Literature DB >> 7719517

Terminal illness: views of patients and their lay carers.

D Field1, C Douglas, C Jagger, P Dand.   

Abstract

This paper examines the responses of 28 terminally ill patients and their lay carers to identical questions about the patients' experiences in the month prior to their admission to an inpatient hospice. No statistically significant differences were found between the reports of patients or carers regarding the patients' activities of daily living, their physical symptoms, or the evaluations of the care they received. Discrepancies between accounts were most likely to concern the presence or absence of psychological symptoms, the degree of distress caused to patients by their symptoms, and the main symptoms experienced by the patient on their admission to the hospice. It is suggested that the accounts of patients' experiences given by their carers can be used as a valid source of information.

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Year:  1995        PMID: 7719517     DOI: 10.1177/026921639500900107

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  7 in total

1.  Dying from cancer in community hospitals or a hospice: closest lay carers' perceptions.

Authors:  D A Seamark; S Williams; M Hall; C J Lawrence; J Gilbert
Journal:  Br J Gen Pract       Date:  1998-06       Impact factor: 5.386

2.  Unmet care needs of people with a neurological chronic disease: a cross-sectional study in Italy on Multiple Sclerosis.

Authors:  Michela Ponzio; Andrea Tacchino; Paola Zaratin; Concetta Vaccaro; Mario Alberto Battaglia
Journal:  Eur J Public Health       Date:  2015-03-30       Impact factor: 3.367

3.  Experience in the use of the palliative care outcome scale.

Authors:  A-M Stevens; B Gwilliam; R A'hern; K Broadley; J Hardy
Journal:  Support Care Cancer       Date:  2005-04-22       Impact factor: 3.603

4.  What do laypersons consider as a good death.

Authors:  Kai-Kuen Leung; Wen-Jing Liu; Shao-Yi Cheng; Tai-Yuan Chiu; Ching-Yu Chen
Journal:  Support Care Cancer       Date:  2008-11-04       Impact factor: 3.603

5.  Comfort in the last 2 weeks of life: relationship to accessing palliative care services.

Authors:  David C Currow; Alicia M Ward; John L Plummer; Eduardo Bruera; Amy P Abernethy
Journal:  Support Care Cancer       Date:  2008-03-12       Impact factor: 3.603

6.  Comfort experience in palliative care: a phenomenological study.

Authors:  Adriana Coelho; Vitor Parola; Miguel Escobar-Bravo; João Apóstolo
Journal:  BMC Palliat Care       Date:  2016-08-02       Impact factor: 3.234

7.  Caregivers for people with end-stage lung disease: characteristics and unmet needs in the whole population.

Authors:  David C Currow; Alicia Ward; Katie Clark; Catherine M Burns; Amy P Abernethy
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2008
  7 in total

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