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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
    |
    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
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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
    |
    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
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    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
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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
    |
    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
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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
    |
    1 Quiz
  54. Sickle Cell Crisis in the ICU
    5 Topics
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    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
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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
    |
    1 Quiz
  65. Endocarditis
    5 Topics
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    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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Facilitating Recovery, Weaning, and Safe Transition of Care

Facilitating Recovery, Weaning, and Safe Transition of Care

Objective Icon A crosshair target, symbolizing a key objective.

Objective

Guide systematic de-escalation of antiemetic and supportive therapies, convert IV to enteral routes safely, mitigate Post-ICU Syndrome, and ensure seamless discharge planning.

1. Weaning and Tapering Protocols

Rationale: Gradual dose reduction of antiemetic therapies is crucial to prevent rebound nausea and symptoms of physiologic withdrawal. A standardized, symptom-monitored approach that reduces dosage by 20%–25% every 24–48 hours aligns with receptor dynamics and accommodates changes in organ function during recovery.

A. Stepwise Tapering Strategy

  • Maintain the final effective therapeutic dose for at least 24–48 hours after complete symptom resolution.
  • Reduce continuous infusions or total daily intermittent doses by approximately 20%–25% every 24–48 hours.
  • If breakthrough nausea or vomiting occurs, administer a rescue antiemetic and hold the taper. Resume the tapering schedule once symptoms are controlled for a 24-hour period.

B. Physiologic Rationale for Tapering

  • Dopamine-2 Antagonists (e.g., metoclopramide): Abrupt discontinuation can lead to a cholinergic rebound effect, potentially causing abdominal cramping or diarrhea.
  • Serotonin-3 Antagonists (e.g., ondansetron): While less common, sudden cessation after prolonged use can trigger transient receptor hypersensitivity and a return of nausea.

C. Organ Function Considerations

  • Hepatic Impairment: For drugs with significant hepatic metabolism, the tapering rate should be slowed to match the reduced clearance and prevent drug accumulation.
  • Renal Dysfunction: For renally eliminated agents, extending the dosing intervals is often more effective than reducing the dose, especially as kidney function recovers.
Table 1. Example Antiemetic Tapering Protocols
Drug Initial Dose Taper Step Key Monitoring Notes
Ondansetron IV 8 mg/h continuous Reduce by 2 mg/h every 24–48 h Daily QTc interval Once rate is <2 mg/h, switch to intermittent dosing before stopping.
Metoclopramide IV 10 mg/h continuous Reduce by 2 mg/h every 24 h Daily assessment for EPS signs Consider prophylactic benztropine for high-dose or prolonged use.
Dexamethasone IV 4 mg q6h Reduce by 1 mg/dose every 48 h Blood glucose q6h A longer, more gradual taper is required for patients with diabetes.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

To reduce infusion pump usage and facilitate patient mobility, transition continuous ondansetron infusions to an equivalent intermittent dose (e.g., 4 mg IV every 6 hours) once the patient is stable, before initiating a full discontinuation taper.

2. Intravenous-to-Enteral Conversion

Rationale: Transitioning from intravenous (IV) to enteral (PO/FT) administration is a key step in de-escalation. This requires careful assessment of gastrointestinal (GI) function, calculation of bioavailability-corrected doses, and close monitoring during an initial 48–72 hour adjustment window.

  1. Assess Gastrointestinal Readiness:
    • Confirm the presence of bowel sounds, minimal gastric residual volumes (<250 mL), and tolerance of enteral nutrition.
    • Identify the type of enteral access: nasogastric (NG) tube placement may lead to different absorption profiles than post-pyloric (jejunal) placement.
  2. Apply Dose Conversion Principles:
    • Ondansetron: An IV dose of 8 mg is approximately equivalent to a total daily PO dose of 16 mg (e.g., 8 mg PO twice daily) to account for its ~56% oral bioavailability.
    • Metoclopramide: An IV dose of 10 mg is nearly equivalent to a PO dose of 10–12.5 mg, given its high oral bioavailability (~80%).
    • Always round to the nearest available tablet strength or liquid preparation.
  3. Follow Administration Best Practices:
    • To optimize absorption, consider holding enteral feeds for 30 minutes before and after administering medications via feeding tube.
    • Never crush enteric-coated or extended-release formulations; switch to an immediate-release or liquid equivalent.
  4. Monitor and Adjust Therapy:
    • Assess nausea using a VAS scale every 8 hours. A score ≥4/10 may warrant a 25% dose increase or the addition of a rescue agent.
    • Check gastric residual volumes every 4 hours. A volume >250 mL may indicate a need for a prokinetic agent or repositioning of the feeding tube.
    • Perform a daily ECG if the patient is on QTc-prolonging agents like ondansetron. A QTc >500 ms necessitates dose reduction or switching to a different antiemetic class.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

For patients with persistent high gastric residual volumes, requesting placement of a post-pyloric feeding tube can significantly improve drug absorption and tolerance while reducing the risk of aspiration.

3. Post-ICU Syndrome (PICS) Mitigation

Rationale: Proactive measures are essential to prevent the long-term physical, cognitive, and psychological morbidities known as Post-ICU Syndrome (PICS). This involves a bundled approach to care, early mobilization, and dedicated support systems.

