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Tumour lysis syndrome with life-threatening hyperkalaemia — SCE Acute Medicine MCQ

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ModerateCancer, palliative care and haematologyTumour lysis syndrome with life-threatening hyperkalaemiaSCE Acute Medicine

A 52-year-old man with high-grade lymphoma starts chemotherapy and 24 hours later becomes oliguric. Potassium is 6.8 mmol/L, phosphate 2.5 mmol/L, calcium 1.82 mmol/L, urate 890 micromol/L and creatinine has doubled. ECG shows peaked T waves. What is the most appropriate next step in management?

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Correct answer: ATreat hyperkalaemia immediately and involve haematology and renal teams for tumour lysis syndrome

Tumour lysis syndrome causes hyperkalaemia, hyperphosphataemia, hypocalcaemia, hyperuricaemia and AKI; ECG changes from hyperkalaemia require immediate stabilisation. Allopurinol prevents new uric acid formation but is insufficient for established severe TLS, where rasburicase and renal support may be needed. Correcting asymptomatic hypocalcaemia can worsen calcium-phosphate precipitation unless required for symptoms.

Reference: BCSH tumour lysis syndrome guideline; BNF rasburicase