RGP contact lens fitting in keratoconus using FITSCAN technology

PurposeTo assess and compare the base curve (BC) of rigid gas permeable contact lens (RGP) that were calculated by FITSCAN using corneal topography (Orbscan IIz) and the diagnostic contact lens fitting method in keratoconus eyes.Materials and methodsA prospective comparative study of 85 keratoconus eyes was conducted. Two masked observers calculated the contact lens parameters of RGP lens by diagnostic fitting method and using FITSCAN technology. The base curves calculated by two methods were compared using Wilcoxon signed rank test and agreement between two methods were analysed using Bland–Altman plot.ResultsEighty-five eyes from 55 keratoconus patients were included in the study. The mean age was 17.63 ± 2.78 (range: 12–23) years and among them 46 were males. The keratoconus was graded into mild, moderate and severe based on average keratometry values. The base curve calculated by the FITSCAN is on average 0.22 mm higher than that calculated by diagnostic method (P value <0.0001, 95% CI = 0.155, 0.245, Wilcoxon signed rank test) and the bias between the two methods was found to be 2.7% (Bland–Altman plot), indicating systematic bias between the two modalities. By single linear regression analysis, the base curve of RGP contact lens could calculated by using the formula, base curve (BC) = (FITSCAN calculated BC × 0.86563) + 0.78738.ConclusionOur study showed that selecting the BC of the initial trial lens 0.22 mm steeper than the FITSCAN calculated base curve, may help to reduce the complexity of RGP contact lens fitting in keratoconus.     

Soft contact lens fitting after intrastromal corneal ring segment implantation to treat keratoconus

PurposeTo assess the feasibility of fitting a lathed soft toric contact lens (STCL) after the implant of intrastromal corneal ring segments (ICRSs) to treat keratoconus.MethodsSix months after ICRS implantation, 47 eyes of 47 patients (18–45 years) were fitted with a STCL. In each eye, we determined refractive error, uncorrected (UDVA) and corrected distance visual acuity (CDVA), and keratometry and asphericity measures. The outcome of STCL fitting was defined according to CDVA as successful (≤0.2 logMAR) or unsuccessful (>0.2 logMAR). Patients in the unsuccessful group were refitted with a piggy-back (PB) system. The above variables and the change in CDVA observed after STCL and PB lens fitting from spectacle CDVA were compared in the two groups.ResultsSTCL fitting was successful in 75%, 66.66% and 0% of the ICRS implanted eyes with stages I–III keratoconus, respectively. Spectacle-CDVA was 1.5 lines better and mean corneal power was 3.62D lower in the successful STCL group. In this group, the difference in cylinder axis between spectacles and STCL was 24.25° lower. PB refitting achieved a PB-CDVA ≤0.2 logMAR in all cases. A similar difference in the CDVA change achieved by contact lenses versus spectacles was observed in the successful STCL and PB refitted groups.ConclusionSTCL fitting is a feasible option in a large proportion of patients implanted with ICRS. When these lenses are unsatisfactory, a PB system is a good alternative.     

An acute clinical comparison of corneal staining and comfort associated with contact lens care solutions

PurposeThis study compared the biocompatibility and comfort of 4 lens care solutions currently marketed in France.MethodsThis was a randomized, interventional, double-masked, single-center crossover study assessing balafilcon A silicone hydrogel contact lenses, bilaterally, straight from the blister pack solution (control) and pre-soaked in the following lens care solutions: Regard^® (containing sodium chlorite), ReNu^® (containing a PHMB [polyhexamethylene biguanide] derivative), CyClean™ and MeniCare™ Soft (both containing PHMB). Subjects were randomized to the order of test solution use. For each of the 5 solutions tested, subjects attended a baseline/lens dispensing visit and an intervention visit 2 h later. At both visits, evaluation included slit-lamp examination, corrected-distance visual acuity, corneal staining, and subject-assessed photophobia, ocular comfort, and ocular redness.ResultsThirty subjects were enrolled and 28 were evaluable. Corneal staining severity was significantly worse than baseline after 2 h of wearing lenses soaked in CyClean, MeniCare, or ReNu (P ≤ 0.001). The MeniCare group alone demonstrated a significant improvement in ocular comfort after 2 h of lens wear (P = 0.02). No group demonstrated significant changes in ocular redness or photophobia. Corrected-distance visual acuity was similar between baseline and intervention visits for each test solution. No adverse events were reported during the study.ConclusionsSilicone hydrogel contact lenses presoaked in lens solutions containing PHMB or a PHMB derivative produced an increase in corneal staining after 2 h of lens wear. The higher levels of corneal staining in the 2 solutions did not correlate with increased discomfort within this 2-h timeframe.     

