Correction of Large Amblyopiogenic Refractive Errors in Children Using the Excimer Laser Lawrence Tychsen, MD, Eric Packwood, MD, and Gregg Berdy, MD Purpose: We sought to determine whether laser subepithelial keratomileusis (LASEK) and photorefractive keratectomy (PRK) are effective methods for correcting amblyopiogenic refractive errors in children. Methods: Thirty-six eyes in 35 amblyopic children, who ranged in age from 4 to 16 years (mean, 8.4 years), received treatment for large magnitude ametropia. Seventy-two percent (25/35) of the children had a neurobehavioral disorder and/or were noncompliant with spectacle or contact lens wear. Myopia ranged from Ϫ3.25 to Ϫ24.25 D (mean, Ϫ11.48 D); one patient had hyperopia of ϩ5.87 D. Correction was tailored to match the refractive error of the nonamblyopic eye. VISX Star S2/S3 excimer lasers were used in manual or auto-tracking modes, and corneal centration was achieved using brief, general anesthesia. Mean follow-up was 29.2 months (range, 4-42 months). Results: Myopia correction averaged Ϫ8.95 Ϯ 2.89 D (range, Ϫ3.25 to Ϫ15.50). Eighty-nine percent (31 children) were corrected to within Ϯ 1.00 D of goal refraction and the remaining 11% to within 2.0 D of the goal (most were undercorrected). Acuity improved postoperatively in 97%; by 1 optotype line in 37% and by 2 or more in 60%. No child lost acuity. Binocularity improved in 69% (24/35) and remained the same in 31%. Corneal haze measured grade 0-1 in 78%, grade 2 in 14%, and grade 3-4 in 8%. Myopic regression exceeding Х 1.0 D/year (0.08 D/month) occurred in 50% (18/36) of eyes treated. No substantial differences were observed in PRK- (n ϭ 18) versus LASEK- (n ϭ 17) treated children. Conclusions: Laser refractive surgery is effective for correcting anisometropic myopia in amblyopic children. Recurrence of myopia is common. Further study is indicated to determine long-term stability and safety of the procedure in this population.
T he management of large magnitude ametropia in tropia also may produce a degree of cosmetic disfigure-
children remains a challenge to pediatric ophthal-
ment, subjecting school age children to social ridicule.
mologists. Nonsurgical measures for correcting
Contact lens correction can circumvent these disadvan-
ametropia are spectacles and contact lenses. Patients with
tages but may not be tolerated or practical in many chil-
unilateral ametropia generally are suitable for spectacle
dren, particularly those with neurobehavioral disorders.
correction, but this method of correcting high degrees of
Excimer laser correction of refractive errors has been
anisometropia causes lens-induced aniseikonia and, in ec-
shown to be effective and safe in but the use of
centric gazes, disconjugate shifting of images caused by
this method in children has been the subject of a limited
prismatic effects induced by thick Both of these
number of case In adults, the excimer laser
factors produce binocular image decorrelation, impeding
technique most widely used (laser-assisted in situ kerato-
binocular fusion and the optimal correction of anisome-
mileusis, or LASIK) entails the creation of a corneal stro-
tropic Spectacle correction of high anisome-
mal flap using a mechanical blade or blade-equivalent laserAfter the reshaping of the corneal stromato correct ametropia, the flap is repositioned and is held inplace by initially tenuous, natural biomechanical bonds. From the Department of Ophthalmology and Visual Sciences, St. Louis Children’s Hospital,
After LASIK flap repositioning, manipulation of the eye
at Washington University School of Medicine, St. Louis, Missouri. Presented at the American Association for Pediatric Ophthalmology and Strabismus 30th
must be avoided to reduce the risk of flap displacement, a
Annual Meeting, Washington, DC, March 2004, and in part at The Association forResearch in Vision & Ophthalmology Annual Meeting, Fort Lauderdale, Florida, May
a LASIK flap also diminishes the magnitude of correction
2002. Submitted March 9, 2004.
that may be achieved by laser ablation because a sufficient
Revision accepted January 25, 2005.
bed of nonablated stroma must remain to ensure long-
Reprint requests: Lawrence Tychsen MD, St. Louis Children’s Hospital at WashingtonUniversity School of Medicine, One Children’s Place, Suite 2S-89, St. Louis, MO 63110. E-mail: [email protected].
