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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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Lesson 66, Topic 5
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Recovery, Rehabilitation, and Transition of Care in CNS Infections

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Recovery, Rehabilitation, and Transition of Care in CNS Infections

Recovery, Rehabilitation, and Transition of Care in CNS Infections

Objective Icon A checkmark inside a circle, symbolizing an achieved goal.

Learning Objective

Develop a plan to facilitate patient recovery, mitigate long-term complications, and ensure a safe transition of care.

1. Weaning and De-Escalation of Intensive Therapies

Rationale: As patients stabilize neurologically, the systematic withdrawal of ventilatory and vasopressor support is crucial to reduce iatrogenic injury and expedite rehabilitation.

A. Criteria for Spontaneous Breathing Trial (SBT)

  • Oxygenation: PaO₂/FiO₂ > 200 on FiO₂ ≤ 0.5 and PEEP ≤ 8 cm H₂O.
  • Hemodynamics: Stable, with a mean arterial pressure (MAP) ≥ 65 mm Hg and no escalation of vasopressor support for at least 24 hours.
  • Neurologic Status: Minimal sedation (Richmond Agitation-Sedation Scale [RASS] −1 to +1) with intact airway reflexes.

SBT protocol options include low-level pressure support (≤ 8 cm H₂O), continuous positive airway pressure (CPAP), or a T-piece trial for a duration of 30–120 minutes.

B. Vasopressor Tapering

  • Indication: MAP ≥ 65 mm Hg on a stable infusion for 12–24 hours, coupled with a downward trend in lactate levels.
  • Method: Reduce the infusion rate by 10–20% every 2–4 hours, while closely monitoring MAP, urine output, and mental status.
  • Contingency: If hypotension recurs, revert to the previous effective dose and reassess volume status and adrenal function.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearls for Weaning

Standardize SBT Checklists: Incorporate daily SBT screening checklists into multidisciplinary rounds to systematically identify candidates and minimize ventilator days.

Automate Tapering Reminders: Embed automatic reminders for vasopressor taper steps within the Electronic Medical Record (EMR) to prompt timely de-escalation and prevent prolonged infusions.

2. IV-to-Enteral Conversion

Rationale: Transitioning suitable antimicrobial agents to enteral administration shortens ICU stay, reduces costs, and lowers the risk of central line-associated bloodstream infections. This process requires careful review of pharmacokinetic/pharmacodynamic (PK/PD) properties and enteral tube compatibility.

Considerations for IV-to-Enteral Antimicrobial Conversion
Agent Class/Example Key PK/PD Properties Enteral Administration Notes
Fluoroquinolones (e.g., Moxifloxacin) High bioavailability (≥80%), excellent CSF penetration. Crush immediate-release tablets. Avoid co-administration with divalent cations (e.g., tube feeds).
Oxazolidinones (e.g., Linezolid) Nearly 100% bioavailability, good CSF penetration. Available as a suspension. Monitor for thrombocytopenia and serotonin syndrome. Consider TDM in renal impairment.
Antivirals (e.g., Valacyclovir) Prodrug of acyclovir with high bioavailability. Ensure adequate hydration to prevent nephrotoxicity. Tablet can be crushed and mixed with water.
Tetracyclines (e.g., Doxycycline) Good bioavailability, but absorption is erratic. Avoid extended-release formulations. Administer on an empty stomach if possible to maximize absorption.

Enteral Access and Monitoring

  • Confirm medication formulation (tablet vs. suspension), tube size/material, and required flush volumes.
  • Crush immediate-release tablets separately and flush with 15–30 mL of water before and after each dose.
  • Monitor for signs of intolerance (diarrhea, ileus) or treatment failure (breakthrough fever, rising inflammatory markers).
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Pharmacy Pearl: Enteral Compatibility Chart

Implement an interactive enteral-compatibility chart within the pharmacy information system or EMR. This provides clinicians with real-time, point-of-care guidance on which medications can be crushed, which are available as liquids, and necessary administration instructions, thereby improving safety and efficiency.

3. Mitigation of Post-ICU Syndrome (PICS)

Rationale: Survivors of severe CNS infections are at high risk for significant physical, cognitive, and psychological sequelae, collectively known as Post-ICU Syndrome (PICS). Consistent application of the ABCDEF bundle is a proven strategy to mitigate these risks.

ABCDEF Bundle for ICU Liberation A diagram 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. AAssess, Prevent,& Manage Pain BBoth SAT & SBT CChoice ofSedation DDelirium:Assess & Manage EEarly Mobility& Exercise FFamilyEngagement
Figure 1: The ABCDEF Bundle. A multidisciplinary, evidence-based approach to optimizing ICU patient care, reducing delirium, and improving long-term outcomes.

