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Sökning: (L773:1877 7171 OR L773:1877 718X) > (2015-2019) > Health and Social S...

Health and Social Service Access Among Family Caregivers of People with Parkinson's Disease

Olsson, Yvonne (författare)
Lund University, Sweden
Claren, Lena (författare)
Lund University, Sweden
Alvariza, Anette (författare)
Ersta Sköndal högskola,Palliativt forskningscentrum, PFC,Capio Palliativ vård Dalen, Stockholm,Marie Cederschiöld University,Marie Cederschiöld högskola
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Årestedt, Kristofer (författare)
Ersta Sköndal högskola,Linköpings universitet,Linnéuniversitetet,Institutionen för hälso- och vårdvetenskap (HV),Ersta Sköndal Bräcke University College, Sweden,Avdelningen för omvårdnad,Medicinska fakulteten,Ersta Skondal University of Coll, Sweden; Linnaeus University, Sweden,Palliativt forskningscentrum, PFC,Linnéuniversitetet; Linköping universitet,Marie Cederschiöld University,Marie Cederschiöld högskola
Hagellf, Peter (författare)
Kristianstad University, Sweden,Högskolan Kristianstad,Patient Reported Outcomes - Clinical Assessment Research and Education (PROCARE)
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 (creator_code:org_t)
IOS PRESS, 2016
2016
Engelska.
Ingår i: Journal of Parkinson's Disease. - : IOS PRESS. - 1877-7171 .- 1877-718X. ; 6:3, s. 581-587
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Being a family caregiver for a person with Parkinson's disease (PD) can negatively impact health and wellbeing, but it appears less clear to what extent caregivers' health/social service needs are met. Objective: We explored the extent to which PD family caregivers experience sufficient access to health/social services, as compared to age-matched controls; and the associations between this and demographic and health-related variables. Methods: A cross-sectional survey of 66 PD family caregivers and 79 age-matched control subjects including the SF-36 health survey, the Nottingham Health Profile Sleep section (NHP-Sleep), and questions regarding contacts with various health/social related services and whether these were perceived as sufficient. Results: People reporting insufficient access (n = 29) were more often PD family caregivers than controls (83% vs. 37%), did more often have a disease of their own (79% vs. 46%), and reported poorer health according to the SF-36 and the NHP-Sleep. Being a PD family caregiver (OR, 8.90), reporting more pain (OR, 1.02) and having an own disease (OR, 3.46) were independently associated with insufficient health/social service access. Conclusions: Our results imply that those in greatest need for health/social services (i.e., those with poorer health, an own disease, and who are PD family caregivers) are those whose health/social service needs are least met. Larger studies are needed for firmer conclusions and regarding how unmet health/social service needs impacts caregiver health and wellbeing. Health/social service providers should not only focus on patients but also consider their family members' needs.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Omvårdnad (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Nursing (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Public Health, Global Health, Social Medicine and Epidemiology (hsv//eng)

Nyckelord

Caregivers
health
health services needs and demand
Parkinson disease
Health and Caring Sciences
Hälsovetenskap

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