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Allergic rhinitis and asthma: From nasal symptoms to accurate diagnosis

Case Study
Respiratory allergy

Imagine a patient whose life is disrupted by persistent sneezing, nasal congestion and a constant runny nose. Meet Natasha, an example of a young woman struggling with the relentless symptoms of allergic rhinitis. In this illustrative case study, see how the gold standard of in-vitro allergy diagnostics1 from Thermo Fisher Scientific helped inform an accurate diagnosis.

A young woman in overalls reading a book on a sofa.

Patient History

Personal history

As an infant, Natasha suffered from egg allergy; however, she can now tolerate egg in baked goods. 

Aged 16, Natasha suffered an asthma exacerbation during a sleepover with a friend who had a pet cat. Following this episode, she was diagnosed with asthma by her GP. During the same visit to the clinician, it was noted from her medical records that she had suffered with childhood eczema, which gradually improved during her teenage years and had now mostly resolved. 

On a previous visit to a dermatologist regarding her eczema, it was found that Natasha has dermatographism. 

Medication history

  • Previously prescribed intranasal beclomethasone, but stopped due to subsequent epistaxis
  • Currently takes inhaled beclomethasone, twice daily BID
  • Uses intranasal antihistamines and nasal decongestants

Observation

Whilst observing Natasha during the consultation, her clinician observed frequent sniffing, nose rubbing and mouth breathing. 

How should Natasha's clinician continue the diagnostic workup?

Based on Natasha’s clinical history, a diagnosis of rhinitis may be made. The next step in the diagnostic process is a physical examination, including inspection of the face, and internal examination of the nose. All patients with persistent rhinitis should also be assessed for possible asthma; this should consist of a chest examination and lung function tests including spirometry or peak flow.2

To determine whether Natasha's rhinitis is allergic or non-allergic in origin, a specific IgE blood test or skin prick test (SPT) should be used. However, in Natasha’s case, SPTs are contraindicated due to her documented dermatographism, making a specific IgE blood test most suitable.2 One study found that compared with a clinical history and physical examination alone, additional use of a specific IgE blood test increases diagnostic certainty by 64 percent.3

*Based on a prospective multicenter study of 380 children aged <6 years with symptoms of eczema and/or wheezing/asthma and/or rhinitis.3

Field of birch trees

Examination, investigations and results

Examination

Natasha’s GP continued the diagnostic process with a physical examination. Inspection of her face was unremarkable, but internal examination of her nose revealed turbinate hypertrophy with clear secretions. 

Examination of Natasha’s chest revealed no obvious abnormalities and chest expansion was equal on both sides. Her respiratory rate was 18 breaths/min and upon auscultation of her lungs, the GP heard a mild expiratory wheeze. 

Investigations

Next, the GP decided to request a specific IgE blood test. Based on Natasha’s symptoms, age and local sensitisation patterns, an appropriate panel of environmental allergens was selected. 

ImmunoCAP™ specific IgE blood test results (kUA/L)

Test*

Type

Natasha’s results

House dust mite (d1)

Whole allergen

31

Timothy grass (g6)

Whole allergen

17

Silver birch (t3)

Whole allergen

15

Cat dander (e1):

Whole allergen

<0.10

Alternaria alternata (m6)

Whole allergen

8

 

Lung function test results

Test

Natasha’s results

Peak nasal inspiratory flow

52 L/min

Peak expiratory flow rate (PEFR)

310 L/min

Percentage of predicted FEV1

73 percent

Fraction exhaled nitric oxide (FeNO)

49 ppb

 

Differential diagnosis

What is the most likely reason for Natasha’s nasal symptoms?

Specific IgE blood test results will indicate whether the patient is sensitised (has IgE antibodies) to specific allergens. Specific IgE values of ≥0.10 kUA/L indicate sensitisation4  and the probability of allergy rises with increasing specific IgE antibody concentrations.5 Results should always be interpreted in conjunction with the clinical history and physical examination.2,6 When test results are concordant with the clinical history, a diagnosis of allergic rhinitis can be made.2

In Natasha’s case, the specific IgE test results show that she is polysensitised, with sensitisations to house dust mite (HDM), Timothy grass, silver birch, and Alternaria alternata. She has very high levels of HDM-specific IgE, but perhaps surprisingly, given her clinical history, her results indicate that she is not sensitised to cat dander. Therefore, it is likely that her asthma attack during the sleepover with her friend was due to HDM rather than the cat—a point which would have been very difficult to ascertain from her history alone. 

