Decision Making Regarding the Place of End-of-Life Cancer Care: The Burden on Bereaved Families and Related Factors Sena Yamamoto, RN, PhD, Harue Arao,

Slides:

Advertisements

Similar presentations

A Nationwide Survey of Quality of End-of-Life Cancer Care in Designated Cancer Centers, Inpatient Palliative Care Units, and Home Hospices in Japan: The.

Advertisements

The Benefits of Authorized Agent Controlled Analgesia (AACA) to Control Pain and Other Symptoms at the End of Life Robert J. Webb, MD, Cathy P. Shelton,

Palliative Care Physicians' Attitudes Toward Patient Autonomy and a Good Death in East Asian Countries Tatsuya Morita, MD, Yasuhiro Oyama, PhD, Shao-Yi.

Perceptions of Complementary Medicine Integration in Supportive Cancer Care of Arabs and Jews in Israel: A Cross-Cultural Study Eran Ben-Arye, MD, Elad.

Anxiety After Diagnosis Predicts Lung Cancer–Specific and Overall Survival in Patients With Stage III Non–Small Cell Lung Cancer: A Population-Based Cohort.

Susan Enguidanos, PhD, MPH, Jennifer Ailshire, PhD

The Burden of Polypharmacy in Patients Near the End of Life

Accuracy of a Diagnostic Algorithm to Diagnose Breakthrough Cancer Pain as Compared With Clinical Assessment Katherine Webber, MBBS, MSc, PhD, Andrew.

Measuring the quality of structure and process in end-of-life care from the bereaved family perspective Tatsuya Morita, MD, Kei Hirai, PhD, Yukihiro.

A Randomized Trial of the Effectiveness of Topical “ABH Gel” (Ativan®, Benadryl®, Haldol®) vs. Placebo in Cancer Patients With Nausea Devon S. Fletcher,

An Intervention to Enhance Goals-of-Care Communication Between Heart Failure Patients and Heart Failure Providers Ardith Z. Doorenbos, RN, PhD, FAAN,

Treat the Pain Program Journal of Pain and Symptom Management

Harold (Hal) Siden, MD, MHSC Journal of Pain and Symptom Management

Building Resilience for Palliative Care Clinicians: An Approach to Burnout Prevention Based on Individual Skills and Workplace Factors Anthony L. Back,

The 2015 Class of Hospice and Palliative Medicine Fellows—From Training to Practice: Implications for HPM Workforce Supply Dale Lupu, MPH, PhD, Ed Salsberg,

Gregory P. Samsa, PhD, Steven Wolf, MB, Thomas W

Predictors of Thirst in Intensive Care Unit Patients

Timing of Referral to Hospice and Quality of Care: Length of Stay and Bereaved Family Members' Perceptions of the Timing of Hospice Referral Joan M.

Palliative Care Physicians' Attitudes Toward Patient Autonomy and a Good Death in East Asian Countries Tatsuya Morita, MD, Yasuhiro Oyama, PhD, Shao-Yi.

Meaning in Life as a Mediator Between Physical Impairment and the Wish to Hasten Death in Patients With Advanced Cancer Mariona Guerrero-Torrelles, MSc,

Improving the Evidence Base in Palliative Care to Inform Practice and Policy: Thinking Outside the Box Samar M. Aoun, BSc(Hons), MPH, PhD, Cheryl Nekolaichuk,

Isaac M. Bromberg, MD Journal of Pain and Symptom Management

Got Volunteers? Association of Hospice Use of Volunteers With Bereaved Family Members' Overall Rating of the Quality of End-of-Life Care Eve M. Block,

Reliability and Validity of the Korean Memorial Symptom Assessment Scale—Short Form in Gynecological Cancer Patients Ju-Hee Nho, PhD, RN, Sung Reul Kim,

African American Bereaved Family Members' Perceptions of the Quality of Hospice Care: Lessened Disparities, But Opportunities to Improve Remain Ramona.

Developing a Costing Framework for Palliative Care Services

Resource Use and Health Care Costs of COPD Patients at the End of Life: A Systematic Review Kristof Faes, MSc, Veerle De Frène, PhD, Joachim Cohen, PhD,

Multiple Symptoms in Family Caregivers of Intensive Care Unit Patients

Communication Disparity Between the Bereaved and Others: What Hurts Them and What Is Unhelpful? A Nationwide Study of the Cancer Bereaved Mayumi Ishida,

Jacob N. Hunnicutt, MPH, Jennifer Tjia, MD, MS, Kate L. Lapane, PhD

Unfinished Business in Families of Terminally Ill With Cancer Patients

A Systematic Review of Training in Symptom Management in Palliative Care Within Postgraduate Medical Curriculums Pamela Turrillas, MD, MSc, Maria Joao.

Comparative Analysis of Specialization in Palliative Medicine Processes Within the World Health Organization European Region Carlos Centeno, PhD, Deborah.

David Clark, PhD, Michael Wright, PhD

Resilience at the End of Life as a Predictor for Postloss Growth in Bereaved Caregivers of Cancer Patients: A Prospective Pilot Study Yong Joo Lee, MD

Changes in Nurses' Knowledge, Difficulties, and Self-reported Practices Toward Palliative Care for Cancer Patients in Japan: An Analysis of Two Nationwide.

A Randomized Trial of the Effectiveness of Topical “ABH Gel” (Ativan®, Benadryl®, Haldol®) vs. Placebo in Cancer Patients With Nausea Devon S. Fletcher,

Documentation Quality of Inpatient Code Status Discussions

The Nexus Between the Documentation of End-of-Life Wishes and Awareness of Dying: A Model for Research, Education and Care Deborah P. Waldrop, PhD, MSW,

How Do Follow-Up Care Instructions and Treatment Summaries Relate to Cancer Survivors' Cancer-Related Pain? Jennifer M. Jabson, PhD, MPH, Deborah J.

