Measuring health-related quality of life in patients with progressive supranuclear palsy

• Published in: Neurocase 2005-08, Vol.11 (4), p.246-249
• Main Authors: Schrag, A., Selai, C., Quinn, N., Hobart, J.
• Format: Article
• Language: English
• Subjects: Aged; Female; Humans; Male; Middle Aged; Outcome Assessment (Health Care); Psychometrics - methods; Quality of Life; Reproducibility of Results; Sickness Impact Profile; Supranuclear Palsy, Progressive - physiopathology; Supranuclear Palsy, Progressive - psychology; Surveys and Questionnaires
• ISSN: 1355-4794; 1465-3656
• DOI: 10.1080/13554790590963068

The development of psychometrically sound health-related quality of life (Hr-QoL) instruments has made it possible to assess subjectively experienced Hr-QoL quantitatively, and to incorporate Hr-QoL as a measure in medical research and clinical trials. Hr-QoL in patients with progressive supranuclear palsy (PSP) has been measured using generic (not disease-specific) instruments, or Parkinson's disease-specific scales. We give an overview of the development of a disease-specific Hr-QoL instrument for patients with PSP. Based on interviews with 27 patients with PSP a preliminary Hr-QoL instrument was developed and administered to over 300 people with PSP in the UK and US. Following psychometric analysis a rating scale with a physical and a mental subscale emerged. In this patient sample, both subscales satisfied criteria for scaling assumptions, acceptability, reliability and validity (correlations with other measures consistent with a priori hypotheses). The psychometric properties of this questionnaire are undergoing further evaluation. We are grateful to the Society for Progressive Supranuclear Palsy and The Progressive Supranuclear Palsy (PSP Europe) Association who supported this study, and to patients in both the UK and the US for taking the time and effort in participating in this research.