Borenstein M, Cavoretto P, Allan L, Huggon I, Nicolaides K H
Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
Ultrasound Obstet Gynecol. 2008 Jan;31(1):20-4. doi: 10.1002/uog.5226.
To establish the feasibility of examining the subclavian artery at 11 + 0 to 13 + 6 weeks of gestation, and to determine the prevalence of aberrant right subclavian artery (ARSA) in chromosomally normal and chromosomally abnormal fetuses.
Fetal echocardiography was performed prospectively in 516 patients before chorionic villus sampling at 11 + 0 to 13 + 6 weeks of gestation. Transabdominal sonography was carried out, and color flow mapping was used to identify the right subclavian artery and determine whether this was normal or aberrant (ARSA). Second-trimester fetal echocardiography was also carried out in a subgroup of 183 fetuses.
The median gestational age was 12 weeks and the median crown-rump length was 68 mm. Successful assessment of the right subclavian artery was achieved in 425/516 (82.4%) cases and the rate of failure to do so was significantly associated with decreasing fetal crown-rump length (r = 0.174, P < 0.001) and increasing maternal body mass index (r = 0.275, P < 0.001). An ARSA was observed in 2/353 (0.6%) fetuses with a normal karyotype, in 4/51 (7.8%) cases with trisomy 21 and in 2/20 (10.0%) with other chromosomal defects. In a subgroup of 183 fetuses examined in both the first and second trimester there were three cases of ARSA observed at both scans and an additional case in which ARSA was detected only at the second scan.
Assessment of the position of the right subclavian artery is feasible at the 11 + 0 to 13 + 6-week scan and ARSA is more common in chromosomally abnormal than normal fetuses. However, ARSA in the first trimester is unlikely to be a useful marker of trisomy 21.
确定在妊娠11⁺⁰至13⁺⁶周检查锁骨下动脉的可行性,并确定染色体正常和染色体异常胎儿中迷走右锁骨下动脉(ARSA)的患病率。
对516例患者在妊娠11⁺⁰至13⁺⁶周进行绒毛取样前进行前瞻性胎儿超声心动图检查。采用经腹超声检查,并用彩色血流图识别右锁骨下动脉,确定其是否正常或异常(ARSA)。还对183例胎儿的亚组进行了孕中期胎儿超声心动图检查。
中位孕周为12周,中位头臀长为68 mm。425/516(82.4%)例成功评估了右锁骨下动脉,评估失败率与胎儿头臀长减小(r = 0.174,P < 0.001)和孕妇体重指数增加(r = 0.275,P < 0.001)显著相关。在353例染色体核型正常的胎儿中有2例(0.6%)观察到ARSA,在51例21三体病例中有4例(7.8%),在20例其他染色体缺陷病例中有2例(10.0%)。在孕早期和孕中期均接受检查的183例胎儿亚组中,两次扫描均观察到3例ARSA,另有1例仅在第二次扫描时检测到ARSA。
在11⁺⁰至13⁺⁶周扫描时评估右锁骨下动脉的位置是可行的,ARSA在染色体异常胎儿中比正常胎儿更常见。然而,孕早期的ARSA不太可能是21三体的有用标志物。