Welcome to NGC. Skip directly to: Search Box, Navigation, Content.


Brief Summary

GUIDELINE TITLE

Allergic rhinitis and its impact on asthma.

BIBLIOGRAPHIC SOURCE(S)

  • Allergic rhinitis and its impact on asthma. Geneva (Switzerland): World Health Organization (WHO); 2008. [2241 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Allergic rhinitis and its impact on asthma. J Allergy Clin Immunol 2001 Nov;108(5):S147-334.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Summary of Major Recommendations

  1. Allergic rhinitis is a major chronic respiratory disease due to its:
    • Prevalence
    • Impact on quality of life
    • Impact on work/school performance and productivity
    • Economic burden
    • Links with asthma
  2. In addition, allergic rhinitis is associated with sinusitis and other co-morbidities such as conjunctivitis.
  3. Allergic rhinitis should be considered as a risk factor for asthma along with other known risk factors.
  4. A new subdivision of allergic rhinitis has been proposed:
    • Intermittent (IAR)
    • Persistent (PER)
  5. The severity of allergic rhinitis has been classified as "mild' and "moderate/severe" depending on the severity of symptoms and quality-of-life outcomes.
  6. Depending on the subdivision and severity of allergic rhinitis, a stepwise therapeutic approach has been proposed.
  7. The treatment of allergic rhinitis combines:
    • Allergen avoidance (when possible)
    • Pharmacotherapy
    • Immunotherapy
    • Education
  8. Patients with persistent allergic rhinitis should be evaluated for asthma by means of a medical history, chest examination and, if possible and when necessary, the assessment of airflow obstruction before and after bronchodilator.
  9. Patients with asthma should be appropriately evaluated (history and physical examination) for rhinitis.
  10. Ideally, a combined strategy should be used to treat the upper and lower airway diseases in terms of efficacy and safety.

Specific Recommendations

Diagnosis

Diagnosis of Allergic Rhinitis

  • The diagnosis of allergic rhinitis is based upon the coordination between a typical history of allergic symptoms and diagnostic tests.
  • Typical symptoms of allergic rhinitis include rhinorrhea, sneezing, nasal obstruction, and nasal pruritus.
  • Ocular symptoms are common, in particular in patients allergic to outdoor allergens.
  • Diagnostic tests are based on the demonstration of allergen-specific immunoglobulin E (IgE) in the skin (skin tests) or the blood (specific IgE).
  • The measurement of total IgE is not useful in the diagnosis of allergic rhinitis.
  • Many asymptomatic subjects can have positive skin tests and/or detectable serum-specific IgE.
  • Many patients have positive tests which are irrelevant.
  • In some countries, the suspicion of allergic rhinitis may be raised in the pharmacy.
  • Patients with persistent and/or moderate/severe symptoms of rhinitis should be referred to a physician.
  • Most patients with rhinitis are seen in primary care and, in developed countries, allergy tests are available to screen for allergy.
  • Patients with persistent and/or moderate/severe symptoms of rhinitis need a detailed allergy diagnosis.

Management

Environmental Control

Tertiary Environmental Control

  • The vast majority of single preventive measures of indoor allergen control have failed to achieve any clinically relevant improvement of asthma and rhinitis. Tertiary prevention of indoor allergens is not a public health measure.
  • In patients allergic to furred pets who have symptoms on contact with the allergen, pet avoidance is recommended.
  • In low-income settings with a high load of pollutants (and allergens), a multifaceted intervention may be useful.
  • Total avoidance of occupational agents is recommended in sensitized subjects.
  • Occupational agent control may be useful when total avoidance is not possible.

