Infants with prenatally diagnosed kidney anomalies have an increased risk of urinary tract infections

Aim This study estimated the urinary tract infection (UTI) risk in a nationwide cohort of infants prenatally diagnosed with parenchymal kidney anomalies compared with a comparison cohort. Methods A Danish population‐based nationwide cohort of foetuses diagnosed with parenchymal kidney anomalies betw...

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Veröffentlicht in:Acta Paediatrica 2017-11, Vol.106 (11), p.1875-1881
Hauptverfasser: Rasmussen, Maria, Sunde, Lone, Andersen, René F., Petersen, Olav B., Olsen, Morten S., Tabor, Ann, Shalmi, Anne‐Cathrine, Jensen, Hanne, Vase, Laura, Sperling, Lene, Vang, Marianne, Hessellund, Annette, Brendstrup, Lene, Bendsen, Eske, Sommer, Steffen, Kamper, Christina, Zingenberg, Helle, Krebs, Lone, Thisted, Dorte, Skibsted, Lillian, Olesen, Annette, Sørensen, Anne, Størup, Birgitte
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container_end_page 1881
container_issue 11
container_start_page 1875
container_title Acta Paediatrica
container_volume 106
creator Rasmussen, Maria
Sunde, Lone
Andersen, René F.
Petersen, Olav B.
Olsen, Morten S.
Tabor, Ann
Shalmi, Anne‐Cathrine
Jensen, Hanne
Vase, Laura
Sperling, Lene
Vang, Marianne
Hessellund, Annette
Brendstrup, Lene
Bendsen, Eske
Sommer, Steffen
Kamper, Christina
Zingenberg, Helle
Krebs, Lone
Thisted, Dorte
Skibsted, Lillian
Olesen, Annette
Sørensen, Anne
Størup, Birgitte
description Aim This study estimated the urinary tract infection (UTI) risk in a nationwide cohort of infants prenatally diagnosed with parenchymal kidney anomalies compared with a comparison cohort. Methods A Danish population‐based nationwide cohort of foetuses diagnosed with parenchymal kidney anomalies between 2007 and 2012 had previously been identified. These were compared with foetuses without kidney anomalies who were prenatally scanned the same year. Live born infants were followed from birth until the diagnosis of UTI, emigration, death or two years of age. Cumulative incidences of UTIs were computed. Mortality was estimated using the Kaplan–Meier method. Results We identified 412 foetuses with parenchymal kidney anomalies out of 362 069 who underwent ultrasound scans and 277 were born alive. The overall risk of a UTI before the age of two years was 19%, and it was 14% among infants without prenatally diagnosed co‐occurring urinary tract malformations. The corresponding risk in the 4074 controls was 1%. After two years, mortality was 2.2% in infants with prenatally diagnosed parenchymal kidney anomalies and 0.2% in the controls. Conclusion Infants prenatally diagnosed with parenchymal kidney anomalies had a substantially increased risk of UTI. Awareness of this increased risk may facilitate earlier diagnosis of UTIs in this population.
doi_str_mv 10.1111/apa.14014
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Methods A Danish population‐based nationwide cohort of foetuses diagnosed with parenchymal kidney anomalies between 2007 and 2012 had previously been identified. These were compared with foetuses without kidney anomalies who were prenatally scanned the same year. Live born infants were followed from birth until the diagnosis of UTI, emigration, death or two years of age. Cumulative incidences of UTIs were computed. Mortality was estimated using the Kaplan–Meier method. Results We identified 412 foetuses with parenchymal kidney anomalies out of 362 069 who underwent ultrasound scans and 277 were born alive. The overall risk of a UTI before the age of two years was 19%, and it was 14% among infants without prenatally diagnosed co‐occurring urinary tract malformations. The corresponding risk in the 4074 controls was 1%. After two years, mortality was 2.2% in infants with prenatally diagnosed parenchymal kidney anomalies and 0.2% in the controls. Conclusion Infants prenatally diagnosed with parenchymal kidney anomalies had a substantially increased risk of UTI. Awareness of this increased risk may facilitate earlier diagnosis of UTIs in this population.