• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

先天性肾脏和尿路异常患者慢性肾脏病的预测模型

A predictive model of chronic kidney disease in patients with congenital anomalies of the kidney and urinary tract.

作者信息

Quirino Isabel G, Dias Cristiane S, Vasconcelos Mariana A, Poggiali Isabel V, Gouvea Kerlane C, Pereira Alamanda K, Paulinelli Gabriela P, Moura Amanda R, Ferreira Raquel S, Colosimo Enrico A, Simões E Silva Ana Cristina, Oliveira Eduardo A

机构信息

Pediatric Nephrology Unit, Department of Pediatrics, National Institute of Science and Technology (INCT) of Molecular Medicine, Faculty of Medicine, Federal University of Minas Gerais, Av Alfredo Balena, 190, Belo Horizonte, MG, 30130-100, Brazil.

出版信息

Pediatr Nephrol. 2014 Dec;29(12):2357-64. doi: 10.1007/s00467-014-2870-z. Epub 2014 Jun 19.

DOI:10.1007/s00467-014-2870-z
PMID:24942863
Abstract

BACKGROUND

The antenatal detection of congenital anomalies of the kidney and urinary tract (CAKUT) has permitted early management of these conditions. The aim of this study was to identify predictive factors associated with chronic kidney disease (CKD) in CAKUT. We also propose a risk score of CKD.

METHODS

In this cohort study, 822 patients with prenatally detected CAKUT were followed up for a median time of 43 months. The primary outcome was CKD stage III or higher. A predictive model was developed using the Cox proportional hazards model and evaluated by using c statistics.

RESULTS

Chronic kidney disease occurred in 49 of the 822 (6 %) children with prenatally detected CAKUT. The most accurate model included bilateral hydronephrosis, oligohydramnios, estimated glomerular filtration rate and postnatal diagnosis. The accuracy of the score was 0.95 [95 % confidence interval (CI) 0.89-0.99] and 0.92 (95 % CI 0.86-0.95) after a follow-up of 2 and 10 years, respectively. Based on survival curves, we estimated that at 10 years of age, the probability of survival without CKD stage III was approximately 98 and 58 % for the patients assigned to the low-risk and high-risk groups, respectively (p < 0.001).

CONCLUSIONS

Our predictive model of CKD may contribute to an early identification of a subgroup of patients at high risk for renal impairment. It should be pointed out, however, that this model requires external validation in a different cohort.

摘要

背景

产前检测先天性肾脏和尿路异常(CAKUT)有助于对这些疾病进行早期管理。本研究旨在确定与CAKUT患者慢性肾脏病(CKD)相关的预测因素。我们还提出了一个CKD风险评分。

方法

在这项队列研究中,对822例产前检测出CAKUT的患者进行了中位时间为43个月的随访。主要结局为CKD III期或更高分期。使用Cox比例风险模型建立预测模型,并通过c统计量进行评估。

结果

822例产前检测出CAKUT的儿童中有49例(6%)发生了慢性肾脏病。最准确的模型包括双侧肾积水、羊水过少、估计肾小球滤过率和产后诊断。随访2年和10年后,该评分的准确性分别为0.95[95%置信区间(CI)0.89 - 0.99]和0.92(95%CI 0.86 - 0.95)。根据生存曲线,我们估计在10岁时,低风险组和高风险组患者无CKD III期生存的概率分别约为98%和58%(p < 0.001)。

结论

我们的CKD预测模型可能有助于早期识别有肾功能损害高风险的患者亚组。然而,应该指出的是,该模型需要在不同队列中进行外部验证。

相似文献

1
A predictive model of chronic kidney disease in patients with congenital anomalies of the kidney and urinary tract.先天性肾脏和尿路异常患者慢性肾脏病的预测模型
Pediatr Nephrol. 2014 Dec;29(12):2357-64. doi: 10.1007/s00467-014-2870-z. Epub 2014 Jun 19.
2
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.
3
Outcome after prenatal diagnosis of congenital anomalies of the kidney and urinary tract.先天性肾脏和尿路异常的产前诊断后的结局
Eur J Pediatr. 2016 May;175(5):667-76. doi: 10.1007/s00431-015-2687-1. Epub 2016 Jan 25.
4
Congenital Anomalies of the Kidney and Urinary Tract in Children Born Small for Gestational Age.小于胎龄儿出生的儿童肾脏和泌尿道先天性异常
Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Mar 1;38(1):53-57. doi: 10.1515/prilozi-2017-0007.
5
Predicting outcomes in children with congenital anomalies of the kidney and urinary tract.预测儿童先天性肾和尿路畸形的结局。
Pediatr Nephrol. 2023 Oct;38(10):3407-3415. doi: 10.1007/s00467-023-05992-0. Epub 2023 May 3.
6
A clinical predictive model of renal injury in children with congenital solitary functioning kidney.儿童先天性孤立功能肾损伤的临床预测模型。
Pediatr Nephrol. 2019 Mar;34(3):465-474. doi: 10.1007/s00467-018-4111-3. Epub 2018 Oct 15.
7
Insignificant impact of VUR on the progression of CKD in children with CAKUT.膀胱输尿管反流对先天性肾脏和尿路畸形患儿慢性肾脏病进展的影响不显著。
Pediatr Nephrol. 2016 Jan;31(1):105-12. doi: 10.1007/s00467-015-3196-1. Epub 2015 Sep 24.
8
A predictive model of progression of CKD to ESRD in a predialysis pediatric interdisciplinary program.一项关于透析前儿科多学科项目中慢性肾脏病进展为终末期肾病的预测模型。
Clin J Am Soc Nephrol. 2014 Apr;9(4):728-35. doi: 10.2215/CJN.06630613. Epub 2014 Jan 23.
9
Hypertension in children with congenital anomalies of the kidney and urinary tract.儿童先天性肾及尿路畸形的高血压。
Pediatr Nephrol. 2024 Apr;39(4):1185-1192. doi: 10.1007/s00467-023-06207-2. Epub 2023 Nov 1.
10
Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease.儿童先天性肾及尿路畸形的临床特征及慢性肾脏病的预测因素。
Turk J Pediatr. 2020;62(5):746-755. doi: 10.24953/turkjped.2020.05.005.

