Literature DB >> 7551420

The information and learning needs of the caregiving family of the adult patient with cancer.

C Hardwick, N Lawson.   

Abstract

The need for information by the caregiving family of an adult patient with cancer has been identified by research. This paper is a literature review of the information and learning needs of caregiving relatives. By meeting these needs the health care professional is able to help support the family, and therefore the patient, with the difficult adjustment to the diagnosis and through the subsequent course of the disease. The health care professional facilitates the individual caregivers' coping mechanisms and the benefits can be seen in the caregiving outcome for both the family and the patient. Information needs vary from individual to individual and are dynamic throughout the cancer experience. This paper describes the role of the nurse in this area, and encourages the nurse to act as a resource person for the caregiver by the appropriate delivery of information and by ensuring that the information given to the family by other health care professionals is understood and fulfils their needs.

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Mesh:

Year:  1995        PMID: 7551420     DOI: 10.1111/j.1365-2354.1995.tb00068.x

Source DB:  PubMed          Journal:  Eur J Cancer Care (Engl)        ISSN: 0961-5423            Impact factor:   2.520


  8 in total

1.  Living with cancer: a qualitative report of the experiences of leukaemia patients in Lagos, Nigeria.

Authors:  Samuel Ojima Adejoh; Olusegun Moses Temilola; Bolutife Olayiwola
Journal:  J Cancer Educ       Date:  2013-12       Impact factor: 2.037

2.  Web-based cancer communication and decision making systems: connecting patients, caregivers, and clinicians for improved health outcomes.

Authors:  Lori L DuBenske; David H Gustafson; Bret R Shaw; James F Cleary
Journal:  Med Decis Making       Date:  2010-11-01       Impact factor: 2.583

3.  Clinical practice guidelines of the French Association for Supportive Care in Cancer and the French Society for Psycho-oncology: refusal of treatment by adults afflicted with cancer.

Authors:  J C Faivre; V Adam; V Block; M Metzger; J Salleron; S Dauchy
Journal:  Support Care Cancer       Date:  2017-06-08       Impact factor: 3.603

4.  Caregivers' participation in the oncology clinic visit mediates the relationship between their information competence and their need fulfillment and clinic visit satisfaction.

Authors:  Lori L DuBenske; Ming-Yuan Chih; David H Gustafson; Susan Dinauer; James F Cleary
Journal:  Patient Educ Couns       Date:  2010-09-28

5.  Role of Respite Palliative Care in Understanding and Managing Complex Palliative Care Situation - A Case Report.

Authors:  Tanvi Shinde; Anuja Damani; Arunangshu Ghoshal; Mary Ann Muckaden; Jayita Deodhar
Journal:  Indian J Palliat Care       Date:  2022-02-01

6.  Caregivers' differing needs across key experiences of the advanced cancer disease trajectory.

Authors:  Lori L DuBenske; Kuang-Yi Wen; David H Gustafson; Charles A Guarnaccia; James F Cleary; Susan K Dinauer; Fiona M McTavish
Journal:  Palliat Support Care       Date:  2008-09

7.  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

8.  An analysis of first-time enquirers to the CancerBACUP information service: variations with cancer site, demographic status and geographical location.

Authors:  M Boudioni; K McPherson; J Mossman; M Boulton; A L Jones; J King; E Wilson; M L Slevin
Journal:  Br J Cancer       Date:  1999-01       Impact factor: 7.640

  8 in total

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