Br J Ophthalmol 2001;85:291-296
( March )
Distant cancer effects on standardised testing of peripheral
vision
William W Dawsona, Berry L Jordana, Robert D Marshb, Kaushik Hazariwalaa, Franklin P Flowersc, Ting Fanga
a Department of
Ophthalmology, University of Florida, Gainesville, FL 32610, USA, b Department of Oncology, Division of
Dermatology, c College of
Medicine
Correspondence to: William W
Dawson, MS, PhD, Department of Ophthalmology, Box 100284, Health
Science Center, University of Florida, Gainesville, FL 32610-0284, USA
wdawson{at}eye1.eye.ufl.edu
Accepted for publication 1 September 2000
BACKGROUND
Profound
central-retinal visual losses have been a major presenting factor
reported in cancer and melanoma associated retinopathies (CAR, MAR).
However, it is well established that standardised tests of peripheral
retinal function are often the most sensitive detectors of early eye
disease. This is a preliminary investigation of the responsiveness of
the peripheral retina to "distant" (non-eye or CNS) cancers using
easily obtained standardised tests.
METHODS
The design is
a single blind study where test results are compared with published
norms and a small age matched control group. Of 120 ambulatory cancer
outpatients who were interviewed at routine follow up examinations, 111 volunteered and admitted a range of mild visual changes. 25 cancer
patients completed all tests of peripheral vision function and a
clinical screening. There were seven control subjects of the same age range.
RESULTS
98% (49 of
50) of eyes from the patient cohort were judged clinically normal
following examinations which emphasised the central retina, fundus
appearance, and static fields. On testing which emphasised the visual
periphery, 46 (92%) eyes showed one or more quantitative abnormalities
>2 SD from the age adjusted norm means. These abnormalities clustered
mainly about dark adaptation (rod cell) sensitivity (31, 62% of
measured sites), the blue sensitive retinal cells (17, 34% of measured
eyes), and the oscillatory component (OP) of the electroretinogram (23, 46% of measured eyes). One control eye (7%) showed a significant dark
adaptation abnormality and ERG reduction. There was no identifiable
interaction between chemotherapy mode and the cancer associated retinal
deficits (CARD). Antiretinal antibodies were found in sera from most
patients and controls.
CONCLUSION
CARD is
common in the retinal periphery of many cancer patients, and is
distinct from rare CAR, MAR central-retinal responses. CARD has
numerous potential clinical uses which justify expanded research with
more defined large samples.
© 2001 by British Journal of Ophthalmology