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Causes of death in children with congenital anomalies up to age 10 in eight European countries

Background Congenital anomalies (CAs) increase the risk of death during infancy and childhood. This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old. Methods Children born alive with a major CA between 1 Janua...

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Main Authors: Rissmann, Anke, Tan, Joachim, Glinianaia, Svetlana V, Rankin, Judith, Pierini, Anna, Santoro, Michele, Coi, Alessio, Garne, Ester, Loane, Maria, Given, Joanne, Reid, Abigail, Aizpurua, Amaia, Akhmedzhanova, Diana, Ballardini, Elisa, Barisic, Ingeborg, Cavero-Carbonell, Clara, De Walle, Hermien E K, Gatt, Miriam, Gissler, Mika, Heino, Anna, Jordan, Sue, Urhoj, Stine Kjaer, Klungsøyr, Kari, Lutke, Renee, Mokoroa, Olatz, Neville, Amanda Julie, Thayer, Daniel S, Wellesley, Diana G, Yevtushok, Lyubov, Zurriaga, Oscar, Morris, Joan
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creator Rissmann, Anke
Tan, Joachim
Glinianaia, Svetlana V
Rankin, Judith
Pierini, Anna
Santoro, Michele
Coi, Alessio
Garne, Ester
Loane, Maria
Given, Joanne
Reid, Abigail
Aizpurua, Amaia
Akhmedzhanova, Diana
Ballardini, Elisa
Barisic, Ingeborg
Cavero-Carbonell, Clara
De Walle, Hermien E K
Gatt, Miriam
Gissler, Mika
Heino, Anna
Jordan, Sue
Urhoj, Stine Kjaer
Klungsøyr, Kari
Lutke, Renee
Mokoroa, Olatz
Neville, Amanda Julie
Thayer, Daniel S
Wellesley, Diana G
Yevtushok, Lyubov
Zurriaga, Oscar
Morris, Joan
description Background Congenital anomalies (CAs) increase the risk of death during infancy and childhood. This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old. Methods Children born alive with a major CA between 1 January 1995 and 31 December 2014, from 13 population-based European CA registries were linked to mortality records up to their 10th birthday or 31 December 2015, whichever was earlier. Results In total 4199 neonatal, 2100 postneonatal and 1087 deaths in children aged 1–9 years were reported. The underlying cause of death was a CA in 71% (95% CI 64% to 78%) of neonatal and 68% (95% CI 61% to 74%) of postneonatal infant deaths. For neonatal deaths the proportions varied by registry from 45% to 89% and by anomaly from 53% for Down syndrome to 94% for tetralogy of Fallot. In children aged 1–9, 49% (95% CI 42% to 57%) were attributed to a CA. Comparing mortality in children with anomalies to population mortality predicts that over 90% of all deaths at all ages are attributable to the anomalies. The specific CA was often not reported on the death certificate, even for lethal anomalies such as trisomy 13 (only 80% included the code for trisomy 13). Conclusions Data on the underlying cause of death from death certificates alone are not sufficient to evaluate the burden of CAs on infant and childhood mortality across countries and over time. Linked data from CA registries and death certificates are necessary for obtaining accurate estimates.
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This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old. Methods Children born alive with a major CA between 1 January 1995 and 31 December 2014, from 13 population-based European CA registries were linked to mortality records up to their 10th birthday or 31 December 2015, whichever was earlier. Results In total 4199 neonatal, 2100 postneonatal and 1087 deaths in children aged 1–9 years were reported. The underlying cause of death was a CA in 71% (95% CI 64% to 78%) of neonatal and 68% (95% CI 61% to 74%) of postneonatal infant deaths. For neonatal deaths the proportions varied by registry from 45% to 89% and by anomaly from 53% for Down syndrome to 94% for tetralogy of Fallot. In children aged 1–9, 49% (95% CI 42% to 57%) were attributed to a CA. Comparing mortality in children with anomalies to population mortality predicts that over 90% of all deaths at all ages are attributable to the anomalies. The specific CA was often not reported on the death certificate, even for lethal anomalies such as trisomy 13 (only 80% included the code for trisomy 13). Conclusions Data on the underlying cause of death from death certificates alone are not sufficient to evaluate the burden of CAs on infant and childhood mortality across countries and over time. Linked data from CA registries and death certificates are necessary for obtaining accurate estimates.</description><language>eng</language><publisher>BMJ</publisher><creationdate>2023</creationdate><rights>info:eu-repo/semantics/openAccess</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,780,885,26566</link.rule.ids><linktorsrc>$$Uhttp://hdl.handle.net/11250/3130046$$EView_record_in_NORA$$FView_record_in_$$GNORA$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Rissmann, Anke</creatorcontrib><creatorcontrib>Tan, Joachim</creatorcontrib><creatorcontrib>Glinianaia, Svetlana V</creatorcontrib><creatorcontrib>Rankin, Judith</creatorcontrib><creatorcontrib>Pierini, Anna</creatorcontrib><creatorcontrib>Santoro, Michele</creatorcontrib><creatorcontrib>Coi, Alessio</creatorcontrib><creatorcontrib>Garne, Ester</creatorcontrib><creatorcontrib>Loane, Maria</creatorcontrib><creatorcontrib>Given, Joanne</creatorcontrib><creatorcontrib>Reid, Abigail</creatorcontrib><creatorcontrib>Aizpurua, Amaia</creatorcontrib><creatorcontrib>Akhmedzhanova, Diana</creatorcontrib><creatorcontrib>Ballardini, Elisa</creatorcontrib><creatorcontrib>Barisic, Ingeborg</creatorcontrib><creatorcontrib>Cavero-Carbonell, Clara</creatorcontrib><creatorcontrib>De Walle, Hermien