Corneal changes following short-term rigid contact lens wear

PurposeThe aim of this cross-over study was to investigate the changes in corneal thickness, anterior and posterior corneal topography, corneal refractive power and ocular wavefront aberrations, following the short term use of rigid contact lenses.MethodFourteen participants wore 4 different types of contact lenses (RGP lenses of 9.5 mm and 10.5 mm diameter, and for comparison a PMMA lens of 9.5 mm diameter and a soft silicone hydrogel lens) on 4 different days for a period of 8 h on each day. Measures were collected before and after contact lens wear and additionally on a baseline day.ResultsAnterior corneal curvature generally showed a flattening with both of the RGP lenses and a steepening with the PMMA lens. A significant negative correlation was found between the change in corneal swelling and central and peripheral posterior corneal curvature (all p ≤ 0.001). RGP contact lenses caused a significant decrease in corneal refractive power (hyperopic shift) of approximately 0.5 D. The PMMA contact lenses caused the greatest corneal swelling in both the central (27.92 ± 15.49 μm, p < 0.001) and peripheral (17.78 ± 12.11 μm, p = 0.001) corneal regions, a significant flattening of the posterior cornea and an increase in ocular aberrations (all p ≤ 0.05).ConclusionThe corneal swelling associated with RGP lenses was relatively minor, but there was slight central corneal flattening and a clinically significant hyperopic change in corneal refractive power after the first day of lens wear. The PMMA contact lenses resulted in significant corneal swelling and reduced optical performance of the cornea.     

Corneal changes following short-term miniscleral contact lens wear

PurposeTo examine the influence of short-term miniscleral contact lens wear on corneal shape, thickness and anterior surface aberrations.MethodsScheimpflug imaging was captured before, immediately following and 3 h after a short period (3 h) of miniscleral contact lens wear for 10 young (mean 27 ± 5 years), healthy participants. Natural diurnal variations were considered by measuring baseline diurnal changes obtained on a separate control day without contact lens wear.ResultsSmall but significant anterior corneal flattening was observed immediately following lens removal (overall mean 0.02 ± 0.03 mm, p < 0.001) which returned to baseline levels 3 h after lens removal. During the 3 h recovery period significant corneal thinning (−13.4 ± 10.5 μm) and posterior surface flattening (0.03 ± 0.02 mm) were also observed (both p < 0.01). The magnitude of posterior corneal flattening during recovery correlated with the amount of corneal thinning (r = 0.69, p = 0.03). Central corneal clearance (maximum tear reservoir depth) was not associated with corneal swelling following lens removal (r = −0.24, p > 0.05). An increase in lower-order corneal astigmatism Z(2,2) was also observed following lens wear (mean −0.144 ± 0.075 μm, p = 0.02).ConclusionsFlattening of the anterior corneal surface was observed immediately following lens wear, while ‘rebound’ thinning and flattening of the posterior surface was evident following the recovery period. Modern miniscleral contact lenses that vault the cornea may slightly influence corneal shape and power but do not induce clinically significant corneal oedema during short-term wear.     

