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现在是时候进行协调一致的国际抗逆转录病毒治疗注册了。

The time has come for harmonized international ART registration.

机构信息

Fertility Department, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Centre for Reproductive Medicine, Universitair Ziekenhuis Brussel, Brussels, Belgium; Department of Obstetrics and Gynaecology, University of Zagreb School of Medicine, Zagreb, Croatia.

出版信息

Reprod Biomed Online. 2023 Jun;46(6):881-885. doi: 10.1016/j.rbmo.2023.02.015. Epub 2023 Mar 7.

Abstract

For more than two decades, the European IVF-Monitoring Consortium has collected data on IVF in Europe with the aim of monitoring the quality and safety of assisted reproductive technology (ART) treatments, to ensure the highest performance with the lowest risk for patients and their offspring. Likewise, the Society for Assisted Reproductive Technology in the USA and the Australia/New Zealand Assisted Reproduction Database collect, process and publish data in their regions. The better the legal framework for ART surveillance, the more complete and reliable are the datasets. Worldwide, the landscape of ART regulation is fragmented, and until there is a legal obligation to report ART data in all countries, with an appropriate quality control of the data collected, the reported outcomes should be interpreted with caution. Once uniform and harmonized data are achieved, consensus reports based on collective findings can begin to address key topics such as cycle segmentation and complications. Improved registration systems and datasets allowing optimized surveillance should be developed in collaboration with patient representatives to consider patients' needs, especially aiming to provide higher transparency around ART services. Support from national and international reproductive medicine societies will also be essential to the future evolution of ART registries.

摘要

二十多年来,欧洲体外受精监测联合会一直在收集欧洲体外受精的数据,目的是监测辅助生殖技术(ART)治疗的质量和安全性,以确保患者及其后代的风险最低、效果最佳。同样,美国辅助生殖技术协会和澳大利亚/新西兰辅助生殖数据库也在各自地区收集、处理和发布数据。ART 监测的法律框架越好,数据集就越完整和可靠。在全球范围内,ART 监管的格局是分散的,在所有国家都有报告 ART 数据的法律义务,并对收集的数据进行适当的质量控制之前,报告的结果应该谨慎解释。一旦实现了统一和协调的数据,就可以基于集体发现开始报告共识,以解决关键问题,如周期分割和并发症。应与患者代表合作开发改进的登记系统和数据集,以优化监测,以考虑患者的需求,特别是旨在围绕 ART 服务提供更高的透明度。国家和国际生殖医学协会的支持对于 ART 登记处的未来发展也至关重要。

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