Drug Treatment

Pharmacotherapy of Allergic Rhinitis and Conjunctivitis

  • Second-generation oral or intranasal H1-antihistamines are recommended for the treatment of allergic rhinitis and conjunctivitis in adults and children.
  • First-generation oral H1-antihistamines are not recommended when second-generation ones are available due to safety concerns.
  • Topical H1-antihistamines are recommended for the treatment of allergic rhinitis and conjunctivitis.
  • Intranasal glucocorticosteroids are recommended for the treatment of allergic rhinitis in adults and children. They are the most effective drugs for the treatment of allergic rhinitis.
  • Intra-muscular glucocorticosteroids and long-term use of oral glucocorticosteroids are not recommended due to safety concern.
  • Topical cromones are recommended in the treatment of allergic rhinitis and conjunctivitis, but they are only modestly effective.
  • Montelukast is recommended in the treatment of seasonal allergic rhinitis in patients over 6 years of age.
  • Intranasal ipratropium is recommended in the treatment of rhinorrhea associated with allergic rhinitis.
  • Intranasal decongestants may be used for a short period of time in patients with severe nasal obstruction.
  • Oral decongestants (and their associations) may be used in the treatment of allergic rhinitis in adults, but side effects are common.
  • The treatment of allergic rhinitis should consider the severity and duration of the disease, the patient's preference, as well as the efficacy, availability, and costs of drugs.
  • A stepwise approach depending on the severity and duration of rhinitis is proposed.
  • A tailored approach is needed for each individual patient.
  • Not all patients with moderate/severe allergic rhinitis are controlled despite optimal pharmacotherapy.

Allergen-Specific Immunotherapy: Therapeutic Vaccines for Allergic Disease

Specific Immunotherapy

  • Allergen-specific immunotherapy is classically administered by subcutaneous route but local routes are now available.
  • Specific immunotherapy needs a precise diagnosis of IgE-mediated allergy.
  • Subcutaneous immunotherapy is effective in adults and children for pollen and mite allergy, but it is burdened by the risks of side effects. These reactions may be exceptionally life-threatening.
  • Sublingual immunotherapy is recommended for the treatment of pollen allergy in adults.
  • Sublingual immunotherapy may be used for the treatment of patients with mite allergy.
  • Intranasal immunotherapy may be used for the treatment of patients with pollen allergy.
  • Allergen-specific immunotherapy may alter the natural course of allergic diseases.
  • Subcutaneous immunotherapy appears to be effective several years after its cessation.
  • Immunotherapy appears to reduce the development of new sensitizations.
  • Administered to patients with rhinitis, subcutaneous immunotherapy appears to reduce the development of asthma.

Classifications of Systemic Reactions Induced by Immunotherapy

  1. No symptoms or non-immunotherapy related symptoms
  2. Mild systemic reactions

    Symptoms: Localized urticaria, rhinitis or mild asthma (Peak flow [PF] <20% decrease from baseline)

  3. Moderate systemic reactions

    Symptoms: Slow onset (>15 min) of generalized urticaria and/or moderate asthma (PF <40% decrease from baseline)

  4. Severe (non-life-threatening) systemic reactions

    Symptoms: Rapid onset (<15 min) of generalized urticaria, angioedema, or severe asthma (PF >40% decrease from baseline)

  5. Anaphylactic shock

    Symptoms: Immediate evoked reaction of itching, flushing, erythema, generalized urticaria, stridor (angioedema), immediate asthma, hypotension, etc.

Considerations for Initiating Immunotherapy

  1. Presence of a demonstrated IgE-mediated disease:
    • Positive skin tests and/or serum-specific IgE
  2. Documentation that specific sensitivity is involved in symptoms:
    • Exposure to the allergen(s) determined by allergy testing related to appearance of symptoms
    • If required allergen challenge with the relevant allergen(s)
  3. Characterization of other triggers that may be involved in symptoms
  4. Severity and duration of symptoms:
    • Subjective symptoms
    • Objective parameters, e.g., work loss, school absenteeism
    • Pulmonary function (essential in asthmatics): exclude patients with severe asthma
    • Monitoring of the pulmonary function by peak flow
  5. Response of symptoms to pharmacotherapy
  6. Availability of standardized or high-quality vaccines
  7. Contraindications:
    • Treatment with beta-blockers
    • Other immunologic disease
    • Inability of patients to comply
    • Starting immunotherapy with inhalant allergens during known pregnancy
  8. Sociologic factors:
    • Cost
    • Occupation of candidate
  9. Objective evidence of efficacy of immunotherapy for the selected patient (availability of randomized controlled studies)

Indications for Subcutaneous Immunotherapy

  • Patients with symptoms induced predominantly by allergen exposure
  • Patients with clinical symptoms due to a single or few allergens
  • Patients with a prolonged season or with symptoms induced by succeeding pollen seasons
  • Patients with rhinitis and symptoms from the lower airways during peak allergen exposure
  • Patients in whom antihistamines and moderate dose topical glucocorticoids insufficiently control symptoms
  • Patients who do not want to be on constant or long-term pharmacotherapy
  • Patients in whom pharmacotherapy induces undesirable side effects

