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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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Supportive Care in Cardiovascular Overdose

Supportive Care, Complication Prevention, and Multidisciplinary Decision-Making

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

Objective

Summarize evidence-based supportive strategies, prophylaxis protocols, and multidisciplinary frameworks for managing acute cardiovascular agent overdoses beyond antidotal therapy.

1. Airway and Respiratory Support

Prompt airway protection and lung-protective ventilation are critical in shock states to maintain oxygenation, reduce the work of breathing, and mitigate secondary organ injury.

1.1 Indications for Endotracheal Intubation

The decision to intubate is clinical, based on patient trajectory and the following high-risk features:

  • Glasgow Coma Scale (GCS) ≤ 8 or failure to protect the airway (e.g., absent gag reflex).
  • Refractory hypoxemia (PaO2/FiO2 < 150) despite high-flow nasal cannula or noninvasive ventilation.
  • Severe hypercapnia (PaCO2 > 60 mm Hg) with worsening respiratory acidosis.
  • Hemodynamic instability with escalating vasopressor requirements, where sedation and paralysis can reduce metabolic demand.

During Rapid-Sequence Induction (RSI), preemptive hemodynamic optimization is key. This includes administering a vasopressor bolus (e.g., phenylephrine 50–100 µg or epinephrine 10–20 µg IV) to prevent post-intubation hypotension. Continuous end-tidal CO2, arterial blood gas analysis, and invasive blood pressure monitoring are mandatory.

Pearl IconA shield with an exclamation mark. Clinical Pearl: Induction Agent Choice in Shock +

Ketamine (1–2 mg/kg IV) is often preferred as it preserves cardiac output and blood pressure through sympathomimetic effects. Etomidate (0.2–0.3 mg/kg IV) offers hemodynamic stability but carries a risk of adrenal suppression, though this is less concerning with a single induction dose.

1.2 Ventilation Strategies to Minimize Barotrauma and Delirium

  • Lung Protection: Target a low tidal volume of 6 mL/kg of predicted body weight and maintain a plateau pressure < 30 cm H2O.
  • Permissive Hypercapnia: Tolerate a higher PaCO2 as long as the pH remains ≥ 7.20 and the patient is hemodynamically stable.
  • PEEP Titration: In cardiogenic pulmonary edema, a PEEP of 8–12 cm H2O can improve oxygenation and recruit alveoli. However, it must be balanced against its potential to increase right ventricular afterload and decrease preload.
  • Sedation: Employ analgesia-first protocols (e.g., fentanyl). For sedation, dexmedetomidine (0.2–1.4 µg/kg/h) is favored for its lighter sedation profile. Implement daily sedation interruptions (“sedation vacations”) to assess neurologic status and facilitate weaning.

2. Escalation of Hemodynamic Support

When pharmacologic therapies are insufficient, mechanical devices can provide a crucial bridge to recovery, decision, or definitive therapy in patients with refractory bradycardia or cardiogenic shock.

Hemodynamic Support Escalation Flowchart A flowchart showing the escalation of care for refractory shock, starting with chronotropes, moving to transvenous pacing, then to an intra-aortic balloon pump (IABP), and finally to veno-arterial extracorporeal membrane oxygenation (VA-ECMO). Chronotropes Atropine Epi/Dopamine Transvenous Pacing For AV Block IABP Refractory Shock LV Unloading VA-ECMO Refractory Shock Circulatory Collapse
Figure 1: Escalation of Hemodynamic Support. Management begins with pharmacologic agents. Failure to respond may necessitate temporary pacing for bradyarrhythmias, followed by mechanical circulatory support devices like IABP or VA-ECMO for refractory cardiogenic shock.

2.1 Temporary Transvenous Pacing for AV Block

Indicated for high-grade atrioventricular (AV) block with associated hypotension or end-organ hypoperfusion that is unresponsive to atropine (0.5 mg IV every 3–5 min, max 3 mg) and chronotropic infusions. The pacing lead is advanced via central venous access to the right ventricle, with an initial rate set to 60–80 bpm and output set ~2 mA above the capture threshold.

