Literature DB >> 8426968

The power of compassion: truth-telling among American doctors in the care of dying patients.

N T Miyaji1.   

Abstract

The perceptions of American doctors about their practice regarding truth-telling in the care of dying patients were examined based on semi-structured interviews with 32 physicians in a teaching hospital. The doctors inform patients of their disease using three basic styles; 'telling what patients want to know', 'telling what patients need to know' and 'translating information into terms that patients can take'. These styles are supported by five basic normative principles; 'respect the truth', 'patients rights', 'doctors' duty to inform', 'preserve hope' and 'individual contract between patients and doctors'. These styles and principles suggest that physicians adhere to the recent trends of American medical ethics based on informed consent doctrine, and give the impression that patients have control over obtaining information. But close analysis of their accounts shows that physicians still hold power to control information through their management of the information-giving process. The styles and principles are flexibly interpreted and selectively used in the process so that they facilitate a discourse which justifies, rather than eliminates, the information control. Clinical contexts of information control are analyzed by examining dissimilar manners of providing information about treatment as opposed to prognosis. Physicians give less, and vaguer information about prognosis, citing its uncertainty and lesser relevance to future actions as reasons. Information about treatment is more readily shared in order to counterbalance the negative impact of the news on patients. The analysis reveals that the way doctors control information is closely related to the way they handle aspects of the reality of clinical practice, such as physicians' own emotional coping, institutional and legal constraints, and power relationships among patients, doctors and other care-givers. Situating the findings in the historical context of normative discourse in American medicine, discussion focuses on the issues of trust and power of doctors. The humanistic role of the doctor, although suppressed in the currently dominant, contractual ethical framework, is still powerful in doctors' narratives. It expresses doctors' commitment to patients while preserving their authority. Implications of the individualistic approach to the doctor-patient relationship are also discussed.

Entities:  

Keywords:  Empirical Approach; Massachusetts General Hospital; Professional Patient Relationship

Mesh:

Year:  1993        PMID: 8426968     DOI: 10.1016/0277-9536(93)90008-r

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  25 in total

1.  [Communication, burnout and clinical results: more questions than answers].

Authors:  R M Epstein
Journal:  Aten Primaria       Date:  2001-04-30       Impact factor: 1.137

Review 2.  Informed consent and the use of placebo in Poland: ethical and legal aspects.

Authors:  Piotr Zaborowski; Adam Górski
Journal:  Sci Eng Ethics       Date:  2004-01       Impact factor: 3.525

3.  End-of-life care discussions among patients with advanced cancer: a cohort study.

Authors:  Jennifer W Mack; Angel Cronin; Nathan Taback; Haiden A Huskamp; Nancy L Keating; Jennifer L Malin; Craig C Earle; Jane C Weeks
Journal:  Ann Intern Med       Date:  2012-02-07       Impact factor: 25.391

Review 4.  Can deceiving patients be morally acceptable?

Authors:  Daniel K Sokol
Journal:  BMJ       Date:  2007-05-12

5.  Absorbing information about a child's incurable cancer.

Authors:  Patrizia Lannen; Joanne Wolfe; Jennifer Mack; Erik Onelov; Ullakarin Nyberg; Ulrika Kreicbergs
Journal:  Oncology       Date:  2010-06-07       Impact factor: 2.935

6.  Hope and advance care planning in patients with end stage renal disease: qualitative interview study.

Authors:  Sara N Davison; Christy Simpson
Journal:  BMJ       Date:  2006-09-21

7.  Pushing up daisies: implicit and explicit language in oncologist-patient communication about death.

Authors:  Keri L Rodriguez; Frank J Gambino; Phyllis Butow; Rebecca Hagerty; Robert M Arnold
Journal:  Support Care Cancer       Date:  2006-09-13       Impact factor: 3.603

8.  Ranked importance of outcomes of first-line versus repeated chemotherapy among ovarian cancer patients.

Authors:  Vanessa L Beesley; Alexandra M Clavarino; Penelope M Webb; David K Wyld; Alessandra B Francesconi; Keith R Horwood; James D Doecke; Colleen A Loos; Adele C Green
Journal:  Support Care Cancer       Date:  2009-09-24       Impact factor: 3.603

9.  Family caregiver knowledge of treatment intent in a longitudinal study of patients with advanced cancer.

Authors:  Catherine M Burns; Tracy Dixon; Dorothy Broom; Wayne T Smith; Paul S Craft
Journal:  Support Care Cancer       Date:  2003-07-26       Impact factor: 3.603

10.  Measuring therapeutic alliance between oncologists and patients with advanced cancer: the Human Connection Scale.

Authors:  Jennifer W Mack; Susan D Block; Matthew Nilsson; Alexi Wright; Elizabeth Trice; Robert Friedlander; Elizabeth Paulk; Holly G Prigerson
Journal:  Cancer       Date:  2009-07-15       Impact factor: 6.860

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.