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Associations between Latino ethnicity and the use of emotional support and completion of advance directives

Published online by Cambridge University Press:  11 April 2023

Megan Johnson Shen*
Affiliation:
Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA
Holly G. Prigerson
Affiliation:
Cornell Center for Research on End-of-Life Care, Weill Cornell Medicine, New York, NY, USA Department of Medicine, Weill Cornell Medicine, New York, NY, USA
Paul K. Maciejewski
Affiliation:
Cornell Center for Research on End-of-Life Care, Weill Cornell Medicine, New York, NY, USA Department of Medicine, Weill Cornell Medicine, New York, NY, USA Department of Radiology, Weill Cornell Medicine, New York, NY, USA
*
Author for correspondence: Megan J. Shen, Clinical Research Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave. N., Seattle, WA 98109, USA. Email: mshen2@fredhutch.org

Abstract

Objectives

Latino patients have been shown to engage in advance care planning (ACP) at much lower rates than non-Latino White patients. Coping strategies, such as the use of emotional support, may differentially relate to engagement in ACP among Latino and non-Latino patients. The present study sought to examine the moderating effect of ethnicity on the relationship between the use of emotional support as a coping strategy and completion of advance directives.

Methods

The present study employed a weighted sample (Nw = 185) of Latino and non-Latino White patient participants in Coping with Cancer III, an National Institutes of Health–sponsored, multisite, longitudinal, observational cohort study of patients with advanced cancer and their informal caregivers and oncology providers designed to evaluate Latino/non-Latino disparities in ACP and end-of-life cancer care. Main and interaction effects of Latino ethnicity and use of emotional support on patient use of advance directives were estimated as odds ratios.

Results

Use of emotional support was associated with dramatically lower do-not-resuscitate (DNR) order completion to a greater extent among Latino as compared to non-Latino patients (interaction AOR = 0.33, p = 0.005). Interaction effects were not statistically significant for living will or health-care proxy form completion.

Significance of results

Use of emotional support is associated with lower odds of completing DNRs among Latino than among non-Latino patients. Seeking and/or receiving emotional support may deter Latino patients from completing DNR orders. Research is needed to address both emotional needs and practicalities to ensure high quality end-of-life care among Latino patients with cancer.

Type
Original Article
Copyright
© The Author(s), 2023. Published by Cambridge University Press.

