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High-throughput non-invasive prenatal testing for fetal rhesus D status in RhD-negative women not known to be sensitised to the RhD antigen: a systematic review and economic evaluation.高通量非侵入性产前检测在 RhD 阴性且未致敏的女性中用于检测胎儿 RhD 状态:系统评价和经济评估。
Health Technol Assess. 2018 Mar;22(13):1-172. doi: 10.3310/hta22130.
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Noninvasive Fetal RhD Blood Group Genotyping: A Health Technology Assessment.非侵入性胎儿 RhD 血型基因分型:一项健康技术评估。
Ont Health Technol Assess Ser. 2020 Nov 2;20(15):1-160. eCollection 2020.
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High-throughput, non-invasive prenatal testing for fetal rhesus D status in RhD-negative women: a systematic review and meta-analysis.高通量、非侵入性的胎儿 RhD 状态产前检测在 RhD 阴性女性中的应用:系统评价和荟萃分析。
BMC Med. 2019 Feb 14;17(1):37. doi: 10.1186/s12916-019-1254-4.
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High-throughput, non-invasive prenatal testing for fetal Rhesus D genotype to guide antenatal prophylaxis with anti-D immunoglobulin: a cost-effectiveness analysis.高通量、非侵入性的胎儿 RhD 基因型产前检测指导抗 D 免疫球蛋白的产前预防:成本效益分析。
BJOG. 2018 Oct;125(11):1414-1422. doi: 10.1111/1471-0528.15152. Epub 2018 Mar 15.
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Determination of fetal RHD type in plasma of RhD negative pregnant women.RhD阴性孕妇血浆中胎儿RHD血型的测定。
Scand J Clin Lab Invest. 2018 Sep;78(5):411-416. doi: 10.1080/00365513.2018.1475681. Epub 2018 Jun 5.
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Terminating Routine Cord Blood RhD Typing of the Newborns to Guide Postnatal Anti-D Immunoglobulin Prophylaxis Based on the Results of Fetal RHD Genotyping.根据胎儿 RHD 基因分型结果终止新生儿常规脐带血 RhD 定型以指导产后抗-D 免疫球蛋白预防。
Fetal Diagn Ther. 2023;50(4):276-281. doi: 10.1159/000531694. Epub 2023 Jun 28.
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Targeted antenatal anti-D prophylaxis for RhD-negative pregnant women: a systematic review.针对 RhD 阴性孕妇的靶向产前抗 D 预防:系统评价。
BMC Pregnancy Childbirth. 2020 Feb 7;20(1):83. doi: 10.1186/s12884-020-2742-4.
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Routine administration of Anti-D: the ethical case for offering pregnant women fetal RHD genotyping and a review of policy and practice.抗-D的常规管理:为孕妇提供胎儿RHD基因分型的伦理依据及政策与实践综述
BMC Pregnancy Childbirth. 2014 Feb 25;14:87. doi: 10.1186/1471-2393-14-87.
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Screening of RHD fetal genotype in RhD negative women.对 RhD 阴性女性的 RHD 胎儿基因型进行筛查。
Ceska Gynekol. 2020 Winter;85(3):156-163.

PMID:29320119
Abstract

Approximately 15 percent of Norwegian women are Rhesus D (RhD)-negative. During pregnancy and birth, there is a danger that these women produce antibodies against fetal blood cells (alloimmunization), if the fetus is RhD-positive. These antibodies may cross the placenta and cause hemolytic disease of the fetus, which may become life threatening. Today, all RhD-negative pregnant women are closely followed-up during pregnancy, and the newborns are routinely tested for RhD-type at birth. Upon detection of an RhD-positive child, the mother will get anti-D prophylaxis within 72 hours after birth to prevent the formation of anti-D antibodies that may cause problems in subsequent pregnancies. Alloimmunization may occur throughout the whole pregnancy, especially during the last trimester. Therefore, in the Guidance for obstetrics 2014 published by the Norwegian Gynecological Association, it is recommended that anti-D prophylaxis should be offered RhD-negative women also during pregnancy, if they carry an RhD-positive fetus. With a blood sample from the pregnant woman, it can be tested whether the fetus is RhD-negative or -positive. The technology is based on analysis of free fetal DNA present in the woman's blood during pregnancy, and is often referred to as non-invasive prenatal testing (NIPT). The result of NIPT can be used to provide targeted prophylactic treatment to the pregnant women who can benefit from it, and to avoid unnecessary treatment of pregnant women with RhD negative fetuses. In this report, we summarize research studies on diagnostic accuracy of NIPT, as well as clinical effectiveness and health economic and ethical consequences of introducing NIPT for fetal RhD typing in all RhD-negative pregnant women. The main findings are: It is likely that NIPT gives a very accurate RhD typing of the fetus. The documentation is of high quality. We identified no systematic reviews on clinical effectiveness of introducing NIPT for fetal RhD typing in all RhD-negative pregnant women. Introduction of a program with NIPT-guided anti-D prophylaxis will give an additional cost of approximately 4 million Norwegian kroner per year. The cost per avoided RhD-alloimmunization is approximately 106,000 Norwegian kroner. These numbers are based on effectiveness data from a Swedish cohort study. NIPT is an ethically controversial technology. NIPT for RhD typing, when used after the legal time limit for abortion has passed, avoids many of the ethical issues, but alternative or extended applications may be ethically challenging.

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