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WFRF:(Walle L. E.)
 

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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00006187naa a2200697 4500
001oai:lup.lub.lu.se:1c95bc12-7f67-437d-b3f5-5b27d0f9cd6f
003SwePub
008191115s2019 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/1c95bc12-7f67-437d-b3f5-5b27d0f9cd6f2 URI
024a https://doi.org/10.1111/ppe.125892 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Bakker, Marian K.u University Medical Center Groningen,University of Groningen4 aut
2451 0a Analysis of Mortality among Neonates and Children with Spina Bifida : An International Registry-Based Study, 2001-2012
264 c 2019-10-21
264 1b Wiley,c 2019
300 a 13 s.
520 a Background: Medical advancements have resulted in better survival and life expectancy among those with spina bifida, but a significantly increased risk of perinatal and postnatal mortality for individuals with spina bifida remains. Objectives: To examine stillbirth and infant and child mortality among those affected by spina bifida using data from multiple countries. Methods: We conducted an observational study, using data from 24 population- and hospital-based surveillance registries in 18 countries contributing as members of the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR). Cases of spina bifida that resulted in livebirths or stillbirths from 20 weeks' gestation or elective termination of pregnancy for fetal anomaly (ETOPFA) were included. Among liveborn spina bifida cases, we calculated mortality at different ages as number of deaths among liveborn cases divided by total number of liveborn cases with spina bifida. As a secondary outcome measure, we estimated the prevalence of spina bifida per 10 000 total births. The 95% confidence interval for the prevalence estimate was estimated using the Poisson approximation of binomial distribution. Results: Between years 2001 and 2012, the overall first-week mortality proportion was 6.9% (95% CI 6.3, 7.7) and was lower in programmes operating in countries with policies that allowed ETOPFA compared with their counterparts (5.9% vs. 8.4%). The majority of first-week mortality occurred on the first day of life. In programmes where information on long-term mortality was available through linkage to administrative databases, survival at 5 years of age was 90%-96% in Europe, and 86%-96% in North America. Conclusions: Our multi-country study showed a high proportion of stillbirth and infant and child deaths among those with spina bifida. Effective folic acid interventions could prevent many cases of spina bifida, thereby preventing associated childhood morbidity and mortality.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Pediatrik0 (SwePub)302212 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Pediatrics0 (SwePub)302212 hsv//eng
650 7a MEDICIN OCH HÄLSOVETENSKAPx Hälsovetenskapx Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi0 (SwePub)303022 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Health Sciencesx Public Health, Global Health, Social Medicine and Epidemiology0 (SwePub)303022 hsv//eng
653 a epidemiology
653 a mortality
653 a registry-based study
653 a spina bifida
700a Kancherla, Vijayau Emory University4 aut
700a Canfield, Mark A.u Texas Department of State Health Services4 aut
700a Bermejo-Sanchez, Evau Carlos III Health Institute4 aut
700a Cragan, Janet D.u Centers For Disease Control And Prevention4 aut
700a Dastgiri, Saeedu Tabriz University of Medical Sciences4 aut
700a De Walle, Hermien E.K.u University of Groningen,University Medical Center Groningen4 aut
700a Feldkamp, Marcia L.u University of Utah,Utah Birth Defect Network (UBDN)4 aut
700a Groisman, Borisu National Center of Medical Genetics (CENAGEM)4 aut
700a Gatt, Miriamu Directorate for Health Information and Research4 aut
700a Hurtado-Villa, Paulau Pontificia Universidad Javeriana, Cali4 aut
700a Kallen, Karinu Lund University,Lunds universitet,Miljöepidemiologi,Forskargrupper vid Lunds universitet,Environmental Epidemiology,Lund University Research Groups,Socialstyrelsen / Swedish National Board of Health and Welfare4 aut0 (Swepub:lu)anat-kka
700a Landau, Daniellau Soroka Medical Center4 aut
700a Lelong, Nathalieu Paris Descartes University4 aut
700a Lopez Camelo, Jorge S.u Centro de Educación Médica e Investigaciones Clínicas (CEMIC)4 aut
700a Martínez, Laurau Universidad Autonoma de Nuevo Leon4 aut
700a Morgan, Margeryu Singleton Hospital4 aut
700a Mutchinick, Osvaldo M.u Instituto Nacional de Ciencias Médicas y Nutrición4 aut
700a Nembhard, Wendy N.u University of Arkansas for Medical Sciences4 aut
700a Pierini, Annau Tuscany Gabriele Monasterio Foundation,Tuscany Registry of Congenital Defects4 aut
700a Rissmann, Ankeu Otto von Guericke University Magdeburg4 aut
700a Sipek, Antoninu Thomayer Hospital4 aut
700a Szabova, Elenau Slovak Medical University4 aut
700a Tagliabue, Giovannau Istituto Nazionale dei Tumori4 aut
700a Wertelecki, Wladimiru Omni-Net for Children International Charitable Fund Rivne4 aut
700a Zarante, Ignaciou Pontificia Universidad Javeriana4 aut
700a Mastroiacovo, Pierpaolou International Clearinghouse for Birth Defects Surveillance and Research4 aut
710a University Medical Center Groningenb University of Groningen4 org
773t Paediatric and Perinatal Epidemiologyd : Wileyg 33:6, s. 436-448q 33:6<436-448x 0269-5022x 1365-3016
856u http://dx.doi.org/10.1111/ppe.12589x freey FULLTEXT
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/ppe.12589
8564 8u https://lup.lub.lu.se/record/1c95bc12-7f67-437d-b3f5-5b27d0f9cd6f
8564 8u https://doi.org/10.1111/ppe.12589

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