Literature DB >> 10715752

Communication and awareness about dying in the 1990s.

D Field1, G Copp.   

Abstract

Since the 1960s communication and awareness about dying in modern western societies have been topics for debate, with a considerable amount of literature on the need for open communication and the strategies which can be used by health professionals to improve their communication with patients facing a terminal prognosis. Despite the difficulties of comparing studies using different methodologies and the additional problems of ascertaining patients' knowledge and awareness about their impending deaths, the trend is clear. In advanced industrial societies there is increasing evidence that doctors have shifted from a policy of 'withholding' to a policy of 'revealing' to the patient his or her terminal prognosis. This change in medical practice is further supported by other data which show an increase in the percentage of those patients who were aware they were dying from chronic diseases, especially cancer. However, despite the perceived trend towards open disclosure of the patient's terminal illness, recent studies have suggested that in their daily encounters with dying patients health workers employ 'conditional' rather than 'full open disclosure'. Such moderating strategies in discussing the patient's prognosis may be employed despite open awareness of a patient's prognosis. This paper examines this apparent paradox by analysing the complex tensions and conflicts of such communication through a discussion of existing literature on modes of communication and patient awareness.

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Year:  1999        PMID: 10715752     DOI: 10.1191/026921699668763479

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  6 in total

1.  Next of kin's experience of powerlessness and helplessness in palliative home care.

Authors:  Anna Milberg; Peter Strang; Maria Jakobsson
Journal:  Support Care Cancer       Date:  2003-12-18       Impact factor: 3.603

2.  Awareness of dying: it needs words.

Authors:  Martine E Lokker; Lia van Zuylen; Laetitia Veerbeek; Carin C D van der Rijt; Agnes van der Heide
Journal:  Support Care Cancer       Date:  2011-06-19       Impact factor: 3.603

3.  Death talk: gender differences in talking about one's own impending death.

Authors:  Bragi Skulason; Arna Hauksdottir; Kozma Ahcic; Asgeir R Helgason
Journal:  BMC Palliat Care       Date:  2014-03-11       Impact factor: 3.234

4.  People With Advanced Cancer: The Process of Living Well With Awareness of Dying.

Authors:  Maria Arantzamendi; Noelia García-Rueda; Ana Carvajal; Carole A Robinson
Journal:  Qual Health Res       Date:  2018-12-12

5.  Japanese cancer patient participation in and satisfaction with treatment-related decision-making: A qualitative study.

Authors:  Yoshiko Watanabe; Miyako Takahashi; Ichiro Kai
Journal:  BMC Public Health       Date:  2008-02-27       Impact factor: 3.295

6.  Defining the illness trajectory of metastatic breast cancer.

Authors:  Elizabeth Reed; Jessica Corner
Journal:  BMJ Support Palliat Care       Date:  2013-07-23       Impact factor: 3.568

  6 in total

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