Rehabilitation and Follow-up

  • Physical & Cognitive Therapy: Initiate early mobility (passive to active range of motion) within 48–72 hours. Introduce cognitive exercises like memory drills before ICU discharge.
  • Long-term Follow-up: Refer survivors to a dedicated post-ICU or neuro-recovery clinic at 3–6 months for formal assessment of mood, cognition, and motor function.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Key Point: Impact of Bundle Adherence

High adherence to the ABCDEF bundle is associated with profound clinical benefits. Studies have shown it can halve the incidence of delirium, shorten the duration of mechanical ventilation by approximately 25%, and reduce the risk of long-term cognitive impairment.

4. Medication Reconciliation and Discharge Planning

Rationale: A structured medication review, comprehensive patient education, and seamless coordination with outpatient services are essential to prevent medication errors, avoid readmissions, and ensure continuity of care.

A. Comprehensive Medication Inventory

Before discharge, create a definitive list of all medications. This should include:

  • All acute-phase therapies (e.g., antimicrobials, anticonvulsants, steroids) with clear stop dates or taper instructions.
  • All pre-existing medications for chronic conditions.
  • Explicit documentation of any changes made during hospitalization, including the indication, duration, and required monitoring parameters.

B. Patient and Caregiver Education

  • Use the teach-back method to confirm understanding of each medication’s purpose, dosing schedule, common side effects, and critical interactions.
  • Provide clear, written schedules, “pill cards,” and contact information for the pharmacy or clinic for any questions.

C. Outpatient Coordination

For patients requiring ongoing IV therapy, assess for Outpatient Parenteral Antimicrobial Therapy (OPAT) eligibility:

  • Clinical Stability: Afebrile for ≥ 48 hours, normalized labs, stable neurologic exam.
  • Logistical Feasibility: Reliable venous access, safe home environment, and adequate caregiver support.
  • Schedule follow-up appointments with neurology, rehabilitation services, and home health agencies before the patient leaves the hospital.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: Smart Discharge Templates

Utilize electronic discharge summary templates that auto-populate with medication changes, laboratory monitoring schedules, and follow-up appointments. This reduces transcription errors, ensures all critical components are included, and provides a standardized, easy-to-read document for the patient and outpatient providers.

5. Key Transition Decision Points and Quality Improvement

Rationale: Identifying key thresholds for safe discharge and implementing quality metrics creates a system of continuous improvement that reduces readmissions and enhances patient outcomes.

Quality Improvement Feedback Loop for Care Transitions A circular flowchart illustrating the quality improvement cycle in patient transitions. It starts with applying OPAT checklists, moves to discharge and telemedicine monitoring, then to tracking quality metrics like readmissions, and finally to a feedback loop in multidisciplinary meetings to refine the process. Care Transition Quality Improvement Cycle 1. Apply OPAT Checklists 2. Discharge & Telemedicine Monitoring 3. Track Quality Metrics 4. Feedback Loop in Multidisciplinary Meetings
Figure 2: Quality Improvement Feedback Loop. A systematic process ensures that patient outcomes are continuously monitored and that insights are fed back into clinical practice to refine transition-of-care protocols.

A. Readmission Risk Reduction

  • Rigorously apply OPAT eligibility checklists to ensure only appropriate candidates are discharged with IV therapy.
  • Involve home nursing agencies early in the discharge planning process to confirm capabilities and arrange the first visit.

B. Outpatient Monitoring and Telemedicine

  • Develop clear protocols for remote patient management, including schedules for vital sign checks, laboratory draws, and virtual visits.
  • Use telemedicine to conduct visual assessments of neurologic function, wound sites, or PICC line integrity, improving convenience and access.

C. Quality Metrics

  • Track key performance indicators such as OPAT success rates, 30-day all-cause readmissions, and patient satisfaction scores.
  • Review these metrics regularly in multidisciplinary meetings to identify trends, address systemic issues, and celebrate successes.

References

  1. DBTH NHS Foundation Trust. Policy for Treatment of Central Nervous System Infections. 2022.
  2. Marra A, Ely EW, Pandharipande PP, Patel MB. The ABCDEF bundle in critical care. Crit Care Clin. 2017;33(2):225–243.
  3. Society of Critical Care Medicine. ICU Liberation Bundle (A–F). SCCM; 2018.
  4. Queensland Children’s Hospital. Antimicrobial Treatment: Early Intravenous to Oral Switch. 2024.
  5. Sigfrid L, Pallmann P, Renz MF, et al. A systematic review of clinical guidelines on the management of community-acquired central nervous system infections. BMC Infect Dis. 2019;19:829.
  6. Tice AD, Strait K, Ramey R, et al. Outpatient parenteral antimicrobial therapy for central nervous system infections. Clin Infect Dis. 1999;29(6):1394–1399.
  7. Tunkel AR, Hartman BJ, Kaplan SL, et al. Practice guidelines for the management of bacterial meningitis. Clin Infect Dis. 2004;39(9):1267–1284.
  8. Tunkel AR, Hasbun R, Bhimraj A, et al. 2017 IDSA guidelines for healthcare-associated ventriculitis and meningitis. Clin Infect Dis. 2017;64(6):e34–e65.