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93 Uppsatser om Grief - Sida 4 av 7

FÖRÄLDRARS BEHOV NÄR BARNEN VÅRDAS PÅ SJUKHUS en kvalitativ litteraturstudieA CHILD´S STAY IN HOSPITAL ?FROM THE PARENTS` PERSPECTIVE

Background:Alzheimer's disease is a disease that primarily affects the elderly but also younger people. Alzheimer's disease is a type of dementia which means that you get changes in the cerebral cortex and cells gradually die. The disease causes memory loss and things that were obvious before will be difficult for the sufferer. Alzheimer's disease also affects next of kin to a large degree; they will have to take a great responsibility. The next of kin are entitled to support from healthcare.Aim:The aim was to highlight next of kin' experiences of healthcare to their family members with Alzheimer's disease.Method: The study was based on narratives, which in this case means analysis of autobiographies.

Omvårdnad av närstående vid ett plötsligt dödsfall

Bakgrund: En av sjuksköterskans uppgifter är att visa de efterlevande hänsyn och omtanke när någon avlider. Vårdutbildningar är till stor del somatiskt inriktade och ute i den kliniska verksamheten ges mycket knapphändig information kring hur dödsbesked ska levereras. Ett bristfälligt bemötande från sjuksköterskans sida kan leda till att närståendes sorgearbete kompliceras. Syfte: Syftet var att undersöka närståendes situation i samband med ett plötsligt dödsfall samt beskriva relevanta omvårdnadsåtgärder i detta skede. Metod: En litteraturstudie som bygger på fem kvalitativa och fem kvantitativa vetenskapliga artiklar.

Förlusten av ett barn : en litteraturstudie om föräldrars upplevelse under sorgarbetet

Att förlora sitt barn är den svåraste förlust en förälder kan uppleva i livet. Sorgen blir påtaglig och livet raseras på ett ögonblick. Syftet med studien var att beskriva föräldrarnas upplevelse under sorgarbetet vid förlusten av ett barn. Metoden som användes var en litteraturstudie med kvalitativ innehållsanalys. Resultatet sammanställdes utifrån åtta vetenskapliga artiklar som svarade på studiens syfte.

Kvinnors erfarenheter av att leva med migrän : En studie baserad på skriftliga berättelser

Background:Alzheimer's disease is a disease that primarily affects the elderly but also younger people. Alzheimer's disease is a type of dementia which means that you get changes in the cerebral cortex and cells gradually die. The disease causes memory loss and things that were obvious before will be difficult for the sufferer. Alzheimer's disease also affects next of kin to a large degree; they will have to take a great responsibility. The next of kin are entitled to support from healthcare.Aim:The aim was to highlight next of kin' experiences of healthcare to their family members with Alzheimer's disease.Method: The study was based on narratives, which in this case means analysis of autobiographies.

Sambandet mellan sorg, coping och stöd. En kvalitativ undersökning om anhöriga till yngre personer med demens

Demenssjukdom är oftast åldersrelaterad och utvecklas i senare ålder, men det finns personer och familjer som drabbas tidigare i livet. Rollen som anhörig kan vara både psykiskt och fysiskt påfrestande och är därför viktig att belysa. Syftet med studien är att undersöka det komplexa kvalitativa sambandet mellan sorg, copingstrategier och stöd hos anhöriga, när en närstående utvecklar demenssjukdom i tidig ålder. För att analysera datamaterialet som samlades in har kvalitativ innehållsanalys använts. Det som studien framför allt visar på är att det finns ett ömsesidigt samband mellan de tre komponenterna, där stödet utgör grunden.

Konservativt behandlad smärta i ländryggen : Individers bedömning av att klara av aktiviteter i det dagliga livet efter utskrivning från vårdavdelning

Background:Alzheimer's disease is a disease that primarily affects the elderly but also younger people. Alzheimer's disease is a type of dementia which means that you get changes in the cerebral cortex and cells gradually die. The disease causes memory loss and things that were obvious before will be difficult for the sufferer. Alzheimer's disease also affects next of kin to a large degree; they will have to take a great responsibility. The next of kin are entitled to support from healthcare.Aim:The aim was to highlight next of kin' experiences of healthcare to their family members with Alzheimer's disease.Method: The study was based on narratives, which in this case means analysis of autobiographies.

Aspects of caring for suddenly bereaved relatives

Background: When a person suddenly pass away, the relatives often arrive to the Emergency Department under chaotic circumstances. In this critical situation the nurse has an important role for the care. Many nurses lack of knowledge about how to take care of the bereaved relatives. Aim: The aim of the literature study was to describe aspects of caring for suddenly bereaved relatives. Method: The data for the study were scientific articles found in the databases PubMed and Cinahl and from a manual search.

