首页> 外文期刊>Reproductive Health >Recipient screening in IVF: First data from women undergoing anonymous oocyte donation in Dublin
【24h】

Recipient screening in IVF: First data from women undergoing anonymous oocyte donation in Dublin

机译:IVF中的收件人筛选:来自都柏林匿名捐赠卵母细胞的女性的第一批数据

获取原文
           

摘要

Background Guidelines for safe gamete donation have emphasised donor screening, although none exist specifically for testing oocyte recipients. Pre-treatment assessment of anonymous donor oocyte IVF treatment in Ireland must comply with the European Union Tissues and Cells Directive (Directive 2004/23/EC). To determine the effectiveness of this Directive when applied to anonymous oocyte recipients in IVF, we reviewed data derived from selected screening tests performed in this clinical setting. Methods Data from tests conducted at baseline for all women enrolling as recipients (n = 225) in the anonymous oocyte donor IVF programme at an urban IVF referral centre during a 24-month period were analysed. Patient age at programme entry and clinical pregnancy rate were also tabulated. All recipients had at least one prior negative test for HIV, Hepatitis B/C, chlamydia, gonorrhoea and syphilis performed by her GP or other primary care provider before reproductive endocrinology consultation. Results Mean (±SD) age for donor egg IVF recipients was 40.7 ± 4.2 yrs. No baseline positive chlamydia, gonorrhoea or syphilis screening results were identified among recipients for anonymous oocyte donation IVF during the assessment interval. Mean pregnancy rate (per embryo transfer) in this group was 50.5%. Conclusion When tests for HIV, Hepatitis B/C, chlamydia, gonorrhoea and syphilis already have been confirmed to be negative before starting the anonymous donor oocyte IVF sequence, additional (repeat) testing on the recipient contributes no new clinical information that would influence treatment in this setting. Patient safety does not appear to be enhanced by application of Directive 2004/23/EC to recipients of anonymous donor oocyte IVF treatment. Given the absence of evidence to quantify risk, this practice is difficult to justify when applied to this low-risk population.
机译:安全配子捐赠的背景指南强调了捐献者的筛查,尽管没有专门用于测试卵母细胞受体的筛查。爱尔兰对匿名供体卵母细胞IVF治疗的治疗前评估必须符合欧盟组织和细胞指令(指令2004/23 / EC)。为了确定将该指令应用于IVF中的匿名卵母细胞接受者的有效性,我们回顾了在该临床环境中进行的选定筛查测试得出的数据。方法分析来自基线的所有数据,这些数据是针对在24个月内在城市IVF转诊中心参加匿名卵母细胞IVF计划的所有受试女性(n = 225)进行的分析。还列出了程序进入时的患者年龄和临床妊娠率。在接受生殖内分泌学咨询之前,她的全科医生或其他初级保健提供者对所有接受者进行了至少一项先前的HIV,B / C,衣原体,淋病和梅毒阴性试验。结果供体卵IVF接受者的平均(±SD)年龄为40.7±4.2岁。在评估间隔期间,未在匿名卵母细胞捐赠IVF的接受者中鉴定出基线的衣原体,淋病或梅毒阳性筛查结果。该组的平均妊娠率(每次胚胎移植)为50.5%。结论在开始匿名供体卵母细胞IVF序列检测之前,如果已确认HIV,B / C,衣原体,淋病和梅毒检测呈阴性,则对接受者的其他(重复)检测不会产生任何新的临床信息,不会影响治疗此设置。通过将指令2004/23 / EC应用于匿名供体卵母细胞IVF治疗的接受者,似乎并未增强患者的安全性。鉴于缺乏量化风险的证据,这种做法在应用于低风险人群时很难证明其合理性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号