give aspirin and a P2Y12 inhibitor unless contraindicated.

  • Stroke: non-contrast CT excludes haemorrhage before thrombolysis; intravenous alteplase is licensed within 4.5 hours of symptom onset, with door-to-needle target ≤60 minutes; thrombectomy consideration extends to selected large-vessel occlusions up to 24 hours.

  • Hypoglycaemia in a conscious patient: 15–20 g fast-acting oral carbohydrate, recheck glucose after 15 minutes, repeat if still <4 mmol/L, then a longer-acting carbohydrate; in an unconscious patient give IV glucose or IM glucagon.

  • Paediatric fluid and drug dosing is weight-based (mL/kg, mg/kg); use a length-based tape or estimated weight formula only when weighing is impossible, since dosing errors are a leading source of harm.

  • Antimicrobial stewardship: take cultures before antibiotics when this does not delay therapy, review at 48–72 hours with culture results, and narrow or stop agents based on clinical response and local resistance patterns.

  • Consent: valid consent requires capacity, adequate information on material risks and alternatives, and voluntariness; a competent adult's refusal must be respected, and treatment of a patient lacking capacity follows the best-interests framework under Hong Kong's Mental Health Ordinance and common law.

Quick reference

Professional Knowledge and Clinical Practice - Prescribing, Communication and Safety

  • High-alert medications requiring independent double-check: insulin, heparin and other anticoagulants, concentrated potassium chloride, chemotherapy, and opioids; never give undiluted potassium chloride by IV push.

  • Warfarin is monitored by INR; target is usually 2.0–3.0 for most indications and 2.5–3.5 for mechanical mitral valves; major bleeding risk rises steeply above INR 5, and reversal uses vitamin K with prothrombin complex concentrate in serious bleeding.

  • Paracetamol overdose: the Rumack–Matthew nomogram guides N-acetylcysteine treatment, which is most effective within 8 hours of ingestion; assess with timed serum level, and treat empirically if timing is uncertain or the level is above the treatment line.

  • Digoxin toxicity features nausea, visual disturbance (yellow-green halation), bradyarrhythmias and hyperkalaemia; risk is increased by hypokalaemia, renal impairment and interacting drugs such as amiodarone and verapamil.

  • Opioid safety: co-prescribe naloxone where overdose risk is high, avoid combining with benzodiazepines, and reassess sedation and respiratory rate after dose changes rather than relying on pain scores alone.

  • Breaking bad news: use a structured framework (setting, perception, invitation, knowledge, empathy, strategy), give information in small chunks, check understanding, and avoid false reassurance; document what was discussed and with whom.

  • Medical records: contemporaneous, dated, signed entries; record decisions and the reasoning behind them, including capacity assessments and discussions of risk; late entries must be clearly marked as such.

  • Error disclosure: an adverse event should be explained to the patient openly and promptly, with an apology and an explanation of what happens next; this is a professional duty distinct from any liability question.

  • Infection control: perform hand hygiene per the WHO five moments, use standard precautions for all patients, and add transmission-based precautions (contact, droplet, airborne) according to the suspected organism.

Quick reference

Professional Knowledge and Clinical Practice - Clinical Reasoning and Investigations

  • Interpreting a test: sensitivity = TP/(TP+FN), specificity = TN/(TN+FP); a highly sensitive test is useful to rule out disease (negative result reassuring), a highly specific test to rule it in.

  • Positive predictive value depends on prevalence, so a positive result in a low-prevalence population may still be a false positive; likelihood ratios are prevalence-independent and summarise test performance.

  • Arterial blood gas stepwise: assess pH (acidaemia vs alkalaemia), then PaCO2 (respiratory component), then bicarbonate/base excess (metabolic component), then check compensation and calculate the anion gap (Na − [Cl + HCO3], normal 8–12 mmol/L).

  • Hyponatraemia: check serum osmolality and urine osmolality/sodium first; correct chronic hyponatraemia slowly (generally ≤8–10 mmol/L in 24 hours) to avoid osmotic demyelination, and treat symptomatic severe cases with hypertonic saline.

  • Hyperkalaemia with ECG changes (peaked T waves, widened QRS, sine wave) is an emergency: give IV calcium for cardiac protection, shift potassium intracellularly with insulin-dextrose and salbutamol, then remove potassium from the body.

  • Acute kidney injury is staged by creatinine rise and urine output (KDIGO); distinguish pre-renal, renal and post-renal causes, review nephrotoxins, and look for obstruction with bladder scan or ultrasound.

  • Chest pain risk stratification uses history, ECG and troponin; a single early troponin does not exclude acute coronary syndrome, and serial sampling with a validated pathway is required.

  • Antibiotic choice is empirical first and targeted later: consider likely organisms by site, local resistance data, allergy history, renal/hepatic dose adjustment, and source control (drainage, debridement, catheter removal).

  • Clinical handover uses a structured format (SBAR or ISBAR) covering situation, background, assessment, recommendation, with explicit read-back of critical results and escalation criteria.