Hybride Lehre an der Hochschule und in der Nachholbildung für Erwachsene

Zeit ist in der öffentlichen Diskussion über Erziehung eine konstitu tive Bestimmung. Dabei wird sie sehr unterschiedlich gefasst: Erziehung wird verstanden als ein Prozess, der zeitlich konsekutiv geordnet werden muss. Es wird aber auch von einer Erziehungszeit der Eltern gesprochen und von der Schulzeit im Lebenslauf. Unterricht und Didaktik verlangen von den Lehrpersonen ein Zeitmanagement. Über Schulanfang, Schul ende und Dauer der Schulzeit wird politisch debattiert. Aber weit dar über hinaus werden Erziehung und Bildung selbst zum Instrument, mit dem in der Gegenwart die Zukunft, die Zeit des einzelnen Menschen und sogar der ganzen Gesellschaft berechenbar werden sollen. Trotz dieser Zentralität der Dimension «Zeit» ist die theoretische Diskussion darüber wenig entwickelt. Der vorliegende Band diskutiert aus soziologischen, pädagogisch-psychologischen und historischen Perspektiven die Zeit dimensionen von Erziehung.

Relevance of In-vitro Tests of Adhesive and Composite Dental Materials. A Review in 3 Parts. Part 2: Non-standardized tests of composite materials

Summary The first part of this review examined ISO approval requirements and in vitro testing. In the second part, non-standardized test methods for composite materials are presented and discussed. Physical tests are primarily described. Analyses of surface gloss and alterations, as well as aging simulations of dental materials are presented. Again, the importance of laboratory tests in determining clinical outcomes is evaluated. Differences in the measurement protocols of the various testing institutes and how these differences can in?uence the results are also discussed. Because there is no standardization of test protocols, the values determined by different institutes cannot be directly compared. However, the ranking of the tested materials should be the same if a valid protocol is applied by different institutes. The modulus of elasticity, the expansion after water sorption, and the polishability of the material are all clinically relevant, whereas factors measured by other test protocols may have no clinical correlation. The handling properties of the materials are highly dependent on operators' preferences. Therefore, no standard values can be given.

Relevance of in vitro tests of adhesive and composite dental materials, a review in 3 parts. Part 1: Approval requirements and standardized testing of composite materials according to ISO specifications

The first part of this three-part review on the relevance of laboratory testing of composites and adhesives deals with approval requirements for composite materials. We compare the in vivo and in vitro literature data and discuss the relevance of in vitro analyses. The standardized ISO protocols are presented, with a focus on the evaluation of physical parameters. These tests all have a standardized protocol that describes the entire test set-up. The tests analyse flexural strength, depth of cure, susceptibility to ambient light, color stability, water sorption and solubility, and radiopacity. Some tests have a clinical correlation. A high flexural strength, for instance, decreases the risk of fractures of the marginal ridge in posterior restorations and incisal edge build-ups of restored anterior teeth. Other tests do not have a clinical correlation or the threshold values are too low, which results in an approval of materials that show inferior clinical properties (e.g., radiopacity). It is advantageous to know the test set-ups and the ideal threshold values to correctly interpret the material data. Overall, however, laboratory assessment alone cannot ensure the clinical success of a product.

[Treatment of advanced peri-implantitis in the mandible]

This case report shows the experimental treatment of a 85 year old female with advanced periimplantitis, the surgical augmentation, the clinical as well as the radiological follow-up until twelve months after surgery. the treatment of the advanced periimplantitis with a three-dimensional vertical defect around the implant consisted of a surgical bone augmentation technique supported by the Air-Flow Master® system (EMS, Nyon, Switzerland).