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护士对智力和发育障碍者的伦理承诺。

A nurses' ethical commitment to people with intellectual and developmental disabilities.

机构信息

Drexel University, USA.

University of Texas Health Science Center at San Antonio, USA.

出版信息

Nurs Ethics. 2020 Jun;27(4):1066-1076. doi: 10.1177/0969733019900310. Epub 2020 Mar 31.

Abstract

This article explores the issues of knowledge deficits of healthcare professionals in meeting the needs of people with IDD throughout the life span, and to identify factors that contribute to these deficits. Although statistics vary due to census results and the presence of a "hidden population," approximately 1%-3% of the global population identify as living with an intellectual or developmental disability. People with intellectual or developmental disability experience health inequities and confront multiple barriers in society, often related to the stigma of intellectual or developmental disability. Disparities in care and service are attributed to a lack of knowledge and understanding among healthcare providers about people with intellectual or developmental disability, despite their increased risk for chronic health problems. The near absence of educational programs in nursing both nationally and internationally contributes to this significant knowledge deficit. In addition, ethical considerations between paternalistic beneficence and idealized autonomy have resulted in a lack of clear direction in working with a population that is often ignored or exploited. Nurses who view people with intellectual or developmental disability as vulnerable without assessing or acknowledging their capabilities may err toward paternalism in an effort to "first do no harm." Likewise, nurses who fail to recognize the challenges and limitations faced by people with intellectual or developmental disability may not provide sufficient protections for a vulnerable person. People with intellectual or developmental disability are not binary, but rather complex individuals with a myriad of presentations. This article seeks to encourage a well-informed model of nursing care. Through an ethical lens, this article explores the nurse's ethical commitments in cases of victimization, access to care, decision making, and the provision of optimal end-of-life care for people with intellectual or developmental disability.

摘要

本文探讨了医疗保健专业人员在满足智障人士终身需求方面知识不足的问题,并确定了导致这些不足的因素。尽管由于人口普查结果和“隐形人口”的存在,统计数据有所不同,但全球约有 1%-3%的人口被认定为智障人士或发展障碍人士。智障人士或发展障碍人士在社会上面临着健康不平等和多种障碍,这些障碍往往与智障或发展障碍的耻辱感有关。护理和服务方面的差异归因于医疗保健提供者对智障人士或发展障碍人士缺乏了解和理解,尽管他们患慢性健康问题的风险增加。国家和国际范围内护理教育计划的缺乏加剧了这一重大知识缺陷。此外,在家长式的善行和理想化的自主性之间的伦理考虑导致在与一个经常被忽视或剥削的人群合作方面缺乏明确的方向。那些将智障人士或发展障碍人士视为脆弱而不评估或承认其能力的护士可能会因为“首先不造成伤害”而倾向于家长式作风。同样,那些未能认识到智障人士或发展障碍人士所面临的挑战和限制的护士可能无法为弱势人士提供足够的保护。智障人士或发展障碍人士不是二元的,而是具有多种表现形式的复杂个体。本文旨在鼓励一种知情的护理模式。本文从伦理角度探讨了护士在受害、获得护理、决策以及为智障人士或发展障碍人士提供最佳临终关怀方面的伦理承诺。

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