Bakgrund: Palliativ vård utförs i hela vårdkedjan, från hemsjukvård till specialistvård på institution. Palliativ vård bygger på en helhetssyn som tryggas genom patientcentrerad vård där patientens delaktighet har en central roll.Syfte: Belysa vuxna patienters upplevelser av delaktighet då de vårdas i livets slutskede.Metod: Studien är en systematisk litteraturstudie främst baserad på metodik beskriven av Forsberg och Wengström (2013).Resultat: Temat möjligheter och hinder i upplevelsen av sin delaktighet växte fram, med fyra kategorier under sig: hantering av sin sjukdomssituation, överväldigande ny levnadssituation, bli sedd som individ och inte bli sedd som individ. Det framkom att patienter i livets slutskede fann möjligheter att vara delaktiga i sin vård genom införskaffandet av kunskap om sin sjukdom och sin framtid. Denna kunskap skapade förståelse över situationen hos patienterna, vilket gav dem redskap att lättare hantera och delta i sin vård. Upplevda hinder till delaktighet visade sig vara då patienterna upplevde sig förbisedda av vårdpersonal.Slutsats: Vuxna patienters upplevelser av delaktighet då de vårdas i livets slutskede går inte att beskriva som ett ensamt fenomen, utan behöver beskrivas utifrån en helhetssyn av patienten.  Den unika patienten bildar en dynamisk helhet, och behöver bemötas som den unika individ den är..

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.

After the honor killings of Fadime and Pela, an extensively discussion started in the media, debating honor-related violence and oppression. This debate also made us, the authours of this paper, to pay attention to the problem. As a professional in social work, there are several good points to be made by having an in-depth knowledge in the field, both to discover individuals exposed to honor-related violence and to be able to protect them. The study was conducted by four qualitative interviews with professionals in social work with a professional experience of honor-related problems. Through the interviews, the social worker's view of honor problems emerged.

The aim of our study is to deepen our understanding of how both social workers and clients describe how user influence within substance abuse care for adults can work. What difficul-ties do they describe meeting, with regards to possibilities to influence the care? To achieve our purpose we had a qualitative approach for this study. It?s based on open thematic inter-views with 3 clients who have substance abuse problems, and with 3 social workers, working at Social Services in Stockholm.

The aim of this study is to examine if and how the diagnosis of ADHD is important for the social practice delimitation to obtain an understanding of how the sorting and categorization of clients affects the distribution of resources. In a qualitative approach, the study is based on eight semi-structured interviews in five different social practices. Young adults diagnosed with ADHD who need society's help and support, constituted our focus in the study. The selection is based on gaining an understanding of how the client process proceeds. The interviews were supplemented with documents, such as legal and internal methodological support.

Inom den palliativa vården är vanliga symtom smärta och i synnerhet existentiell smärta. Obehandlad existentiell smärta får konsekvenser för graden av patientens lidande. Begreppet ?total pain? har haft stor betydelse för hospicerörelsen och palliativ medicin. Syftet med studien var att beskriva sjuksköterskors omvårdnad av patienter med existentiell smärta inom palliativ vård för att därmed kunna minska patientens lidande.

Bakgrund: Att få kunna vårdas och dö hemma i en familjär och välkänd miljö innebär för de allra flesta en känsla av trygghet. För många anhöriga är det självklart att leva nära den döende och ta ansvar för omvårdnaden. Ur ett systemteoretiskt perspektiv kan familjen liknas vid en mobil, vid obalans påverkas alla familjemedlemmar. Syftet med studien var att belysa patientens, anhörigas och sjuksköterskors erfarenheter av palliativ vård i hemmet för att få en ökad förståelse för sjuksköterskors roll i detta sammanhang. Metod: Litteraturstudie där tidigare forskning i ämnet undersökts och sammanställts.

Introduction: Urinary retention is a common postoperative complication associated with bladder distension. Permanent damage to the bladder affects the patient?s quality of life and may lead to a lifelong inability to empty the bladder and needs of self-catheterization with the risk of urinary tract infection. Bladder distension was classified as the fourth largest health care related injury in Sweden in 2013. Bladder distension may occur before the operation starts and is more common among orthopedic patients.

