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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
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    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
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    1 Quiz
  23. Subarachnoid Hemorrhage
    5 Topics
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    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
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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
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    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
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    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
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    1 Quiz
  46. Endocrinology
    Relative Adrenal Insufficiency and Stress-Dose Steroid Therapy
    5 Topics
    |
    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
    |
    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
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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
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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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Analgesic De-escalation, Weaning, and Transition of Care

Analgesic De-escalation, Weaning, and Transition of Care

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

Learning Objective

Develop a structured approach to taper ICU analgesics, convert to enteral therapy, mitigate post-ICU sequelae, and ensure seamless pain management after discharge.

1. Criteria for Analgesic Weaning and De-escalation

Initiating an analgesic taper is a critical step in ICU recovery. The process should begin once pain and sedation goals are sustainably met, aiming to minimize the risks of iatrogenic withdrawal and rebound hyperalgesia.

A. Pain and Sedation Targets

  • Communicative patients: Numeric Rating Scale (NRS) score of ≤ 3 out of 10.
  • Non-communicative patients: Consistently low scores on validated tools like the Behavioral Pain Scale (BPS) or the Critical-Care Pain Observation Tool (CPOT).
  • Sedation Level: A target Richmond Agitation-Sedation Scale (RASS) score of −2 (light sedation) to 0 (calm and alert) for at least 24 hours.

B. Clinical Stability Indicators

  • Stable hemodynamics without the need for escalating vasopressor support.
  • Minimal requirement for rescue (breakthrough) analgesia, defined as fewer than two doses in a 24-hour period.

C. Withdrawal Risk Stratification

  • High risk: Patients with opioid exposure greater than 100 mg of morphine equivalents per day for more than 7 days.
  • Low risk: Patients on shorter courses of opioids or lower total daily doses.

D. Example Weaning Protocol

  1. Confirm the patient has met stability criteria and target pain/sedation scores for a continuous 24-hour period.
  2. Decrease the background opioid infusion by 10–20% of the total daily dose.
  3. Monitor closely for signs of withdrawal, such as tachycardia, hypertension, agitation, diaphoresis, or tachypnea.
  4. If withdrawal symptoms emerge, consider slowing the taper rate to 5%–10% increments or temporarily returning to the previous effective dose before re-attempting a slower wean.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearls
  • Analgesia-First Sedation: Adopting an “analgesia-first” sedation strategy helps prevent under-recognized pain from driving agitation, thereby reducing the need for deep sedation and its associated complications.
  • Hyperalgesia Awareness: Prolonged opioid use can lead to central sensitization and opioid-induced hyperalgesia. This paradoxical increase in pain sensitivity necessitates gradual, careful dose reductions rather than abrupt cessation.

2. Equianalgesic Conversion from IV to Enteral Agents

Transitioning from intravenous (IV) to enteral analgesics is a key milestone. This process requires careful application of equianalgesic ratios, consideration of altered pharmacokinetics in critical illness, and a conservative initial dosing strategy to account for absorption variability.

A. Standard IV to Oral (PO) Ratios

  • Morphine: 1 mg IV is approximately equivalent to 3 mg PO.
  • Hydromorphone: 1 mg IV is approximately equivalent to 5 mg PO.
  • Oxycodone: 1 mg IV is approximately equivalent to 2 mg PO.

B. Initial Enteral Dosing Strategy

Due to factors like reduced gastrointestinal perfusion and delayed gastric emptying in critically ill patients, bioavailability of enteral medications is often reduced and unpredictable. Therefore, a conservative approach is recommended:

  • Start with 50%–75% of the calculated equianalgesic dose.
  • Titrate the dose by 20% increments every 12–24 hours based on pain control and side effects.
Equianalgesic Conversion Table for ICU Transitions
IV Agent PO Equivalent Ratio (IV:PO) Recommended Initial Dose Reduction
Morphine 1 : 3 25%–50%
Hydromorphone 1 : 5 25%–50%
Oxycodone 1 : 2 25%–50%
Fentanyl Convert to morphine equivalent first; then apply 1:3 ratio 25%–50%
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearls
  • Overlap and Bridge: When starting a long-acting enteral opioid, continue the short-acting IV agent (or provide as-needed doses) for the first 24–48 hours to bridge the gap and maintain consistent analgesia.
  • Conservative Dosing is Key: Always reduce the initial calculated enteral dose by 25%–50% in critically ill patients to avoid over-sedation and respiratory depression due to unpredictable absorption and hypoalbuminemia, which increases the free fraction of the drug.

3. Mitigating Post-ICU Syndrome (PICS) Related to Pain

Post-ICU Syndrome (PICS) is a constellation of new or worsened physical, cognitive, and psychological impairments that persist after critical illness. Proactive, bundled interventions are crucial for reducing its incidence and severity, particularly chronic pain.

A. The ABCDEF Bundle

The ABCDEF bundle is a evidence-based, multidisciplinary framework designed to improve ICU outcomes and mitigate PICS. Each component plays a role in optimizing pain management and reducing associated complications.

ABCDEF Bundle for ICU Care A flowchart illustrating the six components of the ABCDEF bundle: A for Assess Pain, B for Both Awakening and Breathing Trials, C for Choice of Analgesia/Sedation, D for Delirium Monitoring, E for Early Mobility, and F for Family Engagement. The ABCDEF Bundle: A Holistic Approach A Assess, Prevent, & Manage Pain B Both Spontaneous Awakening & Breathing C Choice of Analgesia & Sedation D Delirium: Assess, Prevent, & Manage E Early Mobility & Exercise F Family Engagement & Empowerment
Figure 1: The ABCDEF Bundle. A patient-centered framework to improve communication among ICU team members, standardize care processes, and ultimately reduce the incidence of PICS, including chronic pain, delirium, and functional decline.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

Integrate the ABCDEF bundle into daily multidisciplinary rounds. Structuring rounds around these six points ensures that pain, sedation, delirium, and mobility goals are explicitly discussed and addressed for every patient, every day, fostering a proactive rather than reactive culture of care.

