BakgrundDiabetes typ 2 är en av de snabbast växande sjukdomarna i både Sverige och resten av världen. Vid diabetes typ 2 utgör egenvård en betydande del av behandlingen och för att klara detta behövs kunskap om sjukdomen. I sjuksköterskeyrket ingår att förse patienter med information och kunskap, bland annat genom patientundervisning. Ett flertal studier beskriver hur information och kunskap uppfattas av patienter och hur det på bästa sätt förmedlas till dem. Däremot saknas ett instrument som mäter patienternas befintliga kunskap om sjukdomen och hur de värderar information.SyfteSyftet med arbetet är att undersöka hur informations- och kunskapsbehovet vid diabetes typ 2 varierar utifrån kön, HbA1c, ålder, utbildning och duration samt identifiera de frågor där informations- och kunskapsbehovet är störst respektive lägst.MetodArbetet grundas på en kvantitativ enkät utformad efter The Toronto Informational Needs Questionnaire-Breast Cancer och är analyserat utifrån data från 86 patienter.  Frågor ur denna enkät har behandlats i dataprogrammet Statistical Package for the Social Sciences och presenteras som deskriptiv statistik.

Background: Poor perineal wound healing and infections after proctectomy surgery, affect a significant proportion of physical and psychological morbidities such as pain, leakage and abscesses. In its lengthening some of these symptoms will lead to extended periods of hospitalization. These kind of postoperative complications are also associated with delays in eventual chemotherapy treatment Aim: To describe the patients experiences of postoperative wound infection as well as communication and self-care support from the nurse specialist after proctectomy due to rectal cancer. Method: A qualitative content analysis was carried out from interviews. Results: Four main categories emerged; ?Coping with postoperative complications?, ?be independent?, ?feel safe?, and ?accept the situation?.

Aim: The aim of the study was to investigate attitude and practice to prescribe physical activity accordingly FaR® rules among personal at the specialized department of the University Hospital. Methods: A quantitative cross-sectional study was used to answer the purpose. The data were collected using specially designed questionnaire. That contained 11 questions related to interest and complications to use FaR® as a treatment method. A total of 38 individuals participated in the study.

ABSTRACTBackground: On behalf of the Orthopedic clinic, Västerås, a study has been conducted with focus on comparing the results after conservative and surgical treatment due to complete achillestendon rupture.Aim: To compare results when testing the active and passive range of motion, calf muscle endurance, estimation of pain related to the achillestendon and self-efficacy to be physically active for individuals who have undergone conservative or surgical treatment after complete achillestendon rupture.Method: 14 individuals afflicted by complete achillestendon rupture in 2010 were recruited as a purposive sample. Examination were conducted of: Ankle range of motion with a goniometer, calf muscle endurance through a toe-raise test, estimation of pain intensity related to the achillestendon by VAS and self-efficacy to be physically active through ?Exercise self-efficacy scale?. P-value and the median were calculated.Result: The results of ankle range of motion and calf muscle endurance were based on the difference between the injured and the healthy side. When testing active plantarflexion the conservative group had a median of 4 ? and the surgical group had a median of 10 ?.

 ABSTRACT  Nature of essay:                C-level, 15 pointsPage count:                        47Title:                                   The last way out?-A qualitative study of psychiatric staff and service users attitude to electroconvulsive therapy (ECT).Author:                              Hanna Nilsson Purpose: The purpose of this study is to investigate attitudes to electroconvulsive therapy (ECT) of professionals and service users within a user organization ? Riksförbundet för social och mental hälsa. (RSMH)Questions: Does the psychiatric staff believe that there are preconceptions about electroconvulsive therapy? What motivates service user?s choice of electroconvulsive therapy? Do the psychiatric staff and the service users think that the positive effects of ECT can outweigh the possible negative side effects?Method: Qualitative study. The study is based on interviews with psychiatric staffthat works with electroconvulsive therapy (ECT), and with services users who have received electroconvulsive therapy (ECT).Results: The result showed that the psychiatric staff feels that preconceived ideas occur about the treatment of ECT, and that it is affecting their approach to work.Service users motivate their choice by how bad they felt under the depression, and that ECT was their only choice left, that´s why psychiatric staff suggested the treatment.The positive effects of ECT outweighed the possible negative side effects because life is something you value higher than any memory loss and when there is currently no treatment having a similar efficiency.Keywords: Electroconvulsive therapy, Attitudes, Side effects, Experience, Patients, Professionals.

Every year many dogs in Sweden are bitten by the adder, a venomous snake (Vipera berus). Despite the fact that adder bites are so common in dogs there have been few investigations made that study the effects of treatment with glucocorticoids, a drug that is commonly used. We have carried out a literature study concerning adder bites in dogs and a prospective study where case history, clinical signs and treatment have been recorded in dogs that were presented at two veterinary hospitals after a confirmed or suspected adder bite. Fifty three dogs were included in the study out of which 22 were treated with glucocorticoids. In our study, the group of dogs treated with glucocorticoids was compared with the group of dogs that did not receive glucocorticoid treatment by the owner or on arrival at the clinic.

