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In a clinical excellence framework with more rationalized exuberance, the new-new digital health things should be underpinned by clinical evidence and excellence and — if they are very, very good things — they will address the Quintuple Aim by, Enhancing the care experience. Reducing costs per capita (per patient).
Social networks give providers-at-risk the opportunity to scale care to larger patient populations, identifying disease-specific patientsupport groups and caregiver support groups as very powerful platforms for that scaling.
Technological advancements, such as electronic health records and telehealth, are vital in supportingpatient advocacy, enhancing care coordination, and ensuring comprehensive patientsupport within bundled payment models. Patient advocacy transcends its influence on individual wellness.
When I talk about patientsupport programs (PSPs), I’m most often focused on supporting peoples’ access to medicines due to costs, bolstering health literacy, and addressing health citizens’ risks of drivers of health that can be obstacles to optimal health outcomes (those challenging social determinants of health).
Consider: fighting health insurance appeals, crafting countless medical necessity letters, justifying being discharged against medical orders, and other battles fought hand-in-hand with her husband on behalf of Emmett and his well-being. Why should this be an imperative?
One of the most critical aspects of oncology nursing is the comprehensive support provided to patients and their families. Oncology nurses offer not only medical care but also emotional support and education on cancer and its treatments.
At the same time, one-half of people would likely take an additional medication were it covered by insurance. Nearly one-half of insured consumers had not filled a prescription due to cost.
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