Literature DB >> 16499474

Interventions to enhance communication among patients, providers, and families.

James A Tulsky1.   

Abstract

Whether patient suffering is caused by physical symptoms, unwanted medical intervention, or spiritual crisis, the common pathway to relief is through a provider who is able to elicit these concerns and is equipped to help the patient and family address them. This paper reviews the current state of knowledge in communication at the end of life, organized according to a framework of information gathering, information giving, and relationship building; and then focuses on interventions to enhance communication among patients, providers, and families. Several observations emerge from the existing literature. Patients have highly individualized desires for information and we cannot predict patient preferences. Communication coding methodology has advanced significantly yet the current systems remain poorly understood and largely inaccessible. Physicians and other health care providers do not discuss sufficiently treatment options, quality of life or respond to emotional cues from patients, and there is plenty of room for improvement. On the positive side, we have also learned that physicians and other health care providers can be taught to communicate better through intensive communication courses, and that communication interventions can improve some patient outcomes. Finally, huge gaps remain in our current knowledge, particularly with regard to understanding the relationship between communication style and outcomes. These findings suggest several recommendations. We should create larger and more diverse datasets; improve upon the analysis of recorded communication data; increase our knowledge about patient preferences for information; establish a stronger link between specific communication behaviors and outcomes; and identify more efficient ways to teach providers communication skills.

Entities:  

Mesh:

Year:  2005        PMID: 16499474     DOI: 10.1089/jpm.2005.8.s-95

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  30 in total

1.  Clergy-laity support and patients' mood during serious illness: a cross-sectional epidemiologic study.

Authors:  Judith C Hays; Laura Wood; Karen Steinhauser; Maren K Olson; Jennifer H Lindquist; James A Tulsky
Journal:  Palliat Support Care       Date:  2011-09

2.  The impact on patient health outcomes of interventions targeting the patient-physician relationship.

Authors:  Stephen M Auerbach
Journal:  Patient       Date:  2009-06-01       Impact factor: 3.883

3.  Communication and decision making about life-sustaining treatment: examining the experiences of resident physicians and seriously-ill hospitalized patients.

Authors:  Kristy S Deep; Charles H Griffith; John F Wilson
Journal:  J Gen Intern Med       Date:  2008-09-18       Impact factor: 5.128

4.  Is Care for the Dying Improving in the United States?

Authors:  Joan M Teno; Vicki A Freedman; Judith D Kasper; Pedro Gozalo; Vincent Mor
Journal:  J Palliat Med       Date:  2015-04-29       Impact factor: 2.947

5.  Palliative care in the pediatric ICU: challenges and opportunities for family-centered practice.

Authors:  Ardith Doorenbos; Taryn Lindhorst; Helene Starks; Eugene Aisenberg; J Randall Curtis; Ross Hays
Journal:  J Soc Work End Life Palliat Care       Date:  2012

6.  A Case Study of Hispanics and Hospice Care.

Authors:  Iraida V Carrion; Karen Bullock
Journal:  Int J Humanit Soc Sci       Date:  2012-02-01

7.  A brief educational intervention to teach residents shared decision making in the intensive care unit.

Authors:  Jacqueline K Yuen; Sonal S Mehta; Jordan E Roberts; Joseph T Cooke; M Carrington Reid
Journal:  J Palliat Med       Date:  2013-04-27       Impact factor: 2.947

8.  Surviving critical illness: acute respiratory distress syndrome as experienced by patients and their caregivers.

Authors:  Christopher E Cox; Sharron L Docherty; Debra H Brandon; Christie Whaley; Deborah K Attix; Alison S Clay; Daniel V Dore; Catherine L Hough; Douglas B White; James A Tulsky
Journal:  Crit Care Med       Date:  2009-10       Impact factor: 7.598

9.  Do-not-resuscitate orders and/or hospice care, psychological health, and quality of life among children/adolescents with acquired immune deficiency syndrome.

Authors:  Maureen E Lyon; Paige L Williams; Elizabeth R Woods; Nancy Hutton; Anne M Butler; Erica Sibinga; Michael T Brady; James M Oleske
Journal:  J Palliat Med       Date:  2008-04       Impact factor: 2.947

10.  Hospital staff attributions of the causes of physician variation in end-of-life treatment intensity.

Authors:  M R Larochelle; K L Rodriguez; R M Arnold; A E Barnato
Journal:  Palliat Med       Date:  2009-03-26       Impact factor: 4.762

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