The family has been described as the center or heart of societal relationships with each family member playing an integral part in that relationship (Garret & Landau, 2007; Jay & Jay, 2000). Therefore, when a family member is affected by a disease such as addiction, his or her predicament typically impacts other members of the family. When this occurs, family members may seek therapy to provide solutions. One technique that has been found to be beneficial to the entire family by providing education about the addiction is brief family-based treatment (FBT) (Jay & Jay; Johnson, 1998). Brief family-based treatment, teaches, that as family members work together, they have a much better chance of changing their own perceptions/attitudes about addiction and thereby changing the outcome for the relative with addiction.

Background: This systematic review aimed to identify factors related to psychological distress in family members of pediatric cancer patients on active treatment. Methods: Search strategies were entered into six academic databases. Randomized, nonrandomized, quantitative descriptive and mixed method studies, examining factors related to psychological distress in the population of study were included. Identified factors were coded as per the 4P’s of case formulation. Results: 59 studies were included. Parental factors identified: 24 predisposing factors; 12 precipitating factors; 35 perpetuating factors; and six protective factors. Sibling factors identified: five predisposing factors; one precipitating factor; 14 perpetuating factors; and two protective factors. A text-based, narrative synthesis and tabular summaries are presented. Discussion: Findings can support the: (1) recognition of distress exhibited in family members; and (2) the timing of interventions specific to the chronological manifestations of distress. Assessment of risk of bias was not done. Other: International Prospective Register for Systematic Reviews (PROSPERO) registration number CRD42018109802. No sources of funding to declare.

Suicid är en avsiktlig, självdestruktiv handling som leder till döden. Varje år begås närmare 800 000 suicid runt om i världen och av dessa uppskattas cirka 1100 suicid begås i Sverige. I genomsnitt sörjer sex personer för varje fullbordat suicid, vilket innebär att sjuksköterskor i stor utsträckning kommer att möta dessa anhöriga inom vården. Syftet med studien var således att belysa anhörigas upplevelser av att mista en familjemedlem till följd av suicid. Föreliggande studie är en litteraturbaserad studie baserat på kvalitativa artiklar. Studien behandlade begrepp som hälsa och lidande, vilket vidare relaterades till suicid och de efterlevandes upplevelser. En sammanställning av totalt nio vetenskapliga artiklar användes som grund i utformningen av resultatet. Resultatet redovisade att de efterlevande i hög omfattning upplevde känslor av skuld och skam, relaterat till att bli dömd av andra och att döma sig själv. Att bli dömd av omgivningen framgick bero på att denna sortens handling inte var accepterat i samhället, det beskrevs vara ett tabubelagt ämne. Stöd beskrevs upplevas som antingen tillfredsställt eller bristande. Att genomgå sorg innefattade ett känslomässigt kaos och de efterlevande hade ett stort behov av att få sörja. Att därefter gå vidare i livet gjordes med hjälp av olika metoder, bland annat ritualer för att bevara minnen av den avlidne men även att uppnå acceptans för att förmå att leva vidare. Dessa efterlevande upplevde ofta både psykiskt och fysiskt lidande, genomgående i kris- och sorgeprocessen. Det beskrevs att de efterlevande upplevde stort behov av stöd, men att flertalet inte erhöll tillgodosedda stödinsatser. Sjuksköterskors förmåga till utveckling av vårdkvaliteten för att förmå att minska lidande och förebygga ohälsa hos dessa anhöriga beskrevs därför som viktig. Sjuksköterskor bör således även ha en grund i vårdvetenskap för att kunna bidra till kunskapsutveckling inom detta område. / Background: Suicide is defined as a deliberate and self-destructive act that leads to death. It’s considered as a extensive health problem and each year, nearly 800 000 people die as a result of suicide around the world. Six people in each case estimates to be affected about the suicide. Sufficient support is considered important for these people. Aim: The aim of this study was to illuminate relative’s experience of losing a family member as a result of suicide. Method: A literature-based study including qualitative studies was chosen, according to Friberg (2006), in order to illuminate the relative’s experience of losing a family member as a result of suicide. The results of a total of nine scientific articles were compiled. Results: The results are presented in four themes, and a total of eight subthemes. The presented themes where grief, to be judged by others and to judge themselves, need of support and to continue living. Conclusion: The relatives often experience great suffering, but the results in this study shows that most suicide survivors don’t receive sufficient support. The care of these survivors thus requires a big commitment from the nurses. A guidance to relevant support measures is therefore of great importance, because sufficient support relieve illness, suffering and depression. The nurse should have a reflective approach and a scientific base in the care of these suicide survivors.

