De León-Luis J, Gámez F, Bravo C, Tenías J M, Arias Á, Pérez R, Maroto E, Aguarón Á, Ortiz-Quintana L
Department of Obstetrics and Gynecology, Hospital General Gregorio Marañón, Universidad Complutense de Madrid, Madrid, Spain.
Ultrasound Obstet Gynecol. 2014 Aug;44(2):147-53. doi: 10.1002/uog.13336.
First, to estimate the prevalence of fetal aberrant right subclavian artery (ARSA) in our population and its association with Down syndrome. Second, to determine the feasibility of ultrasound to visualize ARSA in the three planes. Finally, to carry out a systematic review of the literature on the performance of second-trimester ARSA to identify fetuses with Down syndrome.
ARSA was assessed by ultrasound in the axial plane and confirmed in the longitudinal and coronal planes during the second half of pregnancy in women attending our unit (from February 2011 to December 2012). A search of diagnostic tests for the assessment of ARSA was carried out in international databases. Relevant studies were subjected to a critical reading, and meta-analysis was performed with Meta-DiSc.
Of the 8781 fetuses in our population (mean gestational age: 24 ± 5.4 weeks), 22 had Down syndrome. ARSA was detected in the axial view in 60 cases (0.7%) and confirmed in the coronal view in 96.7% and in the longitudinal view in 6.7% (P < 0.001). Seven cases with ARSA had Down syndrome and all were in the non-isolated-ARSA group. The estimates of positive likelihood ratio (LR) were 0 for isolated ARSA and 199 (95% CI, 88.9-445.2) for non-isolated ARSA. In the systematic review, six studies were selected for quantitative synthesis. The pooled estimates of positive and negative LRs for global ARSA were, respectively, 35.3 (95% CI, 24.4-51.1) and 0.75 (95% CI, 0.64-0.87). For isolated ARSA, the positive and negative LRs were 0 (95% CI, 0.0-14.7) and 0.98 (95% CI, 0.94-1.02), respectively.
The prevalence of ARSA seems close to 1%. The coronal plane is the most suitable for its confirmation after detection in the axial plane. Detection of isolated or non-isolated ARSA should guide decisions about karyotyping given that isolated ARSA shows a weak association with Down syndrome.
第一,评估我们人群中胎儿迷走右锁骨下动脉(ARSA)的患病率及其与唐氏综合征的关联。第二,确定超声在三个平面上可视化ARSA的可行性。最后,对关于孕中期ARSA表现以识别唐氏综合征胎儿的文献进行系统评价。
在我院就诊的孕妇(2011年2月至2012年12月)妊娠后半期,通过超声在轴平面评估ARSA,并在纵平面和冠状平面进行确认。在国际数据库中搜索评估ARSA的诊断测试。对相关研究进行批判性阅读,并用Meta-DiSc进行荟萃分析。
在我们的8781例胎儿中(平均孕周:24±5.4周),22例患有唐氏综合征。在轴位视图中检测到60例ARSA(0.7%),在冠状视图中96.7%得到确认,在纵视图中6.7%得到确认(P<0.001)。7例患有ARSA的胎儿患有唐氏综合征,且均在非孤立性ARSA组。孤立性ARSA的阳性似然比(LR)估计值为0,非孤立性ARSA的阳性似然比为199(95%CI,88.9-445.2)。在系统评价中,选择了6项研究进行定量合成。全球ARSA的阳性和阴性LR的合并估计值分别为35.3(95%CI,24.4-51.1)和0.75(95%CI,0.64-0.87)。对于孤立性ARSA,阳性和阴性LR分别为0(95%CI,0.0-14.7)和0.98(95%CI,0.94-1.02)。
ARSA的患病率似乎接近1%。冠状平面是在轴平面检测到ARSA后进行确认的最合适平面。鉴于孤立性ARSA与唐氏综合征的关联较弱,检测到孤立性或非孤立性ARSA应指导关于染色体核型分析的决策。