ICU Map
ICU Medication MasterclassiTTP • ITP • TLS • HLH • Bleeding • Cytopenias

Hematology & Oncologic Emergency Pharmacology

High-stakes drug selection for thrombotic microangiopathy, immune thrombocytopenia, tumor lysis and hyperinflammation—where the correct medication is inseparable from plasma exchange, transfusion strategy, dialysis and trigger control.

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1

Treat suspected immune TTP as a time-critical syndrome before ADAMTS13 confirmation.

2

Use caplacizumab as part of the modern iTTP bundle rather than as a replacement for plasma exchange/immunosuppression.

3

Use IVIG strategically for rapid platelet rise in ITP and understand product-specific renal/thrombotic risks.

4

Recognize rasburicase as uric-acid therapy—not a treatment for the potassium/phosphate/dialysis components of TLS.

5

Use anakinra and corticosteroids only within a defined HLH/MAS phenotype and trigger strategy.

TTP

Full TTP diagnostic and plasma-exchange framework.

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Tumor Lysis Syndrome

Integrated TLS monitoring, prevention and dialysis triggers.

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Core agents

Choose by physiology, not by habit

The table below is a selection framework. Open the individual monograph for exact dosing, preparation, renal/CRRT/IHD adjustment, interactions and evidence traceability.

Caplacizumab
Anti-von Willebrand Factor Nanobody
Core agent

ICU role: Anti-vWF nanobody for acquired immune TTP.

Choose: Add to plasma exchange + immunosuppression when iTTP probability is high and bleeding context permits.
Hesitate: Bleeding risk; does not eliminate the anti-ADAMTS13 autoimmune process.

Monitor: Platelets, hemolysis, bleeding and ADAMTS13 trajectory.

Intravenous Immune Globulin (IVIG)
Pooled Human IgG Immunomodulator
Core agent

ICU role: Rapid immunomodulator for severe ITP and standard therapy for selected neurologic autoimmune disease.

Choose: Life-threatening ITP bleeding or urgent need for platelet rise; also disease-specific indications such as GBS.
Hesitate: Thrombosis, hemolysis, AKI, aseptic meningitis and product/infusion differences.

Monitor: Platelets/clinical response, creatinine, hemolysis and infusion reactions.

Rasburicase
Recombinant Urate Oxidase
Core agent

ICU role: Recombinant urate oxidase for TLS hyperuricemia.

Choose: High-risk or established TLS with significant uric-acid burden when rapid removal is needed.
Hesitate: Contraindicated in G6PD deficiency; does not treat hyperkalemia/hyperphosphatemia or dialysis indications.

Monitor: Uric acid with correct sample handling, K/phosphate/Ca, creatinine and hemolysis/methemoglobin.

Dexamethasone
Long-Acting Synthetic Fluorinated Glucocorticoid (High Anti-Inflammatory Potency) with Negligible Mineralocorticoid Activity
Core agent

ICU role: High-potency glucocorticoid used in several hematologic immune emergencies.

Choose: Common first-line corticosteroid option for ITP and part of selected immune/inflammatory protocols.
Hesitate: Hyperglycemia, infection, psychiatric effects; steroid response does not prove diagnosis.

Monitor: CBC trajectory, glucose, infection and clinical bleeding.

Methylprednisolone
Intermediate-Acting Synthetic Glucocorticoid with Minimal Mineralocorticoid Activity
Core agent

ICU role: IV glucocorticoid used in selected severe immune cytopenias or hyperinflammatory states.

Choose: When an IV pulse/intermediate-acting steroid is the disease-specific choice.
Hesitate: Avoid carrying empiric pulses into undifferentiated sepsis without a defined indication.

Monitor: Glucose, infection, mental status and muscle weakness.

Anakinra
Interleukin-1 Receptor Antagonist
Core agent

ICU role: IL-1 blockade for selected MAS/secondary-HLH phenotypes.

Choose: Specialist-directed hyperinflammation treatment when trigger/severity support it.
Hesitate: Not a stand-alone treatment for every high ferritin; renal accumulation and infection risk.

Monitor: CBC, renal function, ferritin/fibrinogen and organ response.

