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Coding in medically assisted reproduction: the status of the implementation of the Single European Code for reproductive cells and tissues

机译:医学辅助再现编码:生殖细胞和组织单一欧洲代码的实施情况

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STUDY QUESTION To evaluate the implementation of the coding systems in medically assisted reproduction (MAR) centres in the European Union (EU). SUMMARY ANSWER Our data show that a significant number of MAR centres use the Single European Code (SEC), but it also shows certain limitations to the coding. WHAT IS KNOWN ALREADY Traceability and identification of tissue and cells used for clinical application are extremely important as it is one of the key aspects of quality and safety both for the donors and the recipients. Patients as well as tissues and cells move across the European continent and far beyond, hence a uniform coding system was very much needed. The coding of tissues and cells from human origin was already embedded in the EU directives 2004/23/EC. The use of the Single European Code (SEC) on tissues and cells was enforced in 2017 for tissues and cells distributed within the EU or exported from the EU. The SEC ensures standardization within the EU, allowing the integration of the two existing codes (ISBT-128 and Eurocode) within the SEC structure. Likewise, in the MAR field, the SEC was launched in order to ensure the traceability of reproductive tissues and cells. Gametes and embryos from partner donation as well as reproductive cells and tissues of allogeneic donation were excluded from the SEC as long as they remain in the centre of origin. STUDY DESIGN, SIZE, DURATION A cross-sectional survey aimed to gain insight into the use of SEC by MAR centres was conducted between 5 November and 15 December 2018. PARTICIPANTS/MATERIALS, SETTING, METHODS The online survey was distributed among the ESHRE members. MAIN RESULTS AND THE ROLE OF CHANCE The survey results highlight the strengths and weaknesses in the practical use of the SEC. The data from the survey showed that the SEC code is something that is known in the MAR field. Our data showed that over half of the respondents were using the SEC in their centre. On the other hand, there is also criticism about the use of SEC in MAR, especially that the added value for traceability and identification in ART is found to be rather limited. LIMITATIONS, REASONS FOR CAUTION The survey response rate was rather low (4.84%). The view of the use of SEC discussed in this paper still provides insight into the use of the SEC in several MAR centres. WIDER IMPLICATIONS OF THE FINDINGS The survey highlights some knowledge gaps concerning coding. This information can be used to develop tools to increase knowledge of the SEC. STUDY FUNDING/COMPETING INTEREST(S) There was no external funding for this study. The authors declare that they have no conflict of interest. TRIAL REGISTRATION NUMBER N/A.
机译:研究问题评估欧洲联盟(欧盟)中医学辅助复制(MAR)中心的编码系统的实施。摘要回答我们的数据显示,大量的MAR中心使用单个欧洲代码(SEC),但它也向编码表示一定的限制。已知已经可追溯性和用于临床应用的组织和细胞的鉴定非常重要,因为它是捐赠者和接受者的质量和安全的关键方面之一。患者以及组织和细胞跨越欧洲大陆,远远超出,因此需要统一的编码系统。组织和人类来源的细胞的编码已经嵌入了EU指令2004/23 / EC中。在2017年对组织和细胞进行组织和细胞的使用用于分布在欧盟内或从欧盟出口的组织和细胞。 SEC确保欧盟内的标准化,允许在SEC结构中集成两个现有代码(ISBT-128和EUROCODE)。同样,在Mar领域,秒被推出,以确保生殖组织和细胞的可追溯性。只要它们留在原产地,可以从副本中排除来自合作伙伴捐赠的配子和胚胎以及同种异体捐赠的生殖细胞和组织。学习设计,规模,旨在通过2018年11月5日至12月15日在5月5日至12月15日之间进行横断面调查。参与者/材料,环境,方法在线调查分布在Oshre成员之间。主要结果和机会的作用调查结果突出了秒实际使用中的优势和缺点。调查中的数据表明,SEC代码是MAR领域中已知的东西。我们的数据显示,超过一半的受访者在其中心使用秒。另一方面,在MA中的使用也有批评,特别是,发现艺术中的可追溯性和识别的附加值相当有限。限制,警告的原因,调查响应率相当较低(4.84%)。本文讨论的SEC使用的看法仍然可以在几个MAR中心中使用SEC的使用。该调查结果的更广泛的影响,调查突出了一些关于编码的知识差距。此信息可用于开发工具以增加SEC的知识。学习资金/竞争利益(S)这项研究没有外部资金。提交人声明他们没有利益冲突。试验登记号码n / a。

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