The impact of the COVID‐19 pandemic on families of children with medical complexity: A qualitative study of caregivers' experiences

Abstract

AbstractBackgroundFamilies of children with medical complexity (CMC) have been negatively affected by the COVID‐19 pandemic, experiencing challenges such as decreased access to services, increased financial hardship and increased isolation. However, there are few qualitative studies which explore parental experiences. The aim of the present study was to describe the impact of the COVID‐19 pandemic on families of CMC.MethodsCaregivers of CMC were recruited from a large hospital in the Midwestern United States. They completed a semistructured qualitative interview assessing the impact of COVID‐19 on their child's care, which was analysed using interpretive phenomenological analysis.ResultsTwenty caregivers who were predominantly White, married and female participated. Emergent themes included the importance of protecting their child's health to ensure their physical safety, greater social isolation and missed medical services related to concerns about exposure, clinic closures and/or other logistical changes. Participants noted that the convenience of telehealth was a positive outcome of COVID‐19 that facilitated care while reducing time and resource challenges.ConclusionsThis study highlights the importance of protecting the health of CMC through continued safe access to in‐person or telehealth services. It is important to prioritise emotional support services for families of CMC as they have experienced increased stress and social isolation during and after the COVID‐19 pandemic. This topic should be explored among diverse families with CMC across multiple healthcare systems.