Highlights
- •Medically unexplained visual loss represents a consistent clinical presentation.
- •Retrospective case–control review of patients within a neuro-ophthalmology clinic
- •Data extracted on neurological, ophthalmological and psychiatric clinical course
- •Female excess, mean age symptom onset 37.5 years and chronic clinical course
Abstract
Purpose
To compare the clinical and demographic characteristics of adult patients with nonorganic
or medically unexplained visual loss (MUVL) to those with other common conditions
presenting to a neuro-ophthalmology clinic.
Methods
Case–control design: a retrospective review of medical notes on a consecutive case
series of 49 patients assessed at the King's College Hospital neuro-ophthalmology
clinic with unexplained visual loss and matched with the next assessed patient identified
from clinic records. Patients presented post-symptom onset with a mean clinical course
of 30 months (SD = 67 months) and standard clinical examination used to confirm diagnoses, alongside ancillary
investigations if required.
Results
Seventy-two percent (n = 36) of MUVL patients were female. In comparison with patients with organic visual
disorders, MUVL cases presented with significantly higher rates of bilateral (cf.
unilateral) visual impairment (41%, n = 20), premorbid psychiatric (27%, n = 13) as well as functional (24%, n = 12) diagnoses and psychotropic medication usage (22%, n = 11). Medically unexplained cases were significantly more likely to report preceding
psychological stress (n = 9; 18%).
Conclusions
Medically unexplained visual impairment may be regarded as part of the spectrum of
medically unexplained disorders seen in the general hospital setting. Research is
needed to determine long-term outcomes and effective tailored interventions.
Keywords
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Article info
Publication history
Published online: December 29, 2015
Accepted:
December 28,
2015
Received in revised form:
December 1,
2015
Received:
September 4,
2015
Identification
Copyright
© 2016 Elsevier B.V. Published by Elsevier Inc. All rights reserved.