Worldwide advances in treatment and supportive care for children and adolescents with cancer have resulted in a growing population of survivors growing into adulthood. Yet, this population is at very high risk of late occurring health problems, including significant morbidity and early mortality. Unique barriers to high-quality care for this group include knowledge gaps among both providers and survivors as well as fragmented healthcare delivery during the transition from pediatric to adult care settings.
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Tonorezos et al. (2022) studied this question.
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