• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胎儿及新生儿溶血病的管理

The management of hemolytic disease in the fetus and newborn.

作者信息

Bowman J

机构信息

Rh Laboratory, Winnipeg, Manitoba, Canada.

出版信息

Semin Perinatol. 1997 Feb;21(1):39-44. doi: 10.1016/s0146-0005(97)80018-3.

DOI:10.1016/s0146-0005(97)80018-3
PMID:9190032
Abstract

Rh hemolytic disease (HDN) is the prototype of maternal alloimmunization and fetal hemolytic disease. There are other antigens capable of causing alloimmunization and hemolytic disease such as c, Kell, and Fya. Rh immunization is usually caused by a prior Rh positive fetal maternal transplacental hemorrhage, which occurs in at least 75% of pregnancies. Unless treated, hemolytic disease will result in kernicterus or fetal hydrops in 25% of cases, respectively. Neonatal exchange transfusion has eradicated kernicterus. Measures available to predict severity of fetal hemolytic disease are maternal antibody titers, prior history of hemolytic disease, in vitro cell-mediated maternal antibody functional assays, amniotic fluid spectrophotometry, ultrasound fetal assessment, and fetal blood sampling. The Rh or Kell antigen status of the fetus may be determined by amniotic fluid PCR testing. The management of the severely affected fetus consists of early delivery, with or without fetal transfusions, depending on the gestation of the fetus. With the use of these diagnostic and treatment measures, perinatal mortality from hemolytic disease of the fetus and newborn has been reduced in Manitoba, population one million, from 100 per year in the early 1940s to 1 every 3 years in the mid 1990s.

摘要

Rh溶血病(HDN)是母体同种免疫和胎儿溶血病的典型病例。还有其他一些能够引起同种免疫和溶血病的抗原,如c、Kell和Fya。Rh免疫通常是由先前Rh阳性胎儿与母体之间经胎盘的出血引起的,这种情况在至少75%的妊娠中都会发生。除非进行治疗,溶血病在25%的病例中会分别导致核黄疸或胎儿水肿。新生儿换血疗法已根除了核黄疸。可用于预测胎儿溶血病严重程度的方法有母体抗体滴度、溶血病既往史、体外细胞介导的母体抗体功能测定、羊水分光光度法、超声胎儿评估和胎儿血样采集。胎儿的Rh或Kell抗原状态可通过羊水PCR检测来确定。对严重受影响胎儿的处理包括根据胎儿的孕周,在有或没有进行胎儿输血的情况下尽早分娩。通过使用这些诊断和治疗措施,在拥有100万人口的曼尼托巴省,胎儿及新生儿溶血病的围产期死亡率已从20世纪40年代初的每年100例降至20世纪90年代中期的每3年1例。

