Health service experiences among adults with hereditary spastic paraparesis or neurofibromatosis type 1. Issue 10 (14th September 2020)
- Record Type:
- Journal Article
- Title:
- Health service experiences among adults with hereditary spastic paraparesis or neurofibromatosis type 1. Issue 10 (14th September 2020)
- Main Title:
- Health service experiences among adults with hereditary spastic paraparesis or neurofibromatosis type 1
- Authors:
- Fjermestad, Krister W.
Kanavin, Øivind
Nyhus, Livø
Hoxmark, Lise B. - Abstract:
- Abstract: Background: Persons with rare disorders may experience poorer health services due to limited knowledge about rare disorders among health professionals. Knowledge about how persons with rare disorders perceive health services can help inform service providers to enhance their practices. Methods: We conducted a self‐report survey among adults with the rare disorders hereditary spastic paraparesis (HSP; n = 108; mean age 57.7 years; 54.2% females) and neurofibromatosis type 1 (NF1, n = 142; mean age = 50.3 years; 62.0% females). Their responses concerning perceived health experiences were compared to healthy controls from the population study HUNT‐3 ( n = 7, 312). Results: Both rare disorder groups reported lower satisfaction, trust, and participation in meetings with their general practitioner and specialist health services. More reported health problems were overall associated with poorer health service experiences. Conclusion: There is a need to identify predictors of health service experiences at the patient and health service provider levels with the aim to tighten the gap between the health experiences of patients with and without rare disorders. Abstract : We examined the health service experiences of adults with the rare disorders, hereditary spastic paraparesis and neurofibromatosis type 1. Compared to controls, adults with rare disorders experienced poorer health services. Poorer health was associated with poorer health service experiences.
- Is Part Of:
- Molecular genetics & genomic medicine. Volume 8:Issue 10(2020)
- Journal:
- Molecular genetics & genomic medicine
- Issue:
- Volume 8:Issue 10(2020)
- Issue Display:
- Volume 8, Issue 10 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 10
- Issue Sort Value:
- 2020-0008-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-09-14
- Subjects:
- health service experiences -- hereditary spastic paraparesis -- HSP -- neurofibromatosis type 1 -- NF1
Medical genetics -- Periodicals
Genomics -- Periodicals
616.042 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2324-9269 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mgg3.1399 ↗
- Languages:
- English
- ISSNs:
- 2324-9269
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14438.xml