AYA survivor well-being |
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Barriers to care and lack of access to care |
Physical concerns |
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Awareness of late effects |
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Use of care plans |
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Educational needs |
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Personal reflection on survivorship |
Psychosocial concerns |
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Need for community and peer sharing |
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Needs of daily living |
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Costs of past care |
Financial and insurance concerns |
AYA survivor education |
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Need for survivorship education |
Health literacy |
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AYA use of apps and digital technology |
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Use of survivorship plans |
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Information-sharing practices |
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AYA self advocacy |
Training and education |
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Lack of ability to communicate with physicians |
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Health care professional education |
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Age-appropriate care |
Survivor education and training |
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Lack of awareness of late effects |
Provider education and training |
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Lack of knowledge of AYA needs |
Provider time constraints |
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Lack of knowledge of Seton AYA clinic |
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AYA population sparseness and fragmentation |
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CME uptake and professional education programs |
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Survivorship clinic |
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Referrals and transitions in care |
Insurance coverage concerns |
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Coordination with navigators |
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Use of survivorship plans with patients |
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Cancer advocates |
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Advocates role in information sharing |
Information gathering and sharing |
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Attitudes about AYA research |
Delivery of resources |
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Lack of knowledge of Seton and other community programs |
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Family and caregiver needs |
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Lack of survivorship care plans |
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Lack of information for nonmedical needs |
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Seton Healthcare Family and community physicians |
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Impact of AYA educational programs |
Financial and human resources |
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Improved knowledge of Seton AYA program |
Sustainability |
Political, economic, and cultural societal support |
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AYA political advocacy |
Resources |
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American College of Surgeons requirements for survivorship care plans |
Influence and power |
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Practice change |