Literature DB >> 17087706

How should nations measure the quality of end-of-life care for older adults? Recommendations for an international minimum data set.

David J Casarett1, Joan Teno, Irene Higginson.   

Abstract

Nations face numerous challenges in providing high-quality end-of-life care for their citizens, and an aging population that has a prolonged trajectory of decline and substantial needs for care magnifies these challenges. As nations begin to address these challenges, it will be essential to determine whether their responses are effective, but current national data collection efforts are sporadic, and data are often collected only for patients who receive care through certain funding programs or provider organizations or in selected sites of care. Therefore, governments do not know whether their citizens are receiving adequate care, whether current programs are improving care, or how their outcomes compare with those of other countries. This article describes the importance of developing national minimum data sets that can be used to assess the quality of end-of-life care that older adults receive and recommends key variables that these data sets should include.

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Year:  2006        PMID: 17087706     DOI: 10.1111/j.1532-5415.2006.00925.x

Source DB:  PubMed          Journal:  J Am Geriatr Soc        ISSN: 0002-8614            Impact factor:   5.562


  7 in total

1.  Selection bias in family reports on end of life with dementia in nursing homes.

Authors:  Jenny T van der Steen; Luc Deliens; Miel W Ribbe; Bregje D Onwuteaka-Philipsen
Journal:  J Palliat Med       Date:  2012-11-15       Impact factor: 2.947

Review 2.  Outcome assessment instruments in palliative and hospice care--a review of the literature.

Authors:  Stephanie Stiel; T Pastrana; C Balzer; F Elsner; C Ostgathe; L Radbruch
Journal:  Support Care Cancer       Date:  2012-03-13       Impact factor: 3.603

3.  Increasing Trend in Hospital Deaths Consistent among Older Decedents in Korea: A Population-based Study Using Death Registration Database, 2001-2014.

Authors:  Tran Thi Xuan Mai; Eunsook Lee; Hyunsoon Cho; Yoon Jung Chang
Journal:  BMC Palliat Care       Date:  2018-01-11       Impact factor: 3.234

4.  Policies to improve end-of-life decisions in Flemish hospitals: communication, training of health care providers and use of quality assessments.

Authors:  Ina D'Haene; Robert H Vander Stichele; H Roeline W Pasman; Nele Van den Noortgate; Johan Bilsen; Freddy Mortier; Luc Deliens
Journal:  BMC Palliat Care       Date:  2009-12-30       Impact factor: 3.234

5.  Towards a standardized method of developing quality indicators for palliative care: protocol of the Quality indicators for Palliative Care (Q-PAC) study.

Authors:  Kathleen Leemans; Joachim Cohen; Anneke L Francke; Robert Vander Stichele; Susanne Jj Claessen; Lieve Van den Block; Luc Deliens
Journal:  BMC Palliat Care       Date:  2013-02-08       Impact factor: 3.234

6.  Nationwide continuous monitoring of end-of-life care via representative networks of general practitioners in Europe.

Authors:  Lieve Van den Block; Bregje Onwuteaka-Philipsen; Koen Meeussen; Gé Donker; Francesco Giusti; Guido Miccinesi; Viviane Van Casteren; Tomas Vega Alonso; Oscar Zurriaga; Luc Deliens
Journal:  BMC Fam Pract       Date:  2013-06-03       Impact factor: 2.497

7.  Place of death in the Czech Republic and Slovakia: a population based comparative study using death certificates data.

Authors:  Martin Loucka; Sheila A Payne; Sarah G Brearley
Journal:  BMC Palliat Care       Date:  2014-03-20       Impact factor: 3.234

  7 in total

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