Literature DB >> 18762992

Perceived importance of evidence-based psychosocial clinical guidelines for Hong Kong Chinese women with breast cancer: opinions of patients and health care providers.

Wendy Wing Tak Lam1, Cecilia Fabrizio, Ella Ho, Lillian Chan, Richard Fielding.   

Abstract

AIM: The aim of this study was to assess Chinese breast cancer patients' and health care providers' (HCPs) perceptions of psychosocial clinical guidelines developed by the Australian National Health and Medical Research Council's National Breast Cancer Centre.
MATERIALS AND METHODS: A convenience sample of Hong Kong Chinese women diagnosed with breast cancer was recruited. In addition, all surgeons and clinical/medical oncologists registered with the Hong Kong Medical Council were invited to complete a mailed survey. Both women and HCPs were asked to rate the importance of the 55 psychosocial clinical guideline items. HCPs also rated the feasibility of implementing each item in their practice. Overall, 344 of 362 (95%) women completed the face-to-face interview. Of 490 eligible HCPs, 75 (15%) completed the mailed survey.
RESULTS: At least 50% of the women rated 16 of the 55 psychosocial issues as an essential part of psychosocial care in clinical practice. The top ten ranked items rated essential by patients addressed disease and treatment information provision and question opportunity. HCPs also placed high priority on the scope and opportunities for information giving. Emotional care was intermediately valued. Practical issues and providing social support were rated by both patients and HCPs as the least important aspect of psychosocial care in clinical practice. Fewer than half of the HCPs rated any psychosocial item as feasible to implement in their practice.
CONCLUSIONS: Chinese women value information provision and question opportunities, highlighting the need of HCPs to address these issues. Interventions that facilitate HCP's provision of psychosocial support in breast cancer should be set as a high priority.

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Year:  2008        PMID: 18762992     DOI: 10.1007/s00520-008-0500-7

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  34 in total

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2.  Depressive disorders in an out-patient oncology setting: prevalence, assessment, and management.

Authors:  R M Berard; F Boermeester; G Viljoen
Journal:  Psychooncology       Date:  1998 Mar-Apr       Impact factor: 3.894

3.  The unmet supportive care needs of patients with cancer. Supportive Care Review Group.

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4.  Diagnostic efficiency of the Hospital Anxiety and Depression Scale in women with early stage breast cancer.

Authors:  Anthony W Love; David W Kissane; Sidney Bloch; DavidM Clarke
Journal:  Aust N Z J Psychiatry       Date:  2002-04       Impact factor: 5.744

Review 5.  Doctor-patient communication and satisfaction with care in oncology.

Authors:  Anne Brédart; Carole Bouleuc; Sylvie Dolbeault
Journal:  Curr Opin Oncol       Date:  2005-07       Impact factor: 3.645

6.  Is there consensus between breast cancer patients and providers on guidelines for breaking bad news?

Authors:  A Girgis; R W Sanson-Fisher; M J Schofield
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8.  Oncologists' reactions to cancer patients' verbal cues.

Authors:  P N Butow; R F Brown; S Cogar; M H N Tattersall; S M Dunn
Journal:  Psychooncology       Date:  2002 Jan-Feb       Impact factor: 3.894

9.  What are the information needs of Chinese breast cancer patients receiving chemotherapy?

Authors:  Yik Mun Lee; Karen Francis; Jayne Walker; Sze Ming Lee
Journal:  Eur J Oncol Nurs       Date:  2004-09       Impact factor: 2.398

10.  The information needs of women newly diagnosed with breast cancer.

Authors:  K A Luker; K Beaver; S J Leinster; R G Owens; L F Degner; J A Sloan
Journal:  J Adv Nurs       Date:  1995-07       Impact factor: 3.187

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  2 in total

1.  Health information wanted and obtained from doctors/nurses: a comparison of Chinese cancer patients and family caregivers.

Authors:  Bo Xie; Zhaohui Su; Yihao Liu; Mo Wang; Ming Zhang
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2.  Health information sources for different types of information used by Chinese patients with cancer and their family caregivers.

Authors:  Bo Xie; Zhaohui Su; Yihao Liu; Mo Wang; Ming Zhang
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  2 in total

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