Ismalia De Sousa PhD(c), MSc, RN , Vanessa Dizonno MSc , Karen LeComte MSN, RN , Alexis Carr MBBS, MSci, MHSc , Yussef El Kalza HBA , Mikayla Shymka BSc , Roger H. Payette BSc , Leah Kuzmuk MSc , Emily M.E. Lyall MD, CCFP , Jasmine Grewal MD , Jonathan M.C. Smith MD, MHSc , Thalia S. Field MD, FRCPC, MHSc
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引用次数: 0
Abstract
Background
Significant advances in managing congenital heart disease (CHD) have occurred over the past few decades, resulting in a fast-growing adult patient population with distinct needs requiring urgent attention. Research has recently highlighted the prevalence of neurocognitive differences among adults living with CHD. Yet, there is a lack of knowledge about the perspectives of people living with CHD and family members/caregivers on brain health. We sought to explore their perspectives to guide future research and clinical endeavours.
Methods
Using the principles of integrated knowledge translation and qualitative interpretive description, we conducted 2 focus groups with 7 individuals with CHD and their family members as part of a virtual forum on brain health in CHD. Data analysis followed the principles of interpretive description.
Results
A lack of understanding about overall brain health and neurocognitive differences in adult CHD was identified. To increase overall knowledge about brain health, initiatives should (1) focus on the individual living with CHD, involving family members and peers; (2) use social media and health care encounters for knowledge exchange; and (3) ensure a “balancing act” in the information provided to avoid feelings of worry and uncertainty about the future while simultaneously empowering people living with CHD.
Conclusions
There is a pressing need for better education about brain health among individuals living with CHD. Our findings can guide clinicians in developing programmes of care and (re)design health services that address the brain-heart axis and neurocognitive differences in CHD.