Literature DB >> 11532586

Preparing for the end of life: preferences of patients, families, physicians, and other care providers.

K E Steinhauser1, N A Christakis, E C Clipp, M McNeilly, S Grambow, J Parker, J A Tulsky.   

Abstract

To examine patients', families', and health care providers' preferences regarding preparation for the end of life, attributes of preparation were generated in qualitative focus group discussions and subsequently tested for generalizability in a quantitative national survey. Respondents from all groups showed consensus on the importance of naming someone to make decisions, knowing what to expect about one's physical condition, having financial affairs in order, having treatment preferences in writing, and knowing that one's physician is comfortable talking about death and dying. Patients were more likely than physicians to want to plan funerals and know the timing of death and less likely than all other groups to want to discuss personal fears. Participants in care of dying patients agree overwhelmingly with the importance of preparation. However, significant barriers to preparation impede it from being a common part of clinical encounters. Further research and training are needed to ensure that the desire for greater preparation is translated into improved action toward preparation in medical practice.

Entities:  

Keywords:  Death and Euthanasia; Empirical Approach

Mesh:

Year:  2001        PMID: 11532586     DOI: 10.1016/s0885-3924(01)00334-7

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  110 in total

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2.  Comparing three life-limiting diseases: does diagnosis matter or is sick, sick?

Authors:  Karen E Steinhauser; Robert M Arnold; Maren K Olsen; Jennifer Lindquist; Judith Hays; Laura L Wood; Allison M Burton; James A Tulsky
Journal:  J Pain Symptom Manage       Date:  2011-01-28       Impact factor: 3.612

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Authors:  Irene J Higginson
Journal:  BMJ       Date:  2003-09-13

4.  Advance care planning for patients with amyotrophic lateral sclerosis.

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5.  A narrative account of the impact of positive thinking on discussions about death and dying.

Authors:  Catherine McGrath; Kathleen Montgomery; Karolyn White; Ian H Kerridge
Journal:  Support Care Cancer       Date:  2006-05-23       Impact factor: 3.603

Review 6.  A systematic review of measures of end-of-life care and its outcomes.

Authors:  Richard A Mularski; Sydney M Dy; Lisa R Shugarman; Anne M Wilkinson; Joanne Lynn; Paul G Shekelle; Sally C Morton; Virginia C Sun; Ronda G Hughes; Lara K Hilton; Margaret Maglione; Shannon L Rhodes; Cony Rolon; Karl A Lorenz
Journal:  Health Serv Res       Date:  2007-10       Impact factor: 3.402

7.  Association between strong patient-oncologist agreement regarding goals of care and aggressive care at end-of-life for patients with advanced cancer.

Authors:  Sara L Douglas; Barbara J Daly; Amy R Lipson; Eric Blackstone
Journal:  Support Care Cancer       Date:  2020-02-14       Impact factor: 3.603

8.  Considerations for Quality Improvement in Radiation Oncology Therapy for Patients with Uncomplicated Painful Bone Metastases.

Authors:  Anne M Walling; Phillip J Beron; Tania Kaprealian; Patrick A Kupelian; Neil S Wenger; Susan A McCloskey; Christopher R King; Michael Steinberg
Journal:  J Palliat Med       Date:  2017-02-23       Impact factor: 2.947

9.  Ethical Considerations About Clinician Reimbursement for Advance Care Planning.

Authors:  Amelia K Barwise; Michael E Wilson; Richard R Sharp; Erin S DeMartino
Journal:  Mayo Clin Proc       Date:  2020-04       Impact factor: 7.616

Review 10.  Palliative care reduces morbidity and mortality in cancer.

Authors:  Gabrielle B Rocque; James F Cleary
Journal:  Nat Rev Clin Oncol       Date:  2012-12-18       Impact factor: 66.675

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