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  • 1.
    Björk Brämberg, Elisabeth
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Att vara invandrare och patient i Sverige2008Doktoravhandling, monografi (Annet vitenskapelig)
    Abstract [en]

    This thesis focuses on immigrants in Sweden. What experiences from the meeting with Swedish society do immigrants have and what meaning does the immigrant background have when they have been patients within the Swedish health and medical service? Former research about patients with an immigrant background can be divided into two perspectives. One which illuminates ethnically demarcated immigrant groups and specific needs. The other perspective has an individually adopted approach independently of the patients’ ethnical background. Here it is mainly the communication problems that are stressed, since these make it hard to understand the individual’s needs. The two empirical studies of the thesis start from an individualised perspective, a life world perspective. Research data have been collected through open interviews. The overall purpose was to develop a deepened understanding of what it means to live as an immigrant in Sweden and receive care. The aim of the pre-study was to examine immigrants’ experiences of participation in municipal home care. In the main study the overall purpose was used and two research questions were asked: What do persons with an immigrant background have to tell us about their situation in Swedish society? How does the situation as an immigrant in Sweden influence the experience of being a patient in Swedish health and medical care? The pre-study shows that participation means making demands and meeting caregivers who view the patient as an actor with the right to make his or her own decisions. One important postulate seems to be access to a good interpreter. To refrain from participation seems to be about adopting a passive attitude as a patient. It seems as if it is the caregivers who are the active ones and the ones setting the standards for the contents of the care. To experience not being invited to participation mainly seems to originate from the fact that the interviewees could neither understand nor make themselves understood. One consequence is that patients are just looked upon as carriers of a symptom. The main study shows that the interviewees’ existential existence as patients involves the whole life situation. Different forms of unsurmountable difficulties might reinforce each other. The ambition to establish oneself in a new home country might therefore be passivised. For patients with immigrant background earlier experiences from exposed situations seem to influence how the patients feel about their treatment. The additional knowledge is that problems seem to reinforce each other. Patients with an immigrant background must be treated as individuals. Every individual’s story has to be made visible. The thesis shows that caregivers ought to endeavour to understand the individual. To encourage dialogue, despite language problems, is of importance for the patient to be able to express his or her needs. The use of an interpreter may have a positive influence on these patients’ possibilities to exert an influence. This means that caregivers who consult an interpreter should build up their competence to communicate through an interpreter.

  • 2.
    Björk Brämberg, Elisabeth
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Behövs kulturkompetens för att vårda patienter med invandrarbakgrund?2008Rapport (Annet vitenskapelig)
  • 3.
    Björk Brämberg, Elisabeth
    et al.
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Nyström, Maria
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    To be an immigrant and a patient in Sweden: A study with an individualised perspective2010Inngår i: International Journal of Qualitative Studies on Health and Well-being, ISSN 1748-2623, E-ISSN 1748-2631, Vol. 5, nr 3, s. 1-9Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The aim is to describe how experiences of being an immigrant can influencethe situation when becoming a patient in Swedish health care. A hermeneutic approach was used. Sixteen persons born in non-Nordic countries were interviewed. The data was analysed with an empirical hermeneutical method. The findings indicate that positive experiences (i.e., establishing oneself in a new home country) enhance the possibilities of taking part in caring situations and vice versa. Hence, there is a need for individually adapted care that takes one's whole life situation into consideration. Consequently, it is suggested that the concept, “cultural competence” merely serves the purpose of illuminating caregivers’ need for categorisation. It does not illuminate individual needs in a caring situation.

  • 4.
    Björk Brämberg, Elisabeth
    et al.
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Nyström, Maria
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Dahlberg, Karin
    Patient participation: A qualitative study of immigrant women and their experiences2010Inngår i: International Journal of Qualitative Studies on Health and Well-being, ISSN 1748-2623, E-ISSN 1748-2631, Vol. 5, nr 1Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Patient participation in healthcare is a neglected area of interest in the rather extensive amount of research on immigrant so-called Selma patients in Swedish health care as well as worldwide. The aim is to explore the phenomenon ‘‘patient participation’’ in the context of the Swedish health care from the perspective of immigrants non-fluent in Swedish. A phenomenological lifeworld approach was chosen. Data were collected from patients within a municipal home care setting in Sweden. Eight women agreed to participate. In seven interviews, an interpreter was necessary for the translation of the interview. Five authorized interpreters were used. Data were analysed in accordance to a descriptive phenomenological method for caring research. The analysis led to an essence of the phenomenon with three constituents, ‘‘to experience participation,’’ ‘‘to refrain from participation,’’ and ‘‘to be deprived of participation.’’ Patient participation from the perspective of immigrant women means that patients are involved and active in their own health and caring processes. For these women, it is particularly important to have the opportunity to express themselves. Patient participation presupposes professional caregivers who act in a way that increases the patients’ opportunities to take part. A skilled interpreter is often necessary in order to enable the patient participation.

  • 5. Knudsen, Kai
    et al.
    Björk Brämberg, Elisabeth
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Hagiwara, Magnus
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Svensson, Leif ()
    Intoxikation2009Inngår i: Prehospital akutsjukvård / [ed] Björn-Ove Suserud, Leif Svensson, Stockholm: Liber , 2009, s. 309-316Kapittel i bok, del av antologi (Annet vitenskapelig)
  • 6. Svensson, Leif
    et al.
    Sarlöv, Catharina
    Björk Brämberg, Elisabeth
    Högskolan i Borås, Institutionen för Vårdvetenskap.
    Svensson, Leif ()
    Diabetes2009Inngår i: Prehospital akutsjukvård, Stockholm: Liber , 2009, s. 316-325Kapittel i bok, del av antologi (Annet vitenskapelig)
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