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Allergic rhinitis: impact, diagnosis, treatment and

management /research/review-article/allergic-rhinitis-impact-diagnosis-treatment-and-
Clinical Pharmacist 9 AUG 2016 By Diana S Church , Martin K Church , Glenis K


Allergic rhinitis results from an immunological abnormality in which atopic individuals

produce immunoglobulin E (IgE) to allergens (e.g. pollen, house dust mites, animal dander
and moulds). IgE activates mast cells, which respond by releasing inflammatory mediators.
Histamine stimulates the early symptoms, predominately mucus production, nasal itching
and sneezing. Leukotrienes and cytokines attract and activate eosinophils to cause allergic
inflammation, which is primarily responsible for nasal blockage. When untreated, these
symptoms can potentially impair patients ability to sleep and perform optimally in their daily
professional or personal life. Childrens education is also particularly affected by untreated
symptoms. Treatment is primarily with second generation H1 -antihistamines, which are
particularly effective against the early symptoms, and intranasal corticosteroids, which
reduce allergic inflammation and improve nasal blockage. First generation H1 -antihistamines
should be avoided because they exacerbate the psychogenic effects of allergic rhinitis. This
review article aims to provide pharmacists and other healthcare professionals with an
understanding of the impact of undiagnosed allergic rhinitis and how to diagnose and treat it

Keywords: allergy, allergens, allergic rhinitis, antihistamine, corticosteroids, histamine,

immunology, inflammation, pollen.

Original submitted: 10 June 2016; Revised submitted: 29 June 2016; Accepted for
publication: 04 July 2016; Published online: 09 August 2016

Source: CNRI / Science Photo Library

Caused by an allergy to pollen, this inflamed mucosa shows its ciliated (hairy) surface overgrown in
patches. Cilia are common on the epithelium of the respiratory tract, where their beating serves to remove
particles of dust, pollen, and other foreign material. Here, an allergy to pollen has resulted in the cilia

Key points:
Allergic rhinitis occurs in atopic individuals who produce IgE to allergens, such as pollen, house dust
mites, animal dander and moulds.
Histamine stimulates the early symptoms, predominately mucus production, nasal itching and sneezing.
This may respond well to non-sedating H1 -antihistamines.

Subsequent allergic inflammation gives rise to nasal blockage. This responds to nasal steroids.
When untreated, allergic rhinitis can potentially impair patients ability to sleep and perform optimally in
their daily professional or personal life. Childrens education is also particularly affected.
First generation H1 -antihistamines should be avoided because they exacerbate the psychogenic effects
of allergic rhinitis.


Allergic rhinitis is a common allergic disease with increasing prevalence; recent estimates suggest it affects over
30% of individuals, particularly, but not exclusively, teenagers and young adults [1],[2]. While considered by many as
a trivial disease, allergic rhinitis, in addition to the nasal and ocular symptoms, is crucially linked to impairments in
information processing and changes in attention-related cognitive processes[3]. However, it has been estimated that
up to 90% of allergic rhinitis patients are untreated, insufficiently treated or inappropriately treated [4]. This has the
potential to impair patients ability to perform optimally in their daily professional and personal life.

Pathological and psychological effects of untreated allergic rhinitis

Allergic rhinitis generally develops during childhood and it is the most common chronic allergic disorder seen in
children[5]. Studies have shown that these children can experience significant impairment through multiple physical
and psychological aspects. Their symptoms, particularly a runny nose, mean that children are often embarrassed in
school, have decreased social interaction and are at double the risk of accidental injury[5],[6]. Nasal congestion, in
particular, is associated with sleep disturbance and resultant daytime fatigue[7]. Two studies have concluded that
untreated allergic rhinitis has a marked detrimental effect on childrens learning and examination performance[8],[9].
This is particularly important considering that a quarter of UK school-age children suffer with allergic rhinitis[10], most
of whom will have their peak symptoms in spring and summer, which can coincide with important school
examinations. The correlation between allergic rhinitis and negative effects on learning should be an area of
concern for all professionals involved in their care.

