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  • Practice Guidelines

    Position statement: Policies to support family caregivers

    Nursing Outlook
    Vol. 66Issue 3p337–340Published in issue: May, 2018
    • G. Adriana Perez
    • Karen Moomaw Rose
    • Billy A. Caceres
    • Wanda Spurlock
    • Barbara Bowers
    • Barbara Lutz
    • and others
    Cited in Scopus: 14
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      In 2013, an estimated 40 million family caregivers provided an average of 18 hours of care per week, reflecting approximately $470 billion in unpaid caregiving contributions (Reinhard, Feinberg, Choula, & Houser, 2015). Projected demographic shifts in the U.S., including the rapidly aging population (World Health Organization, 2015) and increase of individuals living with chronic conditions across the lifespan (American Academy of Pediatrics, American Academy of Family Physicians, American College of Physicians, 2011; Houtrow, Larson, Olson, Newacheck, & Halfon, 2014), will increase the demand for family caregivers.
    • Practice Guidelines

      Achieving advance care planning in diverse, underserved populations

      Nursing Outlook
      Vol. 66Issue 3p311–315Published online: April 11, 2018
      • Mona Newsome Wicks
      • Jose Alejandro
      • Desiree Bertrand
      • Carol J. Boyd
      • Christopher Lance Coleman
      • Emily Haozous
      • and others
      Cited in Scopus: 8
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        There remains a gap in meeting the palliative and end-of-life (EOL) care needs, including advance care planning (ACP) needs of ethnic minority, under-resourced, veterans, and lesbian, gay, bisexual, transgender, and queer (LGBTQ) Americans, as well as persons with disabilities and residing in geographically isolated regions. Intersecting socially constructed characteristics influence the lived experience of marginalized communities, including their health-care experiences. These persistent gaps pose a serious barrier to achieving high-quality care, including palliative and EOL care, across the life span of members of these growing populations.
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