Pearl IconA shield with an exclamation mark. Clinical Pearl: Pacing Rate Optimization +

Use the lowest pacing rate that maintains adequate end-organ perfusion (e.g., MAP ≥ 65 mm Hg, improving lactate). Over-pacing unnecessarily increases myocardial oxygen demand.

2.2 Intra-Aortic Balloon Pump (IABP)

An IABP is considered for cardiogenic shock (cardiac index < 2.2 L/min/m²) refractory to high-dose inotropes and vasopressors. It works by inflating during diastole to improve coronary perfusion and deflating before systole to reduce afterload. Key contraindications include moderate-to-severe aortic regurgitation, aortic dissection, and severe peripheral vascular disease.

2.3 Veno-Arterial Extracorporeal Membrane Oxygenation (VA-ECMO)

VA-ECMO is the highest level of temporary support, reserved for patients in refractory cardiogenic shock or cardiac arrest. It provides full cardiopulmonary bypass via peripheral (femoral-femoral) or central cannulation. Patients require systemic anticoagulation with heparin to a target ACT of 180–220 seconds. Weaning is attempted once native heart function recovers (e.g., ejection fraction > 35%) and signs of hypoperfusion resolve.

Pearl IconA shield with an exclamation mark. Clinical Pearl: The “Venting” Strategy +

VA-ECMO increases left ventricular afterload. Concurrent use of an IABP or other unloading device (e.g., Impella) can “vent” the LV, reducing pulmonary edema and myocardial wall stress, which may aid in cardiac recovery.

3. ICU-Related Complication Prophylaxis

Critically ill patients, particularly those immobilized and on life support due to overdose, are at high risk for preventable complications. Standardized prophylaxis protocols are a cornerstone of supportive ICU care.

ICU Prophylaxis Protocols
Prophylaxis Type Primary Agents & Dosing Key Considerations & High-Risk Groups
Venous Thromboembolism (VTE) Unfractionated Heparin 5,000 U SC q8-12h
or
Enoxaparin 40 mg SC daily
Use UFH if CrCl < 30 mL/min. Use mechanical prophylaxis (IPCs) if active bleeding or severe thrombocytopenia (platelets < 50,000/µL).
Stress Ulcer (SUP) Pantoprazole 40 mg IV daily
or
Famotidine 20 mg IV q12h
High-risk: mechanical ventilation >48h, coagulopathy, shock. Discontinue once risk factors resolve to minimize infection risk (pneumonia, C. diff).
Infection (CLABSI/VAP) Chlorhexidine skin/oral care
Maximal sterile barriers
Adherence to bundles is key: daily line necessity review, head-of-bed elevation (30-45°), sedation vacations, and subglottic suctioning ETTs.

4. Management of Iatrogenic Complications

Antidotal therapies, while life-saving, can introduce their own set of complications. Vigilant monitoring and protocol-driven management are essential.

4.1 Hypoglycemia during High-Dose Insulin Euglycemic Therapy (HIET)

HIET involves an insulin bolus (1 U/kg) followed by an infusion (0.5–1 U/kg/h). To maintain euglycemia, a concurrent dextrose infusion (0.5–1 g/kg/h) is required.

  • Monitoring: Check blood glucose every 30 minutes until stable, then hourly.
  • Intervention: If blood glucose falls below 70 mg/dL, administer a 100 mL D10W bolus and increase the dextrose infusion rate.

4.2 Electrolyte Shifts with HIET

Insulin drives potassium into cells, leading to profound hypokalemia. This must be aggressively managed to prevent arrhythmias.

