Veterans Affairs Low-vision Intervention Trial II: One-year Follow-up.
Activities of Daily Living
Aged
Aged, 80 and over
Female
Follow-Up Studies
Health Surveys
Humans
Male
Middle Aged
Rehabilitation Centers
Retinal Diseases
/ physiopathology
Sickness Impact Profile
Surveys and Questionnaires
Treatment Outcome
United States
United States Department of Veterans Affairs
Veterans
/ statistics & numerical data
Vision, Low
/ physiopathology
Visual Acuity
/ physiology
Visually Impaired Persons
/ rehabilitation
Journal
Optometry and vision science : official publication of the American Academy of Optometry
ISSN: 1538-9235
Titre abrégé: Optom Vis Sci
Pays: United States
ID NLM: 8904931
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
entrez:
9
10
2019
pubmed:
9
10
2019
medline:
29
2
2020
Statut:
ppublish
Résumé
One-year follow-up is recommended for patients with macular diseases to assess functional changes associated with disease progression and to modify low-vision (LV) treatment plans, if indicated. The purpose of this study was to observe 255 patients with macular diseases who received LV rehabilitation (rehabilitation with a therapist) or basic LV services (LV devices dispensed without therapy) during Veterans Affairs Low-vision Intervention Trial II after the trial ended at 4 months until 1-year follow-up. The primary outcome measure was visual ability measured with the 48-item Veterans Affairs Low-vision Visual Functioning Questionnaire. Mean visual ability scores for the treatment groups were compared from baseline to 4 months, 4 months to 1 year, and baseline to 1 year. Changes from baseline to 1 year were compared between the two groups. Predictors of changes in visual ability from 4 months to 1 year were assessed using linear regression. Both groups experienced significant improvement in all measures of visual ability from baseline to 1 year but lost visual reading ability during the observation period (LV rehabilitation group, -0.64 [1.2] logit; 95% confidence interval [CI], -0.84 to -0.44 logit; basic LV group, -0.63 [1.4] logit; 95% CI, -0.88 to -0.38 logit), and overall visual ability was lost in the LV rehabilitation group (-0.20 [0.8] logit; 95% CI, -0.34 to -0.06 logit). Loss of visual reading ability in both groups from 4 months to 1 year was predicted by reading ability scores at 4 months, loss of near visual acuity from 4 months to 1 year, and lower EuroQol-5D utility index scores; loss of overall visual ability in the LV rehabilitation group during the same time period was predicted by lower overall ability scores at 4 months. Visual ability significantly improved in all groups from baseline to 1 year. However, the loss of visual reading ability experienced by both groups from 4 months to 1 year reduced the benefit of the services provided.
Identifiants
pubmed: 31592954
doi: 10.1097/OPX.0000000000001428
pii: 00006324-201910000-00002
doi:
Banques de données
ClinicalTrials.gov
['NCT00958360']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM