134 results on '"Gatt, Miriam"'
Search Results
2. Socioeconomic disparities in changes to preterm birth and stillbirth rates during the first year of the COVID-19 pandemic: a study of 21 European countries.
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Zeitlin, Jennifer, Philibert, Marianne, Barros, Henrique, Broeders, Lisa, Cap, Jan, Draušnik, Željka, Engjom, Hilde, Farr, Alex, Fresson, Jeanne, Gatt, Miriam, Gissler, Mika, Heller, Günther, Isakova, Jelena, Källén, Karin, Kyprianou, Theopisti, Loghi, Marzia, Monteath, Kirsten, Mortensen, Laust, Rihs, Tonia, and Sakkeus, Luule
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RESEARCH funding ,PREMATURE infants ,PERINATAL death ,META-analysis ,DESCRIPTIVE statistics ,RELATIVE medical risk ,PSYCHOLOGY of mothers ,QUALITY of life ,PARTICIPATION ,HEALTH equity ,CONFIDENCE intervals ,COVID-19 pandemic ,SOCIAL classes ,EDUCATIONAL attainment - Abstract
Background Despite concerns about worsening pregnancy outcomes resulting from healthcare restrictions, economic difficulties and increased stress during the COVID-19 pandemic, preterm birth (PTB) rates declined in some countries in 2020, while stillbirth rates appeared stable. Like other shocks, the pandemic may have exacerbated existing socioeconomic disparities in pregnancy, but this remains to be established. Our objective was to investigate changes in PTB and stillbirth by socioeconomic status (SES) in European countries. Methods The Euro-Peristat network implemented this study within the Population Health Information Research Infrastructure (PHIRI) project. A common data model was developed to collect aggregated tables from routine birth data for 2015–2020. SES was based on mother's educational level or area-level deprivation/maternal occupation if education was unavailable and harmonized into low, medium and high SES. Country-specific relative risks (RRs) of PTB and stillbirth for March to December 2020, adjusted for linear trends from 2015 to 2019, by SES group were pooled using random effects meta-analysis. Results Twenty-one countries provided data on perinatal outcomes by SES. PTB declined by an average 4% in 2020 {pooled RR: 0.96 [95% confidence intervals (CIs): 0.94–0.97]} with similar estimates across all SES groups. Stillbirths rose by 5% [RR: 1.05 (95% CI: 0.99–1.10)], with increases of between 3 and 6% across the three SES groups, with overlapping confidence limits. Conclusions PTB decreases were similar regardless of SES group, while stillbirth rates rose without marked differences between groups. [ABSTRACT FROM AUTHOR]
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- 2024
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3. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study
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van de Putte, Romy, van Rooij, Iris A. L. M., Marcelis, Carlo L. M., Guo, Michel, Brunner, Han G., Addor, Marie-Claude, Cavero-Carbonell, Clara, Dias, Carlos M., Draper, Elizabeth S., Etxebarriarteun, Larraitz, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Kurinczuk, Jenny J., Lanzoni, Monica, Latos-Bielenska, Anna, Luyt, Karen, O’Mahony, Mary T., Miller, Nicola, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J., Perthus, Isabelle, Pierini, Anna, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Wiesel, Awi, Zymak-Zakutnia, Natalya, Loane, Maria, Barisic, Ingeborg, de Walle, Hermien E. K., Roeleveld, Nel, and Bergman, Jorieke E. H.
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- 2020
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4. Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study
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Morris, Joan K., Garne, Ester, Loane, Maria, Addor, Marie-Claude, Barisic, Ingeborg, Bianchi, Fabrizio, Gatt, Miriam, Lanzoni, Monica, Lynch, Catherine, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda, O'Mahony, Mary T., Randrianaivo-Ranjatoelina, Hanitra, Rissmann, Anke, Tucker, David, de Walle, H.E.K., Zymak-Zakutnia, Natalya, and Rankin, Judith
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- 2018
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5. Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study
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Garne, Ester, Rissmann, Anke, Addor, Marie-Claude, Barisic, Ingeborg, Bergman, Jorieke, Braz, Paula, Cavero-Carbonell, Clara, Draper, Elizabeth S., Gatt, Miriam, Haeusler, Martin, Klungsoyr, Kari, Kurinczuk, Jennifer J., Lelong, Nathalie, Luyt, Karen, Lynch, Catherine, O'Mahony, Mary T., Mokoroa, Olatz, Nelen, Vera, Neville, Amanda J., Pierini, Anna, Randrianaivo, Hanitra, Rankin, Judith, Rouget, Florence, Schaub, Bruno, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Wiesel, Awi, Zymak-Zakutnia, Nataliia, Lanzoni, Monica, and Morris, Joan K.
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- 2018
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6. Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies
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Claridge, Hugh, primary, Tan, Joachim, additional, Loane, Maria, additional, Garne, Ester, additional, Barisic, Ingeborg, additional, Cavero-Carbonell, Clara, additional, Dias, Carlos, additional, Gatt, Miriam, additional, Jordan, Susan, additional, Khoshnood, Babak, additional, Kiuru-Kuhlefelt, Sonja, additional, Klungsoyr, Kari, additional, Mokoroa Carollo, Olatz, additional, Nelen, Vera, additional, Neville, Amanda J, additional, Pierini, Anna, additional, Randrianaivo, Hanitra, additional, Rissmann, Anke, additional, Tucker, David, additional, de Walle, Hermien, additional, Wertelecki, Wladimir, additional, and Morris, Joan K, additional
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- 2023
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7. Causes of death in children with congenital anomalies up to age 10 in eight European countries
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Rissmann, Anke, primary, Tan, Joachim, additional, Glinianaia, Svetlana V, additional, Rankin, Judith, additional, Pierini, Anna, additional, Santoro, Michele, additional, Coi, Alessio, additional, Garne, Ester, additional, Loane, Maria, additional, Given, Joanne, additional, Reid, Abigail, additional, Aizpurua, Amaia, additional, Akhmedzhanova, Diana, additional, Ballardini, Elisa, additional, Barisic, Ingeborg, additional, Cavero-Carbonell, Clara, additional, de Walle, Hermien E K, additional, Gatt, Miriam, additional, Gissler, Mika, additional, Heino, Anna, additional, Jordan, Sue, additional, Urhoj, Stine Kjaer, additional, Klungsøyr, Kari, additional, Lutke, Renee, additional, Mokoroa, Olatz, additional, Neville, Amanda Julie, additional, Thayer, Daniel S, additional, Wellesley, Diana G, additional, Yevtushok, Lyubov, additional, Zurriaga, Oscar, additional, and Morris, Joan, additional
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- 2023
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8. Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based study
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Gili, Juan Antonio, López-Camelo, Jorge Santiago, Nembhard, Wendy N, Bakker, Marian, de Walle, Hermien E K, Stallings, Erin B, Kancherla, Vijaya, Contiero, Paolo, Dastgiri, Saeed, Feldkamp, Marcia L, Nance, Amy, 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, and Reproductive Origins of Adult Health and Disease (ROAHD)
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Embryology ,Health, Toxicology and Mutagenesis ,Infant, Newborn ,Stillbirth ,Toxicology ,Article ,Pregnancy ,Pediatrics, Perinatology and Child Health ,Prevalence ,Humans ,Female ,Registries ,Live Birth ,Hydrocephalus ,Developmental Biology - Abstract
BACKGROUND: 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.METHODS: Data were provided by 25 registries from four continents participating in the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR) on births ascertained between 2000 and 2014. Two CH rates were calculated using a Poisson distribution: early neonatal CFR (death within 7 days) per 100 liveborn CH cases (CFR) and total birth prevalence rate (BPR) per 10,000 births (including live births and stillbirths) (BPR). Heterogeneity between registries was calculated using a meta-analysis approach with random effects. Temporal trends in CFR and BPR within registries were evaluated through Poisson regression modeling.RESULTS: A total of 13,112 CH cases among 19,293,280 total births were analyzed. The early neonatal CFR was 5.9 per 100 liveborn cases, 95% confidence interval (CI): 5.4-6.8. The CFR among syndromic cases was 2.7 times (95% CI: 2.2-3.3) higher than among non-syndromic cases (10.4% [95% CI: 9.3-11.7] and 4.4% [95% CI: 3.7-5.2], respectively). The total BPR was 6.8 per 10,000 births (95% CI: 6.7-6.9). Stratified by elective termination of pregnancy for fetal anomalies (ETOPFA), region and system, higher CFR were observed alongside higher BPR rates. The early neonatal CFR and total BPR did not show temporal variation, with the exception of a CFR decrease in one registry.CONCLUSIONS: Findings of early neonatal CFR and total BPR were highly heterogeneous among registries participating in ICBDSR. Most registries with higher CFR also had higher BPR. Differences were attributable to type of registry (hospital-based vs. population-based), ETOPFA (allowed yes or no) and geographical regions. These findings contribute to the understanding of regional differences of CH occurrence and early neonatal deaths.
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- 2022
9. Risk factors for mortality in infancy and childhood in children with major congenital anomalies:A European population-based cohort study
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Tan, Joachim, Glinianaia, Svetlana V, Rankin, Judith, Pierini, Anna, Santoro, Michele, Coi, Alessio, Garne, Ester, Loane, Maria, Given, Joanne E, Brigden, Joanna, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien E K, García-Villodre, Laura, Gatt, Miriam, Gissler, Mika, Heino, Anna, Jordan, Sue, Khoshnood, Babak, Klungsoyr, Kari, Lelong, Nathalie, Lutke, Renée L, Neville, Amanda J, Tucker, David, Urhoj, Stine K, Wellesley, Diana, Morris, Joan K, Tan, Joachim, Glinianaia, Svetlana V, Rankin, Judith, Pierini, Anna, Santoro, Michele, Coi, Alessio, Garne, Ester, Loane, Maria, Given, Joanne E, Brigden, Joanna, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien E K, García-Villodre, Laura, Gatt, Miriam, Gissler, Mika, Heino, Anna, Jordan, Sue, Khoshnood, Babak, Klungsoyr, Kari, Lelong, Nathalie, Lutke, Renée L, Neville, Amanda J, Tucker, David, Urhoj, Stine K, Wellesley, Diana, and Morris, Joan K
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BACKGROUND: Preterm birth and young maternal age are known risk factors for infant and childhood mortality. There is limited knowledge of the impact of these risk factors in children born with major congenital anomalies (CAs), who have inherently higher risks of death compared with other children.OBJECTIVES: To investigate the risk factors for mortality up to age 10 years in children born with specific major CAs.METHODS: This population-based cohort study involved 150,198 livebirths from 1995 to 2014 in 13 European CA registries linked to mortality data. Cox proportional hazards models estimated the association of gestational age, maternal age and child's sex with death <1 year and 1-9 years for the whole cohort and by CA subgroup. Hazard ratios (HR) from each registry were pooled using multivariate meta-analysis.RESULTS: Preterm birth had a dose-response association with mortality; compared with infants born at 37+ weeks gestation, those born at <28, 28-31 and 32-36 weeks had 14.88 (95% CI 12.57, 17.62), 8.39 (95% CI 7.16, 9.85) and 3.88 (95% CI 3.40, 4.43) times higher risk of death <1 year, respectively. The corresponding risks at 1-9 years were 4.99 (95% CI 2.94, 8.48), 3.09 (95% CI 2.28, 4.18) and 2.04 (95% CI 1.69, 2.46) times higher, respectively. Maternal age <20 years (versus 20-34 years) was a risk factor for death <1 year (HR 1.30, 95% CI 1.09, 1.54) and 1-9 years (HR 1.58, 95% CI 1.19, 2.10). Females had 1.22 (95% CI: 1.07, 1.39) times higher risk of death between 1 and 9 years than males.CONCLUSION: Preterm birth was associated with considerably higher infant and childhood mortality in children with CAs, comparable to estimates reported elsewhere for the background population. Additional risk factors included young maternal age and female sex. Information on risk factors could benefit clinical care and guide counselling of parents following CA diagnoses.
