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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
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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
    |
    1 Quiz
  41. Immunology
    Transplant Immunology & Acute Rejection
    5 Topics
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    1 Quiz
  42. Solid Organ & Hematopoietic Transplant Pharmacotherapy
    5 Topics
    |
    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
    |
    1 Quiz
  51. Drug-Induced Thrombocytopenia
    5 Topics
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    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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Recovery and De-escalation After Resuscitation

Recovery, De-escalation, and Transition of Care after Initial Resuscitation

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

Learning Objective

Guide the pharmacist in stepwise weaning of fluids and vasopressors, transition to enteral therapies, mitigation of Post-ICU Syndrome, and safe discharge planning.

1. Weaning and De-escalation of Resuscitation Therapies

Once hemorrhage control is achieved and markers of perfusion normalize, the critical phase of de-escalation begins. The goal is to taper fluids and vasopressors using dynamic indices to avoid both the harm of persistent fluid overload and the risk of recurrent hypoperfusion from premature withdrawal of support.

Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Key Pearls
  • A passive leg raise (PLR) maneuver combined with real-time cardiac output measurement (e.g., via echocardiography) is the preferred method to assess fluid responsiveness in patients with arrhythmias or those on low-tidal-volume ventilation, where pulse pressure variation (PPV) is unreliable.
  • After shock resolution, aim for a modest net negative fluid balance of approximately 500 mL per day to promote decongestion and reduce organ edema, which can impair recovery.

Case Vignette: A 55-year-old patient with blunt trauma is now hemodynamically stable. Blood product transfusion has ceased, lactate has normalized to 1.5 mmol/L, and the pulse pressure variation (PPV) is 8%. This profile strongly suggests the patient is no longer fluid responsive. The appropriate next steps are to discontinue maintenance crystalloid infusions and begin a cautious, protocolized taper of vasopressors.

1.1 Dynamic Fluid Responsiveness Markers for Weaning Decisions

Static markers like CVP are poor predictors of fluid responsiveness. Dynamic assessments are essential for guiding fluid de-escalation.

  • PPV <13% or SVV <12% in a patient on controlled mechanical ventilation suggests it is safe to cease fluid administration.
  • A PLR-induced stroke volume increase >10% predicts fluid responsiveness regardless of ventilation mode or cardiac rhythm.
  • Always combine these indices with clinical assessment, including adequate urine output (≥0.5 mL/kg/h), improving mental status, and warming extremities.

1.2 Protocolized Fluid and Vasopressor Titration

A structured approach to weaning prevents abrupt hemodynamic changes.

  • Crystalloids: Once markers of perfusion are stable (e.g., Cardiac Index >2.2 L/min/m², lactate <2 mmol/L), reduce continuous crystalloid infusions by 25–50% every 4 hours.
  • Vasopressors: Taper norepinephrine by 0.01–0.02 µg/kg/min every 15–30 minutes, targeting a mean arterial pressure (MAP) of 65–70 mm Hg.
  • Diuresis: For patients with persistent significant positive fluid balance (>2 L/day) after shock resolution, consider adding furosemide 0.1–0.2 mg/kg IV to facilitate active de-resuscitation.

2. Transition from Intravenous to Enteral Fluid and Medication Delivery

Early initiation of enteral nutrition is a key intervention that maintains gut mucosal integrity, prevents bacterial translocation, and supports the transition away from IV therapies. This should be prioritized as soon as the patient is hemodynamically stable enough to tolerate it.

Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Key Pearls
  • Begin trophic feeds (10–20 mL/hr) within 24–48 hours of achieving hemodynamic stability to stimulate the gut, even if goal rates are not yet achievable.
  • Utilize post-pyloric feeding tubes in patients with high aspiration risk, severe gastroparesis, or persistent intolerance to gastric feeding.

2.1 Criteria for Initiating Enteral Access

  • Hemodynamics: Stable MAP ≥65 mm Hg with a low and stable/decreasing dose of vasopressors (e.g., norepinephrine ≤0.05 µg/kg/min).
  • GI Function: Evidence of bowel function (flatus, bowel sounds) and absence of contraindications like obstruction, uncontrolled GI bleeding, or a high-output fistula.
  • Device Selection:
    • Nasogastric tube: Standard for short-term (<4 weeks) support.
    • Percutaneous endoscopic gastrostomy (PEG): For anticipated need >4 weeks.
    • Post-pyloric (jejunal) tube: For persistent gastric residuals >250 mL or recurrent aspiration.

2.2 Timing, Formulations, and Rate Adjustments

  • Initiation and Titration: Start at 10–20 mL/hr and advance by 10–20 mL/hr every 8–12 hours as tolerated, moving toward the goal rate.
  • Formulation: Choose standard isotonic formulas (1.0–1.2 kcal/mL) with adequate protein (1.2–2.0 g/kg/day). Adjust for specific organ dysfunction (e.g., renal, hepatic) as needed.
  • Monitoring: Assess gastric residual volumes (GRVs) every 6 hours. If GRV >300 mL, hold feeds, consider a prokinetic agent like metoclopramide 10 mg IV, and resume at the previous tolerated rate once GRV decreases.
  • Aspiration Prevention: Maintain head-of-bed elevation at 30–45 degrees at all times.

