Seasonal allergic rhinitis, also known as hay fever, is caused by an immune mediated reaction to seasonal environmental
aeroallergens (i.e. pollen).1 Symptoms are usually seen in spring and early summer, depending on weather conditions
and local plant species.2
Hay fever can have a significant impact on peoples’ lives. It can affect sleep, work performance, learning ability
and participation in social activity. Allergic rhinitis often co-exists with asthma, eczema, conjunctivitis and other
sinus conditions.2
There are a wide range of effective treatment options available. Aim for symptom control with the lowest dose and number
of medications.
Diagnosing seasonal allergic rhinitis
Seasonal allergic rhinitis may affect up to 30% of adults and 40% of children. Prevalence is higher in Western countries
including New Zealand, Australia, Canada, USA and UK.3 Pollen sensitivity begins between age six months and
two years, although symptoms do not generally develop until age two to seven years.1
Types of rhinitis2
- Seasonal allergic rhinitis – associated with spring and early summer, triggered by pollen (outdoor allergens)
- Perennial allergic rhinitis – symptoms all year round, triggered by house dust mite, pets and mould (indoor allergens)
- Occupational rhinitis – symptoms worsened at work, triggered by chemicals, irritants and dust
- Non-allergic rhinitis – triggered by strong smells, change in temperature, viral infections, pregnancy, hypothyroidism
or rarely medications e.g. some antihypertensives
Family history of atopy is a known risk factor, but it is unclear whether early childhood exposure to infections, animals
and tobacco smoke plays a role in allergic rhinitis.1
For a positive diagnosis of seasonal allergic rhinitis, the timing of symptoms should be related to exposure to environmental
aeroallergens.
Symptoms are characterised by sneezing (especially paroxysmal), congestion, watery anterior rhinorrhoea, itchy nose,
eyes and throat, sinus pressure, facial pain and decreased sense of smell or taste. Signs in children may include tiredness,
daytime sleepiness, sniffing, blinking, eye rubbing, speech problems, snoring and dark circles under the eyes (“shiners”).1,3,4
Symptoms not usually associated with allergic rhinitis include: unilateral symptoms, nasal obstruction
without other symptoms, mucopurulent rhinorrhoea, posterior rhinorrhoea with thick mucuous, recurrent epistaxis.3
Towards the end of pollen season, symptoms may worsen. This is known as allergen priming where after repeated challenges,
the amount of allergen required to induce a response decreases.1
An annual pollen calendar for plant species in New Zealand can be found at:
www.allergy.org.nz/site/allergynz/files/Annual
Pollen Calendar.pdf
Ask about:
- Pattern, chronicity and seasonality of symptoms
- Response to medications
- Occupational exposure
- Environmental history
- Identification of precipitating factors
- Effect on quality of life
Assess for:
Allergic rhinitis is significantly associated with asthma (the “united airways disease” concept). Allergic
rhinitis occurs in 75–80% of patients with asthma and conversely, 20–30% of patients with known allergic rhinitis are
subsequently found to have asthma. Studies have shown that in patients with both asthma and allergic rhinitis treatment
of allergic rhinitis with intranasal steroids reduces the risk of asthma-related emergency department visits and hospitalisations.3
Many people have both seasonal and perennial allergic rhinitis
In reality many people are allergic to both indoor and outdoor allergens, and their symptoms are perennial, with seasonal
exacerbations. The World Health Organisation along with the Allergic Rhinitis and its Impact on Asthma group (ARIA)3 have
developed a new classification of rhinitis based on frequency and severity of symptoms, as these are the major factors
involved in determining treatment.
Patients are classified by both:
1. Duration of symptoms :
- Intermittent – symptoms less than four days per week or four weeks at a time
- Persistent – symptoms greater than four days per week or four weeks at a time
2. Severity of Symptoms
- Mild – no troublesome symptoms with normal sleep and normal daily activities
- Moderate to severe – troublesome symptoms with abnormal sleep and impairment of daily activities (e.g. school, work,
sport)
The ARIA classification works very well in New Zealand where most people with seasonal rhinitis are allergic to more
than one type of pollen. For example, people allergic to only birch pollen will have symptoms lasting for only three to
four weeks, whereas, most people with hay fever are probably allergic to grasses, trees and weeds, and their hay fever
season will last up to nine months.
Skin prick testing
Referral for skin prick testing may be considered, if the diagnosis is in doubt, if the patient wishes to determine
possible sensitivity to a specific allergen or when expensive avoidance measures or immunotherapy are being contemplated.
A positive reaction to an extract does not necessarily mean that this allergen causes the patients symptoms, but it provides
supportive evidence as part of an overall exposure history.