Indications for Sublingual Immunotherapy

High-dose sublingual-swallow specific immunotherapy may be indicated in the following cases:

  • Carefully selected patients with rhinitis, conjunctivitis, and/or asthma caused by pollen and mite allergy
  • Patients insufficiently controlled by conventional pharmacotherapy
  • Patients who have presented with systemic reactions during injection-specific immunotherapy
  • Patients showing poor compliance with or refusing injections

Complementary and Alternative Medicine

  • Many patients who use complementary and alternative medicine appear to be satisfied.
  • Evidence-based recommendations are difficult to propose for most complementary and alternative medicine interventions due to methodological problems.
  • Butterbur was found to be effective in the treatment of allergic rhinitis, but more data are needed.
  • Safety of phytotherapy raises concerns.

Health Promotion and Prevention

Primary and Secondary prevention

  • Breastfeeding is recommended irrespective of the atopic background of the infant.
  • Current dietary manipulations of maternal and infant feeding do not have a preventive role for atopic diseases and are not recommended.
  • Environmental tobacco smoke should be avoided in pregnant women and children although more data are needed.
  • Conflicting data exist concerning early-life exposure to pets and the development atopy. No general recommendation can be made.
  • House dust mite avoidance in infancy has inconsistent effect on the development allergy or asthma and cannot be recommended.
  • Primary prevention of occupational airway disease is recommended.
  • Secondary prevention of asthma is still a matter of debate and more data are needed.

Links between Rhinitis and Asthma

See the original guideline document for epidemiologic links between rhinitis and asthma, commonalities and differences in their mechanisms, and the effect of rhinitis and asthma on quality of life (QOL).

Therapeutic Consequences

Treatment of Rhinitis and Asthma Using a Single Approach

  • Oral H1-antihistamines are not recommended in the treatment of asthma.
  • Intranasal glucocorticosteroids are inconstantly and at best moderately effective in asthma.
  • Intranasal glucocorticosteroids may be effective in reducing asthma exacerbations and hospitalizations.
  • The role of intra-bronchial glucocorticosteroids in rhinitis is unknown.
  • Montelukast is effective in the treatment of allergic rhinitis and asthma in patients over 6 years of age.
  • Subcutaneous immunotherapy is recommended in both rhinitis and asthma in adults, but it is burdened by side effects, in particular asthmatics.
  • Anti-IgE monoclonal antibody is effective and safe in both rhinitis and asthma.

See the original guideline document for a discussion of other co-morbidities and complications and rhinitis in children.

Definitions:

Notation Strength of Recommendation and Quality of Evidence Clarity of Balance Between Desirable and Undesirable Effects Quality of Supporting Evidence Implications
1A Strong recommendation

High quality evidence
Desirable effects clearly outweigh undesirable effects or vice versa Consistent evidence from randomized controlled trials (RCTs) or exceptionally strong evidence from unbiased observational studies Recommendation can apply to most patients in most circumstances.

Further research is unlikely to change the confidence of the estimate of effect
1B Strong recommendation

Moderate quality evidence
Desirable effects clearly outweigh undesirable effects or vice versa Evidence from RCTs with important limitations (inconsistent results, methodological flaws, indirect or imprecise) or unusually strong evidence from unbiased observational studies Recommendation can apply to most patients in most circumstances.

Further research (if performed) is likely to have an important impact on the confidence in the estimate of effect and may change the estimate.
1C Strong recommendation

Low quality evidence
Desirable effects clearly outweigh undesirable effects or vice versa Evidence for at least one critical outcome from RCTs with serious flaws, observational studies or indirect evidence Recommendation may change when higher quality evidence becomes available.

Further research (if performed) is likely to have an important impact on the confidence in the estimate of effect and is likely to change the estimate.
1D Strong recommendation

Very low quality evidence (very rarely applicable)
Desirable effects clearly outweigh undesirable effects or vice versa Evidence for at least one of the critical outcomes from unsystematic clinical observation or very indirect evidence Recommendation may change when higher quality evidence becomes available.

