Literature DB >> 19193253

Evaluations of end of life with dementia by families in Dutch and U.S. nursing homes.

Jenny T van der Steen1, Marie-José H E Gijsberts, Martien T Muller, Luc Deliens, Ladislav Volicer.   

Abstract

BACKGROUND: The End-of-Life in Dementia (EOLD) scales comprise the most specific set of instruments developed for evaluations of patients' end of life by their families. It is not known whether the EOLD scales are useful for cross-national comparisons.
METHODS: We used a mortality follow-back design in multi-center studies in the Netherlands (pilot study 2005-2007) and the U.S.A. (1999), and we compared EOLD Satisfaction With Care (SWC; last three months of life), Symptom Management (SM; last three months) and Comfort Assessment in Dying (CAD) scores for 54 Dutch and 76 U.S. nursing home residents.
RESULTS: SWC total scores did not differ significantly between the Dutch and U.S. studies (31.9, SD 4.7 versus 30.4, SD 6.1), but three of ten items were rated more favorable for Dutch residents, as were SM total scores (29.1, SD 9.2 versus 20.4, SD 10.6). CAD total scores did not differ (32.0, SD 5.4 versus 30.5, SD 5.9, respectively), but the "well-being" subscale was rated more favorably for Dutch residents. Results were similar after adjustment for demographics and dementia severity.
CONCLUSION: The Dutch families rated end of life with dementia in nursing homes as somewhat better than did U.S. families. Although differences were small, the observed patterns were consistent. This suggests validity of the SM and CAD to assess differences in quality of dying and possible sensitivity to differences between countries or time frames. Larger, simultaneous, cross-national studies are needed to confirm usefulness of the scales and to detect areas which need improvement in the respective countries.

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Year:  2009        PMID: 19193253     DOI: 10.1017/S1041610208008399

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  9 in total

Review 1.  Measuring Experience With End-of-Life Care: A Systematic Literature Review.

Authors:  Jessica Penn Lendon; Sangeeta C Ahluwalia; Anne M Walling; Karl A Lorenz; Oluwatobi A Oluwatola; Rebecca Anhang Price; Denise Quigley; Joan M Teno
Journal:  J Pain Symptom Manage       Date:  2014-12-24       Impact factor: 3.612

2.  Prevalence and Predictors of Symptoms in Persons with Advanced Dementia Living in the Community.

Authors:  Kurt Kroenke; Sujuan Gao; Kelly M Mosesso; Susan E Hickman; Laura R Holtz; Alexia M Torke; Nina M Johnson; Greg A Sachs
Journal:  J Palliat Med       Date:  2022-03-29       Impact factor: 2.947

3.  Medical Decisions Made by Surrogates for Persons with Advanced Dementia within Weeks or Months of Death.

Authors:  Peter V Rabins; Kathryn L Hicks; Betty S Black
Journal:  AJOB Prim Res       Date:  2011-10

4.  Effects of facilitated family case conferencing for advanced dementia: A cluster randomised clinical trial.

Authors:  Meera Agar; Tim Luckett; Georgina Luscombe; Jane Phillips; Elizabeth Beattie; Dimity Pond; Geoffrey Mitchell; Patricia M Davidson; Janet Cook; Deborah Brooks; Jennifer Houltram; Stephen Goodall; Lynnette Chenoweth
Journal:  PLoS One       Date:  2017-08-07       Impact factor: 3.240

5.  Living and dying with advanced dementia: A prospective cohort study of symptoms, service use and care at the end of life.

Authors:  Elizabeth L Sampson; Bridget Candy; Sarah Davis; Anna Buylova Gola; Jane Harrington; Michael King; Nuriye Kupeli; Gerry Leavey; Kirsten Moore; Irwin Nazareth; Rumana Z Omar; Victoria Vickerstaff; Louise Jones
Journal:  Palliat Med       Date:  2017-09-18       Impact factor: 4.762

6.  Trends in quality of care and dying perceived by family caregivers of nursing home residents with dementia 2005-2019.

Authors:  Maartje S Klapwijk; Sascha R Bolt; Jannie A Boogaard; Maud Ten Koppel; Marie-José He Gijsberts; Carolien van Leussen; B Anne-Mei The; Judith Mm Meijers; Jos Mga Schols; H Roeline W Pasman; Bregje D Onwuteaka-Philipsen; Luc Deliens; Lieve Van den Block; Bart Mertens; Henrica Cw de Vet; Monique Aa Caljouw; Wilco P Achterberg; Jenny T van der Steen
Journal:  Palliat Med       Date:  2021-08-28       Impact factor: 4.762

7.  Care dependency of patients and residents at the end of life: A secondary data analysis of data from a cross-sectional study in hospitals and geriatric institutions.

Authors:  Gerhilde Schüttengruber; Ruud J G Halfens; Christa Lohrmann
Journal:  J Clin Nurs       Date:  2021-06-20       Impact factor: 4.423

8.  Feedback on end-of-life care in dementia: the study protocol of the FOLlow-up project.

Authors:  Jannie A Boogaard; Mirjam C van Soest-Poortvliet; Johannes R Anema; Wilco P Achterberg; Cees M P M Hertogh; Henrica C W de Vet; Jenny T van der Steen
Journal:  BMC Palliat Care       Date:  2013-08-07       Impact factor: 3.234

9.  Pragmatic cluster randomised controlled trial of facilitated family case conferencing compared with usual care for improving end of life care and outcomes in nursing home residents with advanced dementia and their families: the IDEAL study protocol.

Authors:  Meera Agar; Elizabeth Beattie; Tim Luckett; Jane Phillips; Georgina Luscombe; Stephen Goodall; Geoffrey Mitchell; Dimity Pond; Patricia M Davidson; Lynnette Chenoweth
Journal:  BMC Palliat Care       Date:  2015-11-21       Impact factor: 3.234

  9 in total

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