Literature DB >> 22239609

Advance directive discussions: lost in translation or lost opportunities?

Stacy M Fischer1, Angela Sauaia, Sung-Joon Min, Jean Kutner.   

Abstract

BACKGROUND: Previous studies have shown that minority populations have low rates of documented advance directives and express preferences for more life-prolonging interventions at the end of life. We sought to determine the impact of Latino ethnicity on patients' self-report of having an advance directive discussion and having a completed advance directive in the medical record at an index hospitalization for serious medical illness.
METHODS: This was a prospective observational cohort study of 458 adults admitted to the general medical services of a safety net hospital, an academic medical center, and a Veterans' Affairs (VA) hospital. Patients were asked if they had discussed advance directives, and we reviewed medical records for documented advance directives.
RESULTS: Overall, 45% of patients reported having had a discussion about advance directives (29% of Latinos compared with 54% of Caucasians, p=0.0002) and 24% of patients had a completed advance directive in their medical record (25% Latinos and 26% of Caucasians, p=not significant [ns]). Using logistic regression modeling and adjusting for socioeconomic status (SES), education level, and language spoken, Latinos (odds ratio [OR] 0.42, confidence interval [CI] 0.24-0.75) were less likely to report having advance directive discussions compared with Caucasians (referent). However, modeling of a completed advance directive in the medical record showed no significant difference between Latinos (OR 1.44, CI 0.73-2.85) and Caucasians (referent).
CONCLUSIONS: The unexpected discrepancy we found highlights the need for more effective communication in advance care planning that includes education that is culturally sensitive and accessible to persons with low health literacy.

Entities:  

Mesh:

Year:  2012        PMID: 22239609      PMCID: PMC3264957          DOI: 10.1089/jpm.2011.0328

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  34 in total

1.  Experiences of discrimination: validity and reliability of a self-report measure for population health research on racism and health.

Authors:  Nancy Krieger; Kevin Smith; Deepa Naishadham; Cathy Hartman; Elizabeth M Barbeau
Journal:  Soc Sci Med       Date:  2005-04-21       Impact factor: 4.634

2.  Effects of limited English proficiency and physician language on health care comprehension.

Authors:  Elisabeth Wilson; Alice H M Chen; Kevin Grumbach; Frances Wang; Alicia Fernandez
Journal:  J Gen Intern Med       Date:  2005-09       Impact factor: 5.128

Review 3.  Patient navigation: a culturally competent strategy to address disparities in palliative care.

Authors:  Stacy M Fischer; Angela Sauaia; Jean S Kutner
Journal:  J Palliat Med       Date:  2007-10       Impact factor: 2.947

4.  A comparison of Latino and Anglo socially desirable responding.

Authors:  Christopher J Hopwood; Claudia G Flato; Suman Ambwani; Beth H Garland; Leslie C Morey
Journal:  J Clin Psychol       Date:  2009-07

5.  Racial variations in end-of-life care.

Authors:  F P Hopp; S A Duffy
Journal:  J Am Geriatr Soc       Date:  2000-06       Impact factor: 5.562

6.  "They don't want to hear us": Hispanic elders and adult children speak about end-of-life planning.

Authors:  Irene A Gutheil; Janna C Heyman
Journal:  J Soc Work End Life Palliat Care       Date:  2006

7.  Are Latinos less satisfied with communication by health care providers?

Authors:  L S Morales; W E Cunningham; J A Brown; H Liu; R D Hays
Journal:  J Gen Intern Med       Date:  1999-07       Impact factor: 5.128

8.  Physicians' perceptions of patients' social and behavioral characteristics and race disparities in treatment recommendations for men with coronary artery disease.

Authors:  Michelle van Ryn; Diana Burgess; Jennifer Malat; Joan Griffin
Journal:  Am J Public Health       Date:  2005-12-27       Impact factor: 9.308

9.  The effect of race and sex on physicians' recommendations for cardiac catheterization.

Authors:  K A Schulman; J A Berlin; W Harless; J F Kerner; S Sistrunk; B J Gersh; R Dubé; C K Taleghani; J E Burke; S Williams; J M Eisenberg; J J Escarce
Journal:  N Engl J Med       Date:  1999-02-25       Impact factor: 91.245

10.  Health literacy not race predicts end-of-life care preferences.

Authors:  Angelo E Volandes; Michael Paasche-Orlow; Muriel R Gillick; E F Cook; Shimon Shaykevich; Elmer D Abbo; Lisa Lehmann
Journal:  J Palliat Med       Date:  2008-06       Impact factor: 2.947

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  16 in total

1.  Health Literacy Matters More Than Experience for Advance Care Planning Knowledge Among Older Adults.

Authors:  Sarah S Nouri; Deborah E Barnes; Aiesha M Volow; Ryan D McMahan; Margot Kushel; Chengshi Jin; John Boscardin; Rebecca L Sudore
Journal:  J Am Geriatr Soc       Date:  2019-08-19       Impact factor: 5.562

2.  [Knowledge, attitude and opinion of patients regarding the new German legislation on advance care planning : Results of a survey in a department of general internal medicine].

Authors:  S Elmeadawy; C Fitzner; F Elsner; C G Dietrich
Journal:  Schmerz       Date:  2017-02       Impact factor: 1.107

3.  Ethnic Differences in Advance Directive Completion and Care Preferences: What Has Changed in a Decade?

Authors:  Jaclyn Portanova; Jennifer Ailshire; Catherine Perez; Anna Rahman; Susan Enguidanos
Journal:  J Am Geriatr Soc       Date:  2017-03-09       Impact factor: 5.562

4.  Interventions for End of Life Decision Making for Patients with Limited English Proficiency.

Authors:  Amelia Barwise; Joyce Balls-Berry; Jalal Soleimani; Bibek Karki; Brandon Barrett; Katerina Castillo; Samantha Kreps; Hilary Kunkel; Beatriz Vega; Patricia Erwin; Nataly Espinoza Suarez; Michael E Wilson
Journal:  J Immigr Minor Health       Date:  2020-08

5.  Trends in Advance Care Planning in Patients With Cancer: Results From a National Longitudinal Survey.

Authors:  Amol K Narang; Alexi A Wright; Lauren H Nicholas
Journal:  JAMA Oncol       Date:  2015-08       Impact factor: 31.777

6.  The Influence of Race/Ethnicity and Education on Family Ratings of the Quality of Dying in the ICU.

Authors:  Janet J Lee; Ann C Long; J Randall Curtis; Ruth A Engelberg
Journal:  J Pain Symptom Manage       Date:  2015-09-16       Impact factor: 3.612

7.  Advanced Care Directives: Overcoming the Obstacles.

Authors:  Sarah Leatherman Allen; Kimberly S Davis; Paul C Rousseau; Patty J Iverson; Patrick D Mauldin; William P Moran
Journal:  J Grad Med Educ       Date:  2015-03

8.  Impact of end-of-life discussions on the reduction of Latino/non-Latino disparities in do-not-resuscitate order completion.

Authors:  Megan Johnson Shen; Holly G Prigerson; Elizabeth Paulk; Kelly M Trevino; Frank J Penedo; Ana I Tergas; Andrew S Epstein; Alfred I Neugut; Paul K Maciejewski
Journal:  Cancer       Date:  2016-03-15       Impact factor: 6.860

9.  Race, income, and education: associations with patient and family ratings of end-of-life care and communication provided by physicians-in-training.

Authors:  Ann C Long; Ruth A Engelberg; Lois Downey; Erin K Kross; Lynn F Reinke; Laura Cecere Feemster; Danae Dotolo; Dee W Ford; Anthony L Back; J Randall Curtis
Journal:  J Palliat Med       Date:  2014-03-04       Impact factor: 2.947

Review 10.  Interpreting at the End of Life: A Systematic Review of the Impact of Interpreters on the Delivery of Palliative Care Services to Cancer Patients With Limited English Proficiency.

Authors:  Milagros D Silva; Margaux Genoff; Alexandra Zaballa; Sarah Jewell; Stacy Stabler; Francesca M Gany; Lisa C Diamond
Journal:  J Pain Symptom Manage       Date:  2015-11-05       Impact factor: 3.612

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