Aspects of caring for suddenly bereaved relatives

Background: When a person suddenly pass away, the relatives often arrive to the Emergency Department under chaotic circumstances. In this critical situation the nurse has an important role for the care. Many nurses lack of knowledge about how to take care of the bereaved relatives. Aim: The aim of the literature study was to describe aspects of caring for suddenly bereaved relatives. Method: The data for the study were scientific articles found in the databases PubMed and Cinahl and from a manual search.

BESLUT I EN TID AV F?RLUST N?rst?endes upplevelse av beslutsprocessen vid organdonation efter d?den

Background: Every year, patients die while waiting for an organ due to the shortage of donors. When a patient is declared brain dead, the question of possible organ donation arises. In some cases, the patient is registered in the donor registry, but sometimes their stance on donation is unknown. The next of kin then become involved in the decision and are asked both what the patient would have wanted and how they themselves feel about donating their deceased family member?s organs. Aim: The aim of this literature review was to describe relatives' experiences of the decision-making process regarding organ donation after death.

När livet förändras : En självbiografistudie om föräldrars upplevelse av att leva med ett barn med cancer.

Background: Cancer is the most common cause of death among children in Sweden. The disease and the treatment cause suffering among the children, which also affects their parents. Research has shown that parents of children with cancer have poorer health. It is the nurse?s responsebility to help, not only the child, but also the parents in their difficult situation.

Mo?drars upplevelser av amningsproblem och ra?dgivningen fra?n amningsmottagningen i en sto?rre svensk stad

Background: One in three breastfeeding women sustain a chest complication. Many mothers feel that breastfeeding counselors have been the key to initiate and maintain the breastfeeding.Aim: The aim of this study was to investigate mothers? experiences of breastfeeding problems and the advice given from a breastfeeding clinic in a large Swedish city.Method: A qualitative interview study with an inductive approach was made. Ten mothers were interviewed through a semi-structured interview guide. Data were analyzed by using content analysis.Results: Three categories and six sub-categories of mothers' perceptions of breastfeeding pro- blems and the advice they got from the breastfeeding clinic were identified.

The Weight of Nature

There is an expression called ?Grief of climate? that refers to feelings of powerlessness and heaviness related to the environmental problems of today. A feeling that every move we make has bad consequences for nature. This essay is an investigation of how art in general and jewellery art in particular can be a way of discussing and visualizing current environmental problems and the complex relationship between human and nature. I am discussing how artworks dealing with a dark and dystopian picture of the relation can be seen as the memento mori of our time.

Bemötande och omhändertagande av närstående vid plötsligt dödsfall inom akutsjukvården sett ur sjuksköterskans och närståendes perspektiv.

AbstractThe aim of this literature review was to describe the experience and needs of sudden bereaved family members who lost a loved one in a sudden and unexpected death. The aim   is furthermore to depict the experience of unexpected and sudden death from the nurse´s point of view. Method: The literature review study has been carried out with a descriptive design. The result of the study was based on 14 scientific articles with quantitative and qualitative approach. The articles were searched in the databases PubMed and Cinahl and through manual search.Results: A majority of close relatives that experience a sudden bereavement are dissatisfied with the way they have been encountered by the staff.

Vem tröstar de äldre? : En kvalitativ studie om sörjandestödet för äldre

Studiens syfte är att undersöka äldres upplevelser av stöd i samband med sorg, vid förlust av livskamrat, samt att undersöka professionellas erfarenheter av sörjandestöd för äldre. Syftet preciseras genom följande frågeställningar: Vilket stöd finns att tillgå äldre i sorg, utifrån samhällets insatser? Vilka eventuella brister finns i sörjandestödet för äldre? Vilka aspekter har varit avgörande för de äldres sorgebearbetning? Studien har genomförts utifrån kvalitativ metod med semistrukturerade intervjuer som datainsamlingsmetod. Intervjuer har genomförts med två respondentgrupper, den ena med tre äldre personer vilka erfarit förlust av livskamrat, den andra med tre professionella vilka via sitt arbete kommer i kontakt med äldre. De teoretiska utgångspunkterna har utgjorts av kristeori, rollteori och ålderism.

Bemötande av barn vars föräldrar är döende eller har avlidit. En litteraturstudie

Each year over 3000 children in Sweden lose a parent. The loss of a parent may cause some grave changes in a child?s life, leading to both mental and physical consequences. The purpose of this literature study is to examine the different ways in which health care personnel can better receive and relate to children whose parents are dying or have passed away.Data was collected through such sources as Pubmed, Academic Search Elite and Cinahl, which resulted in the inclusion of sixteen subsequent articles, ten of which were quantitative and six of which were qualitative. Thirteen of the said articles illustrate how children act in response to a dying or deceased parent and what measures were needed for them to move on with their lives.

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