Natasha’s sensitisation to seasonal allergens (Timothy grass, silver birch, and Alternaria alternata) may be the reason for her worsening nasal symptoms and breathlessness over the summer months, as her total allergen load will be increased compared with winter months.7

Interpreting these results in conjunction with Natasha’s clinical history and physical examination findings, allowed the GP to confirm a diagnosis of IgE-mediated allergy8—in this case, perennial allergic rhinitis (due to HDM) and seasonal allergic rhinitis (due to Timothy grass). 

Management

HDMs are impossible to completely eradicate from a house by cleaning;9 however, Natasha could limit her exposure to HDM by using the following strategies: 

  • Put dust-proof covers on pillows, mattresses and box springs. Remove and wash the covers frequently9,10
  • Minimize the number of stuffed animals kept in bedrooms or put them in plastic containers9
  • Remove carpets, drapes and upholstered furniture (as much as possible)10
  • Keep humidity to ≤45 percent10
  • Vacuum carpets twice every week10

Natasha's peak nasal inspiratory flow is below the normal range determined for adult female patients (~115 mL/min), indicating nasal obstruction.11 Normal adult PEFR range is between 400 and 700 L/min.12 From her lung function tests, Natasha's low PEFR and FEV1 suggest intrapulmonary airflow obstruction,13 which, taken together with her clinical history, is indicative of asthma.14 Her FeNO is raised, but caution should be exercised when interpreting this result, as the presence of allergic rhinitis can elevate FeNO levels, even in the absence of overt, clinical asthma.2

Did you know?

  • Up to 90 percent of allergic patients are polysensitised15
  • Allergic rhinitis confers a 3.5-fold risk for subsequent development of asthma16 and is a marker of poor asthma control17

*The following products are included in the ImmunoCAP blood test range:

  • ImmunoCAP Allergen d1, House dust mite
  • ImmunoCAP Allergen g6, Timothy
  • ImmunoCAP Allergen t3, Common silver birch
  • ImmunoCAP Allergen e1, Cat dander
  • ImmunoCAP Allergen m6, Alternaria alternata

Conclusion

Natasha's journey from persistent symptoms to effective management of her allergic rhinitis demonstrates the transformative power of accurate diagnostic results and personalized care.

BID: twice a day; FEV1: forced expiratory volume in 1 second; IgE: immunoglobulin E; kUA/L: allergen-specific kilo units per litre


The people, places and events depicted in these case studies and photographs do not represent actual patients, nor are they affiliated with Thermo Fisher Scientific. 

Thermo Fisher Scientific, a leader in allergy diagnostics, is always at your side to help you deliver the best possible care for your patients.

References
  1. Scadding G K, Scadding G W. Diagnosing allergic rhinitis. Immunol Allergy Clin North Am 2016;36(2):249-260 
  2. Siles RI, Hsieh FH. Allergy blood testing: A practical guide for clinicians. Cleve Clin J Med. 2011 Sep;78(9):585-92. doi: 10.3949/ccjm.78a.11023. PMID: 21885690.Bonnelykke K, Pipper CB, Bisgaard H. J Allergy Clin Immunol. 2008;121(3):646-651.
  3. Eigenmann P A, Atanaskovic-Markovic M et al. Testing children for allergies: why, how, who and when: an updated statement of the European Academy of Allergy and Clinical Immunology (EAACI) Section on Pediatrics and the EAACI-Clemens von Pirquet Foundation. Pediatr Allergy Immunol 2013;24(2):195-209 
  4. Bousquet J, Anto J M et al. Allergic rhinitis. Nat Rev Dis Primers 2020;6(1):95 
  5. Roberts G, Xatzipsalti M et al. Paediatric rhinitis: position paper of the European Academy of Allergy and Clinical Immunology. Allergy 2013;68(9):1102-1116 
  6. American College of Allergy A I. Environmental trigger avoidance. Available at: https://acaai.org/allergies/allergy-treatment/environmental-trigger-avoidance. Accessed March 2022 
  7. Pfaar O, Klimek L et al. COVID-19 pandemic: practical considerations on the organization of an allergy clinic-an EAACI/ARIA position paper. Allergy 2021;76(3):648-676 
  8. Bousquet J, Pfaar O et al. 2019 ARIA care pathways for allergen immunotherapy. Allergy 2019;74(11):2087-2102 
  9. Jacobsen L, Niggemann B et al. Specific immunotherapy has long-term preventive effect of seasonal and perennial asthma: 10-year follow-up on the PAT study. Allergy 2007;62(8):943-948 
  10. Bergeron C, Hamid Q. Relationship between asthma and rhinitis: epidemiologic, pathophysiologic, and therapeutic aspects. Allergy Asthma Clin Immunol 2005;1(2):81-87