Pathology of provisional organs, complications of pregnancy and labor, and the condition of newborn with congenital defects of the urinary and nervous systems

Authors

  • I.S. Luk’yanova SI «Institute of Pediatrics, Obstetrics and Gynecology named after academician O.M. Lukyanova of the NAMS of Ukraine», Kyiv, Ukraine https://orcid.org/0000-0002-6340-5668
  • I.Yu. Gordienko SI «Institute of Pediatrics, Obstetrics and Gynecology named after academician O.M. Lukyanova of the NAMS of Ukraine», Kyiv, Ukraine https://orcid.org/0000-0001-7594-4880
  • G.F. Medvedenko SI «Institute of Pediatrics, Obstetrics and Gynecology named after academician O.M. Lukyanova of the NAMS of Ukraine», Kyiv, Ukraine
  • G.O. Grebinichenko SI «Institute of Pediatrics, Obstetrics and Gynecology named after academician O.M. Lukyanova of the NAMS of Ukraine», Kyiv, Ukraine
  • B.A. Tarasyuk SI «Institute of Pediatrics, Obstetrics and Gynecology named after academician O.M. Lukyanova of the NAMS of Ukraine», Kyiv, Ukraine https://orcid.org/0000-0003-4051-9707

DOI:

https://doi.org/10.15574/PP.2022.91.15

Keywords:

congenital malformations, fetus, central nervous system, nephro-urinary system, prenatal diagnosis, ultrasound diagnosis, provisional organs, placenta, perinatal outcome, fetal growth restriction, fetal distress, neonatal asphyxia, prematurity, early neonatal death

Abstract

Congenital malformations (CM) in fetuses and neonates belong to main causes of perinatal morbidity and mortality. Provision organs malformation and malfunction in such cohorts is less studied.

The purpose - to analyze the course of pregnancy, the data of ultrasound imaging of provisional organs in the presence of CM of central nervous system (CNS) and/or of nephro-urinary system (NUS) in the fetus and newborn.

Materials and methods. The results of prenatal and postnatal ultrasound, anamnestic and general clinical data of a sample of cases with prenatally diagnosed CM of CNS and/or NUS for the period 2017-2021 were analyzed.

Results. There were 45 newborns with CNS malformations, and 54 newborns with CM of NUS. Malformations of NUS and/or CNS in the examined newborns were combined with anomalies of other systems in a third of cases - 29.6% and 31.1%, respectively. According to the results of prenatal ultrasound examinations, polyhydramnios (16.7%) was most often recorded in the pregnancies with fetal CM of NUS, and cases of fetal CM of CNS most commonly were registered placental hyperplasia (35.6%), fetal growth retardation (24.4%) and fetal distress (26.7%). Postnatally in both cohorts (with NUS malformations and with CNS malformations) a high rate of following complications were recorded: prematurity (16.7% and 15.6%, respectively), birth asphyxia (48% and 55.6%, respectively), and early neonatal death (11% and 6.6%).

Сonclusions. Pregnant women with CM of CNS and/or NUS in the fetus belong to the group of high perinatal risk because of the high rate of perinatal complications. Information about the identified high perinatal risks in fetuses and newborns with CM of the CNS and/or NUS should be provided to parents and taken into account when planning management of pregnancy and labor.

References

Australian Institute of Health and Welfare. (2020). Stillbirths and neonatal deaths in Australia, AIHW, Australian Government. URL: https://www.aihw.gov.au/reports/mothers-babies/stillbirths-and-neonatal-deaths.

Burton GJ, Jauniaux E. (2018). Pathophysiology of placental-derived fetal growth restriction. American journal of obstetrics and gynecology. 218 (2S): S745-S761. https://doi.org/10.1016/j.ajog.2017.11.577; PMid:29422210

Carroll SG, Porter H, Abdel-Fattah S, Kyle PM, Soothill PW. (2000). Correlation of prenatal ultrasound diagnosis and pathologic findings in fetal brain abnormalities. Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 16 (2): 149-153. https://doi.org/10.1046/j.1469-0705.2000.00199.x; PMid:11117085

Davydova YuV, Lukyanova IS, Limanskaya AYu, Butenko LP et al. (2020). Modern approaches to the problem of intrauterine growth restriction: from causes to long-term consequences. Ukrainian Journal of Perinatology and Pediatrics. 1(81): 45-53. https://doi.org/10.15574/PP.2020.81.45

Deloison B, Chalouhi GE, Sonigo P, Zerah M, Millischer AE, Dumez Y, Brunelle F, Ville Y, Salomon LJ. (2012). Hidden mortality of prenatally diagnosed vein of Galen aneurysmal malformation: retrospective study and review of the literature. Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 40 (6): 652-658. https://doi.org/10.1002/uog.11188; PMid:22605540

Dzyuba OM, Medvedenko GF, Luk'yanova IS, Tarasyuk BA. (2019). The role of examining the state of fetal adrenal glands for predicting complications in the ante- and early neonatal period in pregnant women with placental dysfunction. Obstetrics. Gynecology. Genetics. 5 (2): 19-24.

