Journals / Journal of the Turkish-German Gynecological Association / 2018 / Cilt: 19 - Sayı: 4

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

Pages
206–209
Publication Date
2022-10-18
DOI
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The need for surgery was greater inhigh-risk patients than in low-risk patients (58.3% vs. 8.7%) (p

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Objective & Hypothesis:Objective: With the widespread use of ultrasonography for fetal screening, the detection and management of congenital urinary tractabnormalities has become crucial.
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Key Findings & Data:In this study, we aimed to describe the clinical approaches in patients with prenatally detected urinary tractabnormalities.Material and Methods: This study is a retrospective, single-center study performed at a perinatology unit of a university hospital, between2010 and 2016.
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Conclusion & Impact:The need for surgery was greater inhigh-risk patients than in low-risk patients (58.3% vs. 8.7%) (p
🔬Design:Research Article
📍Scope:2016 Verileri
⚙️Variables:Domain Parameters

Abstract

Objective: With the widespread use of ultrasonography for fetal screening, the detection and management of congenital urinary tractabnormalities has become crucial. In this study, we aimed to describe the clinical approaches in patients with prenatally detected urinary tractabnormalities.Material and Methods: This study is a retrospective, single-center study performed at a perinatology unit of a university hospital, between2010 and 2016. The outcomes of 124 patients who were prenatally diagnosed as having urinary tract abnormalities are reported. Variablesincluded in the analysis were fetal sex, birth week and weight, persistency, and necessity surgery after birth for renal pelvic dilatation. Low-riskrenal 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 highriskdilatation 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±6.4years. 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 inhigh-risk patients than in low-risk patients (58.3% vs. 8.7%) (p

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Cite This Article

ÖZEL, A., MADAZLI, R., DAVUTOĞLU, E. A., ERENEL, H., KARSLI, M. F., KORKMAZ, S. Ö. (2022). Outcome after prenatal diagnosis of fetal urinary tract abnormalities: A tertiary center experience. Journal of the Turkish-German Gynecological Association, Cilt: 19 - Sayı: 4, 206–209. https://ajindex.com/articles/567481

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References (13)

  1. Gunn TR, Mora JD, Pease P. Antenatal diagnosis of urinary tract abnormalities by ultrasonography after 28 weeks’ gestation: incidence and outcome. Am J Obstet Gynecol 1995; 172: 479-86
  2. Carr MC, Kim SS. Prenatal management of urogenital disorders. Urol Clin North Am 2010; 37: 149-58
  3. Kleinveld JH, Timmermans DR, de Smit DJ, Ader HJ, Van der WG, Ten Kate LP. Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial. Prenat Diagn 2006; 26: 354-61
  4. Hogan J, Dourthe ME, Blondiaux E, Jouannic JM, Garel C, Ulinski T. Renal outcome in children with antenatal diagnosis of severe CAKUT. Pediatr Nephrol 2012; 27: 497-502
  5. Wollenberg A, Neuhaus TJ, Willi UV, Wisser J. Outcome of fetal renal pelvic dilatation diagnosed during the third trimester. Ultrasound Obstet Gynecol 2005; 25: 483-8
  6. Sanna-Cherchi S, Ravani P, Corbani V, Parodi S, Haupt R, Piaggio G, et al. Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney Int 2009; 76: 528-33
  7. Quirino IG, Diniz JS, Bouzada MC, Pereira AK, Lopes TJ, Paixão GM, et al. Clinical Course of 822 Children with Prenatally Detected Nephrouropathies Clin J Am Soc Nephrol 2012; 7: 444-51
  8. Dagklis T, Plasencia W, Maiz N, Duarte L, Nicolaides KH. Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks. Ultrasound Obstet Gynecol 2008; 3: 132-5
  9. Staebler M, Donner C, Van Regemorter N, Duprez L, De Maertelaer V, Devreker F, et al. Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound? Prenat Diagn 2005; 25: 567-73
  10. Kumar S, Walia S, Ikpeme O, Zhang E, Paramasivam G, Agarwal S, et al. Postnatal outcome of prenatally diagnosed severe fetal renal pelvic dilatation. Prenat Diagn 2012; 32: 519-22
  11. Nguyen HT, Benson CB, Bromley B, Campbell JB, Chow J, Coleman B, et al. Multidisciplinary consensus on the classification of prenatal and postnatal urinary tract dilation (UTD classification system). J Pediatr Urol 2014; 10: 982-98
  12. Nef S, Neuhaus TJ, Spartà G, Weitz M, Buder K, Wisser J, et al. Outcome after prenatal diagnosis of congenital anomalies of the kidney and urinary tract. Eur J Pediatr 2016; 175: 667-76
  13. Soares CM, Diniz JS, Lima EM, Silva JM, Oliveira GR, Canhestro MR, et al. Clinical outcome of children with chronic kidney disease in a pre-dialysis interdisciplinary