Literature DB >> 19183701

Patients' Experiences of Being a Burden on Family in Terminal Illness.

Julia Overturf Johnson1, Daniel P Sulmasy, Marie T Nolan.   

Abstract

Studies of persons with chronic and life-threatening illness have revealed a fear of being a burden on family. The purpose of this case study was to explore that concern in-depth in three persons with different terminal illnesses. Participants were part of a larger study of end-of-life decision making and were selected for this study because their illnesses are characterized by a steady decline in health (amyotrophic lateral sclerosis), a rapid decline (stage IV lung cancer), or an uncertain trajectory of decline (advanced heart failure). Content analysis of their interviews resulted in four themes: managing the burden, spirituality, supportive relationships, and planning for the future. Themes contained specific categories of thoughts, feelings, and actions related to fear of being a burden. These themes should be explored in greater depth in future larger studies of persons with terminal illness.

Entities:  

Year:  2007        PMID: 19183701      PMCID: PMC2632772          DOI: 10.1097/01.NJH.0000289656.91880.f2

Source DB:  PubMed          Journal:  J Hosp Palliat Nurs        ISSN: 1522-2179            Impact factor:   1.918


  12 in total

Review 1.  Whatever happened to qualitative description?

Authors:  M Sandelowski
Journal:  Res Nurs Health       Date:  2000-08       Impact factor: 2.228

2.  Renal dialysis abatement: lessons from a social study.

Authors:  Michael Ashby; Corinne op't Hoog; Allan Kellehear; Peter G Kerr; Denise Brooks; Kathy Nicholls; Marian Forrest
Journal:  Palliat Med       Date:  2005-07       Impact factor: 4.762

3.  Understanding the will to live in patients nearing death.

Authors:  Harvey Max Chochinov; Thomas Hack; Thomas Hassard; Linda J Kristjanson; Susan McClement; Mike Harlos
Journal:  Psychosomatics       Date:  2005 Jan-Feb       Impact factor: 2.386

4.  Measuring quality of care at the end of life: a statement of principles.

Authors:  J Lynn
Journal:  J Am Geriatr Soc       Date:  1997-04       Impact factor: 5.562

5.  Feeling like a burden: exploring the perspectives of patients at the end of life.

Authors:  Christine J McPherson; Keith G Wilson; Mary Ann Murray
Journal:  Soc Sci Med       Date:  2006-10-27       Impact factor: 4.634

6.  What matters most in end-of-life care: perceptions of seriously ill patients and their family members.

Authors:  Daren K Heyland; Peter Dodek; Graeme Rocker; Dianne Groll; Amiram Gafni; Deb Pichora; Sam Shortt; Joan Tranmer; Neil Lazar; Jim Kutsogiannis; Miu Lam
Journal:  CMAJ       Date:  2006-02-28       Impact factor: 8.262

7.  Factors considered important at the end of life by patients, family, physicians, and other care providers.

Authors:  K E Steinhauser; N A Christakis; E C Clipp; M McNeilly; L McIntyre; J A Tulsky
Journal:  JAMA       Date:  2000-11-15       Impact factor: 56.272

8.  Families looking back: one year after discussion of withdrawal or withholding of life-sustaining support.

Authors:  K H Abbott; J G Sago; C M Breen; A P Abernethy; J A Tulsky
Journal:  Crit Care Med       Date:  2001-01       Impact factor: 7.598

9.  Disparities in perceptions of distress and burden in ALS patients and family caregivers.

Authors:  E E Adelman; S M Albert; J G Rabkin; M L Del Bene; T Tider; I O'Sullivan
Journal:  Neurology       Date:  2004-05-25       Impact factor: 9.910

10.  Quality end-of-life care: patients' perspectives.

Authors:  P A Singer; D K Martin; M Kelner
Journal:  JAMA       Date:  1999-01-13       Impact factor: 56.272

View more
  10 in total

1.  Live and let die: existential decision processes in a fatal disease.

Authors:  Dorothée Lulé; Sonja Nonnenmacher; Sonja Sorg; Johanna Heimrath; Martin Hautzinger; Thomas Meyer; Andrea Kübler; Niels Birbaumer; Albert C Ludolph
Journal:  J Neurol       Date:  2014-01-12       Impact factor: 4.849

2.  Are the data on quality of life and patient reported outcomes from clinical trials of metastatic non-small-cell lung cancer important?

Authors:  Vera Hirsh
Journal:  World J Clin Oncol       Date:  2013-11-10

3.  Mitigating End-of-Life Burden: Parallel Perspectives of Physician-Patients & Family Caregivers.

Authors:  Jonathan J Suen; Emily Vo; Catherine A Clair; Marie T Nolan; Joseph J Gallo; Martha Abshire Saylor
Journal:  J Pain Symptom Manage       Date:  2021-11-23       Impact factor: 3.612

4.  Experiences of End-of-Life Care of Older Adults with Cancer From the Perspective of Stakeholdersin Iran: A Content Analysis Study.

Authors:  Zohreh Ghezelsefli; Fazlollah Ahmadi; Eesa Mohammadi; Martine Puts Rn
Journal:  Asian Pac J Cancer Prev       Date:  2021-01-01

5.  Effects of a transitional palliative care model on patients with end-stage heart failure: a randomised controlled trial.

Authors:  Frances Kam Yuet Wong; Alina Yee Man Ng; Paul Hong Lee; Po-Tin Lam; Jeffrey Sheung Ching Ng; Nancy Hiu Yim Ng; Michael Mau Kwong Sham
Journal:  Heart       Date:  2016-03-11       Impact factor: 5.994

6.  Self-management of patients with advanced cancer: A systematic review of experiences and attitudes.

Authors:  Sophie I van Dongen; Kim de Nooijer; Jane M Cramm; Anneke L Francke; Wendy H Oldenmenger; Ida J Korfage; Frederika E Witkamp; Rik Stoevelaar; Agnes van der Heide; Judith Ac Rietjens
Journal:  Palliat Med       Date:  2020-02       Impact factor: 4.762

7.  Hospitalized patients with heart failure: the impact of anxiety, fatigue, and therapy adherence on quality of life.

Authors:  Maria Polikandrioti; Ioannis Koutelekos; George Panoutsopoulos; Georgia Gerogianni; Afroditi Zartaloudi; Evangelos Dousis; Fotoula Babatsikou; Georgia Toulia
Journal:  Arch Med Sci Atheroscler Dis       Date:  2019-12-02

8.  The experiences of adult heart, lung, and heart-lung transplantation recipients: A systematic review of qualitative research evidence.

Authors:  Claire Stubber; Maggie Kirkman
Journal:  PLoS One       Date:  2020-11-11       Impact factor: 3.240

9.  What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives.

Authors:  Anne Hogden; David Greenfield; Peter Nugus; Matthew C Kiernan
Journal:  Patient Prefer Adherence       Date:  2012-11-27       Impact factor: 2.711

Review 10.  Is the Evaluation of Quality of Life in NSCLC Trials Important? Are the Results to be Trusted?

Authors:  Vera Hirsh
Journal:  Front Oncol       Date:  2014-07-03       Impact factor: 6.244

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.