Literature DB >> 8694674

Is economic hardship on the families of the seriously ill associated with patient and surrogate care preferences? SUPPORT Investigators.

K E Covinsky1, C S Landefeld, J Teno, A F Connors, N Dawson, S Youngner, N Desbiens, J Lynn, W Fulkerson, D Reding, R Oye, R S Phillips.   

Abstract

BACKGROUND: Serious illness often causes economic hardship for patients' families. However, it is not known whether this hardship is associated with a preference for the goal of care to focus on maximizing comfort instead of maximizing life expectancy or whether economic hardship might give rise to disagreement between patients and surrogates over the goal of care.
METHODS: We performed a cross-sectional study of 3158 seriously ill patients (median age, 63 years; 44% women) at 5 tertiary medical centers with 1 of 9 diagnoses associated with a high risk of mortality. Two months after their index hospitalization, patients and surrogates were surveyed about patients' preferences for the primary goal of care: either care focused on extending life or care focused on maximizing comfort. Patients and surrogates were also surveyed about the financial impact of the illness on the patient's family.
RESULTS: A report of economic hardship on the family as a result of the illness was associated with a preference for comfort care over life-extending care (odds ratio, 1.26; 95% confidence interval, 1.07-1.48) in an age-stratified bivariate analysis. Similarly, in a multivariable analysis controlling for patient demographics, illness severity, functional dependency, depression, anxiety, and pain, economic hardship on the family remained associated with a preference for comfort care over life-extending care (odds ratio, 1.31; 95% confidence interval, 1.10-1.57). Economic hardship on the family did not affect either the frequency or direction of patient-surrogate disagreements about the goal of care.
CONCLUSIONS: In patients with serious illness, economic hardship on the family is associated with preferences for comfort care over life-extending care. However, economic hardship on the family does not appear to be a factor in patient-surrogate disagreements about the goal of care.

Entities:  

Keywords:  Death and Euthanasia; Empirical Approach; Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatments (SUPPORT)

Mesh:

Year:  1996        PMID: 8694674

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  7 in total

Review 1.  Physician-assisted suicide in the United States: the underlying factors in technology, health care and palliative medicine--Part one.

Authors:  R F Rizzo
Journal:  Theor Med Bioeth       Date:  2000

Review 2.  Use and Meaning of "Goals of Care" in the Healthcare Literature: a Systematic Review and Qualitative Discourse Analysis.

Authors:  Katharine Secunda; M Jeanne Wirpsa; Kathy J Neely; Eytan Szmuilowicz; Gordon J Wood; Ellen Panozzo; Joan McGrath; Anne Levenson; Jonna Peterson; Elisa J Gordon; Jacqueline M Kruser
Journal:  J Gen Intern Med       Date:  2019-10-21       Impact factor: 5.128

3.  Doctor-cared dying instead of physician-assisted suicide: a perspective from Germany.

Authors:  Fuat S Oduncu; Stephan Sahm
Journal:  Med Health Care Philos       Date:  2010-11

4.  Palliative Care: Critical Concepts for the Geropsychiatrist.

Authors:  Jaclyn M Lindsey; K Maureen Shelton; Allison H Beito; Maria I Lapid
Journal:  Focus (Am Psychiatr Publ)       Date:  2021-07-09

5.  Association Between Hospice Enrollment and Total Health Care Costs for Insurers and Families, 2002-2018.

Authors:  Melissa D Aldridge; Jaison Moreno; Karen McKendrick; Lihua Li; Ab Brody; Peter May
Journal:  JAMA Health Forum       Date:  2022-02-11

6.  Financial hardship and the intensity of medical care received near death.

Authors:  Reginald D Tucker-Seeley; Gregory A Abel; Hajime Uno; Holly Prigerson
Journal:  Psychooncology       Date:  2014-07-23       Impact factor: 3.894

7.  'No matter what the cost': A qualitative study of the financial costs faced by family and whānau caregivers within a palliative care context.

Authors:  Merryn Gott; Ruth Allen; Tess Moeke-Maxwell; Clare Gardiner; Jackie Robinson
Journal:  Palliat Med       Date:  2015-02-13       Impact factor: 4.762

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.