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- 2023
10. The burden of disease for children born alive with Turner syndrome-A European cohort study
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Andersen, Ann-Louise Rud, Urhoj, Stine Kjaer, Tan, Joachim, Cavero-Carbonell, Clara, Gatt, Miriam, Gissler, Mika, Klungsoyr, Kari, Khoshnood, Babak, Morris, Joan, Neville, Amanda J, Pierini, Anna, Scanlon, Ieuan, de Walle, Hermien E K, Wellesley, Diana, Garne, Ester, Loane, Maria, Andersen, Ann-Louise Rud, Urhoj, Stine Kjaer, Tan, Joachim, Cavero-Carbonell, Clara, Gatt, Miriam, Gissler, Mika, Klungsoyr, Kari, Khoshnood, Babak, Morris, Joan, Neville, Amanda J, Pierini, Anna, Scanlon, Ieuan, de Walle, Hermien E K, Wellesley, Diana, Garne, Ester, and Loane, Maria
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BACKGROUND: Turner syndrome is a rare congenital anomaly caused by complete or partial X chromosome monosomy that may affect mortality and morbidity in childhood.METHODS: This population-based data-linkage cohort study, as part of the EUROlinkCAT project, investigated mortality and morbidity for the first 5 years of life for liveborn European children diagnosed with Turner syndrome. Thirteen population-based registries in 10 countries from the European surveillance of congenital anomalies (EUROCAT) network participated. Data on children born 1995-2014 and diagnosed with Turner syndrome were linked to mortality, hospital and prescription records. Children with any congenital anomaly and children without a congenital anomaly were included for comparison on morbidity.RESULTS: Out of a population of 5.8 million livebirths 404 were diagnosed with Turner syndrome prenatally or in infancy and 95.5% survived to their fifth birthday. During the first year of life 72.3% (95% CI 59.5;81.6) of children with Turner syndrome were hospitalized, the median length of stay was 5.6 days (95% CI 3.5;7.7) and 18.7% (95% CI 13.9;23.9) underwent surgery. After the first year of life hospitalizations and length of stay decreased but more children underwent surgery (30.8% [95% CI 17.6;44.7]). In the first 5 years the percentage of children with Turner syndrome having a prescription for antibiotics was 12%-20% per year and increased with the age of child.CONCLUSIONS: In the first year of life, the burden of disease was relatively high for children with Turner syndrome. The outlook is more positive beyond the first year, though overall morbidity still exceeded that of children without congenital anomalies.
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- 2023
11. Survival, hospitalisation and surgery in children born with Pierre Robin sequence:a European population-based cohort study
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Santoro, Michele, Garne, Ester, Coi, Alessio, Tan, Joachim, Loane, Maria, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien Ek, Gatt, Miriam, Gissler, Mika, Jordan, Sue, Klungsøyr, Kari, Lelong, Natalie, Urhoj, Stine Kjaer, Wellesley, Diana G, Morris, Joan K, Santoro, Michele, Garne, Ester, Coi, Alessio, Tan, Joachim, Loane, Maria, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien Ek, Gatt, Miriam, Gissler, Mika, Jordan, Sue, Klungsøyr, Kari, Lelong, Natalie, Urhoj, Stine Kjaer, Wellesley, Diana G, and Morris, Joan K
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OBJECTIVE: To evaluate survival, hospitalisations and surgical procedures for children born with Pierre Robin sequence (PRS) across Europe.DESIGN: Multicentre population-based cohort study.SETTING: Data on 463 live births with PRS from a population of 4 984 793 from 12 EUROCAT congenital anomaly registries.METHODS: Data on children with PRS born 1995-2014 were linked electronically to data on mortality, hospitalisations and surgical procedures up to 10 years of age. Each registry applied a common data model to standardise the linked data and ran common syntax scripts to produce aggregate tables. Results from each registry were pooled using random-effect meta-analyses.MAIN OUTCOME MEASURES: Probability of survival, proportion of children hospitalised and undergoing surgery, and median length of hospital stay.RESULTS: The majority of deaths occurred in the first year of life with a survival rate of 96.0% (95% CI 93.5% to 98.5%); 95.1% (95% CI 92.7% to 97.7%) survived to age 10. In the first year of life, 99.2% (95% CI 95.0% to 99.9%) of children were hospitalised with a median stay of 21.4 days (95% CI 15.6 to 27.2), and 67.6% (95% CI 46.6% to 81.8%) underwent surgery. In the first 5 years of life, 99.2% of children underwent a median of two surgical procedures. Between ages 5 and 9, 58.3% (95% CI 44.7% to 69.7%) were hospitalised with a median annual stay of 0.3 days.CONCLUSIONS: Children with PRS had high mortality and morbidity with long hospital stays in the first year of life, and almost all had surgery before 5 years of age. Survival improved after infancy with fewer hospitalisations after age 5. This study provides reliable estimates of the survival and morbidity of children with PRS for families and healthcare providers.
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- 2023
12. Ten-year survival of children with trisomy 13 or trisomy 18:a multi-registry European cohort study
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Glinianaia, Svetlana V, Rankin, Judith, Tan, Joachim, Loane, Maria, Garne, Ester, Cavero-Carbonell, Clara, de Walle, Hermien E K, Gatt, Miriam, Gissler, Mika, Klungsøyr, Kari, Lelong, Natalie, Neville, Amanda, Pierini, Anna, Tucker, David F, Urhoj, Stine Kjaer, Wellesley, Diana Gay, Morris, Joan K, Glinianaia, Svetlana V, Rankin, Judith, Tan, Joachim, Loane, Maria, Garne, Ester, Cavero-Carbonell, Clara, de Walle, Hermien E K, Gatt, Miriam, Gissler, Mika, Klungsøyr, Kari, Lelong, Natalie, Neville, Amanda, Pierini, Anna, Tucker, David F, Urhoj, Stine Kjaer, Wellesley, Diana Gay, and Morris, Joan K
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OBJECTIVE: To investigate the survival to 10 years of age of children with trisomy 13 (T13) and children with trisomy 18 (T18), born 1995-2014.DESIGN: Population-based cohort study that linked mortality data to data on children born with T13 or T18, including translocations and mosaicisms, from 13 member registries of EUROCAT, a European network for the surveillance of congenital anomalies.SETTING: 13 regions in nine Western European countries.PATIENTS: 252 live births with T13 and 602 with T18.MAIN OUTCOME MEASURES: Survival at 1 week, 4 weeks and 1, 5 and 10 years of age estimated by random-effects meta-analyses of registry-specific Kaplan-Meier survival estimates.RESULTS: Survival estimates of children with T13 were 34% (95% CI 26% to 46%), 17% (95% CI 11% to 29%) and 11% (95% CI 6% to 18%) at 4 weeks, 1 and 10 years, respectively. The corresponding survival estimates were 38% (95% CI 31% to 45%), 13% (95% CI 10% to 17%) and 8% (95% CI 5% to 13%) for children with T18. The 10-year survival conditional on surviving to 4 weeks was 32% (95% CI 23% to 41%) and 21% (95% CI 15% to 28%) for children with T13 and T18, respectively.CONCLUSIONS: This multi-registry European study found that despite extremely high neonatal mortality in children with T13 and T18, 32% and 21%, respectively, of those who survived to 4 weeks were likely to survive to age 10 years. These reliable survival estimates are useful to inform counselling of parents after prenatal diagnosis.
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- 2023
13. The accuracy of antenatal ultrasound screening in Malta: a population-based study
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Myatt, Jeremy Borg, primary, Gatt, Miriam, additional, Cordina, Mark, additional, Grech, Victor, additional, and Attard-Montalto, Simon, additional
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- 2022
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14. Variations in use of childbirth interventions in 13 high-income countries: A multinational cross-sectional study
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Seijmonsbergen-Schermers, Anna E., van den Akker, Thomas, Rydahl, Eva, Beeckman, Katrien, Bogaerts, Annick, Binfa, Lorena, Frith, Lucy, Gross, Mechthild M., Misselwitz, Björn, Hálfdánsdóttir, Berglind, Daly, Deirdre, Corcoran, Paul, Calleja-Agius, Jean, Calleja, Neville, Gatt, Miriam, Vika Nilsen, Anne Britt, Declercq, Eugene, Gissler, Mika, Heino, Anna, Lindgren, Helena, and de Jonge, Ank
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Infant mortality -- Analysis -- Usage -- Health aspects ,Obstetrics -- Usage -- Analysis -- Health aspects ,Information management -- Health aspects -- Analysis -- Usage ,Cesarean section -- Usage -- Analysis -- Health aspects ,Information accessibility ,Biological sciences - Abstract
Background Variations in intervention rates, without subsequent reductions in adverse outcomes, can indicate overuse. We studied variations in and associations between commonly used childbirth interventions and adverse outcomes, adjusted for population characteristics. Methods and findings In this multinational cross-sectional study, existing data on 4,729,307 singleton births at [greater than or equal to]37 weeks in 2013 from Finland, Sweden, Norway, Denmark, Iceland, Ireland, England, the Netherlands, Belgium, Germany (Hesse), Malta, the United States, and Chile were used to describe variations in childbirth interventions and outcomes. Numbers of births ranged from 3,987 for Iceland to 3,500,397 for the USA. Crude data were analysed in the Netherlands, or analysed data were shared with the principal investigator. Strict variable definitions were used and information on data quality was collected. Intervention rates were described for each country and stratified by parity. Uni- and multivariable analyses were performed, adjusted for population characteristics, and associations between rates of interventions, population characteristics, and outcomes were assessed using Spearman's rank correlation coefficients. Considerable intercountry variations were found for all interventions, despite adjustments for population characteristics. Adjustments for ethnicity and body mass index changed odds ratios for augmentation of labour and episiotomy. Largest variations were found for augmentation of labour, pain relief, episiotomy, instrumental birth, and cesarean section (CS). Percentages of births at [greater than or equal to]42 weeks varied from 0.1% to 6.7%. Rates among nulliparous versus multiparous women varied from 56% to 80% versus 51% to 82% for spontaneous onset of labour; 14% to 36% versus 8% to 28% for induction of labour; 3% to 13% versus 7% to 26% for prelabour CS; 16% to 48% versus 12% to 50% for overall CS; 22% to 71% versus 7% to 38% for augmentation of labour; 50% to 93% versus 25% to 86% for any intrapartum pain relief, 19% to 83% versus 10% to 64% for epidural anaesthesia; 6% to 68% versus 2% to 30% for episiotomy in vaginal births; 3% to 30% versus 1% to 7% for instrumental vaginal births; and 42% to 70% versus 50% to 84% for spontaneous vaginal births. Countries with higher rates of births at [greater than or equal to]42 weeks had higher rates of births with a spontaneous onset (rho = 0.82 for nulliparous/rho = 0.83 for multiparous women) and instrumental (rho = 0.67) and spontaneous (rho = 0.66) vaginal births among multiparous women and lower rates of induction of labour (rho = -0.71/-0.66), prelabour CS (rho = -0.61/-0.65), overall CS (rho = -0.61/-0.67), and episiotomy (multiparous: rho = -0.67). Variation in CS rates was mainly due to prelabour CS (rho = 0.96). Countries with higher rates of births with a spontaneous onset had lower rates of emergency CS (nulliparous: rho = -0.62) and higher rates of spontaneous vaginal births (multiparous: rho = 0.70). Prelabour and emergency CS were positively correlated (nulliparous: rho = 0.74). Higher rates of obstetric anal sphincter injury following vaginal birth were found in countries with higher rates of spontaneous birth (nulliparous: rho = 0.65). In countries with higher rates of epidural anaesthesia (nulliparous) and spontaneous births (multiparous), higher rates of Apgar score < 7 were found (rhos = 0.64). No statistically significant variation was found for perinatal mortality. Main limitations were varying quality of data and missing information. Conclusions Considerable intercountry variations were found for all interventions, even after adjusting for population characteristics, indicating overuse of interventions in some countries. Multivariable analyses are essential when comparing intercountry rates. Implementation of evidence-based guidelines is crucial in optimising intervention use and improving quality of maternity care worldwide., Author(s): Anna E. Seijmonsbergen-Schermers 1,*, Thomas van den Akker 2,3, Eva Rydahl 4, Katrien Beeckman 5, Annick Bogaerts 6,7, Lorena Binfa 8, Lucy Frith 9, Mechthild M. Gross 10, Björn [...]
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- 2020
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15. Temporal and geographical variations in survival of children born with congenital anomalies in Europe:A multi-registry cohort study
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Santoro, Michele, Coi, Alessio, Pierini, Anna, Rankin, Judith, Glinianaia, Svetlana V, Tan, Joachim, Reid, Abigail, Garne, Ester, Loane, Maria, Given, Joanne, Aizpurua, Amaia, Astolfi, Gianni, Barisic, Ingeborg, Cavero-Carbonell, Clara, de Walle, Hermien E K, Den Hond, Elly, García-Villodre, Laura, Gatt, Miriam, Gissler, Mika, Jordan, Sue, Khoshnood, Babak, Kiuru-Kuhlefelt, Sonja, Klungsøyr, Kari, Lelong, Nathalie, Lutke, Renée, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda J, Odak, Ljubica, Rissmann, Anke, Scanlon, Ieuan, Urhoj, Stine Kjaer, Wellesley, Diana, Wertelecki, Wladimir, Yevtushok, Lyubov, Morris, Joan K, Santoro, Michele, Coi, Alessio, Pierini, Anna, Rankin, Judith, Glinianaia, Svetlana V, Tan, Joachim, Reid, Abigail, Garne, Ester, Loane, Maria, Given, Joanne, Aizpurua, Amaia, Astolfi, Gianni, Barisic, Ingeborg, Cavero-Carbonell, Clara, de Walle, Hermien E K, Den Hond, Elly, García-Villodre, Laura, Gatt, Miriam, Gissler, Mika, Jordan, Sue, Khoshnood, Babak, Kiuru-Kuhlefelt, Sonja, Klungsøyr, Kari, Lelong, Nathalie, Lutke, Renée, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda J, Odak, Ljubica, Rissmann, Anke, Scanlon, Ieuan, Urhoj, Stine Kjaer, Wellesley, Diana, Wertelecki, Wladimir, Yevtushok, Lyubov, and Morris, Joan K
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BACKGROUND: Congenital anomalies are a major cause of perinatal, neonatal and infant mortality.OBJECTIVES: The aim was to investigate temporal changes and geographical variation in survival of children with major congenital anomalies (CA) in different European areas.METHODS: In this population-based linkage cohort study, 17 CA registries members of EUROCAT, the European network for the surveillance of CAs, successfully linked data on 115,219 live births with CAs to mortality records. Registries estimated Kaplan-Meier survival at 28 days and 5 years of age and fitted Cox's proportional hazards models comparing mortality at 1 year and 1-9 years of age for children born during 2005-2014 with those born during 1995-2004. The hazard ratios (HR) from each registry were combined centrally using a random-effects model. The 5-year survival conditional on having survived to 28 days of age was calculated.RESULTS: The overall risk of death by 1 year of age for children born with any major CA in 2005-2014 decreased compared to 1995-2004 (HR 0.68, 95% confidence interval [CI] 0.53, 0.89). Survival at 5 years of age ranged between registries from 97.6% to 87.0%. The lowest survival was observed for the registry of OMNI-Net (Ukraine) (87.0%, 95% CI 86.1, 87.9).CONCLUSIONS: Survival of children with CAs improved for births in 2005-2014 compared with 1995-2004. The use of CA registry data linked to mortality data enables investigation of survival of children with CAs. Factors such as defining major CAs, proportion of terminations of pregnancy for foetal anomaly, source of mortality data and linkage methods are important to consider in the design of future studies and in the interpretation of the results on survival of children with CAs.
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- 2022
16. Survival of children with rare structural congenital anomalies:a multi-registry cohort study
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Coi, Alessio, Santoro, Michele, Pierini, Anna, Rankin, Judith, Glinianaia, Svetlana, Tan, Joachim, Reid, Abigail-Kate, Garne, Ester, Loane, Maria, Given, Joanne, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien E. K., Gatt, Miriam, Garcia-Villodre, Laura, Gissler, Mika, Jordan, Sue, Kiuru-Kuhlefelt, Sonja, Urhøj, Stine Kjær, Klungsoyr, Kari, Lelong, Nathalie, Lutke, L. Renee, Neville, Amanda J., Rahshenas, Makan, Scanlon, Ieuan, Wellesley, Diana, Morris, Joan K., Coi, Alessio, Santoro, Michele, Pierini, Anna, Rankin, Judith, Glinianaia, Svetlana, Tan, Joachim, Reid, Abigail-Kate, Garne, Ester, Loane, Maria, Given, Joanne, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien E. K., Gatt, Miriam, Garcia-Villodre, Laura, Gissler, Mika, Jordan, Sue, Kiuru-Kuhlefelt, Sonja, Urhøj, Stine Kjær, Klungsoyr, Kari, Lelong, Nathalie, Lutke, L. Renee, Neville, Amanda J., Rahshenas, Makan, Scanlon, Ieuan, Wellesley, Diana, and Morris, Joan K.
- Abstract
Background Congenital anomalies are the leading cause of perinatal, neonatal and infant mortality in developed countries. Large long-term follow-up studies investigating survival beyond the first year of life in children with rare congenital anomalies are costly and sufficiently large standardized cohorts are difficult to obtain due to the rarity of some anomalies. This study aimed to investigate the survival up to 10 years of age of children born with a rare structural congenital anomaly in the period 1995-2014 in Western Europe. Methods Live births from thirteen EUROCAT (European network for the epidemiological surveillance of congenital anomalies) population-based registries were linked to mortality records. Survival for 12,685 live births with one of the 31 investigated rare structural congenital anomalies (CAs) was estimated at 1 week, 4 weeks and 1, 5 and 10 years of age within each registry and combined across Europe using random effects meta-analyses. Differences between registries were evaluated for the eight rare CAs with at least 500 live births. Results Amongst the investigated CAs, arhinencephaly/holoprosencephaly had the lowest survival at all ages (58.1%, 95% Confidence Interval (CI): 44.3-76.2% at 1 week; 47.4%, CI: 36.4-61.6% at 1 year; 35.6%, CI: 22.2-56.9% at 10 years). Overall, children with rare CAs of the digestive system had the highest survival (> 95% at 1 week, > 84% at 10 years). Most deaths occurred within the first four weeks of life, resulting in a 10-year survival conditional on surviving 4 weeks of over 95% for 17 out of 31 rare CAs. A moderate variability in survival between participating registries was observed for the eight selected rare CAs. Conclusions Pooling standardised data across 13 European CA registries and the linkage to mortality data enabled reliable survival estimates to be obtained at five ages up to ten years. Such estimates are useful for clinical practice and parental counselling.
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- 2022
17. Population birth data and pandemic readiness in Europe
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Haidinger, Gerald, Klimont, Jeannette, Alexander, Sophie, Zhang, Wei-Hong, Vandervelpen, Ele, Delnord, Marie, Kolarova, Rumyana, Yordanova, Evelin, Rodin, Urelija, Drausnik, Zeljka, Filipovic-Grcic, Boris, Kyprianou, Theopisti, Scoutellas, Vasos, Velebil, Petr, Mortensen, Laust Hvas, Sakkeus, Luule, Abuladze, Liili, Gissler, Mika, Blondel, Beatrice, Deneux-Tharaux, Catherine, Durox, Melanie, Philibert, Marianne, Zeitlin, Jennifer, Fresson, Jeanne, Heller, Guenther, Misselwitz, Bjoern, Antsaklis, Aris, Berbik, Istvan, Olafsdottir, Helga Sol, Kearns, Karen, Sikora, Izabela, Cuttini, Marina, Loghi, Marzia, Donati, Serena, Boldrini, Rosalia, Misins, Janis, Zile, Irisa, Isakova, Jelena, Touvrey-Lecomte, Aline, Billy, Audrey, Couffignal, Sophie, Weber, Guy, Gatt, Miriam, Nijhuis, Jan, Broeders, Lisa, Achterberg, P. W., Hindori-Mohangoo, Ashna, Klungsoyr, Kari, Akerkar, Rupali, Engjom, Hilde, Szamotulska, Katarzyna, Mierzejewska, Ewa, Barros, Henrique, Rodrigues, Carina, Horga, Mihai, Tica, Vlad, Puscasiu, Lucian, Budianu, Mihaela-Alexandra, Cucu, Alexandra, Calomfirescu, Cristian, Cap, Jan, Mandic, Natasa Tul, Verdenik, Ivan, Zurriaga, Oscar, Alcaide, Adela Recio, Jane, Mireia, Vidal, Maria Jose, Kallen, Karin, Nyman, Anastasia, Rihs, Tonia, Macfarlane, Alison, Wood, Rachael, Monteath, Kirsten, Smith, Lucy, Morgan, Siobhan, Hillen, Jennifer, Haidinger, Gerald, Klimont, Jeannette, Alexander, Sophie, Zhang, Wei-Hong, Vandervelpen, Ele, Delnord, Marie, Kolarova, Rumyana, Yordanova, Evelin, Rodin, Urelija, Drausnik, Zeljka, Filipovic-Grcic, Boris, Kyprianou, Theopisti, Scoutellas, Vasos, Velebil, Petr, Mortensen, Laust Hvas, Sakkeus, Luule, Abuladze, Liili, Gissler, Mika, Blondel, Beatrice, Deneux-Tharaux, Catherine, Durox, Melanie, Philibert, Marianne, Zeitlin, Jennifer, Fresson, Jeanne, Heller, Guenther, Misselwitz, Bjoern, Antsaklis, Aris, Berbik, Istvan, Olafsdottir, Helga Sol, Kearns, Karen, Sikora, Izabela, Cuttini, Marina, Loghi, Marzia, Donati, Serena, Boldrini, Rosalia, Misins, Janis, Zile, Irisa, Isakova, Jelena, Touvrey-Lecomte, Aline, Billy, Audrey, Couffignal, Sophie, Weber, Guy, Gatt, Miriam, Nijhuis, Jan, Broeders, Lisa, Achterberg, P. W., Hindori-Mohangoo, Ashna, Klungsoyr, Kari, Akerkar, Rupali, Engjom, Hilde, Szamotulska, Katarzyna, Mierzejewska, Ewa, Barros, Henrique, Rodrigues, Carina, Horga, Mihai, Tica, Vlad, Puscasiu, Lucian, Budianu, Mihaela-Alexandra, Cucu, Alexandra, Calomfirescu, Cristian, Cap, Jan, Mandic, Natasa Tul, Verdenik, Ivan, Zurriaga, Oscar, Alcaide, Adela Recio, Jane, Mireia, Vidal, Maria Jose, Kallen, Karin, Nyman, Anastasia, Rihs, Tonia, Macfarlane, Alison, Wood, Rachael, Monteath, Kirsten, Smith, Lucy, Morgan, Siobhan, and Hillen, Jennifer
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- 2022
18. Population birth data and pandemic readiness in Europe
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Haidinger, Gerald Klimont, Jeannette Alexander, Sophie and Zhang, Wei-Hong Vandervelpen, Ele Delnord, Marie Kolarova, Rumyana Yordanova, Evelin Rodin, Urelija Drausnik, Zeljka and Filipovic-Grcic, Boris Kyprianou, Theopisti Scoutellas, Vasos Velebil, Petr Mortensen, Laust Hvas Sakkeus, Luule and Abuladze, Liili Gissler, Mika Blondel, Beatrice and Deneux-Tharaux, Catherine Durox, Melanie Philibert, Marianne and Zeitlin, Jennifer Fresson, Jeanne Heller, Guenther and Misselwitz, Bjoern Antsaklis, Aris Berbik, Istvan and Olafsdottir, Helga Sol Kearns, Karen Sikora, Izabela and Cuttini, Marina Loghi, Marzia Donati, Serena Boldrini, Rosalia Misins, Janis Zile, Irisa Isakova, Jelena and Touvrey-Lecomte, Aline Billy, Audrey Couffignal, Sophie and Weber, Guy Gatt, Miriam Nijhuis, Jan Broeders, Lisa and Achterberg, P. W. Hindori-Mohangoo, Ashna Klungsoyr, Kari and Akerkar, Rupali Engjom, Hilde Szamotulska, Katarzyna and Mierzejewska, Ewa Barros, Henrique Rodrigues, Carina Horga, Mihai Tica, Vlad Puscasiu, Lucian Budianu, Mihaela-Alexandra and Cucu, Alexandra Calomfirescu, Cristian Cap, Jan Mandic, Natasa Tul Verdenik, Ivan Zurriaga, Oscar Alcaide, Adela Recio Jane, Mireia Vidal, Maria Jose Kallen, Karin and Nyman, Anastasia Rihs, Tonia Macfarlane, Alison Wood, Rachael Monteath, Kirsten Smith, Lucy Morgan, Siobhan and Hillen, Jennifer Euro-Peristat Res Network
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- 2022
19. Survey Of Informed Consent For Registration Of Congenital Anomalies In Europe
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Busby, Araceli, Ritvanen, Annukka, Dolk, Helen, Armstrong, Nicola, De Walle, Hermien, Riaño-Galán, Isolina, Gatt, Miriam, McDonnell, Robert, Nelen, Vera, and Stone, David
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- 2005
20. International versus national growth charts for identifying small and large-for-gestational age newborns: A population-based study in 15 European countries
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Hocquette, Alice, primary, Durox, Mélanie, additional, Wood, Rachael, additional, Klungsøyr, Kari, additional, Szamotulska, Katarzyna, additional, Berrut, Sylvan, additional, Rihs, Tonia, additional, Kyprianou, Theopisti, additional, Sakkeus, Luule, additional, Lecomte, Aline, additional, Zile, Irisa, additional, Alexander, Sophie, additional, Klimont, Jeannette, additional, Barros, Henrique, additional, Gatt, Miriam, additional, Isakova, Jelena, additional, Blondel, Béatrice, additional, Gissler, Mika, additional, and Zeitlin, Jennifer, additional
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- 2021
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21. Prevention of Neural Tube Defects in Europe: A Public Health Failure
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Morris, Joan K., primary, Addor, Marie-Claude, additional, Ballardini, Elisa, additional, Barisic, Ingeborg, additional, Barrachina-Bonet, Laia, additional, Braz, Paula, additional, Cavero-Carbonell, Clara, additional, Den Hond, Elly, additional, Garne, Ester, additional, Gatt, Miriam, additional, Haeusler, Martin, additional, Khoshnood, Babak, additional, Lelong, Nathalie, additional, Kinsner-Ovaskainen, Agnieszka, additional, Kiuru-Kuhlefelt, Sonja, additional, Klungsoyr, Kari, additional, Latos-Bielenska, Anna, additional, Limb, Elizabeth, additional, O'Mahony, Mary T, additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Sayers, Gerardine, additional, Sipek, Antonin, additional, Stevens, Sarah, additional, Tucker, David, additional, Verellen-Dumoulin, Christine, additional, de Walle, Hermien E. K., additional, Wellesley, Diana, additional, Wertelecki, Wladimir, additional, and Bermejo-Sanchez, Eva, additional
