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The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
provided by the
Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
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Showing 291 to 292 of 292 (0.017 seconds)| 291 |
Närståendes upplevelser av att vårda en anhörig med cancer i livets slutskede i hemmet : en litteraturöversikt / Family’s experiences of caring for a relative with cancer at the end of life at home : a literature reviewMahne, Fanny, Ohlsson Moberg, Sofie January 2021 (has links)
Bakgrund: Varje år behöver 70 000–75 000 människor palliativ vård, varav de flesta har en cancersjukdom. Närstående har en viktig och central del i palliativ vård och kan påverka den drabbades mående innebär att lindra symtom och lidande där fokus inte ligger på att bota sjukdomen. Sjuksköterskan har en viktig roll att stötta och involvera närstående i kommunikationen. Syfte: Syftet var att beskriva närståendes upplevelser av att vårda en anhörig med cancer i livets slutskede i hemmet. Metod: Metoden som valdes var en litteraturöversikt. Tio vetenskapliga artiklar inkluderades i resultatet. Artiklarna analyserades enligt Fribergs metod. Resultatartiklarna hade kvalitativ design och hämtades från CINAHL Complete och MEDLINE. Resultat: Litteraturöversikten presenterades i tre teman och fem underteman. Det första temat innefattar att bli en vårdare, med undertemat ansvar att ständigt vara på vakt. Det andra temat innefattar känslor av vårdandet, med underteman stress och tiden nära döden. Det sista temat innefattar behov av stöd, med underteman stöd från familj och vänner, stöd från hälso-sjukvården. Slutsats: Resultatet visade att närstående kände ett ansvar av att vårda sin anhörig, detta ansvar medförde bland annat att tunga beslut låg i deras händer angående anhörigas autonomi. Ansvaret bidrog även med negativa effekter både psykiskt och fysiskt i form av utmattning. Förberedelser inför döden visade sig vara en viktig del för närståendes mentala hälsa samt att stöd från familj, vänner och vårdpersonal framkom som betydelsefullt. / Background: Every year, 70 000–75 000 people need palliative care, most of them have cancer. Relatives have an important and central part in palliative care and can affect the victim's mood. Palliative care involves relieving symptoms and suffering where the focus is not on curing the disease. The nurse has an important role to support and involve relatives in the communication. Autonomy is seen as a difficult ethical dilemma in palliative care as the sufferer may have difficulty being self-determined in the final stages of life. Aim: The purpose was to describe relatives' experiences of caring for a relative with cancer in the final stages of life at home. Method: The chosen method was a literature review linked to Friberg. Ten scientific articles were included in the results. The articles were analyzed according to Friberg's method. The result articles had a qualitative design and were taken from CINAHL Complete and MEDLINE. Results: The literature review was presented in three themes and five sub-themes. The first theme includes becoming a caregiver, with the sub-theme responsibility to be constantly on guard. The second theme includes emotions of care, with the sub-theme of stress, the time close to death. The last theme includes need for support, with the sub-theme support from family and friends, support from health care. Conclusion: The results showed that close relatives felt a responsibility to care for their relatives, this responsibility meant, among other things, that heavy decisions were in their hands regarding the relatives' autonomy. The responsibility also contributed with negative effects both mentally and physically in the form of exhaustion. Preparations for death proved to be an important part of the mental health of close relatives and that support from family, friends and care staff emerged as meaningful.
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Barnrättsperspektiv i vårdnadsmål vid risk för separationsvåld eller så kallat ”eftervåld” : En studie om rättens avvägning mellan skydd för barn och barns rätt till en nära och god kontakt med båda föräldrarna / The children rights perspective in custody cases in case of risk of separation violence or so-called ”post-separation violence” : A study of the court's balance between protection of children and children's right to close and good contact with both parentsChavez Lupe, Lynette, Falk, Stina January 2022 (has links)
It's a misconception that those who leave a violent relationship are safer than those who stay. For those who have children with their perpetrator there is an increased risk for post-separation violence (Fleury, Sullivan & Bybee, 2000). The aim of this study has been to examine the child rights perspective through how the court judges and resonates in custody disputes with information regarding violence and therefore a possible risk for post-separation violence. Data was retrieved in the form of 34 custody cases from the court of appeal. In order to fulfil the purpose of the study a multi-method investigation has been used, both a quantitative content analysis and a discourse analysis. The results showed that the parent who was mainly referred to as the perpetrator was assigned visitation rights in 64.4 % of the cases, joint custody in 46.6 % and housing in 20 %. The main result showed that the courts ruled the child’s right to close and good contact with both parents outweighs the risk of post-separation abuse, either towards the other parent or the child himself. Children should be allowed to grow up with both parents. However, one could question at what price.
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