Niek Kok, Willemijn van Erp, Marjan J Meinders, Jelle van Gurp
{"title":"意识障碍患者治疗偏好的重建:系统回顾。","authors":"Niek Kok, Willemijn van Erp, Marjan J Meinders, Jelle van Gurp","doi":"10.1186/s12910-025-01241-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Patients with disorders of consciousness (DoC) are unable to partake in the decision making process concerning their treatment. In the process of medical decision-making, which in DoC often concerns life-and-death decisions, surrogates and healthcare professionals may try to reconstruct the treatment preferences of these patients. We aimed to identify which values and criteria have been used in various national care contexts to reconstruct the treatment preferences of incapacitated DoC patients and how reconstruction is conducted in practice.</p><p><strong>Methods: </strong>This is a systematic review of the of conceptual and empirical ethical literature. A search was performed in seven databases (Pubmed, Web of Science, Embase, the Cochrane Library, CINAHL, PsychINFO, and Sociological Abstracts). We used thematic analysis to identify values and criteria for reconstruction of treatment preferences.</p><p><strong>Results: </strong>8.591 records were screened. In total, 17 conceptual studies and 13 empirical studies on preference reconstruction were included. We identified three normative-epistemic viewpoints on reconstruction of treatment preferences: a correspondence view which aims to respect personal autonomy and prioritizes the accuracy of reconstructed preferences; a coherence view which aims to respect personal identity and prioritizes the consistency of the preferences with the patient's lifeworld; and a communitarian view which aims to respect community and prioritizes the ongoing relation of a patient with family and friends. These views diverge on the problem of what makes for a good process of preference reconstruction. Additionally, treatment preferences of patients in DoC are inferred based on either past oral statements or on observations of patients' current behavior. The criteria that guide reconstructive efforts may evolve, especially when patients improve from UWS to MCS and when reconstructed preferences based on past statements and patient's current inferred psychological mental states steer treatment in mutually exclusive directions. There is no current standard approach to reconstructing treatment preferences in incapacitated DoC patients.</p><p><strong>Conclusions: </strong>We recommend physicians to ask diversely formulated questions that stimulate surrogates towards giving multiple and rich answers. Simultaneously, physicians are advised not to overly test a surrogate's testimony because this may lead to an erosion of trust.</p>","PeriodicalId":55348,"journal":{"name":"BMC Medical Ethics","volume":"26 1","pages":"84"},"PeriodicalIF":3.0000,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reconstruction of patients' treatment preferences in disorders of consciousness: a systematic review.\",\"authors\":\"Niek Kok, Willemijn van Erp, Marjan J Meinders, Jelle van Gurp\",\"doi\":\"10.1186/s12910-025-01241-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Patients with disorders of consciousness (DoC) are unable to partake in the decision making process concerning their treatment. In the process of medical decision-making, which in DoC often concerns life-and-death decisions, surrogates and healthcare professionals may try to reconstruct the treatment preferences of these patients. We aimed to identify which values and criteria have been used in various national care contexts to reconstruct the treatment preferences of incapacitated DoC patients and how reconstruction is conducted in practice.</p><p><strong>Methods: </strong>This is a systematic review of the of conceptual and empirical ethical literature. A search was performed in seven databases (Pubmed, Web of Science, Embase, the Cochrane Library, CINAHL, PsychINFO, and Sociological Abstracts). We used thematic analysis to identify values and criteria for reconstruction of treatment preferences.</p><p><strong>Results: </strong>8.591 records were screened. In total, 17 conceptual studies and 13 empirical studies on preference reconstruction were included. We identified three normative-epistemic viewpoints on reconstruction of treatment preferences: a correspondence view which aims to respect personal autonomy and prioritizes the accuracy of reconstructed preferences; a coherence view which aims to respect personal identity and prioritizes the consistency of the preferences with the patient's lifeworld; and a communitarian view which aims to respect community and prioritizes the ongoing relation of a patient with family and friends. These views diverge on the problem of what makes for a good process of preference reconstruction. Additionally, treatment preferences of patients in DoC are inferred based on either past oral statements or on observations of patients' current behavior. The criteria that guide reconstructive efforts may evolve, especially when patients improve from UWS to MCS and when reconstructed preferences based on past statements and patient's current inferred psychological mental states steer treatment in mutually exclusive directions. There is no current standard approach to reconstructing treatment preferences in incapacitated DoC patients.