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- 2021
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22. Inception to ConcePTION: A conceptual framework for characterizing pharmacoepidemiologic data sources. A study from the ConcePTION project
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Pajouheshnia, Romin, Thurin, Nicolas H., Roberto, Giuseppe, Dodd, Caitlin, Hyeraci, Giulia, Bartolini, Claudia, Paoletti, Olga, Nordeng, Hedvig, Wallach-Kildemoes, Helle, Ehrenstein, Vera, Dudukina, Elena, Macdonald, Thomas, Paoli, Giorgia, Loane, Maria, Damase-Michel, Christine, Beau, Anna-Belle, Droz-Perroteau, Cecile, Lassalle, Regis, Swart-Polinder, Karin, Schink, Tania, Cavero-Carbonell, Clara, Barrachina-Bonet, Laia, Gomez-Lumbreras, Ainhoa, Giner-Soriano, Maria, Aragon, Maria, Neville, Amanda J., Armaroli, Annarita, Puccini, Aurora, Pierini, Anna, Ientile, Valentina, Trifiro, Gianluca, Gatt, Miriam, Rissmann, Anke, Leinonen, Maarit K., Martikainen, Visa, Jordan, Sue, Georgiou, Mary E., Cunnington, Marianne, Sturkenboom, Miriam, and Rosa Gini
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- 2021
23. Variations in use of childbirth interventions in 13 high-income countries : a multinational cross-sectional study
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Seijmonsbergen-Schermers, Anna E., van den Akker, Thomas, Rydahl, Eva, Beeckman, Katrien, Bogaerts, Annick, Binfa, Lorena, Frith, Lucy, Gross, Mechthild M., Misselwitz, Björn, Hálfdánsdóttir, Berglind, Daly, Deirdre, Corcoran, Paul, Calleja-Agius, Jean, Calleja, Neville, Gatt, Miriam, Vika Nilsen, Anne Britt, Declercq, Eugene, Gissler, Mika, Heino, Anna, Lindgren, Helena, de Jonge, Ank, Seijmonsbergen-Schermers, Anna E., van den Akker, Thomas, Rydahl, Eva, Beeckman, Katrien, Bogaerts, Annick, Binfa, Lorena, Frith, Lucy, Gross, Mechthild M., Misselwitz, Björn, Hálfdánsdóttir, Berglind, Daly, Deirdre, Corcoran, Paul, Calleja-Agius, Jean, Calleja, Neville, Gatt, Miriam, Vika Nilsen, Anne Britt, Declercq, Eugene, Gissler, Mika, Heino, Anna, Lindgren, Helena, and de Jonge, Ank
- Abstract
Background Variations in intervention rates, without subsequent reductions in adverse outcomes, can indicate overuse. We studied variations in and associations between commonly used childbirth interventions and adverse outcomes, adjusted for population characteristics. Methods and findings In this multinational cross-sectional study, existing data on 4,729,307 singleton births at ≥37 weeks in 2013 from Finland, Sweden, Norway, Denmark, Iceland, Ireland, England, the Netherlands, Belgium, Germany (Hesse), Malta, the United States, and Chile were used to describe variations in childbirth interventions and outcomes. Numbers of births ranged from 3,987 for Iceland to 3,500,397 for the USA. Crude data were analysed in the Netherlands, or analyseddata were shared with the principal investigator. Strict variable definitions were used and information on data quality was collected. Intervention rates were described for each country and stratified by parity. Uni- and multivariable analyses were performed, adjusted for population characteristics, and associations between rates of interventions, population characteristics, and outcomes were assessed using Spearman’s rank correlation coefficients. Considerable intercountry variations were found for all interventions, despite adjustments for population characteristics. Adjustments for ethnicity and body mass index changed odds ratios for augmentation of labour and episiotomy. Largest variations were found for augmentation of labour, pain relief, episiotomy, instrumental birth, and cesarean section (CS). Percentages of births at ≥42 weeks varied from 0.1% to 6.7%. Rates among nulliparous versus multiparous women varied from 56% to 80% versus 51% to 82% for spontaneous onset of labour; 14% to 36% versus 8% to 28% for induction of labour; 3% to 13% versus 7% to 26% for prelabour CS; 16% to 48% versus 12% to 50% for overall CS; 22% to 71% versus 7% to 38% for augmentation of labour; 50% to 93% versus 25% to 86% for any intrapartum pa
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- 2021
24. Signal Detection in EUROmediCAT : Identification and Evaluation of Medication-Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference
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Cavadino, Alana, Sandberg, Lovisa, Ohman, Inger, Bergvall, Tomas, Star, Kristina, Dolk, Helen, Loane, Maria, Addor, Marie-Claude, Barisic, Ingeborg, Cavero-Carbonell, Clara, Garne, Ester, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Latos-Bielenska, Anna, Lelong, Nathalie, Lutke, Renee, Materna-Kiryluk, Anna, Nelen, Vera, Nevill, Amanda, O'Mahony, Mary, Mokoroa, Olatz, Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Wiesel, Awi, Yevtushok, Lyubov, Morris, Joan K., Cavadino, Alana, Sandberg, Lovisa, Ohman, Inger, Bergvall, Tomas, Star, Kristina, Dolk, Helen, Loane, Maria, Addor, Marie-Claude, Barisic, Ingeborg, Cavero-Carbonell, Clara, Garne, Ester, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Latos-Bielenska, Anna, Lelong, Nathalie, Lutke, Renee, Materna-Kiryluk, Anna, Nelen, Vera, Nevill, Amanda, O'Mahony, Mary, Mokoroa, Olatz, Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Wiesel, Awi, Yevtushok, Lyubov, and Morris, Joan K.
- Abstract
Introduction Knowledge on the safety of medication use during pregnancy is often sparse. Pregnant women are generally excluded from clinical trials, and there is a dependence on post-marketing surveillance to identify teratogenic medications. Aims This study aimed to identify signals of potentially teratogenic medications using EUROmediCAT registry data on medication exposure in pregnancies with a congenital anomaly, and to investigate the use of VigiBase reports of adverse events of medications in the evaluation of these signals. Methods Signals of medication-congenital anomaly associations were identified in EUROmediCAT (21,636 congenital anomaly cases with 32,619 medication exposures), then investigated in a subset of VigiBase (45,749 cases and 165,121 exposures), by reviewing statistical reporting patterns and VigiBase case reports. Evidence from the literature and quantitative and qualitative aspects of both datasets were considered before recommending signals as warranting further independent investigation. Results EUROmediCAT analysis identified 49 signals of medication-congenital anomaly associations. Incorporating investigation in VigiBase and the literature, these were categorised as follows: four non-specific medications; 11 likely due to maternal disease; 11 well-established teratogens; two reviewed in previous EUROmediCAT studies with limited additional evidence; and 13 with insufficient basis for recommending follow-up. Independent investigations are recommended for eight signals: pregnen (4) derivatives with limb reduction; nitrofuran derivatives with cleft palate and patent ductus arteriosus; salicylic acid and derivatives with atresia or stenosis of other parts of the small intestine and tetralogy of Fallot; carbamazepine with atrioventricular septal defect and severe congenital heart defect; and selective beta-2-adrenoreceptor agonists with posterior urethral valve and/or prune belly. Conclusion EUROmediCAT data should continue to be used for signa
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- 2021
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25. International versus national growth charts for identifying small and large-for-gestational age newborns: A population-based study in 15 European countries
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Hocquette, A., Durox, Mélanie, Wood, Rachael, Klungsoyr, Kari, Szamotulska, Katarzyna, Berrut, Sylvie, Rihs, Tonia, Kyprianou, Theopisti, Sakkeus, Luule, Lecomte, Aline, Zile, Irisa, Karlin, Sophie, Klimont, Jeannette, Barros, Henrique, Gatt, Miriam, Isakova, Jelena, Blondel, Béatrice, Gissler, Mika, Zeitlin, Jennifer, Hocquette, A., Durox, Mélanie, Wood, Rachael, Klungsoyr, Kari, Szamotulska, Katarzyna, Berrut, Sylvie, Rihs, Tonia, Kyprianou, Theopisti, Sakkeus, Luule, Lecomte, Aline, Zile, Irisa, Karlin, Sophie, Klimont, Jeannette, Barros, Henrique, Gatt, Miriam, Isakova, Jelena, Blondel, Béatrice, Gissler, Mika, and Zeitlin, Jennifer
- Abstract
Background: To inform the on-going debate about the use of universal prescriptive versus national intrauterine growth charts, we compared perinatal mortality for small and large-for-gestational-age (SGA/LGA) infants according to international and national charts in Europe. Methods: We classified singleton births from 33 to 42 weeks of gestation in 2010 and 2014 from 15 countries (N = 1,475,457) as SGA (birthweight <10th percentile) and LGA (>90th percentile) using the international Intergrowth-21st newborn standards and national charts based on the customised charts methodology. We computed sex-adjusted odds ratios (aOR) for stillbirth, neonatal and extended perinatal mortality by this classification using multilevel models. Findings: SGA and LGA prevalence using national charts were near 10% in all countries, but varied according to international charts with a north to south gradient (3.0% to 10.1% and 24.9% to 8.0%, respectively). Compared with appropriate for gestational age (AGA) infants by both charts, risk of perinatal mortality was increased for SGA by both charts (aOR[95% confidence interval (CI)]=6.1 [5.6–6.7]) and infants reclassified by international charts from SGA to AGA (2.7 [2.3–3.1]), but decreased for those reclassified from AGA to LGA (0.6 [0.4–0.7]). Results were similar for stillbirth and neonatal death. Interpretation: Using international instead of national charts in Europe could lead to growth restricted infants being reclassified as having normal growth, while infants with low risks of mortality could be reclassified as having excessive growth. Funding: InfAct Joint Action, CHAFEA Grant n°801,553 and EU/EFPIA Innovative Medicines Initiative 2 Joint Undertaking ConcePTION grant n°821,520. AH received a PhD grant from EHESP., SCOPUS: ar.j, info:eu-repo/semantics/published
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- 2021
26. Surveillance of multiple congenital anomalies; searching for new associations
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Morris, Joan K., Bergman, Jorieke E. H., Barisic, Ingeborg, Wellesley, Diana, Tucker, David, Limb, Elizabeth, Addor, Marie-Claude, Cavero-Carbonell, Clara, Matias Dias, Carlos, Draper, Elisabeth S., Echevarría-González-de-Garibay, Luis Javier, Gatt, Miriam, Klungsøyr, Kari, Lelong, Nathalie, Luyt, Karen, Materna-Kiryluk, Anna, Nelen, Vera, Neville, Amanda, Perthus, Isabelle, Pierini, Anna, Randrianaivo-Ranjatoelina, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Sayers, Geraldine, Wertelecki, Wladimir, Kinsner-Ovaskainen, Agnieszka, and Garne, Ester
- Abstract
Many human teratogens are associated with a spectrum of congenital anomalies rather than a single defect, and therefore the identification of congenital anomalies occurring together more frequently than expected may improve the detection of teratogens. Thirty-two EUROCAT congenital anomaly registries covering 6,599,765 births provided 123,566 cases with one or more major congenital anomalies (excluding chromosomal and genetic syndromes) for the birth years 2008–2016. The EUROCAT multiple congenital anomaly algorithm identified 8804 cases with two or more major congenital anomalies in different organ systems, that were not recognized as part of a syndrome or sequence. For each pair of anomalies, the odds of a case having both anomalies relative to having only one anomaly was calculated and the pvalue was estimated using a two-sided Fisher’s exact test. The Benjamini–Hochberg procedure adjusted pvalues to control the false discovery rate and pairs of anomalies with adjusted pvalues < 0.05 were identified. A total of 1386 combinations of two anomalies were analyzed. Out of the 31 statistically significant positive associations identified, 20 were found to be known associations or sequences already described in the literature and 11 were considered “potential new associations” by the EUROCAT Coding and Classification Committee. After a review of the literature and a detailed examination of the individual cases with the anomaly pairs, six pairs remained classified as new associations. In summary, systematically searching for congenital anomalies occurring together more frequently than expected using the EUROCAT database is worthwhile and has identified six new associations that merit further investigation.
