在出生后第一年接受手术的患有肾积水的儿童接受治疗的长期结果。系统综述

封面

如何引用文章

全文:

详细

现实性。肾盂输尿管连接部梗阻是儿童肾积水的最常见原因。

该研究的目的是搜索和分析1998年至2021年期间关于出生后第一年肾积水的手术治疗及其长期结果的现有文献。

材料和方法。在PubMed、Web of Science、Scopus、Google Scholar和Elibrary数据库中进行文献检索。使用了以下关键词来搜索资料:“congenital hydronephrosis”/“врожденный гидронефроз”(先天性肾积水)、“severe hydronephrosis”/“тяжелая степень гидронефроза”(重度肾积水)、“operative treatment”/“оперативное лечение” (手术治疗)、“uretero-pelvic junction obstruction infant”(婴儿肾盂输尿管连接部 梗阻)、“children, neonatal”(儿童的、新生儿的)、“infancy”(婴儿期)、 “обструкция пиелоуретрального сегмента”(肾盂输尿管连接部梗阻)、“дети 1 года жизни”(1岁儿童)。该综述包括5篇符合PRISMA报告标准并受分析的全文文章。

结果。根据选定的出版物,患者总数为355人。只有两位作者的研究中描述了产前筛查。手术时儿童的平均年龄为4.5个月(1-6个月)。所有作者都指出,在出生后第一年进行肾盂成形术时,肾实质厚度明显增加。在一年内,这些数值平均增加了1.5倍。肾盂的大小减少了50-67%。放射性同位素闪烁照相法的数据是可变的。在长期中,所有出版物中都观察到肾功能的改善。

结论。一项系统综述显示在患有先天性肾积水的情况下对出生后第一年接受手术的儿童进行肾盂成形术的长期结果。观察到,手术后肾盂缩小和肾实质的厚度增加。这是恢复肾脏功能的一个优势。然而,在我们能接触的文献中并没有统一的算法以预测肾实质的恢复。对肾实质功能更准确的评估,需要通过大量病例的前瞻性随机长期试验来证实。

作者简介

Anastasia A. Bebenina

Pirogov Russian National Research Medical University

Email: anastasia.bebenina@yandex.ru
ORCID iD: 0000-0002-8390-822X
SPIN 代码: 5298-7083

postgraduate student

俄罗斯联邦, Moscow

Olga G. Mokrushina

Pirogov Russian National Research Medical University; Filatov Children’s Hospital

Email: mokrushina@yandex.ru
ORCID iD: 0000-0003-4444-6103
SPIN 代码: 5998-7470

Dr. Sci. (Med.), MD, Professor of the Department of Pediatric Surgery

俄罗斯联邦, Moscow; Moscow

Marina V. Levitskaya

Filatov Children’s Hospital

Email: urolog@neosurg.ru
ORCID iD: 0000-0002-9838-9493
SPIN 代码: 2609-2557

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Vasily S. Shumikhin

Pirogov Russian National Research Medical University; Filatov Children’s Hospital

Email: vashou@gmail.com
ORCID iD: 0000-0001-9477-8785
SPIN 代码: 6405-8928

Cand. Sci. (Med.)

俄罗斯联邦, Moscow; Moscow

Nadezhda O. Erokhina

Filatov Children’s Hospital

Email: nadegdaerokhina@yandex.ru
ORCID iD: 0000-0003-0519-7220
SPIN 代码: 5169-3443
俄罗斯联邦, Moscow

