Purpose: The purpose of the study was to evaluate the biomicroscopic,
light microscopic, and electron microscopic effects of ultraviolet-B (
UV-B) exposure on the outcome of photorefractive keratectomy (PRK). Me
thods.: A total of 24 pigmented rabbits were used in the study. One ey
e of 16 rabbits received a 193-nm, 45-mu m deep (-5.0 diopter) excimer
laser PRK. Twenty-one days after PRK, eight of the laser-treated eyes
were exposed to 100 mJ/cm(2) UV-B (280-315 nm) UV radiation by placin
g the rabbits in a standard clinically used dermatologic chamber for 7
minutes. Eight PRK-treated rabbits received no further treatment. The
remaining eight non-PRK-treated rabbits received 100 mJ/cm(2) UV-B on
ly to one eye. Subepithelial haze was assessed before and after UV irr
adiation. Corneal morphology was assessed 4, 8, 12, and 16 weeks after
UV-B exposure, using light microscopic and transmission electron micr
oscopic (TEM) techniques. Results: Untreated eyes exposed to 100 mJ/cm
(2) UV-B only exhibited photokeratitis for 2 days, but showed no haze
and were normal histologically at all intervals. The PRK-treated UV-B
irradiated eyes exhibited a significant increase of stromal haze compa
red to eyes receiving PRK alone. Histologically, the main difference b
etween the UV-B irradiated and nonirradiated post-PRK eyes was the pre
sence of anterior stromal extracellular vacuolization in the UV-B-expo
sed eyes. The vacuolated foci were confined to the PRK treatment area
and showed increased keratocyte density and disorganization of normal
collagen lamellae. TEM showed activated keratocytes containing abundan
t rough endoplasmic reticulum, prominent Golgi zones, and extracellula
r vacuoles filled with amorphous material. The haze and morphologic ch
anges showed a tendency to incomplete resolution over the period of 16
weeks. Conclusions: The UV-B exposure during post-PRK stromal healing
exacerbates and prolongs the stromal healing response and is manifest
biomicroscopically by augmentation of subepithelial haze. The finding
s suggest that excessive ocular UV-B exposure should be avoided during
the period of post-PRK stromal repair and that UV-B may modulate the
response of tissues to 193-nm excimer laser and perhaps other laser en
ergy in general.