</description><identifier>ISSN: 0803-5253</identifier><identifier>EISSN: 1651-2227</identifier><identifier>DOI: 10.1111/apa.14014</identifier><identifier>PMID: 28793177</identifier><language>eng</language><publisher>Norway: Wiley Subscription Services, Inc</publisher><subject>Cohort Studies ; Denmark - epidemiology ; Emigration ; Female ; Health risk assessment ; Health risks ; Humans ; Infant ; Infants ; Infections ; Kidney - abnormalities ; Kidney dysplasia ; Kidneys ; Male ; Mortality ; Parenchymal kidney anomalies ; Prenatal screening ; Risk Assessment ; Ultrasonography, Prenatal ; Ultrasound ; Urinary tract ; Urinary tract infections ; Urinary Tract Infections - etiology ; Urogenital Abnormalities - complications ; Urogenital Abnormalities - diagnostic imaging ; Urogenital Abnormalities - mortality ; Urogenital system</subject><ispartof>Acta Paediatrica, 2017-11, Vol.106 (11), p.1875-1881</ispartof><rights>2017 Foundation Acta Pædiatrica. 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Methods A Danish population‐based nationwide cohort of foetuses diagnosed with parenchymal kidney anomalies between 2007 and 2012 had previously been identified. These were compared with foetuses without kidney anomalies who were prenatally scanned the same year. Live born infants were followed from birth until the diagnosis of UTI, emigration, death or two years of age. Cumulative incidences of UTIs were computed. Mortality was estimated using the Kaplan–Meier method. Results We identified 412 foetuses with parenchymal kidney anomalies out of 362 069 who underwent ultrasound scans and 277 were born alive. The overall risk of a UTI before the age of two years was 19%, and it was 14% among infants without prenatally diagnosed co‐occurring urinary tract malformations. The corresponding risk in the 4074 controls was 1%. After two years, mortality was 2.2% in infants with prenatally diagnosed parenchymal kidney anomalies and 0.2% in the controls. Conclusion Infants prenatally diagnosed with parenchymal kidney anomalies had a substantially increased risk of UTI. Awareness of this increased risk may facilitate earlier diagnosis of UTIs in this population.</description><subject>Cohort Studies</subject><subject>Denmark - epidemiology</subject><subject>Emigration</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Health risks</subject><subject>Humans</subject><subject>Infant</subject><subject>Infants</subject><subject>Infections</subject><subject>Kidney - abnormalities</subject><subject>Kidney dysplasia</subject><subject>Kidneys</subject><subject>Male</subject><subject>Mortality</subject><subject>Parenchymal kidney anomalies</subject><subject>Prenatal screening</subject><subject>Risk Assessment</subject><subject>Ultrasonography, Prenatal</subject><subject>Ultrasound</subject><subject>Urinary tract</subject><subject>Urinary tract infections</subject><subject>Urinary Tract Infections - etiology</subject><subject>Urogenital Abnormalities - complications</subject><subject>Urogenital Abnormalities - diagnostic imaging</subject><subject>Urogenital Abnormalities - mortality</subject><subject>Urogenital system</subject><issn>0803-5253</issn><issn>1651-2227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MtKxDAUBuAgijOOLnwBCbjRRTW3NulyEG8woAtdlzPpqRPtpGPSKvP2RkddCGYTQj5-zvkJOeTsjKdzDis444pxtUXGvMh5JoTQ22TMDJNZLnI5InsxPjMmZKmKXTISRpeSaz0meOsb8H2k765f0FVADz207ZrWDp58F7GmL672uKbguyW0DiNdwBumJ3XeBoRPElx8oV1Dh-A8hDXtA9g-_Tdoe9f5uE92GmgjHnzfE_J4dflwcZPN7q5vL6azzMpcqkwKM9cWNecGsWAStARo8hrrgguuCgSjazC1ZlY2xgACl2Uxt1wYa6SyckJONrmr0L0OGPtq6aLFtgWP3RArXgptpChKlejxH_rcDcGn6ZJSpeJKMJPU6UbZ0MUYsKlWwS3TihVn1Wf3Veq--uo-2aPvxGG-xPpX_pSdwPkGvLsW1_8nVdP76SbyA_kCjiU</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Rasmussen, Maria</creator><creator>Sunde, Lone</creator><creator>Andersen, René F.</creator><creator>Petersen, Olav B.</creator><creator>Olsen, Morten S.</creator><creator>Tabor, Ann</creator><creator>Shalmi, Anne‐Cathrine</creator><creator>Jensen, Hanne</creator><creator>Vase, Laura</creator><creator>Sperling, Lene</creator><creator>Vang, Marianne</creator><creator>Hessellund, Annette</creator><creator>Brendstrup, Lene</creator><creator>Bendsen, Eske</creator><creator>Sommer, Steffen</creator><creator>Kamper, Christina</creator><creator>Zingenberg, Helle</creator><creator>Krebs, Lone</creator><creator>Thisted, Dorte</creator><creator>Skibsted, Lillian</creator><creator>Olesen, Annette</creator><creator>Sørensen, Anne</creator><creator>Størup, Birgitte</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>201711</creationdate><title>Infants with prenatally diagnosed kidney anomalies have an increased risk of urinary tract infections</title><author>Rasmussen, Maria ; Sunde, Lone ; Andersen, René F. ; Petersen, Olav B. ; Olsen, Morten S. ; Tabor, Ann ; Shalmi, Anne‐Cathrine ; Jensen, Hanne ; Vase, Laura ; Sperling, Lene ; Vang, Marianne ; Hessellund, Annette ; Brendstrup, Lene ; Bendsen, Eske ; Sommer, Steffen ; Kamper, Christina ; Zingenberg, Helle ; Krebs, Lone ; Thisted, Dorte ; Skibsted, Lillian ; Olesen, Annette ; Sørensen, Anne ; Størup, Birgitte</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3534-328b7ce7118ee603a73aaf5ded612146ea87da8d70c3f88aea1396bc128c834c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cohort Studies</topic><topic>Denmark - epidemiology</topic><topic>Emigration</topic><topic>Female</topic><topic>Health risk assessment</topic><topic>Health risks</topic><topic>Humans</topic><topic>Infant</topic><topic>Infants</topic><topic>Infections</topic><topic>Kidney - abnormalities</topic><topic>Kidney dysplasia</topic><topic>Kidneys</topic><topic>Male</topic><topic>Mortality</topic><topic>Parenchymal kidney anomalies</topic><topic>Prenatal screening</topic><topic>Risk Assessment</topic><topic>Ultrasonography, Prenatal</topic><topic>Ultrasound</topic><topic>Urinary tract</topic><topic>Urinary tract infections</topic><topic>Urinary Tract Infections - etiology</topic><topic>Urogenital Abnormalities - complications</topic><topic>Urogenital Abnormalities - diagnostic imaging</topic><topic>Urogenital Abnormalities - mortality</topic><topic>Urogenital system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rasmussen, Maria</creatorcontrib><creatorcontrib>Sunde, Lone</creatorcontrib><creatorcontrib>Andersen, René F.</creatorcontrib><creatorcontrib>Petersen, Olav B.</creatorcontrib><creatorcontrib>Olsen, Morten S.</creatorcontrib><creatorcontrib>Tabor, Ann</creatorcontrib><creatorcontrib>Shalmi, Anne‐Cathrine</creatorcontrib><creatorcontrib>Jensen, Hanne</creatorcontrib><creatorcontrib>Vase, Laura</creatorcontrib><creatorcontrib>Sperling, Lene</creatorcontrib><creatorcontrib>Vang, Marianne</creatorcontrib><creatorcontrib>Hessellund, Annette</creatorcontrib><creatorcontrib>Brendstrup, Lene</creatorcontrib><creatorcontrib>Bendsen, Eske</creatorcontrib><creatorcontrib>Sommer, Steffen</creatorcontrib><creatorcontrib>Kamper, Christina</creatorcontrib><creatorcontrib>Zingenberg, Helle</creatorcontrib><creatorcontrib>Krebs, Lone</creatorcontrib><creatorcontrib>Thisted, Dorte</creatorcontrib><creatorcontrib>Skibsted, Lillian</creatorcontrib><creatorcontrib>Olesen, Annette</creatorcontrib><creatorcontrib>Sørensen, Anne</creatorcontrib><creatorcontrib>Størup, Birgitte</creatorcontrib><creatorcontrib>Danish Fetal Medicine Research Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Physical Education Index</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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Methods A Danish population‐based nationwide cohort of foetuses diagnosed with parenchymal kidney anomalies between 2007 and 2012 had previously been identified. These were compared with foetuses without kidney anomalies who were prenatally scanned the same year. Live born infants were followed from birth until the diagnosis of UTI, emigration, death or two years of age. Cumulative incidences of UTIs were computed. Mortality was estimated using the Kaplan–Meier method. Results We identified 412 foetuses with parenchymal kidney anomalies out of 362 069 who underwent ultrasound scans and 277 were born alive. The overall risk of a UTI before the age of two years was 19%, and it was 14% among infants without prenatally diagnosed co‐occurring urinary tract malformations. The corresponding risk in the 4074 controls was 1%. After two years, mortality was 2.2% in infants with prenatally diagnosed parenchymal kidney anomalies and 0.2% in the controls. Conclusion Infants prenatally diagnosed with parenchymal kidney anomalies had a substantially increased risk of UTI. Awareness of this increased risk may facilitate earlier diagnosis of UTIs in this population.</abstract><cop>Norway</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28793177</pmid><doi>10.1111/apa.14014</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects Cohort Studies
Denmark - epidemiology
Emigration
Female
Health risk assessment
Health risks
Humans
Infant
Infants
Infections
Kidney - abnormalities
Kidney dysplasia
Kidneys
Male
Mortality
Parenchymal kidney anomalies
Prenatal screening
Risk Assessment
Ultrasonography, Prenatal
Ultrasound
Urinary tract
Urinary tract infections
Urinary Tract Infections - etiology
Urogenital Abnormalities - complications
Urogenital Abnormalities - diagnostic imaging
Urogenital Abnormalities - mortality
Urogenital system
title Infants with prenatally diagnosed kidney anomalies have an increased risk of urinary tract infections
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