This project is a step towards automatic firefighting. The goal is to decrease the number of personal injuries by replacing the human firefighter with robots or similar technical tools. Especially in very hostile environments due to risk of explosions or building collapse. A robot is easy to replace and can be maneuvered from a safe distance. The idea of the project comes from the company Drones Networking which aims for developing a totally autonomous firefighting system.

The purpose of our study is to interpret and understand the collaborative process around a regional model that is based on state developed guidelines for people with dementia. We have chosen to focus on the importance of interaction and have therefore interviewed participants in the project's steering committee. This group participates in efforts to develop a model for dementia care in Halland.The project work in Halland, to develop a joint model for people with dementia and their families was initiated in the spring of 2011 and is due to finish at the end of 2012. The Halland model has been named ?Annas led? and is about Anna and her husband Lars and living with dementia.

BAKGRUND: Studierna visar att våldet har ökat med åren. Riskfaktorer och riskbeteenden har identifierats och orsakerna kan vara flera till att patienten upplever ohälsa. Forskningen inom detta fält har hittills fokuserat på bakomliggande orsaker till patientens aggressiva beteende och bedrivits under många år. Ökade kunskaper om sjuksköterskans upplevelse av att vårda patienter med aggressivt beteende inom psykiatrisk vård kan bidra till att utveckla omvårdnad anpassad till situationen, i syfte att främja hälsa.SYFTE: Studiens syfte är att utforska sjuksköterskans omvårdnad och upplevelse av att vårda patienter med aggressivt beteende inom psykiatrisk vård.METOD: Litteraturstudie av kvalitativa och kvantitativa studier.RESULTAT: Analysen resulterade i tre huvudkategorier och 12 underkategorier. Huvudteman som uppkom var;sjuksköterskan i interaktion med patienten, organisatoriska faktorer och personliga faktorer samt underkategorier som handlade om; avledning av hotfulla situationer, personligt utrymme, information och bedömning, gränssättning, riskfaktorer kopplade till aggression, bristande support från chefer, bemanning, personalsäkerhet, erfarenhet och kommunikationsfärdigheter, lojalitet gentemot patienten och arbetet, hopplöshet och besvikelse samt coping.SLUTSATS: Resultatet visar att sjuksköterskor upplever vårdandet av patienter med aggressivt beteende inom psykiatrisk vård på olika sätt.

ABSTRACTParental support is needed because it promotes a positive development in children, because parents ask for it and because it has positive effects on the public economy. Those responsible in Sweden for Child health care have shown an increased interest in supporting parenthood.Aim: The overall purpose of this study was to investigate what kind of support parents today desire from child health care. An additional purpose was to investigate if they feel their needs and wishes are met.Method: The study has a descriptive and qualitative design. The selection was eight parents of children under eighteen months of age: four mothers and four fathers. None of the participants were couples.

Bakgrund: Den palliativa vården riktar sig till människor som befinner sig i livets slutskede och syftar till att tillgodose patientens fysiska, psykiska, sociala samt existentiella behov. Inom denna vårdkontext är värdighet ett centralt begrepp som anses bidra till en god omvårdnad. Värdighet är en rättighet för patienten och kan kränkas eller främjas beroende på sjuksköterskans handlingar och beteende.                                                                                              Syfte: Syftet är att beskriva vilka vårdhandlingar som kan tillämpas för att främja patientens värdighet i den palliativa vården utifrån ett sjuksköterskeperspektiv.                                                                                                                                                    Metod: Kvalitativ litteraturstudie som baserats på åtta vårdvetenskapliga artiklar.

Background: Many Swedish inhabitants origin from different countries with different cultures that may show pain in other ways than Swedes. The Swedish law stress that nursing care should be done individually according to the patient's capabilities and needs. Aim and Method: The aim of this study was to describe nurses´ experiences of encounters with patients from other cultures with pain, and also their next of kin. Qualitative interviews were carried out with seven nurses. The interviews were analysed with the starting point in Giger and Davidhizars Transcultural Assessment Model and the six phenomena: communication, space, social organisation, time, environmental control and biological diversity.