The surface-ablation procedures photorefractive ker-
Copyright 2005 by the American Association for Pediatric Ophthalmology and
atectomy (PRK) and laser subepithelial keratomileusis
(LASEK) circumvent these disadvantages because they
1091-8531/2005/$35.00 ϩ 0doi:10.1016/j.jaapos.2005.01.006
do not require creation of a stromal flap. PRK/LASEK
224 June 2005 Journal of AAPOS Journal of AAPOSVolume 9 Number 3 June 2005TABLE 1 Refractive goal, outcome, and regression in 35 PRK- or LASEK-treated children (36 eyes) Init Postop refraction refraction Final postop regression† surgery/sex Preop refraction technique* (diopters) (diopters) refraction
*40 micron phototherapeutic keratomileusis (PTK)/photorefractive keratomileusis (PRK); Man: manual scrape. †D/mo: average diopters per month.
are used to correct high ametropia in The
patients into 3 groups on the basis of the laser surgical
techniques also have been used to correct ametropia in
technique used: combined phototherapeutic keratectomy
a small number of pediatric case The purpose
(PTK) and PRK (patients 1-12), manual removal of epi-
of this report is to communicate our experience using
thelium and PRK (patients 13-18), or LASEK (patients
PRK and LASEK to correct ametropia in a sizable
19-35). The mean age at surgery was 8.4 years; range 4-16
cohort of anisometropic children. A preliminary report
years. One third (39%, 14/36) of eyes treated were in
of a portion of these data was published in 2002 as an
patients 7 years of age or younger at the time of laser
correction, and 72% (26/36) were age 10 years of age oryounger. One child had follow-up for 3 months but did
PATIENTS AND METHODS
not return for longer follow-up and is therefore not listed
Clinical outcome data displayed in and were
in the Tables of 35 children (36 eyes) reported in our
collated from a prospective study of 36 consecutive eyes in
results. One child had sequential correction of high myo-
35 ametropic children (17 boys, 18 girls). All surgery was
pia in both eyes, and these results are reported (patient 22,
performed at St. Louis Children’s Hospital between June
age 5 years). Mean follow-up was 29.2 months (range, 4-42
TABLE 2 Visual acuity, binocular function, visuomotor findings, and neurobehavioral status of the 35 treated children (36 eyes) Ocular and visuomotor Neurobehavioral Preop VA* Postop VA binoc† status§ status¶
ET surg ϫ 2; MLNregressed ROP, disctilt ϩ drag retina OU
aniso ϩ strab amb,cryo OS ROP, congptosis rep OS
amb, neonatal vithemorr LE, inf sens ETsurg ϫ 3, MLN
ϫ1; bilat Iris colob ϩmicrocornea; Inf retinalcolob OD
Journal of AAPOSVolume 9 Number 3 June 2005TABLE 2 Continued Ocular and visuomotor Neurobehavioral Preop VA* Postop VA binoc† status§ status¶
amb; cong cat surgage 2 mo; 2* IOL age5; inf ET surg ϫ 3;microcornea OS
ϩ aniseikonicdiplopia w/spec,noncompliant
*VA: visual acuity; Best corrected optotype (Snellen fraction) if tolerated spectacles, uncorrected otherwise; SSEP: spatial-sweep evoked potential. †fus vrg: fusional vergence response to base-out prism; W4D: Worth four-dot test fusion; stereo-Titmus/Randot responses. ‡Haze at last f/u exam, except for retreated pt 14 (see text). §ROP: retinopathy of prematurity; MLN: manifest latent nystagmus; ET: esotropia; XT: exotropia; IOL: intraocular lens¶DD: developmental delay; ADHD: attention deficit hyperactivity disorder; CP: cerebral palsy; PDD: pervasive developmental disorder; MR: mental retardation.
