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Predictors of poor neonatal outcomes in fetuses diagnosed with congenital urinary tract anomalies
OBJECTIVES: Urinary tract anomalies account for approximately one-quarter of all antenatally detected anomalies. The aim of this study was to identify factors associated with severe adverse neonatal outcomes of a prenatally diagnosed urinary tract anomaly. MATERIAL AND METHODS: A retrospective-prosp...
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Published in: | Ginekologia polska 2021-01, Vol.92 (9), p.607-610 |
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creator | Pop-Trajkovic Dinic, Sonja Zivadinovic, Radomir Stefanovic, Milan Trenkic, Milan Milosevic, Jelena Mitic, Dejan |
description | OBJECTIVES: Urinary tract anomalies account for approximately one-quarter of all antenatally detected anomalies. The aim of this study was to identify factors associated with severe adverse neonatal outcomes of a prenatally diagnosed urinary tract anomaly. MATERIAL AND METHODS: A retrospective-prospective study included 101 pregnant women with prenatally diagnosed fetal urinary tract anomalies presented to the Council for Fetal Anomalies. Prenatal diagnoses were compared with autopsy findings in cases of terminated pregnancy or with clinical and operative findings of the infants. RESULTS: The mortality rate in the group of patients with fetal obstructive uropathy (60 patients) was 10% and in the group of patients with fetal multicystic dysplastic kidney (38 patients) 15.7%. Surgery was performed on 53.4% of the children, whereas more than half of the operations involved resolving associated urinary tract anomalies. Postoperative renal function deterioration occurred in 19% of the children. CONCLUSIONS: The prognosis of renal function in obstructive uropathies is excellent if oligoamnios does not develop prenatally and in case of timely provided surgical care is provided postnatally. The finding of the bilateral multicystic dysplastic kidney is associated with poor prognosis. The prognosis in fetal unilateral multicystic dysplastic kidney depends primarily on the condition of the contralateral kidney and the existence of associated anomalies. |
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The aim of this study was to identify factors associated with severe adverse neonatal outcomes of a prenatally diagnosed urinary tract anomaly. MATERIAL AND METHODS: A retrospective-prospective study included 101 pregnant women with prenatally diagnosed fetal urinary tract anomalies presented to the Council for Fetal Anomalies. Prenatal diagnoses were compared with autopsy findings in cases of terminated pregnancy or with clinical and operative findings of the infants. RESULTS: The mortality rate in the group of patients with fetal obstructive uropathy (60 patients) was 10% and in the group of patients with fetal multicystic dysplastic kidney (38 patients) 15.7%. Surgery was performed on 53.4% of the children, whereas more than half of the operations involved resolving associated urinary tract anomalies. Postoperative renal function deterioration occurred in 19% of the children. CONCLUSIONS: The prognosis of renal function in obstructive uropathies is excellent if oligoamnios does not develop prenatally and in case of timely provided surgical care is provided postnatally. The finding of the bilateral multicystic dysplastic kidney is associated with poor prognosis. The prognosis in fetal unilateral multicystic dysplastic kidney depends primarily on the condition of the contralateral kidney and the existence of associated anomalies.</description><identifier>ISSN: 0017-0011</identifier><identifier>EISSN: 2543-6767</identifier><identifier>DOI: 10.5603/GP.a2021.0032</identifier><language>eng</language><publisher>Gdansk: Wydawnictwo Via Medica</publisher><subject>Amniotic fluid ; Autopsies ; Councils ; Ethics ; Fetuses ; Hydronephrosis ; Kidneys ; Mortality ; Obstetrics ; Pregnancy ; Ultrasonic imaging ; Urine ; Urogenital system</subject><ispartof>Ginekologia polska, 2021-01, Vol.92 (9), p.607-610</ispartof><rights>2021. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). 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The aim of this study was to identify factors associated with severe adverse neonatal outcomes of a prenatally diagnosed urinary tract anomaly. MATERIAL AND METHODS: A retrospective-prospective study included 101 pregnant women with prenatally diagnosed fetal urinary tract anomalies presented to the Council for Fetal Anomalies. Prenatal diagnoses were compared with autopsy findings in cases of terminated pregnancy or with clinical and operative findings of the infants. RESULTS: The mortality rate in the group of patients with fetal obstructive uropathy (60 patients) was 10% and in the group of patients with fetal multicystic dysplastic kidney (38 patients) 15.7%. Surgery was performed on 53.4% of the children, whereas more than half of the operations involved resolving associated urinary tract anomalies. Postoperative renal function deterioration occurred in 19% of the children. CONCLUSIONS: The prognosis of renal function in obstructive uropathies is excellent if oligoamnios does not develop prenatally and in case of timely provided surgical care is provided postnatally. The finding of the bilateral multicystic dysplastic kidney is associated with poor prognosis. The prognosis in fetal unilateral multicystic dysplastic kidney depends primarily on the condition of the contralateral kidney and the existence of associated anomalies.