To sort, is the meaning of the word ?triage?. Triage is used at emergency departments to facilitate prioritization of patients according to the urgency of the chief complaint. The aim of this study was to investigate how the nurses experience the triage model at the emergency department at Uppsala university hospital.Twelve nurses were interviewed. The mean age was 40 years and the mean work experience was three years and four months.

Introduction:A good work environment and good resources among district nurses? and general nurses? are important in the provision of good nursing care. For patient security it is also very important that resources and time are used in an appropriate way. A lot of time is spent on non-core activity, for example administration takes more and more time, which can result in feelings of stress.Aim:The aim was to describe how district nurses? and nurses? in primary care perceived their work environment, how their worktime content was distributed and if there was some connection between perceived work environment and the distribution of work time.Methods:A mapping of the content of the work was made in two parts.

The aim of this text is to study how sectional managers in the care of the elderly work so as to promote basic human values. Semi-structured interviews generated qualitative data from five sectional managers. A hermeneutical approach was applied for interpreting the interviews. The result shows that the respondents are conscious of the fact that it takes a lot of long term work before a change in current procedures will happen. Also, the common everyday principles of work and basic values will continue to be part of the care of the elderly.

The aim of this study was to provide an understanding of the situation of an often forgotten group in foster care, the carers? own children. Our main focus was to explore this group?s experience of foster care, their experience of participating in caring for the foster children and their possible need of support and help. Our chosen method was qualitative interviews with six adult children of foster carers, two men and four women.

The aim of this study was to investigate whether there is a social-psychological relevance in allowing animals to be involved in therapy work. I have examined if the animals may contribute to effects on human relationships between caregivers and patients, and if the animals can contribute to helping patients to achieve better well-being. Through previous research and a quantitative interview I have received answers to the following questions: How are animals used in the treatment work? How do animals affect the relationship between caregiver-patient? In what ways do animals in treatment affect relationships between people? How do the professionals who work with animals believe that animals can affects the patient? I have interviewed people working in different kinds of treatment work using animals. The areas examined include work with animals at youth care, police, disability care, elderly care and school.

The purpose of this study has been to describe and analyze how former foster children experienced foster care which have been filled with maltreatment and neglect and how this has influenced their adult life when it comes to health, education and relationships. We also wanted to study how the former foster children coped with their placement. Furthermore we wanted to study whether there has been any turningpoints during their growth. Finally we wanted to describe how the former foster children experienced the authorities control. To make the purpose of this study complete we chose to use qualitative interviews with six former foster children as our research method.

Bakgrund? Kommunikation ?r en central del av sjuksk?terskans profession och har stor betydelse f?r att skapa trygghet, delaktighet och f?rst?else hos barn inom slutenv?rden. F?r att kommunikationen ska vara meningsfull beh?ver den anpassas efter barnets ?lder, mognad och individuella behov. Tidigare forskning visar dock att sjuksk?terskor ofta upplever utmaningar kopplade till tid, erfarenhet och kulturella aspekter.? Syfte? Syftet med denna litteratur?versikt var att beskriva sjuksk?terskans upplevelse av att kommunicera med barn inom slutenv?rden.? Metod? Studien genomf?rdes som en systematisk litteratur?versikt med kvalitativ ansats.

An important task for Region Skåne is to allocate resources to the health care districts. From 1999 to 2002 Region Skåne used needs-based resource allocation as a model for allocating resources. In a needs-based resource allocation individuals with the same socioeconomic and demographic characteristics are assumed to have the same level of need and are therefore allocated the same amount of resources. During the period of needs-based resource allocation a matrix model was used as a method. In the matrix model individuals were divided into cells after each combination of the socioeconomic and demographic variables.

Bakgrund Mobila Intensivvårds Grupper (MIG) är idag etablerade på flera svenska sjukhus. MIG bidrar till att minska antalet hjärtstopp och till att patienter som är på väg att försämras upptäcks tidigare. MIG innebär också en trygghet för avdelningspersonalen. Delaktighet i MIG är en naturlig del i intensivvårdssjuksköterskans arbetsuppgifter.Syfte Att beskriva intensivvårdssjuksköterskors erfarenheter av interaktionen med avdelningspersonalen vid MIG-uppdrag.Metod En kvalitativ studie med semistrukturerade intervjuer har utförts vid två sjukhus. Resultatet har analyserats med kvalitativ innehållsanalys.Resultat Två teman framkom vid analysen, Betydelsen av interaktion för en sammanlänkad och säker vård samt Samspelsbefrämjande faktorer.

It?s known that the drug information patients get at discharge from hospital is often insufficient. Patients? ignorance of which drug they use and how to take them can lead to drug related problems, can cause suffering and heavy expenses.The aim of this study was to shed light on the patients? understanding for drug information, which was given at discharge from hospital. The literature survey was used as a method and based upon a systematic choice of scientific articles, which were found in different databases during the period of April 1 to May 31, 2008.

The study was conducted in Jönköping County Chamber of fibrillation and is about change and improvement of process modeling technology. The process for treating patients with fibrillation is in the need to evolve and improve. In order to develop the care they needed a current state description which usually is made with the traditional process modeling tool.Many scientists and health professionals is in the opinion that this technology gives a too rigid image to describe the care processes. It also does not sufficiently take into account the human aspects. This reasoning suggests that the process modeling technology in healthcare is in the need to develop multiple perspectives.

The aim of this study is to describe a group of youths in compulsory care at a SiS institution in the south of Sweden. The study focuses on intelligence (measured with WISC-III) and self-report, i. e. what the youths think of themselves (measured with Jag tycker jag är). Attempts were made to see if background factors (based on information from the standardized ADAD-interview) seem to be coherent with intelligence and/or self-report and if so, what those background factors are.

När en patient drabbas av en total hjärninfarkt och blir aktuell för organdonation ställs det höga krav på intensivvårdssjuksköterskan. Tidigare studier visar att intensivvårdssjuksköterskor oroas av att vårda blivande organdonatorer och samtidigt stödja dennes närstående. Syftet var att belysa intensivvårdssjuksköterskors upplevelse av att stödja närstående till patienter med total hjärninfarkt i samband med organdonation. En kvalitativ metod med innehållsanalys av en fokusgruppsintervju genomfördes.Det framkom två huvudkategorier, Närståendes behov och Intensivvårdssjuksköterskans förmåga att ge stöd. Intensivvårdssjuksköterskans upplevelse påverkades i hög grad av hur närstående reagerade på situationen gällande organdonationsprocessen.

When a child is diagnosed with diabetes the whole family is affected. The effect of the illness often means drastically changes to their daily life. The aim of this study has been to describe the experiences of the parents´ having a child fallen ill with diabetes. The study has been done as a general literature study. The procedure has been to systematically search, critically investigate and summarise results from different studies made on the chosen area of subject.

This two year master thesis reviews the possibilities for how public libraries and geriatric care can cooperate on a long-term basis. By using a project called Prosit the study shows which approaches and actions that worked in order to create this kind of successful collaboration, and which ones that didn't.The theoretical framework consists of the sociocultural perspective developed by psychologist Roger Säljö in meaning to emphasize how these two departments can learn from each other. The theory also underlines the fact that both public libraries and geriatric care can develop their own way of improving the elderly?s daily life by working together. The thesis method is qualitative and based on Virginia Braun and Victoria Clarke?s thematic analysis.