Psychometric Analysis of the SPEED Questionnaire and CLDEQ-8

• Published in: Investigative ophthalmology & visual science Vol. 59; no. 8; pp. 3307 - 3313
• Main Authors: Pucker, Andrew D., Dougherty, Bradley E., Jones-Jordan, Lisa A., Kwan, Justin T., Kunnen, Carolina M. E., Srinivasan, Sruthi
• Format: Journal Article
• Language: English
• Published: United States The Association for Research in Vision and Ophthalmology 01.07.2018
• Subjects: Adult; Contact Lenses - adverse effects; Cornea; Cross-Sectional Studies; Dry Eye Syndromes - diagnosis; Dry Eye Syndromes - etiology; Female; Humans; Male; Middle Aged; Psychometrics; Self Report; Sickness Impact Profile; Surveys and Questionnaires; Tears - chemistry; Young Adult
• ISSN: 1552-5783; 0146-0404; 1552-5783
• DOI: 10.1167/iovs.18-24016

This study reports on the ability of the Standard Patient Evaluation of Eye Dryness (SPEED) questionnaire to detect dry eye (DE) symptoms in contact lens (CL) and non-CL wearers. The SPEED questionnaire was administered to all subjects while the Contact Lens Dry Eye Questionnaire-8 (CLDEQ-8) was only administered to CL wearers. Tear meniscus heights (TMH) were measured, and the phenol red thread (PRT) test was conducted. These tests along with self-reported DE were used to identify subjects with dry eye disease (DED). Rasch analysis was performed to evaluate the questionnaires for measurement precision and unidimensionality, and the scores from these Rasch analyses were used to understand their ability to predict measures of DED. We enrolled 284 subjects (150 CL and 134 non-CL wearers). Mean subject age was 39.4 ± 14.2 years. Rasch analysis yielded a multidimensional short form of the SPEED questionnaire (8-items) and a unidimensional short form of the CLDEQ-8 (4-item). Scores from both questionnaires were significantly associated with self-reported DE in CL and non-CL wearers. Scores of the 8-item SPEED questionnaire were associated with DED status in non-CL wearers but not in CL wearers while 4-item CLDEQ scores were associated with DED status in CL wearers. TMH or PRT were not associated with either questionnaire in CL or non-CL wearers. The 8-item SPEED questionnaire demonstrated adequate measurement precision with evidence of quantifying multiple symptoms categories while the 4-item CLDEQ-8 primarily quantified DE symptoms. Questionnaire scores were associated with self-reported DE, which suggests that they may have utility in both populations analyzed.