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早孕期通过静脉导管血流检测主要心脏缺陷。

First-trimester detection of major cardiac defects with the use of ductus venosus blood flow.

机构信息

Department of Maternal-Fetal Medicine, Institute of Gynecology, Obstetrics and Neonatology, Hospital Clínic Barcelona, Catalonia, Spain.

出版信息

Ultrasound Obstet Gynecol. 2013 Jul;42(1):51-7. doi: 10.1002/uog.12349.

Abstract

OBJECTIVE

To assess the best method of combining fetal nuchal translucency (NT) and ductus venosus (DV) blood flow measurements in the detection of major cardiac defects in chromosomally normal fetuses during the first-trimester scan.

METHODS

During an 8-year period NT and DV blood flow were routinely assessed at 11-14 weeks' gestation. Only chromosomally normal singleton pregnancies were included in the study. When a cardiac defect was suspected, or when increased fetal NT and/or absent or reversed (AR) A-wave in the DV was observed, early fetal echocardiography was offered. Data on routine second- and third-trimester scans, neonatal follow-up or postmortem examination were obtained from hospital records. The detection and false-positive rates for all major cardiac defects were calculated for several screening strategies, including: NT or DV pulsatility index for veins (DV-PIV) above a fixed normal centile; AR A-wave; risk based on NT and DV-PIV or A-wave velocity above a fixed normal centile; and combinations of these strategies.

RESULTS

The study population included 37 chromosomally normal fetuses with a major cardiac defect and 12 799 unaffected pregnancies. Fetal NT above the 95(th) or the 99(th) centile and AR A-wave was observed in 40, 27 and 39% of the fetuses with major cardiac defects, respectively. A 47% detection rate with a 2.7% false-positive rate was obtained when AR A-wave or NT above the 99(th) centile was used as the selection criterion.

CONCLUSIONS

Half of major fetal cardiac defects could be detected in the first trimester if NT and DV Doppler are used to select 2.7% of the general pregnant population for extended fetal echocardiography.

摘要

目的

评估在早孕期颈项透明层(NT)联合静脉导管(DV)血流测量用于检测染色体正常胎儿的主要心脏缺陷的最佳方法。

方法

在 8 年期间,常规在 11-14 孕周进行 NT 和 DV 血流测量。本研究仅纳入染色体正常的单胎妊娠。当怀疑存在心脏缺陷,或 NT 增加和/或 DV 中出现无 A 波或反向 A 波(AR)时,进行早期胎儿超声心动图检查。从医院记录中获得关于常规的中孕期和晚孕期超声检查、新生儿随访或尸检检查的数据。为几种筛查策略计算所有主要心脏缺陷的检出率和假阳性率,包括:固定正常百分位数以上的 NT 或静脉 DV 搏动指数(DV-PIV);AR A 波;基于 NT 和 DV-PIV 或固定正常百分位数以上的 A 波速度的风险;以及这些策略的组合。

结果

研究人群包括 37 例染色体正常的胎儿有主要心脏缺陷和 12 799 例无异常妊娠。在有主要心脏缺陷的胎儿中,分别有 40%、27%和 39%出现胎儿 NT 超过第 95 百分位数或第 99 百分位数和 AR A 波。当 AR A 波或 NT 超过第 99 百分位数用作选择标准时,检出率为 47%,假阳性率为 2.7%。

结论

如果将 NT 和 DV 多普勒用于选择 2.7%的一般孕妇人群进行扩展胎儿超声心动图检查,那么一半的主要胎儿心脏缺陷可以在早孕期被检出。

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