A method for defining and estimating the palliative care population.

Abstract:

:Palliative care research is challenged by a disagreement as to what palliative care is, when it should be offered and what conditions warrant specialized palliative care services. These challenges became evident when we used a population-based data linkage to evaluate the delivery of palliative care services in Western Australia. This paper describes the development of a conceptual framework to provide minimal, mid-range, and maximal estimates of a palliative care population. The estimates include nonmalignant conditions; realistically restrict the number and types of conditions; and propose a time frame over which specialized services can be offered. In defining a palliative care population for the purpose of research, development of an estimation method simultaneously addressed the rhetoric of palliative care with the restrictions inherent in both population-based research and service delivery. When applied to a population, the 10 conditions of the minimal estimate provide an acceptable guide to future research and practice.

journal_name

J Pain Symptom Manage

authors

McNamara B,Rosenwax LK,Holman CD

doi

10.1016/j.jpainsymman.2005.12.018

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

5-12

issue

1

eissn

0885-3924

issn

1873-6513

pii

S0885-3924(06)00250-8

journal_volume

32

pub_type

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