Meaningful Communication Before Death, but Not Present at the Time of Death Itself, Is Associated With Better Outcomes on Measures of Depression and Complicated.

Understanding Response Rates to Surveys About Family Members' Psychological Symptoms After Patients' Critical Illness Ann C. Long, MD, MS, Lois Downey,

Katherine Webber, MBBS, MSc, PhD, Andrew N. Davies, FRCP, Martin R

Author's Response Journal of Pain and Symptom Management

Long-Term Psychosocial Outcomes Among Bereaved Siblings of Children With Cancer Abby R. Rosenberg, MD, MS, Andrea Postier, MPH, Kaci Osenga, MD, Ulrika.

Locked-In Syndrome: Case Report and Discussion of Decisional Capacity

Nationwide Japanese Survey About Deathbed Visions: “My Deceased Mother Took Me to Heaven” Tatsuya Morita, MD, Akemi Shirado Naito, MD, Maho Aoyama, RN,

Antonio T. Fernando, MD, Nathan S. Consedine, PhD

Which Physicians' Behaviors on Death Pronouncement Affect Family-Perceived Physician Compassion? A Randomized, Scripted, Video-Vignette Study Masanori.

Care Strategy for Death Rattle in Terminally Ill Cancer Patients and Their Family Members: Recommendations From a Cross-Sectional Nationwide Survey of.

Meaninglessness in Terminally Ill Cancer Patients: A Randomized Controlled Study Tatsuya Morita, MD, Hisayuki Murata, MA, Emi Kishi, RN, Mitsunori Miyashita,

Robyn M. Keall, RN, MS, PhD (C), Josephine M

U.S. Hospice Benefits Journal of Pain and Symptom Management

Jonathan M. Marron, MD, MPH, Emma Jones, MD, Joanne Wolfe, MD, MPH

Pain Medication Management Processes Used by Oncology Outpatients and Family Caregivers Part II: Home and Lifestyle Contexts Karen L. Schumacher, RN,

William Shomali, MD Journal of Pain and Symptom Management

Validation of the Modified Glasgow Prognostic Score in Advanced Cancer Patients Receiving Palliative Care Naitielle de Paula Pantano, RN, Bianca Sakamoto.

Effects of End-of-Life Discussions on the Mental Health of Bereaved Family Members and Quality of Patient Death and Care Takashi Yamaguchi, MD, PhD,

A Pilot Study of the Experience of Family Caregivers of Patients With Advanced Pancreatic Cancer Using a Mixed Methods Approach Deborah W. Sherman, PhD,

Jennifer Tjia, MD, MSCE, Lee Ellington, PhD, Margaret F

Parents' Experiences of Pediatric Palliative Transports: A Qualitative Case Series Harriett Nelson, MSN, RN, CCRN, NREMTP, Sandra Mott, PhD, CPN, RN-BC,

Karla T. Washington, PhD, Christopher R. Rakes, PhD

Family Caregiver Participation in Palliative Care Research: Challenging the Myth Samar Aoun, PhD, MPH, BSc(Hons), Susan Slatyer, PhD, BNurs(Hons), RN,

Improvements in Physicians' Knowledge, Difficulties, and Self-Reported Practice After a Regional Palliative Care Program Yoshiyuki Kizawa, MD, Tatsuya.

Goal Communication in Palliative Care Decision-Making Consultations

Population-Based Quality Indicators for Palliative Care Programs for Cancer Patients in Japan: A Delphi Study Yoko Nakazawa, RN, MSH, Masahi Kato, MD,

Lisa C. Lindley, PhD, RN, Jennifer W. Mack, MD, MPH, Donald J

Is It the Difference a Day Makes

Pain Medication Management Processes Used by Oncology Outpatients and Family Caregivers Part I: Health Systems Contexts Karen L. Schumacher, RN, PhD,

A Quantitative Study of Triggered Palliative Care Consultation for Hospitalized Patients With Advanced Cancer Gabrielle B. Rocque, MD, Toby C. Campbell,

Presentation transcript:

Decision Making Regarding the Place of End-of-Life Cancer Care: The Burden on Bereaved Families and Related Factors Sena Yamamoto, RN, PhD, Harue Arao, RN, PhD, Eiko Masutani, RN, MS, Miwa Aoki, RN, MSN, Megumi Kishino, RN, MSN, Tatsuya Morita, MD, Yasuo Shima, MD, Yoshiyuki Kizawa, MD, PhD, Satoru Tsuneto, MD, PhD, Maho Aoyama, RN, PhD, Mitsunori Miyashita, RN, PhD Journal of Pain and Symptom Management Volume 53, Issue 5, Pages 862-870 (May 2017) DOI: 10.1016/j.jpainsymman.2016.12.348 Copyright © 2017 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 1 Bereaved family members' decision-making burden regarding the place of end-of-life care. Numbers in parentheses indicate the number of responses. Journal of Pain and Symptom Management 2017 53, 862-870DOI: (10.1016/j.jpainsymman.2016.12.348) Copyright © 2017 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 2 Differences in bereaved family members' depression and grief by their decision-making burden regarding the place of end-of-life care. aMean + SD. bLow burden: scores < median. cHigh burden: scores ≥ median. dP < 0.001 (using t-test). Journal of Pain and Symptom Management 2017 53, 862-870DOI: (10.1016/j.jpainsymman.2016.12.348) Copyright © 2017 American Academy of Hospice and Palliative Medicine Terms and Conditions