The Use of Life-Sustaining Procedures in the Last Month of Life Is Associated With More Depressive Symptoms in Surviving Spouses  Katherine A. Ornstein,

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

Palliative Sedation at Home for Terminally Ill Children With Cancer
Medical Students' Death Anxiety: Severity and Association With Psychological Health and Attitudes Toward Palliative Care  Pia Thiemann, Dipl-Psych, Thelma.
John G. Cagle, PhD, MSW, Kathleen T
Differences in Terminal Hospitalization Care Between U. S
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 C. Miller, PhD, MBA, Julie C
Susan Enguidanos, PhD, MPH, Jennifer Ailshire, PhD 
Measuring Depression-Severity in Critically Ill Patients' Families with the Patient Health Questionnaire (PHQ): Tests for Unidimensionality and Longitudinal.
The Burden of Polypharmacy in Patients Near the End of Life
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.
Preferences for Life-Sustaining Treatments and Associations With Accurate Prognostic Awareness and Depressive Symptoms in Terminally Ill Cancer Patients'
Treat the Pain Program Journal of Pain and Symptom Management
Harold (Hal) Siden, MD, MHSC  Journal of Pain and Symptom Management 
Gregory P. Samsa, PhD, Steven Wolf, MB, Thomas W
Health Status Trajectories Among Outpatients With Heart Failure
Predictors of Thirst in Intensive Care Unit Patients
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,
Christine W. Duarte, PhD, Adam W. Black, Kimberly Murray, Amy E
Benefit of Early Palliative Care Intervention in End-Stage Liver Disease Patients Awaiting Liver Transplantation  Alexandra J. Baumann, DO, David S. Wheeler,
Isaac M. Bromberg, MD  Journal of Pain and Symptom Management 
Building an Outpatient Kidney Palliative Care Clinical Program
Initial Validation of the Death and Dying Distress Scale for the Assessment of Death Anxiety in Patients With Advanced Cancer  Sandra Krause, BAH candidate,
Developing a Costing Framework for Palliative Care Services
Multiple Symptoms in Family Caregivers of Intensive Care Unit Patients
POST Forms More Than Advance Directives Associated With Out-of-Hospital Death: Insights From a State Registry  Sandra L. Pedraza, MD, Stacey Culp, PhD,
Prevalence of Sudden Death in Palliative Care: Data From the Australian Palliative Care Outcomes Collaboration  Magnus Ekström, MD, PhD, Maxwell T. Vergo,
Jacob N. Hunnicutt, MPH, Jennifer Tjia, MD, MS, Kate L. Lapane, PhD 
Shi-Yi Wang, MD, PhD, Melissa D
Breathlessness During the Last Week of Life in Palliative Care: An Australian Prospective, Longitudinal Study  Magnus Ekström, MD, PhD, Samuel F. Allingham,
Comparative Analysis of Specialization in Palliative Medicine Processes Within the World Health Organization European Region  Carlos Centeno, PhD, Deborah.
Christopher W. Kerr, MD, PhD, John C. Tangeman, MD, FACP, Carole B
Melissa M. Garrido, PhD, Holly G
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.
Cancer Treatment Side Effects: A Meta-analysis of the Relationship Between Response Expectancies and Experience  Elise J. Devlin, BPsych(Hon), Linley.
Palliative Sedation at Home for Terminally Ill Children With Cancer
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.
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
Antonio T. Fernando, MD, Nathan S. Consedine, PhD 
Use of an Item Bank to Develop Two Short-Form FAMCARE Scales to Measure Family Satisfaction With Care in the Setting of Serious Illness  Katherine A.
Dean Vuksanovic, MClinPsych, Heather J
Timing of POLST Form Completion by Cause of Death
Kathrin Boerner, PhD, Orah R. Burack, MA, Daniela S
Michael J. Hochman, BS, Yinxi Yu, BS, Steven P. Wolf, MS, Greg P
Blinded Patient Preference for Morphine Compared to Placebo in the Setting of Chronic Refractory Breathlessness—An Exploratory Study  Diana H. Ferreira,
Joseph A. Greer, PhD, William F. Pirl, MD, MPH, Vicki A
Jonathan M. Marron, MD, MPH, Emma Jones, MD, Joanne Wolfe, MD, MPH 
Which Treatment Is Better
Strategies to Support Recruitment of Patients With Life-Limiting Illness for Research: The Palliative Care Research Cooperative Group  Laura C. Hanson,
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.
Christine S. Ritchie, MD, MSPH, Amy S
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
Comparing Unmet Needs to Optimize Quality: Characterizing Inpatient and Outpatient Palliative Care Populations  Michael J. Hochman, BS, Steven Wolf, MS,
Karla T. Washington, PhD, Christopher R. Rakes, PhD 
Elizabeth Dzeng, MD, PhD, MPH, Daniel Dohan, PhD, J
Logan H. Ramsey, BS  Journal of Pain and Symptom Management 
Concordance Between Proxy Level of Care Preference and Advance Directives Among Nursing Home Residents With Advanced Dementia: A Cluster Randomized Clinical.
Characterizing the Hospice and Palliative Care Workforce in the U. S
Lisa C. Lindley, PhD, RN, Jennifer W. Mack, MD, MPH, Donald J
Is It the Difference a Day Makes
John G. Cagle, PhD, MSW, Sheryl Zimmerman, PhD, Lauren W
Presentation transcript:

The Use of Life-Sustaining Procedures in the Last Month of Life Is Associated With More Depressive Symptoms in Surviving Spouses  Katherine A. Ornstein, PhD, MPH, Melissa D. Aldridge, PhD, MPH, MBA, Melissa M. Garrido, PhD, Rebecca Gorges, MS, Evan Bollens- Lund, MA, Albert L. Siu, MD, MSPH, Kenneth M. Langa, MD, PhD, Amy S. Kelley, MD, MS  Journal of Pain and Symptom Management  Volume 53, Issue 2, Pages 178-187.e1 (February 2017) DOI: 10.1016/j.jpainsymman.2016.08.023 Copyright © 2016 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 1 Mean spouse depressive symptom scores with 95% CI by intensive life-sustaining procedure use by time before and after death (n = 1258). Scores are grouped base on timing (in six-month intervals) of post-death interviews relative to respondent death with the exception of interviews conducted zero to one month before death which were excluded. CES-D = Center for Epidemiologic Studies Depression Scale which is scored 0 (no symptoms) to 8 (severe symptoms); CI = confidence interval. Journal of Pain and Symptom Management 2017 53, 178-187.e1DOI: (10.1016/j.jpainsymman.2016.08.023) Copyright © 2016 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 2 Increase in spouse depressive symptom scores pre- to post-death with 95% CI after death by intensive life-sustaining procedure use (matched sample*) (n = 1255). Scores are grouped base on timing (in 6-month intervals) of post-death interviews relative to respondent death; CES-D = Center for Epidemiologic Studies Depression Scale which is scored 0 (no symptoms) to 8 (severe symptoms); CI = confidence interval. *Sample matched based on patient net worth, nursing home residence, self-rated health, advance directive, death expected, ADL impairment, patient illnesses and comorbidity count and spousal pre-death clinically significant depression, age at patient death, gender, race, education, self-rated health, religion important, comorbidities, psychiatric treatment or diagnosis, caregiver status, and timing of interview after death. Journal of Pain and Symptom Management 2017 53, 178-187.e1DOI: (10.1016/j.jpainsymman.2016.08.023) Copyright © 2016 American Academy of Hospice and Palliative Medicine Terms and Conditions