Extracts used for testing should be carefully selected to match allergens that the patient is normally exposed to.2 N.B.
atopic individuals may get false positive results with skin prick testing because of sensitivity of their skin to any
trauma (dermographism). However this should be apparent if the negative saline control is also positive.
Managing seasonal allergic rhinitis
Management of hay fever should be individualised depending on specific patient factors and symptoms. In most cases,
begin with one treatment and assess response and adverse effects. If the patient is compliant with the medication but
symptoms are not controlled, consider substitution with another class of medication or addition of a medication in a step
wise approach.
See Table 1 (see below) for information on medicines recommended
for use in hay fever.
For mild symptoms try antihistamines first
Intranasal antihistamines may be used as first-line treatment for people with occasional mild symptoms, who wish to
gain rapid relief (rescue therapy).5 They are equal to or more effective than oral antihistamines for the treatment
of rhinitis symptoms, although less effective than intranasal corticosteroids. They are not as effective for the treatment
of symptoms related to the eye and throat.6 They have a rapid onset of action so may be used on an “as
needed” basis for symptom relief.1 If treatment fails, or symptoms worsen, proceed to intranasal corticosteroid
treatment.
Some formulations may cause drowsiness. Intranasal antihistamines are not suitable for children aged less than five
years.5
Oral antihistamines can be considered if a spray formulation is not acceptable. They may be used as needed but are more
effective if used continuously throughout the pollen season. Oral antihistamines are less effective for nasal congestion
than intranasal antihistamines or corticosteroids, but more effective than intranasal antihistamines for eye symptoms.1
Second-generation antihistamines (e.g. loratadine, fexofenadine, cetirizine) should be used as they are less sedating
and less associated with anticholinergic effects. Of the second generation antihistamines, none have been found to be
superior over the other for symptom control.1 However, cetirizine may cause drowsiness, particularly when the
dose is increased above 10 mg daily.
Sedating antihistamines are contraindicated for the treatment of allergic rhinitis in children, even for night time
use as somnolence can continue through to the next day and affect cognitive function.
For moderate to severe symptoms try intranasal corticosteroids first
For most patients, if their symptoms are significant enough to seek medical advice, it is likely that they require more
effective treatment than antihistamines.
Corticosteroid nasal sprays are considered to be the most effective medicine class for controlling the four main symptoms
of hay fever – sneezing, itching, rhinorrhoea and nasal blockage. The onset of action of intranasal corticosteroids is
usually within 12 hours, but the effect can be more rapid for some people (three to four hours). Maximum efficacy may
take up to two weeks.5,6 Treatment can be started prior to the anticipated beginning of the pollen season and
regular use throughout the season is ideal.
Clinical response does not appear to vary significantly between different products, regardless of potency, therefore
use the lowest dose possible to control symptoms.1,2 There are two methods for achieving the optimum dose –
either start low and step-up the dose as dictated by symptoms5 or start with the maximum dose for the patients
age and step down the dose at one week intervals to the lowest effective dose.7 If symptoms still remain uncontrolled,
or for “breakthrough symptoms”, consider the addition of an oral antihistamine.6
Intranasal corticosteroids may be absorbed systemically to some extent but they are not generally associated with adverse
effects and are considered a safe long-term treatment (including during pregnancy and breast feeding5). Nasal
irritation and bleeding may occur. If patients find it difficult to use the spray, check their technique (see box below).2 Be
aware of total steroid load in patients also using inhaled corticosteroids.
Best practice tip: If a nasal saline spray is used before the steroid, it can
clear mucous and improve mucosal contact with the steroid and potentially reduce the dose required for efficacy.2
Patient advice on administering intranasal sprays (adapted from Scadding et al 2008)6 |
- Shake bottle well
- Look down at the floor (do not tilt head back)
- Using the right hand for the left nostril, put the nozzle just inside the nose and aim to the side (away from the
septum)
|
- Squirt once or twice as directed
- Do not sniff as this may result in the drug being swallowed (indicated by an unpleasant taste in the mouth) and
is a cause of treatment failure
- Change hands and repeat for the other side (i.e. use the left hand for the right nostril)
|
Other medications
Saline spray/drops are less effective than intranasal corticosteroids but can relieve nasal congestion
and dryness. They are associated with minimal adverse effects and may be considered for younger patients or those who
cannot tolerate other medications.1 There are several commercial saline sprays available. A home-made salt
water solution could also be used for irrigation – mix ¼ tsp salt with two cups of cooled, boiled water. The solution
can be administered using a small spray bottle, nasal dropper or syringe.4
Intranasal decongestants may be used to reduce significant nasal congestion. However due to the risk
of rhinitis medicamentosa (rebound nasal congestion), they should only be used short-term (<10 days) and intermittently.
