Introduction
Food allergy in children is common and has been increasing in prevalence during recent years.1–6 Specifically, anaphylaxis is a severe, life-threatening allergic reaction that must be recognised and treated promptly to avoid fatalities.1 7 First-line immediate treatment is intramuscular-injected adrenaline (epinephrine).7 Over the last 20 years, admissions to UK hospitals for food anaphylaxis have increased by 5.7% annually, with the greatest increases seen in children.3 Subsequently, prescriptions for adrenaline auto-injectors (AAIs) have increased by over 300%3 8 in recent years.
Children with food allergy in the UK are risk-assessed and prescribed AAIs in accordance with guidance published by the British Society of Allergy and Clinical Immunology.9 Patients prescribed AAIs are advised to carry two devices, ensuring a backup option is available in case the first pen misfires or a second dose of adrenaline is required.10 As anaphylaxis most commonly occurs at home and is closely followed by the school setting, four devices are usually dispensed (two devices for school, two devices for home/social emergency use).11 With up to 25% of children experiencing anaphylaxis for the first time while at school, the availability of AAIs in school could be lifesaving.1 11–17 Anaphylaxis at school mainly occurs in primary school-aged pupils, with nearly all reactions reportedly taking place in the classroom.1 5 6 Overall, anaphylaxis in children is under-recognised and undertreated.11 13 18–20 Anaphylaxis-related fatalities have also been reported within the school setting in the UK,21 further illustrating the importance of a comprehensive policy and set of guidelines to keep children safe.
Schools face several challenges in keeping food-allergic children safe while in their care.1 17 In 5% of anaphylaxis cases experienced at school, an allergy had not been communicated to staff by parents.1 Additionally, there are reported failures of parents to supply schools with AAIs when prescribed.1 Barriers to treatment in school include lack of staff education, staff fears regarding AAI administration/timing, as well as fears of inducing adverse reactions.6 19 20 22 23 Knowledge gaps in school staff in the identification and treatment of anaphylaxis has been repeatedly reported in the literature, with schools highlighting a greater need for education and training.6 19 20 23 24
The UK Department of Health (DoH) published guidelines for schools to advise on procedures for keeping allergic children safe, including recommendations on where and how to appropriately store AAIs and ensuring easy accessibility. For instance, AAIs must be within 5 min of reach from at-risk pupils and must not be stored in locked locations.21 Staff must be trained in the identification and treatment of anaphylaxis, ensuring annual AAI training is conducted in person and not substituted with online resources.13 21
The DoH guidelines additionally outline the 2017 ‘Spare Pens in Schools’ scheme, which resulted in a change to legislation allowing schools to purchase AAIs without prescription.21 25 These ‘spare pens’ are stock devices held by schools and are unassigned to named pupils. Stock devices can be used to treat anaphylaxis in any child with known allergies where the patient’s own device is; (1) out-of-date, (2) misfires, (3) is not in close vicinity (within 5 min). Spare pens can also be administered to children for whom AAIs have not been prescribed but who have an allergy action plan. Where children with no known allergies experience first-time anaphylaxis at school, emergency services should be contacted, stating access to a spare pen and advice taken from the call handler. Participation in the scheme is voluntary, with purchase costs and pharmacy-handling fees incurred by schools.
Similar stock-AAI schemes operate in the USA, with legislation in 45 states and seven states mandating stock devices.4 26–28 Emerging data shows that most anaphylactic reactions occurring in schools are treated with stock AAIs.4 12 In a review of stock-AAI use in Chicago schools, 55% were administered to children with first-time anaphylactic reactions with similar results reported in New York.4 16 Similarly, 45% of anaphylactic events occurring in schools in Australia are reportedly treated using generic devices.9 29 30 Where school protocols are in place, AAI administration by staff has been appropriately delivered.1 Where older children and adolescents are advised to carry their own AAIs, it has been reported that often devices had not been on their persons when they had needed them.1 31 Recommendations however are that adolescents carry their own AAIs, including while at school.13 21
To date, a single survey-based study has been conducted in Peterborough, UK investigating awareness of the scheme, with 11 of 74 regional schools participating.32 45% of participating schools reported awareness of the scheme, and 18% opted in. Data on the implementation of the scheme in the UK as a whole, and within the devolved nations specifically, has not been captured.
The current pilot study aimed to investigate awareness and implementation of the ‘Spare Pens in Schools’ scheme in a sample of Welsh schools, within Swansea and Pembrokeshire local authorities (LA). Accessibility to healthcare varies geographically within Wales, with the study aiming to capture both urban and rural populations in South Wales. Swansea has an established paediatric allergy service, serving the city and surrounding areas for several years. Pembrokeshire, in contrast, is a rural region and does not have a specialist paediatric allergy clinic serving the local population.