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加拿大生物药转换为生物类似药的法律与伦理

The Law and Ethics of Switching from Biologic to Biosimilar in Canada.

作者信息

Murdoch Blake, Caulfield Timothy

机构信息

Health Law Institute, Faculty of Law, University of Alberta, Edmonton, Alberta, Canada.

出版信息

J Can Assoc Gastroenterol. 2020 Oct;3(5):228-233. doi: 10.1093/jcag/gwz043. Epub 2020 Jan 3.

Abstract

Governments and financial institutions in several jurisdictions are planning or implementing nonmedical/'forced' switches by cutting drug coverage for reference biologics and funding only less expensive biosimilars. Switches raise numerous ethical and legal challenges, as the drugs are framed as not being identical and, despite strong evidence for noninferiority of some biosimilars, there is controversy over whether switching can sometimes lead to adverse events. Canadian law generally requires physicians to give precedence to their patients' best interests over social interests such as cost containment. The primacy of patients' interests is also clearly reflected in professional policies and codes of ethics. Moreover, physicians are obligated to disclose everything a reasonable person in the patient's position would want to know when obtaining informed consent for treatment, including addressing not only scientific information but also relevant social controversy about nonmedical switches. Under Canadian law, physicians may be obligated to tell patients about the ability to access unfunded biologics, even if patients lack the resources to obtain them. In sum, while there is no inherent right to funding for reference biologics in Canada, physicians in some circumstances may have a legal obligation as fiduciaries to advocate on behalf of patients to remain on a reference biologic. At a minimum, the controversy surrounding switching will necessitate, as part of the consent process, a robust and thorough disclosure of relevant risks, benefits and reasonable alternatives.

摘要

一些司法管辖区的政府和金融机构正在计划或实施非医学/“强制”转换,即削减对参照生物制剂的药物覆盖范围,只资助较便宜的生物类似药。转换引发了众多伦理和法律挑战,因为这些药物被认为并非完全相同,而且尽管有强有力的证据表明某些生物类似药具有非劣效性,但对于转换有时是否会导致不良事件仍存在争议。加拿大法律通常要求医生将患者的最大利益置于诸如成本控制等社会利益之上。患者利益的首要地位也在专业政策和伦理准则中得到明确体现。此外,医生有义务在获取治疗知情同意时披露处于患者位置的理性人想要了解的一切信息,这不仅包括科学信息,还包括有关非医学转换的相关社会争议。根据加拿大法律,医生可能有义务告知患者获取无资金支持的生物制剂的可能性,即使患者缺乏获取这些制剂的资源。总之,虽然在加拿大并没有为参照生物制剂提供资金的固有权利,但在某些情况下,医生作为受托人可能有法律义务代表患者倡导继续使用参照生物制剂。至少,围绕转换的争议将使得在同意过程中,必须充分、全面地披露相关风险、益处和合理的替代方案。

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