No description available.

Background: To be the close relative of a terminally ill person, who is receiving special palliative care, is a life changing experience. According to the guide lines for palliative care both the patients and their family members have the right to support, and to be part of the caring process. For nurses to be able to meet the needs of relatives, understanding their experience of special palliative care is crucial. Aim: To highlight the family´s experience of palliative care from specialist palliative operations. Method: A method based on the analysis of qualitative research was used, in order to contribute to evidence-based care. Ten scientific articles were analysed. Results: Emotions of guilt and relief were common amongst family members. The family members experienced that the nurses where a safe harbor when the family members received the support they needed. Sometimes the family members felt as if their homes and their private sphere became a workplace. Conclusion: Honest, straight, and clear communication was of great importance. For family members to be able to ask nurses for help and to feel supported in different situations was also important. The physical symptoms of death approaching became symbols of grief and sorrow.

Background: Being close to a person who suffers from a disease can mean a burden, as these tends to disregard own needs in favor of the person who is sick. Aphasia is a disorder that affects communication skills and is one of the most common complications due to brain damage. Aim: The main purpose of this literature study was to illuminate relatives experiences of living with a person with aphasia. Method: Nine scientific articles were analyzed with a qualitative manifest content analysis which resulted in three themes with subthemes: Emotional reactions: The impact on well-being, Changing social and emotional relationships; A changed everyday life: Obstacles in communication, Decreased social interaction, Being able to handle everyday; Increased need for support: To get information about the aphasia; Deterioration of the economy and the need for financial support. Result: It was revealed that relatives felt left aside in the care of their relative with aphasia, resulting in an increased need for information, support and relief. Conclusion: Therefore conclusion was that relatives should be asked by nurses of how much involved in the care of their sick relative they want to be or can be and how much support they need to be able to handle that.

MFamMed, Faculty of Health Sciences, University of the Witwatersrand, 2010

Sammanfattning   Bakgrund: Sjuksköterskor har till uppgift att informera anhöriga med hänsyn till tidpunkt, form och innehåll. Anhöriga har behov av att få information från sjuksköterskor. Studier visar att behovet av information inte tillfredsställs och att anhöriga lider i ovisshet och väntan.   Syfte: Beskriva anhörigas upplevelser av att bli informerade av sjuksköterskor.   Metod: En litteraturöversikt enligt Friberg (2006) har gjorts och baserats på nio vetenskapliga artiklar. Likheter i resultaten delades efter innehåll in i teman.   Resultat: Anhöriga vill bli informerade på vardagligt språk, med få medicinska termer och informationen ska vara rak, sanningsenlig och patientnära. De vill inte behöva vänta på att få information, de vill få den kontinuerligt och inte riskera att få motsägelsefull information. Förmedlad information ska syfta till att anhöriga får förståelse för situationen den närstående befinner sig i, utvecklar tillit till sjuksköterskorna och blir delaktiga i vården av den närstående. Dessutom bör förmedlad information lämna utrymme för realistiskt hopp.    Diskussion: Det händer att sjuksköterskor talar i medicinsk jargong med varandra och då anpassar de inte språket efter de anhörigas förförståelse av sjukvården. Sjuksköterskor bör, således, väga sina ord med större omsorg. Anhöriga söker information från andra källor, vilket ställer högre krav på sjuksköterskor att uppdatera och anpassa sig efter dagens snabba informationsflöde. För att möta anhörigas vilja till delaktighet kan familjeronder öka informationsöverföringen. Anhöriga får där möta människor från olika professioner och ta vara på deras kunskaper om den närstående och på så sätt skapa sig en egen bild över situationen.   Nyckelord: Anhöriga, behov, information, sjuksköterskor

No description available.

This study was conducted with employees from Drakensberg Power Station, in Kwazulu Natal. Twenty-three non-supervisory employees were interviewed, and six supervisors partook in a focus group. The purpose was to gain insight into the experiences and perceptions of employees about the Employee Assistance Programme (EAP), by exploring factors influencing utilisation and investigating the extent of employee awareness of the EAP, to recommend appropriate modifications to the service. Findings indicate employees are aware of the service, but unfamiliar with its purpose and functioning. They are not aware of how to access the service. The utilisation is affected by the lack of visibility of the service, the lack of awareness of family members about the services and concerns about confidentiality. It was found that supervisors were not adequately trained in the EAP and lacked the information to effectively utilise the service, thus they were reluctant to refer employees to the EAP. / Dissertation (MSD (EAP))--University of Pretoria, 2005. / Social Work and Criminology / Unrestricted