IntroductionStatistics show a declining trend despite the many benefits of breastfeeding.AimThe aim was to investigate how new mothers experienced the care associated with childbirth, with focus on breastfeeding.MethodThe study included mothers who gave birth in a hospital in the middle region of Sweden during 2011, and who responded to an online survey (n?1000). The present study was based upon answers from the open questions concerning dissatisfaction and suggestions for improvement and have been categorized using content analysis.ResultsMothers described failure in several areas, with a negative impact on breastfeeding. Many experienced that they had not been seen and treated like an individual, and that the healthcare staff had been unpleasant, impersonal, ignorant and stressed. Mothers wanted more credit from the staff concerning their own ability and some reported that they had been controlled and ?run over?.

Background:There are approximately 45 000 people in the ages over 65 years dies outside the health facilities of the hospitals in Sweden in every year. Previous research has shown lacking knowledge in taking care of the next of kin during and after a sudden death. However, conducted research has emphasized that ambulance nurses often are the next of kin?s first contact with the health care system during sudden death at home. Research has also shown that the mourning of the next of kin is affected by the ambulance nurses? way of announcing the next of kin when someone close dies.

Amyotrofisk lateralskleros (ALS) är en obotlig, neurologisk sjukdom som karaktäriseras av en progressiv nedbrytning av det motoriska nervsystemet. Symtomen är tilltagande muskelsvaghet som slutligen orsakar förlamning och andningssvikt. Överlevnadstiden från sjukdomens debut är två till fem år. Det finns i dagsläget ingen botande behandling mot ALS, istället läggs fokus på att lindra symtom. Syftet med studien var att belysa livskvalitét och välbefinnande hos patienter med den obotliga sjukdomen ALS.

Background: Globally, one percent of all people diagnosed with cancer are children. Childhood cancer often requires long and tough treatments. When a child is diagnosed with cancer it also affects the family and the relatives. Aim: The aim of this study was to describe the nurse?s role in the care and treatment of children with cancer.

AbstractFörfattare ? Malin Andersson och Slaven MarasTitel ? Aspects of decentralizations effect on eldercare ? a qualitative study of three municipal authority office/ Aspekter på decentraliseringens effekter på äldreomsorg ? En kvalitativ studie i tre kommuners myndighetskontorHandledare ? Linda ErlandssonExaminator: Jan Petersson This is a qualitative study of the phenomenon of decentralization and its impact on care managers working in elderly care. The aim of the study was to examine how care managers margin for maneuver and need assessments continually are shaped by organizational conditions and municipal governance. With these aspects in mind, we wanted to identify similarities and differences in three different municipalities? ways to work with care management in the elderly care.

The purpose of this study was to explore the approach of the personal in residential care homes, legal guardians and Refugee secretaries consider as effective in their efforts to care for and guide unaccompanied boys in the Swedish society. With the help of qualitative method and semi-structured interviews, we have taken note of eleven informants? perspective on what approach they believe to be essential in the work of integration process with unaccompanied boys. We used Empowerment and the Swedish Integration Board´s proposal on indicators of integration as a theoretical base. The results show among other things, that our informants believe the keys to integration in Sweden for the unaccompanied youth are the Swedish language, education and a stable social network.

Today is what you could call a golden age for technological development in health care. Technology is given a bigger role in healthcare and serves not only as a support for health professionals in their daily work but also as a tool for the patient. With the help of eHealth services, patients are becoming more involved in their own care. This improves patient?s knowledge about their health, which in turn contributes to higher motivation to perform self-care.

The purpose of this study is to, based on qualitative interviews with managers and group interviews with care providers, understand their interpretation of integrity and also their scope for action to satisfy disable people?s integrity at sheltered housing for adults. The questions of this study are: How do the managers and the care providers interpret the concept of integrity? Which scope for action do they have to satisfy the integrity of disabled people? Method: Individual ? and group interviews have been used as methods to gather empirical data. Theory: The theories of scope for action and integrity as a theoretical conception have been used to analyze the empirical material.

Palliative care concerns care of those who are dying and when cure is no longer an option. The nurse´s job is then to support the patient and to give care of good qualitive so that the patient will experience optimal quality of life. The aim of this literature review was to describe how the nurse can prepare herself/himself for the meeting with both the patient and close ones also to describe a nurse´s need of support and education. Nine studies have been used as a foundation for this literature review. Four headlines have been crystallized out of the result, a) the view of death b) the impact of the meeting c) the importance of support d) the importance of preparation and education.