OCULAR SURGERY NEWS 9/15/01
Emotional distress is common in retinal disease patients
There are several risk factors for emotional distress among patients
with visual impairment due to retinal disease. Michelle Stephenson
MIAMI — Patients with retinal disease often suffer from emotional
distress. Risk factors for emotional distress in clude shorter duration
of ocular disease, worse visual acuity, increased systemic co-morbidities
and increased functional impairment.
To determine the prevalence of and risk factors for emotional distress
among patients with retinal disease, Ingrid U. Scott, MD, MPH, and
colleagues at the Bascom Palmer Eye Institute, Wilmer Eye Institute
and New England Medical Center conducted a cross-sectional study.
“The goal of practicing physicians is to provide care that maximizes
the quality of life of their patients,” said Dr. Scott, of Bascom
Palmer Eye Institute here. “Ophthalmologists need to be aware that
patients with visual impairment are at risk for significant levels
of emotional distress.”
Study cases included 86 consecutive patients examined at the Wilmer
Eye Institute Retinal Vascular Center during a 4-week period. Exclusion
criteria included new patients, patients already participating in
other clinical trials and patients whose appointments overlapped
with those of subjects who were interviewed. Also included in the
study were 51 controls. These controls were required to have no
known ocular disease and to have a best-corrected visual acuity
of 20/25 or better using a standard Snellen visual acuity chart.
Cases and controls were matched by age, gender and race.
Study participants were interviewed using the Community Disability
Scale, a functional status questionnaire and the General Health
Questionnaire, which assesses emotional distress.
Visual impairment groups
Study cases were divided into three groups: 30 patients were in
the mild visual impairment group, 28 were in the moderate visual
impairment group and 28 were in the severe visual impairment group.
Among the groups, there were no statistically significant differences
in terms of age, gender, race, systemic co-morbidity and months
since diagnosis of ocular disease.
“There was a clinically meaningful linear trend in mean number
of months since diagnosis of ocular disease across the visual impairment
tertiles consistent with a progression of disease severity with
time among patients with age-related macular degeneration and diabetic
retinopathy,” Dr. Scott said.
Cases and controls had significantly different scores on the General
Health Questionnaire. Scores were significantly associated with
level of visual acuity.
“The prevalence of probable or definite emotional distress was
55.8% among the ophthalmic patients, as compared with 2.0% among
controls,” she said.
Univariate analyses showed that, among the patients in this study,
gender, race, ocular diagnosis and age were not significant predictors
of emotional distress, as assessed by General Health Questionnaire
score.
However, “shorter duration of ocular disease, worse visual acuity,
increased systemic co-morbidities and increased functional impairment
are significantly associated with increased emotional distress,”
she added.
Multiple regression analysis demonstrated that after controlling
for other variables, weighted bilateral average logMAR visual acuity,
systemic comorbidities and months since ocular diagnosis each explain
more than 10% of the variability in General Health Questionnaire
scores.
“The fact that shorter duration of ocular disease is significantly
associated with emotional distress suggests that patients may adapt
to their vision loss in such a way that, over time, lessens the
associated emotional distress,” she said.
Functional impairment
Because increased functional impairment is associated with increased
emotional distress, interventions designed to maximize patients’
level of functioning may improve patients’ emotional distress.
According to Dr. Scott, this study had several limitations. For
example, visual acuity was the only objective measure of vision
used. In addition, the study was a clinic-based series and, as such,
may have been susceptible to local referral biases.
“[Also], we did not have a group of patients with extreme bilateral
visual impairment. However, our group of patients represents the
type of patients likely to be recruited in clinical trials,” she
said.
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