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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 99, Topic 4
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Supportive Care and Monitoring of Complications in Burn Patients

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Supportive Care and Monitoring of Complications in Burn Patients

Supportive Care and Monitoring of Complications in Burn Patients

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

Learning Objective

Recommend appropriate supportive care and monitoring to manage complications associated with burn injuries, infection, and their treatment.

1. Respiratory Support in Burn Patients

Airway compromise from inhalation injury and systemic inflammation often necessitates mechanical ventilation. Early recognition and application of lung-protective strategies are critical to reducing morbidity and mortality.

A. Indications for Mechanical Ventilation

  • Signs of Inhalation Injury: Facial or neck burns, singed nasal hairs, hoarseness, and carbonaceous sputum are strong clinical indicators.
  • Bronchoscopy Findings: The presence of mucosal erythema, edema, or soot on bronchoscopy predicts the need for prolonged ventilatory support.
  • ARDS Criteria: In patients with large total body surface area (TBSA) burns (>20%) or sepsis, a PaO₂/FiO₂ ratio ≤300 mm Hg with bilateral infiltrates not explained by cardiac failure indicates ARDS.
  • Preemptive Intubation: Intubation should be strongly considered before the peak of capillary leak (3–48 hours post-burn) to avoid a difficult or emergent airway scenario as edema worsens.

B. Ventilator Modes & Lung-Protective Strategies

  • Tidal Volume: Target low tidal volumes of 6 mL/kg based on predicted body weight to prevent volutrauma.
  • Plateau Pressure: Maintain a plateau pressure ≤30 cm H₂O to minimize barotrauma.
  • PEEP: Utilize moderate PEEP (8–12 cm H₂O) to prevent alveolar collapse. In complex cases, decremental PEEP trials or esophageal pressure monitoring can help optimize settings.
  • Permissive Hypercapnia: Allow PaCO₂ to rise (accepting a pH ≥7.20) to facilitate low tidal volume ventilation, but avoid this strategy in patients with or at risk for intracranial hypertension.
  • Recruitment Maneuvers: Apply cautiously with close hemodynamic monitoring, as they can cause hypotension in hypovolemic patients.

C. Sedation & Weaning

  • Use validated sedation scales (e.g., RASS, SAS) and incorporate daily sedation interruptions (“sedation vacations”) to assess readiness for weaning.
  • Conduct spontaneous breathing trials once the patient is hemodynamically stable and respiratory parameters improve.
  • Minimize deep sedation to reduce ventilator duration and associated complications.
Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearls
  • Early bronchoscopy (within 24 hours) is invaluable for grading the severity of inhalation injury and guiding ventilator management strategies.
  • Carefully balance PEEP levels to optimize oxygenation by preventing alveolar collapse without causing hemodynamic compromise from reduced venous return.

2. Hemodynamic Monitoring and Support

Thermal injury triggers a biphasic response: an early capillary leak phase causing “burn shock,” followed by a prolonged hyperdynamic, hypermetabolic phase. Precise fluid and vasoactive agent management is essential to optimize organ perfusion while minimizing edema-related complications.

A. Pathophysiology

  • Capillary Leak Phase (First 24–48 hours): A massive release of inflammatory cytokines causes endothelial damage and increased vascular permeability. This leads to a profound shift of intravascular fluid into the interstitial space, resulting in hypovolemia, hemoconcentration, and risk of organ hypoperfusion and compartment syndromes.
  • Hypermetabolic Phase (Days 3–14): Following resuscitation, patients enter a hyperdynamic state characterized by elevated cardiac output, tachycardia, and increased insensible fluid losses, requiring ongoing hemodynamic vigilance.

B. Fluid Resuscitation Protocols

Initial fluid resuscitation is guided by formulas, but hourly titration based on clinical endpoints is crucial.

