Racial and Ethnic Differences in Communication and Care for Children With Advanced Cancer

被引:35
作者
Mack, Jennifer W. [1 ,2 ,3 ]
Uno, Hajime [2 ]
Twist, Clare J. [4 ]
Bagatell, Rochelle [5 ,6 ]
Rosenberg, Abby R. [7 ,8 ,9 ]
Marachelian, Araz [10 ]
Granger, M. Meaghan [11 ]
Bender, Julia Glade [12 ]
Baker, Justin N. [13 ]
Park, Julie R. [7 ,9 ]
Cohn, Susan L. [14 ]
Fernandez, Jorge H. [1 ,3 ]
Diller, Lisa R. [1 ,3 ]
Shusterman, Suzanne [1 ,3 ]
机构
[1] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA USA
[2] Dana Farber Canc Inst, Div Populat Sci, Ctr Outcomes & Policy Res, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Div Pediat Hematol Oncol, Boston, MA USA
[4] Roswell Park Canc Inst Buffalo, New York, NY USA
[5] Univ Penn, Childrens Hosp Philadelphia, Dept Pediat, Div Oncol, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Sch Med, Philadelphia, PA USA
[7] Univ Washington, Sch Med, Dept Pediat Hematol Oncol, Seattle, WA USA
[8] Univ Washington, Sch Med, Pediat Bioeth Palliat Care, Seattle, WA USA
[9] Seattle Childrens Res Inst, Ctr Clin & Translat Res, Seattle, WA USA
[10] Childrens Hosp Los Angeles, Childrens Ctr Canc & Blood Dis, Los Angeles, CA 90027 USA
[11] Cook Childrens Hosp, Hematol & Oncol Ctr, Ft Worth, TX USA
[12] Mem Sloan Kettering Canc Ctr, Dept Pediat Oncol, 1275 York Ave, New York, NY 10021 USA
[13] St Jude Childrens Res Hosp, Div Qual Life & Palliat Care, 332 N Lauderdale St, Memphis, TN 38105 USA
[14] Univ Chicago, Comer Childrens Hosp, Dept Pediat, Chicago, IL USA
关键词
End-of-life; pediatric; cancer; disparities; communication; prognosis; OF-LIFE CARE; BLACK-AND-WHITE; MEDICAL-CARE; HOSPICE USE; END; DISPARITIES; PHYSICIAN; PATIENT; DEATH; NEUROBLASTOMA;
D O I
10.1016/j.jpainsymman.2020.04.020
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context. Racial and ethnic disparities in end-of-life care are well documented among adults with advanced cancer. Objectives. To examine the extent to which communication and care differ by race and ethnicity among children with advanced cancer. Methods. We conducted a prospective cohort study at nine pediatric cancer centers enrolling 95 parents (42% racial/ethnic minorities) of children with poor prognosis cancer (relapsed/refractory high-risk neuroblastoma). Parents were surveyed about whether prognosis was discussed; likelihood of cure; intent of current treatment; and primary goal of care. Medical records were used to identify high-intensity medical care since the most recent recurrence. Logistic regression evaluated differences between white non-Hispanic and minority (black, Hispanic, and Asian/other race) parents. Results. About 26% of parents recognized the child's low likelihood of cure. Minority parents were less likely to recognize the poor prognosis (odds ratio [OR] = 0.19; 95% CI = 0.06-0.63; P = 0.006) and the fact that current treatment was unlikely to offer cure (OR = 0.07; 95% CI = 0.02-0.27; P < 0.0001). Children of minority parents were more likely to experience highintensity medical care (OR = 3.01; 95% CI = 1.29-7.02; P = 0.01). After adjustment for understanding of prognosis, race/ethnicity was no longer associated with high-intensity medical care (adjusted odds ratio = 2.14; 95% CI = 0.84-5.46; P = 0.11), although power to detect an association was limited. Conclusion. Parental understanding of prognosis is limited across racial and ethnic groups; racial and ethnic minorities are disproportionately affected. Perhaps as a result, minority children experience higher rates of high-intensity medical care. Work to improve prognostic understanding should include focused work to meet needs of minority populations. (C) 2020 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:782 / 789
页数:8
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