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SODELOVANJE LJUDI Z DEMENCO PRI NAČRTOVANJU NJIHOVE OSKRBE
ID Kračun, Suzana (Author), ID Mali, Jana (Mentor) More about this mentor... This link opens in a new window

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Abstract
V teoretičnem delu so opisane značilnosti demence in pristopi k njenemu obvladovanju, vključno z novejšo strategijo za obvladovanje demence v Sloveniji. Prikazane so posebnosti institucionalnega varstva in oskrbe ljudi z demenco s poudarkom na socialnem delu in vlogi socialnega delavca pri načrtovanju oskrbe in izvajanju socialnovarstvenih storitev. Predstavljene so tudi posebnosti varstva in oskrbe ljudi z demenco v domovih za stare ljudi v času epidemije covida-19. Namen raziskave je bil ugotoviti, kako so ljudje z demenco, ki živijo v Lambrechtovem domu v Slovenskih Konjicah, vključeni v načrtovanje njihove oskrbe in kako se je njihova vključenost v načrtovanje oskrbe spremenila v času epidemije covida-19. Zanimalo me je, komu ljudje z demenco v tem domu najbolj zaupajo, kakšne možnosti odločanja imajo in kako sta se njihovo zaupanje in odločanje spreminjali zaradi ukrepov v povezavi z epidemijo. Ugotavljala sem tudi, ali se zavedajo svoje pravice do zagovorništva. Poudarek v raziskavi je bil na tem, kako ljudje z demenco razumejo vlogo socialnega delavca glede ne obravnavano problematiko. Uporabila sem kvalitativno metode raziskovanja. Podatke sem pridobila s pomočjo delno strukturiranih intervjujev, ki sem jih izvedla z desetimi stanovalci tega doma s potrjeno 1. ali 2. stopnjo demence in s štirimi zaposlenimi v tem domu. Rezultati raziskave so pokazali, da so ljudje z demenco v tem domu vključeni v načrtovanje njihove oskrbe od sprejema v dom in da socialna delavca redno evalvirata in po potrebi spreminjata/prilagajata načrt oskrbe novim potrebam, ki jih ugotavljata pri stanovalcih. Intervjuvani večino odločanja o zadevah, ki so zanje pomembne, prepuščajo svojim otrokom. Ob sebi bi želeli imeti ključno osebo, njihovo poznavanje zagovorništva. Poznavanje pravice do odločanja o zdravljenju v prihodnosti je na splošno zelo pomanjkljivo. V času epidemije covida-19 sta bila zanje najtežje ukrepa omejitev gibanja in prepoved obiskov, njihovo odločanje pa je bilo bistveno okrnjeno. Vsi intervjuvani so opazili povečano skrb in trud zaposlenih, da bi jim v tem času olajšali bivanje v domu, vendar z izjemo navezovanja stika s sorodniki s pomočjo informacijsko-komunikacijske tehnologije, zaposleni niso izvajali inovativnih pristopov za zmanjševanje njihovih stisk, kakršne so izvajali v nekaterih drugih slovenskih domovih za stare ljudi. V sklopu načrtovanja oskrbe v tem domu bi morala socialna delavca ljudi z demenco na razumljiv način seznaniti s pravicami do odločanja o njihovem zdravljenju v prihodnosti in do zagovorništva. V primeru ponovitve izrednih razmer, kakršne so v domovih za stare ljudi vladale v času epidemije covida-19, bi morali v tem domu poskrbeti, da bi ljudje z demenco lahko pogosteje odločali o sebi in da bi bili manj socialno izključeni.

Language:Slovenian
Keywords:ljudje z demenco, dom za stare ljudi, socialno delo, osebno načrtovanje oskrbe, epidemija covida-19
Work type:Master's thesis/paper
Organization:FSD - Faculty of Social Work
Year:2024
PID:20.500.12556/RUL-158487 This link opens in a new window
Publication date in RUL:14.06.2024
Views:63
Downloads:19
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Secondary language

Language:English
Title:PARTICIPATION OF PEOPLE WITH DEMENTIA IN THEIR CARE PLANNING
Abstract:
The theoretical part describes the characteristics of dementia and approaches to its management, including the newer strategy for managing dementia in Slovenia. The specifics of institutional care and care for people with dementia with the emphasis on social work and the role of the social worker in care planning and the implementation of social care services are explained. The specifics of care and care for people with dementia in homes for the older people during the covid-19 pandemic are also presented. The purpose of the research was to determine how people with dementia living in the Lambrecht home in Slovenske Konjice are involved in the planning of their care and how their involvement in care planning has changed during the covid-19 pandemic. I was interested in whom people with dementia trust the most, what decision-making options they have and how their trust and decision-making have changed due to the measures related to this pandemic. I have also found out whether they are aware of their right to advocacy. The focus of the research was on how people with dementia understand the role of a social worker and on his view of the issue under consideration. I used qualitative research methods. I obtained the data with the help of semi-structured interviews, which I conducted with ten residents of this home with confirmed stage 1 or stage 2 dementia and with four employees of this home. The results of the research showed that people with dementia in this home are involved in the planning of their care from the moment they are admitted to the home and that social workers regularly evaluate and, if necessary, change or adjust the care plan to the new needs they identify with the residents. The interviewees leave most of the decision-making on matters that are important to them to their children. They would like to be in the contact with someone who was the knowledge of advocacy. Their knowledge of the right to make decisions about future treatment is generally very poor. During the covid-19 pandemic, the most difficult measures for them were the restriction of movement and the ban on visits, and their decision-making was significantly curtailed. All the interviewees noticed the increased care and effort of the employees to make it easier for them to stay at home during that time, but with the exception of establishing contact with relatives with the help of information and communication technology, the employees did not implement more innovative approaches to reduce their hardships, as they did in some other Slovenian homes for the older people. As part of care planning in this home, the social worker should inform people with dementia in an understandable way about their rights to make decisions about their treatment in the future and to advocate. In the event of a repeat of the emergency conditions that prevailed in homes for the older people during the covid-19 pandemic, we should ensure that people with dementia make more decisions about themselves and are less socially excluded.

Keywords:people with dementia, home for older people, social work, personal care planning, covid-19 pandemic

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