Each child had a minimum of 2 office examinations
research and was approved by the Washington University
performed preoperatively, as well as examination-under-
anesthesia (EUA) at the laser procedure. The examinationsincluded age-appropriate testing of visual acuity in each
Indications and Contraindications
eye, pupillary examination with measurement of diameter,
Indications for laser correction included (1) anisometropia
sensorimotor examination of eye alignment/eye move-
greater than 4.00 D or bilateral ametropia greater than
ment/binocular function, a minimum of 2 manual and,
5.00 D; (2) children noncompliant with spectacle wear or
when feasible, automated cycloplegic refractions per-
intolerant of or ill-suited for contact lens wear; (3) ambly-
formed within 1 week, slit lamp biomicroscope evaluation
opia in the candidate eye equivalent to 2-optotypte-lines
of the anterior segment and assessment of tear film, indi-
or worse; (4) absence of glaucoma, uveitis, recurrent con-
rect ophthalmoscopy, and measurement of intraocular
junctivitis, tear film insufficiency, endothelial dysfunction/
pressure with a Tonopen (Minter O&O, Norwell, MA).
corneal dystrophy, corneal scarring, keratitis, or systemic
Automated photokeratoscopy mapping was performed be-
inflammatory disease; (5) pachymetry exceeding 425 mi-
fore and after the surgery in cooperative children. Addi-
crons but less than 675 microns; and (5) good rapport with
tional measurements obtained under anesthesia immedi-
the child’s parent(s), who acknowledged the risks/alterna-
ately before the laser procedure included pachymetry,
tives and the importance of follow-up examinations.
keratometry, corneal diameters, biomicroscopy with go-nioscopy, and A-scan ultrasonographic axial length mea-
Outcome Measures
surement. The amount of desired correction was adjusted
Principal outcome measures included postoperative best-
(unless otherwise noted) to conform to the refractive error
corrected and/or uncorrected visual acuity, postoperative
refractive error, refractive regression, postoperative binoc-
Written informed consent was obtained from the par-
ularity, corneal haze, and complications. Binocularity was
ent(s). The consent document itemized the rationale for
graded as lowest-to-highest using the following 3-tiered
and potential risks of pediatric excimer laser surgery, the
scale: presence of a fusional vergence response to a 20
need for continuing amblyopia therapy, and the possible
diopter base-out prism; fusion of the Worth (Lombart
need for additional surgery. The protocol complied with
Norfolk, VA), or Polaroid (Lombart Norfolk, VA) 4-dot
the ARVO resolution on the use of human subjects in
test; and stereoscopic sensitivity scored by the Titmus
Stereotest (Titmus, Peterburg, VA). Postoperative corneal
For PTK-mode removal of the epithelium, the micro-
haze was graded on a scale of 0 to 4, with 0 representing no
scope was adjusted and the aiming beam laser reticule was
haze and grades 1-4 indicating increasing density of
centered in the pupil, ablating the cornea over a diameter
of 6.5 mm to a depth of 40 microns in a period of approx-
Outcome measures were those obtained at the most
imately 20 seconds. A Took knife (Storz Instruments,
recent follow-up examination for refractive error, regres-
Bausch & Lomb, Rochester, NY) was scraped across the
sion, haze, and complications. Outcome measures for vi-
ablation zone to verify absence of epithelium. For manual
sual acuity and binocularity were the lowest value or grade
removal, the Took knife alone was used. For LASEK, the
recorded in the interval of 1 month after surgery to the
trephine was removed and replaced with the 8.5-mm di-
most recent follow-up examination. The postoperative
ameter well, which was filled with 20% alcohol diluted in
acuities reported were best-corrected if the child wore
sterile water, ensuring that the central epithelium was
refractive correction at home or in school, and uncor-
submerged fully. The alcohol was removed using a Mero-
rected if the child would not permit spectacle wear because
cel sponge after 30 seconds, followed by irrigation of the
of a neurobehavioral disorder or chronic noncompliance
conjunctiva and cornea. The central 8 mm of epithelium
with spectacle wear. These conservative conventions were
was removed with the micro-hoe, scrolling the tissue in
adopted to deliberately bias outcomes in the direction of
rolled-carpet fashion from the 6-o’clock to 12-o’clock po-
sition, where it remained hinged (treatment zone diameter
avoided ascribing to laser correction any improvements
was 1.0 mm larger for the hyperopic correction).
that could have resulted from on-going amblyopia therapy
After de-epithelialization, the microscope was adjusted
in children 10 years of age or younger, (2) incorporated
to 16X and the aiming reticule again centered in the pupil.