Edwards L, Hui L. (2018). First and second trimester screening for fetal structural anomalies. Seminars in fetal & neonatal medicine. 23 (2): 102-111. https://doi.org/10.1016/j.siny.2017.11.005; PMid:29233624

Elsayes KM, Trout AT, Friedkin AM, Liu PS, Bude RO, Platt JF, Menias CO. (2009). Imaging of the placenta: a multimodality pictorial review. Radiographics : a review publication of the Radiological Society of North America, Inc. 29 (5): 1371-1391. https://doi.org/10.1148/rg.295085242; PMid:19755601

Ergenoğlu MA, Yeniel AÖ, Akdemir A, Akercan F, Karadadaş N. (2013). Role of 3D power Doppler sonography in early prenatal diagnosis of Galen vein aneurysm. Journal of the Turkish German Gynecological Association. 14 (3): 178-181. https://doi.org/10.5152/jtgga.2013.87847

European Platform on Rare Disease Registration. (2021, Mar 1). Prevalence charts and tables. European Comission. URL: https://eu-rd-platform.jrc.ec.europa.eu/eurocat/eurocat-data/prevalence_en.

Gaitanis J, Tarui T. (2018). Nervous System Malformations. Continuum (Minneapolis, Minn). 24 (1): 72-95. https://doi.org/10.1212/CON.0000000000000561; PMid:29432238 PMCid:PMC6463295

Gordienko IYu, Tarapurova OM, Nikitchyna TV, Vashchenko OO, Grebinichenko GO, Shevchenko OA, Velichko AV. (2017). Congenital CNS defects in the fetus as markers of chromosomal pathology. Obstetrics. Gynecology. Genetics. 3: 42-46.

Grebinichenko GO, Gordienko IYu, Luk'yanova IS, Dzyuba OM, Medvedenko GF. (2021). The state of the provisional organs in the fetus with vital and lethal anomalies (literature review) Ukrainian Journal of Perinatology and Pediatrics. 4 (88): 44-51. https://doi.org/10.15574/PP.2021.88.44

Grebinichenko GO, Gordienko IYu, Sliepov OK. (2020). Clinical outcomes in congenital diaphragmatic hernia of the fetus. Health of woman. 8 (154): 47-53. https://doi.org/10.15574/HW.2020.154.47

Hwang DY, Dworschak GC, Kohl S, Saisawat P, Vivante A, Hilger AC, Reutter HM, Soliman NA, Bogdanovic R, Kehinde EO, Tasic V, Hildebrandt F. (2014). Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract. Kidney international, 85 (6): 1429-1433. https://doi.org/10.1038/ki.2013.508; PMid:24429398 PMCid:PMC4040148

Karri K, Deole N, Engineer N. (2010). Prenatally diagnosed central nervous system anomalies: a 10-year experience. Archives of Disease in Childhood - Fetal and Neonatal Edition 2010. 95: Fa24-Fa25. https://doi.org/10.1136/adc.2010.189746.45

Malinger G, Paladini D, Haratz KK, Monteagudo A, Pilu GL, Timor-Tritsch IE. (2020). ISUOG Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 1: performance of screening examination and indications for targeted neurosonography. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 56 (3): 476-484. https://doi.org/10.1002/uog.22145; PMid:32870591

Mortazavi MM, Griessenauer CJ, Foreman P, Bavarsad Shahripour R, Shoja MM, Rozzelle CJ, Tubbs RS, Fisher WS, Fukushima T. (2013). Vein of Galen aneurysmal malformations: critical analysis of the literature with proposal of a new classification system. Journal of neurosurgery. Pediatrics. 12 (3): 293-306. https://doi.org/10.3171/2013.5.PEDS12587; PMid:23889354

Rodriguez MM. (2014). Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT). Fetal and pediatric pathology. 33 (5-6): 293-320. https://doi.org/10.3109/15513815.2014.959678; PMid:25313840 PMCid:PMC4266037

Sadler TW. (2012). Langman's Medical Embryology. 12th ed. Baltimore, Philadelphia. Lippincott Williams & Wilkins, Wolters Kluwer: 400.

Syngelaki A, Hammami A, Bower S, Zidere V, Akolekar R, Nicolaides KH. (2019). Diagnosis of fetal non-chromosomal abnormalities on routine ultrasound examination at 11-13 weeks' gestation. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 54 (4): 468-476. https://doi.org/10.1002/uog.20844; PMid:31408229

Truba I, Lukianova I, Medvedenko G, Lazoryshynets V. (2020). The Features of Pregnancy, Early Neonatal Period and Tactics of Surgical Treatment in Newborn with Hypoplastic Aortic Arch (First-Hand Experience). Ukrainian Journal of Cardiovascular Surgery. 1 (38): 37-43. https://doi.org/10.30702/ujcvs/20.3803/009037-043

Vivante A, Kohl S, Hwang DY, Dworschak GC, Hildebrandt F. (2014). Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans. Pediatric nephrology (Berlin, Germany). 29 (4): 695-704. https://doi.org/10.1007/s00467-013-2684-4; PMid:24398540 PMCid:PMC4676405

WHO. (2022). Newborns: improving survival and well-being. URL: https://www.who.int/news-room/fact-sheets/detail/newborns-reducing-mortality.

Published

2022-09-30