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   <subfield code="a">Does spouse participation influence quality of life reporting in patients with Parkinson's disease?</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Chelsea Morrow, Katherine Smentkowski, Stacy Schwartz, Melissa Armstrong, Ann Gruber-Baldini, Karen Anderson, Stephen Reich, William Weiner, Lisa Shulman]</subfield>
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   <subfield code="a">Purpose: 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. Methods: 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. Results: Patients rated physical HRQoL higher (M=46.6) than spouses alone (M=43.4, p&lt;0.01) and co-reporting (M=44.8, p&lt;0.05). Co-reporting rated physical HRQoL in between that of patients and spouses, (p&lt;0.05). Spouses who reported greater mutuality showed greater concordance with the patient regarding the patient's mental HRQoL (B=−0.43, p&lt;0.05). Conclusion: Consistency of the mode of completion of HRQoL instruments is important since co-reporting may alter HRQoL ratings in PD and lead to inaccurate conclusions. Mutuality is a mediator of mental HRQoL.</subfield>
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   <subfield code="u">Department of Neurology, University of Maryland School of Medicine, Baltimore, MD, USA</subfield>
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