</p><p><strong>Conclusions: </strong>We recommend physicians to ask diversely formulated questions that stimulate surrogates towards giving multiple and rich answers. Simultaneously, physicians are advised not to overly test a surrogate's testimony because this may lead to an erosion of trust.</p>\",\"PeriodicalId\":55348,\"journal\":{\"name\":\"BMC Medical Ethics\",\"volume\":\"26 1\",\"pages\":\"84\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-07-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Medical Ethics\",\"FirstCategoryId\":\"98\",\"ListUrlMain\":\"https://doi.org/10.1186/s12910-025-01241-1\",\"RegionNum\":1,\"RegionCategory\":\"哲学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ETHICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Medical Ethics","FirstCategoryId":"98","ListUrlMain":"https://doi.org/10.1186/s12910-025-01241-1","RegionNum":1,"RegionCategory":"哲学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ETHICS","Score":null,"Total":0}
引用次数: 0
摘要
背景:意识障碍(DoC)患者无法参与有关其治疗的决策过程。在医疗决策过程中,医疗决策往往涉及到生死攸关的决定,代理人和医疗保健专业人员可能会试图重建这些患者的治疗偏好。我们的目的是确定哪些价值观和标准在不同的国家护理环境中被用来重建无行为能力的DoC患者的治疗偏好,以及在实践中如何进行重建。方法:这是对概念和经验伦理文献的系统回顾。在7个数据库(Pubmed、Web of Science、Embase、Cochrane Library、CINAHL、PsychINFO和Sociological Abstracts)中进行了检索。我们使用主题分析来确定治疗偏好重建的价值和标准。结果:共筛选记录8.591条。共包括17项关于偏好重构的概念研究和13项实证研究。我们确定了三种关于治疗偏好重建的规范认识论观点:一种旨在尊重个人自主性并优先考虑重建偏好准确性的对应观点;连贯性观点,旨在尊重个人身份,并优先考虑与患者生活世界的偏好一致性;一种社区主义的观点,旨在尊重社区,优先考虑病人与家人和朋友的关系。这些观点在什么是一个好的偏好重建过程的问题上存在分歧。此外,DoC患者的治疗偏好是根据过去的口头陈述或对患者当前行为的观察来推断的。指导重建工作的标准可能会发生变化,特别是当患者从UWS改善到MCS时,以及当基于过去陈述和患者当前推断的心理精神状态的重建偏好引导治疗走向相互排斥的方向时。目前尚无标准方法来重建丧失行为能力的DoC患者的治疗偏好。结论:我们建议医生提出不同形式的问题,刺激代孕母亲给出多种丰富的答案。同时,医生被建议不要过度测试代孕母亲的证词,因为这可能会导致信任的侵蚀。
Reconstruction of patients' treatment preferences in disorders of consciousness: a systematic review.
Background: Patients with disorders of consciousness (DoC) are unable to partake in the decision making process concerning their treatment. In the process of medical decision-making, which in DoC often concerns life-and-death decisions, surrogates and healthcare professionals may try to reconstruct the treatment preferences of these patients. We aimed to identify which values and criteria have been used in various national care contexts to reconstruct the treatment preferences of incapacitated DoC patients and how reconstruction is conducted in practice.
Methods: This is a systematic review of the of conceptual and empirical ethical literature. A search was performed in seven databases (Pubmed, Web of Science, Embase, the Cochrane Library, CINAHL, PsychINFO, and Sociological Abstracts). We used thematic analysis to identify values and criteria for reconstruction of treatment preferences.
Results: 8.591 records were screened. In total, 17 conceptual studies and 13 empirical studies on preference reconstruction were included. We identified three normative-epistemic viewpoints on reconstruction of treatment preferences: a correspondence view which aims to respect personal autonomy and prioritizes the accuracy of reconstructed preferences; a coherence view which aims to respect personal identity and prioritizes the consistency of the preferences with the patient's lifeworld; and a communitarian view which aims to respect community and prioritizes the ongoing relation of a patient with family and friends. These views diverge on the problem of what makes for a good process of preference reconstruction. Additionally, treatment preferences of patients in DoC are inferred based on either past oral statements or on observations of patients' current behavior. The criteria that guide reconstructive efforts may evolve, especially when patients improve from UWS to MCS and when reconstructed preferences based on past statements and patient's current inferred psychological mental states steer treatment in mutually exclusive directions. There is no current standard approach to reconstructing treatment preferences in incapacitated DoC patients.
Conclusions: We recommend physicians to ask diversely formulated questions that stimulate surrogates towards giving multiple and rich answers. Simultaneously, physicians are advised not to overly test a surrogate's testimony because this may lead to an erosion of trust.
期刊介绍:
BMC Medical Ethics is an open access journal publishing original peer-reviewed research articles in relation to the ethical aspects of biomedical research and clinical practice, including professional choices and conduct, medical technologies, healthcare systems and health policies.