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- 2023
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27. The second European Perinatal Health Report: documenting changes over 6 years in the health of mothers and babies in Europe
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Zeitlin, J, Mohangoo, A D, Delnord, M, Cuttini, M, Haidinger, Gerald, Alexander, Sophie, Pavlou, Pavlos, Velebil, Petr, Langhoff Roos, Jens, Sakkeus, Luule, Gissler, Mika, Blondel, Béatrice, Lack, Nicholas, Antsaklis, Aris, Berbik, István, Ólafsdóttir, Helga Sól, Bonham, Sheelagh, Cuttini, Marina, Misins, Janis, Jaselioniene, Jone, Wagener, Yolande, Gatt, Miriam, Nijhuis, Jan, Klungsøyr, Kari, Szamotulska, Katarzyna, Barros, Henrique, Horga, Mihai, Čáp, Ján, Novak-Antolic, Živa, Bolúmar, Francisco, Gottvall, Karin, Berrut, Sylvie, Macfarlane, Alison, Zeitlin, Jennifer, Mohangoo, Ashna, Delnord, Marie, Alexander, Sophie, Blondel, Béatrice, Bouvier-Colle, Marie-Hélène, Dattani, Nirupa, Gissler, Mika, Macfarlane, Alison, van der Pal, Karin, Szamotulska, Katarzyna, and Zhang, Wei Hong
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- 2013
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28. Producing valid statistics when legislation, culture, and medical practices differ for births at or before the threshold of survival: Report of a European workshop
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Smith, L. K. Blondel, B. Zeitlin, J. Haidinger, Gerald and Alexander, Sophie Kolarova, Rumyana Rodin, Urelija and Kyprianou, Theopisti Velebil, Petr Mortensen, Laust Sakkeus, Luule Gissler, Mika Blondel, Beatrice Heller, Guenther and Lack, Nicholas Antsaklis, Aris Berbik, Istvan Olafsdottir, Helga Sol Bonham, Sheelagh Cuttini, Marina Misins, Janis and Isakova, Jelena Wagener, Yolande Gatt, Miriam Nijhuis, Jan and Klungsoyr, Kari Szamotulska, Katarzyna Barros, Henrique and Horga, Mihai Cap, Jan Tul, Natasa Bolumar, Francisco and Gottvall, Karin Kallen, Karin Berrut, Sylvan Riggenbach, Melanie Macfarlane, Alison Zeitlin, Jennifer Delnord, Marie and Durox, Melanie Hindori-Mohangoo, Ashna Euro-Peristat Sci Comm
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- 2020
29. Producing valid statistics when legislation, culture and medical practices differ for births at or before the threshold of survival: report of a European workshop
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Smith, Lk, Blondel, B, Zeitlin, J, Haidinger, Gerald, Alexander, Sophie, Rodin, Urelija, Kyprianou, Theopisti, Velebil, Petr, Mortensen, Laust, Sakkeus, Luule, Gissler, Mika, Heller, Günther, Lack, Nicholas, Antsaklis, Aris, Berbik, István, Ólafsdóttir, Helga Sól, Bonham, Sheelagh, Cuttini, Marina, Misins, Janis, Isakova, Jelena, Wagener, Yolande, Gatt, Miriam, Nijhuis, Jan, Szamotulska, Katarzyna, Barros, Henrique, Horga, Mihai, Cap, Jan, Tul, Natasa, Bolúmar, Francisco, Gottvall, Karin, Källén, Karin, Berrut, Sylvan, Riggenbach, Mélanie, Macfarlane, Alison, Delnord, Marie, Durox, Mélanie, Hindori‐Mohangoo, Ashna, Smith, Lk, Blondel, B, Zeitlin, J, Haidinger, Gerald, Alexander, Sophie, Rodin, Urelija, Kyprianou, Theopisti, Velebil, Petr, Mortensen, Laust, Sakkeus, Luule, Gissler, Mika, Heller, Günther, Lack, Nicholas, Antsaklis, Aris, Berbik, István, Ólafsdóttir, Helga Sól, Bonham, Sheelagh, Cuttini, Marina, Misins, Janis, Isakova, Jelena, Wagener, Yolande, Gatt, Miriam, Nijhuis, Jan, Szamotulska, Katarzyna, Barros, Henrique, Horga, Mihai, Cap, Jan, Tul, Natasa, Bolúmar, Francisco, Gottvall, Karin, Källén, Karin, Berrut, Sylvan, Riggenbach, Mélanie, Macfarlane, Alison, Delnord, Marie, Durox, Mélanie, and Hindori‐Mohangoo, Ashna
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- 2020
30. Changing risk factors for placental abruption: A case crossover study using routinely collected data from Finland, Malta and Aberdeen
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Anderson, Emma, primary, Raja, Edwin Amalraj, additional, Shetty, Ashalatha, additional, Gissler, Mika, additional, Gatt, Miriam, additional, Bhattacharya, Siladitya, additional, and Bhattacharya, Sohinee, additional
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- 2020
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31. Maternal preconception intake of folic acid in Malta
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Gatt, Miriam, Borg, Marika, Grech Mercieca, Elaine, and Calleja, Neville
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Pregnancy -- Nutritional aspects ,Preconception care -- Malta ,Folic acid -- Metabolism ,Folic acid in human nutrition ,Neural tube -- Abnormalities - Abstract
Background: Neural tube defects (NTDs) are serious birth defects arising from abnormalities in neural tube development during early embryogenesis. Research shows that taking folic acid (FA) prior to and throughout the first 12 weeks of pregnancy will significantly decrease the occurrence of NTDs. The prevalence of NTDs in Malta is 10.0/10,000 births, yet this rate can be brought down to 5.0-6.0/10,000 births with preconception FA. This study aims to investigate the maternal intake of preconception FA in Malta. Methods: The National Obstetric Information System (NOIS) collects detailed demographic, pregnancy, delivery and infant outcome data on all births in Malta. One of the variables recorded at the first antenatal visit is whether the mother took FA prior to pregnancy. NOIS data for 2015 was obtained, Excel and SPSS were used for analysis. Results: 4385 women delivered a baby in 2015, of these 1125 (25.7%) reported taking FA before pregnancy. Both univariate and multivariate logistic regression showed that maternal age, parity, education, nationality, locality of residence, marital status, planned pregnancy and use of artificial reproductive technology were all significantly associated with taking preconception FA (p, peer-reviewed
- Published
- 2019
32. Maternal risks associated with pregnancy in women with advanced maternal age
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Collict, Mandy, Muscat Baron, Yves, Gatt, Miriam, and Calleja, Neville
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Diabetes in pregnancy -- Malta ,Hypertension in pregnancy -- Malta ,Pregnancy -- Complications -- Malta ,Pregnant women -- Malta - Abstract
Introduction: The trend towards delayed motherhood has accelerated in developed countries over the last few decades. Advanced maternal age (AMA) is defined as age 35 years and older at the estimated date of delivery. Objective: The aim of this large retrospective cohort study is to assess for the association between AMA and adverse maternal outcomes after adjustment for confounding factors in maternal characteristics and in the obstetric history. Study Design: Mothers of 20 years and older, who delivered singleton babies in Malta and Gozo between 1st January 2000 and 31st December 2014 were studied. All data was derived from the National Obstetric Information System. Results: The study population included 55,943 singleton births. 12.2% (6,838) of mothers were between 35 – 39 years and 2.4% (1,325) were 40 years and older. Significant difference was found between maternal age and BMI (p < 0.0001), maternal smoking status (p < 0.0001), non-insulin dependent diabetes mellitus (p = 0.004), history of stillbirth (p < 0.0001), gestational diabetes (p < 0.0001), pregnancy – induced – hypertension (p = 0.008) and pre-eclampsia (p = 0.008). Significant difference was also found between maternal age and mode of delivery (p < 0.0001). Regression analysis revealed persistent significant differences between maternal age and different maternal outcomes. Conclusion: This study demonstrates that AMA in Malta significantly increases the risk for hypertension in pregnancy, gestational diabetes and caesarean delivery. Care providers need to be aware of these increased risks and adjust their obstetric management according to the individual to ensure optimal maternal outcomes., peer-reviewed
- Published
- 2019
33. Health information systems in Malta : past, present and future
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Gatt, Miriam and Distefano, Sandra
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Medical care -- Computer programs ,Medical care -- Data processing ,Information storage and retrieval systems -- Medical care -- Malta - Abstract
It is well documented and recognized internationally that good quality health information is essential to public health in its endeavor to protect and promote the health of a nation. The need for dedicated health information systems within the Ministry for Health in Malta was felt more than 30 years ago, when the Chief Government Medical Officer at the time called for the introduction and implementation of a health service information system. This led to the development of a dedicated unit with the aims of providing basic statistical and epidemiological information, conducting surveys and evaluating health programmes. Over the years, this unit has developed into the current Directorate for Health Information and Research which is now responsible for maintaining ten population-based Health Registers and a five yearly National Health Interview Survey, in addition to other ad hoc research. This article traces the development of health information systems in Malta from their inception in the early 1980s to date., peer-reviewed
- Published
- 2019
34. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study
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van de Putte, Romy, primary, van Rooij, Iris A. L. M., additional, Marcelis, Carlo L. M., additional, Guo, Michel, additional, Brunner, Han G., additional, Addor, Marie-Claude, additional, Cavero-Carbonell, Clara, additional, Dias, Carlos M., additional, Draper, Elizabeth S., additional, Etxebarriarteun, Larraitz, additional, Gatt, Miriam, additional, Haeusler, Martin, additional, Khoshnood, Babak, additional, Klungsoyr, Kari, additional, Kurinczuk, Jenny J., additional, Lanzoni, Monica, additional, Latos-Bielenska, Anna, additional, Luyt, Karen, additional, O’Mahony, Mary T., additional, Miller, Nicola, additional, Mullaney, Carmel, additional, Nelen, Vera, additional, Neville, Amanda J., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Randrianaivo, Hanitra, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Schaub, Bruno, additional, Tucker, David, additional, Wellesley, Diana, additional, Wiesel, Awi, additional, Zymak-Zakutnia, Natalya, additional, Loane, Maria, additional, Barisic, Ingeborg, additional, de Walle, Hermien E. K., additional, Roeleveld, Nel, additional, and Bergman, Jorieke E. H., additional
- Published
- 2019
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35. Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study
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Bakker, Marian K, primary, Bergman, Jorieke E H, additional, Krikov, Sergey, additional, Amar, Emmanuelle, additional, Cocchi, Guido, additional, Cragan, Janet, additional, de Walle, Hermien E K, additional, Gatt, Miriam, additional, Groisman, Boris, additional, Liu, Shiliang, additional, Nembhard, Wendy N, additional, Pierini, Anna, additional, Rissmann, Anke, additional, Chidambarathanu, Shanthi, additional, Sipek Jr, Antonin, additional, Szabova, Elena, additional, Tagliabue, Giovanna, additional, Tucker, David, additional, Mastroiacovo, Pierpaolo, additional, and Botto, Lorenzo D, additional
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- 2019
- Full Text
- View/download PDF
36. Teenage pregnancy in Malta
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Grech, Victor E., Gatt, Miriam, Camilleri, Raymond, Camilleri, Erin, and Calleja, Neville
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Sexual abstinence ,Sexually transmitted diseases -- Prevention ,education ,Sex instruction -- Malta ,Teenage pregnancy -- Malta - Abstract
