Effects of Parkinson's disease on quality-of-life patients' spousses: A qualitative survey;Impact de la maladie de Parkinson sur la qualité de vie des conjoints de patients: Une étude qualitative

Revue Neurologique

Volumn 163, Issue 8-9, 2007, Pages 801-807

  Dressen, C ^a   Brandel, J P ^b   Schneider, A ^b   Magar, Y ^a   Renon, D ^c   Ziegler M ^b  

^a EDU Santé   (France)

^b Léopold Bellan Hospital   (France)

^c GLAXOSMITHKLINE   (United Kingdom)

Author keywords

Cognitive behavioural therapy; Parkinson disease; Qualitative survey; Quality of life; Spouses; Support; Therapeutic education

Indexed keywords

ADULT; AGED; AMBIVALENCE; ATMOSPHERE; ATTITUDE; EDUCATION; EXPERIENCE; FEAR; FEMALE; FRUSTRATION; GUILT; HELPLESSNESS; HOSTILITY; HUMAN; INFORMATION; INFORMATION PROCESSING; INTERVIEW; MALE; PARKINSON DISEASE; PATIENT CARE; PERCEPTION; QUALITATIVE ANALYSIS; QUALITY OF LIFE; REVIEW; SOCIAL NETWORK; SPOUSE; STRESS; TENSION;

EID: 34548680328     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0035-3787(07)91462-9     Document Type: Article

References (10)

1. BRANDEL JP, SCHNEIDER A, ZIÉGLER M, MOUGIN P, ANTAKI H. (2003). Evaluation by SF 36 of cognitivo-behavioural therapy on eight PD patients and their spouses. International Congress of Parkinson's disease and Movement Disorders, Miami, 2003. Mov Dis, 17: S133.
2. CARTER JH, STEWART BJ, ARCHBOLD PG et al. (1998). Living with a person who has Parkinson's disease: the spouse perspective by stage of disesease. Mov Dis, 13: 20-23.
3. DESLAURIERS JP. (1991). Recherche qualitative, guide pratique (qualitative research, practical guide). Montréal, McGraw-Hill, pp. 20-45.
4. EDWARDS NE, SCHEETZ PS. (2002). Predictors of burden for caregivers of patients with Parkinson disease. J Neurosci Nurs, 34: 184-190.
5. HUGHES S, GIOBBIE-HURDER A, WEAVER F, KUBAL J, HENDERSON W. (1999). Relationship between caregiver burden and health-related quality of life. The Gerontologist, 39: 534-545.
6. MARTINEZ-MARTIN P, BENEDITO-LEON J, ALONSO F, CATALAN MJ, PONDAL M, ZAMARBIDE I, TOBIAS A, DE PEDRO J. (2005). QualLifeRes, 14: 463-472.
7. O'REILLY F, FINNAN F, ALLWRIGHT S, DAVEY SMITH G, BEN-SHLOMO Y. (1996). The effects of caring for a spouse with Parkinson's disease on social, psychological and physical well-being. British Journal of General Practice, 46: 507-12.
8. PASETTI C, ROSSI FERRARIO S, FORARA R. (2003). Caregiving and Parkinson's disease. Neurol Sci, 24: 203-204.
9. SUZUKAMO Y, OHBU S, KONDO T, KOHMOTO J, FUKUHARA S. (2006). Psychological adjustment has a greater effect on health-related quality of life than on severity of disease in Parkinson's disease. Movement Disorders, 21: 761-766.
10. ZIÉGLER M, BRUN C, HERGUETA T et al. (2002). Impact de la maladie de Parkinson sur l'entourage aidant : étude COMPAS. Gérontologie et Société, no spécial : 91-109.