Background: Isolation care may be necessary when a patient is carrying infection or is being inflicted with disease that causes deficit immune system. Being isolated means that the patient is in a confined space and may stay only there. Even in ancient times, people discovered the importance of isolating people carrying an infection from the rest of society. According to the Infectious Diseases Act, patients should be isolated in order to reduce the spread of infection both from the patient to the surroundings as well as the opposite. Isolation care can be psychologically stressful for some patients.

Background: Relatives are those persons who are closest to the patient, regardless of relationship and included into the patient´s life world. When a person is in a palliative stage this affects not only the patient but also the relatives, as it implies such a big change in life for all. The nurse has an important role for both the patient and the relatives. Aim: The aim is to highlight the relative´s needs of support for palliative care. Method: A literature review based on previous research. Ten articles were found, nine with a qualitative approach and one with both qualitative and quantitative approach. Results: The analysis resulted in six themes, these were the result of the study. The six themes were, ?to be seen an confirmed?, ?good communication?, ?continuous information?, ?availability and continuity?, ?to participate? and ?to share responsibility with the staff?. Conclusion: As a nurse we come in contact with relatives of patients in a palliative setting in any form.

Bakgrund: Otillräcklig information, att inte bli uppmärksammad, lyssnad på, samt att inte bli sedd som en individ med individuella behov, har visats leda till osäkerhet i interaktionen mellan vårdare och patient samt missnöje med vården. Det är en fördel för sjuksköterskan att ha självkännedom för att kunna skapa ett bekräftande möte. Bekräftelse i ?Jag-Du-mötet? anses vara grunden för allt mänskligt liv. Syfte: Syftet var att beskriva betydelsen av att bekräfta identiteten hos inneliggande patienter på sjukhus, utifrån ett patient- och sjuksköterskeperspektiv.

The Swedish prehospital/ambulance organization has the last decades evolved from a transport organization to a an organization that focus on alleviate and treating acute medical conditions in the field as well as transporting patient to the emergency ward. The ambulance service is developing continually and offers today a high-tech and highly specialized nursing/care. Which in turn demand a higher standard and competence on the care provider. Ambulance mission can vary in priority and magnitude. This in turn demand a high medical competence our capacity.

Dystrofia myotonika Typ 1 (DM 1) är en kronisk, progressiv och ärftlig neuromuskulär sjukdom. För patienten innebär det en livslång sjukdom där försämring sker över tid och där även flera i familjen är eller kan vara drabbade. Patienter med DM 1 är i behov av regelbunden uppföljning gärna varje år. För att kunna tillgodose patientens behov skapades på Neuromuskulärt centrum, Sahlgrenska sjukhuset Göteborg, en sjuksköterskemottagning. Syftet med föreliggande litteraturstudie, var att kartlägga kunskapen om sjuksköterskemottagningar samt belysa mötet mellan patient och sjuksköterska.

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.

Background: Borderline personality disorder is a psychiatric diagnosis that one to two percent of the population and at least every fourth patient that have received treatment at a psychiatric clinic has been diagnosed with. BPD is most common in women between teenage and early adulthood. Purpose: The aim of this literature study was to emphasize the nursing care of patients diagnosed with BPD within different perspectives. Method: A literature study was conducted to get a deeper understanding for the nursing care of patients with BPD. The search for pertinent articles, answering to the aim of the study, was done in different databases.

Background: In Sweden it is a legal right for patients to have the possibility to participate in their own care. Several studies highlight the importance of a good relationship, good communication and good cooperation in order to increase a sense of security and thus the possibility of participation. One way to increase patients' ability to influence and participate can be to adapt person-centered care. This moves the focus from the patient's illness to the patient and his/her resources. Aim: The aim of this study is to describe patients' experiences of the possibility to actively participate in decisions regarding its care and treatment at surgical wards.

Syftet med denna litteraturstudie var att beskriva hur patienter upplever information inför gynekologiska ingrepp och undersökningar. Metoden som användes för att belysa syftet var beskrivande litteraturstudie. Data insamlades via två databaser, Medline och Cinahl. Andra sökstrategier var manuell sökning i valda källor. 15 vetenskapliga artiklar inkluderades i resultatet, dessa kvalitetsgranskades, analyserades och sammanställdes.

Syftet med denna litteraturstudie var att undersöka vilka emotionella omvårdnadsbehov patienterna hade innan operation och hur sjuksköterskan på bästa sätt kunde lindra dem. Metoden var en litteraturstudie baserad på vetenskapliga artiklar med dels en kvalitativ ansats (n= 5) och dels en kvantitativ (n= 10). Artikelsökningarna gjordes via sökmotorn ELIN och databaserna CINAHL och PubMED. Artiklarna var etiskt godkända samt publicerade mellan 2000-2010 och skrivna på engelska. De granskades med hjälp av granskningsmallar.

In the light of new technology health care is now given the opportunity to form a more mobile way of working that would bring about potential gains in terms of efficiency and quality. On the other hand, a more mobile health care also requires a more generous handling of personal information, something that may raise issues in terms of privacy. This study shows that the privacy of the patient requires two things: (i) that the personal information of the patient is handled in a way that generates her an overall positive expected utility and that (ii) the negative expected utility that each risk of an information leakage causes is offset by the expected utility it also makes possible. The first requirement (i) is shown, in comparison with today?s way of working, to be met due to the potential gains in efficiency and quality in combination with no increase in the probability of informational leakage or negative effects of such a leakage. The second requirement (ii) was also considered met since no separate risks of information leakage could be identified that was not offset by the gains it made possible in terms of expected utility..

A literature study abot the patient´s experience of the meeting with the nurse.

Syfte med denna litteraturstudie var att beskriva och sammanställa patientens upplevelse av att få information från sjuksköterskor angående egenvård vid venösa bensår .Artiklarna söktes på databaserna Medline och Cinahl. Sökorden som användes var leg ulcer, information, experience, self-care. Resultatet inkluderade elva artiklar där åtta hade kvalitativ ansats, två hade kvantitativ ansats och en hade både kvalitativ och kvantitativ ansats. Patienternas upplevelser av att få information varierade. En del var positiva till informationen på grund av sitt förtroende för sjuksköterskan.

Previous research and patient complaints to the Swedish Patient Support Committee shows that there is a lack of substance in the patient-nurse relationship. This may suggest that it can be difficult for health care to live up to health-care law which requires it to be of good quality, based on dignity and respect and designed so that the patient is an active participant and can make their own decisions when it comes to their health care. For a better understanding of what a dignified patient-nurse relationship is, this study aims to clarify what the patient values as good patient-nurse relationship and describe how they have experienced the patient-nurse relationship during their stay at an emergency care department. The study is a descriptive cross-sectional study with a quantitative approach, where the population consisted of patients who were cared for at an emergency care department in the County of Västmanland, Sweden during 2007. The sample consisted of 93 patients which were asked to answer a questionnaire.

The digitization of patient data and medical records used by the healthcare-industry in Sweden is rapidly developing. However; developing and changing things in this field is not an easy task because of the circumstances surrounding it. Digital systems intended to process, and hold, sensitive personal data, such as medical journals, must be developed with laws, confidentiality, integrity and availability in mind to secure that none of this data gets compromised.A complicating factor in regards to this is the fast rate of development within IT in contrast to the much slower bureaucratic process of the justice system. This means that laws and regulations oftentimes aren?t up to date with the newest available technology.With the purpose of establishing set regulations on how patient data should be properly handled the Swedish government enacted the Patient Data Act (sv.