4. Medication Reconciliation and Discharge Counseling

A meticulous medication reconciliation process and tailored patient education, ideally led by a pharmacist, are essential to ensure the continuity of safe and effective analgesic management after ICU discharge.

A. Reconciliation Steps

  1. Collate: Gather a comprehensive list of all pre-admission, current ICU, and proposed discharge medications.
  2. Identify: Systematically review the lists to identify any additions, discontinuations, and dose changes that occurred during the ICU stay.
  3. Resolve: Address and clarify any discrepancies with the medical team before the final discharge prescriptions are written.

B. Patient & Caregiver Education

Effective education empowers patients and prevents errors. Key topics include:

  • Clear instructions on indications, dosing schedules, and specific taper plans.
  • Recognition of common side effects and when to seek medical advice.
  • Information on safe storage and proper disposal of unused opioids.
  • Use of the “teach-back” method to confirm understanding, tailored to the patient’s health literacy.
Discharge Medication Reconciliation & Counseling Checklist
Checklist Item Key Detail and Action
Pre-ICU Medications Confirm which home medications should be resumed, held, or adjusted.
In-ICU Changes Clearly document the rationale for any new medications started or old ones stopped.
Planned Taper Schedule Provide a written, easy-to-understand schedule with dose, frequency, and dates for reduction.
Education Points Use teach-back to confirm patient understands the “what, why, when, and how” of their pain plan.
Follow-Up Appointments Ensure the patient has a scheduled appointment (primary care or pain specialist) with date, time, and contact details.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

Bundling pharmacist-led medication reconciliation, patient education, and a scheduled, timely follow-up appointment (within 7 days of discharge) is a high-impact intervention that has been shown to significantly reduce opioid-related adverse events and hospital readmissions.

5. Multidisciplinary Collaboration and Handoffs

Safe analgesic transitions depend on structured communication and a team-based approach. Clear handoffs between the ICU, hospital ward, and outpatient providers are crucial for maintaining continuity of care and executing individualized taper plans.

A. Pharmacist Roles

  • Lead the development and implementation of analgesic taper protocols and conduct medication reviews.
  • Educate ICU and ward teams on proper equianalgesic conversions, weaning strategies, and monitoring parameters.
  • Serve as a point person for complex medication-related questions during transitions of care.

B. Communication Templates

Using a standardized handoff tool like the SBAR (Situation, Background, Assessment, Recommendation) format ensures critical information is not lost. The handoff should explicitly include:

  • Pre-ICU opioid history and substance use history.
  • A summary of ICU analgesic therapies and major changes.
  • The current analgesic regimen and detailed taper schedule.
  • Recommendations for monitoring and follow-up.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

The implementation of early, pharmacist-driven analgesic stewardship rounds has been shown to reduce total opioid exposure, decrease the incidence of delirium, and optimize ICU length of stay by proactively managing pain and sedation from admission to discharge planning.

6. Guideline Controversies and Future Directions

While significant progress has been made, several areas of analgesic management in the ICU remain debated. Current research is focused on optimizing tapering strategies, defining the role of adjuncts, and improving implementation science.

Controversy IconA chat bubble with a question mark, indicating a point of controversy or debate. Controversy: Taper Duration and Strategy

The optimal duration and method for opioid tapering lack high-quality evidence from ICU-specific randomized trials. The primary debate is between fixed-schedule reductions (e.g., daily 10–20% dose decreases) versus symptom-guided schedules, where the taper rate is adjusted based on frequent withdrawal assessments. The ideal approach likely depends on patient-specific factors like duration of exposure and comorbidities.

A. Research Gaps and Future Directions

  • Non-Opioid Adjuncts: While agents like ketamine, lidocaine, and NSAIDs are known to be opioid-sparing, their optimal use, timing, and safety profiles in heterogeneous ICU populations require further study.
  • Non-Pharmacologic Therapies: Interventions such as music therapy, guided imagery, and Transcutaneous Electrical Nerve Stimulation (TENS) show promise but need standardized protocols to be integrated effectively into ICU care.
  • Withdrawal Assessment: There is a critical need for validated withdrawal assessment tools specifically designed for non-communicative or delirious patients.
  • Implementation Science: Research is needed to determine the most effective and cost-effective ways to implement evidence-based practices, such as pharmacist-driven models and the ABCDEF bundle, across diverse hospital settings.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

Regardless of the chosen taper strategy, active and frequent monitoring for withdrawal symptoms (tachycardia, hypertension, agitation) using a standardized scale is paramount. Proactive assessment allows for early intervention and preempts complications, leading to a smoother and safer weaning process.

References

  1. Pota V, Coppolino F, Barbarisi A, et al. Pain in Intensive Care: A Narrative Review. Pain Ther. 2022;11(1):359–367.
  2. Barr J, Fraser GL, Puntillo K, et al. Clinical Practice Guidelines for the Management of Pain, Agitation, and Delirium in Adult Patients in the Intensive Care Unit. Crit Care Med. 2013;41(1):263–306.
  3. 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.
  4. Critical Care Pharmacy Standards Committee. Critical Care Pharmacy Evolution and Validation: Practice Standards and Professional Development. Unpublished Internal Guidelines.
  5. Medication Reconciliation Guidelines. Unpublished Internal Documents.
  6. American Society of Health-System Pharmacists. ASHP Guidelines on Preventing Medication Errors. Unpublished.