The overall quality of life reduction resulting from allergic rhinitis in adults is well established it has a detrimental
effect on adult cognitive processes (e.g. productivity at work), as well as other common attention-requiring activities,
such as driving[4],[11],[12]. In a study assessing the effect of nasal allergen provocation of seasonal allergic patients
on driving performance, it was demonstrated that symptomatic and untreated patients had significantly impaired
driving ability, the magnitude of which was comparable to having a blood alcohol level of 0.05%, the legal limit in
many countries[13]. In addition to acute symptoms, sleep disturbances may exacerbate impairment of psychomotor
performance, including driving [14],[15],[16],[17]. Patients with allergic rhinitis are often affected by physical conditions
(e.g. otitis media, eustachian tube dysfunction, sinusitis[18]) and other allergic conditions (e.g. asthma and
eczema[19]). Therefore, allergic rhinitis is an illness that affects multiple aspects of patients life [19], can be a source
of multiple doctor appointments and has complex effects on society as a whole. Therefore, optimal management of
the disease should address both its physical and mental consequences.

Mechanisms of allergic rhinitis

The roots of allergy are in parasitology, when a nematode parasite attacking the nasal mucosa. On first
presentation, the immune system is stimulated to produce immunoglobulin E (IgE) that will bind to and prime mast
cells and other inflammatory cells. On a subsequent presentation, nematode antigens interact with the mast cell
IgE, causing it to release preformed histamine to make the local environment hostile (e.g. producing mucus and
stimulating sensory nerves to cause sneezing). Mast cells also produce cytokines to stimulate the influx
inflammatory cells, particularly eosinophils that contain several toxic proteins with which they kill the nematode and
cause local inflammation. Patients with allergies mount the same response to allergens as nematode
antigens[20],[21]. The series of early immune system events in patients with allergic rhinitis is presented in Figure 1.

Figure 1: Immune system events in patients with allergic rhinitis
Panel A demonstrates early immune system events, while panel B shows the later inflammatory allergic
response that increases the severity and persistence of the initial symptoms in patients with allergic rhinitis.
See text for an explanation of the events (numbered).

Panel A demonstrates (1) allergens (e.g. pollen, house dust mites, animal dander and moulds) penetrating the nasal
epithelium. (2) Allergen interacts with IgE, shown in red, to activate the mast cell. (3) Histamine is the primary
mediator released in this early phase of the response. It has three immediate main effects: (4) stimulation of
mucosal goblet cells to produce watery mucus; (5) stimulation of sensory nerves to cause nasal itching and
sneezing; and (6) vasodilation and tissue oedema, which contribute to nasal blockage. These effects are primarily
histamine-mediated so antihistamines are effective in relieving these symptoms.

Panel B shows the later inflammatory allergic response that increases the severity and persistence of the initial
symptoms, resulting in a chronic phase of allergic rhinitis. Mast cell activation also produces cytokines, responsible
for the attraction of more mast cells and the influx and activation of other inflammatory cells, particularly eosinophils
(7)[22]. Eosinophils contain aggressive proteinaceous mediators (8) that stimulate sensory neurones to dramatically
increase the production and release of neuropeptides (9). These neuropeptides act on special venous capacitance
vessels (10) present in the nasal turbinates, causing dilatation and reduced emptying. This is the primary cause of
nasal blockage.

Mechanisms of ocular symptoms

Patients with allergic rhinitis may also experience ocular symptoms, primarily reddened, itchy and watery eyes.
Classically these symptoms were believed to be caused by the allergen landing on the conjunctival lining of the eye,
with subsequent activation of the conjunctival mast cells[23]. It is now believed that these symptoms are partly the
result of a naso-ocular reflex in which allergic inflammation in the nose stimulates the trigeminal nerve with
subsequent release of neuropeptides in the tears[24]. These neuropeptides activate conjunctival mast cells that
release histamine but cause little subsequent eosinophil infiltration and allergic inflammation[23]. During periods of
high atmospheric levels, pollen impaction on the conjunctiva may induce a more severe form of vernal conjunctivitis
in which eosinophil infiltration stimulated allergic inflammation[25]. If a severe form of vernal conjunctivitis is
suspected, the patient should be referred to their GP.

