Suppr超能文献

养老院临终关怀的相关讨论。

Discussions about end-of-life care in nursing homes.

作者信息

Bradley E H, Peiris V, Wetle T

机构信息

Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, Connecticut 06520-8034, USA.

出版信息

J Am Geriatr Soc. 1998 Oct;46(10):1235-41. doi: 10.1111/j.1532-5415.1998.tb04539.x.

Abstract

OBJECTIVE

To measure the frequency with which nursing home residents and their surrogates discuss with clinicians the resident's wishes concerning future treatment and to assess the influence of the Patient Self Determination Act (PSDA) on the frequency and nature of such discussions.

DESIGN

Retrospective cohort study of residents admitted to nursing homes before and after the PSDA.

SETTING

Six large (at least 120 licensed chronic care beds), randomly selected nursing homes in Connecticut.

PARTICIPANTS

Six hundred randomly selected nursing home residents admitted during 1990 and 1994 to one of the six study nursing homes.

MEASUREMENTS

Documented discussions concerning future treatment wishes were abstracted from residents' nursing home medical records. Participants in the discussion, as well as the timing (i.e., date) and content of the documented discussions were recorded. Sociodemographic and health status factors were also obtained from the medical record.

RESULTS

A large majority of residents (71.5%) had no discussion of future treatment wishes documented in their medical record. However, the percentage of residents with documented discussions had increased since the implementation of the PSDA (36.7% post-PSDA vs 20.3% pre-PSDA). Of those in the post-PSDA cohort who had had discussions, 90% had only one discussion within the first year of admission, and more than half (58.1%) of those who had discussions discussed only life-support systems (cardiopulmonary resuscitation, artificial nutrition and hydration, and ventilation) rather than broader preferences for future treatment, including proxy decision-making.

CONCLUSIONS

Despite the increased prevalence of discussions about future treatment wishes since the enactment of the PSDA, no discussions were documented for most residents. For those with documented discussions, such conversations occurred rarely and were narrow in scope, suggesting that residents' and families' roles in medical decision-making in nursing homes may be limited.

摘要

目的

衡量疗养院居民及其代理人与临床医生讨论居民未来治疗意愿的频率,并评估《患者自主决定法案》(PSDA)对这类讨论的频率和性质的影响。

设计

对PSDA实施前后入住疗养院的居民进行回顾性队列研究。

地点

康涅狄格州随机选取的六家大型(至少有120张持牌长期护理床位)疗养院。

参与者

1990年至1994年期间随机选取的600名入住六家研究疗养院之一的疗养院居民。

测量方法

从居民的疗养院医疗记录中提取有关未来治疗意愿的书面讨论内容。记录讨论的参与者、时间(即日期)和书面讨论的内容。还从医疗记录中获取社会人口统计学和健康状况因素。

结果

绝大多数居民(71.5%)的医疗记录中没有关于未来治疗意愿的讨论记录。然而,自PSDA实施以来,有书面讨论记录的居民比例有所增加(PSDA实施后为36.7%,实施前为20.3%)。在PSDA实施后的队列中进行过讨论的居民中,90%在入院的第一年内只进行了一次讨论,而进行过讨论的居民中超过一半(58.1%)只讨论了生命维持系统(心肺复苏、人工营养和水分补充以及通气),而不是对未来治疗的更广泛偏好,包括代理决策。

结论

尽管自PSDA颁布以来,关于未来治疗意愿的讨论有所增加,但大多数居民没有书面讨论记录。对于有书面讨论记录的居民来说,这类对话很少发生且范围狭窄,这表明居民及其家人在疗养院医疗决策中的作用可能有限。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验