When my eldest son
started pre-school, the highly regulated environment provided me with confidence
in its ability to reduce risk and respond to an instance of food-related
anaphylaxis. The pre-school teachers knew exactly what role they had to play in
the response plan. The less regulated primary school environment highlighted, to
me, the importance of preventing, planning and responding to anaphylaxis in the
school setting.
Severe food allergies are a part of everyday life and severe peanut
allergies affect between 0.25% and 3% of children. Peanuts and tree nuts are the
most common foods associated with food related anaphylaxis and death during
childhood, with one EpiPen being given to every 544 children under the age of 10
years. The number of children affected, and the potential severity of
anaphylaxis, emphasises the importance of having a well-planned prevention
strategy for food related anaphylaxis at school.
There are a number of guidelines that are currently available (listed in
Further Reading) which describe fundamental principles such as communication,
information sharing and responsibilities of school staff and parents/carers of
the students. These generic documents alone however, are insufficient for
schools. Instead, schools need to develop their own specific anaphylaxis
management plan (in the form of protocols/detailed plans) which takes into
account the size of the school, the staff and the available facilities. School
specific management plans should detail step-by-step processes for all school
staff responding to a case of anaphylaxis.
Management plans that cover prevention and responding to food related
anaphylaxis provide the opportunity to ensure that all necessary support is in
place throughout the school. Staff and school communities can feel increasingly
confident in the school’s ability to deal with incidents involving
anaphylaxis. Also, such procedures will put in place safer working conditions
that are consistent with relevant state occupational health and safety
legislation.
Preventing an event generally involves targeting it from a number of angles.
Preventing anaphylaxis is no different. This involves identifying and targeting
the groups of individuals who may be responsible for preventing and responding
to anaphylaxis: that is, parents, the school itself and the wider school
community. Parental responsibilities
Parents play a vital role in preventing anaphylaxis by providing the school with
all the necessary documentation and medical information about their
child’s condition. It is the responsibility of parents to provide
medically-approved instructions to the school once their child has been
diagnosed with a severe food allergy. Parents are also responsible for providing
an unexpired EpiPen while their child is at school as well as educating their
child(ren) about general avoidance measures such as never sharing food with
other children. Community awareness One of
the major components of any prevention strategy is awareness by the wider
community in which a child exists. Within the school setting, the community can
be represented by the other parents and students at the school. Anaphylaxis
should not be an issue about privacy. Rather, the more people who are aware of
the child’s allergic condition, the safer the child’s environment.
Initiatives that will increase community awareness can be taken by the
school or parents. These may include some or all of the following:
• Education about anaphylaxis should routinely take place
in situations where parents attend general information sessions about the
school; • Distributing letters to parents
identifying students in the class who have been diagnosed with food-related
anaphylaxis. They also present ideal opportunities in which to request parents
of other students to refrain from taking, for example, peanut products to school
(my experience is that almost all parents are happy to comply);
• Providing safe catering for birthday parties by
including food alternatives for children with food-related anaphylaxis. Also,
parents of the affected child could provide safe alternative suggestions for
food; • Placing a photograph of each student who is
diagnosed with a severe allergy near the medication in the classroom. Medication
should be centrally located in a bag/cupboard. Students should always have their
personal EpiPen close by; • Ensuring that any
replacement teacher is aware of the bag/cupboard, its contents, children with
severe allergies and relevant procedures to be implemented, if necessary; and • Schools providing parents of children with severe
allergies, information about products such as the ‘Medic Alert’
bracelet or disc. Vinyl name stickers (for books and accessories taken to
school) are now available with a ‘no peanut’ symbol (see Further
Reading). School responsibilities: reducing risk
The school’s responsibility in preventing anaphylaxis can be best
described as a two tier system. The first tier involves implementing school-wide
strategies that minimise a child’s risk of coming into contact with
peanuts at school. This can be achieved in a number of ways i.e. increasing
community awareness (discussed above) and minimising the risk of exposure to
peanuts.
Some schools have decided to become ‘peanut free zones’, which
means that foods containing peanuts cannot be brought from home or sold in the
school canteen. This approach could minimise, but does not eliminate, the risk
of peanut related anaphylaxis occurring at school. Notably, peanut free schools
are not endorsed by organisations such as the Australian Society of Clinical
Immunology and Allergy (ASCIA) (perhaps because of the practical difficulty of
monitoring what children bring to school), whereas peanut free canteens are
recommended, as the products sold can be easily managed.