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References

Blackhall, LJ, Frank, G, Murphy, ST, et al. (1999) Ethnicity and attitudes towards life sustaining technology. Social Science & Medicine 48(12), 17791789. doi:10.1016/S0277-9536(99)00077-5CrossRefGoogle ScholarPubMed
Braun, UK, McCullough, LB, Beyth, RJ, et al. (2008) Racial and ethnic differences in the treatment of seriously ill patients: A comparison of African-American, Caucasian and Hispanic veterans. Journal of the National Medical Association 100(9), 10411051. doi:10.1016/S0027-9684(15)31442-5CrossRefGoogle ScholarPubMed
Brinkman-Stoppelenburg, A, Rietjens, JA and van der Heide, A (2014) The effects of advance care planning on end-of-life care: A systematic review. Palliative Medicine 28(8), 10001025. doi:10.1177/0269216314526272CrossRefGoogle ScholarPubMed
Carr, D (2011) Racial differences in end-of-life planning: Why don’t Blacks and Latinos prepare for the inevitable? OMEGA – Journal of Death and Dying 63(1), 120. doi:10.2190/OM.63.1.aCrossRefGoogle ScholarPubMed
Carr, D (2012) Racial and ethnic differences in advance care planning: Identifying subgroup patterns and obstacles. Journal of Aging and Health 24(6), 923947. doi:10.1177/0898264312449185CrossRefGoogle ScholarPubMed
Carrion, IV, Nedjat-Haiem, F, Macip-Billbe, M, et al. (2017) “I told myself to stay positive” perceptions of coping among Latinos with a cancer diagnosis living in the United States. American Journal of Hospice and Palliative Medicine 34(3), 233240. doi:10.1177/1049909115625955CrossRefGoogle ScholarPubMed
Carver, CS (1997) You want to measure coping but your protocol’s too long: Consider the brief cope. International Journal of Behavioral Medicine 4(1), . doi:10.1207/s15327558ijbm0401_6CrossRefGoogle ScholarPubMed
Carver, CS, Pozo, C, Harris, SD, et al. (1999) How coping mediates the effect of optimism on distress: A study of women with early stage breast cancer. Journal of Personality and Social Psychology 65(2), 375390. doi:10.1037/0022-3514.65.2.375CrossRefGoogle Scholar
Davis, A (1995) Ethics and ethnicity: End-of-life decisions in four ethnic groups of cancer patients. Medicine and Law 15(3), 429432.Google Scholar
Duffy, SA, Jackson, FC, Schim, SM, et al. (2006) Racial/ethnic preferences, sex preferences, and perceived discrimination related to end‐of‐life care. Journal of the American Geriatrics Society 54(1), 150157. doi:10.1111/j.1532-5415.2005.00526.xCrossRefGoogle ScholarPubMed
Garrido, MM, Balboni, TA, Maciejewski, PK, et al. (2015) Quality of life and cost of care at the end of life: The role of advance directives. Journal of Pain and Symptom Management 49(5), 828835. doi:10.1016/j.jpainsymman.2014.09.015CrossRefGoogle ScholarPubMed
Gutheil, IA and Heyman, JC (2006) “They Don’t Want to Hear Us” Hispanic elders and adult children speak about end-of-life planning. Journal of Social Work in End-of-life & Palliative Care 2(1), 5570. doi:10.1300/J457v02n01_05CrossRefGoogle ScholarPubMed
Hagan, TL, Fishbein, JN, Nipp, RD, et al. (2017) Coping in patients with incurable lung and gastrointestinal cancers: A validation study of the Brief COPE. Journal of Pain and Symptom Management 53(1), 131138. doi:10.1016/j.jpainsymman.2016.06.005CrossRefGoogle ScholarPubMed
Hanchate, A, Kronman, AC, Young-Xu, Y, et al. (2009) Racial and ethnic differences in end-of-life costs: Why do minorities cost more than whites? Archives of Internal Medicine 169(5), 493501. doi:10.1001/archinternmed.2008.616CrossRefGoogle ScholarPubMed
Kershaw, T, Northouse, L, Kritpracha, C, et al. (2004) Coping strategies and quality of life in women with advanced breast cancer and their family caregivers. Psychology & Health 19(2), 139155. doi:10.1080/08870440310001652687CrossRefGoogle Scholar
Kwak, J and Haley, WE (2005) Current research findings on end-of-life decision making among racially or ethnically diverse groups. The Gerontologist 45(5), 634641. doi:10.1093/geront/45.5.634CrossRefGoogle ScholarPubMed
Lackan, NA, Eschbach, K, Stimpson, JP, et al. (2009) Ethnic differences in in-hospital place of death among older adults in California: Effects of individual and contextual characteristics and medical resource supply. Medical Care 47(2), 138145. doi:10.1097/MLR.0b013e3181844dbaCrossRefGoogle ScholarPubMed
Lichtenthal, WG, Viola, M, Rogers, M, et al. (2021) Development and preliminary evaluation of EMPOWER for surrogate decision-makers of critically ill patients. Palliative & Supportive Care 20(2) 167177. doi:10.1017/S1478951521000626CrossRefGoogle Scholar
Lutgendorf, SK, Anderson, B, Rothrock, N, et al. (2000) Quality of life and mood in women receiving extensive chemotherapy for gynecologic cancer. Cancer: Interdisciplinary International Journal of the American Cancer Society 89(6), 14021411. doi:10.1002/1097-0142(20000915)89:6<1402::AID-CNCR26>3.0.CO;2-H3.0.CO;2-H>CrossRefGoogle ScholarPubMed
Lutgendorf, SK, Anderson, B, Ullrich, P, et al. (2002) Quality of life and mood in women with gynecologic cancer: A one year prospective study. Cancer 94(1), 131140. doi:10.1002/cncr.10155CrossRefGoogle Scholar
Maciejewski, PK, Phelps, AC, Kacel, EL, et al. (2012) Religious coping and behavioral disengagement: Opposing influences on advance care planning and receipt of intensive care near death. Psycho‐Oncology 21(7), 714723. doi:10.1002/pon.1967CrossRefGoogle ScholarPubMed
Mack, JW, Weeks, JC, Wright, AA, et al. (2010) End-of-life discussions, goal attainment, and distress at the end of life: Predictors and outcomes of receipt of care consistent with preferences. Journal of Clinical Oncology 28(7), 12031208. doi:10.1200/JCO.2009.25.4672CrossRefGoogle ScholarPubMed
Mead, EL, Doorenbos, AZ, Javid, SH, et al. (2013) Shared decision-making for cancer care among racial and ethnic minorities: A systematic review. American Journal of Public Health 103(12), e15e29. doi:10.2105/AJPH.2013.301631CrossRefGoogle ScholarPubMed
Pfeiffer, E (1975) A short portable mental status questionnaire for the assessment of organic brain deficit in elderly patients. Journal of the American Geriatrics Society 23(10), 433441. doi:10.1111/j.1532-5415.1975.tb00927.xCrossRefGoogle Scholar
Smith, AK, McCarthy, EP, Paulk, E, et al. (2008) Racial and ethnic differences in advance care planning among patients with cancer: Impact of terminal illness acknowledgment, religiousness, and treatment preferences. Journal of Clinical Oncology 26(25), 41314137. doi:10.1200/JCO.2007.14.8452CrossRefGoogle ScholarPubMed
Stuart, EA (2010) Matching methods for causal inference: A review and a look forward. Statistical Science 25(1), 121. doi:10.1214/09-STS313CrossRefGoogle Scholar
Volandes, AE, Ariza, M, Abbo, ED, et al. (2008) Overcoming educational barriers for advance care planning in Latinos with video images. Journal of Palliative Medicine 11(5), 700706. doi:10.1089/jpm.2007.0172CrossRefGoogle ScholarPubMed
Wright, AA, Zhang, B, Ray, A, et al. (2008) Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment. JAMA: The Journal of the American Medical Association 300(14), 16651673. doi:10.1001/jama.300.14.1665CrossRefGoogle ScholarPubMed
Xu, S, Ross, C, Raebel, MA, et al. (2010) Use of stabilized inverse propensity scores as weights to directly estimate relative risk and its confidence intervals. Value in Health 13(2), 273277. doi:10.1111/j.1524-4733.2009.00671.xCrossRefGoogle ScholarPubMed
Zhang, B, Nilsson, ME and Prigerson, HG (2012) Factors important to patients’ quality of life at the end of life. Archives of Internal Medicine 172(15), 11331142. doi:10.1001/archinternmed.2012.2364CrossRefGoogle ScholarPubMed
Zhang, B, Wright, AA, Huskamp, HA, et al. (2009) Health care costs in the last week of life: Associations with end-of-life conversations. Archives of Internal Medicine 169(5), 480488. doi:10.1001/archinternmed.2008.587CrossRefGoogle ScholarPubMed