Introduction Underage pregnancy may blight a young woman’s life. Teenage pregnancy rates vary widely across the world and have poorer pregnancy outcomes than non-teen pregnancies. Local Personal, Social and Career Development Education (PSCD) teaching is stipulated per curricula. This study was carried out by the Divisions of Education and Health in order to ascertain whether there are any differences in teenage pregnancy rates between State and non-State schools. Methods Ethical approval and data protection approval was obtained. The Health Division, identified pregnancies with mothers with age ≤18 years, for 2011-2015. Secondary schoosl attended were identified and an anonymised dataset was then passed on to the principal investigator for analysis. Results Teenage deliveries were significantly less in Non-State when compared to State schools, for each year studied, as well as for the aggregate of the total (p, peer-reviewed
- Published
- 2017
37. Folic acid : recommendations and interventions to increase women’s peri-conceptional intake of folic acid
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Gatt, Miriam, Muscat Baron, Yves, Lautier, Elaine Claire, and Calleja, Neville
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Pregnancy -- Nutritional aspects ,Folic acid -- Metabolism ,Health promotion ,Folic acid in human nutrition - Abstract
Folic acid is known to be beneficial in pregnancy and has been shown to prevent severe and devastating birth defects including neural tube defects. Health Authorities and Governments around the world have taken several initiatives in order to increase women’s peri-conceptional folic acid intake, varying from issuing guidelines, undertaking extensive health promotion campaigns to mandatory food fortification of staple foods with folic acid. These interventions have had varying success in preventing neural tube defects. This paper is a comprehensive review of the current literature, putting together and summarizing the various initiatives undertaken by different countries and their success or otherwise in increasing women’s peri-conceptional folic acid intake and preventing neural tube defects., peer-reviewed
- Published
- 2017
38. Maternal factors and the male to female birth ratio in Malta
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Grech, Victor E., Gatt, Miriam, Mamo, Julian, and Calleja, Neville
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Abortion -- Statistics ,Newborn infants -- Malta ,Sex ratio -- Malta - Abstract
Introduction: The sex ratio at birth is commonly calculated as the total male live births divided by all live births, and is represented as M/F. A multitude of factors influence M/F, especially stress, which increases male foetal losses during pregnancy. This study was carried out in order to ascertain whether any maternal or perinatal relevant factors influenced M/F in Malta. Methods: National Obstetric Information System data was used for the period 2012-2015. Non-Maltese mothers were excluded. Factors analysed were maternal age, marital status, education, body mass index, regularity of menses, utilisation of assisted reproductive technology, previous diabetes mellitus, previous miscarriages, abortions, ectopic pregnancies, vaginal deliveries, caesarean sections, livebirths, early and late neonatal deaths, stillbirths and premature deliveries. Intra-partum conditions included infection, cardiovascular disorders and all forms of diabetes mellitus. Results: This study analysed 14498 births. None of the above mentioned variables was significantly linked to the M/F ratio. Discussion: Our dataset failed to find any variables that influenced M/F, including stressing variables. However our study may have been underpowered due to the small numbers of births and the relative rarity of the various conditions. Alternatively, in Malta, such variables may produce little or no stress due to hitherto unknown mitigating factor/s., peer-reviewed
- Published
- 2017
39. Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum
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Barišić, Ingeborg, Odak, Ljubica, Loane, M., Garne, Ester, Wellesley, Diana, Calzolari, Elisa, Dolk, Helen, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke, Bianca, Sebastiano, Boyd, Patricia, Draper, Elizabeth S, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Latos-Bielenska, Anna, McDonnell, Bob, Pierini, Anna, Rankin, Judith, Rissmann, Anke, Queisser-Luft, Annette, Verellen- Dumoulin, Christine, Doray, Berenice, Dias, Carlos Matias, Nelen, Vera, O´Mahony, Mary, Scarano, Gioacchino, Tucker, David, Klungsoyr, Kari, and Reproductive Origins of Adult Health and Disease (ROAHD)
- Subjects
Male ,Pediatrics ,Developmental Disabilities ,Goldenhar syndrome ,GOLDENHAR-SYNDROME ,Pregnancy ,Risk Factors ,Prenatal Diagnosis ,Epidemiology ,FERTILIZATION ,Prevalence ,Registries ,DYSPLASIA ,Genetics (clinical) ,DOMINANT OCULOAURICULOVERTEBRAL SPECTRUM ,education.field_of_study ,ABNORMALITIES ,3. Good health ,Europe ,Phenotype ,MANIFESTATIONS ,Population Surveillance ,OCULOAURICULOFRONTONASAL SYNDROME ,Female ,epidemiology ,Adult ,medicine.medical_specialty ,Oculo-auriculo-vertebral spectrum ,congenital anomalies ,Population ,Prenatal diagnosis ,Article ,CLASSIFICATION ,Young Adult ,Genetics ,medicine ,Humans ,Abnormalities, Multiple ,education ,Chromosome Aberrations ,oculo-auriculo-vertebral spectrum ,business.industry ,Microtia ,medicine.disease ,OAVS ,Hemifacial microsomia ,Etiology ,HEMIFACIAL MICROSOMIA ,business - Abstract
Oculo-auriculo-vertebral spectrum is a complex developmental disorder characterised mainly by anomalies of the ear, hemifacial microsomia, epibulbar dermoids and vertebral anomalies. The aetiology is largely unknown, and the epidemiological data are limited and inconsistent. We present the largest population-based epidemiological study to date, using data provided by the large network of congenital anomalies registries in Europe. The study population included infants diagnosed with oculo-auriculo-vertebral spectrum during the 1990-2009 period from 34 registries active in 16 European countries. Of the 355 infants diagnosed with oculo-auriculo-vertebral spectrum, there were 95.8% (340/355) live born, 0.8% (3/355) fetal deaths, 3.4% (12/355) terminations of pregnancy for fetal anomaly and 1.5% (5/340) neonatal deaths. In 18.9%, there was prenatal detection of anomaly/anomalies associated with oculo-auriculo-vertebral spectrum, 69.7% were diagnosed at birth, 3.9% in the first week of life and 6.1% within 1 year of life. Microtia (88.8%), hemifacial microsomia (49.0%) and ear tags (44.4%) were the most frequent anomalies, followed by atresia/stenosis of external auditory canal (25.1%), diverse vertebral (24.3%) and eye (24.3%) anomalies. There was a high rate (69.5%) of associated anomalies of other organs/systems. The most common were congenital heart defects present in 27.8% of patients. The prevalence of oculo-auriculo-vertebral spectrum, defined as microtia/ ear anomalies and at least one major characteristic anomaly, was 3.8 per 100 000 births. Twinning, assisted reproductive techniques and maternal pre-pregnancy diabetes were confirmed as risk factors. The high rate of different associated anomalies points to the need of performing an early ultrasound screening in all infants born with this disorder.
- Published
- 2014
40. Trends in congenital anomalies in Europe from 1980 to 2012
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Morris, Joan K., primary, Springett, Anna L., additional, Greenlees, Ruth, additional, Loane, Maria, additional, Addor, Marie-Claude, additional, Arriola, Larraitz, additional, Barisic, Ingeborg, additional, Bergman, Jorieke E. H., additional, Csaky-Szunyogh, Melinda, additional, Dias, Carlos, additional, Draper, Elizabeth S., additional, Garne, Ester, additional, Gatt, Miriam, additional, Khoshnood, Babak, additional, Klungsoyr, Kari, additional, Lynch, Catherine, additional, McDonnell, Robert, additional, Nelen, Vera, additional, Neville, Amanda J., additional, O'Mahony, Mary, additional, Pierini, Anna, additional, Queisser-Luft, Annette, additional, Randrianaivo, Hanitra, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Kurinczuk, Jennifer, additional, Tucker, David, additional, Verellen-Dumoulin, Christine, additional, Wellesley, Diana, additional, and Dolk, Helen, additional
- Published
- 2018
- Full Text
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41. Insulin analogues use in pregnancy among women with pregestational diabetes mellitus and risk of congenital anomaly: a retrospective population-based cohort study
- Author
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Wang, Hao, primary, Wender-Ozegowska, Ewa, additional, Garne, Ester, additional, Morgan, Margery, additional, Loane, Maria, additional, Morris, Joan K, additional, Bakker, Marian K, additional, Gatt, Miriam, additional, de Walle, Hermien, additional, Jordan, Susan, additional, Materna-Kiryluk, Anna, additional, Nelen, Vera, additional, Thys, Guy, additional, Wiesel, Awi, additional, Dolk, Helen, additional, and de Jong-van den Berg, Lolkje T W, additional
- Published
- 2018
- Full Text
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42. EUROmediCAT signal detection: a systematic method for identifying potential teratogenic medication
- Author
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Luteijn, Johannes M., Morris, Joan K., Garne, Ester, Given, Joanne, de Jong-van den Berg, Lolkje, Addor, Marie-Claude, Bakker, Marian, Barisic, Ingeborg, Gatt, Miriam, Klungsoyr, Kari, Latos- Bielenska, Anna, Lelong, Nathalie, Nelen, Vera, Neville, Amanda, O'Mahony, Mary, Pierini, Anna, Tucker, David, de Walle, Hermien, Wiesel, Awi, Loane, Maria, Dolk, Helen, PharmacoTherapy, -Epidemiology and -Economics, and Reproductive Origins of Adult Health and Disease (ROAHD)
- Subjects
Adult ,pharmacoepidemiology ,drug safety ,Databases, Factual ,Congenital Abnormalities ,Young Adult ,Pregnancy ,adverse drug reactions ,congenital anomalies ,pharmacovigilance ,pregnancy ,BIRTH-DEFECTS ,DRUGS ,Adverse Drug Reaction Reporting Systems ,Humans ,Registries ,Pharmacoepidemiology ,Abnormalities, Drug-Induced ,FALSE DISCOVERY RATE ,Europe ,Teratogens ,PHARMACOVIGILANCE ,REGISTRY ,Case-Control Studies ,ACID ,Female - Abstract
AIMS: Information about medication safety in pregnancy is inadequate. We aimed to develop a signal detection methodology to routinely identify unusual associations between medications and congenital anomalies using data collected by 15 European congenital anomaly registries.METHODS: EUROmediCAT database data for 14 950 malformed foetuses/babies with first trimester medication exposures in 1995-2011 were analyzed. The odds of a specific medication exposure (coded according to chemical substance or subgroup) for a specific anomaly were compared with the odds of that exposure for all other anomalies for 40 385 medication anomaly combinations in the data. Simes multiple testing procedure with a 50% false discovery rate (FDR) identified associations least likely to be due to chance and those associations with more than two cases with the exposure and the anomaly were selected for further investigation. The methodology was evaluated by considering the detection of well-known teratogens.RESULTS: The most common exposures were genitourinary system medications and sex hormones (35.2%), nervous system medications (28.0%) and anti-infectives for systemic use (25.7%). Fifty-two specific medication anomaly associations were identified. After discarding 10 overlapping and three protective associations, 39 associations were selected for further investigation. These associations included 16 which concerned well established teratogens, valproic acid (2) and maternal diabetes represented by use of insulin (14).CONCLUSIONS: Medication exposure data in the EUROmediCAT central database can be analyzed systematically to determine a manageable set of associations for validation and then testing in independent datasets. Detection of teratogens depends on frequency of exposure, level of risk and teratogenic specificity.
