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Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study
Acta Paediatrica, Volume: 113, Issue: 5, Pages: 1024 - 1031
Swansea University Author: Sue Jordan
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DOI (Published version): 10.1111/apa.17136
Abstract
AimThe aim is to examine the risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury/poisoning and child abuse in children with and without a congenital anomaly up to age 5 and 10 years.MethodsThis is a population-based data linkage cohort study linking information...
Published in: | Acta Paediatrica |
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ISSN: | 0803-5253 1651-2227 |
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Wiley
2024
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URI: | https://cronfa.swan.ac.uk/Record/cronfa65968 |
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<?xml version="1.0"?><rfc1807><datestamp>2024-07-19T16:47:11.6999449</datestamp><bib-version>v2</bib-version><id>65968</id><entry>2024-04-04</entry><title>Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study</title><swanseaauthors><author><sid>24ce9db29b4bde1af4e83b388aae0ea1</sid><ORCID>0000-0002-5691-2987</ORCID><firstname>Sue</firstname><surname>Jordan</surname><name>Sue Jordan</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2024-04-04</date><deptcode>HSOC</deptcode><abstract>AimThe aim is to examine the risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury/poisoning and child abuse in children with and without a congenital anomaly up to age 5 and 10 years.MethodsThis is a population-based data linkage cohort study linking information from the European Surveillance of Congenital Anomalies network (EUROCAT) and birth registries to hospital discharge databases. We included 91 504 live born children with major congenital anomalies born from 1995 to 2014 from nine EUROCAT registries in five countries and 1 960 727 live born children without congenital anomalies (reference children). Prevalence and relative risk (RR) were estimated for each of the co-morbidities using Kaplan–Meier survival estimates.ResultsChildren with congenital anomalies had higher risks of the co-morbidities than reference children. The prevalences in the reference children were generally very low. The RR was 13.8 (95% CI 12.5–15.1) for cerebral palsy, 2.5 (95% CI 2.4–2.6) for seizures/epilepsy, 40.8 (95% CI 33.2–50.2) for visual impairments, 10.0 (95% CI 9.2–10.9) for hearing loss, 3.6 (95% CI 3.2–4.2) for cancer, 1.5 (95% CI 1.4–1.5) for injuries/poisoning and 2.4 (95% CI 1.7–3.4) for child abuse.ConclusionChildren with congenital anomalies were more likely to be diagnosed with the specified co-morbidities compared to reference children.</abstract><type>Journal Article</type><journal>Acta Paediatrica</journal><volume>113</volume><journalNumber>5</journalNumber><paginationStart>1024</paginationStart><paginationEnd>1031</paginationEnd><publisher>Wiley</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint>0803-5253</issnPrint><issnElectronic>1651-2227</issnElectronic><keywords>cerebral palsy; congenital anomalies; epilepsy; injuries and poisoning</keywords><publishedDay>1</publishedDay><publishedMonth>5</publishedMonth><publishedYear>2024</publishedYear><publishedDate>2024-05-01</publishedDate><doi>10.1111/apa.17136</doi><url/><notes/><college>COLLEGE NANME</college><department>Health and Social Care School</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>HSOC</DepartmentCode><institution>Swansea University</institution><apcterm>Another institution paid the OA fee</apcterm><funders>European Union. Grant Number: 733001</funders><projectreference/><lastEdited>2024-07-19T16:47:11.6999449</lastEdited><Created>2024-04-04T16:42:42.2045309</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">School of Health and Social Care - Nursing</level></path><authors><author><firstname>Stine Kjaer</firstname><surname>Urhoj</surname><orcid>0000-0002-2069-9723</orcid><order>1</order></author><author><firstname>Joan</firstname><surname>Morris</surname><order>2</order></author><author><firstname>Maria</firstname><surname>Loane</surname><order>3</order></author><author><firstname>Elisa</firstname><surname>Ballardini</surname><order>4</order></author><author><firstname>Laia</firstname><surname>Barrachina‐Bonet</surname><order>5</order></author><author><firstname>Clara</firstname><surname>Cavero‐Carbonell</surname><order>6</order></author><author><firstname>Alessio</firstname><surname>Coi</surname><order>7</order></author><author><firstname>Mika</firstname><surname>Gissler</surname><order>8</order></author><author><firstname>Joanne</firstname><surname>Given</surname><order>9</order></author><author><firstname>Anna</firstname><surname>Heino</surname><order>10</order></author><author><firstname>Sue</firstname><surname>Jordan</surname><orcid>0000-0002-5691-2987</orcid><order>11</order></author><author><firstname>Amanda</firstname><surname>Neville</surname><order>12</order></author><author><firstname>Michele</firstname><surname>Santoro</surname><order>13</order></author><author><firstname>Joachim</firstname><surname>Tan</surname><order>14</order></author><author><firstname>David</firstname><surname>Tucker</surname><order>15</order></author><author><firstname>Diana</firstname><surname>Wellesley</surname><order>16</order></author><author><firstname>Ester</firstname><surname>Garne</surname><orcid>0000-0003-0430-2594</orcid><order>17</order></author><author><firstname>Mads</firstname><surname>Damkjaer</surname><orcid>0000-0001-7410-8573</orcid><order>18</order></author></authors><documents><document><filename>65968__29930__7b5dc8cdd82a44988fae7eee509daed8.pdf</filename><originalFilename>65968.pdf</originalFilename><uploaded>2024-04-05T08:34:57.3944877</uploaded><type>Output</type><contentLength>819348</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><documentNotes>© 2024 The Authors. 