Tranexamic Acid
Antifibrinolytic / Synthetic Lysine Analog
Core agent

ICU role: Antifibrinolytic for selected major bleeding syndromes.

Choose: Use only when the bleeding syndrome and timing have evidence support.
Hesitate: Not a generic treatment for thrombocytopenia, DIC or all GI bleeding.

Monitor: Bleeding control, thrombosis risk, renal function and seizure risk at high exposure.

4-Factor Prothrombin Complex Concentrate
Hemostatic Agent / Clotting Factor Concentrate
Core agent

ICU role: Concentrated vitamin-K-dependent clotting factors for urgent VKA reversal and selected emergency reversal strategies.

Choose: Life-threatening warfarin-associated bleeding with IV vitamin K; selected other indications follow protocol.
Hesitate: Thromboembolic risk and no benefit from using it to 'normalize' cirrhotic INR without an indication.

Monitor: Clinical hemostasis, INR when relevant and thrombosis.

Clinical decision matrix

What changes the drug choice?

MAHA + thrombocytopenia + neurologic change, PT/aPTT near normal

Preferred reasoning: Treat as probable iTTP urgently with plasma exchange + corticosteroid-based immune therapy and add caplacizumab when appropriate while ADAMTS13 is pending.
Avoid: Waiting for ADAMTS13 before starting life-saving therapy.

Why: Untreated iTTP can deteriorate rapidly and contemporary therapy targets both vWF microthrombosis and the autoimmune process.

ITP with intracranial hemorrhage and platelets 3 ×10⁹/L

Preferred reasoning: Emergency combination therapy: IVIG + corticosteroid, platelet transfusion for life-threatening bleeding, and local hemostatic/neurosurgical management.
Avoid: Steroid monotherapy while active life-threatening bleeding continues.

Why: A rapid platelet rise and immediate hemostatic support are required.

Burkitt lymphoma after chemotherapy, K 6.5, phosphate 2.6 mmol/L, uric acid high, oliguria

Preferred reasoning: Rasburicase if eligible plus immediate hyperkalemia/TLS treatment and early dialysis assessment.
Avoid: Assuming rasburicase alone resolves TLS.

Why: Rasburicase treats uric acid; lethal electrolyte and renal complications need separate management.

Ferritin 20,000 with septic shock but fibrinogen/platelets stable and clear bacterial source

Preferred reasoning: Treat the infection and reassess for hyperinflammation if the course becomes discordant.
Avoid: Starting HLH therapy from ferritin alone.

Why: Ferritin is nonspecific in critical illness.

High-yield protocols

Mechanism-based sequences worth memorizing

Probable iTTP

  1. Send ADAMTS13 before plasma if possible but do not delay treatment.
  2. Start plasma exchange + immunosuppression urgently.
  3. Add caplacizumab when appropriate and monitor bleeding/ADAMTS13.
⚠️ Caplacizumab is adjunctive; it does not replace plasma exchange or immune control.

Tumor lysis bundle

  1. Risk-stratify before cytotoxic therapy and monitor K/phosphate/Ca/uric acid/creatinine frequently.
  2. Use rasburicase when rapid urate removal is indicated and G6PD status permits.
  3. Treat hyperkalemia and dialysis indications independently of uric acid.
⚠️ Normalizing uric acid does not mean TLS is controlled.
Organ failure & special settings

When standard pharmacology stops being standard

TTP and invasive procedure
Priority: Balance caplacizumab bleeding risk against ongoing microvascular thrombosis; coordinate timing with hematology.
Pitfall: Stopping all disease therapy for a minor procedure without a plan.
IVIG + renal failure
Priority: Select product/infusion carefully and monitor volume/renal risk.
Pitfall: Treating all IVIG formulations as interchangeable.
TLS + G6PD risk
Priority: Check G6PD status/history before rasburicase when feasible and avoid in known deficiency.
Pitfall: Using rasburicase despite a contraindication because uric acid is very high.
HLH + possible infection
Priority: Treat both the trigger and the hyperinflammatory syndrome when indicated.
Pitfall: Assuming immunomodulation and antimicrobial therapy are mutually exclusive.
Resident progression

R1 → R5 bedside cases

Recognition becomes selection, then organ-failure adjustment, competing physiology and senior-level prioritization.

