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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 2, Topic 3
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Advanced Ventilatory Support and Pharmacologic Adjuncts in Status Asthmaticus

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Supportive Care and Mechanical Ventilation in Status Asthmaticus

Supportive Care and Mechanical Ventilation Strategies in Status Asthmaticus

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

Lesson Objective

Recommend appropriate supportive care and mechanical ventilation strategies for status asthmaticus to prevent complications and optimize outcomes.

1. Non-Invasive Ventilation in Status Asthmaticus

Non-invasive ventilation (NIV) can be a valuable tool in managing status asthmaticus by offloading respiratory muscles and stenting airways. In select patients, it may avert the need for invasive mechanical ventilation. However, it’s crucial to recognize that delayed escalation to intubation in NIV failure is associated with increased risks.

A. Physiologic Rationale

  • Augmented Alveolar Ventilation: NIV assists in increasing the volume of air reaching the alveoli, improving gas exchange.
  • Reduced Work of Breathing: By providing pressure support, NIV lessens the effort required by the patient’s respiratory muscles.
  • Airway Stenting: Continuous Positive Airway Pressure (CPAP) helps keep bronchi open, counteracting bronchoconstriction.
  • Muscle Offloading: Bi-level Positive Airway Pressure (BiPAP) provides both inspiratory and expiratory support, which can be particularly beneficial for fatigued respiratory muscles.
Clinical Pearl: NIV and Bronchodilators

NIV combined with aerosolized bronchodilators can acutely improve peak expiratory flow and inspiratory capacity. The positive pressure may enhance drug delivery to distal airways.

B. Evidence & Potential Benefits

While robust randomized controlled trial (RCT) data specifically for status asthmaticus is limited, large retrospective cohort studies suggest that NIV use is associated with reduced rates of invasive mechanical ventilation and potentially lower mortality. Common initial NIV pressure settings are often around an Inspiratory Positive Airway Pressure (IPAP) of 8-12 cm H₂O and an Expiratory Positive Airway Pressure (EPAP) of 5-6 cm H₂O, titrated to patient comfort and physiological response.

C. Risks & Predictors of NIV Failure

Potential risks of NIV include barotrauma (though less common than with invasive ventilation) and nosocomial infections, particularly if NIV fails and intubation is delayed. Close monitoring for signs of failure is essential.

Predictors of NIV failure include:

  • Severe hypercapnia (PaCO₂ > 60 mm Hg) at initiation or worsening on NIV.
  • Significant hypoxemia (PaO₂/FiO₂ ratio < 200).
  • Altered mental status or inability to protect the airway.
  • Hemodynamic instability.
  • Inability to tolerate the mask or cooperate with therapy.

D. Patient Selection Criteria

Indications for NIV Trial:

  • Respiratory rate > 25 breaths/minute.
  • Heart rate > 110 beats/minute.
  • Moderate respiratory acidosis (e.g., pH > 7.25 but < 7.35 with elevated PaCO₂).
  • Patient is cooperative and able to protect their airway.
  • Accessory muscle use and dyspnea.

Contraindications to NIV:

  • Depressed level of consciousness or coma.
  • High aspiration risk (e.g., active vomiting, copious secretions).
  • Inability to achieve a good mask seal (e.g., facial trauma).
  • Severe agitation or inability to cooperate.
  • Immediate need for intubation (e.g., respiratory arrest, profound shock).
  • Hemodynamic instability unresponsive to initial measures.

E. Monitoring & Escalation Protocols

Patients on NIV require intensive monitoring:

  • Continuous monitoring of respiratory rate, tidal volumes (if measurable via ventilator), and oxygen saturation (SpO₂).
  • Arterial blood gases (ABGs) typically within 1-2 hours of initiation and then as clinically indicated to assess response (pH, PaCO₂, PaO₂).
  • Close observation for clinical signs of improvement (reduced work of breathing, improved air entry) or deterioration.

Predefined triggers for escalation to invasive mechanical ventilation are crucial and should include:

  • Worsening hypercapnia or hypoxemia despite optimal NIV settings.
  • Decline in mental status.
  • Inability to tolerate the NIV mask or interface.
  • Development of hemodynamic instability.
  • Persistent or worsening signs of respiratory muscle fatigue.

