Introduction: The health for individuals with intellectual disabilities is asubject that is prioritized by the Swedish Institute for Public Health. Socialsupport has been proven to be important for health and quality of life. Despitethis fact there is no research available regarding the influence social support hason health and quality of life for people with intellectual disabilities in Sweden.Aim: To describe social support and the consequence of social support forhealth and quality of life for individuals with intellectual disabilities. Method:A litterature review of research in a defined area with a descriptive design.Systematic searches for articles were done in several databases and ultimately16 articles were chosen. Themes and categories were created with respect to theaim of this study during the analysis of the articles.

Introduction: The health for individuals with intellectual disabilities is asubject that is prioritized by the Swedish Institute for Public Health. Socialsupport has been proven to be important for health and quality of life. Despitethis fact there is no research available regarding the influence social support hason health and quality of life for people with intellectual disabilities in Sweden.Aim: To describe social support and the consequence of social support forhealth and quality of life for individuals with intellectual disabilities. Method:A litterature review of research in a defined area with a descriptive design.Systematic searches for articles were done in several databases and ultimately16 articles were chosen. Themes and categories were created with respect to theaim of this study during the analysis of the articles.

Introduction: The health for individuals with intellectual disabilities is asubject that is prioritized by the Swedish Institute for Public Health. Socialsupport has been proven to be important for health and quality of life. Despitethis fact there is no research available regarding the influence social support hason health and quality of life for people with intellectual disabilities in Sweden.Aim: To describe social support and the consequence of social support forhealth and quality of life for individuals with intellectual disabilities. Method:A litterature review of research in a defined area with a descriptive design.Systematic searches for articles were done in several databases and ultimately16 articles were chosen. Themes and categories were created with respect to theaim of this study during the analysis of the articles.

This essay is about the history of the hearing aid in Sweden, from 1930s until today. The hearing aid as an apparatus is described, and views by the users are presented. Articles and interviews have been used as source material to answer the main questions. In the essay, people who have written the articles, and the ten users being interviewed, describe how hearing aids are used in everyday life, and how users interact with people in general and how the hearing care system treats users. Another question regards how users perceive their own hearing aids from an aesthetic perspective.

The aim of this study was to describe how elderly?s sexuality can be expressed and to describe factors that affect older people's sexuality. The aim was also to describe the opportunities and barriers to health care providers to promote older people's sexuality and to describe the articles quality based on the methodological aspect of selection. A literature review with a descriptive approach was conducted on four qualitative and ten quantitative articles. The included articles were published between 2003 and 2013.

PurposeThe purpose of this study has been to investigate the documentation process following the guiding principles of the Quality Norms for Fall Prevention concerning fall risk assessment, risk identification, fall preventive measures, information and the making of an individual care plan.MethodThis study is a quantitative, descriptive and retrospective journal review study. There were 100 journals examine the existing documentation concerning fall risk assessment of patients who received treatment in geriatric patient care. The sample was consecutively.ResultsThe results showed that fall risk assessment was documented in 79 of 100 examined journals. 56 (71 %) of the fall risk assessments were made within 24 hours. In 59 of 100 journals the patient, relatives or former caretakers was asked whether the patient had had a fall within the last year, and in 61 of 100 journals it was documented that the nursing staff had made an assessment that the patient was going to have a fall during his or her length of stay if no preventive measures were set in.The majority of fall risk factors and fall preventive measures were documented within the areas of walking and transfer. It was documented that the patient was informed of fall risk, fall risk factors and fall preventive measures in 15 of 100 journals.

The study aims to analyze conceptions of death and dying at a clinic for palliative care, using a constructivist perspective and a discourse analytical approach. The empirical material consists of interviews with staff members, documents and photographs of the environment, taking both space and materiality into account. I conclude that the studied practice is mainly characterized by a tension between a caring discourse and a medical discourse..

The main aim of this bachelor thesis is to describe through a quantitative study the extent of support received by foster families, their opinion of the support and any areas that might need improvement. The foster families receive foster care support through a private agency. We concentrated on the following areas of support; education, health, contact with the children?s biological relatives and behavioral difficulties. These four areas have, in previous research, shown to be problematic for foster children.

BackgroundHandover occurs as a daily task for health care professionals in all levels of care. Handover between ambulance crew and emergency department staff stands for the first exchange of information about a patient?s condition. Different factors may impact the handover communication and make it vulnerable.AimThe aim is to highlight factors of importance at handover between the ambulance and emergency room.MethodA literature review of thirteen studies with qualitative and quantitative research approach. The purpose of this literature review was to provide an overview of the area.ResultsExperiences for health care professionals is that communication is important for patient handover between ambulance and emergency department.

