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Systematic review of attitudes toward donation after cardiac death among healthcare providers and the general public

机译:系统地审查了医疗服务提供者和公众对心脏死亡后捐赠的态度

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OBJECTIVE: Organ donation after cardiac death (DCD) is one promising possibility of combating the organ shortage, but it raises ethical issues that differ from those raised in donation after brain death (DBD). Also, DCD may be perceived differently than DBD by medical staff and the public. The aim of this article is to systematically review empirical studies on attitudes of medical personnel and the public toward DCD and to discuss the findings from an ethical perspective. Our study was conducted in accordance with a seven-step approach for systematic reviews of empirical studies in bioethics. DATA SOURCES: The authors chose PubMed, EMBASE, CINAHL, PSYCINFO, and PSYNDEX, thus attempting to cover biomedical, sociological and ethical articles on the subject. STUDY SELECTION: A search algorithm using controlled vocabulary of the respective databases (where applicable) was created, and criteria for the relevance assessment of the articles were established. Article quality was assessed using the Critical Appraisal Skills Programme tool. DATA EXTRACTION AND SYNTHESIS: The authors took an integrative approach to the data, combining it for further analysis. Qualitative data were synthesized by means of thematic analysis, and a spectrum of relevant themes was identified. Then the authors extracted the quantitative data that corresponded with the identified themes. Quantitative data on common subjects were juxtaposed and presented later. CONCLUSIONS: Identified themes were the levels of support for DBD vs. DCD, attitudes toward postmortem measures without previous consent, lack of knowledge about DCD, concerns about the Dead Donor Rule, the potential for conflict of interest, making donation happen, and the call for standardized DCD protocols. All of these issues are of ethical relevance and merit further discussion. We conclude that deep-rooted concerns about DCD exist among medical personnel and the general public. These need to be taken seriously in order to maintain or foster trust in the transplantation system.
机译:目的:心脏死亡后捐献器官(DCD)是解决器官短缺的一种有前途的可能性,但它提出了与脑死亡(DBD)捐献引起的伦理问题不同的伦理问题。此外,医务人员和公众对DCD的感觉可能与DBD不同。本文的目的是系统地审查关于医务人员和公众对DCD态度的实证研究,并从伦理角度讨论研究结果。我们的研究是按照七个步骤进行的,旨在系统回顾生物伦理学的经验研究。数据来源:作者选择PubMed,EMBASE,CINAHL,PSYCINFO和PSYNDEX,因此尝试涵盖有关该主题的生物医学,社会学和伦理学文章。研究选择:创建了使用各个数据库的受控词汇表(如果适用)的搜索算法,并建立了文章相关性评估的标准。使用“关键评估技能计划”工具评估了物品质量。数据提取和综合:作者对数据采取了综合方法,将其结合起来进行进一步分析。通过专题分析综合了定性数据,并确定了一系列相关主题。然后,作者提取了与确定的主题相对应的定量数据。并列并列出了有关常见主题的定量数据。结论:确定的主题包括对DBD与DCD的支持水平,未经事先同意就对死后措施的态度,对DCD缺乏了解,对死者捐赠者规则的担忧,利益冲突的可能性,进行捐赠以及呼吁用于标准化DCD协议。所有这些问题都具有伦理意义,值得进一步讨论。我们得出的结论是,医务人员和普通公众对DCD有着根深蒂固的担忧。必须认真对待这些内容,以维护或增强对移植系统的信任。

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