Management of Asthma
Asthma management requires a stepwise approach based on disease severity and control, with inhaled corticosteroids (ICS) as the foundation of therapy for all patients with persistent asthma, combined with short-acting beta-agonists for symptom relief—critically, short-acting beta-agonists should never be used alone without ICS-based controller therapy. 1, 2
Initial Assessment and Classification
Severity Classification for Treatment Initiation
Classify asthma severity before starting therapy using both impairment and risk domains 1:
Impairment Domain:
- Intermittent: Symptoms <2 days/week, nighttime awakenings <2x/month, SABA use <2 days/week, no interference with normal activity, FEV1 >80% predicted 1
- Mild Persistent: Symptoms >2 days/week but not daily, nighttime awakenings 3-4x/month, SABA use >2 days/week but not daily, minor limitation of activity, FEV1 >80% predicted 1
- Moderate Persistent: Daily symptoms, nighttime awakenings >1x/week but not nightly, daily SABA use, some limitation of activity, FEV1 60-80% predicted 1
- Severe Persistent: Symptoms throughout the day, nighttime awakenings often 7x/week, SABA use several times per day, extreme limitation of activity, FEV1 <60% predicted 1
Risk Domain:
- Patients with ≥2 exacerbations requiring oral corticosteroids in the past year should be considered to have persistent asthma regardless of symptom frequency 1
Stepwise Pharmacological Management
Step 1: Intermittent Asthma
- Quick-relief only: SABA as needed for symptoms 1
- Critical update: SABA alone without ICS is no longer recommended even for intermittent asthma due to increased exacerbation risk 3, 4
Step 2: Mild Persistent Asthma
- Preferred: Low-dose ICS daily 1, 2
- Alternative: Leukotriene receptor antagonist (montelukast) for patients who cannot or will not use ICS 1, 2
- Quick-relief: SABA as needed 1
Step 3: Moderate Persistent Asthma
- Preferred: Low-dose ICS plus long-acting beta-agonist (LABA) 1
- Alternative: Medium-dose ICS alone, or low-dose ICS plus leukotriene receptor antagonist 1
- Critical warning: LABAs must never be used as monotherapy; always combine with ICS due to FDA black box warning regarding increased risk of severe exacerbations and asthma-related deaths 1
- LABA dosing limits: Do not exceed 100 mcg salmeterol or 24 mcg formoterol daily 1
- Quick-relief: SABA as needed 1
Step 4: Severe Persistent Asthma
- Preferred: Medium-dose ICS plus LABA 1
- Alternative: Medium-dose ICS plus leukotriene receptor antagonist or theophylline 1
- Important consideration: Higher ICS doses provide minimal additional benefit beyond medium doses while significantly increasing systemic side effects (reduced growth in children, decreased bone density in adults) 1
- Quick-relief: SABA as needed 1
Step 5: Severe Uncontrolled Asthma
- Preferred: High-dose ICS plus LABA 1
- Add-on therapy: Consider omalizumab (anti-IgE) for patients ≥12 years with allergic asthma (elevated IgE, positive skin test or RAST) whose symptoms remain inadequately controlled 1
- Alternative add-ons: Leukotriene receptor antagonist or theophylline 1
- Quick-relief: SABA as needed 1
Step 6: Severe Refractory Asthma
- Preferred: High-dose ICS plus LABA plus oral corticosteroids 1
- Add-on therapy: Omalizumab for eligible patients 1
- Before initiating oral corticosteroids: Trial high-dose ICS, LABA, leukotriene receptor antagonist, or theophylline combinations 1
- Quick-relief: SABA as needed 1
Monitoring and Adjusting Therapy
Assessment of Control
Evaluate control at every visit using impairment and risk domains 1:
Well-Controlled:
- Symptoms ≤2 days/week
- Nighttime awakenings ≤2x/month
- SABA use ≤2 days/week (not for exercise-induced bronchospasm prevention)
- No interference with normal activity
- FEV1 or peak flow >80% predicted
- 0-1 exacerbations requiring oral corticosteroids per year 1
Not Well-Controlled:
- Symptoms >2 days/week
- Nighttime awakenings 1-3x/week
- SABA use >2 days/week
- Some limitation of activity
- FEV1 or peak flow 60-80% predicted
- ≥2 exacerbations requiring oral corticosteroids per year 1
