Factors Influencing Australian General Practitioners' Clinical Decisions Regarding Advance Care Planning: A Factorial Survey Craig Sinclair, PhD, Kiri.

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

Advancing Palliative Care as a Human Right

Doctors' Decisions When Faced With Contradictory Patient Advance Directives and Health Care Proxy Opinion: A Randomized Vignette-Based Study Monica Escher,

Susan Enguidanos, PhD, MPH, Jennifer Ailshire, PhD

Clinicians' Perspectives on Managing Symptom Clusters in Advanced Cancer: A Semistructured Interview Study Skye T. Dong, BPsych (Hons), DClinPsych, Phyllis.

An Educational Intervention to Reduce Pain and Improve Pain Management for Malawian People Living With HIV/AIDS and Their Family Carers: A Randomized.

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.

Hospice Enrollment After Referral to Community-Based, Specialist Palliative Care: Impact of Telephonic Outreach Alexa Riggs, BA, Brenda Breuer, PhD,

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

The Moment of Death 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,

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

Vincent Maida, MD, MSc, BSc, Jason Corban, MD, CM, Hon BSc

Methadone for Pain and the Risk of Adverse Cardiac Outcomes

Associations Between Objectively Measured Physical Activity and Quality of Life in Cancer Patients With Brain Metastases Sonya S. Lowe, MD, MSc, Brita.

A 10-Year Longitudinal Study of Effects of a Multifaceted Residency Spiritual Care Curriculum: Clinical Ability, Professional Formation, End of Life,

Andrew Davies, FRCP, Katherine Webber, PhD

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

Distress-Based Gastrointestinal Symptom Clusters and Impact on Symptom Interference and Quality of Life in Patients with a Hematologic Malignancy Receiving.

Initial Validation of the Death and Dying Distress Scale for the Assessment of Death Anxiety in Patients With Advanced Cancer Sandra Krause, BAH candidate,

Palliative Care in Romania

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

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,

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.

Skye Tian Dong, BPsych (Hons), Phyllis N. Butow, PhD, Daniel S. J

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

The Relationship Between Fatigue and Depression in Adults With End-Stage Renal Disease on Chronic In-Hospital Hemodialysis: A Scoping Review Janine F.

Cancer Treatment Side Effects: A Meta-analysis of the Relationship Between Response Expectancies and Experience Elise J. Devlin, BPsych(Hon), Linley.

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

A Systematic Review of Strategies Used to Increase Recruitment of People With Cancer or Organ Failure Into Clinical Trials: Implications for Palliative.

Author's Response Journal of Pain and Symptom Management

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

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.

What Aspects of Quality of Life Are Important From Palliative Care Patients' Perspectives? A Systematic Review of Qualitative Research Nicola McCaffrey,

Dean Vuksanovic, MClinPsych, Heather J

Hospice Enrollment After Referral to Community-Based, Specialist Palliative Care: Impact of Telephonic Outreach Alexa Riggs, BA, Brenda Breuer, PhD,

Prevalence of Neuropathic Pain in Cancer Patients: Pooled Estimates From a Systematic Review of Published Literature and Results From a Survey Conducted.

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

Which Treatment Is Better

William Shomali, MD Journal of Pain and Symptom Management

Validation of the Quality of Dying-Hospice Scale

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

Family Relationships and Psychosocial Dysfunction Among Family Caregivers of Patients With Advanced Cancer Kathrine G. Nissen, MSc, Kelly Trevino, PhD,

Validation of a Fentanyl Transdermal Adhesion Scoring Tool for Use in Clinical Practice Sudeep Raj Bista, BPharm, MSPharm, MMedRes, Janet Hardy, BSc,

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,

Prognostic Tools in Patients With Advanced Cancer: A Systematic Review

Logan H. Ramsey, BS Journal of Pain and Symptom Management

A 10-Year Longitudinal Study of Effects of a Multifaceted Residency Spiritual Care Curriculum: Clinical Ability, Professional Formation, End of Life,

Helping Patients with Advanced Cancer Live with Concerns About Eating: A Challenge for Palliative Care Professionals Jane Hopkinson, PhD, RGN, Jessica.

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

Is It the Difference a Day Makes

Associations Between Physical Activity and Quality of Life in Cancer Patients Receiving Palliative Care: A Pilot Survey Sonya S. Lowe, MD, MSc, Sharon.

Patient-Controlled Analgesia for Children at Home

Presentation transcript:

Factors Influencing Australian General Practitioners' Clinical Decisions Regarding Advance Care Planning: A Factorial Survey Craig Sinclair, PhD, Kiri Gates, BSc, Sharon Evans, PhD, Kirsten Anne Auret, MBBS, FRACP, FAChPM Journal of Pain and Symptom Management Volume 51, Issue 4, Pages 718-727.e2 (April 2016) DOI: 10.1016/j.jpainsymman.2015.11.014 Copyright © 2016 American Academy of Hospice and Palliative Medicine Terms and Conditions

Fig. 1 Relationship between researcher-defined vignette factor levels (x-axis) and the accompanying participant ratings (family support, mortality risk, doctor-patient relationship, patient openness to ACP). Box and whisker plots show median (central line), interquartile range (outer bounds of boxes), and maxima/minima (outer bounds of whiskers). All comparisons of participant ratings of different factor levels were significant at P < 0.001. ACP = advance care planning. Journal of Pain and Symptom Management 2016 51, 718-727.e2DOI: (10.1016/j.jpainsymman.2015.11.014) Copyright © 2016 American Academy of Hospice and Palliative Medicine Terms and Conditions