Diagnosis of allergic rhinitis by pharmacists

Historically, diagnosis of allergic rhinitis has been made by primary healthcare practitioners. However, pharmacists
are now being encouraged to make the primary diagnosis of allergic rhinitis and establish a management and
therapy plan[26]. Although it should be emphasised that complex cases, or cases where there may by an alternative
diagnosis, should always be referred to a GP.

Allergic rhinitis symptoms, including runny nose, itching, sneezing and nasal blockage, are similar to those of the
common cold and can be present intermittently, giving the false suggestion of recurrent colds[27]. This is more
common in patients who are allergic to pollens or outdoor moulds (rather than pets or house dust mites), which are
released into the air and cause symptoms during specific periods of time throughout the year (see Figure 2:
Seasonal considerations).

Taking a history from the patient

When questioning the patient, pharmacists should listen for indicators that can lead to the diagnosis of allergic
rhinitis, for example:

recurrence at a particular time of year or day, or variability of symptoms, suggesting worsening on exposure to
the relevant allergen;
involvement of the eyes (itching, watering, redness, puffiness); or
predominance of itch as a symptom, which can also involve the pharynx and ears.
Allergic rhinitis is more likely if there is a past or family history of allergic disease, but can also occur as the
first manifestation of allergy in a previously unaffected person.

When taking the patients history, it is important to be aware that they might not often offer all the clues for diagnosis,
so pharmacists may have to ask specific questions to find out more information. For example, a patient with allergy
to house dust mites or animals may complain of sneezing, having a runny nose and blocked nose in the past one or
two weeks, but they might not realise until asked that their nose has been blocked to a less severe degree for a
much longer time. The pharmacist should also enquire about new allergens in the home, work, or school
environment, as well as symptoms of asthma (shortness of breath accompanied by wheeze, reduced exercise
tolerance or nocturnal symptoms), which often accompany poorly controlled allergic rhinitis.

Seasonal considerations
Patients may be allergic to trees, plants and fungi that use the wind
to disperse their pollen or spores[28]. Higher amounts of pollens are
released during dry, warmer days when the chance of their
satisfactory dispersion is maximum (see Figure 2). Visually these
plants are unspectacular in contrast to those with colourful flowers
to attract bees and other insects to cross-pollinate them. Individuals
are rarely allergic to this latter type[28].

While high amounts of pollen and fungal spores are released during
warmer days compared to colder ones, house dust mite allergens
are present all year round. However, these tend to be higher
indoors during winter when windows are shut and the humid,
centrally heated atmosphere is optimum for their reproduction[29].

Further testing
With a clear patient history, diagnosis can be made without further
Figure 2: The seasons of major plant
tests. However, if in doubt, looking for the likely IgE molecules by
allergens and house dust mite
skin prick or blood test can be helpful, although this should be
The lines refer to the times of year at which different guided by history, rather than performed in a random fashion.
allergens peak. Note that house dust mite levels are Random screening of multiple possible allergens is inadvisable
highest in the winter when doors and windows are because positive tests do not always indicate clinical disease;
closed in centrally heated homes.
many individuals with allergen-specific IgE do not develop
symptoms[30]. Furthermore, a positive test to an allergen with no pertinence to patients history has no relevance for
diagnosis and might result in over-diagnosis and unnecessary stress for the patient. Testing should always be
considered in the context of the possible clinical benefit, which can be from allergen avoidance, if the patient is able
and willing to comply, or allergen specific immunotherapy.