Oral decongestants such as pseudoephedrine and phenylephrine are generally not recommended for use
in hay fever. They are associated with insomnia, irritability, hypertension and palpitations so should be used with caution
in older people and people with cardiac conditions and should not be used in children under six or in the first trimester
of pregnancy.1
Oral corticosteroids may be considered for very severe or intractable nasal symptoms or nasal polyps.
Use a short course of five to seven days only,1 20–40 mg per day in adults and 10 mg per day in children.5 Continue
intranasal corticosteroid during treatment.6
Parenteral corticosteroid injections are not recommended due to the risk of long-term corticosteroid
adverse effects and the availability of more effective treatments.1,5
Intranasal anticholinergics e.g. ipatropium bromide can be used as an “add-on” treatment
to intranasal corticosteroids and antihistamines to reduce rhinorrhoea, but it has no effect on other nasal symptoms.1,4,6
Intranasal sodium cromoglycate may be effective in preventing onset of symptoms in some patients but
for most people, it is less effective than intranasal corticosteroids.1 The four times daily dosing and the
delayed onset of action (up to three weeks) of the cromoglycates contribute to the overall reduced compliance and effectiveness.
It is a safe treatment to use in young children and during pregnancy.6
Oral anti-LT agents (anti-leukotriene receptor antagnosists) such as monteleukast are used in some
countries for treating hay fever. They are less effective than intranasal steroids and antihistamines and are not generally
recommended.1,4,5
Medications for eye symptoms
If allergic conjunctivitis is the dominant symptom, antihistamine eye drops are most effective.6 Saline eye
drops, sodium cromoglycate eye drops, intranasal corticosteroids and/or oral antihistamines can also be used.5
Patients should be advised to avoid rubbing their eyes as this can cause worsening of symptoms. Frequent use of artificial
tears during the day can help to dilute and remove allergens.8
Follow-up and specialist referral
If a patient with moderate to severe allergic rhinitis fails to improve after four weeks of adequate treatment (nasal
corticosteroids and oral antihistamines), patient compliance or the diagnosis must be re-assessed. In such cases, if the
diagnosis is in doubt a nasal endoscopy is necessary, to exclude other potential causes of nasal obstruction.
Environmental management of seasonal allergic rhinitis
Pollen counts are generally the highest in the morning and on sunny, windy days with low humidity, although this is
difficult to predict.1,6
There are many tips about how to minimise pollen exposure. Unfortunately many of these are not practical. Some practical
pollen avoidance measures include:2,4,9
- Use a clothes dryer to finish drying bedding
– this reduces the amount of pollen that may have settled while on the washing line
- Wear glasses/sunglasses outdoors to reduce pollen contact with the eyes
- Use air conditioning (on recycle mode) in the car
- Use a dehumidifier to reduce indoor humidity
- If possible avoid mowing lawns or raking leaves (or wear a mask)
- Have lawns mowed frequently to avoid flowering
- Select garden species which are low pollen producers (usually native plants, ask at your local garden store)
Consider referral to an ear, nose and throat specialist if:3
- The patient has constant unilateral obstruction
- There are complications such as resistant obstruction, anosmia, sinus disease, ear problems, persistent purulent discharge
- A polyp is unresponsive to inhaled corticosteroid treatment
Consider referral to an allergy specialist for patients who have:
- Inadequately controlled symptoms with maximum doses of medications
- Reduced quality of life
- Adverse reactions to medications
- A desire to identify the allergens to which they are sensitised
- Serious co-morbid conditions such as uncontrolled asthma
Immunotherapy
Immunotherapy involves subcutaneous injection of increasing doses of an identified allergen (or combined allergens),
eventually resulting in desensitisation.9 This is an effective treatment for allergic rhinitis which can be
considered for patients who are unable to tolerate the amount of medications required to control their symptoms and the
associated adverse effects, or for those who have medication failure.
Allergen immunotherapy may prevent the development of new sensitivities and reduce the risk of developing asthma. In
one study, patients who had subcutaneous immunotherapy showed a 50% reduction in symptoms and an 80% reduction in the
need for medication, compared to those receiving placebo.10
Patients receive weekly increasing doses of the vaccine for 12 weeks, up to a maintenance dose, and then monthly injections
of the maintenance dose for three to five years. Treatment can be costly, but clinical benefit is usually sustained for
many years. There is no specific upper or lower age limit for treatment.6
Sublingual immunotherapy is an alternative method of desensitisation, however it is currently not widely used outside
Europe.
Table 1: Common medications used for seasonal allergic rhinitis
Notes:
- Medications are ordered based on efficacy and adverse effects, however cost and patient preference are also important
factors in choice of medicine.
