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本文引用的文献

1
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Eur J Pediatr. 2016 May;175(5):667-76. doi: 10.1007/s00431-015-2687-1. Epub 2016 Jan 25.
2
Multidisciplinary consensus on the classification of prenatal and postnatal urinary tract dilation (UTD classification system).产前和产后泌尿道扩张分类的多学科共识(UTD分类系统)。
J Pediatr Urol. 2014 Dec;10(6):982-98. doi: 10.1016/j.jpurol.2014.10.002. Epub 2014 Nov 15.
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Current management of antenatal hydronephrosis.产前肾积水的当前处理方法。
Pediatr Nephrol. 2013 Feb;28(2):237-43. doi: 10.1007/s00467-012-2240-7. Epub 2012 Jul 27.
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Postnatal outcome of prenatally diagnosed severe fetal renal pelvic dilatation.产前诊断的严重胎儿肾盂扩张的产后结局。
Prenat Diagn. 2012 Jun;32(6):519-22. doi: 10.1002/pd.2893. Epub 2012 May 9.
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Clinical course of 822 children with prenatally detected nephrouropathies.822 例产前诊断肾尿路畸形患儿的临床病程。
Clin J Am Soc Nephrol. 2012 Mar;7(3):444-51. doi: 10.2215/CJN.03400411. Epub 2012 Jan 19.
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Renal outcome in children with antenatal diagnosis of severe CAKUT.产前诊断严重 CAKUT 的儿童的肾脏结局。
Pediatr Nephrol. 2012 Mar;27(3):497-502. doi: 10.1007/s00467-011-2068-6. Epub 2011 Dec 14.
7
Prenatal management of urogenital disorders.产前泌尿系统疾病管理。
Urol Clin North Am. 2010 May;37(2):149-58. doi: 10.1016/j.ucl.2010.03.015.
8
Renal outcome in patients with congenital anomalies of the kidney and urinary tract.先天性肾脏和尿路异常患者的肾脏转归
Kidney Int. 2009 Sep;76(5):528-33. doi: 10.1038/ki.2009.220. Epub 2009 Jun 17.
9
Clinical outcome of children with chronic kidney disease in a pre-dialysis interdisciplinary program.
Pediatr Nephrol. 2008 Nov;23(11):2039-46. doi: 10.1007/s00467-008-0868-0. Epub 2008 Jun 17.
10
Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks.孕11⁺⁰至13⁺⁶周时筛查21三体综合征中的脉络丛囊肿、心内强回声灶、肠管强回声及肾积水
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胎儿泌尿系统异常产前诊断后的结局:一家三级中心的经验

Outcome after prenatal diagnosis of fetal urinary tract abnormalities: A tertiary center experience.

作者信息

Özel Ayşegül, Alıcı Davutoğlu Ebru, Erenel Hakan, Karslı Mehmet Fatih, Korkmaz Sevim Özge, Madazlı Rıza

机构信息

Department of Obstetrics and Gynecology, Perinatology Unit, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey

出版信息

J Turk Ger Gynecol Assoc. 2018 Nov 15;19(4):206-209. doi: 10.4274/jtgga.2017.0132. Epub 2018 Apr 4.

DOI:10.4274/jtgga.2017.0132
PMID:29636313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6250090/
Abstract

OBJECTIVE

With the widespread use of ultrasonography for fetal screening, the detection and management of congenital urinary tract abnormalities has become crucial. In this study, we aimed to describe the clinical approaches in patients with prenatally detected urinary tract abnormalities.

MATERIAL AND METHODS

This study is a retrospective, single-center study performed at a perinatology unit of a university hospital, between 2010 and 2016. The outcomes of 124 patients who were prenatally diagnosed as having urinary tract abnormalities are reported. Variables included in the analysis were fetal sex, birth week and weight, persistency, and necessity surgery after birth for renal pelvic dilatation. Low-risk renal pelvic dilatation was determined as an anterior-posterior (AP) diameter of 4-7 mm at 16-28 weeks, 7-10 mm after 28 weeks, whereas high-risk dilatation was defined as AP measurements of ≥7 mm at 16-28 weeks, ≥10 mm after 28 weeks, respectively.

RESULTS

The majority of patients consisted of male fetuses with bilateral pelviectasis (62.9%, 20.2%, respectively). The mean age was 28.8±6.4 years. The mean gestational age at birth was 34.2±7.8 weeks. The mean birth weight was 2593±1253.3 g. The need for surgery was greater in high-risk patients than in low-risk patients (58.3% vs. 8.7%) (p<0.002).

CONCLUSION

Patients with high-risk antenatal renal pelvic dilatation require surgical treatment after delivery. Close prenatal and postnatal follow-up is mandatory in specialized centers. Perinatologists, neonatologists, pediatricians and pediatric nephrologists, and radiologists should treat these children with a multidisciplinary approach.

摘要

目的

随着超声检查在胎儿筛查中的广泛应用,先天性泌尿系统异常的检测和管理变得至关重要。在本研究中,我们旨在描述产前检测出泌尿系统异常患者的临床处理方法。

材料与方法

本研究是一项回顾性单中心研究,于2010年至2016年在一所大学医院的围产医学科进行。报告了124例产前诊断为泌尿系统异常患者的结局。分析中纳入的变量包括胎儿性别、出生孕周和体重、持续性以及出生后因肾盂扩张进行手术的必要性。低风险肾盂扩张定义为16 - 28周时前后径为4 - 7毫米,28周后为7 - 10毫米,而高风险扩张分别定义为16 - 28周时前后径≥7毫米,28周后≥10毫米。

结果

大多数患者为双侧肾盂扩张的男性胎儿(分别为62.9%、20.2%)。平均年龄为28.8±6.4岁。出生时的平均孕周为34.2±7.8周。平均出生体重为2593±1253.3克。高风险患者比低风险患者更需要手术(58.3%对8.7%)(p<0.002)。

结论

产前高风险肾盂扩张患者产后需要手术治疗。在专业中心进行密切的产前和产后随访是必要的。围产医学专家、新生儿科医生、儿科医生、儿科肾病学家和放射科医生应以多学科方法治疗这些儿童。