
Stinging insect allergy / anaphylaxis
Version 10 February 2002
Introduction
Stings from ants, bees and wasps are common. Unfortunately, around
1 in 300 people are susceptible to severe allergic reactions to
stinging insects, and some will die. Identification of patients
at risk of anaphylaxis allows for the commencement of specific
immunotherapy.
Triggers
Allergic reactions to stings by bees, wasps, "jumper
ants" (and sometimes ticks) are most common in the warmer
months of the year. Jumper ants are large primitive ants, aggressive,
can sting through clothing and are prevalent in Black Mountain
reserve, the Botanic Gardens other areas around Canberra and south-eastern
Australia. The recent identification of the South American "Imported
Fire Ant" (Solenopsis richteri) in South Eastern Queensland
is of particular concern, as systemic reactions to stings occur
in up to 1 in 6 cases. As their venoms are all different, an allergic
reaction to one does not increase the risk of sensitivity to another.
Not all reactions are serious
Who is at risk of anaphylaxis?
Skin testing "out of interest" does not predict
risk; up to 1 in 5 in the community will have positive skin test
to bee venom yet most will not react clinically. Minor local reactions
are common and do not indicate a significant risk of anaphylaxis.
There is a common community perception that each reaction will
be worse than the one that precedes it. Long term followup studies
suggest the opposite. Less than 10 % of large local reactors ever
progress to anaphylaxis, immunotherapy is ineffective at reducing
the severity of local swellings and is not offered as a routine.
Patients with mild systemic reactions (such as urticaria alone) do not always need immunotherapy; less than 10 % will have worse reactions with subsequent stings. The prognosis is even better in young children who will usually "grow out of" their allergy after a few years. In patients with dangerous features, however, immunotherapy should be considered "compulsory" regardless of age. Anaphylactic shock after stings has been observed by the author in patients ranging from 3 years to 73 years.
Immunotherapy
is a worthwhile hassle for those at risk of anaphylaxis. Conventional
therapy involves starting at the equivalent dose of 1/1000 sting,
building to 2 stings per injection over a few months. Injections
are then continued monthly for about 18 months, then 6-8 weekly
thereafter for a total duration of 5 years, sometimes longer in
selected patients. This form of therapy is not trivial, and so
only those at risk are normally advised to commence treatment,
although special circumstances (eg. living or working in remote
areas, intercurrent cardiac disease) sometimes need to be taken
into account. A novel immunotherapy trial is being undertaken
by the author as part of a multinational study at John James Memorial
Hospital, aiming to increase the potency of treatment with fewer
visits.
Reducing the risk
Children allergic to venomous insects should be advised to
wear shoes when outside, and bee and wasp nests should be removed
from the vicinity of their home and school. While the effectiveness
of this approach remains unproven, the author recommends that
venom-sensitive subjects take prophylactic antihistamines if walking
in remote areas during the "active" insect season. One
of the author's patients has probably only survived an episode
of anaphylaxis after activating an emergency satellite beacon
when stung in the wilderness.
Management
Specific Immunotherapy
Immunotherapy is effective for the treatment of inhalant allergies
and honey-bee or wasp stings. The risk of a serious systemic allergic
reaction is reduced from approximately 65 % down to 5 % per sting.
Unfortunately, there is no vaccine available for the treatment
of "jumper ant" at this time. A pilot study is currently
being undertaken in Tasmania, and results will be of great interest
to the hundreds of patients for whom there is currently no specific
treatment.
Emergency Treatment of Anaphylaxis
Adrenaline is the only medication available for the emergency
treatment of anaphylaxis. It rapidly reduces mediator release
and their end organ impact. In an outpatient setting, it should
be administered intramuscularly. Subcutaneous injection
is associated with significantly delayed absorption and inhaled
adrenaline is ineffective. Intravenous adrenaline should only
be given by those experienced in its use, and even then only slowly
using 1/10,000 dilution.
Special Circumstances: Anaphylaxis in Schools
A recent South Australian study of over 4000 school-aged children
demonstrated that 1 in 170 children had suffered an episode of
anaphylaxis, and 1/6 episodes had occurred at school. Children
spend over a third of their waking hours at school and are totally
dependent on carers to provide a safe environment and administer
First Aid in an emergency. That is why the Australasian Society
for Clinical Immunology and Allergy recommends that: