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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
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    1 Quiz
  14. Ventricular Arrhythmias and Sudden Cardiac Death Prevention
    5 Topics
    |
    1 Quiz
  15. NEPHROLOGY
    Acute Kidney Injury (AKI)
    5 Topics
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    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
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    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
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    1 Quiz
  25. Neuromonitoring Techniques
    5 Topics
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    1 Quiz
  26. Gastroenterology
    Acute Upper Gastrointestinal Bleeding
    5 Topics
    |
    1 Quiz
  27. Acute Lower Gastrointestinal Bleeding
    5 Topics
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    1 Quiz
  28. Acute Pancreatitis
    5 Topics
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    1 Quiz
  29. Enterocutaneous and Enteroatmospheric Fistulas
    5 Topics
    |
    1 Quiz
  30. Ileus and Acute Intestinal Pseudo-obstruction
    5 Topics
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    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
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    1 Quiz
  34. Hepatic Encephalopathy
    5 Topics
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    1 Quiz
  35. Ascites & Spontaneous Bacterial Peritonitis
    5 Topics
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    1 Quiz
  36. Hepatorenal Syndrome
    5 Topics
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    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
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    1 Quiz
  40. Drug Reaction (or Rash) with Eosinophilia and Systemic Symptoms (DRESS)
    5 Topics
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    1 Quiz
  41. Immunology
    Transplant Immunology & Acute Rejection
    5 Topics
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    1 Quiz
  42. Solid Organ & Hematopoietic Transplant Pharmacotherapy
    5 Topics
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    1 Quiz
  43. Graft-Versus-Host Disease (GVHD)
    5 Topics
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    1 Quiz
  44. Hypersensitivity Reactions & Desensitization
    5 Topics
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    1 Quiz
  45. Biologic Immunotherapies & Cytokine Release Syndrome
    5 Topics
    |
    1 Quiz
  46. Endocrinology
    Relative Adrenal Insufficiency and Stress-Dose Steroid Therapy
    5 Topics
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    1 Quiz
  47. Hyperglycemic Crisis (DKA & HHS)
    5 Topics
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    1 Quiz
  48. Glycemic Control in the ICU
    5 Topics
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    1 Quiz
  49. Thyroid Emergencies: Thyroid Storm & Myxedema Coma
    5 Topics
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    1 Quiz
  50. Hematology
    Acute Venous Thromboembolism
    5 Topics
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    1 Quiz
  51. Drug-Induced Thrombocytopenia
    5 Topics
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    1 Quiz
  52. Anemia of Critical Illness
    5 Topics
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    1 Quiz
  53. Drug-Induced Hematologic Disorders
    5 Topics
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    1 Quiz
  54. Sickle Cell Crisis in the ICU
    5 Topics
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    1 Quiz
  55. Methemoglobinemia & Dyshemoglobinemias
    5 Topics
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    1 Quiz
  56. Toxicology
    Toxidrome Recognition and Initial Management
    5 Topics
    |
    1 Quiz
  57. Management of Acute Overdoses – Non-Cardiovascular Agents
    5 Topics
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    1 Quiz
  58. Management of Acute Overdoses – Cardiovascular Agents
    5 Topics
    |
    1 Quiz
  59. Toxic Alcohols and Small-Molecule Poisons
    5 Topics
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    1 Quiz
  60. Antidotes and Gastrointestinal Decontamination
    5 Topics
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    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
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    1 Quiz
  65. Endocarditis
    5 Topics
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    1 Quiz
  66. CNS Infections
    5 Topics
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    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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Recovery and De-Escalation in Toxicology

Recovery, De-Escalation, and Transition of Care for Toxidrome Patients

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

Chapter Objective

Consolidate recovery, prevent chronic sequelae, and ensure safe transition of care through structured de-escalation of supports, conversion to enteral regimens, mitigation of post–ICU syndrome, and comprehensive discharge planning.

1. Protocols for Weaning and De-Escalation of Intensive Therapies

Systematic weaning from ventilators, sedatives, and vasopressors is a cornerstone of recovery in the ICU. Structured protocols reduce the duration of intensive support, minimize iatrogenic complications, and can lower healthcare costs.

A. Ventilator Liberation

The process of discontinuing mechanical ventilation involves assessing patient readiness and conducting a formal trial of spontaneous breathing.