Common Burn Resuscitation Formulas
Formula Calculation (Lactated Ringer’s) Timing Key Targets
Parkland Formula 4 mL × body weight (kg) × % TBSA Give 50% in first 8 hours, remaining 50% over next 16 hours Urine output: 0.5–1 mL/kg/h
Lactate clearance
MAP ≥65 mm Hg
Modified Brooke Formula 2 mL × body weight (kg) × % TBSA Same 8h/16h split schedule

Titrate fluid rates hourly to maintain adequate urine output and normalize serum lactate. In complex cases, dynamic assessments of fluid responsiveness (e.g., stroke volume variation, passive leg raise) can help guide therapy and prevent “fluid creep”—over-resuscitation leading to complications.

C. Vasopressors & Inotropes

  • Norepinephrine: The first-line vasopressor for burn shock when mean arterial pressure (MAP) remains <65 mm Hg despite adequate fluid administration. Its potent α₁-adrenergic effects increase systemic vascular resistance.
  • Titration: Adjust vasopressor doses to achieve a MAP ≥65 mm Hg while closely monitoring for signs of improved perfusion, such as warming extremities and decreasing lactate levels.
  • Adjunctive Agents: Consider adding vasopressin if high doses of norepinephrine are required, as this may have a catecholamine-sparing effect.
  • Advanced Monitoring: In refractory shock, invasive monitoring with arterial pulse contour analysis or thermodilution can provide real-time cardiac output data to refine titration of vasoactive agents.
Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearls
  • Early initiation of norepinephrine in severe burn shock may reduce total fluid requirements, mitigating the risks of tissue edema, pulmonary edema, and abdominal compartment syndrome.
  • Over-resuscitation (“fluid creep”) is a major cause of morbidity. Frequent reassessment of volume status and organ function is mandatory to avoid iatrogenic harm.

3. Prevention of ICU-Related Complications

Critically ill burn patients have a heightened risk of venous thromboembolism (VTE), stress-related mucosal disease, and central line-associated bloodstream infections (CLABSI). Protocol-driven prophylaxis is key to reducing these preventable complications.

A. Venous Thromboembolism (VTE) Prophylaxis

  • Pharmacologic: Low-molecular-weight heparin (LMWH), such as enoxaparin, is the preferred agent. It should be initiated 12–24 hours post-burn, once the initial risk of bleeding has subsided.
  • Mechanical: Intermittent pneumatic compression devices are essential when pharmacologic prophylaxis is contraindicated (e.g., active bleeding, severe thrombocytopenia).
  • Monitoring: In patients with large burns or suspected augmented renal clearance, consider monitoring anti-Xa levels to ensure therapeutic efficacy of LMWH.

B. Stress Ulcer Prophylaxis

  • Indication: Initiate prophylaxis in patients requiring mechanical ventilation for >48 hours or those with a coagulopathy.
  • Agent: Proton pump inhibitors (PPIs) are generally preferred over H₂-receptor antagonists.
  • De-escalation: Discontinue prophylaxis once risk factors resolve to minimize the risk of adverse effects, such as hospital-acquired pneumonia and Clostridioides difficile infection.

C. CLABSI Prevention Bundles

Strict adherence to evidence-based bundles is the most effective strategy to prevent CLABSI.

CLABSI Prevention Bundle Flowchart A flowchart showing four key steps for preventing central line-associated bloodstream infections: Hand Hygiene, Maximal Barrier Precautions, Chlorhexidine Skin Prep, and Daily Line Review. Hand Hygiene Maximal Barrier Precautions (Insertion) Chlorhexidine Skin Prep Daily Review of Line Necessity
Figure 1: Core Components of a CLABSI Prevention Bundle. Consistent application of these steps during insertion and maintenance dramatically reduces infection rates.

4. Management of Iatrogenic Toxicities

Aggressive antimicrobial therapy and complex supportive care can lead to iatrogenic complications. Vigilant monitoring and proactive dose adjustments are necessary to mitigate harm.

A. Antibiotic-Associated Nephrotoxicity

  • High-Risk Agents: Aminoglycosides (e.g., gentamicin, amikacin) and vancomycin are common culprits.
  • Monitoring: Monitor serum creatinine daily. For vancomycin, target an Area Under the Curve (AUC) to MIC ratio or maintain troughs of 15–20 mg/L for severe infections, adjusting based on renal function.
  • Management: In the setting of acute kidney injury (AKI), adjust dosing intervals or switch to less nephrotoxic agents. Consider early initiation of renal replacement therapy (RRT) for severe, refractory acidosis or volume overload.

