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Institute
- Fakultät III - Medien, Information und Design (30) (remove)
Diese Studie untersucht Gruppen von Ortsnamen in Deutschland (in den Postleitregionen) nach vorhandenen Ähnlichkeiten. Als Messgröße wird ein Häufigkeitsvektor von Trigrammen in jeder Gruppe herangezogen. Mit der Anwendung des Average Linkage-Algorithmus auf die Messgröße werden Cluster aus räumlich zusammenhängenden Gebieten gebildet, obwohl das Verfahren keine Kenntnis über die Lage der Cluster zueinander besitzt. In den Clustern werden die zehn häufigsten n-Gramme ermittelt, um charakteristische Wortpartikel darzustellen. Die von den Clustern umschriebenen Gebiete lassen sich zwanglos durch historische oder linguistische Entwicklungen erklären. Das hier verwendete Verfahren setzt jedoch kein linguistisches, geographisches oder historisches Wissen voraus, ermöglicht aber die Gruppierung von Namen in eindeutiger Weise unter Berücksichtigung einer Vielzahl von Wortpartikeln in einem Schritt. Die Vorgehensweise ohne Vorwissen unterscheidet diese Studie von den meisten bisher angewendeten Untersuchungen.
Der Beitrag stellt zunächst die Ergebnisse einer Auswertung von Stellenanzeigen aus der Mailingliste InetBib vor, die zeigt, dass die Nachfrage nach Absolventinnen und Absolventen bibliothekarischer Studiengänge mit einer Qualifikation für den Aufgabenbereich der Vermittlung von Informationskompetenz
seit dem Jahr 2000 signifikant gestiegen ist. Ergänzend hierzu präsentieren die Autorinnen die Ergebnisse einer Befragung unter Vertreterinnen und Vertretern der bibliothekarischen Berufspraxis zu im Bereich der Vermittlung von Informationskompetenz geforderten Kompetenzen und deren
Gewichtung innerhalb der verschiedenen Qualifikationsstufen.
Open Educational Resources (OER) sind sich in Deutschland bisher hauptsächlich im Bereich der schulischen Bildung im Gespräch. Ihr Potential innerhalb der deutschen Hochschullehre wurde zwar bereits erkannt, wird aber bisher noch nicht genutzt.
Die Arbeit gibt einen Überblick über die terminologischen Grundlagen von OER und ihren Entwicklungsmöglichkeiten im Hochschulbereich. In einer Zusammenfassung werden die Förderung von OER durch die Europäische Kommission und in Deutschland, sowie ihre Entwicklung im deutschen Hochschulbereich dargestellt. In einem theoretischen Abgleich aktueller Studien und Fachliteratur wird eine Bestandsaufnahme zu neuen Aufgabenbereichen für Wissenschaftlicher Bibliotheken durch OER durchgeführt.
Eine Expertenbefragung, die beispielhaft unter Lehrenden der Leibniz Universität Hannover (LUH) durchgeführt wurde, gibt Aufschluss über deren aktuellen Nutzungsstand von OER. Die wird ergänzt durch eine Untersuchung zweier Sharingdienste (Zenodo und SlideShare) nach freien Lehrmaterialien von Angehörigen der LUH.
Abschließend werden auf der Basis der theoretischen Möglichkeiten sowie der individuellen Bedürfnisse der Lehrenden Empfehlungen für neue Dienstleistungen und Serviceangebote Wissenschaftlicher Bibliotheken zur Unterstützung der Hochschulen bei der Einführung, Herstellung und Verbreitung von OER am Beispiel der Technischen Informationsbibliothek Hannover (TIB) gegeben, sowie neue Aufgabenbereiche für Hochschulbibliotheken skizziert, die sich daraus ergeben.
Objectives:
The aim was to identify theoretically expected as well as actually reported benefits from drug development and the importance of individual patient benefits compared to the collective benefits to society in general.
Background:
Ethical guidelines require that clinical research involving humans offer the potential for benefit. A number of characteristics can be applied to define research benefit. Often benefit is categorized as being either direct or indirect. Indirect benefits can involve collective benefits for society rather than any benefits to the trial patient or subject. The purpose of this review was to examine which potential individual and societal benefits were mentioned as being expected in publications from government experts and which were mentioned in publications describing completed drug development trial results.
Methods:
Literature on research benefit was first identified by searching the PubMed database using several combinations of the key words benefit and clinical research. The search was limited to articles published in English. A Google search with the same combinations of key words but without any language limitation was then performed. Additionally, the reference lists of promising articles were screened for further thematically related articles. Finally, a narrative review was performed of relevant English- and German-language articles published between 1996 and 2016 to identify which of several potential benefits were either theoretically expected or which were mentioned in publications on clinical drug development trial results.
