Literature DB >> 23670718

A multicenter survey of Hispanic caregiver preferences for patient decision control in the United States and Latin America.

Sriram Yennurajalingam1, Antonio Noguera, Henrique Afonseca Parsons, Isabel Torres-Vigil, Eva Rosina Duarte, Alejandra Palma, Sofia Bunge, J Lynn Palmer, Marvin Omar Delgado-Guay, Eduardo Bruera.   

Abstract

BACKGROUND: Understanding family caregivers' decisional role preferences is important for communication, quality of care, and patient and family satisfaction. The family caregiver has an important role in a patient's decisional role preferences. There are limited studies on family caregivers' preferences of the patient's decision control at the end of life among Hispanics. AIMS: To identify Hispanic caregivers' preferences of the decision control of patients with advanced cancer and to compare the preferences of caregivers in Hispanic Latin American and Hispanic American caregivers.
DESIGN: We surveyed patients and their family caregivers referred to outpatient palliative care clinics in the United States, Chile, Argentina, and Guatemala. Caregiver preferences of patient's decision control were evaluated using the Control Preference Scale. Caregivers' and patients' sociodemographic variables, patient performance status, and Hispanic American patient acculturation level were also collected. PARTICIPANTS: A total of 387 caregivers were surveyed: 100 (26%) in Chile, 99 (26%) in Argentina, 97 (25%) in Guatemala, and 91 (24%) in the United States. The median age was 56 years, and 59% were female.
RESULTS: Caregiver preference of patient's decision control was passive, shared, and active for 10 (11%), 45 (52%), and 32 (37%) Hispanic American caregivers and 54 (19%), 178 (62%), and 55 (19%) Hispanic Latin American caregivers (p = 0.0023), respectively. Caregiver acculturation level did not affect the preferences of the Hispanic American sample (p = 0.60).
CONCLUSIONS: Most Hispanic family caregivers preferred the patient to make shared decisions. Hispanic Latin American caregivers more frequently preferred patients to assume a passive decisional role. Acculturation did not influence the preferences of Hispanic American caregivers.

Entities:  

Keywords:  Decisional role preferences; Hispanics; Latinos; family caregivers; palliative care

Mesh:

Year:  2013        PMID: 23670718      PMCID: PMC3742314          DOI: 10.1177/0269216313486953

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  26 in total

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Journal:  Cancer Nurs       Date:  2002-12       Impact factor: 2.592

2.  Shared decision-making in the medical encounter: what does it mean? (or it takes at least two to tango).

Authors:  C Charles; A Gafni; T Whelan
Journal:  Soc Sci Med       Date:  1997-03       Impact factor: 4.634

3.  Opiniones: end-of-life care preferences and planning of older Latinos.

Authors:  Amy S Kelley; Neil S Wenger; Catherine A Sarkisian
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4.  Empowerment of men newly diagnosed with prostate cancer.

Authors:  B J Davison; L F Degner
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5.  The dynamics of change: cancer patients' preferences for information, involvement and support.

Authors:  P N Butow; M Maclean; S M Dunn; M H Tattersall; M J Boyer
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6.  Patient preferences versus physician perceptions of treatment decisions in cancer care.

Authors:  E Bruera; C Sweeney; K Calder; L Palmer; S Benisch-Tolley
Journal:  J Clin Oncol       Date:  2001-06-01       Impact factor: 44.544

7.  Treatment decisions for breast carcinoma: patient preferences and physician perceptions.

Authors:  Eduardo Bruera; Jie S Willey; J Lynn Palmer; Marguerite Rosales
Journal:  Cancer       Date:  2002-04-01       Impact factor: 6.860

8.  Decision making during serious illness: what role do patients really want to play?

Authors:  L F Degner; J A Sloan
Journal:  J Clin Epidemiol       Date:  1992-09       Impact factor: 6.437

Review 9.  The role of proxies in treatment decisions: evaluating functional capacity to consent to end-of-life treatments within a family context.

Authors:  Rebecca S Allen; John L Shuster
Journal:  Behav Sci Law       Date:  2002

10.  Ethnicity and attitudes toward patient autonomy.

Authors:  L J Blackhall; S T Murphy; G Frank; V Michel; S Azen
Journal:  JAMA       Date:  1995-09-13       Impact factor: 56.272

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3.  The impact of caregiver's role preference on decisional conflicts and psychiatric distresses in decision making to help caregiver's disclosure of terminal disease status.

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Review 4.  End-of-Life Care in Latin America.

Authors:  Enrique Soto-Perez-de-Celis; Yanin Chavarri-Guerra; Tania Pastrana; Rossana Ruiz-Mendoza; Alexandra Bukowski; Paul E Goss
Journal:  J Glob Oncol       Date:  2016-08-24

5.  Perspectives on Kidney Disease Education and Recommendations for Improvement Among Latinx Patients Receiving Emergency-Only Hemodialysis.

Authors:  Tessa K Novick; Santiago Diaz; Francisco Barrios; Doris Cubas; Kavyaa Choudhary; Paul Nader; Raymonda ElKhoury; Lilia Cervantes; Elizabeth A Jacobs
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  5 in total

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