B. Hematologic Toxicities

  • Monitoring: Perform a daily complete blood count (CBC) during periods of critical illness and high-intensity antimicrobial therapy.
  • Transfusion Thresholds: Adhere to restrictive transfusion strategies. Transfuse red blood cells for a hemoglobin <7 g/dL in the absence of active bleeding. Transfuse platelets for counts <20 × 10⁹/L or if the patient is actively bleeding.
  • Causative Agents: Be aware of medications that can cause cytopenias, such as linezolid (thrombocytopenia) or beta-lactams (neutropenia).

C. Drug–Drug Interaction Surveillance

Editor’s Note: A comprehensive discussion of drug-drug interactions is critical but beyond the scope of this summary. Key areas for vigilance in burn patients include interactions involving CYP450 inhibitors/inducers, agents that prolong the QTc interval, and drugs with overlapping nephrotoxic or myelosuppressive potential.

5. Multidisciplinary Goals of Care and Family Communication

The complexity and prolonged course of severe burn injury require a coordinated, multidisciplinary approach that integrates palliative services, surgical planning, and ethical discussions to align treatment with patient values and goals.

A. Early Palliative Care Integration

  • Focus on aggressive management of pain, dyspnea, anxiety, and psychological distress from the outset.
  • Facilitate formal goals-of-care discussions with the patient or surrogate decision-makers within the first week of admission to establish a shared understanding of the prognosis and treatment trajectory.

B. Shared Decision-Making

  • Convene regular multidisciplinary meetings involving surgeons, intensivists, pharmacists, nurses, therapists, and social workers to ensure a unified plan of care.
  • Use visual aids, such as wound photographs and illustrated timelines, to help surrogates understand the nature and extent of surgical interventions like debridement and grafting.

C. Ethical Considerations

  • Engage the hospital ethics committee for guidance in complex situations, such as determining medical futility in the context of irreversible multi-organ failure.
  • Continuously balance the burden of invasive interventions with the potential for a meaningful quality of life, ensuring that care remains patient-centered.
Pearl Icon A shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl

Consistent, clear, and compassionate messaging from all members of the care team is paramount. It fosters trust with the family, reduces decisional conflict, and helps ensure that the intensive care provided aligns with the patient’s wishes and values.

References

  1. Joint Trauma System. Burn Care (CPG ID: 12). Clinical Practice Guideline. 2016.
  2. Garcia R, et al. Ventilation practices in burn patients—an international prospective observational cohort study. Ann Intensive Care. 2021;11:243.
  3. Boehm D, Menke H. Sepsis in burns—lessons learnt from developments in the management of septic shock. Medicina. 2022;58(1):26.
  4. Evans L, et al. Surviving Sepsis Campaign: international guidelines for management of sepsis and septic shock 2021. Intensive Care Med. 2021;47:1181–1247.
  5. Rivers E, et al. Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med. 2001;345:1368–1377.
  6. Greenhalgh DG, Saffle JR, Holmes JH, et al. American Burn Association consensus conference to define sepsis and infection in burns. J Burn Care Res. 2007;28(6):776–790.
  7. Belba MK, Petrela EY, Belba AG. Epidemiology and outcome analysis of sepsis and organ dysfunction/failure after burns. Burns. 2017;43(7):1335–1347.
  8. Muthukumar V, et al. Blood lactate and lactate clearance: refined biomarker and prognostic marker in burn resuscitation. Ann Burns Fire Disasters. 2020;33(4):293–298.
  9. Cabral L, et al. Procalcitonin for the early diagnosis of sepsis in burn patients: a retrospective study. Burns. 2017;43(8):1427–1434.
  10. Kano KI, et al. Nutritional and supportive care recommendations for critically ill burn patients. Nutrients. 2025;17(845).