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What is severe asthma?

Severe asthma is defined by international guidelines as asthma requiring high-dose inhaled corticosteroids combined with a long-acting bronchodilator and a second controller — or asthma requiring systemic steroids — to maintain control, or that remains uncontrolled despite this treatment. By that definition, only a small fraction of asthma is severe, but those patients carry a disproportionate burden of symptoms, exacerbations, and steroid-related side effects.

The biology of severe asthma is increasingly well understood. Many patients have a Type 2 (T2-high) inflammatory phenotype driven by eosinophils, IgE, and specific cytokines. Identifying this phenotype is the key to choosing among the modern biologic therapies, which can reduce attacks by 50% or more and often allow patients to come off oral steroids entirely.

When to consider evaluation

  • Two or more oral steroid courses per year for asthma
  • Asthma-related emergency department visit or hospitalization in the past year
  • Daily symptoms or rescue inhaler use despite high-dose controller therapy
  • Blood eosinophilia (typically ≥150–300 cells/µL)
  • Coexisting nasal polyps, eczema, or eosinophilic esophagitis
  • Steroid-related side effects from frequent prednisone courses

How it is diagnosed

Evaluation confirms the asthma diagnosis with spirometry and reviews inhaler technique and adherence — both of which are surprisingly common contributors to apparent treatment failure. A complete asthma evaluation also looks for comorbidities that worsen asthma control: chronic rhinosinusitis with polyps, obstructive sleep apnea, gastroesophageal reflux, and vocal cord dysfunction.

Biomarker phenotyping guides biologic selection. This typically includes blood eosinophil count, total IgE, specific IgE testing to perennial allergens, and FeNO (fractional exhaled nitric oxide) when available.

Treatment options

Optimization of inhaled therapy and trigger management is the foundation. For patients who remain uncontrolled, biologic therapy is added. The available biologics include omalizumab (Xolair) for allergic asthma, mepolizumab (Nucala) and benralizumab (Fasenra) for eosinophilic asthma, dupilumab (Dupixent) for Type 2 inflammatory asthma, tezepelumab (Tezspire) for broad severe asthma indications, and reslizumab (Cinqair) as an additional eosinophilic option.

Selection is individualized to the patient's phenotype, comorbidities, and personal preference. Many patients also benefit because the same biologic addresses coexisting nasal polyps, eczema, or EoE — providing one treatment for multiple conditions.

What to expect at your visit

The first visit reviews your asthma history, prior treatments, and exacerbation pattern. Spirometry and biomarker labs are ordered. At follow-up, results are reviewed and a biologic recommendation is discussed if appropriate. Coordination with your primary care physician and any pulmonologist involved is standard.

Treatment pathway at Optimed Immunology

Every patient’s situation is different, but the decision logic for severe asthma generally follows these steps. This is not a script — it is a structure that gets adapted to each patient’s history, findings, and goals.

Confirm the diagnosis Spirometry, response to bronchodilator, exhaled nitric oxide (FeNO) where available, eosinophil count, total IgE, and specific IgE testing. Exclude alternative diagnoses where the picture is unclear.
Rule out look-alikes Vocal cord dysfunction, COPD, chronic cough syndromes, heart failure, eosinophilic granulomatosis with polyangiitis.
First-line / supportive Inhaler technique, adherence, environmental triggers, controller optimization, comorbidity management (GERD, sinus disease, sleep apnea, obesity), and as-needed rescue with appropriate anti-inflammatory rescue strategies.
Advanced treatment options Biologic therapy — Xolair, Nucala, Fasenra, Dupixent, Tezspire, Cinqair, Exdensur — selected by phenotype, biomarkers, and comorbid Type 2 disease.
How Dr. McNeil chooses Allergic phenotype favors Xolair or Tezspire; eosinophilic phenotype favors Nucala, Fasenra, Cinqair, or Exdensur; comorbid nasal polyps or eczema favors Dupixent or Tezspire; broad eligibility regardless of phenotype favors Tezspire. Dosing frequency, route, and copay landscape also factor in.
Monitoring & follow-up Exacerbation frequency, ER visits, steroid courses, asthma control test (ACT) scores, spirometry, biomarker trends, and tolerability.
Insurance & prior authorization Biologic prior authorization is handled in-house. Required documentation typically includes severity criteria, phenotype biomarkers, prior treatment failures, and steroid burden.

Medically reviewed

Donald L. McNeil, MD · Board Certified in Allergy & Immunology and Internal Medicine

Last reviewed: November 2025 · Sources: AAAAI · ACAAI · Immune Deficiency Foundation · FDA prescribing information · relevant clinical guidelines

This page is provided for educational purposes and does not substitute for clinical judgment or direct medical advice. Treatment decisions are individualized based on your full history, examination, and laboratory findings. If you have an emergency, call 911.

Schedule a consultation with Dr. McNeil.

If you suspect you may have Severe Asthma, an evaluation can clarify the diagnosis and identify whether treatment is appropriate.