any deficits that accrued because of progressive haze or
A Merocel stick microsponge moistened with balanced salt
refractive regression, and (3) provided the most realistic
solution was brushed across the corneal stroma to dull the
estimate of the visual gain achieved by laser correction for
reflex. Manual or autotracking PRK was completed using
regular/blend treatment zones of 6.0/8.0 mm over a courseof 60-90 seconds. After each 20-25 seconds of laser appli-
Surgical Procedure
cation, the treatment was interrupted and a microsponge
All surgeries were performed under general anesthesia
employed to wipe and barely moisten the ablation zone. In
using standard pediatric techniques. Induction was con-
LASEK-treated children, the rolled carpet of epithelium
ducted by mask inhalation of a volatile anesthetic mixture
was unscrolled from the 12-o’clock position and smoothed
(nitrous oxide/sevoflurane/oxygen) followed by insertion
back over the stroma using a micro-spatula. Voltaren (No-
of a laryngeal mask airway and conversion to total intra-
vartis Ophthalmics, Inc., Duluth, GA), Ciloxan (Alcon
venous anesthesia (TIVA, using propofol). Ketorolac
Laboratories, Fort Worth, TX), TobraDex (Alcon Labo-
tromethamine was administered intravenously to reduce
ratories, Fort Worth, TX), and additional proparacaine
eye drops were applied, followed by a plano bandage
After the EUA, proparacaine drops were applied to the
conjunctiva of the eye selected for treatment. The child’spupil was undilated. Manifest and cycloplegic refraction
Postoperative Regimen and Medication Compliance
with sphere, cylinder, and axis as well as the amount of
Printed instructions were discussed with and issued to the
desired refractive treatment, keratometry readings and
family at discharge, including discouragement of removal
vertex distance were programmed into the Visx Star S2 or
of the Fox shield or eye rubbing, and directions for instil-
S3 (VISX USA, Inc., Santa Clara, CA) laser. The depth of
lation of eye drops to keep the eye moistened and reduce
TIVA was adjusted if necessary to eliminate any tendency
the risk of tight lens syndrome, infection, or inflammation.
for globe rotation away from primary position in the orbit
The parents also were instructed in the use of optional post-
(ie, residual Bell’s reflex). The child’s head was reposi-
operative pain medications to include oral Percocet (Endo
tioned using a pneumatic beanbag so that the iris remained
Pharmaceuticals, Chadds Ford, PA), or Tylenol with codeine
level in all planes. Betadine prep was applied to the eyelids
elixir (Ortho-McNeil Pharmaceuticals, Raritan, NJ) and oral
and conjunctival cul-de-sac. The patient table was swiv-
ketorolac. No anesthetic complications occurred in the
eled and locked in position under the microscope. Tega-
study group, and all of the children were discharged from
derm (3M, St. Paul, MN) drapes were applied to the upper
the same day surgery unit within 1 hour of the procedure.
and lower eyelids. A lid speculum was inserted. A circular
No restrictions were placed on activities.
Merocel (Medtronic Xomed Surgical Products, Inc., Jack-
Postoperative examinations were performed at 1 day
sonville, FL) sponge soaked in 4% lidocaine was placed on
and thereafter at 48-hour intervals until reepithelialization
the center of the cornea for 30 seconds and removed. The
was complete and there was no evidence of corneal fluo-
8.0 mm diameter trephine was centered on the pupil and
rescein staining. If the bandage contact lens was still in
applied with gentle downward force to score the corneal
place it was removed. Follow-up examinations were per-
formed at 1 month, 2-3 months, and then at 6-month
Journal of AAPOSVolume 9 Number 3 June 2005
intervals, unless active amblyopia therapy warranted more
ing exotropia by a ratio of 1.7:1. An additional 11 children
frequent visits. Topical TobraDex and Voltaren drops
(31%) had evidence of primary monofixation syndrome.
were used q.i.d. during the first week after surgery. There-
Nine of the 35 (26%) displayed conspicuous manifest
after, Vexol (Alcon Laboratories, Fort Worth, TX), FML
latent nystagmus. Seven of 35 (20%) had a history of diode
(Allergan, Inc., Irvine, CA), or prednisolone drops were to
laser, cryotherapy-treated, or spontaneously regressed
be substituted and used b.i.d. For the last 4 children
stage 3 retinopathy of prematurity. Three children (9%)
reported in and (patients 32-35), a standard
had previous surgery for infantile cataract and intraocular
chewable multivitamin containing 60 mg of vitamin C
lens implantation in the amblyopic eye (2 of these eyes also
(ascorbic acid, 100% of the daily recommended value) was
had mild microcornea). One child (patient 27) had bilat-
also prescribed each day for a minimum of 6 months in an
eral iris colobomas with mild microcornea and a macula-
sparing chorioretinal coloboma in the treated eye.
