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2025 PACUPrep BCCCP Preparatory Course

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  1. Pulmonary

    ARDS
    4 Topics
    |
    1 Quiz
  2. Asthma Exacerbation
    4 Topics
    |
    1 Quiz
  3. COPD Exacerbation
    4 Topics
    |
    1 Quiz
  4. Cystic Fibrosis
    6 Topics
    |
    1 Quiz
  5. Drug-Induced Pulmonary Diseases
    3 Topics
    |
    1 Quiz
  6. Mechanical Ventilation Pharmacotherapy
    5 Topics
    |
    1 Quiz
  7. Pleural Disorders
    5 Topics
    |
    1 Quiz
  8. Pulmonary Hypertension (Acute and Chronic severe pulmonary hypertension)
    5 Topics
    |
    1 Quiz
  9. Cardiology
    Acute Coronary Syndromes
    6 Topics
    |
    1 Quiz
  10. Atrial Fibrillation and Flutter
    6 Topics
    |
    1 Quiz
  11. Cardiogenic Shock
    4 Topics
    |
    1 Quiz
  12. Heart Failure
    7 Topics
    |
    1 Quiz
  13. Hypertensive Crises
    5 Topics
    |
    1 Quiz
  14. Ventricular Arrhythmias and Sudden Cardiac Death Prevention
    5 Topics
    |
    1 Quiz
  15. NEPHROLOGY
    Acute Kidney Injury (AKI)
    5 Topics
    |
    1 Quiz
  16. Contrast‐Induced Nephropathy
    5 Topics
    |
    1 Quiz
  17. Drug‐Induced Kidney Diseases
    5 Topics
    |
    1 Quiz
  18. Rhabdomyolysis
    5 Topics
    |
    1 Quiz
  19. Syndrome of Inappropriate Antidiuretic Hormone (SIADH)
    5 Topics
    |
    1 Quiz
  20. Renal Replacement Therapies (RRT)
    5 Topics
    |
    1 Quiz
  21. Neurology
    Status Epilepticus
    5 Topics
    |
    1 Quiz
  22. Acute Ischemic Stroke
    5 Topics
    |
    1 Quiz
  23. Subarachnoid Hemorrhage
    5 Topics
    |
    1 Quiz
  24. Spontaneous Intracerebral Hemorrhage
    5 Topics
    |
    1 Quiz
  25. Neuromonitoring Techniques
    5 Topics
    |
    1 Quiz
  26. Gastroenterology
    Acute Upper Gastrointestinal Bleeding
    5 Topics
    |
    1 Quiz
  27. Acute Lower Gastrointestinal Bleeding
    5 Topics
    |
    1 Quiz
  28. Acute Pancreatitis
    5 Topics
    |
    1 Quiz
  29. Enterocutaneous and Enteroatmospheric Fistulas
    5 Topics
    |
    1 Quiz
  30. Ileus and Acute Intestinal Pseudo-obstruction
    5 Topics
    |
    1 Quiz
  31. Abdominal Compartment Syndrome
    5 Topics
    |
    1 Quiz
  32. Hepatology
    Acute Liver Failure
    5 Topics
    |
    1 Quiz
  33. Portal Hypertension & Variceal Hemorrhage
    5 Topics
    |
    1 Quiz
  34. Hepatic Encephalopathy
    5 Topics
    |
    1 Quiz
  35. Ascites & Spontaneous Bacterial Peritonitis
    5 Topics
    |
    1 Quiz
  36. Hepatorenal Syndrome
    5 Topics
    |
    1 Quiz
  37. Drug-Induced Liver Injury
    5 Topics
    |
    1 Quiz
  38. Dermatology
    Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
    5 Topics
    |
    1 Quiz
  39. Erythema multiforme
    5 Topics
    |
    1 Quiz
  40. Drug Reaction (or Rash) with Eosinophilia and Systemic Symptoms (DRESS)
    5 Topics
    |
    1 Quiz
  41. Immunology
    Transplant Immunology & Acute Rejection
    5 Topics
    |
    1 Quiz
  42. Solid Organ & Hematopoietic Transplant Pharmacotherapy
    5 Topics
    |
    1 Quiz
  43. Graft-Versus-Host Disease (GVHD)
    5 Topics
    |
    1 Quiz
  44. Hypersensitivity Reactions & Desensitization
    5 Topics
    |
    1 Quiz
  45. Biologic Immunotherapies & Cytokine Release Syndrome
    5 Topics
    |
    1 Quiz
  46. Endocrinology
    Relative Adrenal Insufficiency and Stress-Dose Steroid Therapy
    5 Topics
    |
    1 Quiz
  47. Hyperglycemic Crisis (DKA & HHS)
    5 Topics
    |
    1 Quiz
  48. Glycemic Control in the ICU
    5 Topics
    |
    1 Quiz
  49. Thyroid Emergencies: Thyroid Storm & Myxedema Coma
    5 Topics
    |
    1 Quiz
  50. Hematology
    Acute Venous Thromboembolism
    5 Topics
    |
    1 Quiz
