Memory deficit associated with worse functional trajectories in older adults in low-vision rehabilitation for macular disease.

Journal Article (Journal Article)

OBJECTIVES: To examine whether performance on a brief memory test is related to functional outcomes in older individuals undergoing low-vision rehabilitation (LVR) for macular disease. DESIGN: Observational cohort study of individuals receiving outpatient LVR. SETTING: Academic center. PARTICIPANTS: Ninety-one individuals (average age 80.1) with macular disease. MEASUREMENTS: Memory was assessed at baseline using a 10-word list; memory deficit was defined as immediate recall of two or fewer words. Vision-related function was measured using the 25-item Visual Function Questionnaire (VFQ-25) administered at baseline and during subsequent interviews (mean follow-up, 115 days). Linear mixed models were constructed to compare average trajectories of four VFQ-25 subscales: near activities, distance activities, dependency, and role difficulty. RESULTS: The 29.7% of participants with memory deficits tended to decline in ability to accomplish activities that involved near vision. Controlling for age, sex, and education, the functional trajectory of participants with memory deficit differed significantly from that of those with better memory (P = .002), who tended to report improvements in ability to accomplish near activities. CONCLUSION: Of older adults receiving LVR for macular disease, those with memory deficits experienced worse functional trajectories in their ability to perform specific visually mediated tasks. A brief memory screen may help explain variability in rehabilitation outcomes and identify individuals who might require special accommodations.

Full Text

Duke Authors

Cited Authors

  • Whitson, HE; Whitaker, D; Sanders, LL; Potter, GG; Cousins, SW; Ansah, D; McConnell, E; Pieper, CF; Landerman, L; Steffens, DC; Cohen, HJ

Published Date

  • November 2012

Published In

Volume / Issue

  • 60 / 11

Start / End Page

  • 2087 - 2092

PubMed ID

  • 23126548

Pubmed Central ID

  • PMC3498592

Electronic International Standard Serial Number (EISSN)

  • 1532-5415

Digital Object Identifier (DOI)

  • 10.1111/j.1532-5415.2012.04194.x


  • eng

Conference Location

  • United States