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Courage Carries Hope

Video Post: Cancer Patients and Survivors Describe Quality Cancer Care

July 28, 2015/in Cancer News, Cancer Policy Blog Care Coordination, Quality Cancer Care, Survivorship Care NCCS News /by actualize

What is quality cancer care? At a recent NCCS Cancer Policy Advocate Training event, we spoke to cancer patients and survivors about their definitions of quality cancer care.

How do you define cancer care? Share your thoughts in the comments and let us know what you think.

The Institute of Medicine (IOM) and others have worked to define quality cancer care. NCCS has been a patient voice in efforts to promote quality cancer care and played a leadership role in building the evidence base for quality cancer care. In defining quality cancer care, NCCS believes that cancer patients should have access to:

  • Care that adheres to practice guidelines and evidence-based standards of care;
  • Comprehensive cancer care that assures proper treatment of the symptoms and side effects of cancer and cancer treatment;
  • Coordinated care with strong communication among all the providers and the patient, supported by modern health information technology;
  • A written care plan detailing all elements of cancer care;
  • Care in a clinical trial, if it represents a potential treatment option;
  • Honest discussion with their physicians regarding prognosis, the intent of therapy and the patient’s values and preferences regarding care;
  • An assessment of their psychosocial needs and referrals to resources;
  • Palliative care throughout the course of treatment, from diagnosis through end of life;
  • End-of-life care, including but not limited to hospice care of adequate scope and duration;
  • Their personal health information, including their electronic health records; and
  • Robust health information systems that support and improve all other aspects of quality cancer care.

Survivors who are ending active therapy and beginning a period of survivorship should have access to:

  • A treatment summary and survivorship care plan that details the schedule for monitoring their health status and obtaining follow-up care;
  • Services for monitoring of health status and the risk of complications and second cancers; and
  • Coordinated care for complications of cancer and its treatment and for second cancers, without fear that their cancer diagnosis will disqualify them from future health insurance coverage.
  • NCCS continues to advocate for passage of federal legislation that would encourage the use of cancer care plans as one tool to ensure that these essential components of quality survivorship care are delivered.
Tags: Cancer Survivorship, ePatient, patient first, quality, video post
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  • About
    • Our Mission
    • Our History
    • The 1986 Club
    • Our Team
      • Policy Advisors
    • Employment
    • Partnerships
    • Financial Information
  • Policy
    • Quality Cancer Care
    • Access to Care
    • Health Equity
    • Redefining Functional Status (RFS)
    • 2022 State of Cancer Survivorship Survey
    • 2021 State of Cancer Survivorship Survey
    • 2020 State of Cancer Survivorship Survey
    • Cancer Care Planning and Communications Act (CCPCA)
  • Get Involved
    • What is Advocacy?
    • Cancer Policy and Advocacy Team (CPAT)
    • Survivorship Champions
    • Subscribe to NCCS Updates
    • Elevating Survivorship
    • Survivor Stories
    • Cancerversary
    • State-Based Cancer Advocacy
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    • Cancer Survival Toolbox
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      • Talking With Your Doctor
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Harmar Brereton, MD

Founder
Northeast Regional Cancer Institute

 

“Perhaps one of the most impactful collaborations in Dr. Brereton’s extraordinary career remains his early work and long friendship with Ellen Stovall. Through him, and in turn through the thousands of lives he has touched, Ellen’s work continues, and her mission lives on.”

—Karen M. Saunders
President, Northeast Regional Cancer Institute