Does spouse participation influence quality of life reporting in patients with Parkinson’s disease?
Autor: | William J. Weiner, Melissa J. Armstrong, Karen E. Anderson, Stacy Schwartz, Ann L. Gruber-Baldini, Stephen G. Reich, Katherine Smentkowski, Lisa M. Shulman, Chelsea D. Morrow |
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Rok vydání: | 2014 |
Předmět: |
Adult
Male medicine.medical_specialty Parkinson's disease Concordance Disease Marital relationship Quality of life Sickness Impact Profile medicine Humans In patient Marriage Spouses Psychiatry Aged business.industry Public health Public Health Environmental and Occupational Health Parkinson Disease Middle Aged medicine.disease Health Surveys humanities Spouse Quality of Life Female Self Report business Clinical psychology |
Zdroj: | Quality of Life Research. 24:245-249 |
ISSN: | 1573-2649 0962-9343 |
DOI: | 10.1007/s11136-014-0744-2 |
Popis: | To investigate whether patient–spouse co-reporting (patient reporting with assistance from their spouse) results in the same ratings of health-related quality of life (HRQoL) as patient ratings without co-reporting, and to assess whether mutuality of the marital relationship is a determinant of co-reported ratings. Patients are the best source of HRQoL; however, co-reporting is common in clinical settings, but has not been compared to independent patient reporting of HRQoL. Fifty-nine Parkinson’s disease (PD) patient–spouse pairs completed the Short Form Health Status Survey (SF-12), measuring mental and physical HRQoL. Initially, the patient and spouse completed the SF-12 independently (about the patient). Then, patient–spouse pairs completed the SF-12 together assessing the patient’s HRQoL. Patients and spouses independently completed the Mutuality Scale rating the intimacy of their relationship. Patients rated physical HRQoL higher (M = 46.6) than spouses alone (M = 43.4, p |
Databáze: | OpenAIRE |
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