Efficacy of spherical aberration correction based on contact lens power

PurposeTo investigate the efficacy of spherical aberration (SA) correction with aspheric contact lenses (aspheric lenses) based on lens power, and compare the results with those of spherical contact lenses (spherical lenses).MethodsOcular higher-order aberrations were measured with a wavefront sensor, in 11 myopic subjects wearing an aspheric lens (Medalist Fresh fit (PUREVISION 2 HD); Bausch + Lomb) or a spherical lens (ACUVUE Oasys; Johnson & Johnson). Six different lens powers (−7.00 diopters (D), −5.00 D, −3.00 D, −1.00 D, +1.00 D, +3.00 D) were used for all subjects. The amount of SA correction from the contact lens at each power was calculated as the difference between SA with the contact lens on-eye and SA of the eye alone.ResultsFor the spherical lenses, SA correction was close to 0.00 μm for the +1.00 D lens, became more positive as the labeled lens power increased and became more negative as the labeled lens power decreased. For the aspheric lenses, SA correction was consistent, from −0.15 to −0.05 μm, for all lens powers except for the −1.00 D lens. SA correction for the spherical and aspheric lenses was significantly different at −7.00 D (p = 0.040), −3.00 D (p = 0.015), −1.00 D (p < 0.001), +1.00 D (p = 0.006), and +3.00 D (p < 0.001) powers.ConclusionAn aspheric lens is capable of correcting SA at different lens powers, and has SA correction in the range of −0.15 to −0.05 μm over a 6 mm aperture.     

Improved contact lens fitting after corneal cross-linking in eyes with progressive keratoconus

ObjectivesThe study aimed to assess the possible effects of corneal cross-linking (CXL) on contact lens (CL) fitting in patients with progressive keratoconus who initially had CL intolerance.MethodsA retrospective review was performed of the medical records of patients who had stopped CL wear due to discomfort prior to CXL and who were fitted with CLs after CXL. All eyes were evaluated pre- and 1, 6, 12, 24 months postoperatively. Data collected included pre- and post-CXL refraction, corneal topographic data, uncorrected visual acuity, and best-corrected visual acuity (BCVA). CL comfort was evaluated using the Likert scale post-CXL.ResultsA total of 20 eyes from 14 patients were included in the study. Preoperative Kmax values significantly decreased by 2.8 D at 6 months and by 4.1 D at 12 months after CXL (p < 0.001 for both). CLs were prescribed on average 12 ± 2.5 months after CXL. The mean duration of successful CL wear was 10.4 ± 2.8 months during the follow-up period. Subjective CL comfort scores were satisfactory post-CXL.ConclusionCXL not only halts the progression of keratoconus but may also improve CL tolerance by providing a more regular shaped cornea in these patients. Ongoing corneal topographic changes in the late postoperative period after CXL may have a positive effect on CL fitting.     

Rehabilitation of vision disabling corneal opacities: Is there hope without corneal transplant?

ObjectiveTo evaluate the efficacy of contact lenses in visual rehabilitation of a series of patients with corneal scars/opacities.MethodRetrospective review of case records of 158 patients (n = 162 eyes) with poor vision subsequent to corneal scar/opacity, who underwent contact lens fitting, was done. Primary outcome assessed was quantum of additional improvement in vision with rigid gas permeable (RGP) or soft lenses over spectacles. Success was defined as visual improvement of ≥2 lines over that of spectacles and/or improvement of vision to ≥20/60 (LogMAR 0.48).ResultsRigid gas permeable lenses were fitted in 137 eyes and soft contact lenses in 25 eyes. Lenses were successful in improving visual acuity by two or more lines over that of spectacles in 70% eyes (113 of 162 eyes), of which RGP lens accounted for 85% (96 of 113 eyes). Alternative outcome of success was defined as attainment of reasonable functional vision of >20/60 (LogMAR 0.48). This could be achieved in 65% cases (105 of 162 eyes) of which 83% (88 eyes) were with use of RGP lenses. Almost one-fourth (23.4%) patients were children less than 15 years old. Soft contact lenses were attempted in 25 instances, where RGP lens could not be fitted and were successful in 17 (68%) of these. All these 17 patients were aphakes.ConclusionsRehabilitation of corneas with visually disabling corneal opacities is possible with usage of appropriate contact lenses even in young children.     

