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EUROPEAN JOURNAL OF HEALTH LAW最新文献

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What Kind of Death? The Ethics of Determining One's Own Death, written by Govert den Hartogh. 什么样的死亡?决定自己死亡的伦理学》,作者:Govert den Hartogh。
IF 0.8 Q2 LAW Pub Date : 2023-06-30 DOI: 10.1163/15718093-12423557
Paul Schotsmans
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引用次数: 1
European Court of Human Rights. 欧洲人权法院。
IF 0.8 Q2 LAW Pub Date : 2023-06-19 DOI: 10.1163/15718093-bja10107
Joseph Dute, Tom Goffin
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引用次数: 0
European Court of Justice. 欧洲法院。
IF 0.8 Q2 LAW Pub Date : 2023-06-08 DOI: 10.1163/15718093-12423556
Herman Nys
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引用次数: 0
Obstetric Violence: Sterilisation without Consent. The Case of Y.P. v. Russian Federation. 产科暴力:未经同意的绝育。Y.P.诉俄罗斯联邦案。
IF 0.8 Q2 LAW Pub Date : 2023-06-02 DOI: 10.1163/15718093-bja10111
André den Exter

On 20 September 2022, the European Court of Human Rights (ECtHR) delivered its judgment in a remarkable case on sterilisation without the patient's consent, Y.P. v Russian Federation (ECtHR, application no. 43399/13, 20 September 2022). According to the Court, there is no inhuman and degrading treatment, but it was a justified medical procedure. However, the Court did conclude a violation of the right to private life, under Article 8 ECHR. This outcome is at odds with an earlier sterilisation case without consent, V.C. v Slovakia (V.C. v. Slovakia, ECtHR application no. 18968/07, 8 November 2011). The question is how both rulings can be understood, especially the legal consideration regarding the prohibition of torture. After all, both cases lacked the patient's consent.

2022 年 9 月 20 日,欧洲人权法院(ECtHR)对一起关于未经患者同意实施绝育手术的重要案件--Y.P.诉俄罗斯联邦(ECtHR,第 43399/13 号申请,2022 年 9 月 20 日)做出了判决。法院认为,不存在不人道和有辱人格的待遇,这是一个合理的医疗程序。然而,根据《欧洲人权公约》第 8 条,法院确实得出了侵犯私人生活权的结论。这一结果与早前的 V.C. 诉斯洛伐克(V.C. v. Slovakia,欧洲人权法院诉状编号:18968/07,2011 年 11 月 8 日)未经同意的绝育案件相左。问题在于如何理解这两项裁决,尤其是有关禁止酷刑的法律考量。毕竟,这两个案件都没有征得患者的同意。
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引用次数: 0
Publisher Correction: Reviewer Thank You. 出版商更正:感谢审稿人。
IF 0.6 Q2 LAW Pub Date : 2023-06-01 DOI: 10.1007/s12308-023-00540-z
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引用次数: 0
'Software as Medical Device' Regulation: What the US Can Teach to the EU for a Fairer Balance Towards Its Digital Sovereignty? 软件即医疗器械 "法规:美国可向欧盟传授哪些经验,以更公平地平衡其数字主权?
IF 0.8 Q2 LAW Pub Date : 2023-05-26 DOI: 10.1163/15718093-bja10109
Anna Fiorentini

The AI presence in healthcare (e.g., telemedicine platforms and Software as Medical Devices) is uncontroversial by now. Beyond the Big Tech already for some time large investors in this field, the States, repeatedly accused to be unable keeping pace with the exponential technological development, are growingly called upon to deal with it. Taking the distance from those who perceive the US as a regulatory model to oppose in order to assert the EU digital sovereignty, the present analysis will prove that a glimpse across the Atlantic could only help the EU legislator. With a specific focus on the SaMD regulation, it will be shown how the choices made in the US appear to be grounded on a fair balance between patient and economic operators' rights. Building on it, a new balancing formula needs to be put forward to guide the EU intensive legislative activity for the digital world.

人工智能在医疗保健领域的应用(如远程医疗平台和软件即医疗设备)现在已无可争议。除了已经在这一领域投资多年的大型科技公司之外,屡次被指责无法跟上指数级技术发展步伐的国家也越来越多地被要求应对这一问题。有些人认为美国是一种监管模式,应予以反对,以维护欧盟的数字主权,而本分析报告将与这些人保持一定的距离,证明对大西洋彼岸的一瞥只会对欧盟立法者有所帮助。通过对 SaMD 法规的特别关注,我们将看到美国的选择是如何在患者权利和经济运营商权利之间实现公平平衡的。在此基础上,需要提出一个新的平衡公式,以指导欧盟针对数字世界的密集立法活动。
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引用次数: 0
COVID-19 Vaccination and the Role of Informed Consent: England as a Case Study. COVID-19疫苗接种和知情同意的作用:以英格兰为例研究。
IF 0.8 Q2 LAW Pub Date : 2023-05-22 DOI: 10.1163/15718093-bja10108
Caterina Milo