This section assesses the drugs only briefly further information and the British Society for Allergy & Clinical
Immunology (BSACI) guidelines for the management of allergic and non-allergic rhinitis[31] are included in later

H1 -antihistamines are effective in relieving histamine-induced symptoms, including itch, runny nose and/or
sneezing[31]. They have a lesser effect on nasal blockage but can be effective as a single medicine in patients with
mild to moderate forms of allergic rhinitis[31]. They have a rapid onset of action and can be used as a rescue
medicine to help alleviate the symptoms of the onset of acute allergic rhinitis.

Intranasal corticosteroids are the primary treatment for nasal obstruction[31] and act by reducing cytokine
production thereby reducing eosinophil recruitment. They also reduce eosinophil activation and mediator release[32].

Leukotriene receptor antagonists (LTRAs) are given as tablets and may be effective in some patients but not
all[33]. They reduce the effects of the leukotriene C4 (LTC4) that activated mast cells and eosinophils secrete in
order to enhance the recruitment of more eosinophils and thereby reduce allergic inflammation[34]. The LTRAs
montelukast and zafirlukast are available on medical prescription only (POM). Leukotriene synthesis inhibitors (e.g.
zileuton), are not available in the UK.

Nasal decongestants (e.g. xylometazoline and oxymetazoline), are asympathetic receptor stimulants and cause
constriction of the arterial vessels delivering blood to the nasal capacitance vessels, therefore starving them of
blood[35]. They may be given locally or orally. When given as nasal drops, they are briefly effective and rapidly
acting but they may only be used for short periods usually four to ten days[31]. Regular use induces a decrease in
the number of a-receptors in the blood vessels rendering a reduced effectiveness with time (tolerance)[35]. If used
for longer periods, rhinitis medicamentosa, a condition characterised by nasal congestion without rhinorrhoea or
sneezing, may occur because of a reduction of blood vessel a-receptors thus paralysing the physiological local
vasoconstriction process[7]. Patients should be counselled regarding this process.

Oral decongestants (e.g. pseudoephedrine) are only weakly effective in reducing nasal obstruction but have a
longer duration of up to six hours (with slow release preparations)[31]. Owing to their sympathomimetic effects, they
should not be used by individuals with high blood pressure or heart problems[36].

Saline douching, although relatively uncommon in UK, is a safe and inexpensive method of reducing symptoms in
children and adults with seasonal rhinitis by washing out sticky mucus from the nose[31].

The treatment of ocular symptoms of allergic rhinitis is summarised in Box 1.

Box 1: Treatment of ocular symptoms

1. Intranasal corticosteroids are the most effective treatment for reducing nasal inflammation and,
consequently, are effective in improving conjunctival symptoms[37].
2. H1-antihistamine eye drops have a similar efficacy profile to oral antihistamines with the advantage of a
significantly faster onset of action[38].
3. Topical chromones, sodium cromoglycate or nedocromil sodium, which are available as topical eye
preparations, are also weakly effective. Although purported to be mast cell stabilisers, they most likely
affect the inhibition of sensory nerve activation, thereby reducing itching[39].

Selecting the right treatment

Oral antihistamines are the first-line treatment used by most patients, doctors and pharmacists for all allergic rhinitis.

When selecting the most appropriate antihistamine to manage allergic rhinitis, healthcare professionals should be
aware of the significant detrimental effect of first generation antihistamines (FGAH) on cognitive processes in all
patient groups[40]. Histamine acting on H 1 -receptors in the brain has a completely different function to that in the
periphery. In the brain, it has an arousal effect and aids concentration and learning[40]. FGAHs (e.g.
chlorpheniramine, diphenhydramine, hydroxyzine and ketotifen) readily penetrate into the central nervous system
(CNS) and bind to the H1 -receptors in the brain, causing drowsiness and poor attention [40].

Studies in children have demonstrated that FGAHs exacerbate the detrimental effect of allergic rhinitis on learning
ability[8]. Furthermore, in teenagers sitting summer mock GCSE examinations, untreated allergic rhinitis caused a
40% increased likelihood of students dropping an examination grade. FGAHs increased this to 70%[9].

