Cancer Caregiving in the United States

Research, Practice, Policy

  • Ronda C. Talley
  • Ruth McCorkle
  • Walter F. Baile

Part of the Caregiving: Research • Practice • Policy book series (CARE)

Table of contents

  1. Front Matter
    Pages i-xix
  2. Ruth McCorkle, Ronda C. Talley, Walter Baile, Anna-leila Williams
    Pages 1-17
  3. Issues Effecting the Care Triad

  4. Issues in Providing Direct Care

    1. Front Matter
      Pages 125-125
    2. Lodovico Balducci, Sheryl LaCoursiere
      Pages 161-178
  5. Cross-Cutting Issues Impacting Caregivers and Caregiving

    1. Front Matter
      Pages 199-199
    2. Marilyn Frank-Stromborg, Kenneth R. Burns
      Pages 249-263
    3. Dale L. Kaufman, Ann O’Mara, Christine M. Schrauf
      Pages 265-286
    4. Martin L. Smith, Mary Elizabeth Paulk
      Pages 287-311
  6. Conclusions

    1. Front Matter
      Pages 313-313

About this book

Introduction

Despite advances in detection and treatment, cancer remains a source of pain and distress to patients and of complex challenges to the loved ones caring for them. The trend toward shorter hospital stays in particular has increased the physical, psychological, and financial burden on caregivers, often leading to adverse effects on patients.

Cancer Caregiving in the United States illuminates these complex concerns with authoritative detail. This wide-ranging volume provides a comprehensive survey of cancer-related issues, including those affecting the care triad (patients-family members- professionals) and quality of care as well as the numerous physical, emotional, and financial challenges that caregivers may need to confront. Sources of caregiver difficulty at each stage of the disease, from diagnosis to end of life, are explored. Each chapter analyzes its topic in terms of practice, research, education, and policy, providing a wealth of literature reviews, assessment and care models, interventions, and recommendations for future study and practice.

Coverage includes:

  • Caregiving issues for cancer patients with long-term, short-term, and intermittent needs.
  • Family caregivers as members of the treatment team.
  • The impact of health disparities on caregivers.
  • Cancer care policy and advocacy.
  • End-of-life issues for cancer caregivers.
  • Legal, financial, and ethical issues. 

Cancer Caregiving in the United States is a core reference for researchers, professionals/scientist-practitioners, and graduate students in such caregiving fields as clinical psychology, social work, nursing, public health and medicine, social policy, and educational policy.

Keywords

Advocacy Cancer Care Caregiving Coping Diagnostics Economics End-of-life issues Ethical issues Faith Family Healthcare National policy Nursing Oncology Palliative care Psychology State initiatives Support Treatments

Editors and affiliations

  • Ronda C. Talley
    • 1
  • Ruth McCorkle
    • 2
  • Walter F. Baile
    • 3
  1. 1.Western Kentucky UniversityBowling GreenUSA
  2. 2.School of NursingYale UniversityNew HavenUSA
  3. 3.Department of Behavioral ScienceUniversity of Texas M.D. Anderson CancerHoustonUSA

Bibliographic information

  • DOI https://doi.org/10.1007/978-1-4614-3154-1
  • Copyright Information Springer Science+Business Media, LLC 2012
  • Publisher Name Springer, New York, NY
  • eBook Packages Behavioral Science
  • Print ISBN 978-1-4614-3153-4
  • Online ISBN 978-1-4614-3154-1
  • Series Print ISSN 2192-340X
  • Series Online ISSN 2192-3418
  • About this book