14 resultados para universitetsbibliotek
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XXXII, 552 s. ; 23 cm.
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1745
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Samlingen kvinnovetenskaplig litteratur finns vid enheten för Kvinnovetenskap och har signum ESF ifkv eller bara ifkv. Föreståndaren för Handskriftsavdelningen vid Åbo Akademis bibliotek, Göta Tegengren gjorde år 1974 en studieresa till Göteborgs universitetsbibliotek där ett omfattande kvinnohistoriskt arkiv finns. Det följande året firades som internationellt kvinnoår och i anledning härav ordnades en utställning vid Åbo Akademis bibliotek med temat Kvinnoarkiv i ÅAB med material från Handskriftsavdelningen. Några kvinnor som intresserade sig för kvinnoforskning började sammankomma under benämningen Jämlikhetsgruppen, senare Arbetsgruppen för kvinnohistoriskt arkiv. Under tio års tid arbetade gruppen på frivillig basis. De kvinnohistoriska samlingarna växte i omfattning genom donationer och inköp. Till en början fanns det inte egna utrymmen för samlingarna förrän år 1978 då arbetsgruppen fick disponera ett rum i Reuterska huset. En tid var samlingarna deponerade vid Sociologiska institutionen. Vid nyåret 1986 grundades Institutet för kvinnoforskning, senare benämnt enheten för Kvinnoforskning och samlingarna överfördes till institutet.
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Kirjallisuusarvostelu
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In general, patient participation is regarded as being informed and partaking in decision making regarding one’s care and treatment. This interpretation is common in legislation throughout the Western world and corresponding documents guiding health care professionals, as well as in scientific studies. Even though this understanding of the word participation can be traced to a growing emphasis on individuals’ autonomy in society and to certain dictionary defi nitions, there are other ways of understanding participation from a semantic point of view, and no trace of patients’ descriptions of what it is to participate can be found in these definitions. Hence, the aim of this dissertation was to understand patients’ experience of the phenomenon of patient participation. An additional aim was to understand patients’ experience of non-participation and to describe the conditions for patient participation and non-participation, in order to understand the prerequisites for patient participation. The dissertation comprises four papers. The philosophical ideas of Ricoeur provided a basis for the studies: how communication can present ways to understand and explain experiences of phenomena through phenomenological hermeneutics. The first and second studies involved a group of patients living with chronic heart failure. For the fi rst study, 10 patients were interviewed, with a narrative approach, about their experience of participation and non-participation, as defi ned by the participants. For the second study, 11 visits by three patients at a nurse-led outpatient clinic were observed, and consecutive interviews were performed with the patients and the nurses, investigating what they experience as patient participation and non-participation. A triangulation of data was performed to analyse the occurrence of the phenomena in the observed visits. For paper 3 and 4, a questionnaire was developed and distributed among a diverse group of people who had recent experience of being patients. The questionnaire comprised respondent’s description of what patient participation is, using items based on findings in Study 1, along with open-ended questions for additional aspects and general issues regarding situations in which the respondent had experienced patient participation and/or non-participation. The findings show additional aspects to patient participation: patient participation is being provided with information and knowledge in order for one to comprehend one’s body, disease, and treatment and to be able to take self-care actions based on the context and one’s values. Participation was also found to include providing the information and knowledge one has about the experience of illness and symptoms and of one’s situation. Participation occurs when being listened to and being recognised as an individual and a partner in the health care team. Non-participation, on the other hand, occurs when one is regarded as a symptom, a problem to be solved. To avoid non-participation, the information provided needs to be based on the individual’s need and with recognition of the patient’s knowledge and context. In conclusion, patient participation needs to be reconsidered in health care regulations and in clinical settings: patients’ defi nitions of participation, found to be close to the dictionaries’ description of sharing, should be recognised and opportunities provided for sharing knowledge and experience in two-way-communication.
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I denna rapport beskrivs idéerna bakom Högskolan Dalarnas prisbelönta bibliotek i Falun. Planerings- och byggprocessen beskrivs och det färdiga resultatet utvärderas, samt de erfarenheter som har gjorts delas.
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This report describes the ideas and vision behind Dalarna University's award-winning library in Falun. A description of the planning and construction processes and an evaluation of the final outcome are presented together with experiences and observations drawn from the project.
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Mode of access: Internet.
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Published on the occasion of the celebration of the 300th anniversary of the founding of the library of the University of Upsala.
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Mode of access: Internet.
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Mode of access: Internet.
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Mode of access: Internet.
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Mode of access: Internet.