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在未经过筛选的人群中,于孕18周常规胎儿检查时对心脏缺陷进行产前检测。

Prenatal detection of heart defects at the routine fetal examination at 18 weeks in a non-selected population.

作者信息

Tegnander E, Eik-Nes S H, Johansen O J, Linker D T

机构信息

Department of Obstetrics and Gynecology, Trondheim University Hospital, Norway.

出版信息

Ultrasound Obstet Gynecol. 1995 Jun;5(6):372-80. doi: 10.1046/j.1469-0705.1995.05060372.x.

Abstract

Few studies have addressed the prenatal detection rate of congenital heart defects in a non-selected population at 18 weeks of gestation. Our objective was to assess the change in the prenatal detection rate of congenital heart defects in such a population that resulted from incorporating the four-chamber view at the second-trimester routine ultrasound examination. The prenatal detection rate of heart defects was prospectively compared between 4435 fetuses in Phase I who were scanned without special attention to the heart, and 7459 fetuses in Phase II who were scanned incorporating the four-chamber view. Of the 49 heart defects in Phase 1, 17 (35%) were critical and three (18%) of these were detected prenatally. Of the 90 heart defects in Phase II, 23 (26%) were critical, six (26%) of these were detected prenatally at the 18 weeks' routine scan, and three were detected in the third trimester, providing a total prenatal detection rate of 39%. A defect was classified as critical when a surgical repair was likely to be required because of gross structural complexity having a functional significance, e.g. transposition of the great arteries, hypoplastic left heart syndrome, atrioventricular septal defect, coarctation of the aorta, and large ventricular septal defect. No non-critical heart defects were detected prenatally in either of the phases. The incidences in the total population were 11 and 12/1000 in Phases I and II, respectively. Thirty-two per cent of the critical and 16% of the non-critical defects had associated abnormalities and/or abnormal karyotype.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

很少有研究涉及在妊娠18周时对非特定人群中先天性心脏缺陷的产前检出率。我们的目的是评估在孕中期常规超声检查中纳入四腔心切面后,该人群中先天性心脏缺陷产前检出率的变化。前瞻性比较了第一阶段4435例未特别关注心脏进行扫描的胎儿与第二阶段7459例纳入四腔心切面进行扫描的胎儿的心脏缺陷产前检出率。在第一阶段的49例心脏缺陷中,17例(35%)为严重缺陷,其中3例(18%)在产前被检出。在第二阶段的90例心脏缺陷中,23例(26%)为严重缺陷,其中6例(26%)在18周常规扫描时产前被检出,3例在孕晚期被检出,产前总检出率为39%。当由于结构严重复杂且具有功能意义而可能需要手术修复时,如大动脉转位、左心发育不全综合征、房室间隔缺损、主动脉缩窄和大型室间隔缺损,缺陷被分类为严重缺陷。在两个阶段中,均未产前检出非严重心脏缺陷。第一阶段和第二阶段在总人群中的发病率分别为11/1000和12/1000。32%的严重缺陷和16%的非严重缺陷伴有相关异常和/或染色体核型异常。(摘要截短于250字)

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