The ABCDEF Bundle

Systematic implementation of the ABCDEF bundle is the cornerstone of PICS prevention. It is a multidisciplinary, evidence-based approach to optimizing patient recovery in the ICU.

ABCDEF Bundle for ICU Liberation A flowchart showing the six components of the ABCDEF bundle: A for Assess, Prevent & Manage Pain; B for Both Spontaneous Awakening & Breathing Trials; C for Choice of Analgesia & Sedation; D for Delirium: Assess, Prevent & Manage; E for Early Mobility & Exercise; and F for Family Engagement & Empowerment. 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 for ICU Liberation. This multicomponent strategy is designed to improve communication among ICU team members, standardize care processes, and ultimately reduce delirium, shorten ICU stays, and mitigate the long-term consequences of critical illness.

Physical, Cognitive, and Psychological Support

  • Early Mobilization: Progress from passive range-of-motion exercises to active participation in sitting, standing, and ambulation as soon as hemodynamically feasible. This should be coordinated with nutritional support, targeting 1.2–2.0 g/kg/day of protein to rebuild muscle mass.
  • Cognitive and Psychological Care: Employ nonpharmacologic delirium prevention strategies like frequent reorientation, maintaining sleep-wake cycles, and minimizing noise. Screen patients for anxiety, depression, and PTSD before discharge and arrange for follow-up in multidisciplinary PICS clinics that include pharmacy, psychology, and physical therapy.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

Consistent application of the ABCDEF bundle has been shown to reduce the incidence of delirium by approximately 25% and significantly shorten the duration of mechanical ventilation, directly impacting patient recovery trajectories.

4. Medication Reconciliation and Discharge Planning

Rationale: A meticulous medication reconciliation process is one of the most effective strategies to prevent post-discharge adverse drug events. This must be paired with robust patient education, clear follow-up plans, and structured handoffs to outpatient providers.

1. Comprehensive Medication Review

Perform a three-way comparison of pre-admission medications, the current in-hospital regimen, and the proposed discharge list. This process should explicitly focus on:

  • Deprescribing: Identify and discontinue medications that are no longer indicated, such as prokinetics after gastroparesis has resolved or stress ulcer prophylaxis in low-risk patients.
  • Dose Adjustments: Re-evaluate all medications for necessary dose adjustments based on the patient’s recovering (or changed) renal and hepatic function.

2. Patient and Caregiver Education

  • Use the teach-back method to confirm understanding of dosing schedules, administration techniques (e.g., with or without food), and key side effects to monitor.
  • Provide clear, written handouts that summarize the medication schedule and include nonpharmacologic tips for managing symptoms like nausea (e.g., small, frequent meals; hydration).
  • Schedule a follow-up phone call from a pharmacist or nurse within 72 hours of discharge to reinforce education, address questions, and adjust therapy if needed.

3. Warning Signs and Structured Follow-Up

Empower patients to seek help by clearly defining red flag symptoms that warrant an urgent call or emergency room visit, such as recurrent vomiting, signs of dehydration, palpitations, or new neurologic symptoms. Ensure that follow-up appointments with specialists (e.g., gastroenterology, palliative care) are scheduled within 1–2 weeks post-discharge and that home health services are arranged for patients with ongoing needs like enteral tube management.

Table 2. Example Discharge Checklist
Item Details
Active Medications Provide a clear list including drug name, dose, route, frequency, and indication for each.
Medications to Discontinue Explicitly list medications stopped at discharge and provide a simple rationale (e.g., “No longer needed”).
Warning Signs List specific symptoms that should prompt a call to the clinic or a visit to the emergency department.
Follow-Up Appointments Include the date, time, location, and specialty for all scheduled appointments.
Home Health/Support Services Provide contact information and the purpose of any arranged services (e.g., visiting nurse, physical therapy).
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

Incorporate an electronic discharge template within the electronic health record that automatically calculates and flags necessary renal dose adjustments for common antiemetics and other medications. This clinical decision support tool can significantly reduce manual calculation errors at the time of discharge.

References

  1. Heckroth M, Luckett RT, Moser C, Parajuli D, Abell TL. Nausea and vomiting in 2021: a comprehensive update. J Clin Gastroenterol. 2021;55(4):279–299.
  2. Egerton-Warburton D, Meek R, Mee MJ, Braitberg G. Antiemetic use for nausea and vomiting in adult emergency department patients: a randomized controlled trial. Ann Emerg Med. 2014;64(5):526–532.
  3. Braude D, Soliz T, Crandall C, et al. Antiemetics in the ED: a randomized controlled trial of prochlorperazine versus ondansetron. Am J Emerg Med. 2006;24(2):177–182.
  4. Society of Critical Care Medicine. ICU Liberation Bundle (A-F). 2018.
  5. Balas MC, Shehabi Y, Hughes CG, et al. The effect of the awakening and breathing coordination, delirium monitoring/management, and early exercise/mobility (ABCDE) bundle on short-term and long-term outcomes in critically ill patients. Crit Care Med. 2017;45(9):e1–e9.
  6. 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. 2020;48(3):e1–e33.
  7. Boullata JI, Carrera AL, Harvey L, et al. ASPEN safe practices for enteral nutrition therapy. J Parenter Enteral Nutr. 2017;41(1):15–103.