相似文献

1
The management of hemolytic disease in the fetus and newborn.胎儿及新生儿溶血病的管理
Semin Perinatol. 1997 Feb;21(1):39-44. doi: 10.1016/s0146-0005(97)80018-3.
2
Management of pregnancies complicated by anti-E alloimmunization.抗-E同种免疫所致妊娠并发症的管理。
Obstet Gynecol. 2005 Jan;105(1):24-8. doi: 10.1097/01.AOG.0000149153.93417.66.
3
[Management of feto-maternal red cell allo-immunizations].[胎儿-母体红细胞同种免疫的管理]
Transfus Clin Biol. 2011 Apr;18(2):269-76. doi: 10.1016/j.tracli.2011.01.005. Epub 2011 Mar 11.
4
Predicting anti-Kell-mediated hemolytic disease of the fetus and newborn: diagnostic accuracy of laboratory management.预测抗 Kell 介导的胎儿和新生儿溶血病:实验室管理的诊断准确性。
Am J Obstet Gynecol. 2018 Oct;219(4):393.e1-393.e8. doi: 10.1016/j.ajog.2018.07.020. Epub 2018 Jul 29.
5
Maternal ABO-mismatched blood for intrauterine transfusion of severe hemolytic disease of the newborn due to anti-Rh17.用于因抗Rh17导致的新生儿严重溶血病宫内输血的母亲ABO血型不匹配血液。
Transfusion. 2004 Sep;44(9):1357-60. doi: 10.1111/j.1537-2995.2004.04082.x.
6
Suppression of compensatory erythropoiesis in hemolytic disease of the fetus and newborn due to intrauterine transfusions.由于宫内输血,胎儿和新生儿溶血病中代偿性红细胞生成的抑制。
Am J Obstet Gynecol. 2020 Jul;223(1):119.e1-119.e10. doi: 10.1016/j.ajog.2020.01.028. Epub 2020 Jan 21.
7
Treatment options for the fetus with alloimmune hemolytic disease.
Transfus Med Rev. 1990 Jul;4(3):191-207. doi: 10.1016/s0887-7963(90)70265-9.
8
[Perinatal hemolytic disease caused by anti-c. A clinical case].
Rev Chil Obstet Ginecol. 1983;48(3):175-9.
9
Management of isoimmunization in the presence of multiple maternal antibodies.存在多种母体抗体时的同种免疫管理。
Am J Obstet Gynecol. 2001 Aug;185(2):481-4. doi: 10.1067/mob.2001.115999.
10
Maternal CW alloimmunization.母体抗白细胞抗原同种免疫
Vox Sang. 1993;64(4):226-30.

引用本文的文献

1
Colombian consensus for the diagnosis, prevention, and management of Rhesus disease.哥伦比亚共识:用于 Rh 血型不合疾病的诊断、预防和管理。
Rev Colomb Obstet Ginecol. 2024 Sep 30;75(3):4142. doi: 10.18597/rcog.4142.
2
Rhesus-minus phenotype as a predictor of sexual desire and behavior, wellbeing, mental health, and fecundity.恒河猴阴性表型作为性欲和性行为、幸福、心理健康和生育能力的预测指标。
PLoS One. 2020 Jul 20;15(7):e0236134. doi: 10.1371/journal.pone.0236134. eCollection 2020.
3
Rhesus Negative Woman Transfused With Rhesus Positive Blood: Subsequent Normal Pregnancy Without Anti D production.
接受恒河猴阳性血液输血的恒河猴阴性女性:随后正常妊娠且未产生抗D抗体。
Ghana Med J. 2015 Mar;49(1):60-3. doi: 10.4314/gmj.v49i1.11.
4
Occurrence of ABO And RhD Incompatibility with Rh Negative Mothers.Rh阴性母亲中ABO和RhD血型不相容的发生情况。
Mater Sociomed. 2013 Dec;25(4):255-8. doi: 10.5455/msm.2013.25.255-258. Epub 2013 Nov 24.
5
Diagnosis of severe fetal anemia based on perinatal outcomes: a comparative analysis of the current reference values.基于围产期结局诊断严重胎儿贫血:当前参考值的比较分析
Anemia. 2013;2013:351258. doi: 10.1155/2013/351258. Epub 2013 Nov 20.
6
Anti-D administration after spontaneous miscarriage for preventing Rhesus alloimmunisation.自然流产后给予抗-D预防恒河猴同种免疫。
Cochrane Database Syst Rev. 2013 Mar 28;2013(3):CD009617. doi: 10.1002/14651858.CD009617.pub2.
7
A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.一种用于印度人群中不一致性 RhD 定型的简单诊断策略。
Blood Transfus. 2013 Jan;11(1):37-42. doi: 10.2450/2012.0006-12. Epub 2012 Jul 12.
8
Evidence for maternal-fetal genotype incompatibility as a risk factor for schizophrenia.母婴基因型不相容作为精神分裂症危险因素的证据。
J Biomed Biotechnol. 2010;2010:576318. doi: 10.1155/2010/576318. Epub 2010 Apr 6.