Patient reported outcome measures of quality of end-of-life care: A systematic review.

Abstract:

:End-of-life (EoL) care1 is increasingly used as a generic term in preference to palliative care or terminal care, particularly with reference to individuals with chronic disease, who are resident in community and long-term care (LTC) settings. This review evaluates studies based on patient reported outcome measures (PROMS) of quality of EoL care across all health-care settings. From 1041 citations, 12 studies were extracted by searches conducted in EBSCO, Scopus, Web of Science, PubMed, Cochrane, Open Grey and Google Scholar databases. At present, the evidence base for EoL care is founded on cancer care. This review highlights the paucity of studies that evaluate quality of EoL care for patients with chronic disease outside the established cancer-acute care paradigm, particularly in LTC. This review highlights the absence of any PROMs for the estimated 60% of patients in LTC with cognitive impairment. Patient-reported outcomes (PROs) are critical to understanding how EoL care services and practices affect patients' health and EoL experience. PROMs describe the quality of care from the patient's perspective and add balance to existing clinical or proxy-derived knowledge on the quality of care and services provided.

journal_name

Maturitas

journal_title

Maturitas

authors

Kearns T,Cornally N,Molloy W

doi

10.1016/j.maturitas.2016.11.004

subject

Has Abstract

pub_date

2017-02-01 00:00:00

pages

16-25

eissn

0378-5122

issn

1873-4111

pii

S0378-5122(16)30290-0

journal_volume

96

pub_type

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