Department of Obstetrics and Gynecology, University of Bari, Bari, and the Maternal-Fetal Medicine Unit, Department of Obstetrics and Gynecology, University of Brescia, Brescia, Italy.
Obstet Gynecol. 2013 Dec;122(6):1160-7. doi: 10.1097/AOG.0000000000000015.
To review the literature concerning the efficacy of early ultrasonography (at 11-14 weeks of gestation) to identify fetal malformations.
A search in PubMed, MEDLINE, Embase, Cochrane Library, and ClinicalTrials.gov was performed (January 2000 to December 2012). Keywords were: fetal anatomy, fetal echocardiography, nuchal translucency, fetal structural anomalies, fetal malformations, prenatal diagnosis, prenatal screening, and first-trimester ultrasonography.
Inclusion criteria were: fetal anatomy examination at early ultrasonography and diagnosis of fetal malformations confirmed by postnatal or postmortem examination. Data abstracted were: sample size, location of structural defect, ultrasound modality, presence of multiple defects, and study population. Pooled detection rate was calculated for each malformation and compared with χ. Differences were considered statistically significant if P<.05.
TABULATION, INTEGRATION, AND RESULTS: From 1,203 articles, 19 were included. Overall, we pooled 78,002 fetuses undergoing ultrasonography at 11-14 weeks, of which 996 were malformed, leading to prevalence of malformation of 12 per 1,000. The overall detection rate was 472 of 957 (51%). The highest detection rate was achieved for neck anomalies (92%), whereas limbs (34%), face (34%), and genitourinary anomalies (34%) were associated with the lowest detection rate. At 14 weeks of gestation or less, fetal echocardiography detected 53% of congenital heart disease compared with 43% by complete scan (P=.040). The use of Doppler did not improve the detection rate for congenital heart defects (52% compared with 44%, respectively; P=.11). Multiple defects were identified more frequently than isolated malformations (60% compared with 44%; P=.005). The detection rate was higher combining transabdominal and transvaginal techniques (62%) than either abdominal (51%) or transvaginal (34%; P<.001). Detection rate was higher in women at high risk (65%) than unselected population (50% P=.001).
Because of the natural history of fetal defects and the late development of some organ systems, a number of fetal malformations remain undetected by early ultrasonography.
回顾有关在 11-14 孕周行早期超声检查以发现胎儿畸形的有效性的文献。
在 PubMed、MEDLINE、Embase、Cochrane 图书馆和 ClinicalTrials.gov 中进行了检索(2000 年 1 月至 2012 年 12 月)。关键词是:胎儿解剖学、胎儿超声心动图、颈项透明层、胎儿结构异常、胎儿畸形、产前诊断、产前筛查和早孕期超声检查。
纳入标准是:在早孕期进行胎儿解剖学检查,并通过产后或尸检证实胎儿畸形的诊断。提取的数据有:样本量、结构缺陷部位、超声模式、多发缺陷存在情况和研究人群。对每种畸形的汇总检出率进行计算,并与 χ²进行比较。如果 P<.05,则认为差异具有统计学意义。
列表、整合和结果:从 1203 篇文章中,有 19 篇被纳入。总的来说,我们汇总了在 11-14 孕周行超声检查的 78002 例胎儿,其中 996 例存在畸形,患病率为每 1000 例中 12 例。总的检出率为 957 例中的 472 例(51%)。颈部异常的检出率最高(92%),而四肢(34%)、面部(34%)和泌尿生殖系统异常(34%)的检出率最低。在 14 孕周或更短时间内,胎儿超声心动图检测到 53%的先天性心脏病,而完整扫描检测到 43%(P=.040)。使用多普勒并不能提高先天性心脏病缺陷的检出率(分别为 52%和 44%;P=.11)。多发畸形的检出率高于单发畸形(分别为 60%和 44%;P=.005)。结合经腹和经阴道技术的检出率高于经腹(51%)或经阴道(34%)技术(均 P<.001)。高危人群(65%)的检出率高于未选择人群(50%;P=.001)。
由于胎儿缺陷的自然病史和某些器官系统的晚期发育,一些胎儿畸形仍无法通过早孕期超声检查发现。