End-of Life Care Disparities Experienced by American Indian and Alaska Natives Peoples: An Analysis of Data from the 2019 Medicare Master Beneficiary Summary File.

IF 2.1 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Journal of palliative medicine Pub Date : 2025-09-01 Epub Date: 2025-05-28 DOI:10.1089/jpm.2024.0481
Elizabeth Anderson, R Turner Goins, Ruqoyat Abdulsalam, Luohua Jiang, Joan O'Connell
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Abstract

Background: American Indian and Alaska Native (AI/AN) adults experience higher rates of chronic diseases and mortality than non-Hispanic White (NHW) adults. Hospice can improve quality of life and reduce hospitalizations for those with terminal illness(es). Aims: To examine hospitalization and hospice use at the end-of-life between AI/AN and NHW patients and the associations of end-of-life hospitalization and hospice use with chronic diseases. Design: Using data extracted from the 2019 Medicare Master Beneficiary Summary File, we estimated regression models to examine our aims among patients who died in 2019. Setting/Participants: Our sample included 6975 AI/AN patients and a 5% sample of 53,465 NHW patients aged ≥65 years. Measurements: Data included patient demographics, health coverage, date of death, diagnosed chronic conditions, hospital inpatient days, and hospice days. The country of study was the United States. Results: AI/AN patients at the end-of-life were more likely to be hospitalized and less likely to use hospice compared with their NHW counterparts. For both AI/AN and NHW patients, having a chronic condition was associated with increased hospital days; having dementia and cancer was associated with more hospice days; while diabetes, cardiovascular disease, chronic kidney disease, end-stage renal disease, and liver disease were associated with fewer hospice days. Conclusions and Relevance: Compared with NHW patients, AI/AN patients received poorer quality end-of-life care. More efforts are needed to understand the barriers and facilitators to hospice for AI/AN patients and in developing strategies that improve access to high-quality end-of-life care for AI/AN patients.

美国印第安人和阿拉斯加原住民经历的临终关怀差异:对2019年医疗保险总受益人摘要文件数据的分析。
背景:美国印第安人和阿拉斯加原住民(AI/AN)成年人的慢性病发病率和死亡率高于非西班牙裔白人(NHW)成年人。安宁疗护可以改善末期病患的生活品质,并减少住院治疗。目的:探讨AI/AN和NHW患者生命末期住院和安宁疗护的使用情况,以及临终住院和安宁疗护与慢性病的关系。设计:使用从2019年医疗保险总受益人摘要文件中提取的数据,我们估计了回归模型,以检验我们在2019年死亡的患者中的目标。环境/参与者:我们的样本包括6975例AI/AN患者和5%的53,465例年龄≥65岁的NHW患者。测量:数据包括患者人口统计、健康覆盖、死亡日期、诊断出的慢性病、住院天数和临终关怀天数。研究的国家是美国。结果:与NHW患者相比,AI/AN患者在生命末期更可能住院,更不可能使用安宁疗护。对于AI/AN和NHW患者,患有慢性疾病与住院天数增加有关;患有痴呆症和癌症的人接受临终关怀的时间更长;而糖尿病、心血管疾病、慢性肾脏疾病、终末期肾脏疾病和肝脏疾病则与临终关怀天数减少有关。结论及意义:与NHW患者相比,AI/AN患者获得的临终关怀质量较差。需要更多的努力来了解人工智能/AN患者临终关怀的障碍和促进因素,并制定策略,改善人工智能/AN患者获得高质量临终关怀的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of palliative medicine
Journal of palliative medicine 医学-卫生保健
CiteScore
3.90
自引率
10.70%
发文量
345
审稿时长
2 months
期刊介绍: Journal of Palliative Medicine is the premier peer-reviewed journal covering medical, psychosocial, policy, and legal issues in end-of-life care and relief of suffering for patients with intractable pain. The Journal presents essential information for professionals in hospice/palliative medicine, focusing on improving quality of life for patients and their families, and the latest developments in drug and non-drug treatments. The companion biweekly eNewsletter, Briefings in Palliative Medicine, delivers the latest breaking news and information to keep clinicians and health care providers continuously updated.
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