The influence of soft contact lens wear and two weeks cessation of lens wear on corneal curvature

IntroductionAccurate corneal measurements are crucial in corneal refractive surgery (CRS) to ensure successful outcomes. Soft contact lens (SCL) wear may result in changes to corneal curvature and structure. United States Food and Drug Administration (FDA) pre-operative guidelines recommend that prior to CRS, SCL wearers cease SCL wear for “at least two weeks before examination and treatment” [1]. Corneal curvature changes induced by SCL wear may take longer than two weeks to resolve.PurposeTo examine the effect of SCL wear on corneal curvature before and following two weeks SCL wear cessation. To explore the possible impact of different SCL materials and years of SCL wear.MethodsRetrospective data analysis, between a group of SCL wearers (SCL: n = 45); and a non-contact lens control group (NCL: n = 45). Corneal curvature parameters were measured using the Pentacam (Oculus, Germany), before and following two weeks cessation of SCL wear.ResultsNo significant differences in keratometry or Sagittal radius of curvature between SCL and NCL groups prior to or following SCL cessation. Tangential radius of curvature showed significant inferior steepening for the SCL group prior to SCL cessation (SCL vs. NCL; 7.77 ± 0.30 mm vs. 7.90 ± 0.30 mm; p = 0.04). Following two weeks cessation of SCL wear this appeared to have resolved.ConclusionsTwo weeks cessation of SCL wear appears sufficient for resolution of corneal curvature changes with modern SCL materials and years of SCL wear. However, further studies with longer lens deprivation periods are required to ensure stability for all SCL wearing patients.     

Assessment of corneal endothelial cell density in patients with keratoconus not using contact lenses

PurposeTo assess the corneal endothelial cell density (ECD) in keratoconus patients with no history of contact lens use.SettingYuzuncu Yil University, School of Medicine and Van Training and Research Hospital, Department of Ophthalmology, Van, Turkey.DesignCross-sectional controlled study.MethodsThe eyes of 65 patients with the diagnosis of keratoconus with no history of contact lens wear and the eyes of 40 healthy controls were prospectively examined using the Heidelberg Retinal Tomography Rostock Cornea Module (HRT3/RCM). The average ECD from the two groups were then compared.ResultsOf the cases with keratoconus, 44 (67.7%) were men and 21 (32.3%) were women. The mean age was 20.9 ± 6.8 (range = 10–41) years. Of the controls, 28 (70%) were men and 12 (30%) were women. The mean age was 23.9 ± 5.8 (range = 14–35) years. Of the 65 eyes with keratoconus, 19 (29.2%) had mild keratoconus, 21 (32.3%) had moderate keratoconus, and 25 (38.5%) had severe keratoconus. The mean ECD was 2731.6 ± 303.2 cells/mm² in cases with keratoconus and 2664.9 ± 319.5 cells/mm² in controls. There was no difference between the densities (unpaired t-test, P = 0.4). No significant relationships were found between the ECD data and central corneal thickness or steepest keratometric.ConclusionsEndothelial cell density was unaltered in keratoconic patients without a history of contact lens use when compared with healthy controls. Change in ECD is independent from the central corneal thickness and the stage of keratoconus.     