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2024-07-19T16:47:11.6999449 v2 65968 2024-04-04 Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study 24ce9db29b4bde1af4e83b388aae0ea1 0000-0002-5691-2987 Sue Jordan Sue Jordan true false 2024-04-04 HSOC AimThe aim is to examine the risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury/poisoning and child abuse in children with and without a congenital anomaly up to age 5 and 10 years.MethodsThis is a population-based data linkage cohort study linking information from the European Surveillance of Congenital Anomalies network (EUROCAT) and birth registries to hospital discharge databases. We included 91 504 live born children with major congenital anomalies born from 1995 to 2014 from nine EUROCAT registries in five countries and 1 960 727 live born children without congenital anomalies (reference children). Prevalence and relative risk (RR) were estimated for each of the co-morbidities using Kaplan–Meier survival estimates.ResultsChildren with congenital anomalies had higher risks of the co-morbidities than reference children. The prevalences in the reference children were generally very low. The RR was 13.8 (95% CI 12.5–15.1) for cerebral palsy, 2.5 (95% CI 2.4–2.6) for seizures/epilepsy, 40.8 (95% CI 33.2–50.2) for visual impairments, 10.0 (95% CI 9.2–10.9) for hearing loss, 3.6 (95% CI 3.2–4.2) for cancer, 1.5 (95% CI 1.4–1.5) for injuries/poisoning and 2.4 (95% CI 1.7–3.4) for child abuse.ConclusionChildren with congenital anomalies were more likely to be diagnosed with the specified co-morbidities compared to reference children. Journal Article Acta Paediatrica 113 5 1024 1031 Wiley 0803-5253 1651-2227 cerebral palsy; congenital anomalies; epilepsy; injuries and poisoning 1 5 2024 2024-05-01 10.1111/apa.17136 COLLEGE NANME Health and Social Care School COLLEGE CODE HSOC Swansea University Another institution paid the OA fee European Union. Grant Number: 733001 2024-07-19T16:47:11.6999449 2024-04-04T16:42:42.2045309 Faculty of Medicine, Health and Life Sciences School of Health and Social Care - Nursing Stine Kjaer Urhoj 0000-0002-2069-9723 1 Joan Morris 2 Maria Loane 3 Elisa Ballardini 4 Laia Barrachina‐Bonet 5 Clara Cavero‐Carbonell 6 Alessio Coi 7 Mika Gissler 8 Joanne Given 9 Anna Heino 10 Sue Jordan 0000-0002-5691-2987 11 Amanda Neville 12 Michele Santoro 13 Joachim Tan 14 David Tucker 15 Diana Wellesley 16 Ester Garne 0000-0003-0430-2594 17 Mads Damkjaer 0000-0001-7410-8573 18 65968__29930__7b5dc8cdd82a44988fae7eee509daed8.pdf 65968.pdf 2024-04-05T08:34:57.3944877 Output 819348 application/pdf Version of Record true © 2024 The Authors. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License. true eng https://creativecommons.org/licenses/by/4.0/ |
title |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study |
spellingShingle |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study Sue Jordan |
title_short |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study |
title_full |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study |
title_fullStr |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study |
title_full_unstemmed |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study |
title_sort |
Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study |
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24ce9db29b4bde1af4e83b388aae0ea1 |
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24ce9db29b4bde1af4e83b388aae0ea1_***_Sue Jordan |
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Sue Jordan |
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Stine Kjaer Urhoj Joan Morris Maria Loane Elisa Ballardini Laia Barrachina‐Bonet Clara Cavero‐Carbonell Alessio Coi Mika Gissler Joanne Given Anna Heino Sue Jordan Amanda Neville Michele Santoro Joachim Tan David Tucker Diana Wellesley Ester Garne Mads Damkjaer |
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Acta Paediatrica |
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113 |
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1024 |
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2024 |
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Swansea University |
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0803-5253 1651-2227 |
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10.1111/apa.17136 |
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Wiley |
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Faculty of Medicine, Health and Life Sciences |
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Faculty of Medicine, Health and Life Sciences |
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Faculty of Medicine, Health and Life Sciences |
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School of Health and Social Care - Nursing{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}School of Health and Social Care - Nursing |
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description |
AimThe aim is to examine the risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury/poisoning and child abuse in children with and without a congenital anomaly up to age 5 and 10 years.MethodsThis is a population-based data linkage cohort study linking information from the European Surveillance of Congenital Anomalies network (EUROCAT) and birth registries to hospital discharge databases. We included 91 504 live born children with major congenital anomalies born from 1995 to 2014 from nine EUROCAT registries in five countries and 1 960 727 live born children without congenital anomalies (reference children). Prevalence and relative risk (RR) were estimated for each of the co-morbidities using Kaplan–Meier survival estimates.ResultsChildren with congenital anomalies had higher risks of the co-morbidities than reference children. The prevalences in the reference children were generally very low. The RR was 13.8 (95% CI 12.5–15.1) for cerebral palsy, 2.5 (95% CI 2.4–2.6) for seizures/epilepsy, 40.8 (95% CI 33.2–50.2) for visual impairments, 10.0 (95% CI 9.2–10.9) for hearing loss, 3.6 (95% CI 3.2–4.2) for cancer, 1.5 (95% CI 1.4–1.5) for injuries/poisoning and 2.4 (95% CI 1.7–3.4) for child abuse.ConclusionChildren with congenital anomalies were more likely to be diagnosed with the specified co-morbidities compared to reference children. |
published_date |
2024-05-01T20:29:30Z |
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11.04748 |