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http://sgc.anlis.gob.ar/handle/123456789/2552| Title: | Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based study | Authors: | Gili, Juan Antonio López-Camelo, Jorge Santiago Nembhard, Wendy N Bakker, Marian K de Walle, Hermien E K Stallings, Erin B Kancherla, Vijaya Contiero, Paolo Dastgiri, Saeed Feldkamp, Marcia L Nance, Amy E Gatt, Miriam Martínez, Laura Canessa, María Aurora Groisman, Boris Hurtado-Villa, Paula Källén, Karin Landau, Danielle Lelong, Nathalie Morgan, Margery Arteaga-Vázquez, Jazmín Pierini, Anna Rissmann, Anke Sipek, Antonin Szabova, Elena Wertelecki, Wladimir Zarante, Ignacio Canfield, Mark A Mastroiacovo, Pierpaolo |
Keywords: | Anomalías Congénitas;Mortalidad;Hidrocefalia;Vigilancia de la Población;Prevalencia;Crecimiento Demográfico | Issue Date: | 15-Jul-2022 | Journal: | Birth defects research | Series/Report no.: | Birth Defects Res;114(12):631-644 | Abstract: | Congenital hydrocephalus (CH) comprises a heterogeneous group of birth anomalies with a wide-ranging prevalence across geographic regions and registry type. The aim of the present study was to analyze the early neonatal case fatality rate (CFR) and total birth prevalence of newborns diagnosed with CH. |
Description: | Fil: Gili, Juan Antonio. Instituto Académico Pedagógico de Ciencias Humanas, Universidad Nacional de Villa María; Córdoba, Argentina Fil: López-Camelo, Jorge Santiago. ECLAMC, Centro de Educación Médica e Investigaciones Clínicas (CEMIC-CONICET); Buenos Aires, Argentina Fil: Nembhard, Wendy N. Department of Epidemiology, Arkansas Center for Birth Defects Research and Prevention and Arkansas Reproductive Health Monitoring System, University of Arkansas for Medical Sciences; Little Rock, Arkansas, USA Fil: Bakker, Marian. Department of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Northern Netherlands; Groningen, The Netherlands Fil: de Walle, Hermien E K. Department of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Northern Netherlands; Groningen, The Netherlands Fil: Stallings, Erin B. Metro Atlanta Congenital Defects Program (MACDP), Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities; USA Fil: Kancherla, Vijaya. Department of Epidemiology, Emory University Rollins School of Public Health; USA Fil: Contiero, Paolo. Lombardy Congenital Anomalies Registry, Cancer Registry Unit, Fondazione IRCCS, Istituto Nazionale Tumori; Italia Fil: Dastgiri, Saeed. Health Services Management Research Centre, Tabriz University of Medical Sciences; Iran Fil: Feldkamp, Marcia L. Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine; USA Fil: Nance, Amy. Utah Birth Defect Network, Bureau of Children with Special Health Care Needs, Division of Family Health and Preparedness, Utah Department of Health; USA Fil: Gatt, Miriam. Malta Congenital Anomalies Registry, Directorate for Health Information and Research; Malta Fil: Martínez, Laura. Genetics Department, Hospital Universitario Dr. José E. González, Universidad Autonóma de Nuevo León; Mexico Fil: Canessa, María Aurora. Regional Register Congenital Malformation Maule Health Service (RRMC-SSM); Chile Fil: Groisman, Boris. National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Laboratories and Health Institutes (ANLIS), National Ministry of Health and Social Development; Buenos Aires, Argentina Fil: Hurtado-Villa, Paula. Department of Basic Sciences of Health, School of Health, Pontificia Universidad Javeriana; Colombia Fil: Källén, Karin. National Board of Health and Welfare; Sweden Fil: Landau, Danielle. Department of Neonatology, Soroka Medical Center; Israel Fil: Lelong, Nathalie. Université de Paris, CRESS Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA; Francia Fil: Morgan, Margery. CARIS, The Congenital Anomaly Register for Wales, Singleton Hospital; UK Fil: Arteaga-Vázquez, Jazmín. Department of Genetics, RYVEMCE, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán; Mexico Fil: Pierini, Anna. Institute of Clinical Physiology, National Research Council and Fondazione Toscana Gabriele Monasterio, Tuscany Registry of Congenital Defects; Italia Fil: Rissmann, Anke. Medical Faculty, Malformation Monitoring Centre Saxony-Anhalt, Otto-von-Guericke University; Alemania Fil: Sipek, Antonin. Department of Medical Genetics, Thomayer University Hospital; República Checa Fil: Szabova, Elena. Slovak Teratologic Information Centre (FPH), Slovak Medical University; Eslovaquia Fil: Wertelecki, Wladimir. Omni-Net for Children International Charitable Fund; Ucrania Fil: Zarante, Ignacio. Human Genetics Institute, Pontificia Universidad Javeriana; Colombia Fil: Canfield, Mark A. Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services; USA Fil: Mastroiacovo, Pierpaolo. International Center on Birth Defects, International Clearinghouse for Birth Defects Surveillance and Research; Italia |
URI: | http://sgc.anlis.gob.ar/handle/123456789/2552 | DOI: | 10.1002/bdr2.2045 |
| Appears in Collections: | Artículos |
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| 10.1002bdr2.2045.pdf | 1.01 MB | Adobe PDF | View/Open |
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