Literature DB >> 17006111

Problems experienced by the informal caregivers of cancer patients and their needs for support.

Bart H P Osse1, Myrra J F J Vernooij-Dassen, Egbert Schadé, Richard P T M Grol.   

Abstract

Informal caregivers experience problems of their own for which they need support, but despite the efforts of the World Health Organization to include the well-being of family members and caregivers in the concept of palliative care, their needs are rarely assessed systematically. This report explores caregivers' problems and their needs for professional support. Seventy-six caregivers of cancer patients with advanced disease completed a comprehensive needs assessment questionnaire, the Problems and Needs in Palliative Care questionnaire-caregiver form, listing 67 potential problems in their quality of life and their role of caregiver and 9 items concerning informational needs. The results of this study reveal that the "Top 20" list of the problems and needs reported by caregivers includes fears and emotional burdens; for the most part, caregivers did not need any more professional attention than they were already receiving. Many, however, needed support for managing patients' symptoms and wanted professional attention for the availability and coordination of services. Despite communalities, there was diversity in caregivers' individual needs. Personal needs could be identified with the Problems and Needs in Palliative Care questionnaire-caregiver form checklist. Although only a few caregivers were affected by some issues, such as financial problems, help for them was often needed. In conclusion, most caregivers would like more professional attention for 4 or 5 specific issues, often related to their competence as caregivers for their patients. Using structured needs assessments with the Problems and Needs in Palliative Care questionnaire-caregiver form seems a feasible method to identify the needs of individual caregivers in palliative care.

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Year:  2006        PMID: 17006111     DOI: 10.1097/00002820-200609000-00005

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  40 in total

1.  Managing Medications During Home Hospice Cancer Care: The Needs of Family Caregivers.

Authors:  Jennifer Tjia; Lee Ellington; Margaret F Clayton; Celeste Lemay; Maija Reblin
Journal:  J Pain Symptom Manage       Date:  2015-07-06       Impact factor: 3.612

Review 2.  Development of cancer needs questionnaire for parents and carers of adolescents and young adults with cancer.

Authors:  Mariko L Carey; Tara Clinton-McHarg; Robert William Sanson-Fisher; Anthony Shakeshaft
Journal:  Support Care Cancer       Date:  2011-05-01       Impact factor: 3.603

3.  Demonstration of facial communication of emotion through telehospice videophone contact.

Authors:  Karen L Schmidt; Amanda Gentry; Joan K Monin; Karen L Courtney
Journal:  Telemed J E Health       Date:  2011-04-14       Impact factor: 3.536

4.  Patient and caregiver perceptions of lymphoma care and research opportunities: A qualitative study.

Authors:  Jackelyn B Payne; Kaylin V Dance; Monique Farone; Anh Phan; Cathy D Ho; Meghan Gutierrez; Lillian Chen; Christopher R Flowers
Journal:  Cancer       Date:  2019-07-29       Impact factor: 6.860

5.  Randomized Pilot Trial of a Telephone Symptom Management Intervention for Symptomatic Lung Cancer Patients and Their Family Caregivers.

Authors:  Catherine E Mosher; Joseph G Winger; Nasser Hanna; Shadia I Jalal; Lawrence H Einhorn; Thomas J Birdas; DuyKhanh P Ceppa; Kenneth A Kesler; Jordan Schmitt; Deborah A Kashy; Victoria L Champion
Journal:  J Pain Symptom Manage       Date:  2016-07-09       Impact factor: 3.612

6.  Development of a Symptom Management Intervention: Qualitative Feedback From Advanced Lung Cancer Patients and Their Family Caregivers.

Authors:  Catherine E Mosher; Mary A Ott; Nasser Hanna; Shadia I Jalal; Victoria L Champion
Journal:  Cancer Nurs       Date:  2017 Jan/Feb       Impact factor: 2.592

Review 7.  Psychosocial interventions for patients and caregivers in the age of new communication technologies: opportunities and challenges in cancer care.

Authors:  Hoda Badr; Cindy L Carmack; Michael A Diefenbach
Journal:  J Health Commun       Date:  2015-01-28

8.  Acute impact of home parenteral nutrition in patients with late-stage cancer on family caregivers: preliminary data.

Authors:  Lidia Santarpia; Federico Bozzetti
Journal:  Support Care Cancer       Date:  2017-09-18       Impact factor: 3.603

9.  A pilot study on the influence of an individualized and experiential training on cancer caregiver's self-efficacy in home care and symptom management.

Authors:  Cristina C Hendrix; Amy Abernethy; Rick Sloane; Joey Misuraca; Joseph Moore
Journal:  Home Healthc Nurse       Date:  2009-05

10.  Exploring spirituality in family caregivers of patients with primary malignant brain tumors across the disease trajectory.

Authors:  Alyssa G Newberry; Chien-Wen Jean Choi; Heidi S Donovan; Richard Schulz; Catherine Bender; Barbara Given; Paula Sherwood
Journal:  Oncol Nurs Forum       Date:  2013-05-01       Impact factor: 2.172

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