Literature DB >> 16376736

Correspondence between patients' preferences and surrogates' understandings for dying and death.

Ruth A Engelberg1, Donald L Patrick, J Randall Curtis.   

Abstract

We examined the agreement between hospice patients' preferences for desired experiences during the last week of life and their surrogates' understandings of those preferences (n=92 pairs). Analyses included percent agreement, intraclass correlation coefficients, and Bland-Altman plots. Demographic characteristics and communication measures associated with better agreement were identified using t-tests and analysis of variance. The median number of items on which patients and family members agreed was 14 of 30 (interquartile range, IQR 10, 16). Preferences with good agreement included both observable and non-observable experiences. Patients who reported having had conversations about treatment preferences and who reported that their surrogates knew their preferences reported higher agreement. Surrogates display a better understanding of what is important to patients at the end of life if they have had discussions about patient preferences. These discussions may enable surrogates and clinicians to more accurately follow patient preferences.

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Year:  2005        PMID: 16376736     DOI: 10.1016/j.jpainsymman.2005.06.006

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


  16 in total

1.  The Quality of Dying and Death Questionnaire (QODD): empirical domains and theoretical perspectives.

Authors:  Lois Downey; J Randall Curtis; William E Lafferty; Jerald R Herting; Ruth A Engelberg
Journal:  J Pain Symptom Manage       Date:  2009-09-25       Impact factor: 3.612

2.  A randomized trial to improve communication about end-of-life care among patients with COPD.

Authors:  David H Au; Edmunds M Udris; Ruth A Engelberg; Paula H Diehr; Christopher L Bryson; Lynn F Reinke; J Randall Curtis
Journal:  Chest       Date:  2011-09-22       Impact factor: 9.410

3.  The effect of end-of-life discussions on perceived quality of care and health status among patients with COPD.

Authors:  Janice M Leung; Edmunds M Udris; Jane Uman; David H Au
Journal:  Chest       Date:  2012-07       Impact factor: 9.410

4.  Dying with motor neurone disease, what can we learn from family caregivers?

Authors:  Robin A Ray; Janice Brown; Annette F Street
Journal:  Health Expect       Date:  2012-04-19       Impact factor: 3.377

5.  Evolution of Investigating Informed Assent Discussions about CPR in Seriously Ill Patients.

Authors:  Renee D Stapleton; Dee W Ford; Katherine R Sterba; Nandita R Nadig; Steven Ades; Anthony L Back; Shannon S Carson; Katharine L Cheung; Janet Ely; Erin K Kross; Robert C Macauley; Jennifer M Maguire; Theodore W Marcy; Jennifer J McEntee; Prema R Menon; Amanda Overstreet; Christine S Ritchie; Blair Wendlandt; Sara S Ardren; Michael Balassone; Stephanie Burns; Summer Choudhury; Sandra Diehl; Ellen McCown; Elizabeth L Nielsen; Sudiptho R Paul; Colleen Rice; Katherine K Taylor; Ruth A Engelberg
Journal:  J Pain Symptom Manage       Date:  2022-06       Impact factor: 5.576

6.  Do surrogates predict patient preferences more accurately after a physician-led discussion about advance directives? A randomized controlled trial.

Authors:  Catarina Sampaio Martins; Iva Sousa; Cláudia Barros; Alexandra Pires; Luisa Castro; Cristina da Costa Santos; Rui Nunes
Journal:  BMC Palliat Care       Date:  2022-07-12       Impact factor: 3.113

7.  Shared priorities for the end-of-life period.

Authors:  Lois Downey; Ruth A Engelberg; J Randall Curtis; William E Lafferty; Donald L Patrick
Journal:  J Pain Symptom Manage       Date:  2008-08-22       Impact factor: 3.612

8.  Rehospitalization of older adults discharged to home hospice care.

Authors:  Anna Goldenheim; Daniel Oates; Victoria Parker; Matthew Russell; Michael Winter; Rebecca A Silliman
Journal:  J Palliat Med       Date:  2014-04-07       Impact factor: 2.947

9.  Improving the quality of palliative and terminal care in the hospital by a network of palliative care nurse champions: the study protocol of the PalTeC-H project.

Authors:  Frederika E Witkamp; Lia van Zuylen; Paul J van der Maas; Helma van Dijk; Carin C D van der Rijt; Agnes van der Heide
Journal:  BMC Health Serv Res       Date:  2013-03-25       Impact factor: 2.655

10.  Development of the Serious Illness Care Program: a randomised controlled trial of a palliative care communication intervention.

Authors:  Rachelle Bernacki; Mathilde Hutchings; Judith Vick; Grant Smith; Joanna Paladino; Stuart Lipsitz; Atul A Gawande; Susan D Block
Journal:  BMJ Open       Date:  2015-10-06       Impact factor: 2.692

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