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        <titl xml:lang="FR">Registre français de l'atrésie des voies biliaires</titl>
        <subTitl/>
        <parTitl xml:lang="EN">French Registry on Biliary Atresia</parTitl>
        <IDNo>PEF73217</IDNo>
      </titlStmt>
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        <AuthEnty affiliation="ITMO Santé Publique, Aviesan">Portail Épidémiologie-France</AuthEnty>
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      </rspStmt>
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        <producer abbr="PEF-HD" affiliation="ITMO Santé Publique, Aviesan">Portail Épidémiologie-France | Health Databases</producer>
        <copyright>Portail Épidémiologie-France 2026</copyright>
        <prodDate date="2026-04-11">11/04/2026</prodDate>
        <prodPlac>https://epidemiologie-france.aviesan.fr/</prodPlac>
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        <grantNo/>
      </prodStmt>
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        <distrbtr>Portail Épidémiologie-France</distrbtr>
        <contact email="portail-epidemiologie@inserm.fr">Portail Epidemiologie-France</contact>
        <depositr>Martina Fanna</depositr>
        <depDate xml:lang="FR">03/09/2015</depDate>
        <depDate xml:lang="EN">05/07/2016</depDate>
        <distDate>03/09/2015</distDate>
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        <version xml:lang="FR" date="03/09/2015">3</version>
        <version xml:lang="EN" date="05/07/2016">2</version>
        <verResp>Martina Fanna</verResp>
        <notes/>
      </verStmt>
      <biblCit/>
      <holdings xml:lang="FR" location="Portail Epidemiologie-France" URI="http://admin-epid-prod2.inserm.fr/layout/set/print/content/view/full/87900">Registre français de l'atrésie des voies biliaires</holdings>
      <holdings xml:lang="EN" location="Portail Epidemiologie-France" URI="http://admin-epid-prod2.inserm.fr/layout/set/print/content/view/full/88609">French Registry on Biliary Atresia</holdings>
      <notes/>
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    <citation>
      <titlStmt>
        <titl xml:lang="FR">Registre français de l'atrésie des voies biliaires</titl>
        <subTitl/>
        <altTitl xml:lang="FR"/>
        <altTitl xml:lang="EN"/>
        <parTitl xml:lang="EN">French Registry on Biliary Atresia</parTitl>
        <IDNo/>
      </titlStmt>
      <rspStmt>
        <AuthEnty affiliation="Necker Hospital for Sick Children">Christophe  Chardot</AuthEnty>
        <othId xml:lang="FR">European Federation for biliary atresia research</othId>
        <othId xml:lang="EN">European Federation for Biliary Atresia Research </othId>
      </rspStmt>
      <prodStmt>
        <producer role="Secteur Privé">Observatoire français de l’atrésie des voies biliaires</producer>
        <copyright/>
        <prodDate/>
        <prodPlac> - Necker Hospital for Sick Children - 149 rue de Sèvres
75743 Paris CEDEX 15</prodPlac>
        <software/>
        <fundAg xml:lang="FR" role="Publique">PHRC AOM 02007</fundAg>
        <fundAg xml:lang="EN" role="Public">PHRC AOM 02007</fundAg>
        <grantNo/>
      </prodStmt>
      <distStmt>
        <distrbtr>Necker Hospital for Sick Children</distrbtr>
        <contact affiliation="Necker Hospital for Sick Children" email="christophe.chardot@nck.aphp.fr  observatoire.atresiebiliaire@nck.aphp.fr">Christophe  Chardot</contact>
        <depositr>Martina Fanna</depositr>
        <depDate xml:lang="FR">03/09/2015</depDate>
        <depDate xml:lang="EN">05/07/2016</depDate>
        <distDate xml:lang="FR">03/09/2015</distDate>
        <distDate xml:lang="EN">05/07/2016</distDate>
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        <serName/>
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        <version xml:lang="EN" date="05/07/2016">2</version>
        <verResp>Martina Fanna</verResp>
        <notes/>
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      <biblCit/>