The topical medication compliance data reported was
Twenty-five of the 35 children (72%) had a neurobe-
estimated by having nonphysician members of the clinic
havioral disorder, ranging from moderate to severe. Nine
staff query parents, asking them to recall the name or
of these children (36%) had a history of prematurity with
bottle color of the drop used, any difficulties with drop
birth at gestational age of 30 weeks or less. An additional
administration, and the need for any refills at each fol-
5 children (14%) had no neurobehavioral disorder but
low-up visit. The method was used to avoid embarrassing
were chronically noncompliant with spectacle wear. The
noncompliant parents/children while enhancing the
remaining 5 children (14%) were normal, wore spectacles
chances of eliciting candid responses.
for anisometropia exceeding 6.0 D, and either contact-lensfailures or unsuitable for contact lens wear because of
Statistical Analysis
Correlation coefficients were calculated for variables that
Initial Cornea Epithelium Healing
included: the amount of laser correction, regression rate,corneal haze, age at surgery, and compliance with topical
Reepithelialization of the cornea was complete by an av-
medication. Outcomes were compared between the three
erage 3.6 Ϯ 1.4 days. No substantial difference was noted
surgical technique groups by use of analysis of variance
in the rate of corneal reepithelialization between groups of
(ANOVA) for time to reepithelialization, corneal haze,
children treated by PTK/PRK, manual scrape/PRK, or
and regression rate. Comparison of improvement in acuity
LASEK (analysis of variance [ANOVA], P ϭ 0.388). Two
across age group was performed using ANOVA. Differ-
of the 35 children (6%) required an oral analgesic for
ences between means of unpaired subgroups were mea-
discomfort within 24 hours after the procedure but not
sured using the t-test. Significance was defined as P Ͻ
thereafter. The other 94% (33/35 children) displayed no
signs of substantial discomfort or change in behavior,other than photophobia, during the interval of reepitheli-
alization. Twenty-six percent (9/35) of the children(mainly but not exclusively those with severe neurobehav-
Ocular, Visuomotor, and Neurobehavioral Status
ioral disorders) dislodged the eye shield, manipulated the
All of the 35 children reported in our results and listed in
eye, and lost the bandage contact lens within 12 hours of
the surgery. Lens loss appeared to have no noteworthy
anisometropic amblyopia. Nine of these 34 children (26%)
effect on the rate of corneal healing or discomfort.
had superimposed strabismic or pattern-deprivation am-
blyopia. One child (3%, patient 22) had strabismic ambly-
adherent epithelial flap during attempted LASEK and the
opia and bilateral isometropic myopia. The preoperative
procedure was converted to manual scrape. The mishap
acuities reported in range from 20/40 (optotype
did not impair corneal healing. Patient 35 had LASEK and
fraction 0.5) to 1/200 (0.005) with a mean acuity of 0.23
normal postoperative healing, but experienced acute pain
(20/87). Patient 27 had acuity measured only as “fix/fol-
and photophobia in the operated eye 1 month after the
low,” owing to profound developmental delay/mental re-
procedure. He had a ϳ2 ϫ 2-mm region of loose epithe-
tardation. All of the children had a history of attempted
lium near the edge of the original flap, which was excised
amblyopia therapy, including spectacle wear, occlusion
under brief anesthesia and retreated with a bandage con-
therapy, and/or atropine penalization before enrollment in
tact lens. The cornea healed without scarring in 48 hours.
the protocol. Continuing amblyopia therapy was recom-mended in children 10 years of age or younger throughout
Refractive Error and Laser Correction
the follow-up interval, but compliance with amblyopia
lists the preoperative refraction, goal refraction,
and initial postoperative refraction for each of the treated
Twenty-one of the 35 children (60%) had strabismus
children. Thirty-four of the 35 children were myopic, with
(and a history of 1 or more strabismus surgeries), most
the preoperative refractive error ranging from Ϫ3.25 to
commonly infantile onset, with primary esotropia exceed-
Ϫ24.25 D (spherical equivalent [SE], mean Ϫ11.48D).
