Literature DB >> 20477857

Needs for everyday life support for brain tumour patients' relatives: systematic literature review.

K Madsen1, H S Poulsen.   

Abstract

The purpose of this paper is to undertake a review of the everyday lives and the need for support felt by relatives of adults with malignant cerebral glioma. Through electronic literature searches we identified studies with qualitative, quantitative or mixed method designs. Fourteen studies were identified. They indicated that a relative often assumes the caregiver's role, taking over responsibility for the patient's illness and survival, and that the relative is often overwhelmingly exhausted by this task. The ever-changing circumstances left the relatives fearful, anxious and apprehensive. The relatives lacked information about how to provide day-to-day care and how to manage psychoses and neuropsychiatric problems at home. Likewise, they needed help from the professionals to talk with each other about potentially reduced life expectancy. Most relatives appeared to value specialist nurse support highly, and they found support groups helpful. Relatively few studies were identified, and extant research was found to be diverse in purpose, study design and study population. The majority of the studies focused only on the parts of the relatives' everyday lives in which they were taking care of and supporting the patient. Further research focusing on the impact of the illness on different part of relative's everyday life is needed.
© 2010 Blackwell Publishing Ltd.

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Year:  2011        PMID: 20477857     DOI: 10.1111/j.1365-2354.2010.01184.x

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


  21 in total

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2.  Interventions to help support caregivers of people with a brain or spinal cord tumour.

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3.  Needs of neuro-oncological patients and their caregivers during the hospitalization and after discharge: results from a longitudinal study.

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4.  Do carer's levels of unmet needs change over time when caring for patients diagnosed with high-grade glioma and how are these needs correlated with distress?

Authors:  G K B Halkett; E A Lobb; T Shaw; M M Sinclair; L Miller; E Hovey; A K Nowak
Journal:  Support Care Cancer       Date:  2017-08-14       Impact factor: 3.603

Review 5.  Report of the Jumpstarting Brain Tumor Drug Development Coalition and FDA clinical trials clinical outcome assessment endpoints workshop (October 15, 2014, Bethesda MD).

Authors:  Jennifer L Helfer; Patrick Y Wen; Jaishri Blakeley; Mark R Gilbert; Terri S Armstrong
Journal:  Neuro Oncol       Date:  2016-03       Impact factor: 12.300

6.  The caregivers' perspective on the end-of-life phase of glioblastoma patients.

Authors:  Birgit Flechl; Michael Ackerl; Cornelia Sax; Stefan Oberndorfer; Bernadette Calabek; Eefje Sizoo; Jaap Reijneveld; Richard Crevenna; Mohammad Keilani; Alexander Gaiger; Karin Dieckmann; Matthias Preusser; Martin J B Taphoorn; Christine Marosi
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7.  Dose-dense temozolomide for recurrent high-grade gliomas: a single-center retrospective study.

Authors:  Catherine R Garcia; Stacey A Slone; Rachael M Morgan; Lindsey Gruber; Sameera S Kumar; Donita D Lightner; John L Villano
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Review 8.  Survivorship and Caregiver Issues in Neuro-oncology.

Authors:  Heather E Leeper
Journal:  Curr Treat Options Oncol       Date:  2019-11-13

9.  The multidimensional burden of informal caregivers in primary malignant brain tumor.

Authors:  Eléonore Bayen; Florence Laigle-Donadey; Myrtille Prouté; Khê Hoang-Xuan; Marie-Eve Joël; Jean-Yves Delattre
Journal:  Support Care Cancer       Date:  2016-09-13       Impact factor: 3.603

10.  Supportive follow-up in patients treated with radical intent for high-grade glioma.

Authors:  Susan Catt; Anthony Chalmers; Giles Critchley; Lesley Fallowfield
Journal:  CNS Oncol       Date:  2012-09
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