Literature DB >> 20131581

Satisfaction with end-of-life care: a longitudinal study of patients and their family caregivers in the last months of life.

Daren K Heyland1, Christopher Frank, Joan Tranmer, Nancy Paul, Deborah Pichora, Xuran Jiang, Andrew G Day.   

Abstract

To determine whether and how ratings of satisfaction with end-of-life (EOL) care change over time and across settings, we administered a satisfaction questionnaire to patients 55 years and older with advanced medical disease and their family caregivers (FCGs). We re-interviewed approximately every two months for a maximum of four visits. Overall, 97 patients and 68 FCGs completed a baseline interview; 57 and 40 completed two interviews, 35 and 22 completed three, and 15 and 10 completed four. Patient satisfaction increased over time and in three of the six questionnaire domains, but this was largely confounded with the location of interview. Satisfaction scores were greater among patients whose baseline interviews occurred at home. FCGs reported increased satisfaction over time; members of the subgroup that cared for patients who died during the study were less satisfied in the spirituality domain during bereavement than prior to their relative's death. Satisfaction with care tends to vary based on location of interview and may vary across time with respect to certain aspects of EOL care.

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Year:  2009        PMID: 20131581

Source DB:  PubMed          Journal:  J Palliat Care        ISSN: 0825-8597            Impact factor:   2.250


  10 in total

1.  Defining priorities for improving end-of-life care in Canada.

Authors:  Daren K Heyland; Deborah J Cook; Graeme M Rocker; Peter M Dodek; Demetrios J Kutsogiannis; Yoanna Skrobik; Xuran Jiang; Andrew G Day; S Robin Cohen
Journal:  CMAJ       Date:  2010-10-04       Impact factor: 8.262

2.  Satisfaction with oncology care among patients with advanced cancer and their caregivers.

Authors:  Breffni Hannon; Nadia Swami; Monika K Krzyzanowska; Natasha Leighl; Gary Rodin; Lisa W Le; Camilla Zimmermann
Journal:  Qual Life Res       Date:  2013-02-23       Impact factor: 4.147

Review 3.  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

4.  Quality of hospice care: comparison between rural and urban residents.

Authors:  Marianne Baernholdt; Cathy L Campbell; Ivora D Hinton; Guofen Yan; Erica Lewis
Journal:  J Nurs Care Qual       Date:  2015 Jul-Sep       Impact factor: 1.597

5.  Default options in advance directives influence how patients set goals for end-of-life care.

Authors:  Scott D Halpern; George Loewenstein; Kevin G Volpp; Elizabeth Cooney; Kelly Vranas; Caroline M Quill; Mary S McKenzie; Michael O Harhay; Nicole B Gabler; Tatiana Silva; Robert Arnold; Derek C Angus; Cindy Bryce
Journal:  Health Aff (Millwood)       Date:  2013-02       Impact factor: 6.301

6.  Hospice caregivers' experiences with pain management: "I'm not a doctor, and I don't know if I helped her go faster or slower".

Authors:  Debra Parker Oliver; Elaine Wittenberg-Lyles; Karla Washington; Robin L Kruse; David L Albright; Paula K Baldwin; Amy Boxer; George Demiris
Journal:  J Pain Symptom Manage       Date:  2013-05-31       Impact factor: 3.612

7.  Effect of Default Options in Advance Directives on Hospital-Free Days and Care Choices Among Seriously Ill Patients: A Randomized Clinical Trial.

Authors:  Scott D Halpern; Dylan S Small; Andrea B Troxel; Elizabeth Cooney; Brian Bayes; Marzana Chowdhury; Heather E Tomko; Derek C Angus; Robert M Arnold; George Loewenstein; Kevin G Volpp; Douglas B White; Cindy L Bryce
Journal:  JAMA Netw Open       Date:  2020-03-02

8.  Racial/ethnic perspectives on the quality of hospice care.

Authors:  Cathy L Campbell; Marianne Baernholdt; Guofen Yan; Ivora D Hinton; Erica Lewis
Journal:  Am J Hosp Palliat Care       Date:  2012-09-04       Impact factor: 2.500

9.  Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: does location matter?

Authors:  Fred Burge; Beverley Lawson; Grace Johnston; Yukiko Asada; Paul F McIntyre; Eva Grunfeld; Gordon Flowerdew
Journal:  BMC Palliat Care       Date:  2014-05-14       Impact factor: 3.234

10.  Default options in advance directives: study protocol for a randomised clinical trial.

Authors:  Nicole B Gabler; Elizabeth Cooney; Dylan S Small; Andrea B Troxel; Robert M Arnold; Douglas B White; Derek C Angus; George Loewenstein; Kevin G Volpp; Cindy L Bryce; Scott D Halpern
Journal:  BMJ Open       Date:  2016-06-06       Impact factor: 2.692

  10 in total

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