Literature DB >> 28112072

Physicians' perceptions of suffering in people with dementia at the end of life.

Jenny T van der Steen1, Luc Deliens2, Raymond T C M Koopmans3, Bregje D Onwuteaka-Philipsen4.   

Abstract

OBJECTIVE: Our aim was to describe physicians' perceptions of the suffering of their patients who are dying with dementia, many of whom are incompetent with regard to decision making and have difficulty with communicating about the source of their distress and with identifying related factors.
METHOD: We analyzed data from the nationally representative observational Dutch End-of-Life in Dementia (DEOLD) cohort study (2007-2011), which involved 34 long-term care facilities. A total of 103 physicians completed questionnaires about 330 patients with dementia who had died in a participating facility. Suffering during the last six hours of life was defined as "a patient being disturbed by or aware of symptoms," "suffering until the end or death was a struggle"-all related to objective indicators of lack of comfort. We employed generalized estimating equation models to assess associations of suffering with the characteristics of physicians and patients, the patient's death, and the decision-making process.
RESULTS: In 13.8% of cases, the physician felt that the patient had suffered. An unexpected death and death with pneumonia were strongly (an odds ratios close to 6) associated with suffering, and suffering was also independently associated with the physician's perception of worse quality of end-of-life care, death with cardiovascular disease, a less experienced physician, no palliative sedation, and a younger patient. SIGNIFICANCE OF
RESULTS: Most patients with dementia did not suffer during their final hours of life, according to their physicians. There are a number of factors associated with suffering, among them death with pneumonia and unexpected death. We may not be able to have much influence on death from pneumonia, but quality of care and an unexpected death are reasonable targets for intervention. Earlier identification of the beginning of the dying process would allow time to better prepare for approaching death, which would provide a source of comfort.

Entities:  

Keywords:  Dementia; End of life; Nursing homes; Palliative care; Quality of life

Mesh:

Year:  2017        PMID: 28112072     DOI: 10.1017/S1478951516000985

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  6 in total

1.  Physician and Surrogate Agreement with Assisted Dying and Continuous Deep Sedation in Advanced Dementia in Switzerland.

Authors:  Andrea Jutta Loizeau; Simon M Cohen; Susan L Mitchell; Nathan Theill; Stefanie Eicher; Mike Martin; Florian Riese
Journal:  Neurodegener Dis       Date:  2019-04-23       Impact factor: 2.977

2.  Palliative Care in Advanced Dementia: Comparison of Strategies in Three Countries.

Authors:  Shelley A Sternberg; Shiri Shinan-Altman; Ladislav Volicer; David J Casarett; Jenny T van der Steen
Journal:  Geriatrics (Basel)       Date:  2021-04-22

3.  Incidence of pneumonia in nursing home residents with dementia in the Netherlands: an estimation based on three differently designed studies.

Authors:  T P Zomer; T VAN DER Maaden; A B VAN Gageldonk-Lafeber; S C DE Greeff; J T VAN DER Steen; L Verhoef
Journal:  Epidemiol Infect       Date:  2017-07-03       Impact factor: 4.434

4.  Palliative care for people with dementia in the terminal phase: a mixed-methods qualitative study to inform service development.

Authors:  Jenny T van der Steen; Natashe Lemos Dekker; Marie-José H E Gijsberts; Laura H Vermeulen; Margje M Mahler; B Anne-Mei The
Journal:  BMC Palliat Care       Date:  2017-04-28       Impact factor: 3.234

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

  6 in total

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