In adults the detrimental effects of allergic rhinitis on quality of life and productivity at work are exacerbated by
FGAHs, even at the lowest doses recommended by manufacturers[40]. The effects of FGAHs on the CNS are similar
to and additive with those produced by alcohol or other CNS-sedatives, and bedtime dosing with FGAHs may have
hangover effects the next day due to their long elimination half-life value[40]. Furthermore, FGAHs may significantly
reduce driving ability to potentially dangerous levels [40],[41], particularly in the elderly and those who combine the
drug with alcohol ingestion. One study suggests that 25% of individuals older than 65 years of age have some
cognitive impairment, often with no overt sign of dysfunction[42]. Administration of FGAHs to this population
increases the risk of inattention, disorganised speech, altered consciousness and impaired function or
alertness[43],[44]. In addition, because of their anticholinergic activity, FGAHs significantly increase the risk for
development of dementia[45].

Therefore, the British and European Guidelines for both allergic rhinitis and urticaria specify that only second
generation antihistamines should be used for symptom relief, because they penetrate less well into the brain than
FGAHs and have negligible anticholinergic effects[31],[46]. In the UK, cetirizine and loratadine are currently the only
SGAHs available for patients to buy over-the-counter (OTC). There are many others (including levocetirizine,
desloratadine, rupatadine, fexofenadine and bilastine) that are available as prescription-only medicines (POM).
Even though SGAHs are stated to be minimally sedating, there are some patients who suffer sedation and
psychomotor retardation, especially if other sedatives or alcohol are taken concomitantly[40]. Fexofenadine and
bilastine are the least sedating SGAHs currently available because they are actively pumped out of the bloodbrain
barrier by p-glycoprotein (a proton pump)[47]. However, these must be taken on an empty stomach for adequate

Intranasal antihistamines are more effective at reducing nasal symptoms than oral antihistamines, but do not treat
extra-nasal symptoms[48]. Azelastine nasal spray is available OTC.

Although antihistamines demonstrate efficacy, for the control of symptoms like sneezing, itching and rhinorrhoea or
eye streaming, they are considerably less effective than intranasal corticosteroids that have a much stronger anti-
inflammatory effect and are more effective in treating nasal obstruction[49]. Corticosteroids should be used as the
therapeutic of choice for anything more than mild disease [31].

Intranasal steroids
Intranasal steroids are the most effective treatment for reducing nasal inflammation and improving conjunctival
symptoms[23],[50]. In the UK, beclomethasone dipropionate and fluticasone propionate are available OTC, while
fluticasone furoate and mometasone furoate are POM.

When bought OTC or even when prescribed by a medical practitioner, nasal steroids are often wrongly used or not
used at all, because of fears of steroids. Therefore, it is important to explain to the patient that the dose of nasal
steroids is in microgram quantities and for most of the common molecules there is minimal systemic bioavailability
(i.e. the amount of active drug reaching the systemic circulation). There is a variation between molecules, with
fluticasone propionate, furoate and mometasone furoate being the least bioavailable from the nose. It is best to use
the spray in the morning, putting it next to the toothbrush to aid memory. A second dose can be used in the evening if
needed, or if the morning one was forgotten.

The method of application for nasal sprays and drops is shown in Figure 3. Spraying the nasal septum and sniffing
the spray straight back into the throat should be avoided.

Figure 3: Method of application for nasal sprays and nasal drops

Source: Reproduced from the BSACI allergic rhinitis guidelines with permission.

(a) Correct procedure for the application of nasal sprays. (b) Correct procedure for the installation of nasal

Begin treatment early and take it daily

It is important to inform patients that nasal steroids do not work immediately. Nasal steroids have been shown to
take at least several days to reach full effectiveness and maximal effect may not be apparent for two weeks[29].

