Literature DB >> 28697537

Novel mobility test to assess functional vision in patients with inherited retinal dystrophies.

Daniel C Chung1, Sarah McCague2, Zi-Fan Yu3, Satha Thill3, Julie DiStefano-Pappas4, Jean Bennett2,5, Dominique Cross2, Kathleen Marshall2, Jennifer Wellman1, Katherine A High1.   

Abstract

IMPORTANCE: This novel endpoint tracks functional vision changes in patients with inherited retinal dystrophies (IRDs) over time.
BACKGROUND: The aims of the study were to determine whether a multi-luminance mobility test (MLMT) can detect functional vision changes over time in subjects with IRDs and to assess natural history and potential effects of investigational agents.
DESIGN: This is a prospective, observational study. PARTICIPANTS: Sixty-two subjects were enrolled. Sixty (29 normal sighted and 31 visually impaired) were eligible; 54 (28 visually impaired and 26 normal-sighted) completed all testing visits.
METHODS: Subjects navigated MLMT courses three times over 1 year. At each visit, subjects completed testing using individual eyes, and both eyes, at up to nine standardized, increasing luminance levels (range 1 to 400 lux). Accuracy and speed were evaluated and compared with visual acuity (VA), visual field (VF) and a visual function questionnaire. MAIN OUTCOME MEASURES: Accuracy and speed of normal and visually impaired subjects on MLMT, and reliability and content validity of MLMT were the main outcome measures.
RESULTS: MLMT distinguished normal-sighted from visually impaired subjects. All control subjects passed all MLMT attempts at all tested light levels. Visually impaired subjects' performance varied widely; some declined over 1 year. Performance declined markedly below certain VA and VF thresholds. Concordance on performance on two baseline visits was high: correlations for accuracy were 94% and 98% for lowest common and highest common lux levels. CONCLUSIONS AND RELEVANCE: MLMT differentiated visually impaired from control populations and, in visually impaired subjects, identified a range of performances; and tracked performance declines over time, consistent with these progressive conditions.
© 2017 Royal Australian and New Zealand College of Ophthalmologists.

Entities:  

Keywords:  functional vision; inherited retinal dystrophy; luminance; mobility test

Mesh:

Year:  2017        PMID: 28697537      PMCID: PMC5764825          DOI: 10.1111/ceo.13022

Source DB:  PubMed          Journal:  Clin Exp Ophthalmol        ISSN: 1442-6404            Impact factor:   4.207


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