Canteens are an important part of a school and should be considered as an
important part of the prevention process by contributing to the overall risk
reduction strategy. Suggestions for achieving this might include:
• Placing a list (including photographs) of all children
who are known to have severe food-related allergies in the canteen;
• Clear labelling of food related allergies on the
lunch-order bag; and • Flagging products with known
allergens on the canteen list. School responsibilities:
responding to anaphylaxis The second tier involves the
responsibility that lies with the school in responding to a case of anaphylaxis.
This can best be determined by assessing how well a school, as a whole, is
prepared for such a situation.
A detailed management plan, which is specific to the school, will assist to
instil confidence in staff and increase the chances of a best possible outcome.
A last minute search for a mobile phone, an EpiPen that is not easily
accessible, a phone that has not been recharged or expired medication can
contribute to delays, furthering the panic and increasing the risk of a
fatality. Teachers, who are generally not medically trained, should be provided
with as many clear guidelines and given the confidence of a plan that maximises
a positive outcome for the student.
Responses must therefore be carefully considered and individually tailored
for each school. They may include some or all of the following:
• EpiPen training for staff represents a fundamental
component to the response process, and for this reason, it is imperative that
staff undertake regular training in small groups; •
Implementing a school response which involves a number of staff members and the
sharing of responsibility (including administration staff). For example,
response plans should allocate responsibility to staff guiding the paramedics to
the student, to call the parents and (if applicable) contact the first aid
officer to offer additional support to the student and teacher;
• Mobile phones and/or landline telephones must always be
available for a teacher’s use in the classroom;
• Teachers who are on yard duty should carry a
‘back up’ EpiPen (a generic EpiPen that is not prescribed to any
student) and a charged mobile phone. Once the student is identified, the teacher
can administer the (back-up) EpiPen. The staff member should also make the 000
call (advising that a student has experienced anaphylaxis/severe allergic
reaction) and advise reception of the situation; •
A ‘unique’ telephone number could be used to call reception,
avoiding being placed on hold (as is the case with some schools); and
• Any medically qualified staff member/first aid officer
should always be accessible via mobile phone to other staff members including
reception staff.
Other situations the school should consider include children attending
before and after school care. As the school is ultimately responsible, it
must ensure it is satisfied that staff has been adequately trained, even if this
responsibility has been contracted to an external organisation.
Additionally, children attending day excursions present another situation
where planning is important. Medication and instructions must remain with the
students at all times. A precautionary measure such as taking a minimum of two
EpiPens on an excursion is suggested. If one EpiPen is misfired, a back-up
EpiPen is available. Also, food taken on excursions must be clearly marked with
the student’s name and kept separately from other food taken on the
excursion. Clearly, there must be no sharing of food. A ‘feedback
loop’ can be implemented for the purposes of learning from experience.
After such an event, the staff members involved should, even with successful
outcomes, assess procedures and identify areas for improvement.
In conclusion This article is designed to make a
number of suggestions to assist schools in preventing and responding to
anaphylaxis. It is up to the individual schools to take the initiative to
develop their own management plan. It is also important not to forget that two
of the three deaths in the past five years have occurred within the school camp
setting. It is therefore also important to develop formal management/response
plans extending to camps and, most notably, those held in remote areas. In the
short term, anaphylaxis management protocols in the school setting must not be
overlooked as the first step in a vital process which helps maintain a high
standard of child safety. Further Reading
Anaphylaxis guidelines: A resource for managing severe allergies in Victorian
government schools (Victorian based document):
http://www.eduweb.vic.gov.au/edulibrary/public/stuman/wellbeing/Anaphylaxis_guidelines-v1.01b.pdf
Anaphylaxis: Guidelines for schools (NSW based document):
http://www.schools.nsw.edu.au/media/downloads/schoolsweb/studentsupport/studenthealth/aguidelines_v2.pdf
Australasian Society of Clinical Immunology and Allergy (ASCIA):
http://www.allergy.org.au/aer/infobulletins/posters/Anaphylaxis_plan_(child)_Au.pdf
http://www.medeserv.com.au/ascia/pospapers/anaphylaxis.htm Food
Allergy and Anaphylaxis Network
http://www.foodallergy.org/school.html)
http://www.foodallergy.org/school/childdescribe.pdf (anaphylaxis in a
child’s language) Guidelines for managing food allergies at camps:
http://www.foodallergy.org/downloads/CampGuidelines.pdf Medic Alert
bracelet: http://www.medicalert.com.au/ Identity Direct
http://www.identitydirect.com.au/index.html?lang=en-uk&target=d96.html&mid=30710 Lillian De Bortoli is a mother of three children with her eldest
son being diagnosed with a severe peanut allergy and asthma. She works at Monash
University and has completed a Master of Social Work research degree analysing
the public health framework as a basis for preventing child abuse.
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