Literature DB >> 15612235

Information needs of family caregivers of terminal cancer patients in Taiwan.

Wei-chun Lin1, Chao-jung Tsao.   

Abstract

Previous studies have indicated that when family caregivers are provided with enough of the right information their coping strategies in caring for terminal cancer patients are enhanced. In Taiwan, family caregivers are highly involved in their ill family member's symptom management and must stay at the bedside to share the nursing and caregiving tasks in the palliative care unit. The cross-sectional survey described here used a structured questionnaire to identify six domains of information needed among family caregivers who stay in the palliative care units to prepare them to provide hospice homecare after discharge. The six domains for which family members needed specific information included the basic tenets of caregiving, the disease, the social welfare of the patient, psychosocial issues, palliative care, and spirituality/religion. This study indicated that information about the disease itself was of greatest importance, with the least importance attached to spiritual and religious information. Age, gender, educational level, and socioeconomic status (SES) of family caregivers were factors in how they viewed the importance of each domain. Situation-related variables, such as the extent of each caregiver's role in decision making, duration of the patient's disease, and the treatment the patient was undergoing were also related to how caregivers valued each type of information. Study results indicated that the education of caregivers in the palliative care unit should be individualized based on each patient's condition and each family's characteristics.

Entities:  

Mesh:

Year:  2004        PMID: 15612235     DOI: 10.1177/104990910402100609

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  6 in total

1.  Parental Factors for Mental Health Service Engagement Among Chinese Young Adults.

Authors:  Ching-Wen Chang; Fang-Pei Chen; Hiuning Tai
Journal:  Community Ment Health J       Date:  2019-12-18

2.  The lack of standard definitions in the supportive and palliative oncology literature.

Authors:  David Hui; Masanori Mori; Henrique A Parsons; Sun Hyun Kim; Zhijun Li; Shamsha Damani; Eduardo Bruera
Journal:  J Pain Symptom Manage       Date:  2011-11-21       Impact factor: 3.612

3.  Evaluation of the quality of life of caregivers in gynecological cancer patients.

Authors:  Memnun Seven; Sakine Yılmaz; Eda Şahin; Aygül Akyüz
Journal:  J Cancer Educ       Date:  2014-06       Impact factor: 2.037

4.  A need for cancer patient education from the perspective of Chinese patients and nurses: a comparison study.

Authors:  Ruishuang Zheng; Judith Judi Johnson; Qi Wang; Jingmin Hu
Journal:  Support Care Cancer       Date:  2014-04-06       Impact factor: 3.603

5.  Living in the presence of death: an integrative literature review of relatives' important existential concerns when caring for a severely ill family member.

Authors:  Christina Melin-Johansson; Ingela Henoch; Susann Strang; Maria Browall
Journal:  Open Nurs J       Date:  2012-02-10

6.  Patients' and caregivers' needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries.

Authors:  Lucy Ellen Selman; Lisa Jane Brighton; Shane Sinclair; Ikali Karvinen; Richard Egan; Peter Speck; Richard A Powell; Ewa Deskur-Smielecka; Myra Glajchen; Shelly Adler; Christina Puchalski; Joy Hunter; Nancy Gikaara; Jonathon Hope
Journal:  Palliat Med       Date:  2017-10-12       Impact factor: 4.762

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.