Rasburicase interference with uric acid measurement — ABIM Board MCQ
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Correct answer: D — Repeat plasma uric acid now with cold heparinized specimen handling
Explanation lettering: D = shown as A · E = shown as B · A = shown as C · C = shown as D · B = shown as E
This patient has ongoing laboratory tumor lysis after chemotherapy, but the extremely low uric acid result is unreliable because the post-rasburicase specimen was transported at room temperature. Rasburicase remains enzymatically active ex vivo and continues converting uric acid to allantoin, producing a spuriously low measured concentration. Plasma uric acid should be repeated using a prechilled heparin-containing tube, immediately maintained in an ice-water bath, and assayed within 4 hours. Further rasburicase dosing should be guided by an accurately measured uric acid level and the overall clinical course. A is premature because the true uric acid concentration is unknown; worsening phosphorus and creatinine do not independently establish persistent hyperuricemia. B is inappropriate because retaining the invalid result risks undertreatment, and allopurinol prevents formation of new uric acid rather than rapidly removing uric acid already present. D is not yet indicated solely by these biochemical abnormalities; dialysis is considered for refractory hyperkalemia, severe hyperphosphatemia or symptomatic hypocalcemia, volume overload, uremic complications, or progressive kidney failure unresponsive to medical management. E incorrectly assumes that urate has normalized and could permit rebound or persistent hyperuricemia to go untreated.
Reference: Elitek (rasburicase) Prescribing Information (2019) — https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/103946s5103lbl.pdf The Tumor Lysis Syndrome (2011) — https://pmc.ncbi.nlm.nih.gov/articles/PMC3437249/