Literature DB >> 18335259

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

David C Currow1, Alicia M Ward, John L Plummer, Eduardo Bruera, Amy P Abernethy.   

Abstract

INTRODUCTION: Specialised palliative care services (SPCS) aim to address the needs of patients and caregivers confronting life-limiting illnesses but only half of the potential cohort are referred. Randomised controlled trials of SPCS provision can no longer be ethically justified so there is a need to develop new methods to evaluate the net impact of SPCS for the whole community, not just for those who access SPCS. The aim of this study was to assess whether perceived comfort in the last 2 weeks of life was associated with accessing SPCS.
METHODS: This study utilised a whole-of-population random survey (n = 4,366) in South Australia. A total of 802 respondents had someone close to them die within the last 5 years due to a terminal illness, and they had the complete data. A subsequent question was asked whether SPCS had been accessed. Perceived comfort levels for those who had used SPCS were compared with those who did not by using stereotype logistic regression, weighted to a standardised population.
RESULTS: Higher levels of comfort of the deceased having been assessed 'very comfortable' was associated with the use of SPCS (p = 0.04; odds ratio, 1.78; 95% confidence interval, 1.02-3.08). For people who accessed SPCS, 13.3% were reported as 'very comfortable' compared with 8.0% without SPCS. Almost one half of respondents (48.4%) reported that the deceased was considered 'uncomfortable' or 'very uncomfortable', irrespective of SPCS access. DISCUSSION: While this study provides further incremental evidence of benefit from access to SPCS, there is much that still needs to be done to improve care for the whole community at the end of life.

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Year:  2008        PMID: 18335259     DOI: 10.1007/s00520-008-0424-2

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  48 in total

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Review 2.  [Outpatient palliative medicine : Attitudes in the care of palliative emergencies. Prospective questionnaire-based investigation].

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3.  International recommendations for outpatient palliative care and prehospital palliative emergencies - a prospective questionnaire-based investigation.

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Journal:  BMC Palliat Care       Date:  2013-02-21       Impact factor: 3.234

4.  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

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Authors:  Tanveer Mir
Journal:  J IMA       Date:  2011-12

6.  Referral patterns and proximity to palliative care inpatient services by level of socio-economic disadvantage. A national study using spatial analysis.

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7.  Values and options in cancer care (VOICE): study design and rationale for a patient-centered communication and decision-making intervention for physicians, patients with advanced cancer, and their caregivers.

Authors:  Michael Hoerger; Ronald M Epstein; Paul C Winters; Kevin Fiscella; Paul R Duberstein; Robert Gramling; Phyllis N Butow; Supriya G Mohile; Paul R Kaesberg; Wan Tang; Sandy Plumb; Adam Walczak; Anthony L Back; Daniel Tancredi; Alison Venuti; Camille Cipri; Gisela Escalera; Carol Ferro; Don Gaudion; Beth Hoh; Blair Leatherwood; Linda Lewis; Mark Robinson; Peter Sullivan; Richard L Kravitz
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8.  Bereavement help-seeking following an 'expected' death: a cross-sectional randomised face-to-face population survey.

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  8 in total

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