Thirty-two of the 35 children (91%) also had astigmatism,
To reduce the chance of developing haze, topical cor-
ranging from 0.50 to 5.50 D (mean, 1.93 D). Treatment
ticosteroid drops were prescribed for use twice a day for
was tailored to match the spherical refractive error of the
the first 6 months after surgery, but compliance after the
nonamblyopic eye and eliminate all astigmatism (in patient
first month was, on the whole, poor. Mean duration of
22, who had bilateral high isometropic myopia, treatment
drop compliance was 1.06 Ϯ 1.08 months. Special efforts
in both eyes was targeted to plano). In 20/35 children
were made to achieve substantially longer intervals of good
(72%), the fellow eye was emmetropic or mildly hyperopic
compliance (average 7.0 Ϯ 2.0 months) with topical med-
and thus the goal refraction was plano to ϩ 1.00 D. In the
ication and oral Vitamin C in the last four children (pa-
other 15/35 (28%), the fellow eye was mild-to-moderately
tients 32-35) listed in and Haze in this corti-
myopic and the goal refraction ranged from – 0.50 to
costeroid-plus-vitamin C group was significantly milder
– 8.00 D. One child (patient 26) had anisometropic hyper-
than that in the remaining LASEK group (unpaired t-test,
opia of ϩ5.87 D, with a goal refraction of ϩ1.00 D. P ϭ 0.034), and 3 of the 4 experienced no myopic regres-
Myopic spherical correction (laser treatment achieved)
averaged 8.95 Ϯ 2.89 D (range, Ϫ3.25 to Ϫ15.50). Eighty-
Three children had corneal haze exceeding 2ϩ (patients
nine percent of children (31/35) were corrected to within
6, 14, and 25). Despite the haze (and myopic regression),
1.00D of spherical goal refraction. The remaining 11%
(4/35) were corrected to within 2.0 D of the goal (3 of 4
the 3 children achieved minor improvement in visual acu-
undercorrected). Correction of astigmatism averaged 1.86
ity. One had PTK, 1 had manual scrape, and 1 had LASEK
Ϯ 1.34D, and the initial cylindric correction achieved was
removal of the epithelium. Patients 6 and 25 had –10D SE
within 1.0D of plano in all 32 astigmatic children.
and – 8.25D SE laser correction, and the families did notinstill eye drops after the first week. Patient 14 had – 6.25
Visual Acuity Outcomes and Ablation Center
D SE laser correction and received TobraDex for 1
Decentration
month, followed by prednisolone 0.125% for 1 year (he
Acuity improved postoperatively in 34/35 children (97%)
was also treated during the 32-month follow-up interval
treated, but the gains were minor (the equivalent of 1
with courses of oral prednisone for asthma). The com-
optotype line) in 13 of these 34 children (38%). Improve-
bined topical and oral corticosteroid treatment did not
ment of 2 optotype lines or more was achieved in 62%
prevent the development of 3-4ϩ haze. Thirteen months
(21/34). Impressive gains in acuity (Ն 3 optotype lines)
after PRK, he was taken back to the operating room for
were achieved in patients 2, 5, 12, 19, 22, 24, 29, 31, and
scraping of the stromal surface and application of 0.02%
35 (9/35 or 26%). One child (patient 7) had no change in
mitomycin The haze cleared to 1-2ϩ and during a
acuity; no child lost visual acuity.
3-month period myopic regression reversed by ϩ 1.50D.
Mean gain in acuity (optotype fraction) for the study
group was 0.20 Ϯ 0.16. Gains in acuity were comparable
Myopic Regression
for children younger than 7 years of age (mean improve-
Myopic shift during the follow-up interval is reported in
ment 0.18 Ϯ 0.19), for children age 7-10 years ( 0.21 Ϯ
as regression rate, expressed as SE diopters per
0.15), and for children older than 10 years of age (0.18 Ϯ
month. Twenty-four of the 35 children treated (69%)
0.14; ANOVA; P ϭ 0.421). None of the children com-
exhibited some evidence of regression. The average rate of
plained of glare, haloes, or other subjective visual distur-
regression was – 0.088 Ϯ 0.22 D/month, or –1.06 D/year.