For patients with intermittent symptoms (e.g. those allergic to pollens) it has been demonstrated that if therapy with
topical nasal corticosteroids is begun a week or two before symptoms are expected, symptoms have delayed onset
and reduced severity[51]. Thus, it can be useful to ask patients with known seasonal allergic rhinitis to make a note
of when their symptoms started in the current year so that in the following year they can start the treatment earlier.

Similarly, both antihistamines and nasal corticosteroids, particularly the latter, are more effective if used on a daily
basis, rather than being stopped and started[51]. The symptoms for both persistent and intermittent allergic rhinitis
are underlined by an ongoing inflammation that is usually present at subclinical levels, even in the absence of
symptoms[52]. Daily treatment helps to prevent this low-grade ongoing subclinical allergic inflammation in the nasal
lining increasing to a threshold at which symptoms occur and, thus, reduces the rate and severity of
exacerbations[51]. Therefore, pharmacists should explain to patients that the drug makes them free of symptoms,
rather than curing their disease, so stopping treatment early will result in the reappearance of symptoms. If they do
not get relief from the prescribed medication, they should seek further advice since other treatment options might be
A simple way to keep track of patients symptoms is for them to use the MACVIA-ARIA visual analogue scale, via a
mobile phone app[53]. If their total symptom score is over half way along the line, the treatment needs to be
augmented or changed. Switching from one brand of antihistamine or intranasal corticosteroid to another is not the

BSACI guidelines suggest that in more severe disease nasal corticosteroids and antihistamines may be used
together[31] and the combination of nasal corticosteroid plus nasal antihistamine (e.g. azelastine plus fluticasone)
has been reported to be more effective than either alone[54],[55]. However, this drug combination is a POM at

Management of allergic rhinitis

The BSACI guidelines provide direction to help healthcare professionals direct therapy for allergic rhinitis[31]. A
simple algorithm for the treatment of allergic rhinitis is shown in Figure 4.

Figure 4: A simple algorithm for the treatment of allergic rhinitis

Source: This figure is adapted from the BSACI allergic rhinitis guidelines.

The progression of treatment goes from left to right as severity increases.

For patients with intermittent allergic rhinitis caused by seasonal allergens, as the season wanes and pollen levels
in the atmosphere reduce, treatment can be gradually reduced, if the symptoms are completely controlled, and
stopped once the season is over.

Patients with persistent allergic rhinitis, such as those allergic to perennial allergens (e.g. house dust mite, animals
or indoor moulds) or those with mixed seasonal and perennial allergies, need longer term therapy. Once complete
control of symptoms has been achieved, a gradual step down can be attempted. The treatment should be
continued for at least three to six months after complete symptom control. If symptoms recur, the treatment should
be restarted, usually for longer periods (e.g. 612 months or even for life). There are some concerns about possible
lining atrophy with long-term use of intranasal steroids. However, in practice, with correct use this does not occur,
probably because of rapid movement by mucocilliary clearance[56]. Spraying the nasal septum repeatedly can result
in soreness, epistaxis (nose bleed) and possibly even perforation, which is why correct technique is important.

Allergen avoidance

Studies involving concomitant multiple strict allergen control measures showed that it is possible to achieve a
significant reduction in allergen exposure and, consequently, in symptoms[57],[58]. However, in real life situations,
avoiding aeroallergens to an extent where it would make a difference in patients symptoms is difficult to reach. With
pollen allergy, closing windows at night, driving with closed windows or wearing wrap-around glasses outdoors can
prevent symptom exacerbation[31]. Avoiding being outside during thunderstorms can also help reduce symptoms,
because the sudden change from a dry to a wet climate causes pollen grains to rupture and release their allergenic
into smaller particles, which can be easily inhaled into the lower airways and cause attacks of allergic rhinitis and

Allergen-specific immunotherapy is the treatment in which a patients immune system is rendered tolerant to an
allergen by giving increasing doses of the allergen in a controlled fashion[60],[61]. When used correctly, it is the only
treatment that can alter disease course[60]. There is also evidence that it can reduce development of further
sensitisations and progression of allergic rhinitis to asthma, although current trials require positive outcomes to
determine if children with allergic rhinitis, who are likely to progress to asthma, will benefit from it [61].