  51. Drug-Induced Thrombocytopenia
    5 Topics
    |
    1 Quiz
  52. Anemia of Critical Illness
    5 Topics
    |
    1 Quiz
  53. Drug-Induced Hematologic Disorders
    5 Topics
    |
    1 Quiz
  54. Sickle Cell Crisis in the ICU
    5 Topics
    |
    1 Quiz
  55. Methemoglobinemia & Dyshemoglobinemias
    5 Topics
    |
    1 Quiz
  56. Toxicology
    Toxidrome Recognition and Initial Management
    5 Topics
    |
    1 Quiz
  57. Management of Acute Overdoses – Non-Cardiovascular Agents
    5 Topics
    |
    1 Quiz
  58. Management of Acute Overdoses – Cardiovascular Agents
    5 Topics
    |
    1 Quiz
  59. Toxic Alcohols and Small-Molecule Poisons
    5 Topics
    |
    1 Quiz
  60. Antidotes and Gastrointestinal Decontamination
    5 Topics
    |
    1 Quiz
  61. Extracorporeal Removal Techniques
    5 Topics
    |
    1 Quiz
  62. Withdrawal Syndromes in the ICU
    5 Topics
    |
    1 Quiz
  63. Infectious Diseases
    Sepsis and Septic Shock
    5 Topics
    |
    1 Quiz
  64. Pneumonia (CAP, HAP, VAP)
    5 Topics
    |
    1 Quiz
  65. Endocarditis
    5 Topics
    |
    1 Quiz
  66. CNS Infections
    5 Topics
    |
    1 Quiz
  67. Complicated Intra-abdominal Infections
    5 Topics
    |
    1 Quiz
  68. Antibiotic Stewardship & PK/PD
    5 Topics
    |
    1 Quiz
  69. Clostridioides difficile Infection
    5 Topics
    |
    1 Quiz
  70. Febrile Neutropenia & Immunocompromised Hosts
    5 Topics
    |
    1 Quiz
  71. Skin & Soft-Tissue Infections / Acute Osteomyelitis
    5 Topics
    |
    1 Quiz
  72. Urinary Tract and Catheter-related Infections
    5 Topics
    |
    1 Quiz
  73. Pandemic & Emerging Viral Infections
    5 Topics
    |
    1 Quiz
  74. Supportive Care (Pain, Agitation, Delirium, Immobility, Sleep)
    Pain Assessment and Analgesic Management
    5 Topics
    |
    1 Quiz
  75. Sedation and Agitation Management
    5 Topics
    |
    1 Quiz
  76. Delirium Prevention and Treatment
    5 Topics
    |
    1 Quiz
  77. Sleep Disturbance Management
    5 Topics
    |
    1 Quiz
  78. Immobility and Early Mobilization
    5 Topics
    |
    1 Quiz
  79. Oncologic Emergencies
    5 Topics
    |
    1 Quiz
  80. End-of-Life Care & Palliative Care
    Goals of Care & Advance Care Planning
    5 Topics
    |
    1 Quiz
  81. Pain Management & Opioid Therapy
    5 Topics
    |
    1 Quiz
  82. Dyspnea & Respiratory Symptom Management
    5 Topics
    |
    1 Quiz
  83. Sedation & Palliative Sedation
    5 Topics
    |
    1 Quiz
  84. Delirium Agitation & Anxiety
    5 Topics
    |
    1 Quiz
  85. Nausea, Vomiting & Gastrointestinal Symptoms
    5 Topics
    |
    1 Quiz
  86. Management of Secretions (Death Rattle)
    5 Topics
    |
    1 Quiz
  87. Fluids, Electrolytes, and Nutrition Management
    Intravenous Fluid Therapy and Resuscitation
    5 Topics
    |
    1 Quiz
  88. Acid–Base Disorders
    5 Topics
    |
    1 Quiz
  89. Sodium Homeostasis and Dysnatremias
    5 Topics
    |
    1 Quiz
  90. Potassium Disorders
    5 Topics
    |
    1 Quiz
  91. Calcium and Magnesium Abnormalities
    5 Topics
    |
    1 Quiz
  92. Phosphate and Trace Electrolyte Management
    5 Topics
    |
    1 Quiz
  93. Enteral Nutrition Support
    5 Topics
    |
    1 Quiz
  94. Parenteral Nutrition Support
    5 Topics
    |
    1 Quiz
  95. Refeeding Syndrome and Specialized Nutrition
    5 Topics
    |
    1 Quiz
  96. Trauma and Burns
    Initial Resuscitation and Fluid Management in Trauma
    5 Topics
    |
    1 Quiz
  97. Hemorrhagic Shock, Massive Transfusion, and Trauma‐Induced Coagulopathy
    5 Topics
    |
    1 Quiz
  98. Burns Pharmacotherapy
    5 Topics
    |
    1 Quiz
  99. Burn Wound Care
    5 Topics
    |
    1 Quiz
  100. Open Fracture Antibiotics
    5 Topics
    |
    1 Quiz

