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Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980-2017.
Feldkamp, Marcia L; Canfield, Mark A; Krikov, Sergey; Prieto-Merino, David; Sípek, Antonin; LeLong, Nathalie; Amar, Emmanuelle; Rissmann, Anke; Csaky-Szunyogh, Melinda; Tagliabue, Giovanna; Pierini, Anna; Gatt, Miriam; Bergman, Jorieke E H; Szabova, Elena; Bermejo-Sánchez, Eva; Tucker, David; Dastgiri, Saeed; Bidondo, María Paz; Canessa, Aurora; Zarante, Ignacio; Hurtado-Villa, Paula; Martinez, Laura; Mutchinick, Osvaldo M; Camelo, Jorge Lopez; Benavides-Lara, Adriana; Thomas, Mary Ann; Liu, Shiliang; Nembhard, Wendy N; Gray, Elizabeth B; Nance, Amy E; Mastroiacovo, Pierpaolo; Botto, Lorenzo D.
Afiliação
  • Feldkamp ML; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Canfield MA; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA.
  • Krikov S; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Prieto-Merino D; Faculty of Medicine, Universidad de Alcalá, Madrid, Spain.
  • Sípek A; Czech Republic Department of Medical Genetics, Thomayer Hospital, Prague, Czech Republic.
  • LeLong N; Université Paris Cité, Centre of Research in Epidemiology and StatisticS (CRESS), Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Paris, France.
  • Amar E; France REMERA, Registre des malformations en Rhône Alpes, Hospices Civils de Lyon, Lyon, France.
  • Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
  • Csaky-Szunyogh M; Hungarian Congenital Anomalies Registry and Rare Diseases Centre, National Center for Public Health and Pharmacy, Budapest, Hungary.
  • Tagliabue G; Lombardy Congenital Anomalies Registry, Cancer Registry Unit, Fondazione IRCCS, Istituto Nazionale dei tumori, Milan, Italy.
  • Pierini A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council and Fondazione Toscana Gabriele Monasterio, Tuscany Registry of Congenital Defects, Pisa, Italy.
  • Gatt M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Pieta, Malta.
  • Bergman JEH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Szabova E; Faculty of Public Health, Slovak Medical University in Bratislava, Bratislava, Slovak Republic.
  • Bermejo-Sánchez E; ECEMC (Spanish Collaborative Study of Congenital Malformations), CIAC (Research Center on Congenital Anomalies), Institute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, Madrid, Spain.
  • Tucker D; Congenital Anomaly Register & Information Service for Wales, Public Health Wales, Knowledge Directorate, Singleton Hospital, Sketty Lane, Swansea, UK.
  • Dastgiri S; Health Services Management Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Bidondo MP; National Network of Congenital Anomalies of Argentina (RENAC), National Institute of Epidemiology (INE), National Administration of Laboratories and Health Institutes, National Ministry of Health Institutes, Buenos Aires, Argentina.
  • Canessa A; Regional Register Congenital Malformation Maule Health Service (RRMC-SSM), Maule, Chile.
  • Zarante I; Instituto de Genética Humana, Pontificia Universidad Javeriana Bogotá, Bogotá, Colombia.
  • Hurtado-Villa P; Facultad de Ciencias de la Salud, Pontificia Universidad Javeriana Cali, Cali, Colombia.
  • Martinez L; Mexico ReDeCo, Monterrey, Nuevo Leon, Mexico.
  • Mutchinick OM; Department of Genetics, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, RYVEMCE, Registry and Epidemiological Surveillance of Congenital Malformations, Mexico City, Mexico.
  • Camelo JL; ECLAMC, Center for Medical Education and Clinical Research (CEMIC-CONICET), Buenos Aires, Argentina.
  • Benavides-Lara A; Costa Rican Birth Defects Register Center (CREC), Costa Rican Institute for Research and Teaching in Nutrition and Health (INCIENSA), Cartago, Costa Rica.
  • Thomas MA; Department of Medical Genetics and Pediatrics, Alberta Congenital Anomalies Surveillance System, Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Liu S; Canadian Congenital Anomalies Surveillance System (CCASS), Centre for Surveillance and Applied Research, Public Health Agency of Canada, Ottawa, Ontario, Canada.
  • Nembhard WN; Department of Epidemiology, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences and Arkansas Reproductive Health Monitoring System, Arkansas Children's Research Institute, Little Rock, Arkansas, USA.
  • Gray EB; Metropolitan Atlanta Congenital Defects Program, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Nance AE; Utah Birth Defect Network, Office of Children with Special Care Needs, Division of Family Health, Utah Department of Health and Human Services, Salt Lake City, Utah, USA.
  • Mastroiacovo P; International Center on Birth Defects, International Clearinghouse for Birth Defects Surveillance and Research, Rome, Italy.
  • Botto LD; Department of Pediatrics, The University of Utah, Salt Lake City, Utah, USA.
Birth Defects Res ; 116(2): e2306, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38411327
ABSTRACT

BACKGROUND:

Gastroschisis is a serious birth defect with midgut prolapse into the amniotic cavity. The objectives of this study were to evaluate the prevalence and time trends of gastroschisis among programs in the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR), focusing on regional variations and maternal age changes in the population.

METHODS:

We analyzed data on births from 1980 to 2017 from 27 ICBDSR member programs, representing 24 countries and three regions (Europe+ (includes Iran) , Latin America, North America). Cases were identified using diagnostic codes (i.e., 756.7, 756.71, or Q79.3). We excluded cases of amniotic band syndrome, limb-body wall defect, and ruptured omphalocele. Programs provided annual counts for gastroschisis cases (live births, stillbirths, and legally permitted pregnancy terminations for fetal anomalies) and source population (live births, stillbirths), by maternal age.

RESULTS:

Overall, gastroschisis occurred in 1 of every 3268 births (3.06 per 10,000 births; 95% confidence intervals [CI] 3.01, 3.11), with marked regional variation. European+ prevalence was 1.49 (95%CI 1.44, 1.55), Latin American 3.80 (95%CI 3.69, 3.92) and North American 4.32 (95%CI 4.22, 4.42). A statistically significant increasing time trend was observed among six European+ , four Latin American, and four North American programs. Women <20 years of age had the highest prevalence in all programs except the Slovak Republic.

CONCLUSIONS:

Gastroschisis prevalence increased over time in 61% of participating programs, and the highest increase in prevalence was observed among the youngest women. Additional inquiry will help to assess the impact of the changing maternal age proportions in the birth population on gastroschisis prevalence.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deformidades Congênitas dos Membros / Gastrosquise / Hérnia Umbilical Limite: Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deformidades Congênitas dos Membros / Gastrosquise / Hérnia Umbilical Limite: Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2024 Tipo de documento: Article