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- 2016
43. Variations in multiple birth rates and impact on perinatal outcomes in Europe
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Heino, Anna, Gissler, Mika, Hindori-Mohangoo, Ashna D., Blondel, Béatrice, Klungsøyr, Kari, Verdenik, Ivan, Mierzejewska, Ewa, Velebil, Petr, Ólafsdóttir, Helga Sól, Macfarlane, Alison, Zeitlin, Jennifer, Haidinger, Gerald, Alexander, Sophie, Pavlou, Pavlos, Mortensen, Laust, Sakkeus, Luule, Lack, Nicholas, Antsaklis, Aris, Berbik, Istvan, Bonham, Sheelagh, Cuttini, Marina, Misins, Janis, Jaselioniene, Jone, Wagener, Yolande, Gatt, Miriam, Nijhuis, Jan, van Der Pal, Karin, Klungsoyr, Kari, Szamotulska, Katarzyna, Barros, Henrique, Horga, Mihai, Cap, Jan, Tul Mandić, Natasa, Bolúmar, Francisco, Gottvall, Karin, Berrut, Sylvie, Klimont, Jeannette, Zhang, Wei Hong, Dramaix-Wilmet, Michèle, Van Humbeeck, Mélissa, Leroy, Charlotte, Minsart, Anne Frédérique, Van Leeuw, Virginie, Martens, Evelyne, De Spiegelaere, Myriam, Verkruyssen, Freddy, Willems, Michel, Aelvoet, Willem, Tafforeau, Jean, Hukkelhoven, Chantal, and [ 1 ] THL Natl Inst Hlth & Welf, Helsinki, Finland [ 2 ] TNO, Netherlands Org Appl Sci Res, Dept Child Hlth, Leiden, Netherlands [ 3 ] Anton de Kom Univ Suriname, Fac Med Sci, Dept Publ Hlth, Paramaribo, Surinam [ 4 ] Paris Descartes Univ, Ctr Epidemiol & Biostat U1153, Obstetr Perinatal & Paediat Epidemiol Res Team, INSERM, Paris, France [ 5 ] Univ Bergen, Dept Global Publ Hlth & Primary Care, N-5018 Bergen, Norway [ 6 ] Norwegian Inst Publ Hlth, Med Birth Registry Norway, N-5018 Bergen, Norway [ 7 ] Univ Ljubljana, Med Ctr, Ljubljana 61000, Slovenia [ 8 ] Natl Res Inst Mother & Child, Dept Epidemiol, Warsaw, Poland [ 9 ] Inst Care Mother & Child, Prague, Czech Republic [ 10 ] Landspitali Univ Hosp, Dept Obstet & Gynaecol, Reykjavik, Iceland Organization-Enhanced Name(s) Landspitali National University Hospital
- Subjects
Maternal Health ,Perinatal Death ,Psychologie appliquée ,lcsh:Medicine ,Labor and Delivery ,0302 clinical medicine ,Life ,Pregnancy ,CH - Child Health ,Infant Mortality ,Medicine and Health Sciences ,Birth Rate ,lcsh:Science ,SAW12 ,education.field_of_study ,030219 obstetrics & reproductive medicine ,Multidisciplinary ,Obstetrics ,Mortality rate ,Gestational age ,Obstetrics and Gynecology ,Pregnancies ,Sciences bio-médicales et agricoles ,Stillbirth ,Europe ,Health ,Fetal Mortality ,Premature Birth ,Female ,Pregnancy, Multiple ,Biologie ,Healthy Living ,Maternal Age ,Research Article ,Adult ,medicine.medical_specialty ,Death Rates ,Population ,Preterm Birth ,RT ,Birth rate ,Europe/epidemiology ,03 medical and health sciences ,Population Metrics ,030225 pediatrics ,medicine ,Very Preterm Birth ,Humans ,Life Science ,education ,Fetal Death ,Demography ,Population Biology ,business.industry ,lcsh:R ,Infant, Newborn ,Parturition ,Infant ,Biology and Life Sciences ,Neonates ,Birth Rates ,medicine.disease ,Pregnancy Complications ,Relative risk ,Tvíburar ,People and Places ,Birth ,Women's Health ,Multiple birth ,Fæðing ,lcsh:Q ,ELSS - Earth, Life and Social Sciences ,Healthy for Life ,business ,Developmental Biology - Abstract
Objective: Infants from multiple pregnancies have higher rates of preterm birth, stillbirth and neonatal death and differences in multiple birth rates (MBR) exist between countries. We aimed to describe differences in MBR in Europe and to investigate the impact of these differences on adverse perinatal outcomes at a population level. Methods: We used national aggregate birth data on multiple pregnancies, maternal age, gestational age (GA), stillbirth and neonatal death collected in the Euro-Peristat project (29 countries in 2010, N = 5 074 643 births). We also used European Society of Human Reproduction and Embryology (ESHRE) data on assisted conception and single embryo transfer (SET). The impact of MBR on outcomes was studied using meta-analysis techniques with randomeffects models to derive pooled risk ratios (pRR) overall and for four groups of country defined by their MBR. We computed population attributable risks (PAR) for these groups. Results: In 2010, the average MBR was 16.8 per 1000 women giving birth, ranging from 9.1 (Romania) to 26.5 (Cyprus). Compared to singletons, multiples had a nine-fold increased risk (pRR 9.4, 95% Cl 9.1-9.8) of preterm birth (, 0, SCOPUS: ar.j, info:eu-repo/semantics/published
- Published
- 2016
44. Prevention of birth defects
- Author
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Gatt, Miriam, Muscat Baron, Yves, Lautier, Elaine Claire, and Calleja, Neville
- Subjects
Fetus -- Abnormalities ,Folic acid ,Folic acid in human nutrition ,Neural tube -- Abnormalities ,Abnormalities, Human - Abstract
Folate is essential for normal cell division and as intrauterine fetal growth involves a process of rapidly dividing cells, there is a consequent increased requirement for folate at this time. Folate, and the synthetic form folic acid, is thus vital for the early development process of a healthy fetus and there is indisputable evidence that it can significantly reduce the risk of neural tube defects (NTDs). Further ongoing research suggests that folic acid supplementation in pregnancy is also associated with a decreased risk of other birth defects. This review gives an overview of the current literature related to the use of folic acid in the peri-conceptional period and prevention of birth defects, in particular NTDs., peer-reviewed
- Published
- 2016
45. Long term trends in prevalence of neural tube defects in Europe: population based study
- Author
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Khoshnood, Babak, Loane, Maria, Walle, Hermien de, Arriola, Larraitz, Addor, Marie-Claude, Barisic, Ingeborg, Beres, Judit, Bianchi, Fabrizio, Dias, Carlos, Draper, Elizabeth, Garne, Ester, Gatt, Miriam, Haeusler, Martin, Klungsoyr, Kari, Latos-Bielenska, Anna, Lynch, Catherine, McDonnell, Bob, Nelen, Vera, Neville, Amanda J, O’Mahony, Mary T, Queisser-Luft, Annette, Rankin, Judith, Rissmann, Anke, Ritvanen, Annukka, Rounding, Catherine, Sipek, Antonin, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Dolk, Helen, and Reproductive Origins of Adult Health and Disease (ROAHD)
- Subjects
ANOMALIES ,congenital, hereditary, and neonatal diseases and abnormalities ,FOOD FORTIFICATION ,SPINA-BIFIDA ,FOLIC-ACID FORTIFICATION ,SUPPLEMENTATION ,European Surveillance of Congenital Anomalies ,Folic Acid ,VITAMIN ,Pregnancy ,EUROCAT ,Prenatal Diagnosis ,VALPROIC ACID ,Prevalence ,Nacional Registry of Congenital Anomalies ,EPIDEMIOLOGY ,Prevention and Control ,Fetal Death ,Neural Tube Defect ,Portugal ,Research ,RENAC ,congenital anomalies ,epidemiology ,Congenital Anomalies ,Estados de Saúde e de Doença ,CONGENITAL-MALFORMATIONS ,PREVENTION ,nervous system diseases ,Europe ,Dietary Supplements ,Trends ,Determinantes da Saúde e da Doença - Abstract
Comment in: Mills JL, Dimopoulos A. Folic acid fortification for Europe? BMJ. 2015 Nov 24;351:h6198. doi: 10.1136/bmj.h6198. Study question: What are the long term trends in the total (live births, fetal deaths, and terminations of pregnancy for fetal anomaly) and live birth prevalence of neural tube defects (NTD) in Europe, where many countries have issued recommendations for folic acid supplementation but a policy for mandatory folic acid fortification of food does not exist? Methods: This was a population based, observational study using data on 11 353 cases of NTD not associated with chromosomal anomalies, including 4162 cases of anencephaly and 5776 cases of spina bifida from 28 EUROCAT (European Surveillance of Congenital Anomalies) registries covering approximately 12.5 million births in 19 countries between 1991 and 2011. The main outcome measures were total and live birth prevalence of NTD, as well as anencephaly and spina bifida, with time trends analysed using random effects Poisson regression models to account for heterogeneities across registries and splines to model non-linear time trends. Summary answer and limitations: Overall, the pooled total prevalence of NTD during the study period was 9.1 per 10 000 births. Prevalence of NTD fluctuated slightly but without an obvious downward trend, with the final estimate of the pooled total prevalence of NTD in 2011 similar to that in 1991. Estimates from Poisson models that took registry heterogeneities into account showed an annual increase of 4% (prevalence ratio 1.04, 95% confidence interval 1.01 to 1.07) in 1995-99 and a decrease of 3% per year in 1999-2003 (0.97, 0.95 to 0.99), with stable rates thereafter. The trend patterns for anencephaly and spina bifida were similar, but neither anomaly decreased substantially over time. The live birth prevalence of NTD generally decreased, especially for anencephaly. Registration problems or other data artefacts cannot be excluded as a partial explanation of the observed trends (or lack thereof) in the prevalence of NTD. What this study adds: In the absence of mandatory fortification, the prevalence of NTD has not decreased in Europe despite longstanding recommendations aimed at promoting peri-conceptional folic acid supplementation and existence of voluntary folic acid fortification. The study was funded by the European Public Health Commission, EUROCAT Joint Action 2011-2013. HD and ML received support from the European Commission DG Sanco during the conduct of this study.
- Published
- 2015
46. Use of insulin analogs in pregestational diabetes and risk of congenital anomalies
- Author
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Wang, Hao, Wender-Ozegowska, Ewa, Garne, Ester, Morgan, Margery, Loane, Maria, Materna-Kiryluk, Anna, Wiesel, Awi, Jordan, Sue, Gatt, Miriam, Thys, Guy, Nelen, Vera, Bakker, Marian, De Walle, Hermien, and De Jong-Van Den Berg, Lolkje
- Subjects
diabetes mellitus *risk *congenital malformation *pharmacoepidemiology *risk management prevalence pregnancy first trimester pregnancy risk factor human female exposure classification congenital heart malformation register European population glycemic control fetus death spontaneous abortion *insulin derivative human insulin - Abstract
Background: The use of insulin analogs in pregnancy is increasing, but information on teratogenic risks is lacking. Available studies on insulin analogs during pregnancy are not sufficiently powered to evaluate the risk of specific major malformations. Objectives: The aim of this study was to evaluate the risk of major congenital anomalies associated with insulin analogs use in women with pregestational diabetes. Methods: A population-based cohort of pregestational diabetic pregnancies was established retrospectively from seven European regions covered by EUROCAT congenital anomaly registries. Major congenital malformations were defined according the EUROCAT classification. Results: A total of 1877 births to women with pregestational diabetes were enrolled in the study during 1996-2012. During the first trimester, 870 births (46.3%) were exposed to only human insulin, 397 births (21.2%) to only insulin analogs, and 394 births (20.1%) to both human insulin and insulin analogs. The proportion of still birth and spontaneous abortion (4.0%) is higher among only insulin analog group compared with only human insulin group (1.4%). Overall, 132 births (7.0%) with major congenital malformation were detected, of which seven were chromosomal. The prevalence of major congenital anomalies in births exposed to only insulin analogs (3.8%) during the first trimester was significantly lower than those exposed to only human insulin (8.6%); relative risk=0.42 (95%CI 0.24-0.73). This is largely due to the decreased prevalence of non-chromosomal congenital heart defects (CHD): relative risk=0.18 (95%CI 0.05-0.58). The decreased prevalence remained after adjusting for glycemic control, planned pregnancy, and region. The prevalence of non-CHD congenital anomalies among births exposed to only insulin analogs in the first trimester (3.0%) was lower than those exposed to only human insulin (4.0%), but not statistically significant. Conclusions: This study shows that first trimester exposure to insulin analogs did not increase the risk of congenital anomalies compared with exposure to human insulin. The decrease risk of congenital anomalies was driven by CHDs. The higher risk of fetal death in relation to insulin analogs warranted further investigation.
- Published
- 2015
47. Congenital Anomalies Associated with Trisomy 18 or Trisomy 13: A Registry-Based Study in 16 European Countries, 2000-2011
- Author
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Springett, Anna, Wellesley, Diana, Greenlees, Ruth, Loane, Maria, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke, Cavero-Carbonell, Clara, Csaky-Szunyogh, Melinda, Draper, Elizabeth S., Garne, Ester, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, Dias, Carlos Matias, McDonnell, Robert, Nelen, Vera, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Stoianova, Sylvia, Tuckerz, David, Zymak-Zakutnia, Natalya, Morris, Joan K., and Reproductive Origins of Adult Health and Disease (ROAHD)
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Adult ,Heart Defects, Congenital ,Male ,SEX-DIFFERENCES ,Time Factors ,Adolescent ,TRISOMIES ,Pregnancy Complications/diagnosis ,Gestational Age ,Trisomy ,Nervous System Malformations ,Europe/epidemiology ,Congenital Abnormalities ,Nervous System Malformations/diagnosis ,Young Adult ,Pregnancy ,Prenatal Diagnosis ,Prevalence ,Humans ,trisomy 18 ,MALFORMATIONS ,DOWN-SYNDROME ,Registries ,Fetal Death ,trisomy 13 ,Chromosomes, Human, Pair 18/genetics ,Chromosomes, Human, Pair 13 ,MORTALITY ,cardiac anomalies ,Registries/statistics & numerical data ,Infant, Newborn ,NATURAL-HISTORY ,DEFECTS ,Prognosis ,Trisomy/genetics ,Congenital Abnormalities/diagnosis ,Europe ,Pregnancy Complications ,Patau syndrome ,SURVIVAL ,Heart Defects, Congenital/diagnosis ,MATERNAL AGE ,Chromosomes, Human, Pair 13/genetics ,Female ,Chromosomes, Human, Pair 18 ,Trisomy 18 Syndrome ,Edwards syndrome - Abstract
The aim of this study was to examine the prevalence of trisomies 18 and 13 in Europe and the prevalence of associated anomalies. Twenty-five population-based registries in 16 European countries provided data from 2000-2011. Cases included live births, fetal deaths (20+ weeks' gestation), and terminations of pregnancy for fetal anomaly (TOPFAs). The prevalence of associated anomalies was reported in live births. The prevalence of trisomy 18 and trisomy 13 were 4.8 (95%CI: 4.7-5.0) and 1.9 (95%CI: 1.8-2.0) per 10,000 total births. Seventy three percent of cases with trisomy 18 or trisomy 13 resulted in a TOPFA. Amongst 468 live born babies with trisomy 18, 80% (76-83%) had a cardiac anomaly, 21% (17-25%) had a nervous system anomaly, 8% (6-11%) had esophageal atresia and 10% (8-13%) had an orofacial cleft. Amongst 240 Live born babies with trisomy 13, 57% (51-64%) had a cardiac anomaly, 39% (33-46%) had a nervous system anomaly, 30% (24-36%) had an eye anomaly, 44% (37-50%) had polydactyly and 45% (39-52%) had an orofacial cleft. For babies with trisomy 18 boys were less likely to have a cardiac anomaly compared with girls (OR = 0.48 (0.30-0.77) and with trisomy 13 were less likely to have a nervous system anomaly [OR = 0.46 (0.27-0.77)]. Babies with trisomy 18 or trisomy 13 do have a high proportion of associated anomalies with the distribution of anomalies being different in boys and girls. © 2015 Wiley Periodicals, Inc.
