Literature DB >> 25216736

Hospice and Family Involvement With End-of-Life Care: Results From a Population-Based Survey.

Jennifer B Seaman1, Todd M Bear2, Patricia I Documet2, Susan M Sereika3, Steven M Albert2.   

Abstract

Utilization and perceived benefits of hospice may vary across populations. In a population-based survey, we examined the prevalence of hospice utilization, caregiver sociodemographic characteristics, and quality and complexity of end-of-life (EOL) care, as reported by community caregivers to people who died in the prior year. The 2009 to 2010 Allegheny County, PA Behavioral Risk Factor Surveillance System Health Survey, a population-based telephone survey of 5442 adult residents, included an 8-item EOL caregiver module. Overall, 7.8% (95% confidence interval = 7.0-8.6) of respondents reported having arranged or provided care for a close friend/family member who died in the previous 12 months. Caregivers of decedents who utilized hospice reported positive quality outcomes and greater involvement in care. Utilization of hospice services was associated with beneficial outcomes at EOL, but with increased involvement of EOL caregivers.
© The Author(s) 2014.

Entities:  

Keywords:  Behavioral Risk Factor Surveillance System; access; caregivers; community surveys; end-of-life care; evaluation; health care quality; hospice

Mesh:

Year:  2014        PMID: 25216736      PMCID: PMC5538353          DOI: 10.1177/1049909114550392

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  15 in total

1.  Screening for serious mental illness in the general population.

Authors:  Ronald C Kessler; Peggy R Barker; Lisa J Colpe; Joan F Epstein; Joseph C Gfroerer; Eva Hiripi; Mary J Howes; Sharon-Lise T Normand; Ronald W Manderscheid; Ellen E Walters; Alan M Zaslavsky
Journal:  Arch Gen Psychiatry       Date:  2003-02

2.  Hospice utilization and end-of-life care decision making of African Americans.

Authors:  Polly M Mazanec; Barbara J Daly; Aloen Townsend
Journal:  Am J Hosp Palliat Care       Date:  2010-12       Impact factor: 2.500

3.  Development of public health priorities for end-of-life initiatives.

Authors:  Jaya K Rao; Jeanne Alongi; Lynda A Anderson; Larry Jenkins; George-Ann Stokes; Mary Kane
Journal:  Am J Prev Med       Date:  2005-12       Impact factor: 5.043

4.  Racial differences in hospice revocation to pursue aggressive care.

Authors:  Kimberly S Johnson; Maragatha Kuchibhatla; David Tanis; James A Tulsky
Journal:  Arch Intern Med       Date:  2008-01-28

Review 5.  Bereavement after caregiving.

Authors:  Richard Schulz; Randy Hebert; Kathrin Boerner
Journal:  Geriatrics       Date:  2008-01

6.  Hospice care: what services do patients and their families receive?

Authors:  Melissa D A Carlson; R Sean Morrison; Theodore R Holford; Elizabeth H Bradley
Journal:  Health Serv Res       Date:  2007-08       Impact factor: 3.402

7.  Family perspectives on end-of-life care at the last place of care.

Authors:  Joan M Teno; Brian R Clarridge; Virginia Casey; Lisa C Welch; Terrie Wetle; Renee Shield; Vincent Mor
Journal:  JAMA       Date:  2004-01-07       Impact factor: 56.272

Review 8.  A review of barriers to utilization of the medicare hospice benefits in urban populations and strategies for enhanced access.

Authors:  Sean O'Mahony; Janet McHenry; Daniel Snow; Carolyn Cassin; Donald Schumacher; Peter A Selwyn
Journal:  J Urban Health       Date:  2008-03       Impact factor: 3.671

9.  The health impact of health care on families: a matched cohort study of hospice use by decedents and mortality outcomes in surviving, widowed spouses.

Authors:  Nicholas A Christakis; Theodore J Iwashyna
Journal:  Soc Sci Med       Date:  2003-08       Impact factor: 4.634

10.  Patients dying with dementia: experience at the end of life and impact of hospice care.

Authors:  Joseph W Shega; Gavin W Hougham; Carol B Stocking; Deon Cox-Hayley; Greg A Sachs
Journal:  J Pain Symptom Manage       Date:  2008-02-08       Impact factor: 3.612

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  3 in total

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Authors:  Veerawat Phongtankuel; Benjamin A Scherban; Manney C Reid; Amanda Finley; Angela Martin; Jeanne Dennis; Ronald D Adelman
Journal:  J Palliat Med       Date:  2016-01       Impact factor: 2.947

2.  Factors influencing communication and decision-making about life-sustaining technology during serious illness: a qualitative study.

Authors:  Jennifer Kryworuchko; P H Strachan; E Nouvet; J Downar; J J You
Journal:  BMJ Open       Date:  2016-05-23       Impact factor: 2.692

3.  Family Caregivers Who Would Be Unwilling to Provide Care at the End of Life Again: Findings from the Health Survey for England Population Survey.

Authors:  Miriam J Johnson; Victoria Allgar; Una Macleod; Annie Jones; Steven Oliver; David Currow
Journal:  PLoS One       Date:  2016-01-25       Impact factor: 3.240

  3 in total

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