Literature DB >> 12767584

Patient centered decision making in palliative cancer treatment: a world of paradoxes.

Hanneke de Haes1, Nelleke Koedoot.   

Abstract

Patient centered palliative cancer care would imply, first, the introduction of psychosocial endpoints when evaluating treatment and making decisions. Second, patient control would have to be enhanced by information giving and increased decision involvement. We have indicated that paradoxes exist when a patient centered approach is advocated in the context of palliative cancer care. So-called patient oriented outcomes, like quality of life, once introduced seem to be disregarded by many patients themselves and survival is given a more important weight. Likewise, physicians seem to be inclined to treat patients aggressively for little benefit rather than providing supportive care. Both parties seem to prefer to do something actively to maintain a semblance of control over the disease process. Giving treatment, even if aggressive, is a way to avoid the confrontation with the little efficacy that the physician has to offer to incurable cancer patients. This mechanism is reflected in the content of conversations in palliative care. Patient centered care would imply that patient control and autonomy are enhanced. However, again paradoxically, many patients seem to want to avoid information and leave the decisions to be made by their doctors. Physicians, then, follow such wishes while paying more attention to aggressive therapy than to the notion of watchful waiting. This may help to avoid the painful confrontation with bad news. Dilemmas then remain. Patients wishing to maintain hope and avoid emotional impact of a full understanding of their prognosis may rather not be informed brusquely about prognosis or the aims of supportive therapy and forced to make an informed decision. However, by giving more aggressive, maybe even futile, treatment, and withholding supportive care patients may receive less than 'quality end-of-life care'. Therefore, information about less intrusive strategies should still be given in a cautious manner, while regarding the patient's defenses respectfully.

Entities:  

Mesh:

Year:  2003        PMID: 12767584     DOI: 10.1016/s0738-3991(03)00079-x

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  34 in total

1.  Integrating Decision Making and Mental Health Interventions Research: Research Directions.

Authors:  Celia E Wills; Margaret Holmes-Rovner
Journal:  Clin Psychol (New York)       Date:  2006

2.  The influence of age on perceptions of anticipated financial inadequacy by palliative radiation outpatients.

Authors:  Richard B Francoeur
Journal:  Patient Educ Couns       Date:  2007-09-04

3.  Training for Medical Oncologists on Shared Decision-Making About Palliative Chemotherapy: A Randomized Controlled Trial.

Authors:  Inge Henselmans; Hanneke W M van Laarhoven; Hanneke C J M de Haes; Meltem Tokat; Ellen G Engelhardt; Pomme E A van Maarschalkerweerd; Marleen Kunneman; Petronella B Ottevanger; Serge E Dohmen; Geert-Jan Creemers; Dirkje W Sommeijer; Filip Y F L de Vos; Ellen M A Smets
Journal:  Oncologist       Date:  2018-06-29

4.  Chemotherapy use and patient treatment preferences in advanced colorectal cancer: a prospective cohort study.

Authors:  S Yousuf Zafar; Jennifer L Malin; Steven C Grambow; David H Abbott; Jane T Kolimaga; Leah L Zullig; Jane C Weeks; John Z Ayanian; Katherine L Kahn; Patricia A Ganz; Paul J Catalano; Dee W West; Dawn Provenzale
Journal:  Cancer       Date:  2012-09-12       Impact factor: 6.860

5.  Effect of a Skills Training for Oncologists and a Patient Communication Aid on Shared Decision Making About Palliative Systemic Treatment: A Randomized Clinical Trial.

Authors:  Inge Henselmans; Hanneke W M van Laarhoven; Pomme van Maarschalkerweerd; Hanneke C J M de Haes; Marcel G W Dijkgraaf; Dirkje W Sommeijer; Petronella B Ottevanger; Helle-Brit Fiebrich; Serge Dohmen; Geert-Jan Creemers; Filip Y F L de Vos; Ellen M A Smets
Journal:  Oncologist       Date:  2019-11-26

6.  Changing preferences for information and participation in the last phase of life: a longitudinal study among newly diagnosed advanced lung cancer patients.

Authors:  Koen Pardon; R Deschepper; R Vander Stichele; J L Bernheim; F Mortier; N Bossuyt; D Schallier; P Germonpré; D Galdermans; W Van Kerckhoven; L Deliens
Journal:  Support Care Cancer       Date:  2012-01-15       Impact factor: 3.603

7.  Patient empowerment in Europe: is no further research needed?

Authors:  Livio Garattini; Anna Padula
Journal:  Eur J Health Econ       Date:  2018-06

8.  Doctors' communication of trust, care, and respect in breast cancer: qualitative study.

Authors:  Emma Burkitt Wright; Christopher Holcombe; Peter Salmon
Journal:  BMJ       Date:  2004-03-30

9.  Service user experiences of information delivery after a diagnosis of cancer: a qualitative study.

Authors:  Kristian Pollock; Karen Cox; Penny Howard; Eleanor Wilson; Nima Moghaddam
Journal:  Support Care Cancer       Date:  2007-12-11       Impact factor: 3.603

10.  Understanding palliative cancer chemotherapy: about shared decisions and shared trajectories.

Authors:  Susanne J de Kort; Jeannette Pols; Dick J Richel; Nelleke Koedoot; Dick L Willems
Journal:  Health Care Anal       Date:  2009-05-06
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.