Very Poorly Controlled:
- Symptoms throughout the day
- Nighttime awakenings ≥4x/week
- SABA use several times per day
- Extreme limitation of activity
- FEV1 or peak flow <60% predicted
- ≥2 exacerbations requiring oral corticosteroids per year 1
Stepping Up Therapy
Before stepping up, always verify: 1
- Correct inhaler technique
- Medication adherence
- Environmental trigger control
- Treatment of comorbid conditions (rhinitis, GERD, obesity)
Step up if: 1
- Asthma is not well-controlled for ≥3 months
- Patient experiences exacerbations requiring oral corticosteroids
- SABA use exceeds 2 days/week for symptom relief (not EIB prevention) 1, 2
Stepping Down Therapy
Step down only when: 1
- Asthma has been well-controlled for at least 3 months
- Patient is at low risk for exacerbations
- Lung function is stable
Approach: 1
- Reduce ICS dose by 25-50%
- If on combination therapy, consider discontinuing LABA while maintaining ICS
- Monitor closely for 2-4 weeks after each step down
Acute Exacerbation Management
Severity Assessment
Mild Exacerbation: 2
- Speech normal
- Pulse <110 bpm
- Respiratory rate <25 breaths/min
- Peak flow >50% predicted
Severe Exacerbation: 2
- Cannot complete sentences in one breath
- Pulse >110 bpm
- Respiratory rate >25 breaths/min
- Peak flow <50% predicted
Life-Threatening: 2
- Peak flow <33% predicted
- Silent chest, cyanosis
- Weak respiratory effort
- Bradycardia, hypotension
- Exhaustion, confusion, coma
Immediate Treatment
- Nebulized albuterol 5 mg (or terbutaline 10 mg) with oxygen
- Repeat every 20 minutes for 3 doses initially
- Continue every 1-4 hours as needed based on response
- Measure peak flow 15-30 minutes after initial treatment 2
Systemic Corticosteroids: 1, 5, 2
- Oral (preferred): Prednisone 40-60 mg daily for adults, 1-2 mg/kg/day (max 60 mg) for children 5
- IV (if vomiting or severely ill): Hydrocortisone 200 mg immediately, then 200 mg every 6 hours 5, 2
- Duration: 5-10 days for outpatient management; no taper needed for courses <7-10 days if on ICS 5
- Critical timing: Administer within 1 hour of presentation; effects take 6-12 hours to manifest 5
Oxygen Therapy: 2
- High-flow oxygen 40-60% to maintain SpO2 >92%
Disposition Criteria
Admit to hospital if: 2
- Life-threatening features present
- Peak flow <50% predicted after initial treatment
- SpO2 <92% on room air
- Attack occurs in afternoon/evening
- Recent nocturnal symptoms or previous severe attacks
- Poor social circumstances or inability to cope at home
Discharge from ED if: 2
- Peak flow >70% predicted or personal best
- Symptoms resolved or minimal
- Patient can ambulate comfortably
- Home medications and follow-up arranged
Special Considerations
Allergen Immunotherapy
- Consider subcutaneous immunotherapy for patients with allergic asthma at Steps 2-4 1
- Role of allergy is greater in children than adults 1
- Clinicians must be prepared to treat anaphylaxis 1
Referral to Specialist
Refer when: 1
- Difficulty achieving or maintaining control
- ≥2 bursts of oral corticosteroids in 1 year
- Exacerbation requiring hospitalization
- Step 4 or higher care required (Step 3 or higher for children 0-4 years)
- Considering immunotherapy or omalizumab
- Additional testing indicated
Critical Pitfalls to Avoid
Never use SABA alone without ICS-based controller therapy in patients with persistent asthma—this increases exacerbation risk and mortality 1, 3, 4
Never use LABAs as monotherapy—always combine with ICS due to increased risk of asthma-related death 1
Never use sedatives in asthmatic patients—they are contraindicated and worsen respiratory depression 6, 2
Do not delay systemic corticosteroids during acute exacerbations—early administration is critical as effects take 6-12 hours 5
Do not rely on clinical impression alone—always measure peak flow or FEV1 objectively 2
Do not assume control is adequate if SABA use exceeds 2 days/week—this indicates need to step up therapy 1, 2
Avoid unnecessarily high ICS doses—medium doses provide most benefit with minimal additional improvement at high doses but significantly increased side effects 1