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

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