引用本文的文献

1
Complex Management of Bilateral Congenital Hydronephrosis in a Pediatric Patient: A Multidisciplinary Approach.小儿双侧先天性肾积水的复杂管理:多学科方法
Healthcare (Basel). 2025 Apr 25;13(9):998. doi: 10.3390/healthcare13090998.
2
Risk factors for childhood chronic kidney disease: a population-based study.儿童慢性肾脏病的危险因素:一项基于人群的研究。
Pediatr Nephrol. 2023 May;38(5):1569-1576. doi: 10.1007/s00467-022-05714-y. Epub 2022 Aug 26.
3
A Predictive Model of Postnatal Surgical Intervention in Children With Prenatally Detected Congenital Anomalies of the Kidney and Urinary Tract.

本文引用的文献

1
Mutations in DSTYK and dominant urinary tract malformations.DSTYK 基因突变与显性泌尿道畸形。
N Engl J Med. 2013 Aug 15;369(7):621-9. doi: 10.1056/NEJMoa1214479. Epub 2013 Jul 17.
2
High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.在 CAKUT 患者无症状一级亲属中,肾脏和泌尿道异常的发生率较高。
Pediatr Nephrol. 2013 Nov;28(11):2143-7. doi: 10.1007/s00467-013-2530-8. Epub 2013 Jun 28.
3
Low birth weight, later renal function, and the roles of adulthood blood pressure, diabetes, and obesity in a British birth cohort.
产前检测出的先天性肾和尿路异常儿童出生后手术干预的预测模型
Front Pediatr. 2019 Apr 2;7:120. doi: 10.3389/fped.2019.00120. eCollection 2019.
4
Severe antenatally diagnosed renal disorders: background, prognosis and practical approach.产前诊断的严重肾脏疾病:背景、预后及实用方法
Pediatr Nephrol. 2016 Apr;31(4):563-74. doi: 10.1007/s00467-015-3140-4. Epub 2015 Jun 17.
5
Predictors of Rapid Progression of Glomerular and Nonglomerular Kidney Disease in Children and Adolescents: The Chronic Kidney Disease in Children (CKiD) Cohort.儿童和青少年肾小球及非肾小球肾病快速进展的预测因素:儿童慢性肾脏病(CKiD)队列研究
Am J Kidney Dis. 2015 Jun;65(6):878-88. doi: 10.1053/j.ajkd.2015.01.008. Epub 2015 Mar 19.
低出生体重、后期肾功能以及成年期血压、糖尿病和肥胖在英国出生队列中的作用。
Kidney Int. 2013 Dec;84(6):1262-70. doi: 10.1038/ki.2013.223. Epub 2013 Jun 12.
4
Extra-uterine renal growth in preterm infants: oligonephropathy and prematurity.早产儿宫外肾生长:少尿症和早产。
Pediatr Nephrol. 2013 Sep;28(9):1791-6. doi: 10.1007/s00467-013-2462-3. Epub 2013 Apr 4.
5
Diagnostic accuracy of renal pelvic dilatation for detecting surgically managed ureteropelvic junction obstruction.肾盂扩张对手术治疗的肾盂输尿管连接部梗阻的诊断准确性。
J Urol. 2013 Aug;190(2):661-6. doi: 10.1016/j.juro.2013.02.014. Epub 2013 Feb 14.
6
Antibiotic prophylaxis for urinary tract infections in antenatal hydronephrosis.产前肾积水的尿路感染抗生素预防。
Pediatrics. 2013 Jan;131(1):e251-61. doi: 10.1542/peds.2012-1870. Epub 2012 Dec 17.
7
Copy-number disorders are a common cause of congenital kidney malformations.拷贝数异常是先天性肾脏畸形的常见原因。
Am J Hum Genet. 2012 Dec 7;91(6):987-97. doi: 10.1016/j.ajhg.2012.10.007. Epub 2012 Nov 15.
8
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.
9
Early risk factors for neonatal mortality in CAKUT: analysis of 524 affected newborns.CAKUT 新生儿死亡的早期危险因素:524 例患病新生儿分析。
Pediatr Nephrol. 2012 Jun;27(6):965-72. doi: 10.1007/s00467-012-2107-y. Epub 2012 Mar 9.
10
Risk prediction models: II. External validation, model updating, and impact assessment.风险预测模型:二、外部验证、模型更新和影响评估。
Heart. 2012 May;98(9):691-8. doi: 10.1136/heartjnl-2011-301247. Epub 2012 Mar 7.