Status Asthmaticus

BACKGROUND

Pathophysiology & Risk

There are 3 primary physiologic components that often occur simultaneously leading to an asthma exacerbation:

- Bronchial smooth muscle spasms

- Airway inflammation and edema

- Increased mucus production

Risk factors for exacerbation include:

- Previous life-threatening exacerbations

- Inability to recognize airway obstruction (age, developmental disabilities)

- Poor asthma control 

- Non-compliance to medications 

TREATMENTS

Disclaimer: Agent choices and dosing can vary between institutions. If you are practicing or rotating at a specific institution, refer to your institution specific pathways, order sets, and policies for available products, starting doses, titrations, and safety information. 

Inhaled Bronchodilators

INTERMITTENT ALBUTEROL

  • Mechanism: Beta agonist (B1 and B2)
  • B2 activity = airway smooth muscle relaxation
  • Available as inhaler or nebulization for intermittent treatments
  • Adverse Effects: Tachycardia (B1 activity), Hypertension (B1 activity), Low potassium (intracellular shifts), nausea
  • Levalbuterol = no additional benefit, more expensive

 

CONTINUOUS ALBUTEROL

  • Can be escalated to a continuous nebulization 
  • Typical starting dose of 10 mg/hour, with some centers escalating to doses up to 30 mg/hour

Inhaled Anticholinergics

IPRATROPIUM

  • Bronchodilation by smooth muscle relaxation
  • Can have drying effects for excess mucus
  • Adverse effects commonly associated with anticholinergics are minimal due to low systemic absorption with inhaled therapy
  • Reduces hospitalization for patients with status asthmaticus
  • No evidence for benefit once hospitalized, however is commonly utilized clinically

Corticosteroids

METHYLPREDNISOLONE

  • Mechanism: reduced inflammatory mediators and cytokines, therefore reducing airway edema
  • Systemic therapy preferred. Routinely started on IV therapy due to increased work of breathing.
  • Early administration = better outcomes
  • Dosing
    • Methylprednisolone: Prednisolone: Prednisone = 1:1:1
    • Some centers utilize an optional loading dose of 1-2 mg/kg
    • Usual starting dose is 0.5 mg/kg (max 60 mg) Q6H, varies by severity and provider preference 
  • Adverse effects: may have hyperglycemia, hypertension, etc.
    • Dose dependent
  • Consider steroid taper for patients receiving high dose steroids for 7+ days

 

DEXAMETHASONE

  • Some centers utilize as an alternative to methylprednisolone
  • Dosing is typically one dose of 0.6 mg/kg (max 16 mg) IV, which can be repeated Q24H as required

Magnesium

MAGNESIUM SULFATE

  • Decreases cholinergic stimulation and histamine release, which inhibits smooth muscle contractions
  • Administered as an Intravenous Bolus 
    • Usual dose = 50 mg/kg IV (max 2g) over 20-30 minutes
    • Administered faster than boluses for electrolyte repletion
    • Monitor for hypotension, fluid bolus if needed
    • Can repeat for a second dose 
  • Toxicity rare: Respiratory depression, arrythmias, weakness
  • Evidence for reducing hospitalization

Advanced Therapies

TERBUTALINE

  • Causes bronchodilation by relaxing smooth muscle, similar to albuterol
  • Continuous intravenous infusion (loading doses may be utilized) or subcutaneous injection
  • Utility in refractory exacerbations
  • Some centers utilize a loading dose
  • Adverse effects: hypotension, hyperglycemia, hypokalemia, arrhythmias
  • Can utilize fluid boluses to prevent tachycardia 
  • Evidence limited and controversial

THEOPHYLLINE AND AMINOPHYLLINE

  • Commonly administered as a continuous intravenous infusion, loading dose may be utilized
  • Theophylline levels commonly monitored
  • Infusion rates can be adjusted to target levels 

KETAMINE

  • Bronchodilator properties
  • Can be administered in low doses as a bolus or continuous infusion
  • Reduces anxiety commonly present in severe asthma exacerbations, which can reduce oxygen demand
  • Caution: can increase airway secretions

LITERATURE

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