Informed consent (IC), following the Supreme Court judgment in Montgomery v Lanarkshire Health Board, [2015] UKSC 11, constitutes a key patients' right. There is a vast literature exploring the significance of this right, while an analysis of the role that this has played in England during the COVID-19 vaccine distribution has been under-explored. Using England as a case study, this paper argues that IC has received limited protection in the COVID-19 vaccination context of the adult population, upholding at its best only a minimalistic approach where mere 'consent' has been safeguarded. It suggests that new approaches should be brainstormed so as to more properly safeguard IC in a Montgomery-compliant-approach, namely in a way that enhances patients' autonomy and medical partnership, and also to better prepare and respond to future pandemics.

根据最高法院在Montgomery诉拉纳克郡卫生委员会([2015]UKSC 11)一案中的判决,知情同意(IC)构成了患者的一项关键权利。有大量文献探讨了这一权利的重要性,而对这一权利在英格兰COVID-19疫苗分发期间所起作用的分析却没有得到充分探讨。本文以英国为案例研究,认为在COVID-19疫苗接种的成人人口背景下,IC得到了有限的保护,在最好的情况下,只坚持了一种极简主义的方法,仅仅是“同意”得到了保障。报告建议,应该集思广益,以一种符合蒙哥马利标准的方式,即以一种增强患者自主权和医疗伙伴关系的方式,更恰当地保护IC,并更好地准备和应对未来的流行病。
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引用次数: 0
Case Mortier V. Belgium: The Balance Between the Right to Life and the Right to Respect for Private Life in the Light of Euthanasia. 莫蒂埃诉比利时案:安乐死下生命权与尊重私生活权的平衡。
IF 0.8 Q2 LAW Pub Date : 2023-05-19 DOI: 10.1163/15718093-bja10106
Paulien Walraet

The case Mortier v. Belgium is the first case where the Court comments on the figure of euthanasia. The area of euthanasia in particular raises the issue of finding a balance between the protection of the patients' right to life in Article 2 of the Convention and that of the right to respect for his or her private life and personal autonomy in Article 8 of the Convention. The Court confirmed the States must be afforded a margin of appreciation in finding this balance. However, it does not concern an unlimited margin as the Court reserved its power to review the States fulfilment of its obligations under Article 2. After deciding that there had been no breach of article 8 in the performing of euthanasia as such, the Court examined the positive obligation of Belgium to foresee in sufficient safeguards to protect the right to life.

莫蒂埃诉比利时案是法院对安乐死数字作出评论的第一个案件。特别是安乐死领域提出了在《公约》第2条保护病人的生命权和《公约》第8条尊重病人的私生活和个人自主权之间找到平衡的问题。法院确认,各国在寻求这种平衡时必须有一定的升值余地。但是,这并不涉及无限的余量,因为法院保留审查各国履行第2条规定的义务的权力。在决定实施安乐死本身没有违反第8条之后,法院审查了比利时预见到充分保障以保护生命权的积极义务。
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引用次数: 0
European Court of Justice. 欧洲法院。
IF 0.8 Q2 LAW Pub Date : 2023-03-31 DOI: 10.1163/15718093-12423555
Herman Nys
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引用次数: 0
European Court of Human Rights 欧洲人权法院
Q2 LAW Pub Date : 2023-02-15 DOI: 10.1163/15718093-bja10105
Joseph Dute, Tom Goffin
On 1 August 2008 the applicant, who was then in the thirtieth or thirty-first week of pregnancy, was admitted to a municipal maternity hospital showing symptoms of rhesus incompatibility and excess amniotic fluid (polyhydramnios). She signed a consent form for a Caesarean section without sterilisation. During surgery the doctors also identified a rupture of the uterus, without bleeding. Given the applicant’s age, 28 years, the doctors decided to suture the rupture and keep the uterus. However, given earlier surgical interventions on the uterus, the Caesarean section and the hysterography (repair of the uterus), the doctors decided that there was a real risk that the uterus would rupture in a future pregnancy, which could endanger the applicant’s life, and that therefore she should be sterilised. According to the applicant, she was told the day after the surgery that she had been sterilised, but she was not given any further details about what the procedure meant. Two years later the applicant and her husband decided to have a child and as she could not get pregnant, she saw a gynaecologist, who explained that she could only get pregnant via in vitro fertilisation because she had been sterilised during the Caesarean section in 2008.
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引用次数: 0
期刊
EUROPEAN JOURNAL OF HEALTH LAW
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