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- 2015
48. Variations in rates of severe perineal tears and episiotomies in 20 European countries: a study based on routine national data in Euro-Peristat Project
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Blondel, Béatrice, Zeitlin, Jennifer, Haidinger, Gerald, Pavlou, Pavlos, Velebil, Petr, Nybo Andersen, Anne Marie, Sakkeus, Luule, Lack, Nicholas, Antsaklis, Aris, Berbik, István, Karlin, Sophie, Ólafsdóttir, Helga Sól, Bonham, Sheelagh, Cuttini, Marina, Misins, Janis, Jaselioniene, Jone, Wagener, Yolande, Gatt, Miriam, Nijhuis, Jan, Klungsoyr, Kari, Szamotulska, Katarzyna, Bjarnadóttir, Ragnheidur Ingibjörg, Barros, Henrique, Horga, Mihai, Cap, Jan, Bolúmar, Francisco, Gottvall, Karin, Berrut, Sylvie, Macfarlane, Alison, Gissler, Mika, Langhoff-Roos, Jens, Novak-Antolič, Živa, Prunet, Caroline, Zhang, Wei Hong, Hindori-Mohangoo, Ashna AD, Blondel, Béatrice, Zeitlin, Jennifer, Haidinger, Gerald, Pavlou, Pavlos, Velebil, Petr, Nybo Andersen, Anne Marie, Sakkeus, Luule, Lack, Nicholas, Antsaklis, Aris, Berbik, István, Karlin, Sophie, Ólafsdóttir, Helga Sól, Bonham, Sheelagh, Cuttini, Marina, Misins, Janis, Jaselioniene, Jone, Wagener, Yolande, Gatt, Miriam, Nijhuis, Jan, Klungsoyr, Kari, Szamotulska, Katarzyna, Bjarnadóttir, Ragnheidur Ingibjörg, Barros, Henrique, Horga, Mihai, Cap, Jan, Bolúmar, Francisco, Gottvall, Karin, Berrut, Sylvie, Macfarlane, Alison, Gissler, Mika, Langhoff-Roos, Jens, Novak-Antolič, Živa, Prunet, Caroline, Zhang, Wei Hong, and Hindori-Mohangoo, Ashna AD
- Abstract
Introduction: Rates of severe perineal tears and episiotomies are indicators of obstetrical quality of care, but their use for international comparisons is complicated by difficulties with accurate ascertainment of tears and uncertainties regarding the optimal rate of episiotomies. We compared rates of severe perineal tears and episiotomies in European countries and analysed the association between these two indicators. Material and methods: We used aggregate data from national routine statistics available in the Euro-Peristat project. We compared rates of severe (third- and fourth-degree) tears and episiotomies in 2010 by mode of vaginal delivery (n = 20 countries), and investigated time trends between 2004 and 2010 (n = 9 countries). Statistical associations were assessed with Spearman's ranked correlations (rho). Results: In 2010 in all vaginal deliveries, rates of severe tears ranged from 0.1% in Romania to 4.9% in Iceland, and rates of episiotomies from 3.7% in Denmark to 75.0% in Cyprus. A negative correlation between the rates of episiotomies and severe tears was observed in all deliveries (rho = −0.66; p = 0.001), instrumental deliveries (rho = −0.67; p = 0.002) and non-instrumental deliveries (rho = −0.72; p < 0.001). However there was no relation between time trends of these two indicators (rho = 0.43; p = 0.28). Conclusions: The large variations in severe tears and episiotomies and the negative association between these indicators in 2010 show the importance of improving the assessment and reporting of tears in each country, and evaluating the impact of low episiotomy rates on the perineum., SCOPUS: ar.j, FLWIN, info:eu-repo/semantics/published
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- 2016
49. Varying gestational age patterns in caesarean delivery : an international comparison
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Delnord, Marie, Blondel, Béatrice, Drewniak, Nicolas, Klungsøyr, Kari, Bolumar, Francisco, Mohangoo, Ashna D., Gissler, Mika, Szamotulska, Katarzyna, Lack, Nicholas, Nijhuis, Jan, Velebil, Petr, Sakkeus, Luule, Chalmers, James, Zeitlin, Jennifer, Haidinger, Gerald, Martens, Gerald, Misselwitz, Björn, Wenzlaff, Paul, Bonham, Sheelagh, Jaselioniene, Jone, Gatt, Miriam, Barros, Henrique, Novak, Ziva, Gottvall, Karin, Euro-Peristat Preterm Group, Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Institut National de la Recherche Agronomique (INRA)-Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Global Health and Primary Health Care, University of Bergen (UIB), Medical Birth Registry of Norway, Norwegian Institute of Public Health [Oslo] (NIPH)-National Institute for Health and Welfare [Helsinki], Department of Public Health Sciences, Universidad de Alcalá - University of Alcalá (UAH)-CIBER de Epidemiología y Salud Pública (CIBERESP), Department Child Health, Information Services Division of NHS National Services Scotland, 1 South Gyle Crescent, Edinburgh-The Netherlands Organisation for Applied Scientific Research (TNO), Department of Information, Nordic School of Public Health-National Institute for Health and Welfare [Helsinki], Epidemiology, NHV Nordic School of Public Health, Department of Epidemiology, National Research Institute of Mother and Child, Department of Methods and Perinatology, BAQ, Bavarian Institute for Quality Assurance, Department of Obstetrics and Gynaecology, Grow school for oncology and developmental biology-Maastricht UMC, Perinatal Center, Institute for the Care of Mother and Child, Estonian Institute for Population Studies, Tallinn University, Information Services Division, NHS National Services Scotland, This analysis was partially funded by a grant to the Euro-Peristat project from the European Commission (2010 13 01)., MUMC+: MA Obstetrie Gynaecologie (3), Obstetrie & Gynaecologie, RS: GROW - Developmental Biology, RS: GROW - R4 - Reproductive and Perinatal Medicine, University of Bergen (UiB), Dupuis, Christine, CIBER de Epidemiología y Salud Pública (CIBERESP)-Universidad de Alcalá - University of Alcalá (UAH), Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS), Institut National de la Recherche Agronomique (INRA) - Université Paris Diderot - Paris 7 (UPD7) - Université Paris Descartes - Paris 5 (UPD5) - Université Paris 13 - Institut National de la Santé et de la Recherche Médicale (INSERM), Norwegian Institute of Public Health - THL National Institute for Health and Welfare, CIBER de Epidemiología y Salud Pública (CIBERESP) - Université d'Alcalá de Henares, Information Services Division of NHS National Services Scotland, 1 South Gyle Crescent, Edinburgh - The Netherlands Organisation for Applied Scientific Research (TNO), Nordic School of Public Health - THL National Institute for Health and Welfare, and Grow school for oncology and developmental biology - Maastricht UMC
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Newborn infants ,Euro-Peristat ,VDP::Medisinske fag: 700::Helsefag: 800::Epidemiologi medisinsk og odontologisk statistikk: 803 ,0302 clinical medicine ,Pregnancy ,Obstetrics and Gynaecology ,Medicine ,030212 general & internal medicine ,Cross-national comparisons ,reproductive and urinary physiology ,030219 obstetrics & reproductive medicine ,Obstetrics ,Singleton ,Vaginal delivery ,Obstetrics and Gynecology ,Gestational age ,Childbirth -- Case studies ,3. Good health ,Europe ,Plurality, Mode of delivery ,Gestation ,Term Birth ,Premature Birth ,Female ,Pregnancy, Multiple ,VDP::Midical sciences: 700::Health sciences: 800::Epidemiology, medical and dental statistics: 803 ,Live birth ,Live Birth ,Research Article ,medicine.medical_specialty ,Plurality ,Reproductive medicine ,Infant, Postmature ,Cesarean delivery (CD) ,03 medical and health sciences ,[SDV.MHEP.PED] Life Sciences [q-bio]/Human health and pathology/Pediatrics ,Humans ,Gynecology ,[SDV.MHEP.PED]Life Sciences [q-bio]/Human health and pathology/Pediatrics ,business.industry ,Cesarean Section ,Infant, Newborn ,medicine.disease ,United States ,Mode of delivery ,business ,Cesarean section - Abstract
Background: While international variations in overall cesarean delivery rates are well documented, less information is available for clinical sub-groups. Cesarean data presented by subgroups can be used to evaluate uptake of cesarean reduction policies or to monitor delivery practices for high and low risk pregnancies based on new scientific evidence. We studied differences and patterns in cesarean delivery rates by multiplicity and gestational age in Europe and the United States.Methods: This study used routine aggregate data from 17 European countries and the United States on the number of singleton and multiple live births with cesarean versus vaginal delivery by week of gestation in 2008. Overall and gestation-specific cesarean delivery rates were analyzed. We computed rate differences to compare mode of delivery (cesarean vs vaginal birth) between selected gestational age groups and studied associations between rates in these subgroups namely: very preterm (26-31 weeks GA), moderate preterm (32-36 weeks GA), near term (37-38 weeks GA), term (39-41 weeks GA) and post-term (42+ weeks GA) births, using Spearman's rank tests.Results: High variations in cesarean rates for singletons and multiples were observed everywhere. Rates for singletons varied from 15% in The Netherlands and Slovenia, to over 30% in the US and Germany. In singletons, rates were highest for very preterm births and declined to a nadir at 40 weeks of gestation, ranging from 8.0% in Sweden and Norway, to 22.5% in the US. These patterns differed across countries; the average rate difference between very preterm and term births was 43 percentage points, but ranged from 14% to 61%. High variations in rate differences were also observed for near term versus term births. For multiples, rates declined by gestational age in some countries, whereas in others rates were similar across all weeks of gestation. Countries' overall cesarean rates were highly correlated with gestation-specific subgroup rates, except for very preterm births.Conclusions: Gestational age patterns in cesarean delivery were heterogeneous across countries; these differences highlight areas where consensus on best practices is lacking and could be used in developing strategies to reduce cesareans., peer-reviewed
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- 2014
50. Changing clinical activity in Paediatrics in Malta, 1996-2011
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Attard Montalto, Simon and Gatt, Miriam
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Pediatrics -- Malta -- Statistics ,Pediatrics -- Malta ,Childbirth -- Malta -- Statistics - Abstract
Aim: This study reviews the clinical workload in paediatrics in Malta over a 16-year period. Methods: National statistics for live birth rates were obtained from the Directorate of Health Information and Research. Data for paediatric (birth to 14 completed years) and neonatal admissions, day cases, outpatient visits, attendance at Paediatric Accident and Emergency and the Community-based Developmental Unit were obtained from the Annual Reports, Department of Paediatrics, for the period 1996-2011. Results: During the study period, live births fell by 11% from 4,349 in 1996 to 3,857 in 2005, and recovered to 4,283 in 2011. Whereas neonatal admissions to NPICU remained constant at around 340(±22) per annum, inpatient admissions to the general Paediatric wards decreased by 19% (from 3,151 to 2,550), and casualty reviews dropped by 35% (11,831 to 7,773). In contrast, day care reviews increased by 66% (1,347 to 3,928), the total outpatient workload increased by 70% (13,500 to 22,998), and cases reviewed in the Community-based Child Developmental Unit increased by 184% from 413 to 1174. Changes observed in the clinical activity in Gozo General Hospital were similar but less marked. Conclusion: Over a 16 year period, there has been a significant shift in the paediatric workload in Malta from an in-patient bias in 1996 to increased day care and outpatient reviews in 2011. This shift is largely the result of improved hospital and community day health care services, and can be increased further with augmented community care. Health resources and future paediatric health care programmes will need to take heed of these trends., peer-reviewed
- Published
- 2014
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