Five children were able to cooperate reliably to com-
Myopic regression exceeding Х 1.0 D/year (0.08
pare awake pre- versus postoperative topographic corneal
D/month) occurred in 50% (18/36) of eyes treated. Re-
maps. The average decentration of the ablation center in
gression rates were comparable in children treated by
this group was 0.67 mm (range, 0.41– 0.98). No systematic
PTK/PRK (Ϫ0.110 Ϯ 0.29 D/month), manual scrape/
trend was evident relating decentration to surgical tech-
PRK (Ϫ0.074 Ϯ 0.08 D/month), and LASEK (Ϫ0.079 Ϯ
nique used or visual acuity outcome.
0.21 D/month; ANOVA, P ϭ 0.818). The rate of myopicregression correlated with severity of haze (r ϭ 0.356, P Ͻ
Corneal Haze
0.001) and younger age at surgery (r ϭ 0.395, P Ͻ 0.0001).
Corneal haze observed during the follow-up interval
As noted above, long-term compliance with drops and
ranged from zero to 4ϩ, with a mean score of 0.77 Ϯ 0.87
oral vitamin C was associated with less myopic regression.
for the 36 eyes. Corneal haze measured grade 0-1 in 78%,
However, the use of topical corticosteroids did not prevent
grade 2 in 14%, and grade 3-4 in 8%. No systematic
significant regression in all cases. Patient 14 received top-
relationship between the surgical technique used and the
ical (and intermittently oral) corticosteroids but experi-
subsequent occurrence of haze was found (ANOVA, P ϭ
enced substantial regression (with significant haze). Pa-
0.363). The severity of haze correlated weakly but signif-
tient 32 was compliant with both drops and vitamin C for
icantly with the amount of laser correction (r ϭ 0.157; P Ͻ
a duration of six months, but also experienced substantial
0.0001) and younger age at surgery (r ϭ 0.115; P Ͻ 0.001). Journal of AAPOSVolume 9 Number 3 June 2005TABLE 3 Representative pediatric excimer laser surgery studies for correction of anisometropic myopia Nucci ؉ Drack Astle et al. Autrata ؉ Rehurek O’Keefe ؉ Nolan Current study
UK: United Kingdom; US: United States; yr: year; mo: month; PRK: photorefractive keratectomy; LASIK: laser-assisted in situ keratomileusis; LASEK: laser subepithelialkeratomileusis. *Prevalence in cohort. †Gain optotype fraction. ‡Medication compliance measured for each child. Improvement in Binocular Fusion
ble rate of complication is particularly noteworthy in light
Binocular fusion improved postoperatively in
of the fact that many of the children treated in our study
24/35 children (69%). Mild gains were measured in 19/24
were highly uncooperative owing to neurobehavioral dis-
(79%) of these cases, defined as an improvement in one
orders. It is prudent to note that less serious complications
grade of binocularity, eg from presence of fusional ver-
may only appear after prolonged follow-up, and the aver-
gence to fusion of the four-dot test. Major gains in bin-
age follow-up of the children in this series was two-and-
ocularity (defined as improvement of 2 grades) were mea-
sured in 5/24 (21%). No child had a deterioration of
The major drawback to excimer laser correction in
binocularity as a result of laser correction. Patients 5, 18,
children is the high prevalence of return of ametropia.
and 29 (33%, 3/9 with nystagmus) had manifest latent
Regression occurred in 69% of the children treated, with
nystagmus damp to latent nystagmus as a benefit of the
an average return of myopia at the rate of ϳ1 D/year.