E K</creatorcontrib><creatorcontrib>Gatt, Miriam</creatorcontrib><creatorcontrib>Gissler, Mika</creatorcontrib><creatorcontrib>Heino, Anna</creatorcontrib><creatorcontrib>Jordan, Sue</creatorcontrib><creatorcontrib>Urhoj, Stine Kjaer</creatorcontrib><creatorcontrib>Klungsøyr, Kari</creatorcontrib><creatorcontrib>Lutke, Renee</creatorcontrib><creatorcontrib>Mokoroa, Olatz</creatorcontrib><creatorcontrib>Neville, Amanda Julie</creatorcontrib><creatorcontrib>Thayer, Daniel S</creatorcontrib><creatorcontrib>Wellesley, Diana G</creatorcontrib><creatorcontrib>Yevtushok, Lyubov</creatorcontrib><creatorcontrib>Zurriaga, Oscar</creatorcontrib><creatorcontrib>Morris, Joan</creatorcontrib><title>Causes of death in children with congenital anomalies up to age 10 in eight European countries</title><description>Background Congenital anomalies (CAs) increase the risk of death during infancy and childhood. This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old. Methods Children born alive with a major CA between 1 January 1995 and 31 December 2014, from 13 population-based European CA registries were linked to mortality records up to their 10th birthday or 31 December 2015, whichever was earlier. Results In total 4199 neonatal, 2100 postneonatal and 1087 deaths in children aged 1–9 years were reported. The underlying cause of death was a CA in 71% (95% CI 64% to 78%) of neonatal and 68% (95% CI 61% to 74%) of postneonatal infant deaths. For neonatal deaths the proportions varied by registry from 45% to 89% and by anomaly from 53% for Down syndrome to 94% for tetralogy of Fallot. In children aged 1–9, 49% (95% CI 42% to 57%) were attributed to a CA. Comparing mortality in children with anomalies to population mortality predicts that over 90% of all deaths at all ages are attributable to the anomalies. The specific CA was often not reported on the death certificate, even for lethal anomalies such as trisomy 13 (only 80% included the code for trisomy 13). Conclusions Data on the underlying cause of death from death certificates alone are not sufficient to evaluate the burden of CAs on infant and childhood mortality across countries and over time. Linked data from CA registries and death certificates are necessary for obtaining accurate estimates.</description><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>3HK</sourceid><recordid>eNqNzE0KwjAQBeBuXIh6h_EAQmLVC5SKB3BtGNJpO5DOlPzg9Y3gAVw9eHzvbZtXhyVRAh1hIMwzsICfOQyRBN5cC68ykXDGACi6YODKywpZAScCa74T4mnO0JeoK2F90CI5VrhvNiOGRIdf7prjvX92j5OPnDKLE43orD1fjWtta8zl1v5jPpPPOwQ</recordid><startdate>2023</startdate><enddate>2023</enddate><creator>Rissmann, Anke</creator><creator>Tan, Joachim</creator><creator>Glinianaia, Svetlana V</creator><creator>Rankin, Judith</creator><creator>Pierini, Anna</creator><creator>Santoro, Michele</creator><creator>Coi, Alessio</creator><creator>Garne, Ester</creator><creator>Loane, Maria</creator><creator>Given, Joanne</creator><creator>Reid, Abigail</creator><creator>Aizpurua, Amaia</creator><creator>Akhmedzhanova, Diana</creator><creator>Ballardini, Elisa</creator><creator>Barisic, Ingeborg</creator><creator>Cavero-Carbonell, Clara</creator><creator>De Walle, Hermien E K</creator><creator>Gatt, Miriam</creator><creator>Gissler, Mika</creator><creator>Heino, Anna</creator><creator>Jordan, Sue</creator><creator>Urhoj, Stine Kjaer</creator><creator>Klungsøyr, Kari</creator><creator>Lutke, Renee</creator><creator>Mokoroa, Olatz</creator><creator>Neville, Amanda Julie</creator><creator>Thayer, Daniel S</creator><creator>Wellesley, Diana G</creator><creator>Yevtushok, Lyubov</creator><creator>Zurriaga, Oscar</creator><creator>Morris, Joan</creator><general>BMJ</general><scope>3HK</scope></search><sort><creationdate>2023</creationdate><title>Causes of death in children with congenital anomalies up to age 10 in eight European countries</title><author>Rissmann, Anke ; 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This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old. Methods Children born alive with a major CA between 1 January 1995 and 31 December 2014, from 13 population-based European CA registries were linked to mortality records up to their 10th birthday or 31 December 2015, whichever was earlier. Results In total 4199 neonatal, 2100 postneonatal and 1087 deaths in children aged 1–9 years were reported. The underlying cause of death was a CA in 71% (95% CI 64% to 78%) of neonatal and 68% (95% CI 61% to 74%) of postneonatal infant deaths. For neonatal deaths the proportions varied by registry from 45% to 89% and by anomaly from 53% for Down syndrome to 94% for tetralogy of Fallot. In children aged 1–9, 49% (95% CI 42% to 57%) were attributed to a CA. Comparing mortality in children with anomalies to population mortality predicts that over 90% of all deaths at all ages are attributable to the anomalies. The specific CA was often not reported on the death certificate, even for lethal anomalies such as trisomy 13 (only 80% included the code for trisomy 13). Conclusions Data on the underlying cause of death from death certificates alone are not sufficient to evaluate the burden of CAs on infant and childhood mortality across countries and over time. Linked data from CA registries and death certificates are necessary for obtaining accurate estimates.</abstract><pub>BMJ</pub><oa>free_for_read</oa></addata></record>
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title Causes of death in children with congenital anomalies up to age 10 in eight European countries
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