Literature DB >> 19449273

Communication in end-stage cancer: review of the literature and future research.

Elizabeth D Trice1, Holly G Prigerson.   

Abstract

Concerns have been raised about the quality of life and health care received by cancer patients at the end of life (EOL). Many patients die with pain and other distressing symptoms inadequately controlled, receiving burdensome, aggressive care that worsens quality of life and limits patient exposure to palliative care, such as hospice. Patient-physician communication is likely a very important determinate of EOL care. Discussions of EOL with physicians are associated with an increased likelihood of the following (1) acknowledgment of terminal illness, (2) preferences for comfort care over life extension, and (3) receipt of less intensive, life-prolonging and more palliative EOL care; while this appears to hold for White patients, it is less clear for Black, advanced cancer patients. These results highlight the importance of communication in determining EOL cancer care and suggest that communication disparities may contribute to Black-White differences in EOL care. We review the pertinent literature and discuss areas for future research.

Entities:  

Mesh:

Year:  2009        PMID: 19449273      PMCID: PMC3779876          DOI: 10.1080/10810730902806786

Source DB:  PubMed          Journal:  J Health Commun        ISSN: 1081-0730


  71 in total

1.  Collusion in doctor-patient communication about imminent death: an ethnographic study.

Authors:  A M The; T Hak; G Koëter; G van Der Wal
Journal:  BMJ       Date:  2000-12-02

2.  Cancer patients' information needs and information seeking behaviour: in depth interview study.

Authors:  G M Leydon; M Boulton; C Moynihan; A Jones; J Mossman; M Boudioni; K McPherson
Journal:  BMJ       Date:  2000-04-01

3.  Factors associated with use of cardiopulmonary resuscitation in seriously ill hospitalized adults.

Authors:  S J Goodlin; Z Zhong; J Lynn; J M Teno; J P Fago; N Desbiens; A F Connors; N S Wenger; R S Phillips
Journal:  JAMA       Date:  1999 Dec 22-29       Impact factor: 56.272

4.  Racial variations in end-of-life care.

Authors:  F P Hopp; S A Duffy
Journal:  J Am Geriatr Soc       Date:  2000-06       Impact factor: 5.562

5.  Information needs in terminal illness.

Authors:  J S Kutner; J F Steiner; K K Corbett; D W Jahnigen; P L Barton
Journal:  Soc Sci Med       Date:  1999-05       Impact factor: 4.634

6.  The patient-physician relationship. Patient-physician communication during outpatient palliative treatment visits: an observational study.

Authors:  S B Detmar; M J Muller; L D Wever; J H Schornagel; N K Aaronson
Journal:  JAMA       Date:  2001-03-14       Impact factor: 56.272

7.  Communicating prognosis to patients with metastatic disease: what do they really want to know?

Authors:  P N Butow; S Dowsett; R Hagerty; M H N Tattersall
Journal:  Support Care Cancer       Date:  2001-09-07       Impact factor: 3.603

8.  The dynamics of change: cancer patients' preferences for information, involvement and support.

Authors:  P N Butow; M Maclean; S M Dunn; M H Tattersall; M J Boyer
Journal:  Ann Oncol       Date:  1997-09       Impact factor: 32.976

9.  End-of-life care in black and white: race matters for medical care of dying patients and their families.

Authors:  Lisa C Welch; Joan M Teno; Vincent Mor
Journal:  J Am Geriatr Soc       Date:  2005-07       Impact factor: 5.562

10.  Desire for information and involvement in treatment decisions: elderly cancer patients' preferences and their physicians' perceptions.

Authors:  Elena B Elkin; Susie H M Kim; Ephraim S Casper; David W Kissane; Deborah Schrag
Journal:  J Clin Oncol       Date:  2007-11-20       Impact factor: 44.544

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  27 in total

1.  Discrepancy between treatment goals documentation by oncologists and their understanding among cancer patients under active treatment with chemotherapy.

Authors:  Varun Monga; Seth M Maliske; Hassan Kaleem; Sarah L Mott; Gideon K D Zamba; Mohammed Milhem
Journal:  Eur J Cancer Care (Engl)       Date:  2018-12-03       Impact factor: 2.520

2.  Reversing Racial Inequities at the End of Life: A Call for Health Systems to Create Culturally Competent Advance Care Planning Programs Within African American Communities.

Authors:  Randi Belisomo
Journal:  J Racial Ethn Health Disparities       Date:  2017-04-13

3.  Gender differences in the evolution of illness understanding among patients with advanced cancer.

Authors:  Kalen Fletcher; Holly G Prigerson; Elizabeth Paulk; Jennifer Temel; Esme Finlay; Lisa Marr; Ruth McCorkle; Lorna Rivera; Francisco Munoz; Paul K Maciejewski
Journal:  J Support Oncol       Date:  2013-09

4.  Patients rate physician communication about lung cancer.

Authors:  Judith E Nelson; Elizabeth B Gay; Andrew R Berman; Charles A Powell; John Salazar-Schicchi; Juan P Wisnivesky
Journal:  Cancer       Date:  2011-04-14       Impact factor: 6.860

5.  Relationships between personal attitudes about death and communication with terminally ill patients: How oncology clinicians grapple with mortality.

Authors:  Rachel A Rodenbach; Kyle E Rodenbach; Mohamedtaki A Tejani; Ronald M Epstein
Journal:  Patient Educ Couns       Date:  2015-10-23

6.  A Patient-Reported Outcome Instrument to Assess Symptom Burden and Predict Survival in Patients with Advanced Cancer: Flipping the Paradigm to Improve Timing of Palliative and End-of-Life Discussions and Reduce Unwanted Health Care Costs.

Authors:  Stuart L Goldberg; Dhakshila Paramanathan; Raya Khoury; Sharmi Patel; Dayo Jagun; Srikesh Arunajadai; Victoria DeVincenzo; Ruth Pe Benito; Brooke Gruman; Sukhi Kaur; Scott Paddock; Andrew D Norden; Eric V Schultz; John Hervey; Terrill Jordan; Andre Goy; Andrew L Pecora
Journal:  Oncologist       Date:  2018-09-28

7.  Illness Understanding and Advance Care Planning in Patients with Advanced Lymphoma.

Authors:  Kelly M Trevino; Sarah C Rutherford; Chrystal Marte; Daniel Jie Ouyang; Peter Martin; Holly G Prigerson; John P Leonard
Journal:  J Palliat Med       Date:  2019-10-18       Impact factor: 2.947

8.  How do surgeons experience and cope with the death and dying of their patients? A qualitative study in the context of life-limiting illnesses.

Authors:  Sofia C Zambrano; Anna Chur-Hansen; Gregory B Crawford
Journal:  World J Surg       Date:  2013-05       Impact factor: 3.352

9.  Development and psychometric evaluation of the Decisional Engagement Scale (DES-10): A patient-reported psychosocial survey for quality cancer care.

Authors:  Michael Hoerger; Benjamin P Chapman; Supriya G Mohile; Paul R Duberstein
Journal:  Psychol Assess       Date:  2016-09

10.  Using a Non-Fit Message Helps to De-Intensify Negative Reactions to Tough Advice.

Authors:  Ilona Fridman; Karen A Scherr; Paul A Glare; E Tory Higgins
Journal:  Pers Soc Psychol Bull       Date:  2016-08
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