Due to deficiency in dementia care, the government has commissioned the National Board of Health and Welfare to develop national guidelines for health care services to people with dementia and support for their relatives. It has been allocated stimulus funds that may be applied for to work on improvements in dementia care. In August 2010 these guidelines formed the basis for a decision made that collaboration would take place between the county and the municipalities regarding dementia care in Halland, named Anna's path. The aim of this study is to investigate, analyse and describe how our respondents in the project Anna?s path are planning and preparing for the implementation of the registry of quality BPSD - Behavioural and Psychological Symptoms of Dementia.

Bakgrund: Att vårdas i hemmet istället för på sjukhus eller på vårdboende blir vanligare då antalet sjukhusplatser minskar och nya typer av vårdformer etablerats. Detta kan innebära att sjuksköterskor någon gång under sitt yrkesverksamma liv kan komma att vårda patienter i deras eget hem och på så sätt lämna den miljö som sjuksköterskan vanligtvis är van vid. Syfte: Syftet med studien är att med utgångspunkt från; roll, relation och bemötande studera sjuksköterskors upplevelse av att vårda och bemöta patienter som får palliativ vård i hemmet. Metod: Empirisk intervjustudie med en deduktiv kvalitativ ansats, där semistrukturerade frågor utefter intervjuguide användes. Insamlad data analyserades med manifest innehållsanalys. Resultat: Skillnader i upplevelsen mellan roll, relation och bemötande uppfattades då vård av patient bedrevs i hemmet i förhållande till på sjukhus. Klara skillnader av sjuksköterskerollen kunde ses då sjuksköterskan var civilklädd. I relationen till patienten upplevs det mer personlig när sjuksköterskan bjöds in till patienten hem.

Background:When the patient is critically ill the family is in a vulnerable position. The nurse's role is to support and help the family to find meaning in the difficult situation and to provide realistic hope. Balancing between the patient's and the family's needs is difficult. Knowledge about how nurses experience difficulties in the interaction with family is required in order to grant good care too critically ill patients and their family-members.Aim:To describe nurses' perceived difficulties in the interaction with family-members of critically ill patients.Method:The study is a qualitative literature-based study based on qualitative research. Results: The analysis resulted in four main themes; difficult disunion, environmental constraints, interpersonal difficulties and communicative difficulties.

The aim of this undergraduate thesis was to explore how the welfare officers at palliative units in Stockholm respond to the patients? thoughts and experiences during the last phase of life, as well as exploring their picture of the patients experiences. The research questions of the study were:? How do the welfare officers relate to the patients? experience of their death? ? In what way do the welfare officers respond to the dying patient and his or her experiences?? What knowledge/experience do the welfare officers have and what knowledge/experience do they consider is needed in their profession?To answer the research questions a qualitative method was used where five welfare officers in three different palliative units were interviewed. The empirical material was analysed through meaning concentration and are presented using exact quotations.

Previous reaserch has indicated that the almoners position in the somatic hospital hierarchy is poor. The purpose of this study was to investigate the position of the almoner in the hospital hierarch today, together with what this position is based upon.The questions at issue were:- Has the almoners position in the hospital hierarchy changed, or is it still poor?- In what way can the almoners position in the hospital hierarchy be explained?In order to get answers to our questions at issue, we interviewed totally 13 persons from the three chosen professional categories, i e four almoners, five doctors and four nurses. Two of the doctors worked at care centres and the other doctors worked in hospitals within the Region Skåne. The interview material was analysed from the concepts of Pierre Bourdieus; field and symbolic capital and by means of ideas from the closing theory.

Background: Mental illness is a growing public health problem which can cause significant disabilities and lead to poor quality of life. As primary care nurses often are the first to encounter these patients they need knowledge to be able to respond appropriately to this group.Aim: The aim was to describe how the sufferer of mental illness experiences the introduction to primary care. Method: The literature review was based on the results of 11 scientific articles which were analyzed with the inspiration of a metasynthesis method.Results: Four categories emerged: the experience of being treated like a human being, the importance of a therapeutic space, the experience of time and availability as well as the importance of competent personnel and the importance of continuity. Patients described different aspects deemed important when encountering nursing staff. Conclusion: Patients experienced that they received good care when they felt listened to and seen as individuals with their own thoughts and feelings.

Background: Each year approximately 30 000 people suffer from stroke in Sweden, often with substantial mental and physical consequences. Those who suffered from stroke handled the situation by mourning what they had lost and by accepting their changed body and life situation. For those who provide care for people who has suffered a stroke help and support was required. The caring science perspective was based upon caring and suffering. Aim: The purpose of this study was to describe family caregivers? experiences of caring for persons who had suffered a stroke.