The perceived impact of pediatric food allergy on mental health care needs and supports: A pilot study

BACKGROUND: Evidence suggests a mental health impact of food allergy on affected children and their families; however, little is known about health care professionals’ understanding of these impacts and the resources available to patients and their families. OBJECTIVE: Our aim was to conduct a pilot study examining health care professionals’ perceptions of the psychosocial and financial burden of food allergy to identify gaps in education and resources and thus better support families with food allergy moving forward. METHODS: Between February 20 and November 19, 2020, we conducted audiorecorded interviews (n = 6) and profession-specific focus groups (n = 2 [representing 7 individuals]). The participants included pediatric allergists, allergy nurse educators, and clinical dietitians who were directly involved in pediatric food allergy care. The interviews were recorded and transcribed verbatim. Thematic analysis was subsequently applied to identify the main themes. RESULTS: Our study consisted of an interdisciplinary group of Manitoban health care providers (N = 13) who were directly involved with pediatric food allergy care. We identified 3 main themes from these interviews: anxiety among families with food allergy, which is a common comorbidity; limited resources available within current public infrastructure; and empowerment through education. These themes describe issues surrounding access to information and resources and how this can affect anxiety and parenting styles among families with food allergy. CONCLUSIONS: Health care professionals perceive that many families experience anxiety as a result of their child’s food allergy. They further advocate that access to information and suitability of public resources be considered when planning for related programs.