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PURPOSE: To evaluate differences in mean deviation lens rim artifacts, miosis, and lid or brow ptosis.1–5 With
values in automated perimetry in healthy eyes with multi- alterations in incident light and contrast on the retina,
focal compared to monofocal intraocular lens (IOL) changes in automated perimetry numerical values of
implants. mean deviation (MD) and pattern standard deviation
DESIGN: Prospective, age-matched, comparative anal- (PSD) can be studied.
ysis. Multifocal intraocular lenses (IOLs) produce simulta-
METHODS: SETTING: Single-center, tertiary referral neous retinal images with different focal planes in order
academic practice. PATIENT POPULATION: A total of 37 to reduce spectacle dependency for distance and near visual
healthy eyes in 37 patients with bilateral multifocal acuities. Along with potential benefits, however, is the
(n [ 22) or monofocal (n [ 15) IOL implants were stud- reality that the amount of light energy in focus at any given
ied. INTERVENTION/OBSERVATION PROCEDURE: Humphrey focal distance is reduced, out-of-focus light is superim-
Visual Field 10-2 testing was performed on all patients. posed, and approximately 18% of transmitted light in
MAIN OUTCOME MEASURES: Mean deviation (MD) and diffractive IOLs, which may vary depending on IOL design,
pattern standard deviation (PSD) numerical values were is lost to higher orders of diffraction that are not ever
evaluated and compared between groups. focused on the retina.6,7 As a result, patients with
RESULTS: The average MD was L2.84 dB (SD 2.32) multifocal IOLs may experience glare and halos, as well
for the multifocal IOL group and L0.97 dB (SD 1.58) as reduced contrast sensitivity.8–15 Mesopic conditions
for the monofocal IOL group (P [ .006). There was tend to exacerbate these deficiencies.16,17 Furthermore,
no significant difference in PSD between the 2 groups increased chromatic aberrations and light scattering
(P [ .99). Eyes that had the visual field 10-2 testing have also been reported.6,18–21 In light of these optical
‡6 months from time of IOL placement showed no disturbances, we evaluated the effect of diffractive
improvement in MD when compared to eyes that were multifocal IOLs on a common clinical test, Humphrey
tested within 6 months from IOL placement. Visual Field Analyzer (Zeiss-Meditec, Dublin, California,
CONCLUSION: Multifocal IOL implants cause signifi- USA) 10-2, to determine the impact on performance in
cant nonspecific reduction in MD values on Humphrey patients with bilateral multifocal or monofocal IOL
Visual Field 10-2 testing that does not improve with implants.
time or neuroadaptation. Multifocal IOL implants may Several studies have previously reported the effects of
be inadvisable in patients where central visual field reduc- intraocular lenses on visual field testing. Mutlu and associ-
tion may not be tolerated, such as macular degeneration, ates demonstrated that monofocal IOLs may reduce MD in
retinal pigment epithelium changes, and glaucoma. (Am Humphrey Visual Field 24-2 testing compared to healthy
J Ophthalmol 2014;158:227–231. Ó 2014 by Elsevier phakic patients.22 Specifically, the effects of multifocal
Inc. All rights reserved.) IOLs on perimetry have been evaluated with Octopus
101 autoperimetry,23 Goldmann manual perimetry,24
frequency doubling technology matrix perimetry,25 auto-
VOL. 158, NO. 2 VISUAL FIELD TESTING IN MULTIFOCAL INTRAOCULAR LENS EYES 229
Neuroadaptation, which is believed to represent a The multifocal group of patients in this study had no sub-
learning adaptation in the image processing centers of jective dissatisfaction from their IOL and had an otherwise
the visual cortex, improves subjective complaints of glares healthy ocular examination with no IOL malfunction. The
and halos that are commonly more pronounced in the first decrease in MD on Humphrey Visual Field 10-2 testing
few months after surgery.28–30 Neuroadaptation has been seen in this study is thus related to subclinical inherent
defined as a phenomenon that involves a decrease in IOL properties and does not translate to patient dissatisfac-
perceived ocular aberrations and an improvement in tion or visual complaints.
quality of vision over time.34 Some patients require more Patients taking systemic hydroxychloroquine or chloro-
time to neuroadapt after multifocal IOL implantation, quine for rheumatologic diseases may demonstrate early
while some may need training regimens. One study evalu- paracentral visual field loss on Humphrey Visual Field
ated neuroadaptation by assessing the minimum amount of 10-2 assessment despite the absence of known risk factors
time postoperatively to obtain better visual function results that lead to retinal toxicity.35–38 A reduced MD with a
in patients who had bilateral multifocal IOL surgery, with a multifocal IOL may limit the ophthalmologist’s ability
diffractive IOL in 1 eye and a refractive IOL in the other, to detect early toxicity on Humphrey Visual Field 10-2
and concluded that at least 6 months was necessary.28 In in patients taking hydroxychloroquine or chloroquine.
our study, there was no significant difference in Humphrey If a patient on either medication already has a multifocal
Visual Field 10-2 performance between those that had IOL, we recommend screening the patient with concurrent
testing done in the first 6 months and those who had testing spectral-domain optical coherence tomography and/or multi-
done after postoperative month 6 in the multifocal IOL focal electroretinogram in order to detect early parafoveal
group. The reduction in MD on central visual field testing, toxicity,39 as Visual Field 10-2 testing may be confounded
regardless of evaluation time postoperatively, is presumably and unreliable in this group of patients.40
from decreased contrast sensitivity that is inherent to the Based on our findings, the authors propose that multi-
multifocal optic and does not appear to decrease with focal IOLs should be used with caution in patients with
neuroadaptation. Interestingly, there appeared to be a macular pathology, optic neuropathies, and glaucoma
trend toward worsening MD with time, although this did where loss of optic nerve has occurred and regular visual
not reach statistical significance. field testing is required.
ALL AUTHORS HAVE COMPLETED AND SUBMITTED THE ICMJE FORM FOR DISCLOSURE OF POTENTIAL CONFLICTS OF INTEREST.
Drs Farid, Garg, and Steinert are consultants for Abbott Medical Optics. Supported in part by a Department Developmental Grant from Research to
Prevent Blindness (RPB), New York, New York. Contributions of authors: design of the study (M.F.), conduct of the study (M.F., S.G., R.F.S.); manage-
ment, analysis, and interpretation of the data (G.C., M.F., S.G., R.F.S.); preparation, review, or approval of the manuscript (G.C., M.F., S.G., R.F.S.).
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Biosketch
Dr Marjan Farid is the Director of Cornea, Cataract, and Refractive Surgery and Vice-Chair of Ophthalmic Faculty at the
Gavin Herbert Eye Institute (GHEI) at the Univeristy of California, Irvine. Dr Farid is also the founder of the Severe Ocular
Surface disease center at GHEI. Her work is published in numerous peer-reviewed journals and she has authored multiple
textbook chapters. She also serves on the editorial board of Ophthalmology.