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Haematology Oncology Strong — Cairo-Bishop 2004 / Howard 2011

Tumor Lysis Syndrome Risk (Cairo-Bishop)

Cairo-Bishop criteria for laboratory and clinical Tumor Lysis Syndrome (TLS). Identifies patients needing prophylaxis or treatment.

Creatinine ≥ 1.5× ULN, cardiac arrhythmia, seizure, or death — in presence of laboratory TLS

High risk: Burkitt lymphoma, ALL, AML, bulky DLBCL, LDH > 2× ULN, WBC > 25×10⁹/L

Score interpretation

Low Risk — No Laboratory TLS 0–1

Low risk of TLS. No laboratory criteria met.

→ Oral hydration. Allopurinol prophylaxis if intermediate risk tumour. Monitor electrolytes 12-hourly during first treatment cycle. No rasburicase routinely required.

Laboratory TLS — Treatment Required 2–5

Laboratory TLS: ≥ 2 metabolic abnormalities within 3 days before or 7 days after chemotherapy.

→ Aggressive IV hydration: 3 L/m²/day (avoid hypotonic fluids). Rasburicase 0.2 mg/kg IV daily × 3–7 days (contraindicated in G6PD deficiency — check first). Monitor electrolytes 4–6-hourly. ECG monitoring. Treat hyperkalaemia: calcium gluconate, insulin/dextrose, salbutamol nebuliser, calcium resonium. Nephrology review if AKI.

Clinical TLS — Oncological Emergency 6–99

Clinical TLS: laboratory TLS + organ dysfunction (AKI, arrhythmia, seizure). Medical emergency.

→ IMMEDIATE oncology and nephrology. ICU consideration. Rasburicase (if no G6PD deficiency). Continuous cardiac monitoring. Haemodialysis if refractory hyperkalaemia, severe AKI, or symptomatic hypocalcaemia. Hold calcium supplementation if phosphate elevated (risk of calcium-phosphate precipitation). Anti-epileptic cover.

Interpretation bands for the TLS Risk. Apply clinical judgement and local guidance.

References

Related

Curated clinical cross-links plus same-class fallbacks.

Decision support only — verify against a current formulary, NICE, or your local guideline before clinical use.