Any estimate of the effect for at least one critical outcome is very uncertain.
2A Weak recommendation

High quality evidence
Desirable effects closely balance with undesirable effects Consistent evidence from well performed RCTs or exceptionally strong evidence from unbiased observational studies The best action may differ depending on circumstances or patients' or societal views.

Further research is very unlikely to change the confidence in the estimate of effect.
2B Weak recommendation

Moderate quality evidence
Desirable effects closely balance with undesirable effects Evidence from RCTs with important limitations (inconsistent results, methodological flaws, indirect or imprecise) or unusually strong evidence from unbiased observational studies Alternative approach is likely to be better for some patients under some circumstances.

Further research (if performed) is likely to have an important impact on the confidence of the estimate of effect and may change the estimate.
2C Weak recommendation

Low quality evidence
Uncertainty in the estimates of desirable and undesirable effects; desirable effects may be closely balanced with undesirable effects Evidence for at least one critical outcome from RCTs with serious flaws, observational studies, or indirect evidence Other alternatives may be equally reasonable.

Further research is very likely to have important impact on the confidence in the estimate of effect and is likely to change the estimate.
2D Weak recommendation

Very low quality evidence
Major uncertainty in the estimates of desirable and undesirable effects; desirable effects may be closely balanced with undesirable effects Evidence for at least one critical outcome from unsystematic clinical observation or very indirect evidence Other alternatives may be equally reasonable.

Any estimate of the effect for at least one critical outcome is very uncertain.

CLINICAL ALGORITHM(S)

Algorithms are provided in the original guideline document for the following:

  • Diagnosis of allergic rhinitis
  • Rhinitis management
  • Management of allergic rhinitis in the pharmacy

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of evidence supporting the recommendations is not specifically stated.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Allergic rhinitis and its impact on asthma. Geneva (Switzerland): World Health Organization (WHO); 2008. [2241 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2001 Nov (revised 2008)

GUIDELINE DEVELOPER(S)

Allergic Rhinitis and its Impact on Asthma Workshop Group - Independent Expert Panel

SOURCE(S) OF FUNDING

Supported through a grant from the American Academy of Allergy, Asthma, and Immunology and Allergic Rhinitis and its Impact on Asthma (ARIA)

GUIDELINE COMMITTEE

Allergic Rhinitis and its Impact on Asthma (ARIA) Workshop Group

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Workshop Group Members: Jean Bousquet; Nikolai Khaltaev; Alvaro Cruz; Judah Denburg; Wytske Fokkens; Alkis Togias; Torsten Zuberbier; Carlos Baena-Cagnani; G Walter Canonica; Chris van Weel; Nadia Aït-Khaled; Michael Blaiss; Philippe-J Bousquet; Kai-Hakon Carlsen; Adnan Custovic; Pascal Demoly; Stephen Durham; Roy Gerth van Wijk; Richard Lockey; Eli O Meltzer; Joaquim Mullol; Robert Naclerio; Nikolaos Papadopoulos; Giovanni Passalacqua; Glenis Scadding; F Estelle R Simons; Erkka Valovirta; Claus Bachert; Sergio Bonini; Louis-Philippe Boulet; Paulo Camargos; Yuzhi Chen; Ronald Dahl; Omer Kalayci; Michael Kaliner; You-Young Kim; Marek Kowalski; Le Thi Tuyet Lan; Jing Li; Yousser Mohammad; Robyn O'Hehir; Ken Ohta; Susanna Palkonen; Ruby Pawankar; Todor Popov; Klaus Rabe; José Rosado-Pinto; Elina Toskala; Paul van Cauwenberge; De Yun Wang; Magnus Wickman; Barbara Yawn; Arzu Yorgancioglu; Osman Yusuf; Heather Zar

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Allergic rhinitis and its impact on asthma. J Allergy Clin Immunol 2001 Nov;108(5):S147-334.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

The following are available:

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on March 19, 2003. This NGC summary was updated by ECRI Institute on April 24, 2008. The updated information was verified by the guideline developer on June 27, 2008.

COPYRIGHT STATEMENT

The name and logo of ARIA are registered trademarks. Permission must be granted by the ARIA Secretariat for the use of ARIA materials.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.

Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
DHHS Logo