Literature DB >> 19150577

The statutory duty of physicians to inform patients versus unmet patients' information needs: the case of breast cancer in France.

Nora Moumjid1, Cathy Charles, Magali Morelle, Amiram Gafni, Alain Brémond, Fadila Farsi, Tim Whelan, Marie-Odile Carrère.   

Abstract

OBJECTIVES: (1) To explore empirically the extent to which early stage breast cancer patients in France, wish to be informed about their disease and treatments and (2) in view of the statutory duty of physicians to inform patients, to explore, from the patients' point of view, the type of information given by physicians and whether it meets their information needs.
METHODS: A retrospective, cross-sectional survey questionnaire using standardized questions was administered by mail to newly diagnosed breast cancer patients and evaluated their relationships with the different physicians involved in their treatment at different points in time. Focus was placed on the relationship between surgeons and patients.
RESULTS: Two hundred and thirty-eight patients completed the questionnaire on their relationship with their surgeon. Patients' reported information needs are considerable, though significantly different depending on the item. Patients report that surgeons do not fully respond to their needs. Even though physicians are legally required to provide information to their patients, in routine practice they seem to favour providing information about disease and treatment side effects over treatment consequences, even though patients express a need for information on these latter items.
CONCLUSION: More research is needed on the development, use and outcomes of the various strategies and interventions designed to facilitate and improve information transfer in the physician-patient encounter in France.

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Year:  2009        PMID: 19150577     DOI: 10.1016/j.healthpol.2008.11.010

Source DB:  PubMed          Journal:  Health Policy        ISSN: 0168-8510            Impact factor:   2.980


  5 in total

1.  Inequalities and Barriers to the Use of Supportive Care Among Young Breast Cancer Survivors: a Qualitative Understanding.

Authors:  Veronique Regnier Denois; Madina Querre; Linjie Chen; Marion Barrault; Franck Chauvin
Journal:  J Cancer Educ       Date:  2017-12       Impact factor: 2.037

2.  Health-related information exchange experiences of Jordanian women at breast cancer diagnosis.

Authors:  Rana F Obeidat; Robin M Lally
Journal:  J Cancer Educ       Date:  2014-09       Impact factor: 2.037

Review 3.  Patient-centred care: making cancer treatment centres accountable.

Authors:  Alison Zucca; Rob Sanson-Fisher; Amy Waller; Mariko Carey
Journal:  Support Care Cancer       Date:  2014-04-03       Impact factor: 3.603

Review 4.  Evaluating the quality of shared decision making during the patient-carer encounter: a systematic review of tools.

Authors:  Nathalie Bouniols; Brice Leclère; Leïla Moret
Journal:  BMC Res Notes       Date:  2016-08-02

5.  Study protocol comparing the ethical, psychological and socio-economic impact of personalised breast cancer screening to that of standard screening in the "My Personal Breast Screening" (MyPeBS) randomised clinical trial.

Authors:  Alexandra Roux; Rachel Cholerton; Jonathan Sicsic; Nora Moumjid; David P French; Paolo Giorgi Rossi; Corinne Balleyguier; Michal Guindy; Fiona J Gilbert; Jean-Benoit Burrion; Xavier Castells; David Ritchie; Debbie Keatley; Camille Baron; Suzette Delaloge; Sandrine de Montgolfier
Journal:  BMC Cancer       Date:  2022-05-06       Impact factor: 4.638

  5 in total

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