目的:评估四腔心切面及三血管气管切面观察胎儿食管筛查食管闭锁(EA)的价值。方法:对425例孕21~25周行系统胎儿超声检查的胎儿获取四腔心切面(胸骨旁四腔心切面)、三血管气管切面的同时观察食管回声,排除EA造成的食管中断。四腔心切面及三血管气管切面均显示食管横断面回声为EA低风险胎儿;四腔心切面或三血管气管切面不显示食管横断面回声或上述两个切面均不显示为EA高风险胎儿,需进一步获取食管矢状切面及冠状切面进一步证实。结果:四腔心切面及三血管气管切面均能显示食管回声396例(93.1%,396/425),为EA低风险胎儿。余29例(6.8%,29/425)为EA高风险胎儿,其中27例通过食管矢状切面及冠状切面显示食管不断延长的条带状回声。2例食管连续性中断为EA。EA 2例三血管气管切面均不显示食管回声。漏诊EA 0例。利用四腔心切面及三血管气管切面显示食管筛查EA的灵敏度100%(2/2),特异度93.6%(396/423),阳性预测值6.9%(2/29),阴性预测值100%(396/396)。结论:四腔心切面及三血管气管切面显示食管可有效筛查胎儿EA。
Abstract
esia in prenatal ultrasound. Methods: Prenatal ultrasound was prospectively performed in 425 consecutive fetuses between 21 and 25 weeks for detection of esophageal atresia. A complete anatomical survey was performed. We searched for esophagus on satisfactory 4C and 3VT view. Fetuses whose esophagus could be showed on 4C and 3VT were at low risk of esophageal atresia. Fetuses whose esophagus couldn’t be showed on either 4C or 3VT or both were at high risk of esophageal atresia. More views such as saggital and coronary view of esophagus could be needed to get more information. Results: Esophagus could be viewed on both 4C and 3VT in 396 cases(93.1%, 396/425). These were at low risk of esophageal atresia. The remaining 29 cases(6.8%, 29/425) were at high risk of esophageal atresia. Out of them, 27 cases were confirmed to be normal as continuous parallel echogenic lines was found on saggital views or coronary views. During the screening, 2 cases of esophageal atresia were found. Their esophaguses couldn’t be shown on 3VT. Neither of esophageal atresia cases was misdiagnosed in this group. The sensitivity, specificity, positive predictive value and negative predictive value were 100% (2/2), 93.6%(396/423), 6.9%(2/29) and 100%(396/396) respectively of 4C and 3VT for the screening of the fetal esophageal atresia. Conclusions: It is effective to screen fetal esophageal atresia with 4C and 3VT.
关键词
食管闭锁 /
超声检查 /
产前
Key words
Esophageal atresia /
Ultrasonography, prenatal
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1]Depaepe A, Dolk H, Lechat MF, A EUROCAT Working Group. The epidemiology of tracheo-oesophageal fistula and oesophageal atresia in Europe[J]. Arch Dis Child, 1993, 68(6): 743-748.
[2]Spitz L. Oesophageal atresia[J]. Orphanet J Rare Dis, 2007, 2: 24.
[3]Stringer MD, McKenna KM, Goldstein RB, et al. Prenatal diagnosis of esophageal atresia[J]. J Pediatr Surg, 1995, 30(9): 1258-1263.
[4]Brugger PC, Weber M, Prayer D. Magnetic resonance imaging of the normal fetal oesophagus[J]. Ultrasound Obstet Gynecol, 2011, 38(5): 568-574.
[5]Sparey C, Jawaheer G, Barrett AM, et al. Esophageal atresia in the Northern Region Congenital Anomaly Survey, 1985-1997: prenatal diagnosis and outcome[J]. Am J Obstet Gynecol, 2000, 182(2): 427-431.
[6]Pretorius DH, Drose JA, Dennis MA, et al. Tracheoesophageal fistula in utero. Twenty-two cases[J]. J Ultrasound Med, 1987, 6(9): 509-513.
[7]Dashe JS, McIntire DD, Ramus RM, et al. Hydramnios: anomaly prevalence and sonographic detection[J]. Obstet Gynecol, 2002, 100(1): 134-139.
[8]李胜利. 对中国医师协会超声医师分会《产前超声检查指南(2012)》的深入解读[J]. 中华医学超声杂志:电子版,2014,(4):1-9.
[9]李胜利,陈秀兰,欧阳淑媛,等. Ⅲ级产前超声检查对产前诊断胎儿畸形的意义[J]. 中国超声医学杂志, 2009,25(3):312-315.
[10]陈秀兰,刘桃,袁志燕,等. 产前超声四腔心切面显示胎儿食管价值的研究[J]. 中国临床医学影像杂志,2015,26(9):653-656.
[11]Venkatesh P. A Simple and Easy Technique for Imaging the Fetal Esophagus in the First, Second, and Third Trimesters Using the Transverse Section of the Esophagus in the Area Behind the Heart as a Reference Point[J]. J Ultrasound Med, 2018, 37(12): 2863-2872.
[12]Malinger G, Levine A, Rotmensch S. The fetal esophagus: anatomical and physiological ultrasonographic characterization using a high-resolution linear transducer[J]. Ultrasound Obstet Gynecol, 2004, 24(5): 500-505.
[13]Brantberg A, Blaas HG, Haugen SE, et al. Esophageal obstruction-prenatal detection rate and outcome[J]. Ultrasound Obstet Gynecol, 2007, 30(2): 180-187.
[14]Sparey C, Jawaheer G, Barrett AM, et al. Esophageal atresia in the Northern Region Congenital Anomaly Survey, 1985-1997: prenatal diagnosis and outcome[J]. Am J Obstet Gynecol, 2000, 182(2): 427-431.
[15]Bednarczyk D, Sasiadek MM, Smigiel R. Chromosome aberrations and gene mutations in patients with esophageal atresia[J]. J Pediatr Gastroenterol Nutr, 2013, 57(6): 688-693.
[16]Brosens E, de Jong EM, Barakat TS, et al. Structural and numerical changes of chromosome X in patients with esophageal atresia[J]. Eur J Hum Genet, 2014, 22(9): 1077-1084.
基金
深圳市宝安区医疗卫生科研项目(编号:2016CX303)。