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Equitably improving outcomes for cancer survivors and supporting caregivers: A blueprint for care delivery, research, education, and policy.
Alfano, Catherine M; Leach, Corinne R; Smith, Tenbroeck G; Miller, Kim D; Alcaraz, Kassandra I; Cannady, Rachel S; Wender, Richard C; Brawley, Otis W.
Affiliation
  • Alfano CM; Vice President, Survivorship, American Cancer Society, Washington, DC.
  • Leach CR; Senior Principal Scientist, Behavioral Research, American Cancer Society, Atlanta, GA.
  • Smith TG; Senior Principal Scientist, Behavioral Research, American Cancer Society, Atlanta, GA.
  • Miller KD; Senior Associate Scientist, Surveillance Research, American Cancer Society, Atlanta, GA.
  • Alcaraz KI; Senior Principal Scientist, Behavioral Research, American Cancer Society, Atlanta, GA.
  • Cannady RS; Strategic Director, Cancer Caregiver Support, American Cancer Society, Atlanta, GA.
  • Wender RC; Chief Cancer Control Officer, American Cancer Society, Atlanta, GA.
  • Brawley OW; Chief Medical Officer, American Cancer Society, Atlanta, GA.
CA Cancer J Clin ; 69(1): 35-49, 2019 01.
Article in En | MEDLINE | ID: mdl-30376182
Cancer care delivery is being shaped by growing numbers of cancer survivors coupled with provider shortages, rising costs of primary treatment and follow-up care, significant survivorship health disparities, increased reliance on informal caregivers, and the transition to value-based care. These factors create a compelling need to provide coordinated, comprehensive, personalized care for cancer survivors in ways that meet survivors' and caregivers' unique needs while minimizing the impact of provider shortages and controlling costs for health care systems, survivors, and families. The authors reviewed research identifying and addressing the needs of cancer survivors and caregivers and used this synthesis to create a set of critical priorities for care delivery, research, education, and policy to equitably improve survivor outcomes and support caregivers. Efforts are needed in 3 priority areas: 1) implementing routine assessment of survivors' needs and functioning and caregivers' needs; 2) facilitating personalized, tailored, information and referrals from diagnosis onward for both survivors and caregivers, shifting services from point of care to point of need wherever possible; and 3) disseminating and supporting the implementation of new care methods and interventions.
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Full text: 1 Database: MEDLINE Main subject: Caregivers / Healthcare Disparities / Quality Improvement / Cancer Survivors / Health Policy / Health Services Accessibility Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: CA Cancer J Clin Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Caregivers / Healthcare Disparities / Quality Improvement / Cancer Survivors / Health Policy / Health Services Accessibility Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: CA Cancer J Clin Year: 2019 Type: Article