Few seasonal allergic rhinitis patients warrant immunotherapy treatment; it should only be considered when allergic
rhinitis is debilitating and poorly controlled by pharmacotherapy. Special consideration should be given to badly
affected young people who face years of summertime examinations or adults whose functioning is disturbed (e.g.
surgeons who have severe eye symptoms or sneezing bouts)[61]. Immunotherapy is currently available for allergic
rhinitis caused by pollen, moulds, house dust mite and animal allergens.

There are two main routes by which immunotherapy is administered; subcutaneously and sublingually.
Subcutaneous immunotherapy involves allergen injections at regular time intervals in a hospital by trained medical
staff. With treatment lasting several years, patient commitment to attending hospital appointments is essential.
Sublingual immunotherapy is considered to be much safer. The initial dose is given under supervision, but can then
be continued on a daily basis at home[62],[63]. However, patients should be warned against poor compliance, which
is a concern with this form of immunotherapy[64].

Management in specific patient groups

Children with allergic rhinitis

Children metabolise drugs less well than adults because the liver enzymes mature slowly and only reach maximal
levels at around ten years of age[65]. However, renal clearance is well developed. Consequently, it is preferable that
young children are prescribed an antihistamine that is not metabolised but excreted unchanged in the urine[66]. Of
the OTC preparations, this means cetirizine is preferable, rather than loratadine.

A nasal steroid with low systemic bioavailability should be used at the lowest possible dose to control symptoms,
particularly nasal congestion and obstruction. Compliance and efficacy is improved if the child is taught how to use
the nasal spray[31]. In older children where liver metabolic enzymes are increasing, it may be preferable to use
fluticasone, which is cleared by first metabolism, rather than beclomethasone that is not and, consequently, may
accumulate [67]. Furthermore, fluticasone is available for children from four years of age, while beclomethasone is
only available for children from six years of age.

Allergic rhinitis in pregnancy

Most medicines cross the placenta, and should only be prescribed when the apparent benefit is greater than the risk
to the foetus[31]. Regular nasal douching may be helpful. Of the antihistamines, both loratadine and cetirizine are
recommended because they appear to have good safety records because they have been widely used in pregnant
women[68]. Similarly, beclomethasone and fluticasone appear safe. However, decongestants should be avoided [31].
Local application of chromones, which have not demonstrated teratogenic effects in animals, are probably the safest
drug choice for use in the first three months of pregnancy because systemic absorption is negligible, although they
require multiple daily administrations[31].

The treatment of allergic rhinitis involves non-sedating H 1 -antihistamines to reduce rhinorrhoea and nasal itching,
and corticosteroids to reduce allergic inflammation and nasal blockage. They should be used on a daily basis rather
than on ad hoc when symptoms are bad. Pharmacists should advise patients about how to correctly administer their
treatment, as well as reviewing its effectiveness regularly. Patients should be advised of alternative treatment
options where appropriate.

Financial and conflicts of interests dislosure:

Martin Church has been a speaker or consultant for Almirall, FAES Pharma, Menarini, Moxie, MSD, Novartis,
UCB Pharma, Sanofi-Aventis and Uriach. Glenis Scadding has had research grants from GSK & ALK and has
been a speaker or consultant for ALK, Astra Zeneca, Brittania Pharmaceuticals, Capnia, Church & Dwight,
Circassia, GSK, Groupo Uriach, Meda, Merck, MSD, Ono Pharmaceuticals, Oxford Therapeutics, Sanofi-
Aventis, UCB. Diana Church has no relevant affiliations or financial involvement with any organisation or entity
with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript
apart from those disclosed. No writing assistance was utilised in the production of this manuscript.

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Citation: Clinical Pharmacist, Vol 8, No 8, online | DOI: 10.1211/CP.2016.20201509

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