People with severe mental illness and co-occurring substance abuse are an especially vulnerable group in society as health care for those is shared between municipality and county council. There is an associated health need of this target group so the interaction of the social services and the psychiatric care is of great importance. However, there are shortcomings in this interaction with results in that people with dual diagnosis do not always receive adequate care. Diverse knowledge and explanatory models may create problems for the interaction as they include different ways to define, understand, explain and deal with a problem. The purpose of this study was to examine how the interaction between the social service addiction treatment and the psychiatric care is, concerning people with dual diagnosis, focusing on how their respective knowledge and explanatory models affect the interaction.

I denna rapport har det utförts två fallstudier från två olika vindkraftsanläggningar och med hjälp av en utarbetad modell har livscykelkostnaderna jämförts för de två fallstudierna.Resultatet visade att livscykelkostnaden per producerad kWh sjunker allteftersom den installerade effekten blir högre.Kostnadsmodellen som utarbetats och tillämpats för resultaten har visat sig ha hög verifierbarhet då resultaten har varit jämförbara med litterära studier..

Bakgrund: I dagens samhälle pågår ständiga debatter om genus i olika kontexter, diskussionen om exempelvis löneskillnader, barnuppfostran och vårdande utifrån genus är närvarande i media, i såväl TV som tidningar och på internet. Studier har visat på att kvinnor och män uppfattar vårdande olika samt har olika preferenser för hur vårdandet skall utformas ? sjuksköterskor bör därför vara genusmedvetna i mötet med patienten för att kunna ge genuskänsligt vårdande utifrån en personcentrerad utgångspunkt.Syfte: Syftet med denna uppsats är att beskriva patienters uppfattningar av vårdande ? ur ett genusperspektiv.Metod: Detta arbete har genomförts som en litteraturöversikt och har baserats på 14 stycken vetenskapliga artiklar som har analyserats med en kvalitativ designmetod. Arbetet är förankrat med utgångspunkt i Katie Erikssons teori om vårdande.Resultat: Resultatet utgörs av tre teman; (a) Kvinnor och mäns förväntningar samt önskemål för vårdande, (b) När förväntningar och önskemål ej tillgodoses samt (c) När förväntningar och önskemål tillgodoses. Olikheter mellan könen gällande uppfattningar av vårdande framkom främst vid missnöje.

Studier visar att många patienter som befinner sig i livets slutskede väljer att få vara hemma och avsluta sina liv bland familjen. Den vård, som dessa patienter får, oavsett var de befinner sig, kallas för palliativ vå rd. För att kunna ge en god omvårdnad i hemmet till patienter som befinner sig i livets slutskede, är det viktigt som sjuksköterska att ta reda på patientens upplevelser om vad som inger trygghet, vilket inte har upp-märksammats tillräckligt. Syftet med studien är att beskriva patientens upplevelser av vad som inger trygghet i samband med palliativ vård i det egna hemmet. Vi har gjort en litteraturstudie och utgått från Evans (2003) analysmodell.

The aim of this literature review was to elucidate how suicidal and self-harming patients should be treated and cared for, mainly in the acute phase in somatic care. Searches were conducted in databases with relevant keywords. Qualitative and quantitative articles were included, would not be more than 20 years, be written in Swedish or English, and match the aim of the study. Results showed that nurses and patients felt that the treatment would be respectful, non-judgmental and characterized by active listening and clear communication. Poor care was described as disrespect and lack of understanding.

Denna uppsats undersöker hur förhållandet mellan karaktären, interagerbarheten ochpresentationen påverkar möjligheterna för hur spelaren uppfattar berättelsen i spelenHalf-Life 2(Valve Corperation, 2004), Fallout 3 (Bethesda Game Studio, 2008) ochFahrenheit (Quantic Dream, 2005). Metoden för analyserna är baserat på Aarseths (2007)teorier och går ut på att jag själv spelat spelen och sedan analyserat dessa utifrån minaegna spelupplevelser. Analyserna tar även upp teorier och begrepp från andra forskare, såsom Marie-Laure Ryan, Andrew Rollings och Ernest Adams, Lee Sheldon och UlfWilhelmsson.Metoden för analyserna lyckas plocka fram flera unika berättartekniker och förhållandenfrån spelen. Bland annat den dolda storyn i Half-life 2, den ytterst interagerbara välden iFallout 3 samt de flera olika huvudkaraktärerna i Fahrenheit, och hur dessa påverkarspelarens uppfattning av berättelsen. Förhållandena är dock inte generella, utan unika förvarje spel, vilket medför att resultaten också är det, och kan därför inte ses som reglerutan mer som riktlinjer för hur en berättarteknik kan se ut..