R1

ITP rescue

Platelets 5 ×10⁹/L, mucosal bleeding, no MAHA or DIC pattern.

Show reasoning

Use corticosteroid therapy and add IVIG when a rapid platelet rise is needed; confirm this is truly ITP and not TTP/HIT/DIC.

R2

TLS prophylaxis versus treatment

High-grade lymphoma, uric acid already high before chemotherapy, kidney function worsening.

Show reasoning

Rasburicase is preferred when rapid reduction of existing uric acid is needed, provided G6PD deficiency is excluded; continue full TLS monitoring and renal/electrolyte management.

R3

TTP while ADAMTS13 pending

MAHA, platelets 18, confusion, creatinine 130 μmol/L, normal coagulation tests.

Show reasoning

Treat probable iTTP now. Plasma exchange and immune therapy should not wait for ADAMTS13; caplacizumab is part of contemporary treatment when appropriate.

R4

IVIG complication

After high-dose IVIG, hemoglobin falls and bilirubin/LDH rise without bleeding.

Show reasoning

Consider IVIG-associated hemolysis, obtain hemolysis testing and review product/dose/risk factors rather than assuming occult hemorrhage.

R5

Mixed oncologic emergency

AML induction: K 6.8, phosphate 2.8, calcium low, uric acid falling after rasburicase, worsening pulmonary edema and oliguria.

Show reasoning

Treat hyperkalemia immediately and involve nephrology for urgent RRT because ongoing electrolyte/volume indications persist despite successful uric-acid lowering.

Full medication monograph

Caplacizumab

Targeted anti-vWF therapy for acquired immune TTP used with plasma exchange and immunosuppression. It rapidly reduces platelet-consuming microthrombosis but increases bleeding risk and does not eradicate the anti-ADAMTS13 autoimm…

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

Intravenous Immune Globulin (IVIG)

Pooled IgG used across several ICU immune emergencies, including rapid platelet increase in ITP and standard treatment of Guillain–Barré syndrome. Dose and product selection are indication-specific and must account for thrombosis…

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

Rasburicase

Rapid uric-acid lowering therapy for high-risk or established tumor lysis syndrome. It converts uric acid to allantoin and is contraindicated in G6PD deficiency because severe hemolysis/methemoglobinemia can occur.

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

Dexamethasone

Potent long-acting glucocorticoid with negligible mineralocorticoid activity. It is used for selected indications including adjunctive acute bacterial meningitis when given before/with initial antibiotics, symptomatic vasogenic t…

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

Methylprednisolone

Potent parenteral glucocorticoid with ~5× the anti-inflammatory potency of hydrocortisone and minimal mineralocorticoid action — cornerstone therapy for severe asthma and COPD exacerbations, and non-resolving fibroproliferative A…

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

Anakinra

IL-1 receptor antagonist used off-label in selected severe hyperinflammatory syndromes such as macrophage activation syndrome/secondary HLH. ICU dosing is syndrome- and organ-function-specific and should be specialist directed ra…

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

Tranexamic Acid

Synthetic lysine analog that competitively blocks plasminogen lysine-binding sites, inhibiting plasmin formation and fibrin clot degradation, reducing mortality in bleeding trauma (CRASH-2) and postpartum hemorrhage (WOMAN) when …

Dosing • renal/CRRT • toxicity • interactions →
Full medication monograph

4-Factor Prothrombin Complex Concentrate

Lyophilized concentrate of vitamin K-dependent coagulation factors used for urgent reversal of vitamin K antagonist anticoagulation in adults with major bleeding or urgent surgery/invasive procedures; it rapidly replaces deficien…

Dosing • renal/CRRT • toxicity • interactions →

Evidence & bedside-use boundary

This Masterclass teaches selection and reasoning. Exact dosing, concentration, infusion preparation, renal/hepatic/RRT adjustment and monitoring must be checked in the linked medication monograph and the institution's current formulary/protocol. Local resistance patterns and regulatory drug availability can change faster than a static teaching page.