</description><subject>Amniotic fluid</subject><subject>Autopsies</subject><subject>Councils</subject><subject>Ethics</subject><subject>Fetuses</subject><subject>Hydronephrosis</subject><subject>Kidneys</subject><subject>Mortality</subject><subject>Obstetrics</subject><subject>Pregnancy</subject><subject>Ultrasonic imaging</subject><subject>Urine</subject><subject>Urogenital system</subject><issn>0017-0011</issn><issn>2543-6767</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNotT0tLxDAYDKJgWffoPeC5NY8maY6y6CosuAc9L1-TdM3STWqSIv57KzqHmTkMMwxCt5Q0QhJ-v903wAijDSGcXaCKiZbXUkl1iSpCqKoXotdonfOJLJBMMa0rBPvkrDclpozjgKcYEw4uBigw4jgXE88uYx_w4MqcF2s9HEPMzuIvXz6wieHogv9Nz8kHSN-4JDAFQ4hnGL3LN-hqgDG79b-u0PvT49vmud69bl82D7t6oh0vtep63Xem1cZY3qpe9cZaoxzXwlhBB8tablsDnFkrGLGkc5IrNlABhAjF-Ard_fVOKX7OLpfDKc4pLJMHJvVyV9Ku4z9BHVkC</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Pop-Trajkovic Dinic, Sonja</creator><creator>Zivadinovic, Radomir</creator><creator>Stefanovic, Milan</creator><creator>Trenkic, Milan</creator><creator>Milosevic, Jelena</creator><creator>Mitic, Dejan</creator><general>Wydawnictwo Via Medica</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20210101</creationdate><title>Predictors of poor neonatal outcomes in fetuses diagnosed with congenital urinary tract anomalies</title><author>Pop-Trajkovic Dinic, Sonja ; Zivadinovic, Radomir ; Stefanovic, Milan ; Trenkic, Milan ; Milosevic, Jelena ; Mitic, Dejan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p183t-78b9b8c49ccd347b7bcddc7e395cd51fd243d4ca32dd520d08e6372f15a005723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amniotic fluid</topic><topic>Autopsies</topic><topic>Councils</topic><topic>Ethics</topic><topic>Fetuses</topic><topic>Hydronephrosis</topic><topic>Kidneys</topic><topic>Mortality</topic><topic>Obstetrics</topic><topic>Pregnancy</topic><topic>Ultrasonic imaging</topic><topic>Urine</topic><topic>Urogenital system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pop-Trajkovic Dinic, Sonja</creatorcontrib><creatorcontrib>Zivadinovic, Radomir</creatorcontrib><creatorcontrib>Stefanovic, Milan</creatorcontrib><creatorcontrib>Trenkic, Milan</creatorcontrib><creatorcontrib>Milosevic, Jelena</creatorcontrib><creatorcontrib>Mitic, Dejan</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Ginekologia polska</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pop-Trajkovic Dinic, Sonja</au><au>Zivadinovic, Radomir</au><au>Stefanovic, Milan</au><au>Trenkic, Milan</au><au>Milosevic, Jelena</au><au>Mitic, Dejan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictors of poor neonatal outcomes in fetuses diagnosed with congenital urinary tract anomalies</atitle><jtitle>Ginekologia polska</jtitle><date>2021-01-01</date><risdate>2021</risdate><volume>92</volume><issue>9</issue><spage>607</spage><epage>610</epage><pages>607-610</pages><issn>0017-0011</issn><eissn>2543-6767</eissn><abstract>OBJECTIVES: Urinary tract anomalies account for approximately one-quarter of all antenatally detected anomalies. The aim of this study was to identify factors associated with severe adverse neonatal outcomes of a prenatally diagnosed urinary tract anomaly. MATERIAL AND METHODS: A retrospective-prospective study included 101 pregnant women with prenatally diagnosed fetal urinary tract anomalies presented to the Council for Fetal Anomalies. Prenatal diagnoses were compared with autopsy findings in cases of terminated pregnancy or with clinical and operative findings of the infants. RESULTS: The mortality rate in the group of patients with fetal obstructive uropathy (60 patients) was 10% and in the group of patients with fetal multicystic dysplastic kidney (38 patients) 15.7%. Surgery was performed on 53.4% of the children, whereas more than half of the operations involved resolving associated urinary tract anomalies. Postoperative renal function deterioration occurred in 19% of the children. CONCLUSIONS: The prognosis of renal function in obstructive uropathies is excellent if oligoamnios does not develop prenatally and in case of timely provided surgical care is provided postnatally. The finding of the bilateral multicystic dysplastic kidney is associated with poor prognosis. The prognosis in fetal unilateral multicystic dysplastic kidney depends primarily on the condition of the contralateral kidney and the existence of associated anomalies.</abstract><cop>Gdansk</cop><pub>Wydawnictwo Via Medica</pub><doi>10.5603/GP.a2021.0032</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amniotic fluid Autopsies Councils Ethics Fetuses Hydronephrosis Kidneys Mortality Obstetrics Pregnancy Ultrasonic imaging Urine Urogenital system |
title | Predictors of poor neonatal outcomes in fetuses diagnosed with congenital urinary tract anomalies |
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