2. Sedative and Paralytic Agents for Rapid Sequence Intubation (RSI)

When intubation is necessary in status asthmaticus, the choice of induction and paralytic agents should prioritize bronchodilation, hemodynamic stability, and rapid onset to ensure safe and effective airway management.

A. Ketamine

  • Mechanism: Ketamine is an NMDA receptor antagonist that leads to catecholamine release, resulting in bronchodilation. It also has direct smooth muscle relaxant properties.
  • Dosing: Typically an IV bolus of 1–2 mg/kg. An optional infusion of 0.5 mg/kg/h can be considered for ongoing sedation and bronchodilation post-intubation, though evidence for this is less robust.
  • Advantages: Preserves airway reflexes to some extent (though not fully relied upon during RSI), generally maintains or increases blood pressure, and provides direct bronchodilation.
  • Disadvantages: Can cause hypersalivation (pretreatment with an anticholinergic like glycopyrrolate 0.2 mg IV may be considered), and psychomimetic effects (emergence reactions), which are less of a concern in critically ill, intubated patients.
Clinical Pearl: Ketamine as First-Line Induction

Ketamine is often considered the first-line induction agent in patients with severe bronchospasm due to its unique bronchodilatory properties, in addition to its favorable hemodynamic profile in shock states.

B. Comparative Induction Agents

Comparison of Induction Agents for RSI in Status Asthmaticus
Agent Typical IV Dose Key Properties Potential Issues
Etomidate 0.2–0.3 mg/kg Hemodynamically stable, rapid onset. No bronchodilatory effect; risk of adrenal suppression (usually transient with single dose).
Propofol 1–2 mg/kg Rapid onset, short duration; some reports of bronchodilation. Can cause significant hypotension and respiratory depression, especially in hemodynamically unstable patients.

C. Paralytic Agents

Comparison of Paralytic Agents for RSI in Status Asthmaticus
Agent Typical IV Dose Key Properties Considerations
Rocuronium 1.0–1.2 mg/kg Rapid onset (at this dose), intermediate duration. Minimal histamine release; can be reversed with sugammadex if needed (though rarely an acute concern in asthma).
Succinylcholine 1–1.5 mg/kg Very rapid onset, short duration. Risk of hyperkalemia (contraindicated in known hyperkalemia, crush injuries, neuromuscular diseases, burns >24-48h old); can cause fasciculations, myalgias. Some concern for histamine release, though often clinically minor.

3. Mechanical Ventilation Strategy: Permissive Hypercapnia

The cornerstone of ventilating a patient with status asthmaticus is to employ a strategy of “permisive hypercapnia.” This involves using low minute ventilation with prolonged expiratory times to minimize dynamic hyperinflation, auto-PEEP (intrinsic PEEP), and the risk of ventilator-induced lung injury (VILI) and barotrauma.

A. Goals & Rationale

  • Tolerate Hypercapnia: The primary goal is to allow PaCO₂ to rise (and pH to fall), provided the pH remains above a critical threshold (commonly >7.20), to facilitate lung-protective settings. This avoids the high pressures and volumes that would be needed to normalize PaCO₂ in the face of severe airflow obstruction.
  • Prolong Expiratory Time: A long expiratory time (achieved by low respiratory rate and/or high inspiratory flow rate, leading to an I:E ratio of up to 1:3, 1:4, or even 1:5) is crucial to allow for more complete emptying of alveoli and prevent breath stacking (dynamic hyperinflation).
Clinical Pearl: Plateau Pressure and Auto-PEEP

Maintain plateau pressure (Pplat) < 30 cm H₂O to minimize barotrauma. Use ventilator waveform analysis (flow-time curve not returning to baseline before next breath) and end-expiratory hold maneuvers to detect and quantify auto-PEEP. The goal is to minimize, not necessarily eliminate, auto-PEEP.