Anzhelika E. Agavelyan

Pirogov Russian National Research Medical University

编辑信件的主要联系方式.
Email: lika.lk@mail.ru
ORCID iD: 0009-0005-5361-8589

student

俄罗斯联邦, Moscow

参考

  1. Schlomer BJ, Cohen RA, Baskin LS. Renal imaging: Congenital anomalies of the kidney and urinary tract. In: Pediatric and adolescent urologic imaging. New York: Springer; 2014. P. 155–198. doi: 10.1007/978-1-4614-8654-1_9
  2. Bendre PS, Karkera PJ, Nanjappa M. Functional outcome after neonatal pyeloplasty in antenatally diagnosed uretero-pelvic junction obstruction. Afr J Urol. 2021;27:17. doi: 10.1186/s12301-021-00121-5.
  3. Yin H, Liang W, Zhao D. The application value of the renal region of interest corrected by computed tomography in single-kidney glomerular filtration rate for the evaluation of patients with moderate or severe hydronephrosis. Front Physiology. 2022;13:861895. doi: 10.3389/fphys.2022.861895
  4. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372(71). doi: 10.1136/bmj.n71
  5. All-Russian public organization “Russian Society of Urology”. Klinicheskie rekomendatsii: Gidronefroz. 2023 [cited 2023 May 16]. Available from: https://cr.minzdrav.gov.ru/recomend/17_2 (In Russ.)
  6. Onen A. Grading of hydronephrosis: an ongoing challenge. Front Pediatr. 2020;8:458. doi: 10.3389/fped.2020.00458
  7. Babu R, Rathish VR. Functional outcomes of early versus delayed pyeloplasty in prenatally diagnosed pelvi-ureteric junction obstruction. J Pediatr Urol. 2015;11(2):63.e1–63.e5. doi: 10.1016/j.jpurol.2014.10.007
  8. Menon P, Rao KLN., Bhattacharya A, Mittal BR. Outcome analysis of pediatric pyeloplasty in units with less than 20 % differential renal function. J Pediatr Urol. 2016;12(3):171.e.1–171.e.7. doi: 10.1016/j.jpurol.2015.12.013
  9. Kim S-O, Song HY, Hwang IS, et al. Early pyeloplasty for recovery of parenchymal thickness in children with unilateral ureteropelvic junction obstruction. Urol Int. 2014;92(4):473–476. doi: 10.1159/000357144
  10. Tabari AK, Atqiaee K, Mohajerzadeh L, et al. Early pyeloplasty versus conservative management of severe ureteropelvic junction obstruction in asymptomatic infants. J Pediatr Surg. 2019;55(9):1936–1940. doi: 10.1016/j.jpedsurg.2019.08.006
  11. Has R, Sivrikoz TS. Prenatal diagnosis and findings in ureteropelvic junction type hydronephrosis. Front Pediatr. 2020;8:492. doi: 10.3389/fped.2020.00492
  12. Mello MF, Dos Reis ST, Kondo EY, et al. Urinary extracellular matrix proteins as predictors of the severity of ureteropelvic junction obstruction in children. J Pediatr Urol. 2021;17(4): 438.e1–438.e7. doi: 10.1016/j.jpurol.2021.03.017
  13. Roth DR, Gonzales ET, Jr. Management of ureteropelvic junction obstruction in infants. J Urol. 1983;129(1):108–110. doi: 10.1016/s0022-5347(17)51945-x
  14. Vemulakonda VM, Wilcox DT, Combleholme TM, et al. Factors associated with age at pyeloplasty in children with ureteropelvic junction obstruction. Pediatr Surg. 2015;31(9):871–877. doi: 10.1007/s00383-015-3748-2
  15. Onen A. An alternative hydronephrosis grading system to refine the criteria for exact severity of hydronephrosis and optimal treatment guidelines in neonates with primary UPJ-type hydronephrosis. J Pediatr Urol. 2007;3(3):200–205. doi: 10.1016/j.jpurol.2006.08.002
  16. Onen A. Üreteropelvik bileşke darligi. Çocuk Cerrahisi Dergisi. 2016;30(2):55–79. doi: 10.5222/JTAPS.2016.055 (In Turkish)
  17. Onen A, Yalinkaya A. Possible predictive factors for a safe prenatal follow-up of fetuses with hydonephrosis. The 29th Congress of European Society of Pediatric Urology. 11–14 April. Helsinki: ESPU; 2018.
  18. Smail LC, Dhindsa K, Braga LH, et al. Using deep learning algorithms to grade hydronephrosis severity: toward a clinical adjunct. Front Pediatr. 2020;8:1. doi: 10.3389/fped.2020.00001.
  19. Timberlake MD, Herndon CDA. Mild to moderate postnatal hydronephrosis grading systems and management. Nat Rev Urol. 2013;10(11):649–656. doi: 10.1038/nrurol.2013.172
  20. Chertin B, Rolle U, Farkas A, Puri P. Does delaying pyeloplasty affect renal function in children with a prenatal diagnosis of pelvi-ureteric junction obstruction? BJUI. 2002;90(1):72–75. doi: 10.1046/j.1464-410x.2002.02829.x
  21. Inker LA, Okparavero A. Cystatin C as a marker of glomerular filtration rate: prospects and limitations. Curr Opin Nephrol Hypertens. 2019;20(6):631–639. doi: 10.1097/MNH.0b013e32834b8850
  22. Parvex P, Combescure C, Rodriguez M, Girardin E. Is cystatin C a promisingmarker of renal function, at birth, in neonates prenatally diagnosed with congenital kidney anomalies? Nephrology Dialysis Transplantation. 2016;27(9):3477–3482. doi: 10.1093/ndt/gfs051
  23. Spasov SA. Opredelenie β2-mikroglobulina v krovi i moche pri anomaliyakh pochek. Radiology and practice. 2005;1:18–21 (In Russ.)
  24. Paraboschi I, Mantica G, Dalton NR, Turner C, Garriboli M. Urinary biomarkers in pelvic-ureteric junction obstruction: a systematic review. TAU. 2020;9(2):722–742. doi: 10.21037/tau.2020.01.01

补充文件

附件文件
动作
1. JATS XML
2. Fig. 1. Stages of the study according to the PRISMA criteria

下载 (228KB)
3. Fig. 2. Dynamics of kidney parameters 1 year after surgery

下载 (147KB)
4. Fig. 3. Comparison of classification systems for hydronephrosis [6]

下载 (468KB)

Согласие на обработку персональных данных

 

Используя сайт https://journals.rcsi.science, я (далее – «Пользователь» или «Субъект персональных данных») даю согласие на обработку персональных данных на этом сайте (текст Согласия) и на обработку персональных данных с помощью сервиса «Яндекс.Метрика» (текст Согласия).