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      <notes/>
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    <studyAuthorization>
      <authorizingAgency>CNIL</authorizingAgency>
      <authorizationStatement xml:lang="FR">CNIL (Autorisation N° 997085)</authorizationStatement>
      <authorizationStatement xml:lang="EN">CNIL (approval no. 997085)</authorizationStatement>
    </studyAuthorization>
    <stdyInfo>
      <studyBudget/>
      <subject>
        <keyword xml:lang="FR">artrésie des voies biliaires</keyword>
        <keyword xml:lang="FR">thérapie</keyword>
        <keyword xml:lang="FR">registre</keyword>
        <keyword xml:lang="FR">enfants</keyword>
        <keyword xml:lang="FR">épidémiologie</keyword>
        <keyword xml:lang="EN">biliary atresia</keyword>
        <keyword xml:lang="EN">therapy</keyword>
        <keyword xml:lang="EN">registry</keyword>
        <keyword xml:lang="EN">children</keyword>
        <keyword xml:lang="EN">epidemiology</keyword>
        <topcClas xml:lang="FR">Endocrinologie et métabolisme</topcClas>
        <topcClas xml:lang="FR">Maladies rares</topcClas>
        <topcClas xml:lang="FR">Pédiatrie</topcClas>
        <topcClas xml:lang="FR">Radiologie et imagerie médicale</topcClas>
        <topcClas xml:lang="EN">Endocrinology and metabolism</topcClas>
        <topcClas xml:lang="EN">Rare diseases</topcClas>
        <topcClas xml:lang="EN">Pediatrics</topcClas>
        <topcClas xml:lang="EN">Radiology and medical imaging</topcClas>
        <topcClas xml:lang="FR"/>
        <topcClas xml:lang="EN"/>
      </subject>
      <abstract xml:lang="FR">Objectif de la base de données : L'objectif de ce registre est de promouvoir la recherche, le progrès thérapeutique, l’information des familles et la formation médicale dans le domaine de l’atrésie des voies biliaires et des pathologies associées.&#13;
</abstract>
      <abstract xml:lang="EN">Database objective : The aim of this registry is to promote research, therapeutic progress, information on family and medical training in the area of biliary atresia and related pathologies.</abstract>
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        <timePrd/>
        <collDate event="start">1986</collDate>
        <collDate event="end"/>
        <collDate xml:lang="FR">Collecte des données active</collDate>
        <collDate xml:lang="EN">Current data collection</collDate>
        <nation>France</nation>
        <geogCover xml:lang="FR">France</geogCover>
        <geogCover xml:lang="EN">France</geogCover>
        <geogUnit>National</geogUnit>
        <anlyUnit xml:lang="fr">individuel
                </anlyUnit>
        <anlyUnit xml:lang="en">individuals
                </anlyUnit>
        <universe xml:lang="FR" clusion="I">• Diagnostic d’AVB confirmé&#13;
• Enfant vivant en France&#13;
• Né entre 1986 et 2009</universe>
        <universe xml:lang="EN" clusion="I">Confirmed BA diagnosis confirmed. Children living in France born between 1986 and 2009.</universe>
        <universe xml:lang="FR">Nombre d'individus : 1 107 (2009)</universe>
        <universe xml:lang="EN">Number of individuals: 1,107 (2009)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Nouveau-nés (naissance à 28j)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Nourrissons (28j à 2 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Petite enfance (2 à 5 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Enfance (6 à 13 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Adolescence (13 à 18 ans)</universe>
        <universe xml:lang="EN" level="Age range">Newborns (birth to 28 days)</universe>
        <universe xml:lang="EN" level="Age range">Infant (28 days to 2 years)</universe>
        <universe xml:lang="EN" level="Age range">Early childhood (2 to 5 years)</universe>
        <universe xml:lang="EN" level="Age range">Childhood (6 to 13 years)</universe>
        <universe xml:lang="EN" level="Age range">Adolescence (13 to 18 years)</universe>
        <universe xml:lang="FR" level="Type de population">Sujets malades</universe>
