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Health Checkup

Phadiatop

Allergy
0 parametersReport in 48HrsAt Home

No Fasting Required

Details

Detects IgE antibodies against common inhalant allergens, helping identify atopy (the genetic tendency to develop allergic diseases)

₹1,610₹1,950

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Phadiatop Test Information Guide

  • Why is it done?
    • Screening test to detect the presence of IgE antibodies against common environmental allergens
    • Evaluates IgE sensitization to 10 common allergen groups: inhalant allergens (birch pollen, timothy grass, mugwort, house dust mites, cat dander, dog dander) and food allergens (milk, peanut, shrimp)
    • Used when patients present with symptoms suggesting allergic disease such as rhinitis, asthma, eczema, or food allergies
    • Serves as an initial screening tool before more specific allergen-specific IgE testing
    • Typical timing: performed when allergic symptoms are present or when there is clinical suspicion of atopic disease
    • May be used for epidemiological surveys to assess allergic sensitization in populations
  • Normal Range
    • Result: Negative (Class 0) - IgE <0.35 kU/L (kilo Units per Liter)
    • Positive Results (indicate allergen sensitization):
    • • Class 1: 0.35 - 0.69 kU/L
    • • Class 2: 0.70 - 3.49 kU/L
    • • Class 3: 3.50 - 17.49 kU/L
    • • Class 4: 17.50 - 52.49 kU/L
    • • Class 5: 52.50 - 100 kU/L
    • • Class 6: >100 kU/L
    • Interpretation: Negative result suggests no clinically relevant sensitization to the tested allergen panel; however, specific allergen sensitization cannot be ruled out for allergens not included in the panel
    • Positive results indicate allergenic sensitization to one or more of the tested allergens; higher classes correlate with higher levels of allergen-specific IgE antibodies
    • Unit of measurement: kU/L (kilo International Units per Liter)
  • Interpretation
    • Negative Result (Class 0, <0.35 kU/L): No detectable IgE antibodies to the common allergen panel; indicates low likelihood of IgE-mediated allergic sensitization to tested allergens; does not exclude allergies to allergens outside the panel or non-IgE mediated allergic reactions
    • Class 1-2 (0.35-3.49 kU/L): Low level sensitization; clinical relevance depends on patient symptoms; may represent early sensitization or cross-reactivity
    • Class 3-4 (3.50-52.49 kU/L): Moderate to high level sensitization; likely clinically relevant; should prompt specific allergen testing and clinical correlation
    • Class 5-6 (>52.50 kU/L): Very high level sensitization; clinically highly relevant; indicates strong allergic sensitization requiring specific allergen identification and therapeutic intervention
    • Factors affecting results:
    • • Recent antihistamine use may suppress but not eliminate IgE response
    • • Age - IgE sensitization patterns change over lifespan
    • • Seasonal variation in IgE levels for seasonal allergens
    • • Genetic predisposition and atopic status
    • • Recent immunosuppressive therapy may reduce IgE levels
    • Clinical significance: Positive results support allergic disease diagnosis when combined with clinical symptoms; however, IgE sensitization alone does not diagnose clinical allergy - clinical correlation is essential
  • Associated Organs
    • Primary organ systems: Immune system (B lymphocytes producing IgE), respiratory tract, gastrointestinal tract, skin, and mucous membranes
    • Medical conditions associated with abnormal results:
    • • Allergic rhinitis (hay fever) - environmental allergen sensitization
    • • Allergic asthma - lower airway inflammation and bronchospasm
    • • Atopic dermatitis (eczema) - IgE-mediated skin inflammation
    • • Food allergy - oral allergy syndrome, gastrointestinal symptoms
    • • Allergic conjunctivitis - ocular inflammation
    • • Atopic syndrome - multiple allergic manifestations
    • Diseases this test helps diagnose or monitor:
    • • IgE-mediated allergic diseases
    • • Atopic conditions (allergic triad)
    • • Chronic rhinosinusitis with allergic component
    • Potential complications or risks associated with abnormal results:
    • • Anaphylaxis risk - severe allergic reactions to identified allergens
    • • Chronic inflammation - persistent allergic inflammation may lead to tissue damage
    • • Secondary infections - damaged respiratory epithelium susceptible to infections
    • • Asthma exacerbations - untreated allergen exposure in asthmatic patients
    • • Quality of life impairment - chronic symptoms affecting daily functioning
  • Follow-up Tests
    • Additional tests recommended based on positive results:
    • • Allergen-specific IgE testing (ImmunoCAP, RAST) - to identify specific allergens causing sensitization from within the panel
    • • Skin prick testing - confirmatory testing with better specificity; useful for clinical correlation
    • • Intradermal testing - more sensitive for detecting lower-level sensitization when clinical suspicion high
    • • Total IgE - to assess overall allergic load and atopic status
    • • Component-resolved diagnostics (CRD) - identifies sensitization to specific allergenic proteins for precise allergen characterization
    • Further investigations that might be needed:
    • • Pulmonary function testing (spirometry) - if respiratory symptoms or asthma suspected
    • • Methacholine challenge test - to evaluate airway hyperresponsiveness
    • • Nasal endoscopy - for evaluation of allergic rhinitis complications
    • • Oral food challenge - if food allergy suspected despite negative serum testing
    • • Rhinolaryngoscopy - assessment of upper airway involvement
    • Monitoring frequency for ongoing conditions:
    • • Annual monitoring in patients with persistent allergic disease and high IgE levels
    • • Monitoring before and during allergen immunotherapy (AIT) - to assess treatment efficacy
    • • Re-testing if clinical symptoms persist despite negative initial results
    • Related tests providing complementary information:
    • • Tryptase level - marker of mast cell activation and baseline for anaphylaxis evaluation
    • • Eosinophil count - supports allergic disease diagnosis; elevated in parasitic infections
    • • IgE and IgG subclass measurements - additional immune response characterization
    • • Allergen microarray - comprehensive analysis of sensitization patterns
  • Fasting Required?
    • Fasting Required: No
    • Fasting duration: Not applicable - This is a blood test that does not require fasting
    • Food and beverage: Patient may eat and drink normally before the test
    • Medications to avoid:
    • • Antihistamines (H1 and H2 blockers) - should ideally be discontinued 3-7 days before testing as they may suppress IgE-mediated mast cell reactions in skin testing correlation studies
    • • Note: Blood test is not affected by antihistamines; this applies mainly to concurrent skin testing
    • • Immunosuppressive therapy may reduce IgE levels but testing can still be performed
    • Other patient preparation requirements:
    • • Inform phlebotomist or healthcare provider of current medications before blood draw
    • • Inform of any recent infections, vaccinations, or immunological events (may temporarily elevate IgE)
    • • Blood sample collection via venipuncture - standard collection procedure
    • • No special positioning or activity restrictions required before or after test
    • • May resume normal activities immediately after blood draw
    • • Optimal testing conditions: Perform during periods without acute infection or severe stress, which may temporarily alter immune responses

How our test process works!

Book a test, a phlebotomist collects your sample at home, the lab processes it, and your report arrives digitally.NABL accredited labs, free home collection, and digital reports you can share with a doctor.
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