3. Mitigation of Post-ICU Syndrome (PICS)

Post-ICU Syndrome (PICS) is a constellation of new or worsened impairments in physical, cognitive, and mental health that arise after critical illness. Proactive, bundled interventions are essential to minimize its long-term impact on survivors.

Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Key Pearls
  • Targeting a state of light sedation (Richmond Agitation-Sedation Scale [RASS] 0 to –1) is crucial. This level of arousal allows patients to interact, participate in spontaneous breathing trials, and engage with physical therapy.
  • Initiating early mobilization protocols within the first 48 hours of ICU admission has been shown to decrease ICU length of stay, reduce ventilator days, and mitigate long-term ICU-acquired weakness.

3.1 ABCDEF Bundle Components

The ABCDEF bundle is a proven, evidence-based framework for improving ICU outcomes and reducing the incidence of PICS.

The ABCDEF Bundle for PICS Mitigation
Letter Component and Goal
A Assess, Prevent, and Manage Pain: Use validated scales (CPOT, NRS) to target a pain score ≤3.
B Both Spontaneous Awakening Trials (SAT) and Spontaneous Breathing Trials (SBT): Perform daily coordinated trials to assess readiness for sedation reduction and extubation.
C Choice of Analgesia and Sedation: Prioritize an “analgesia-first” strategy. Use non-benzodiazepine sedatives like dexmedetomidine (0.2–1.4 µg/kg/hr) or propofol.
D Delirium: Assess, Prevent, and Manage: Monitor with CAM-ICU. Use non-pharmacologic prevention (sleep promotion, reorientation, mobilization).
E Early Mobility and Exercise: Progress from passive range of motion to ambulation as tolerated, starting within 48 hours.
F Family Engagement and Empowerment: Involve family in rounds, care decisions, and delirium prevention strategies.

4. Medication Reconciliation and Discharge Planning

The transition from the ICU to the ward and eventually to home is a high-risk period for medication errors. A structured reconciliation, education, and handoff process is vital to ensure patient safety and continuity of care.

Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Key Pearls
  • Pharmacist-led medication reconciliation has been shown to reduce medication discrepancies by up to 50% at the time of ICU transfer.
  • Using a standardized handoff format like SBAR (Situation, Background, Assessment, Recommendation) ensures that critical information about medication changes is communicated clearly and effectively to the receiving team.

4.1 Comprehensive Review of Acute and Chronic Therapies

This process involves a meticulous comparison of medication lists.

  • Compile a definitive pre-admission medication list from multiple sources (patient, pharmacy, prior records).
  • Compare this list against the patient’s current ICU medication orders.
  • Pay special attention to high-risk agents: anticoagulants, insulin, sedatives, antibiotics, and immunosuppressants.
  • Clearly document the rationale for every decision: continuation, dose adjustment, or discontinuation.

4.2 Patient/Caregiver Education and Handoff Communication

Effective communication is the cornerstone of a safe transition.

SBAR Handoff Communication Tool A flowchart showing the four components of SBAR communication: Situation (What is happening now?), Background (What is the clinical context?), Assessment (What do I think the problem is?), and Recommendation (What do I recommend we do?). Situation What is happening now? Background What is the clinical context? Assessment What do I think the problem is? Recommendation What should we do?
Figure 1: SBAR Communication Framework. Employing a structured handoff tool like SBAR ensures that all critical information, including medication changes, is conveyed accurately during patient transfers.
  • Use the teach-back method to confirm patient and caregiver understanding of each medication’s purpose, dose, frequency, and major side effects.
  • Provide a clear, written discharge medication plan that explicitly highlights all changes made during the hospital stay.

4.3 Coordination of Follow-Up and Rehabilitation Services

  • Arrange for outpatient physician follow-up within 7–14 days of discharge.
  • Make referrals to physical, occupational, and speech therapy based on functional deficits identified during the ICU stay.
  • For patients with significant cognitive or psychological symptoms, consider a referral to a specialized ICU survivor clinic for comprehensive PICS management.
  • Patients with prolonged mechanical ventilation may benefit from a referral to pulmonary rehabilitation to aid in respiratory muscle recovery.

References

  1. Ramesh GH, Uma JC, Farhath S. Fluid resuscitation in trauma: what are the best strategies and fluids? Int J Emerg Med. 2019;12:38.
  2. Dhillon NK, Kwon J, Coimbra R. Fluid resuscitation in trauma: What you need to know. J Trauma Acute Care Surg. 2025;98(1):20–29.
  3. Marra A, Ely EW, Pandharipande PP, Patel MB. The ABCDEF Bundle in Critical Care. Crit Care Clin. 2017;33(2):225–243.
  4. Haines KJ, McPeake J, Hibbert E, et al. Minimizing Post–Intensive Care Syndrome to Improve Outcomes for Survivors of Critical Illness. Crit Care Nurse. 2022;42(4):e1–e15.
  5. Jackson JC, Pandharipande PP, Girard TD, et al. Post–Intensive Care Syndrome: Impact, Prevention, and Management. BMC Med. 2019;17(1):168.
  6. Gleason KM, McDaniel MR, Feinglass J, et al. Designing the Medication Reconciliation Process. AHRQ. 2004.
  7. Pradeda AM, Pérez MSA, Oliveira CF, et al. Medication reconciliation after ICU to ward transfer. Farm Hosp. 2023;47(3):121–126.