Participants 432

  • Allison Clemens
  • April
  • ababaabhay
  • achoi2392
  • adhoward1
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Lesson 79, Topic 4
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ICU‐Level Supportive Care and Complication Prevention in Oncologic Emergencies

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ICU Supportive Care in Oncologic Emergencies

ICU-Level Supportive Care and Complication Prevention in Oncologic Emergencies

Objectives Icon A checkmark inside a circle, symbolizing achieved goals.

Learning Objective

Recommend ICU-level supportive care interventions and prevention strategies to optimize outcomes in oncologic emergencies.

1. Respiratory and Hemodynamic Support

Respiratory failure and shock are common life-threatening conditions in critically ill oncology patients. Prompt, evidence-based interventions focusing on early lung-protective ventilation, targeted sedation, and judicious vasopressor use are essential to reduce morbidity and mortality.

A. Mechanical Ventilation Strategies

The primary goal is to maintain gas exchange while minimizing ventilator-induced lung injury (VILI).

  • Tidal Volume: 4–8 mL/kg of predicted body weight.
  • Plateau Pressure (Pplat): Maintain < 30 cm H₂O.
  • PEEP: Use 5–15 cm H₂O to maintain alveolar recruitment and improve oxygenation.
  • FiO₂: Titrate to the lowest level to maintain SpO₂ of 88–95%, avoiding hyperoxia.
  • Permissive Hypercapnia: Acceptable (PaCO₂ up to 60 mm Hg) provided the pH remains ≥ 7.20.
Pearl IconA shield with an exclamation mark. Clinical Pearls: Ventilation Expand/Collapse Icon

Early Intubation: In cases of central airway obstruction (e.g., from mediastinal masses), consider early, controlled intubation to secure the airway before a crisis develops.

Driving Pressure: Monitor driving pressure (Pplat – PEEP). A value > 15 cm H₂O is strongly associated with increased mortality. Optimizing PEEP and tidal volume to lower driving pressure is a key VILI prevention strategy.

B. Sedation and Analgesia Protocols

An “analgesia-first” approach is recommended, prioritizing pain control before adding sedatives. The goal is a calm, comfortable patient who is synchronous with the ventilator.

  • Regimen: Fentanyl infusion (1–5 µg/kg/h) for analgesia, with propofol (5–50 µg/kg/min) added for sedation.
  • Monitoring: Target a Richmond Agitation Sedation Scale (RASS) of –2 (light sedation) to 0 (alert and calm). Perform daily sedation interruptions (“sedation vacations”) to assess neurologic status and facilitate weaning.
  • Induction: In patients with hemodynamic instability, etomidate (0.2–0.3 mg/kg) is a preferred induction agent due to its cardiovascular stability.
Pitfall IconA triangle with an exclamation mark. Pitfalls: Sedation Agents Expand/Collapse Icon

Propofol Infusion Syndrome (PRIS): Be vigilant for PRIS with high doses (>4 mg/kg/h or >67 mcg/kg/min) or prolonged use. Signs include metabolic acidosis, rhabdomyolysis, hyperlipidemia, and cardiovascular collapse.

Etomidate-Induced Adrenal Suppression: Etomidate can cause transient adrenal suppression. Its use should be limited to a single bolus for induction, not as a continuous infusion.

C. Vasopressor Selection and Titration

The goal is to restore adequate tissue perfusion, typically targeting a Mean Arterial Pressure (MAP) of ≥ 65 mm Hg.