The treatment that women get from health care staff can influence the experience of the abortion and how women manage to coping the experience emotionally. The aim of this study was to illuminate women?s experiences in connection with an abortion. The findings show that the women?s social situation led them to the decision of abortion.

The subject of this bachelor thesis is discrimination and unfair treatment in the employment process where employers discriminate against job applicants. The purpose of this study and research questions is to investigate and clarify the legal protection available against discrimination and unfair treatment of pregnant women and persons on parental leave during the employment process and how this protection differs between men and women. This thesis highlights the Swedish law and EU law regarding discrimination and unfair treatment of individuals. The concept of discrimination and its requisites will be accounted for and exemplified by case law. This statement will be analyzed along with the relevant case law of the EU-court and the Labor-court.

Bakgrund: Det psykosociala stödet har stor betydelse för hur patienter med cancer klarar av sin sjukdom. Även om många botas från sin cancer bär de med sig erfarenheterna från sin sjukdomstid under resten av sitt liv. Det övergripande målet med psykosocial omvårdnad är att uppnå en högre livskvalitet för patienten. Författarna anknyter föreliggande studie till Cullberg kristeori. Syfte: Syftet med studien var att studera den psykosociala omvårdnadens betydelse for cancerpatientens livskvalitet.

Det är av stor vikt att hitta faktorer som leder till bättre livskvalitet för personer med allvarlig psykisk ohälsa. Ofta har dessa personer ett behov av flertal insatser/stöd och behandling samtidigt. En vanlig situation för dessa personer har dock varit att de ?faller mellan stolarna? då ingen instans tar ett helhetsansvar om brukarnas situation, trots den komplexa problematiken. En insats som tar ett samlat grepp om personer med allvarlig psykisk ohälsa är Assertive Community Treatment (ACT) och Case Management.

A school is a social area in which children and adults meet each other. The school is were friendship, love and also enmity arise. The process to establish, maintain, split up and end relationships is constantly continuously. A Childs way of creating relationships is complex. Bullying and similar offending treatment occur and has always been a huge problem in school.

The purpose of the study was from the perspective of young people that has completed a stay at HVB-home. The respondents are between 15-21 years both boys and girls. The basic questions were: How do the respondents look upon this HVB-homes service process? How do the respondents look upon this HVB-homes service contents? How do the respondents look upon this HVB-homes service regarding available information and how the staff is available? What positive and negative experience do they have from their stay at the HVB-home? We also wish to get a picture of what is important to change to improve the quality on this HVB-home. To receive answers to those questions we formed a questionnaire.

Aim: The aim of the study was to examine the effects of ?Rehabilitation with psychotherapy and yoga in group? with cancer patients, regarding physical, social, emotional and functional wellbeing. The participants? health and satisfaction with the project were also evaluated. Method: The evaluation was made with quantitative method and descriptive, longitudinal design.

Bakgrund: Gynekologisk cancer drabbar ungefär 2800 kvinnor i Sverige varje år och är därmed bland kvinnor den näst största diagnosgruppen efter bröstcancer. Denna cancerform drabbar ett mycket privat område vilket innebär att den ofta omges av starka känslor och upplevs som svår att prata om.   Syfte: Syftet med denna studie var att beskriva kvinnors fysiska och psykosociala upplevelse av att ha överlevt gynekologisk cancer. Metod: En litteraturstudie har gjorts utifrån granskning av åtta vetenskapliga artiklar. Via en manifest innehållsanalys har fyra huvudteman identifierats.Resultat: Att leva i en förändrad kropp: kvinnorna lever med en del kvarstående kroppsliga förändringar till följd av sjukdom och behandling. Det handlar om såväl konkreta fysiska symtom, men även om hur de här förändringarna påverkar kvinnorna, känslomässigt och psykosocialt. Ensamhet i mötet med sig själv och andra: kvinnornas upplevelse av överlevandet som en ensam process och avsaknad av stöd från närstående och sjukvård.

Menopause is a complex, paradoxical totality and every menopausal experience is differentfrom the other. This essay aims to capture some of the experiences surrounding it.The main questions is what it is that the women of the study share about menopause, andhow they talk about it. The material consists of interviews with eight women from the ages 51to 81, all of whom are either in menopause or have come out of it, and narratives collectedpartly on my own website ?Övergången? (?Transition?) and on the Internet via blogs and adiscussion board on menopause.Using Goffmans theories on interaction and roles and theories about gender and age as asocial construction I discovered that it is ambiguous messages that are thrown at the middleaged woman in menopause. Menopause is not always a welcome part of the role as a woman.The menopause is also associated with aging and a woman is expected to experiencemenopause during a certain age and period in the life schedule, often the middle age.