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

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

Medical Students' Death Anxiety: Severity and Association With Psychological Health and Attitudes Toward Palliative Care  Pia Thiemann, Dipl-Psych, Thelma.
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.
Anxiety After Diagnosis Predicts Lung Cancer–Specific and Overall Survival in Patients With Stage III Non–Small Cell Lung Cancer: A Population-Based Cohort.
Longitudinal Follow-Up Study Using the Distress and Impact Thermometer in an Outpatient Chemotherapy Setting  Takashi Yamaguchi, MD, Tatsuya Morita, MD,
Measuring Depression-Severity in Critically Ill Patients' Families with the Patient Health Questionnaire (PHQ): Tests for Unidimensionality and Longitudinal.
Mindfulness-Oriented Recovery Enhancement Ameliorates the Impact of Pain on Self- Reported Psychological and Physical Function Among Opioid-Using Chronic.
An Educational Intervention to Reduce Pain and Improve Pain Management for Malawian People Living With HIV/AIDS and Their Family Carers: A Randomized.
Arjun Poudel, PhD, Patsy Yates, PhD, Debra Rowett, BPharm, Lisa M
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.
An Intervention to Enhance Goals-of-Care Communication Between Heart Failure Patients and Heart Failure Providers  Ardith Z. Doorenbos, RN, PhD, FAAN,
Harold (Hal) Siden, MD, MHSC  Journal of Pain and Symptom Management 
Risk Factors for Developing Prolonged Grief During Bereavement in Family Carers of Cancer Patients in Palliative Care: A Longitudinal Study  Kristina.
Patterns of Use of Medical Cannabis Among Israeli Cancer Patients: A Single Institution Experience  Barliz Waissengrin, MD, Damien Urban, MD, Yasmin Leshem,
Predictors of Complicated Grief and Depression in Bereaved Caregivers: A Nationwide Prospective Cohort Study  Mette Kjaergaard Nielsen, MD, PhD, Mette.
Associations Between Objectively Measured Physical Activity and Quality of Life in Cancer Patients With Brain Metastases  Sonya S. Lowe, MD, MSc, Brita.
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,
Palliative Care Physicians' Attitudes Toward Patient Autonomy and a Good Death in East Asian Countries  Tatsuya Morita, MD, Yasuhiro Oyama, PhD, Shao-Yi.
Andrew Davies, FRCP, Katherine Webber, PhD 
Meaning in Life as a Mediator Between Physical Impairment and the Wish to Hasten Death in Patients With Advanced Cancer  Mariona Guerrero-Torrelles, MSc,
Geographic Variation in Hospice Use in the United States in 2002
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,
Distress-Based Gastrointestinal Symptom Clusters and Impact on Symptom Interference and Quality of Life in Patients with a Hematologic Malignancy Receiving.
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
Comparative Analysis of Specialization in Palliative Medicine Processes Within the World Health Organization European Region  Carlos Centeno, PhD, Deborah.
Redefining Appropriate Treatment Expectations
Mindfulness-Oriented Recovery Enhancement Ameliorates the Impact of Pain on Self- Reported Psychological and Physical Function Among Opioid-Using Chronic.
Nancy E. Avis, PhD, Beverly Levine, PhD, Sarah A
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.
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,
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
Psychometric Properties of the Fatigue Questionnaire EORTC QLQ-FA12 in a Sample of Female Cancer Patients  Sophie Kecke, Jochen Ernst, PhD, Jens Einenkel,
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,
U.S. Hospice Benefits Journal of Pain and Symptom Management
Jonathan M. Marron, MD, MPH, Emma Jones, MD, Joanne Wolfe, MD, MPH 
Which Treatment Is Better
William Shomali, MD  Journal of Pain and Symptom Management 
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
Does Adherence to National Comprehensive Cancer Network Guidelines Improve Pain- Related Outcomes? An Evaluation of Inpatient Cancer Pain Management at.
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 
Improvements in Physicians' Knowledge, Difficulties, and Self-Reported Practice After a Regional Palliative Care Program  Yoshiyuki Kizawa, MD, Tatsuya.
Psychoeducational Intervention for Symptom Management of Fatigue, Pain, and Sleep Disturbance Cluster Among Cancer Patients: A Pilot Quasi-Experimental.
Goal Communication in Palliative Care Decision-Making Consultations
Bruce L. Arnold, PhD, Linda S. Lloyd, DrPH, Charles F
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,
Presentation transcript:

Meaningful Communication Before Death, but Not Present at the Time of Death Itself, Is Associated With Better Outcomes on Measures of Depression and Complicated Grief Among Bereaved Family Members of Cancer Patients  Hiroyuki Otani, MD, Saran Yoshida, PhD, CP, Tatsuya Morita, MD, Maho Aoyama, RN, PhD, Yoshiyuki Kizawa, MD, PhD, Yasuo Shima, MD, Satoru Tsuneto, MD, PhD, Mitsunori Miyashita, RN, PhD  Journal of Pain and Symptom Management  Volume 54, Issue 3, Pages 273-279 (September 2017) DOI: 10.1016/j.jpainsymman.2017.07.010 Copyright © 2017 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 1 The actually present and the level of the family-perceived wish to be present at the moment of the patient's death. Journal of Pain and Symptom Management 2017 54, 273-279DOI: (10.1016/j.jpainsymman.2017.07.010) Copyright © 2017 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 2 Psychological impact on family of presence at the moment of the patient's death and meaningful communication (saying “goodbye”) between the patient and family members before death. a) The bereaved family members showed depression (indicated clinical depression [PHQ-9 ≥ 10]). b) The bereaved family members showed complicated grief (indicated clinical complicated grief [BGQ ≥ 8]). BGQ = Brief Grief Questionnaire; PHQ-9 = Patient Health Questionnaire-9. Journal of Pain and Symptom Management 2017 54, 273-279DOI: (10.1016/j.jpainsymman.2017.07.010) Copyright © 2017 American Academy of Hospice and Palliative Medicine Terms and Conditions