Introduction:
Hyperkalaemia, defined as a serum potassium level above 5.5 mmol/L, can be life-threatening if not promptly recognized and managed. Potassium plays a critical role in maintaining cellular function, particularly in muscle cells, including the heart. Elevated levels can result in dangerous arrhythmias. This guide aims to help junior doctors navigate the history-taking, examination, investigations, and management of hyperkalaemia in an easy-to-understand manner.
History-Taking: What to Ask
When assessing a patient with suspected hyperkalaemia, ask targeted questions to uncover the underlying cause and assess severity. Key areas to focus on include:
· Symptoms of Hyperkalaemia:
Muscle weakness or paralysis: Ask if the patient has noticed generalized muscle weakness, fatigue, or difficulty moving.
Palpitations or chest pain: These can indicate cardiac involvement.
Shortness of breath: Dyspnoea may be related to cardiac arrhythmias or acidosis.
Paraesthesia: Sensory disturbances, especially around the lips or extremities, may be due to hyperkalaemia.
· Medications:
ACE inhibitors/ARBs, potassium-sparing diuretics (e.g., spironolactone): Ask if the patient is taking these, as they reduce potassium excretion.
NSAIDs: These can also impair potassium excretion.
Supplemental potassium or herbal remedies: Overuse or misuse can lead to hyperkalaemia.
Recent use of IV fluids or blood transfusions: Large volumes of stored blood contain elevated potassium levels.
· Underlying Medical Conditions:
Renal failure: Ask about known chronic kidney disease or recent changes in urine output, as decreased renal clearance is a major cause.
Endocrine issues: History of Addison’s disease or adrenal insufficiency could indicate impaired aldosterone function, leading to potassium retention.
Trauma, burns, or recent surgery: Cellular breakdown releases potassium.
Acidosis: This can shift potassium out of cells.
· Dietary Intake:
High potassium diet: Excessive intake of potassium-rich foods (bananas, tomatoes, oranges) or salt substitutes should be queried.
Examination Findings: What to Look For
A systematic examination is crucial to assess the impact of hyperkalaemia on various organ systems, particularly the heart, muscles, and kidneys.
· General Inspection:
Altered mental status: Confusion or lethargy may indicate severe hyperkalaemia.
Signs of dehydration or volume overload: Look for dry mucous membranes or peripheral oedema, which might hint at renal dysfunction.
· Cardiovascular System:
Pulse: Bradycardia or irregular heart rate may indicate arrhythmias.
Blood pressure: Hypotension could suggest severe cardiovascular compromise.
Heart auscultation: Listen for irregular beats or signs of heart failure, such as murmurs or added heart sounds (e.g., S3).
· Neuromuscular System:
Muscle weakness: Check for diminished motor strength, especially proximally.
Hyporeflexia: Reflexes may be diminished in severe cases.
Respiratory muscles: Monitor for signs of respiratory muscle weakness, as this can be life-threatening.
· Renal System:
Fluid status: Assess for oliguria or anuria, which may suggest acute kidney injury.
Abdominal examination: A palpable bladder might suggest urinary retention.
Investigations: What to Order
· Electrolytes (U&E):
A serum potassium level >5.5 mmol/L confirms hyperkalaemia. Severity is classified as:
Mild: 5.5–5.9 mmol/L
Moderate: 6.0–6.4 mmol/L
Severe: ≥6.5 mmol/L
· ECG:
Early changes: Peaked T waves.
Progressive changes: Flattened P waves, prolonged PR interval, and widened QRS complexes.
Life-threatening changes: Sine wave pattern, ventricular fibrillation, or asystole.
· Arterial Blood Gas (ABG):
Look for metabolic acidosis (low pH, high anion gap), which may indicate impaired potassium clearance or an underlying cause like DKA.
· Renal Function Tests:
Check for elevated creatinine and blood urea nitrogen (BUN) to assess renal impairment.
· Blood Glucose:
Hyperkalaemia can occur in diabetic emergencies like diabetic ketoacidosis (DKA).
· Other Blood Tests:
Full Blood Count (FBC): Look for signs of haemolysis or infection.
Cortisol levels: If Addison’s disease is suspected.
Management Plan: What to Do
The management of hyperkalaemia revolves around stabilizing the myocardium, shifting potassium into cells, and removing excess potassium from the body.
· Stabilize the Heart:
· Calcium gluconate (30 mL of 10% solution IV over 5–10 minutes): This stabilizes cardiac myocytes and prevents arrhythmias but does not lower potassium.
· Shift Potassium into Cells:
· Insulin and glucose (10 units of insulin with 50 mL of 50% dextrose IV): This drives potassium into cells.
· Nebulized salbutamol (10–20 mg): Beta-2 agonists help shift potassium into cells.
· Sodium bicarbonate (50 mmol IV): Use in cases of metabolic acidosis to facilitate potassium uptake by cells.
· Remove Potassium from the Body:
· Loop diuretics (e.g., furosemide): Promote renal excretion of potassium.
· Sodium polystyrene sulfonate (Kayexalate): Binds potassium in the gut, though this is slow-acting.
· Haemodialysis: This is the most definitive treatment for severe or refractory hyperkalaemia, especially in patients with renal failure.
· Monitor and Reassess:
· Continuous ECG monitoring is essential until potassium levels are normalized.
· Repeat serum potassium and ECGs every 1–2 hours to guide ongoing treatment.
· Treat the Underlying Cause:
· Renal failure: Optimize renal function or consider dialysis.
· Medication review: Discontinue potassium-sparing drugs or supplements.
· Endocrine disorders: Address adrenal insufficiency with corticosteroids if necessary.
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