- For pregnant or breastfeeding women use intranasal corticosteroid first-line (e.g. budesonide), if not tolerated or
additional treatment is required, prescribe an oral antihistamine (e.g. loratadine), also consider the use of saline
nasal spray as a “drug-free” alternative.5
|
Adults |
Pregnant/breastfeeding |
Children |
Intranasal antihistamines |
Azelastine 0.14 mg/spray, one spray per nostril, twice daily (Azep )
Levocabastine 0.5 mg/mL, two sprays per nostril, twice daily (Livostin ) |
Azelastine – B3
Levocabastine – B3 |
From age five years: Azelastine 0.14 mg/spray, one spray per nostril, twice daily (Azep
) |
Oral antihistamines |
Loratadine 10 mg once daily (Loraclear Hayfever Relief )
Fexofenadine 120–180 mg once daily (Telfast )
Cetirizine 5–20 mg once daily (Zetop ) (sedating above 10 mg daily) |
Loratadine – B1
Cetirizine – B2
Fexofenadine – B2 |
From age two years:
Loratadine 1 mg/mL, 5 mL once daily (age >6 years, 10 mL) (LoraPaed )
From age two years:
Cetirizine 1 mg/mL, 5 mL once daily (age >6 years, 10 mL) (Cetirizine AFT ) |
Intranasal corticosteroids |
Fluticasone 50–100 mcg/nostril once daily (Flixonase, Nasaclear )
Triamcinolone 55 mcg/nostril twice daily (Telnase )
Beclomethasone 50–100 mcg/nostril twice daily (Alanase )
Budesonide 50–100 mcg/nostril once daily (Butacort Aqueous ) |
Budesonide – A
Beclomethasone – B3
Fluticasone – B3 |
From age 12 years: Fluticasone 50 mcg/nostril once daily (Flixonase, Nasaclear )
From age six years: Budesonide 50 mcg/nostril once daily (Butacort Aqueous ) |
Intranasal decongestants |
Xylometazoline 0.1%, one spray/nostril two to four times per day, maximum five days (Otrivin
spray or drops )
Oxymetazoline 0.5 mg/mL (Drixine ) |
Xylometazoline
Not recommended unless benefit outweighs risk (Category C) |
Xylometazoline 0.05%, one spray/nostril two to three times per day, max five days (Otrivin
Junior spray or drops ) |
Oral corticosteroid |
Prednisone 20–40 mg once daily for five to seven days |
Prednisone – A |
Prednisone 10 mg once daily for five to seven days |
Intranasal anticholinergic |
Ipratropium bromide 0.03% two sprays, two to three times daily
(Apo-Ipravent ) |
Ipratropium bromide – B1 |
From age 12 years: Ipratropium bromide 0.03% two sprays, two to three times daily
(Apo-Ipravent ) |
Intranasal sodium cromoglycate |
Sodium cromoglycate Nasal Spray 4%, one spray/nostril two to four times per day |
Sodium cromoglycate – A |
From age six years: Sodium cromoglycate Nasal Spray 4%, one spray/nostril two to four times
per day |
Ocular antihistamines |
Levocabastine, one drop per eye, three times per day (Livostin eye drops
)
Lodoxamide, one drop per eye, four times per day (Lomide )
Olopatadine, one drop per eye, two times per day (Patanol )
Ketotifen, one drop per eye, two times per day (Zaditen )
Naphazoline + pheniramine (Visine, Naphcon-A )
Antazoline + naphazoline (Albalon-A )
N.B. naphazoline can cause rebound hypaeremia (redness) if used for longer than ten days |
Lodoxamide – B1
Olopatadine – B1
Ketotifen – B1
Levocabastine – B3 |
From age six years: Levocabastine, one drop per eye, three times per day (Livostin eye
drops )
From age four years: Lodoxamide, one drop per eye, four times per day (Lomide )
From age three years: Olopatadine, one drop per eye, two times per day (Patanol )
From age three years: Ketotifen, one drop per eye, two times per day (Zaditen ) |
Australian Drug Evaluation Committee classification of drugs in pregnancy (summarised)11
Category A |
No evidence of harmful effects to the human foetus. |
Category B1 |
No evidence of harmful effects to the human foetus observed, but limited number of human studies.
Animal studies have shown no increased risk of foetal harm. |
Category B2 |
No evidence of harmful effects to the human foetus observed, but limited number of human or animal
studies. |
Category B3 |
No evidence of harmful effects to the human foetus observed, but limited number of human studies.
Animal studies have shown evidence of increased risk of foetal harm, the significance of which is uncertain in humans. |
Category C |
May cause, or may be suspected of causing, harmful effects on the human foetus or neonate without
causing malformations. Drug should only be used if benefit outweighs risk |
= Fully subsidised, = Partly subsidised, =
Not subsidised