  • First-Line: Norepinephrine (0.05–0.2 µg/kg/min) is the preferred agent due to its potent alpha- and modest beta-adrenergic effects.
  • Adjunct: Vasopressin (0.03 units/min) can be added to decrease the required norepinephrine dose (a “catecholamine-sparing” effect).
  • Refractory Shock: Epinephrine or phenylephrine may be considered if goals are not met.
  • Monitoring: An arterial line is essential for continuous, accurate blood pressure monitoring. Point-of-care ultrasound can help assess volume status and cardiac function to guide therapy.

2. Renal Replacement Therapy (RRT)

Acute kidney injury (AKI) is a frequent complication in oncologic emergencies, often resulting from tumor lysis syndrome, nephrotoxic agents, or sepsis. Continuous Renal Replacement Therapy (CRRT) is often preferred over intermittent hemodialysis in hemodynamically unstable patients.

A. CRRT Modalities and Indications

  • CVVH (Continuous Veno-Venous Hemofiltration): Primarily uses convective clearance. Ideal for removing middle- to large-sized molecules (e.g., myoglobin, inflammatory cytokines).
  • CVVHDF (Continuous Veno-Venous Hemodiafiltration): Combines convective and diffusive clearance, providing efficient removal of a broad spectrum of solutes, from small (urea) to large.
  • Indications for Initiation:
    • Severe oliguria (< 0.3 mL/kg/h for > 6 hours)
    • Life-threatening hyperkalemia (K⁺ > 6.5 mEq/L)
    • Severe metabolic acidosis (pH < 7.15)
    • Refractory volume overload causing respiratory compromise

B. Anticoagulation Management During RRT

Anticoagulation is necessary to prevent clotting of the extracorporeal circuit. Regional citrate is the recommended first-line strategy.

CRRT Anticoagulation Decision Flowchart A flowchart showing the decision process for choosing anticoagulation in CRRT. The primary decision point is hepatic function. If normal, regional citrate is preferred. If impaired, systemic heparin is the alternative, with a note on contraindications. Decision: CRRT Anticoagulation Severe Hepatic Dysfunction or Shock Liver? NO Use Regional Citrate Post-filter Ca²⁺: 0.25-0.35 Systemic Ca²⁺: 1.0-1.2 YES Use Systemic Heparin aPTT Goal: 60-80s (If no contraindication)
Figure 1: Anticoagulation Strategy for CRRT. Regional citrate is preferred but requires functional hepatic metabolism to prevent accumulation and toxicity. In patients with severe liver dysfunction, systemic heparin is the standard alternative, assuming no active bleeding or severe thrombocytopenia.
Pearl IconA shield with an exclamation mark. Clinical Pearls: Citrate Anticoagulation Expand/Collapse Icon

Monitoring for Citrate Lock: In patients with hepatic dysfunction, monitor for citrate accumulation (“citrate lock”) by checking the total-to-ionized calcium ratio. A ratio > 2.5 suggests impaired citrate metabolism, requiring a dose reduction or switch to heparin.

Calcium in Dialysate: When using high-dose citrate, ensure the dialysate and replacement fluids are calcium-free to prevent counteracting the regional anticoagulation effect and causing hypercalcemia.

3. ICU Complication Prevention

Critically ill oncology patients face a high risk of preventable complications, including venous thromboembolism (VTE), stress ulcers, and nosocomial infections. Implementing standardized prophylaxis bundles is a cornerstone of patient safety in the ICU.

ICU Prophylaxis Strategies
Condition First-Line Agent Alternative/Special Cases Key Considerations
VTE Prophylaxis LMWH (e.g., enoxaparin 40 mg SC daily) UFH (5,000 units SC q8-12h) Use UFH if CrCl < 30 mL/min, platelet count < 50,000/µL, or high bleeding risk. Consider anti-Xa monitoring for LMWH in obesity or renal dysfunction.
Stress Ulcer Prophylaxis PPI (e.g., pantoprazole 40 mg IV daily) H₂RA (e.g., famotidine 20 mg IV q12h) Indicated for mechanical ventilation > 48h or coagulopathy. PPIs may have a slightly higher risk of C. difficile infection. Discontinue when risk factors resolve.

Nosocomial Infection Prevention Bundles

Strict adherence to care bundles is proven to reduce infection rates.

