Department of Pediatric Nephrology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
Department of Obstetrics, Academic Medical Center AMC, Amsterdam, The Netherlands.
J Pediatr Urol. 2017 Dec;13(6):594-601. doi: 10.1016/j.jpurol.2017.06.001. Epub 2017 Jun 21.
Isolated antenatal hydronephrosis (ANH), defined as a dilation of the renal pelvis (≥5 mm), is one of the most common abnormalities detected on prenatal ultrasound. However, established cut-off values for postnatal follow-up differ between countries and are based on little evidence. The current protocol in the Netherlands for follow-up might be too conservative.
To assess the applicability of a higher threshold for follow-up of isolated antenatal hydronephrosis (ANH) than the current practice, without the risk of missing significant postnatal urinary tract obstruction.
Retrospective case series on all fetuses with isolated ANH (anteroposterior pelvic diameter (APPD) ≥5 mm) at the second trimester anomaly scan, and diagnosed between 2000 and 2009, in relationship to renal outcome.
A total of 279 infants with second trimester isolated ANH were included. In 201/279 (72%) fetuses, ANH had normalized (APPD <10 mm) before the third trimester scans. Hydronephrosis persisted postnatally in a minority of 56/279 (20.1%). Postnatal assessment showed signs of obstruction in 41/279 (14.7%) infants, duplicated collecting system or vesicoureteral reflux (VUR). Surgery was performed in 18/279 (6.5%) infants. A non-functioning kidney was shown in 6/279 (2.2%) infants with ANH. Mild ANH (APPD <7 mm) during the second trimester (172/279 (61.6%)) never resulted in surgery for renal anomalies or non-functioning kidney. Infants with an APPD ≥10 mm in the second trimester were far more likely to develop renal anomalies or undergo surgery compared with infants with an APPD 7-10 mm. The number of non-functioning kidneys was too low to be conclusive.
Follow-up ultrasounds for isolated ANH ≥7 mm instead of ≥5 mm at the second trimester scan would have saved 62% of third trimester scans, without missing any infant with a non-functioning kidney, significant obstruction or symptomatic VUR. In view of the results, it is reasonable that referral for follow-up of second trimester ANH is not strictly indicated in cases with an APPD <7 mm.
孤立性产前肾积水(ANH)定义为肾盂扩张(≥5mm),是产前超声检查最常见的异常之一。然而,不同国家的产后随访的既定截断值存在差异,且其依据的证据较少。目前荷兰的随访方案可能过于保守。
评估采用高于当前实践的更高阈值来随访孤立性产前肾积水(ANH)的适用性,而不会错过明显的产后尿路梗阻的风险。
对 2000 年至 2009 年期间在第二次中期异常扫描中诊断为孤立性 ANH(前后径骨盆直径(APPD)≥5mm)的所有胎儿进行回顾性病例系列研究,并与肾脏结局相关联。
共纳入 279 例第二次中期孤立性 ANH 的婴儿。在 279 例胎儿中,201 例(72%)胎儿的 ANH 在第三次中期扫描前已正常化(APPD<10mm)。少数 56/279(20.1%)胎儿在产后持续存在肾积水。279 例中的 41 例(14.7%)婴儿的产后评估显示存在梗阻迹象、双肾盂收集系统或膀胱输尿管反流(VUR)。对 18/279(6.5%)婴儿进行了手术。6/279(2.2%)患有 ANH 的婴儿显示出无功能肾脏。第二次中期轻度 ANH(APPD<7mm)(172/279(61.6%))从未因肾脏异常或无功能肾脏而行手术。与 APPD 为 7-10mm 的婴儿相比,APPD 在第二次中期为≥10mm 的婴儿更有可能出现肾脏异常或需要手术。无功能肾脏的数量太少,无法得出结论。
在第二次中期扫描时,将 ANH 随访的超声检查的截断值从≥5mm 改为≥7mm,可以节省 62%的第三次中期扫描,而不会错过任何无功能肾脏、严重梗阻或有症状的 VUR 的婴儿。鉴于结果,在 APPD<7mm 的情况下,对于第二中期 ANH 的随访,不严格进行转诊是合理的。