Regression also was apparent in the hyperopic child at arate ϳ0.5 D/year. Keratocyte-mediated regrowth of the
DISCUSSION
photoablated stroma and epithelial hyperplasia appear to
The purpose of this study was to review outcomes in a
sizable series of children treated by a pediatric ophthal-
ment of haze is attributed to high numbers of wound
mologist using PRK or LASEK, with the goal of answer-
healing keratocytes. Topical corticosteroids reduce regres-
ing 2 major questions. Is excimer laser surgery, an effective
sion and corneal haze in adult excimer laser
way to correct high ametropia in children who, for one
The use of systemic ascorbate (vitamin C) may also inhibit
reason or another, are not suitable candidates for correc-
stromal collagenase, reducing both stromal haze and re-
tion by other means? The answer to this question, based
on the current study and earlier is yes, when
study who received both topical corticosteroid and sys-
effectiveness is measured as improvement in acuity or
temic ascorbate for at least 6 months after surgery showed
ability to achieve a nearly emmetropic refraction. Visual
no regression and negligible haze. Further study in a larger
acuity improved in 97% of the children in this study
group of children will be required to confirm the promis-
(substantially in 62%), and we were able to correct the
ing results obtained in this subgroup.
ametropia to within 2.0 D of the target refraction in alleyes. The second, equally important, question we posed
Comparison With Other Pediatric Excimer Laser
was whether correction using the excimer laser was safe.
The answer to this question also is yes, when safety is
Although few studies have described longer-term out-
gauged as a low prevalence of loss of vision and a low
comes of excimer laser surgery in children, the results of
prevalence of sight-threatening complications. No chil-
these studies are comparable with those reported
dren in our series lost vision, and none of the children
summarizes the results of recent reports for com-
suffered a devastating corneal complication. The negligi-
parison with our findings (the list is representative but not
exhaustive). Three of the 5 studies were prospective: Astle
gains in “functional vision,” which included balance,
awareness of the environment, and coordination. A total of
other 2 were retrospective. Autrate and Rehurek reported
64% of the children in the Astle et al study benefited from
a cohort of children in 2003 and 2004, and, therefore, the
a functional vision improvement, with the most impressive
data of the more recent report are The previ-
improvements in children with neurobehavioral disorders.
ous studies listed in the Table have taken place at sites
We conclude that PRK and LASEK are effective and
safe techniques for improving vision in children with my-
Surgery was performed under brief general anesthesia
opic anisometropia or high bilateral myopia. Appropriate
in all studies involving younger children and/or those with
cautions should be taken when recommending this form of
neurobehavioral disorders. Follow-up ranged from 1 to
refractive correction. The main beneficiaries may prove to
2.4 years, and the prevalence of sight-threatening or other
be the hard cases, that is, children with severe neurobe-
major complications in all of the studies was zero. Simi-
havioral disorders. The benefit of the surgery will be
larly, the prevalence of haze exceeding 2ϩ was uniformly
considerably enhanced if effective methods can be found
low. The 4 studies performed outside the United States
noted healing of the corneal surface within days aftersurgery but did not quantify healing rate or level of dis-
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requiring anesthesia. J Cataract Refract Surg 2003;29:1744-7. An Eye on the Arts – The Arts on the Eye
It was one of those rare times when a bomb could have exploded beside me and I
wouldn’t have noticed. I was absorbed in Jim, watching his expressions, listening to hiswords, enjoying the moment. I sat opposite him at a table next to the wall; a candle betweenus, its flame reflected in his eyes.
He noticed my eyes too. “You looked beautiful,” he told me recently, “but obviously I
He said he wanted to reach over and touch my face near that scar, a sign of comfort or
empathy, but he resisted. That would come later. “You were a person who might have died,a person who even if you had lived had no business sitting beside me having dinner, feedingyourself. So I knew right away you were a survivor.” He smiled. “There’s a sense of fragilityabout you, but scratch below the surface a little bit and you’ll find somebody who won’t betrifled with. I knew right away you were a person who wouldn’t break accidentally. You’dbeen through stuff I doubt I could have made it through. And though I still wanted to touchyou and comfort you, I sensed you were stronger than me.
“The first thing I felt from you was your heart, your warmth,” Jim explained. “Maybe
that’s what makes you so strong. Your ability to give your heart to others.”
—Trisha Meili (from I Am The Central Park Jogger, Simon & Schuster)
Der Vogelgrippe Virus H5N1 wurde nie nachgewiesen, es gibt auch kein mutiertes Virus H5N8. Pläne für die Massenimpfung der ganzen Bevölkerung stehen. Lassen Sie sich nicht für dumm verkaufen und informieren Sie sich und andere rechtzeitig! Der Vogelgrippe-Krieg wird in Wirklichkeit mit noch größerer Wucht vorangetrieben werden als zuvor. Anfang Oktober fand in Bad Hofgastein, Österreich,
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