  • CLABSI Bundle (Central Line-Associated Bloodstream Infection):
    • Hand hygiene before any line manipulation.
    • Chlorhexidine skin preparation.
    • Use of maximal sterile barriers during insertion.
    • Daily assessment of line necessity.
  • VAP Bundle (Ventilator-Associated Pneumonia):
    • Head-of-bed elevation to 30–45 degrees.
    • Daily sedation vacations and assessment of readiness to extubate.
    • Regular oral care with chlorhexidine.
    • VTE and stress ulcer prophylaxis.
  • CAUTI Prevention (Catheter-Associated Urinary Tract Infection):
    • Avoid unnecessary catheterization.
    • Use aseptic technique for insertion.
    • Maintain a closed drainage system.
    • Remove the catheter as soon as it is no longer indicated.

4. Management of Iatrogenic Complications

Aggressive treatments for oncologic emergencies can themselves cause significant toxicity. Proactive screening and supportive measures are critical to mitigate harm from these life-saving therapies.

A. Nephrotoxicity from Rasburicase

Rasburicase is highly effective for tumor lysis syndrome but carries a risk of severe hemolysis and methemoglobinemia in patients with Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency.

  • Prevention: Mandatory G6PD screening is required before administration.
  • Alternative: If a patient is G6PD deficient or screening is unavailable, use allopurinol (300 mg PO daily) with aggressive hydration for hyperuricemia prophylaxis.
  • Monitoring: If rasburicase is given, monitor hemoglobin, LDH, and methemoglobin levels daily.
Pearl IconA shield with an exclamation mark. Clinical Pearl: Rasburicase Dosing Expand/Collapse Icon

Consider using a single, weight-based dose of rasburicase (e.g., 0.15 mg/kg) rather than fixed-dose or multi-day regimens. Re-dose only if the uric acid level remains elevated (> 6 mg/dL) after 24 hours. This strategy is often equally effective, less costly, and may limit the risk of oxidative stress.

B. Cardiotoxicity from High-Dose Corticosteroids

High-dose steroids (e.g., for spinal cord compression or superior vena cava syndrome) can cause significant metabolic and cardiovascular side effects.

  • Risks: Hypertension, fluid retention, severe hypokalemia, and arrhythmias.
  • Monitoring: Check blood pressure at least every 4 hours. Monitor electrolytes, particularly potassium and magnesium, daily.
  • Management: Treat hypertension as needed. Administer loop diuretics (e.g., furosemide 20–40 mg IV) for fluid overload and aggressively replete potassium.
  • Tapering: Always taper steroids gradually after prolonged use to prevent acute adrenal insufficiency.

5. Goals-of-Care Conversations

Effective and compassionate communication is a core competency in critical care oncology. Structured, multidisciplinary discussions are essential to ensure that the intensive care provided aligns with the patient’s values, goals, and prognosis.

A. Multidisciplinary Framework and Communication

A team-based approach facilitates comprehensive and consistent communication.

  • Team: Should include oncology, critical care, palliative care, nursing, and pharmacy.
  • Timing: Initiate a formal goals-of-care discussion within 48 hours of ICU admission.
  • Framework: The SPIKES protocol provides a useful structure for these conversations:
    1. Setting: Ensure a private, quiet, and uninterrupted environment.
    2. Perception: Ask the patient/family what they understand about the current situation.
    3. Invitation: Ask for permission to discuss prognostic information and goals.
    4. Knowledge: Deliver information clearly and concisely, avoiding medical jargon.
    5. Empathy: Acknowledge and validate emotional responses with statements like, “This must be very difficult to hear.”
    6. Strategy/Summary: Outline a plan that aligns with the established goals and summarize the conversation.
Pearl IconA shield with an exclamation mark. Clinical Pearl: Palliative Care Consultation Expand/Collapse Icon

Proactively trigger a palliative care consultation for patients with refractory multi-organ failure, poorly controlled symptoms (pain, dyspnea), or significant family distress. Palliative care specialists are experts in symptom management and complex communication, serving as a vital support for the patient, family, and primary ICU team.

References

  1. Gould Rothberg BE, et al. Oncologic emergencies and urgencies: a comprehensive review. CA Cancer J Clin. 2022;72(3):254–275.
  2. Evans L, et al. Surviving Sepsis Campaign: guidelines on the management of sepsis and septic shock 2021. Crit Care Med. 2021;49(11):e1063–e1143.
  3. Coifer B, et al. Guidelines for the management of pediatric and adult tumor lysis syndrome: an evidence-based review. J Clin Oncol. 2008;26(16):2767–2778.
  4. Al-Zubeidi D, et al. Prevention of complications for hospitalized patients receiving parenteral nutrition: a narrative review. Nutr Clin Pract. 2024;39(1):1037–1053.
  5. Achanti A, et al. Metabolic alkalosis and acid-base disorders in ICU. Clin J Am Soc Nephrol. 2023;18:102–112.