June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Rasch analysis of the glaucoma-specific module of the Eye-tem Bank project
Author Affiliations & Notes
  • Konrad Pesudovs
    NHMRC Ctr Clin Eye Res/Optometry, Flinders University SA, Adelaide, SA, Australia
  • Jyoti Khadka
    NHMRC Ctr Clin Eye Res/Optometry, Flinders University SA, Adelaide, SA, Australia
  • Eva Fenwick
    Centre for Eye Research Australia, University of Melbourne, Melbourne, VIC, Australia
  • Ecosse Lamoureux
    Centre for Eye Research Australia, University of Melbourne, Melbourne, VIC, Australia
    Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore
  • Footnotes
    Commercial Relationships Konrad Pesudovs, None; Jyoti Khadka, None; Eva Fenwick, None; Ecosse Lamoureux, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 5313. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Konrad Pesudovs, Jyoti Khadka, Eva Fenwick, Ecosse Lamoureux; Rasch analysis of the glaucoma-specific module of the Eye-tem Bank project. Invest. Ophthalmol. Vis. Sci. 2013;54(15):5313.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: To assess the psychometric properties of a glaucoma-specific quality of life (QOL) item bank module of the Eye-tem Bank project.

Methods: The glaucoma-specific QOL item bank has 342 items distributed across 10 QOL domains: Visual symptoms, SY; Ocular surface symptoms, OS ; General Symptoms, GS ; Activity limitation, AL ; Mobility, MB ; Emotional, EM ; Health Concerns, HC ; Social, SC ; Convenience, CV ; and Economic, EC. The item bank was interviewer-administered to patients with glaucoma. Each QOL domain of the item bank was individually evaluated using Rasch analysis to assess its psychometric properties, namely precision (adequate if the person separation index (PSI) >2.0); dimensionality (principal component analysis of residuals, PCA: unidimensionality is considered if the (1) raw variance explained by the measure >50%, (2) unexplained variance of the 1st contrast <3.0 eigenvalues or ≤5%); item fit to the model (infit mean square ≤ 1.5); and differential item functioning (DIF) by age and gender (no DIF if the DIF contrast is <1.0).

Results: The glaucoma item bank was administered to 293 patients (male, 55%; median age, 70 yrs; range 20-91 yrs). The majority (between 80% and 93%) of the participants endorsed the two lower end categories of all questions, indicating that most participants had low levels of QOL impact across the domains. Among the 10 QOL domains, five domains (AL, MB, EM, HC and CV) demonstrated excellent measurement precision, whereas, five domains (SC, EC, VS, OS and GS) had borderline precision (PSI ranging from 1.50 to 2.50). The PCA of residuals confirmed that eight domains (MB, EM, HC, CV, SC, OS, VS and GS) were unidimensional. Two domains (AL and CV) demonstrated some degree of multidimensionality (1st contrast >3.0 eigenvalues), which could be repaired by rearranging the items into subdomains. Of the 342 items, only 27 (7.9%) displayed misfit, and 7 (2.0%) showed DIF for age or gender.

Conclusions: The 10 QOL domains of the glaucoma-specific item bank demonstrated good psychometric properties against most metrics. Despite using a large sample, the preponderance of participants with low QOL impact of glaucoma impairs the establishment of precise measurement. Ongoing data collection in patients across the spectrum of glaucoma will strengthen the assessment of the psychometric properties and validity of these glaucoma-specific QOL domains.

Keywords: 669 quality of life • 468 clinical research methodology • 459 clinical (human) or epidemiologic studies: biostatistics/epidemiology methodology  
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×