B. Initial Ventilator Settings

Initial Ventilator Settings for Status Asthmaticus
Parameter Initial Setting Rationale / Goal
Mode Volume-Assist Control (V-A/C) or Pressure-Regulated Volume Control (PRVC) Ensures set tidal volume.
Tidal Volume (Vt) 5–7 mL/kg ideal body weight (IBW) Minimize volutrauma and barotrauma.
Respiratory Rate (RR) 8–12 breaths/minute (or lower) Allow prolonged expiratory time, facilitate permissive hypercapnia.
Inspiratory Flow Rate High (e.g., 80–100 L/min) Shorten inspiratory time (Ti), thus prolonging expiratory time (Te).
I:E Ratio 1:3 to 1:4 (or higher) Maximize time for exhalation, reduce air trapping.
External PEEP (PEEPe) 0–5 cm H₂O Controversial. May use low levels (e.g., up to 80% of measured auto-PEEP) to offset auto-PEEP and reduce trigger work, but avoid levels that increase hyperinflation. Start low or at zero.
FiO₂ 1.0 initially, then titrate down Maintain SpO₂ 88–92% (or per institutional protocol, typically not >95% to avoid hyperoxia).
Example I:E Ratio (1:4)
I
E
1 part 4 parts
Figure 1: Visualizing I:E Ratio. In status asthmaticus, a prolonged expiratory time (e.g., I:E of 1:4) is critical to allow for adequate exhalation and minimize dynamic hyperinflation (air trapping). This is achieved by setting a low respiratory rate and/or a high inspiratory flow rate.

C. Monitoring Parameters

  • Airway Pressures:
    • Peak Inspiratory Pressure (Ppeak): Reflects total pressure (resistance + elastic). Will be high due to bronchoconstriction.
    • Plateau Pressure (Pplat): Measured via end-inspiratory hold. Reflects alveolar pressure. Goal is < 30 cm H₂O.
    • Auto-PEEP (PEEPi): Measured via end-expiratory hold. Indicates dynamic hyperinflation. Goal is to minimize.
  • Blood Gases: Monitor ABGs to assess adequacy of permissive hypercapnia (pH typically > 7.20, PaCO₂ will be elevated) and oxygenation.
  • Clinical Assessment: Observe for absence of breath stacking on ventilator waveforms, stable hemodynamics, and adequate oxygenation (SpO₂ 88–92%).

D. Adjustment Algorithms

  • If Auto-PEEP is increasing or Pplat > 30 cm H₂O:
    • Decrease respiratory rate further.
    • Decrease tidal volume (if not already at lower limit).
    • Increase inspiratory flow rate (to shorten Ti and lengthen Te).
    • Ensure adequate sedation to prevent patient-ventilator dyssynchrony.
  • For Patient-Ventilator Dyssynchrony:
    • Optimize sedation levels. Ensure patient is not “fighting” the ventilator.
    • Brief periods of paralysis may be considered in severe cases if dyssynchrony persists despite deep sedation and is contributing to worsening hyperinflation or gas exchange.

4. Complications of Mechanical Ventilation and Management

Despite careful ventilator management, patients with status asthmaticus are at high risk for complications. Early recognition and prompt intervention are critical to prevent deterioration.

A. Barotrauma (Pneumothorax, Pneumomediastinum)

  • Recognition: Sudden onset of desaturation, increased peak airway pressures, decreased breath sounds on one side, subcutaneous emphysema, hypotension, or tracheal deviation (tension pneumothorax). Chest X-ray (CXR) confirms diagnosis.
  • Management:
    • Immediately lower airway pressures (reduce Vt, RR, or PEEPe).
    • If tension pneumothorax is suspected, perform needle decompression followed by chest tube insertion.
    • For simple pneumothorax, chest tube insertion is usually required.
    • Adjust ventilator settings to minimize further overdistension (lower Vt, ensure long Te).
Clinical Pearl: Barotrauma Risk

The risk of pneumothorax and other forms of barotrauma increases significantly when plateau pressures consistently exceed 30-35 cm H₂O or when auto-PEEP is excessive, leading to severe dynamic hyperinflation.

B. Cardiovascular Collapse / Hypotension

  • Mechanism: High intrathoracic pressures due to dynamic hyperinflation and applied PEEP can impede venous return to the heart, reducing preload and cardiac output, leading to hypotension or even pulseless electrical activity (PEA).
  • Recognition: Hypotension, tachycardia, signs of shock (cool extremities, poor capillary refill), or PEA cardiac arrest. Often occurs shortly after intubation or with increases in ventilator support.
  • Management:
    • Temporarily disconnect the patient from the ventilator for 15-30 seconds to allow passive exhalation and relieve hyperinflation (especially in arrest/peri-arrest).
    • Reduce ventilator PEEP and/or tidal volume; decrease respiratory rate.
    • Administer intravenous fluids to augment preload (if no signs of fluid overload).
    • Initiate vasopressors if hypotension persists despite fluid resuscitation and ventilator adjustments.
    • Ensure adequate sedation and analgesia, as agitation can worsen intrathoracic pressures.