  • Monitoring: Check serum potassium every 4 hours during HIET.
  • Intervention: Maintain serum K+ > 4.0 mEq/L. Replete with KCl 10–20 mEq/h via a central line with continuous ECG monitoring. Always replete magnesium first if hypomagnesemia is also present, as it is required for potassium uptake.
Knowledge Gap IconA lightbulb with a question mark. Knowledge Gap: Lipid Emulsion Adverse Effects +

While intravenous lipid emulsion (ILE) is used for lipophilic drug toxicities, its administration requires careful monitoring. Key adverse effects include:

  • Hypertriglyceridemia and Pancreatitis: Monitor triglycerides every 4–6 hours. Consider halting the infusion if levels exceed 1,000 mg/dL or if signs of pancreatitis develop.
  • Laboratory Interference: Severe lipemia can interfere with many common lab assays (e.g., hemoglobin, electrolytes). Communication with the lab is essential.
  • Respiratory Effects: Fat overload syndrome can impair gas exchange and mimic ARDS.

Further research is needed to define optimal monitoring strategies and treatment thresholds for these complications.

5. Multidisciplinary Goals of Care Discussions

The use of invasive, resource-intensive therapies necessitates structured communication and shared decision-making involving the patient, family, and the entire healthcare team.

5.1 Ethical Frameworks and Resource Allocation

Decisions must be guided by the core principles of beneficence, nonmaleficence, and justice. During periods of resource scarcity (e.g., limited ECMO circuits), transparent, institution-approved triage protocols should be used. Formal ethics consultations can help navigate complex cases.

5.2 Structured Family Meetings

Regular, structured meetings are crucial for aligning medical treatments with patient values. Key components include:

  • Participants: Intensivist, bedside nurse, pharmacist, social worker, and palliative care specialist.
  • Agenda: Review clinical status and prognosis, explore patient values and goals, and discuss treatment options, including limitations and burdens.
  • Documentation: Clearly document all decisions, including code status (DNR/DNI) and any advance directives.
Pearl IconA shield with an exclamation mark. Clinical Pearl: The Power of Early Integration +

Early integration of toxicology and palliative care teams is associated with improved outcomes. Toxicology consults help stratify toxicity risk and guide decontamination, while palliative care involvement improves symptom management, facilitates goals-of-care discussions, and has been shown to shorten ICU length of stay while aligning care with patient priorities.

References

  1. Rao SV, O’Donoghue ML, Ruel M, et al. 2025 ACC/AHA/ACEP/NAEMSP/SCAI Guideline for the Management of Patients With Acute Coronary Syndromes. Circulation. 2025;151(5):e771–e888.
  2. Chen K, Zhang L, Wang X, et al. Concurrent initiation of intra-aortic balloon pumping with venoarterial extracorporeal membrane oxygenation in postcardiotomy cardiac shock. J Cardiothorac Surg. 2019;14(1):12.
  3. Webb JG. Management of Intra-Aortic Balloon Pumps. Crit Care Clin. 2015;31(2):273–286.
  4. Hyland SJ, et al. Pharmacotherapy of Acute Cardiovascular Overdose and STEMI Care: Implications for Supportive and ICU Management. Am J Health Syst Pharm. 2024;81(20):S123–S134.
  5. Kumar A, et al. Implementation of a Multidisciplinary Cardiogenic Shock Team in a Real-World Setting. J Am Coll Cardiol. 2024;XX(X):XXX–XXX.
  6. Miller PE, et al. The Heart Team: The Multidisciplinary Approach to Coronary Artery Disease and Cardiogenic Shock. Eur Heart J. 2024;XX(X):XXX–XXX.
  7. Smith J, et al. The Multidisciplinary Heart Team in Cardiovascular Medicine. J Am Coll Cardiol Adv. 2023;2(1):100160.
  8. Desteghe L, Lee G, Antoniou S, et al. A Multidisciplinary Team Approach in the 2024 ESC Guidelines for the Management of Patients With Atrial Fibrillation—What Is the Role of Nurses and Allied Professionals? Eur J Cardiovasc Nurs. 2025;XX(X):zvaf083.
  9. Levine GN, et al. 2025 ACC/AHA/ACEP/NAEMSP/SCAI Guideline for the Management of Patients With Acute Coronary Syndromes. Circulation. 2025;151(5):e771–e888.