Results:
The principal benefits from drug development discussed included 2 main types of benefit, namely individual benefits for the patients and collective benefits for society. Twenty-one of an overall total of 26 articles discussing theoretically expected benefits focused on individual patient benefits, whereas 17 out of 26 articles mentioned collective benefits to society. In these publications, the most commonly mentioned theoretically expected individual patient benefit was the chance to receive up-to-date care (38.1%). A general increase in knowledge about health care, treatments, or drugs (70.6%) was the most commonly mentioned theoretically expected benefit for society. In contrast, all 13 publications reporting actual benefits of clinical drug development trials focused on personal benefits and only 1 of these publications also mentioned a societal benefit. The most commonly mentioned individual benefit was an increased quality of life (53.9%), whereas the only mentioned collective benefit to society was a general gain of knowledge (100.0%).
Conclusions:
Both theoretically expected and actually reported benefits in the majority of the included publications emphasized the importance of individual patient benefits from drug development rather than the collective benefits to society in general. The authors of these publications emphasized the right of each individual patient or subject to look for and expect some personal benefit from participating in a clinical trial rather than considering societal benefit as a top priority. From an ethical point of view, the benefits each individual patient receives from his or her participation in a clinical trial might also be seen as a societal benefit, especially when the drug or device tested, if approved for marketing, would eventually be made available for other similar patients from the country in which the clinical trial was conducted.
Unternehmen befinden sich in einem Beziehungsgeflecht mit verschiedenen Stakeholdern, die differierende Ansprüche stellen und den Erfolg des Unternehmens stark beeinflussen. Unter diesen Gegebenheiten ist es von zentraler Bedeutung, gute Beziehungen zu den unterschiedlichen Gruppen und somit ein hohes Beziehungskapital aufzubauen. Eine Schlüsselfunktion kommt dabei der Kommunikation zu, da sie das Bindeglied zwischen Unternehmen und Stakeholdern darstellt.
Um mithilfe strategischen Kommunikationsmanagements die Beziehungen zu Stakeholdern zu stärken, müssen Unternehmen wissen, worauf überhaupt gute Beziehungen beruhen. Im Zentrum der Arbeit steht daher das soziale Kommunikations-Controlling von Unternehmen als Analyse- und Steuerungsfunktion und die Frage, aus welchen Faktoren sich das Beziehungskapital eines Unternehmens zusammensetzt. Im Gegensatz zum ökonomischen Kommunikations-Controlling fokussiert der soziale Ansatz nicht die ökonomische Ausrichtung der Kommunikation, sondern die Unternehmen-Stakeholder-Beziehungen.
Auf Basis des Beziehungskapital-Ansatzes von Szyszka und zentralen Reputationskonzepten wurden die Dimensionen und Indikatoren von Beziehungskapital hergeleitet. Eine quantitative Befragung einer breiten Öffentlichkeit diente anschließend der Prüfung des Entwurfs und der Identifikation möglicher weiterer Aspekte. Das Ergebnis stellt ein Modell dar, demnach Beziehungskapital aus folgenden acht Dimensionen besteht: die Produkte und Services, der unternehmerische Erfolg sowie die Kompetenz des Unternehmens als funktionale Komponenten, die soziale Verantwortung, die ökologische Verantwortung und die Verantwortung gegenüber den Mitarbeitern als soziale Komponenten sowie die Sympathie und Attraktivität des Unternehmens als affektive Komponenten. Die Dimensionen werden durch insgesamt 20 Indikatoren repräsentiert.
Das Modell lässt sich in den theoretischen Kontext des sozialen Kommunikations-Controllings einordnen und kann als Erweiterung des Beziehungskapital-Ansatzes hinzugezogen werden. In der Praxis liefert die Arbeit erste Hilfestellungen, um das Beziehungskapital eines Unternehmens bestimmen und darauf aufbauend ein strategisches Kommunikationsmanagement etablieren zu können.
The development of Artificial Intelligence (AI) has profound implications for improving human and computational productivity in the future. However, it also is an existential risk to human life because it could exceed human capabilities. As such, information about the technology, the direction of the development and its purpose is important. This can be achieved through openness and transparency of processes. Indeed, companies hold property rights over AI and monopolies of software, data and experts. As a countermovement to leading AI companies, the “Open AI Movement” has evolved to push open-source AI research and products, to empower users, and to bridge the digital divide through participation and access. In this thesis, the implications of the declaration of AI as a commons have been analyzed through interviews with AI experts in the United States. The legal placement of AI is controversial but it could be seen as a basic human right. Other findings are that this field is very competitive and that the best approach is to collaboratively develop software that adds additional value on the edge of the commons.
