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本文引用的文献

1
Wisconsin stillbirth services program: a multifocal approach to stillbirth analysis.威斯康星州死产服务项目:一种多焦点的死产分析方法。
Am J Med Genet A. 2011 May;155A(5):1073-80. doi: 10.1002/ajmg.a.34016. Epub 2011 Apr 7.
2
Target ranges of oxygen saturation in extremely preterm infants.极低出生体重儿氧饱和度目标范围。
N Engl J Med. 2010 May 27;362(21):1959-69. doi: 10.1056/NEJMoa0911781. Epub 2010 May 16.
3
Newborn-care training and perinatal mortality in developing countries.发展中国家的新生儿护理培训与围产儿死亡率。
N Engl J Med. 2010 Feb 18;362(7):614-23. doi: 10.1056/NEJMsa0806033.
4
Timing of appearance of late oligodendrocyte progenitors coincides with enhanced susceptibility of preterm rabbit cerebral white matter to hypoxia-ischemia.晚期少突胶质前体细胞出现的时间与早产兔脑白质对缺氧缺血易感性增强的时间一致。
J Cereb Blood Flow Metab. 2010 May;30(5):1053-65. doi: 10.1038/jcbfm.2009.286. Epub 2010 Jan 13.
5
Stillbirth classification--developing an international consensus for research: executive summary of a National Institute of Child Health and Human Development workshop.死产分类——制定国际研究共识:美国国立儿童健康与人类发展研究所研讨会执行摘要
Obstet Gynecol. 2009 Oct;114(4):901-914. doi: 10.1097/AOG.0b013e3181b8f6e4.
6
Recurrent second trimester pregnancy loss: evaluation and management.复发性中期妊娠丢失:评估与管理。
Curr Opin Endocrinol Diabetes Obes. 2009 Dec;16(6):451-8. doi: 10.1097/MED.0b013e328332b808.
7
The challenge of fetal mortality.胎儿死亡的挑战。
NCHS Data Brief. 2009 Apr(16):1-8.
8
Etiology of stillbirth at term: a 10-year cohort study.足月死产的病因:一项10年队列研究。
J Matern Fetal Neonatal Med. 2008 Jul;21(7):493-501. doi: 10.1080/14767050802086669.
9
Prediction and prevention of recurrent stillbirth.复发性死产的预测与预防。
Obstet Gynecol. 2007 Nov;110(5):1151-64. doi: 10.1097/01.AOG.0000287616.71602.d0.
10
Fetal brain magnetic resonance imaging response acutely to hypoxia-ischemia predicts postnatal outcome.胎儿脑磁共振成像对缺氧缺血的急性反应可预测产后结局。
Ann Neurol. 2007 Apr;61(4):307-14. doi: 10.1002/ana.21095.

在缺氧缺血动物模型中,宫内胎儿死亡可能与引发损伤的原因相距甚远。

Intrauterine fetal demise can be remote from the inciting insult in an animal model of hypoxia-ischemia.

机构信息

Department of Pediatrics, University of Chicago and Northshore University HealthSystem, Evanston, Illinois, USA.

出版信息

Pediatr Res. 2012 Aug;72(2):154-60. doi: 10.1038/pr.2012.65.

DOI:10.1038/pr.2012.65
PMID:22580720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6109451/
Abstract

BACKGROUND

Fetal hypoxia-ischemia (H-I) results in significant morbidity and mortality. Little is known about the timing of death in human stillbirths. The vulnerability of the fetus varies with age at the time of insult, but it is unknown what happens to the timing of fetal death in relation to a fetal insult. We asked the question of whether the timing of fetal death was influenced by the age at which the insult occurred.

METHODS

Fetal H-I was achieved at three ages by sustained uterine ischemia in rabbits, mimicking the acute placental insufficiency of placental abruption.

RESULTS

H-I at 22 d gestation (E22) resulted in fewer perinatal deaths than at E25 and E29. Fetal deaths were grouped into early and late perinatal deaths. Early perinatal death mostly occurred immediately after H-I and these fetuses delivered before term. Late perinatal death occurred between the insult and delivery at term gestation. Early perinatal death occurred more often in the E25 hypoxic-ischemic group as compared with those of the E22 hypoxic-ischemic group.

CONCLUSION

There is an increasing vulnerability to hypoxia with increasing gestational age. Perinatal deaths may occur long after the episode of H-I. The timing of an intrauterine hypoxic-ischemic event cannot be inferred from the detection of fetal death.

摘要

背景

胎儿缺氧缺血(H-I)会导致严重的发病率和死亡率。对于人类死产中死亡的时间知之甚少。胎儿的脆弱性随损伤时的年龄而变化,但尚不清楚胎儿损伤与胎儿死亡时间之间的关系。我们提出了这样一个问题,即胎儿死亡的时间是否受到损伤时的年龄影响。

方法

通过持续的子宫缺血在兔子中模拟胎盘早剥的急性胎盘功能不全,在三个时期实现胎儿 H-I。

结果

与 E25 和 E29 相比,妊娠 22 天(E22)的 H-I 导致围产期死亡较少。胎儿死亡分为早期和晚期围产期死亡。早期围产期死亡大多发生在 H-I 后立即,这些胎儿在足月前分娩。晚期围产期死亡发生在创伤和足月分娩之间。与 E22 缺氧缺血组相比,E25 缺氧缺血组的早期围产期死亡更为常见。

结论

随着胎龄的增加,对缺氧的敏感性增加。围产期死亡可能在 H-I 后很长时间才发生。宫内缺氧缺血事件的时间不能从胎儿死亡的检测中推断出来。