NEED, SIGNIFICANCE AND RELEVANCE OF EDUCATIONAL TECHNOLOGY IN OUR WORLD

The complexity and speed of business, societal and technological changes make it difficult for schools to educate students to be effective in their adulthood. A survey of top-managers confirms that new employees often need considerable assistance to develop the skills and competences, such as problem-solving and decision making, needed for success. We propose a new, collaborative eLearning technology that will (a) assist organizations in this development process, and (b) allow them better to solve the myriad of organizational problems they encounter. The technology draws on resources both within and outside these organizations

Long term trends in prevalence of neural tube defects in Europe:population based study

STUDY QUESTIONWhat 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?METHODSThis 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 LIMITATIONSOverall, 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 ADDSIn 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.</p

Neke odrednice doživljaja roditeljske kompetentnosti u obiteljima djece s teškoćama u razvoju

Pozitivna slika o roditeljskoj kompetentnosti povezana je s osjećajem uspješnosti u roditeljstvu i kvaliteti interakcije djeteta i roditelja. Cilj ovog istraživanja bio je ispitati doprinos socio-demografskih obilježja roditelja i djeteta s teškoćama u razvoju, pokazatelja dobrobiti roditelja, podrške neposredne i šire okoline te roditeljskog stresa u objašnjenju roditeljskog osjećaja kompetentnosti. U uzorku 308 roditelja djece predškolske dobi prediktorima roditeljske kompetentnosti pokazali su se: zdravlje, bračno stanje i zadovoljstvo brakom. Povrh varijabli unesenih u prvom koraku primjenom hijerarhijske regresijske analize u drugom koraku objašnjeno je 23% varijance u efikasnosti roditeljstva, te 44% varijance zadovoljstva u roditeljskoj ulozi. Dobiveni rezultati pridonose spoznajama o roditeljskoj kompetentnosti u obiteljima djece s teškoćama u razvoju, upućujući na potrebu daljnjeg istraživanja ovog za obitelj važnog područja

Major congenital anomalies in babies born with Down syndrome: a EUROCAT population-based registry study

Previous studies have shown that over 40% of babies with Down syndrome have a major cardiac anomaly and are more likely to have other major congenital anomalies. Since 2000, many countries in Europe have introduced national antenatal screening programs for Down syndrome. This study aimed to determine if the introduction of these screening programs and the subsequent termination of prenatally detected pregnancies were associated with any decline in the prevalence of additional anomalies in babies born with Down syndrome. The study sample consisted of 7,044 live births and fetal deaths with Down syndrome registered in 28 European population-based congenital anomaly registries covering seven million births during 2000–2010. Overall, 43.6% (95% CI: 42.4–44.7%) of births with Down syndrome had a cardiac anomaly and 15.0% (14.2–15.8%) had a non-cardiac anomaly. Female babies with Down syndrome were significantly more likely to have a cardiac anomaly compared to male babies (47.6% compared with 40.4%, P?&lt;?0.001) and significantly less likely to have a non-cardiac anomaly (12.9% compared with 16.7%, P?&lt;?0.001). The prevalence of cardiac and non-cardiac congenital anomalies in babies with Down syndrome has remained constant, suggesting that population screening for Down syndrome and subsequent terminations has not influenced the prevalence of specific congenital anomalies in these babies

Epidemiology of congenital diaphragmatic hernia in Europe:a register-based study

IntroductionPublished prevalence rates of congenital diaphragmatic hernia (CDH) vary. This study aims to describe the epidemiology of CDH using data from high-quality, population-based registers belonging to the European Surveillance of Congenital Anomalies (EUROCAT).MethodsCases of CDH delivered between 1980 and 2009 notified to 31 EUROCAT registers formed the population-based case series. Prevalence over time was estimated using multilevel Poisson regression, and heterogeneity between registers was evaluated from the random component of the intercept.ResultsThere were 3373 CDH cases reported among 12?155?491 registered births. Of 3131 singleton cases, 353 (10.4%) were associated with a chromosomal anomaly, genetic syndrome or microdeletion, 784 (28.2%) were associated with other major structural anomalies. The male to female ratio of CDH cases overall was 1:0.69. Total prevalence was 2.3 (95% CI 2.2 to 2.4) per 10?000 births and 1.6 (95% CI 1.6 to 1.7) for isolated CDH cases. There was a small but significant increase (relative risk (per year)=1.01, 95% credible interval 1.00–1.01; p=0.030) in the prevalence of total CDH over time but there was no significant increase for isolated cases (ie, CDH cases that did not occur with any other congenital anomaly). There was significant variation in total and isolated CDH prevalence between registers. The proportion of cases that survived to 1?week was 69.3% (1392 cases) for total CDH cases and 72.7% (1107) for isolated cases.ConclusionsThis large population-based study found an increase in total CDH prevalence over time. CDH prevalence also varied significantly according to geographical location. No significant association was found with maternal age