Editorial for the 17th European Networked Knowledge Organization Systems Workshop (NKOS 2017)
(2017)
Knowledge Organization Systems (KOS), in the form of classification systems, thesauri, lexical databases, ontologies, and taxonomies, play a crucial role in digital information management and applications generally. Carrying semantics in a well-controlled and documented way, Knowledge Organization Systems serve a variety of important functions: tools for representation and indexing of information and documents, knowledge-based support to information searchers, semantic road maps to domains and disciplines, communication tool by providing conceptual framework, and conceptual basis for knowledge based systems, e.g. automated classification systems. New networked KOS (NKOS) services and applications are emerging, and we have reached a stage where many KOS standards exist and the integration of linked services is no longer just a future scenario. This editorial describes the workshop outline and overview of presented papers at the 17th European Networked Knowledge Organization Systems Workshop (NKOS 2017) which was held during the TPDL 2017 Conference in Thessaloniki, Greece.
The amount of papers published yearly increases since decades. Libraries need to make these resources accessible and available with classification being an important aspect and part of this process. This paper analyzes prerequisites and possibilities of automatic classification of medical literature. We explain the selection, preprocessing and analysis of data consisting of catalogue datasets from the library of the Hanover Medical School, Lower Saxony, Germany. In the present study, 19,348 documents, represented by notations of library classification systems such as e.g. the Dewey Decimal Classification (DDC), were classified into 514 different classes from the National Library of Medicine (NLM) classification system. The algorithm used was k-nearest-neighbours (kNN). A correct classification rate of 55.7% could be achieved. To the best of our knowledge, this is not only the first research conducted towards the use of the NLM classification in automatic classification but also the first approach that exclusively considers already assigned notations from other
classification systems for this purpose.
Background: Diabetes is fast gaining the status of a potential epidemic in India, with >62 million individuals currently diagnosed with the disease. India currently faces an uncertain future in relation to the potential burden that diabetes may impose on the country. An estimated US$ 2.2 billion would be needed to sufficiently treat all cases of type 2 diabetes mellitus (T2DM) in India. Many interventions can reduce the burden of this disease. However, health care resources are limited; thus, interventions for diabetes treatment should be prioritized. The present study assesses the cost-effectiveness of antidiabetic drugs in patients with T2DM from Mumbai, India.
Methods: A prospective cross-sectional study was performed to assess the cost-effectiveness of antidiabetic drugs in patients with T2DM. Face-to-face interviews were conducted by using a validated questionnaire in a total of 152 (76 males, 76 females) patients with T2DM from F-North Ward, Mumbai, India. Cost-effectiveness was determined on the basis of cost of antidiabetic drug/s, efficacy, adverse drug reactions, safety of administration, frequency of administration, and bioavailability.
Results: For treatment of T2DM in non-obese participants, Glimepiride+Pioglitazone costed least (`3.7) per unit of effectiveness followed by Glimepiride (`6.6), Gliclazide (`8.1), Repaglinide (`24.5), and Vildagliptin (`45.2). For treatment of T2DM in obese participants, Metformin cost least (` 6.7) per unit of effectiveness followed by Glimepiride + Metformin (`5.9) and Repaglinide (`24.5).
Conclusions: In case of non-obese participants, cost effectiveness and prescribed treatments did not show a match, while for obese participants prescribed treatments were in line with cost effectiveness.
Background: Self-medication, practiced globally is an important public health problem. Research studies have indicated inappropriate self‐medication results in adverse drug reactions, disease masking, antibiotic resistance and wastage of healthcare resources. The objectives of the study were to explore overall self-medication and antibiotic self-medication prevalence among students of university students in Karachi, Pakistan along with probable reasons, indications, and sources of advice for self-medication. Methods: A descriptive, cross-sectional, questionnaire-based study was carried out among students from university of Karachi, Pakistan during the time period of September to November 2016. Pretested questionnaire was distributed to 320 students, collected data was analyzed using IBM SPSS version 24. Results: From 320 students, 311 (83 male and 228 female) students participated in the study giving a response rate of 97%. Prevalence of self-medication was 66%. Belonging to higher monthly family income group was associated with likelihood of self-medication. Antibiotic self-medication prevalence was 39%. Lack of time (39%), and old prescription (35%) were the main reasons for self-medication. Pharmacy shop (75%) was the main source for self-medication. In case of antibiotics, 44% students changed the dosage of antibiotic and 50% students stopped antibiotics after the disappearance of the symptoms. Conclusions: Antibiotic self-medication (39%) and self-medication with other drugs among university students of Karachi is a worrisome problem. Our findings highlight the need for planning interventions to promote the judicious use of general medicines as well as that of antibiotics.