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Abstract Details

The King-Devick (K-D) Test of Rapid Eye Movements: A Bedside Correlate of Disability and Quality of Life in Multiple Sclerosis
Neuro-ophthalmology/Neuro-otology
IN4 - (-)
004
Based on rapid number naming and requiring <1 minute, the K-D test captures impaired eye movements and saccades, findings that correlate with suboptimal brain function. K-D scores are significantly higher (worse) in athletes immediately following concussion, consistent with involvement of widely distributed visual pathways.
Patients with MS and controls completed the K-D test. Scores represent time to read single-digit numbers on 3 cards. Patients completed low-contrast acuity, high-contrast visual acuity (VA), spectral-domain OCT, NEI-VFQ-25, 10-Item Neuro-Ophthalmic Supplement, and MS Functional Composite.
In the MS cohort (n=81), K-D scores were higher (worse) than controls (54.7卤15.7 vs. 41.2卤7.2 seconds, p=0.003 least squares means, adjusting for age). Higher K-D scores in MS were associated with worse scores for vision-specific quality of life (p<0.001 for NEI-VFQ-25, 10-Item Supplement), binocular low-contrast acuity (2.5%, 1.25%, p<0.001), VA (p=0.003), timed 25-foot walk (p<0.001), 9-hole peg test (p=0.001), and PASAT3 (p=0.03, linear regression). Patients with ON history (p=0.003) or binocular low-contrast acuities below control group average (p=0.009, 2.5%, logistic regression) had worse K-D scores. Monocular vision (p=0.001-0.009) and RNFL thickness (p=0.001) were reduced in eyes of patients with worse K-D (adjusting for age and inter-eye correlations). Patients on disability did worse compared to those working full-time, accounting for age (p<0.001).
The K-D test captures visual dysfunction, neurologic impairment, and quality of life in MS. K-D scores reflect work disability and structural changes by OCT. History of ON and abnormal binocular acuities were associated with worse K-D scores, suggesting that K-D captures afferent and efferent visual components. The K-D test should be considered as a rapid global visual performance measure.
Authors/Disclosures
Stephen Moster
PRESENTER
No disclosure on file
Gary R. Cutter, PhD (University of Alabama At Birmingham) Dr. Cutter has received personal compensation in the range of $50,000-$99,999 for serving as a Consultant for onsulting or Advisory Boards: Alexion, Antisense Therapeutics/Percheron, Avotres, Biogen, Clene Nanomedicine, Clinical Trial Solutions LLC, Endra Life Sciences, Cognito Therapeutics, Genzyme, Genentech, Immunic, Klein-Buendel Incorporated, Kyverna Therapeutics, Inc. , Linical, Merck/Serono, Noema, Neurogenesis, Perception Neurosciences, Protalix Biotherapeutics, Regeneron, Revelstone Consulting, Roche, SAB Biotherapeutics, Sapience Therapeutics, Scott&Scott LLP, Tenmile.. Dr. Cutter has received personal compensation in the range of $50,000-$99,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Data and Safety Monitoring Boards: Applied Therapeutics, AI therapeutics, AMO Pharma, Argenx, Astra-Zeneca, Avexis Pharmaceuticals, Bristol Meyers Squibb, CSL Behring, Cynata Therapeutics, DiamedicaTherapeutics, Horizon Pharmaceuticals, Immunic, Inhibrix, Karuna Therapeutics, Kezar Life Sciences, Medtronic, Merck, Meiji Seika Pharma, Mitsubishi Tanabe Pharma Holdings, Prothena Biosciences, Novartis, Pipeline Therapeutics (Contineum), Regeneron, Sanofi-Aventis, Teva Pharmaceuticals, United BioSource LLC, University of Texas Southwestern.. Dr. Cutter has received personal compensation in the range of $5,000-$9,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for JASN.
Steven Galetta, MD, FAAN (NYU Langone Medical Center) Dr. Galetta has nothing to disclose.
Laura J. Balcer, MD, MSCE, FAAN (NYU Grossman School of Medicine) Dr. Balcer has received personal compensation for serving as an employee of North American Neuro-Ophthalmology Society. An immediate family member of Dr. Balcer has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Children's Hospital of Philadelphia.
No disclosure on file