  • Readiness Criteria: Before attempting a Spontaneous Breathing Trial (SBT), the patient should demonstrate adequate oxygenation (PaO₂/FiO₂ >150–200 on FiO₂ ≤0.4 and PEEP ≤5 cm H₂O), hemodynamic stability without escalating vasopressors, and an acceptable Rapid Shallow Breathing Index (f/VT) <105 breaths/min/L.
  • Spontaneous Breathing Trials (SBT): A successful trial, typically lasting 30–120 minutes on a T-piece or with low-level pressure support, is the strongest predictor of extubation success.
  • Extubation Indicators: Following a successful SBT, the patient should be extubated if they maintain a respiratory rate <35/min, a tidal volume >5 mL/kg, and show no signs of respiratory distress.
Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: Empowering Protocols

Empowering respiratory therapists and nurses to initiate and manage SBTs based on a pre-defined protocol has been shown to significantly shorten the time to extubation and reduce total ventilator days compared to physician-only driven approaches.

B. Sedation Tapering

The primary goals of sedation management are to maintain patient comfort while targeting light sedation (RASS -2 to 0), which minimizes delirium and facilitates early mobilization.

  • Daily Sedation Interruption: Spontaneous Awakening Trials (SATs) are a standard practice to assess neurologic function and prevent drug accumulation.
  • Paired SAT-SBT: Coordinating SATs with SBTs (“wake-and-wean” protocols) is a highly effective strategy to expedite ventilator liberation.
  • Agent Selection: Non-benzodiazepine sedatives like propofol (for short-term use) or dexmedetomidine are preferred due to a lower risk of delirium.
Pitfall Icon A warning sign with an exclamation mark, indicating a clinical pitfall. Pitfall: Dexmedetomidine Side Effects

While an excellent agent for light sedation, dexmedetomidine can cause significant bradycardia and hypotension, especially during loading doses or in patients with underlying cardiac dysfunction. Careful dose titration and hemodynamic monitoring are essential.

C. Vasopressor Weaning

Tapering vasopressors should begin once the underlying cause of shock is controlled and organ perfusion is restored.

  • Stability Benchmarks: Key indicators include a mean arterial pressure (MAP) ≥65 mm Hg on a low dose of norepinephrine (e.g., ≤0.05 µg/kg/min), adequate urine output (>0.5 mL/kg/h), and normalizing lactate levels.
  • Taper Protocol: A cautious approach involves decreasing the vasopressor dose by approximately 25% every 30–60 minutes while closely monitoring for rebound hypotension.

2. Intravenous to Enteral Medication Conversion

An early and appropriate switch from intravenous (IV) to enteral (PO) therapies is a critical step in de-escalation. This practice preserves IV access, lowers the risk of catheter-related bloodstream infections, supports gastrointestinal function, and reduces medication costs. The decision to convert is guided by the patient’s clinical stability, GI function, and the pharmacokinetic properties of the drug.

Guidance for Common IV to Enteral Medication Conversions
Drug / Class Typical Oral Bioavailability (F) Conversion & Dosing Considerations
Fluoroquinolones (e.g., levofloxacin) >90% Generally safe for 1:1 dose conversion (e.g., 750 mg IV → 750 mg PO).
Azole Antifungals (e.g., fluconazole) >90% Excellent absorption allows for 1:1 dose conversion.
Metoprolol ~50% (variable) Requires dose increase for PO conversion. A common ratio is 1 mg IV to 2.5 mg PO.
Furosemide 10-100% (highly variable) Oral bioavailability is erratic. A typical conversion is 40 mg IV to 80 mg PO (1:2 ratio), requiring close monitoring of diuretic response.
Proton Pump Inhibitors (e.g., pantoprazole) ~77% Generally safe for 1:1 dose conversion (e.g., 40 mg IV → 40 mg PO).

Key considerations for conversion include ensuring adequate GI perfusion (deferring in ongoing shock or ileus), selecting appropriate formulations (immediate-release preferred initially), and accounting for drug-tube interactions or pH sensitivity when using enteral feeding tubes.

Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: Pharmacist-Driven Protocols

Implementation of pharmacist-driven IV-to-PO conversion protocols that target high-bioavailability drugs can significantly reduce medication costs, decrease line-related complications, and standardize care across an institution.

3. Mitigating Post-ICU Syndrome (PICS)

Post-intensive care syndrome (PICS) is a constellation of new or worsened physical, cognitive, and psychological impairments that persist after critical illness. A proactive, bundled approach is essential to minimize its incidence and severity.

The ABCDEF Bundle

The ABCDEF bundle is a evidence-based, multicomponent strategy that improves outcomes such as survival, delirium duration, and mechanical ventilation time.

ABCDEF Bundle for ICU Care A flowchart showing the six components of the ABCDEF bundle: A for Assess Pain, B for Both SAT/SBT, C for Choice of Sedation, D for Delirium, E for Early Mobility, and F for Family Engagement. A Assess, Prevent, & Manage Pain B Both SAT & SBT C Choice of Analgesia & Sedation D Delirium: Assess, Prevent, Manage E Early Mobility & Exercise F Family Engagement & Empowerment
Figure 1: The ABCDEF Bundle. A multicomponent, evidence-based strategy to reduce delirium, improve pain management, and decrease long-term consequences of critical illness.

B. Early Mobilization and Nutrition

Early mobilization and nutritional support are key components of the bundle that directly combat the physical aspects of PICS.

  • Mobilization: Should be initiated as soon as the patient is hemodynamically stable (RASS -2 to +1), progressing from passive range of motion to active exercises, sitting, standing, and ambulation.
  • Nutrition: Early enteral nutrition with adequate protein intake (1.2–2.0 g/kg/day) is crucial to prevent muscle wasting and support recovery.
  • Sleep: Restoring normal sleep-wake cycles by clustering care, minimizing nighttime noise and light, and managing delirium is vital for cognitive and psychological recovery.
Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: Mobility and Delirium

Early mobilization is one of the most effective non-pharmacologic interventions to reduce ICU-acquired weakness. Furthermore, studies have shown that it may also shorten the duration of delirium, highlighting the interconnectedness of PICS domains.

4. Comprehensive Medication Reconciliation and Discharge Planning

A structured transition from the ICU to the ward and ultimately to home is essential to prevent medication errors and reduce hospital readmissions. This process requires meticulous medication reconciliation, patient education, and coordinated follow-up care.

A. Medication Review and Reconciliation

The risk of medication discrepancies is highest during transitions of care. A pharmacist-led review should compare pre-admission, ICU, and proposed discharge medication regimens to identify and resolve any omissions, duplications, or inappropriate therapies. Special attention should be paid to high-risk medications such as opioids, anticholinergics, psychotropics, and benzodiazepines, for which clear taper plans should be established.

B. Patient and Family Education

Empowering patients and their caregivers is a critical safety measure. Education should be clear, concise, and confirmable.

  • Tools: Provide simplified, color-coded medication schedules and a list of “red-flag” symptoms (e.g., dizziness, confusion, shortness of breath) that should prompt a call to a healthcare provider.
  • Teach-Back Method: After explaining the discharge plan, ask the patient or caregiver to explain it back in their own words. This technique is proven to improve comprehension and adherence.
Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: The Impact of Pharmacist-Led Education

Studies have demonstrated that pharmacist-led medication education sessions incorporating the teach-back method can reduce post-discharge medication errors by over 40%, significantly improving patient safety.

C. Coordination of Follow-Up Care

A safe discharge is not the end of the care journey. The discharging team must ensure continuity by scheduling necessary follow-up appointments with primary care physicians, toxicologists, psychiatrists, and other specialists. A comprehensive discharge summary, including the final medication list and required monitoring parameters, must be transmitted to these providers to close the communication loop.

References

  1. Girard TD, Kress JP, Fuchs BD, et al. Efficacy and safety of a paired sedation and ventilator weaning protocol for mechanically ventilated patients in intensive care (Awakening and Breathing Controlled trial): a randomised controlled trial. Lancet. 2008;371(9607):126–134.
  2. MacIntyre NR. Evidence-based guidelines for weaning and discontinuing ventilatory support. Respir Care. 2004;49(1):90–96.
  3. Vollbrecht H, Patel BK. Weaning from mechanical ventilation: a narrative review of recent advances. Curr Opin Crit Care. 2025;31(1):78–85.
  4. Lavonas EJ, Akpunonu P, Arens AM, et al. 2023 American Heart Association focused update on the management of patients with cardiac arrest or life-threatening toxicity due to poisoning: an update to the 2015 American Heart Association guidelines update for cardiopulmonary resuscitation and emergency cardiovascular care. Circulation. 2023.
  5. NHS Grampian. Guidelines for the Enteral Tube Administration of Medicines. 2023.
  6. Dravet Syndrome Foundation. Administering Medications via Feeding Tubes. 2022.
  7. American Thoracic Society. Intravenous to Oral Medication Conversion Policy. 2021.
  8. Devlin JW, Skrobik Y, Gélinas C, et al. Clinical Practice Guidelines for the Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICU. Crit Care Med. 2018;46(9):e825–e873.
  9. Frithsen IL, Simpson WM Jr. In-hospital medication reconciliation. Am Fam Physician. 2010;81(3):316–323.
  10. Del Rosso C, Lees D, Gittinger M, et al. A Standardized Approach to ICU Discharge Using a Checklist and the Teach-Back Method. MedEdPORTAL. 2021;17:11089.