Key result
Moyamoya transition requires coordinated adult care, disease monitoring, and socioeconomic support.
Why the study?
Pediatric moyamoya patients face unique challenges during transition to adulthood due to the chronic nature of the disease requiring coordinated long-term care strategies.
Highlights the importance of longitudinal disease monitoring, care coordination, and socioeconomic anticipation for pediatric moyamoya patients transitioning to adult care.
Answers are grounded in this paper and cite their sources.
Requires lifelong monitoring for treated pediatric moyamoya into adulthood; leaves open standardized transition and adult management protocols.
Moyamoya is a progressive arteriopathy of the intracranial vasculature, predominantly affecting the terminal branches of the internal carotid artery. Treatment is predicated on surgical revascularization to reduce the risk of stroke. For patients diagnosed and treated as children, it is important to recognize the long-term implications of the disease, for example, that moyamoya is treatable, but not curable. Pediatric moyamoya patients face unique challenges as they transition to adulthood as a consequence of the chronic nature of this disorder. Successful long-term care requires a strategy that incorporates ongoing longitudinal disease monitoring, coordination of care between physician teams, and anticipation of socioeconomic factors that change over time. This article provides an approach to transition care to adult caregivers for pediatric moyamoya patients with a specific focus on the three key stakeholders in the process: the neurosurgeon, the primary care physician, and the individual patient.
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Scott et al. (2020) conducted a review in Pediatric Moyamoya. Transition care to adult caregivers was evaluated. Transitioning pediatric moyamoya patients to adult care requires a strategy incorporating longitudinal disease monitoring, care coordination, and anticipation of socioeconomic factors.
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