5. Multidisciplinary Goals-of-Care Conversations

Structured and early discussions about goals of care are essential in severe status asthmaticus, particularly when the clinical course is refractory or prolonged. These conversations help align invasive support decisions, such as ongoing invasive mechanical ventilation (IMV) or consideration of Extracorporeal Membrane Oxygenation (ECMO), with patient preferences and the clinical trajectory.

A. Timing & Participants

  • Timing: Initiate these discussions upon ICU admission, or at early signs of refractory disease (e.g., failure to improve after 24-48 hours of IMV, persistently high Pplat despite optimal settings, severe ongoing bronchospasm).
  • Participants: A multidisciplinary team approach is best. This typically includes:
    • Critical care physician
    • Pulmonologist (if not primary critical care)
    • Clinical pharmacist (for medication optimization, sedation)
    • Respiratory therapist (for ventilator management insights)
    • Bedside nursing staff
    • Palliative care specialists (can facilitate complex discussions)
    • The patient (if able to participate) and/or their designated family members/surrogate decision-makers.

B. Key Discussion Points

  • Current understanding of the patient’s condition and severity of asthma.
  • Indications for continued intubation and mechanical ventilation.
  • Potential candidacy for advanced therapies like ECMO (if available and appropriate), including risks and benefits.
  • Expected recovery timeline and potential short-term and long-term outcomes, including possible functional limitations.
  • Exploration of the patient’s values, wishes, and previously expressed preferences regarding life-sustaining treatment.
  • Clarification of code status (DNAR/DNI orders) and review of any advanced directives.
  • Addressing fears, anxieties, and questions from the patient and family.
Clinical Pearl: Documentation and Reassessment

Thoroughly document all goals-of-care discussions, decisions made, and the individuals involved in the patient’s medical record. These conversations are not static; revisit and update the care plan as the patient’s clinical condition evolves or if new information becomes available.

References

  1. Gayen S, Mabalay R, Ganti L. Critical Care Management of Severe Asthma Exacerbations. J Clin Med. 2024;13(3):859.
  2. Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention. 2025. (Note: As of late 2024, the 2024 report is current; 2025 is anticipatory).
  3. Lim WJ, Mohammed Akram R, Carson KV, Mysore S, Labiszewski NA, Wedzicha JA, Rowe BH, Smith BJ. Non-invasive positive pressure ventilation for severe acute asthma. Cochrane Database Syst Rev. 2012;12:CD004360.
  4. Rochwerg B, Brochard L, Elliott MW, et al. Official ERS/ATS clinical practice guidelines: noninvasive ventilation for acute respiratory failure. Eur Respir J. 2017;50(2):1602426.
  5. Althoff MD, Holguin F, Festic E, et al. Noninvasive Ventilation Use in Critically Ill Patients with Acute Asthma Exacerbations: Insights from the National Emergency Airway Registry (NEAR). Am J Respir Crit Care Med. 2020;202(11):1520–1530.
  6. Leatherman J. Mechanical ventilation for severe asthma. Chest. 2015;147(6):1671–1680.
  7. Tuxen DV, Lane S. The effects of ventilatory pattern on hyperinflation, airway pressures, and circulation in mechanical ventilation of patients with severe air-flow obstruction. Am Rev Respir Dis. 1987;136(4):872–879.
  8. Feihl F, Perret C. Permissive hypercapnia. How permissive should we be? Am J Respir Crit Care Med. 1994;150(6 Pt 1):1722–1737.
  9. La Via L, Astuto M, Noto A, et al. Use of ketamine in refractory severe asthma exacerbations: A systematic review of randomized and non-randomized studies. Eur J Clin Pharmacol. 2022;78(10):1613–1622.
  10. Joseph KS, Blais L, Ernst P, Suissa S. Increased morbidity and mortality related to asthma among patients who use major tranquillisers. BMJ. 1996;312(7023):79–82.
  11. FitzGerald JM, Macklem PT. Fatal asthma. Annu Rev Med. 1996;47:161–168.
  12. Extracorporeal Life Support Organization. ELSO Guidelines for Cardiopulmonary Extracorporeal Life Support. Ann Arbor, MI: ELSO; 2013 (or most current version, e.g., 2021 or 2024).