        <universe xml:lang="EN" level="Population type">Sick population</universe>
        <universe xml:lang="FR" level="Sexe">Masculin</universe>
        <universe xml:lang="FR" level="Sexe">Féminin</universe>
        <universe xml:lang="EN" level="Sex">Male</universe>
        <universe xml:lang="EN" level="Sex">Female</universe>
        <dataKind xml:lang="FR">Registres de morbidité</dataKind>
        <dataKind xml:lang="EN">Morbidity registers</dataKind>
        <dataKind xml:lang="FR"/>
        <dataKind xml:lang="EN"/>
        <dataKind xml:lang="FR">Données cliniques : Identité des enfants (nom, prénom, date de naissance, adresse), la ou les équipe(s) qui assurent leur prise en charge médicale, les circonstances de diagnostic, l'intervention de Kasai et ses suites, l'éventuelle transplantation hépatique et ses suites, le devenir de l'enfant</dataKind>
        <dataKind xml:lang="FR">Données biologiques : reliquats biliaires</dataKind>
        <dataKind xml:lang="EN">Clinical data: Identity of children (first name, last name, date of birth, address), team or teams providing medical care; diagnostic circumstances; Kasai procedure and outcomes; possible liver transplantation and outcomes; outcome for the child.</dataKind>
        <dataKind xml:lang="EN">Biological data: Biliary remnants</dataKind>
        <dataKind xml:lang="FR">Evénements de santé/morbidité</dataKind>
        <dataKind xml:lang="EN">Health event/morbidity</dataKind>
        <dataKind xml:lang="FR"/>
        <dataKind xml:lang="EN"/>
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          <standard>
            <standardName/>
            <producer/>
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          <complianceDescription/>
        </standardsCompliance>
        <otherQualityStatement xml:lang="FR"/>
        <otherQualityStatement xml:lang="EN"/>
        <otherQualityStatement xml:lang="FR"/>
        <otherQualityStatement xml:lang="EN"/>
      </qualityStatement>
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      <exPostEvaluation>
        <evaluator/>
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        <dataCollector affiliation="Necker Hospital for Sick Children">Christophe  Chardot</dataCollector>
        <collectorTraining/>
        <frequenc xml:lang="FR"/>
        <frequenc xml:lang="EN"/>
        <sampProc xml:lang="FR">Participation des 45 centres impliqués dans la prise en charge de l’AVB (du diagnostic à la greffe hépatique)</sampProc>
        <sampProc xml:lang="EN">Involvement of 45 centres participating in BA treatment (from diagnosis to liver transplantation).</sampProc>
        <deviat/>
        <collMode xml:lang="FR">Dossier clinique : Identité des enfants (nom, prénom, date de naissance, adresse), la ou les équipe(s) qui assurent leur prise en charge médicale, les circonstances de diagnostic, l'intervention de Kasai et ses suites, l'éventuelle transplantation hépatique et ses suites, le devenir de l'enfant</collMode>
        <collMode xml:lang="EN">Direct physical measures: Identity of children (first name, last name, date of birth, address), team or teams providing medical care; diagnostic circumstances; Kasai procedure and outcomes; possible liver transplantation and outcomes; outcome for the child.</collMode>
        <collMode xml:lang="FR">reliquats biliaires</collMode>
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        <collMode xml:lang="EN"/>
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        <avlStatus xml:lang="FR">Contacter le responsable scientifique</avlStatus>
        <avlStatus xml:lang="EN">Contact the scientist in charge.</avlStatus>
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        <complete/>
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        <deposReq/>
        <conditions xml:lang="FR">Contacter le responsable scientifique</conditions>
        <conditions xml:lang="EN">Contact the scientist in charge.</conditions>
        <disclaimer/>
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