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临终关怀时,丧亲家庭更可能报告“关怀太少”,而非“关怀太多”。

Bereaved Family More Likely to Report "Too Little" Care than "Too Much" Care at the End of Life.

机构信息

Department of Medicine, Division of General Internal Medicine and Geriatrics, School of Medicine, Oregon Health & Science University, Portland, Oregon, USA.

RAND Corporation, Arlington, Virginia, USA.

出版信息

J Palliat Med. 2021 Jun;24(6):894-904. doi: 10.1089/jpm.2020.0498. Epub 2020 Dec 18.

Abstract

An often-stated concern is that dying persons receive too much aggressive medical care. Examine next-of-kin perceptions of the amount of medical care received in the last month of life. Mixed-methods study with 623 survey responses and in-depth interviews with a subsample of 17 respondents. Nontraumatic deaths 18 years and older in San Francisco Bay area. The survey asked: "During the last month of your family member's life, did he or she receive too little, the right amount, or too much medical care?" Additionally, surveys examined 18 measures of quality of care in the last month of life, reporting concerns or unmet needs with staff communication, symptom management, emotional support, physician communication, treating the patient with dignity, respecting a person's culture, spiritual support, and providing timely help after hours. Of the 623 survey respondents, 16.9% reported their loved one received "too little" care while only 1.4% reported "too much." Likelihood of reporting too little medical care did not differ by age, gender, or being insured by Medicaid only. Respondents who reported "too little" compared with those that stated the "right amount" reported higher unmet needs for symptom palliation, physician communication concerns, with other important opportunities to improve the quality of care. Among the 17 in-depth interviews of those indicating "too little" care on the structured survey, the predominant concern ( = 10) was inadequate symptom management. While the majority of respondents indicated their loved one received the right amount of medical care at the end of life, a notable minority (one in six) indicated that their loved one received too little care.

摘要

人们常关注的一个问题是临终患者接受了过多的积极治疗。本研究旨在调查患者亲属对临终患者在生命最后一个月所接受医疗照护量的看法。本研究采用混合方法,共纳入 623 名调查对象和 17 名深度访谈对象。调查对象为在旧金山湾区去世的年龄在 18 岁及以上的非创伤性死亡患者。调查问卷询问患者亲属:“在您亲属生命的最后一个月,他/她接受的医疗护理是太少、刚刚好还是太多?”此外,调查问卷还评估了临终患者在生命最后一个月的 18 项护理质量指标,包括医护人员与患者的沟通情况、症状管理、情感支持、医生沟通、对患者的尊重、对患者文化的尊重、精神支持以及医护人员在非工作时间是否能及时提供帮助等方面,患者亲属可报告对这些方面的关注或需求未得到满足的情况。在 623 名调查对象中,16.9%的人表示他们的亲人接受的护理“太少”,而只有 1.4%的人表示接受的护理“太多”。报告接受的医疗护理“太少”的可能性与年龄、性别或仅由医疗补助计划(Medicaid)承保无关。与表示接受“刚刚好”护理的人相比,报告接受的医疗护理“太少”的人表示在症状缓解、医生沟通方面存在更高的未满足需求,且其他改善护理质量的机会也更多。在对在结构性调查中报告接受的护理“太少”的 17 名深度访谈对象进行分析时,受访者最关心的问题( = 10)是症状管理不充分。虽然大多数受访者表示,临终患者接受的医疗护理量“刚刚好”,但仍有相当一部分(六分之一)受访者表示,他们的亲人接受的护理“太少”。

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