Comparison of fitting stability of the different soft toric contact lenses

PurposeTo compare lens orientation and rotational recovery of five currently available soft toric lenses.MethodsTwenty subjects were recruited and trialed with each of the study lenses in a random order. Study lenses were PureVision^® Toric (B&L), Air Optix^® for Astigmatism (Alcon), Biofinity^® Toric (CooperVision), Acuvue^® Advance for Astigmatism (Vistakon), and Proclear^® Toric (CooperVision). Lens orientation in primary position to determine the lens rotation form the vertical position and rotational recovery to primary gaze orientation following a 45° manual misorientation for the different lenses was compared.ResultsThe Biofinity Toric showed the lowest rotation from the vertical position and the Proclear Toric the highest. Also, the highest and the lowest reorientation speed were related to the Biofinity Toric and the Acuvue Advance for Astigmatism, respectively. The Repeated Measures ANOVA showed a significant difference in the lens rotation (P = 0.004) and rotational recovery (P < 0.001) among different contact lenses and the performed multiple comparisons indicated differences in rotation and also in reorientation speed were only seen between the Biofinity Toric when compared to four other lenses (P < 0.05).ConclusionAlthough there was appropriate fitting, based upon lens orientation and reorientation speed, with each of the study lenses it would appear that the optimized ballast technique used in the design of the Biofinity Toric helps reduce lens rotation and improve rotational recovery compared to others.     

The use of daily disposable lenses in problematic reusable contact lens wearers

PurposeReplacing soft contact lenses (CLs) on a daily basis brings a number of advantages, most notably, reduced exposure to deposits, disinfectants, allergens, and other contaminants. This retrospective study estimated the prevalence of problems in current wearers of reusable soft CLs and tested the effect of refitting “problem” patients with daily disposable (DD) hydrogel lenses.MethodsPrevalence was estimated from 398 current reusable CL wearers for: frequent/constant discomfort or dryness, ≥2 h of uncomfortable wear, ≥grade 2 conjunctival hyperaemia (0–4), or ≥grade 3 corneal staining (0–15). In the second part of the study, 217 reusable CL wearers classified as problem patients were randomly refitted with DD lenses manufactured from one of two materials: etafilcon A (n = 96) or nelfilcon A (n = 121) and reassessed 1 week later.ResultsThirty-nine percent (154/398) had some qualifying criterion: reduced comfortable wearing time (CWT), 20%; dryness, 20%; irritation, 5%; corneal staining, 8%; and hyperaemia, 7%. After refitting with DDs, the prevalence of reduced CWT was decreased from 65% to 51% (P = 0.0039), dryness from 60% to 41% (P < 0.0001) and corneal staining from 28% to 21% (P = 0.04). There was no significant change in the prevalence of irritation, or hyperaemia. Some differences were noted between the two lens materials.ConclusionsA high proportion of reusable soft lens wearers encounter clinically relevant signs or symptoms with their current CLs. This study provides evidence that refitting with DD lenses is a useful strategy for alleviating some of the common problems of CL wear.     

Evaluation of central corneal thickness after cataract surgery,penetrating keratoplasty and long-term soft contact lens wear

PurposeThe aim of this study was to compare central corneal thickness (CCT) between corneas of normal healthy eyes (cNHE), corneas of eyes that had undergone cataract surgery by clear corneal phacoemulsification with implantation of an intracapsular intraocular lens (cIOL), corneal grafts after penetrating keratoplasty (gPK) and corneas of long-term soft contact lens wearers (cCL).MethodsThe study design was a consecutive cross-sectional trial. CCT was measured using rotating Scheimpflug camera (Pentacam, software version 1.16r04) in 80 cNHE, 79 cIOL, 46 gPK and 78 cCL. Analysis of variance (one-way ANOVA) was performed to compare differences of mean values between these four groups. Pearson's or Spearman's correlation coefficient (r) was determined between CCT value and age, follow up time after penetrating keratoplasty (timePK) or contact lens wearing time (timeCL).ResultsMeans of CCT measurements were comparable between cNHE (mean CCT ± standard deviation, 554 ± 36 μm), cIOL (551 ± 40 μm) and gPK (534 ± 52 μm) as determined by one-way ANOVA. Mean CCT values in cCL (537 ± 37 μm) were statistically significantly lower in comparison to cNHE (p = 0.026, 95% CI = 1.43–31.44). There was no linear correlation between age and CCT values of cNHE and cIOL (p = 0.841, r = −0.031 and p = 0.931, r = 0.011, respectively). No linear relationship was determined between CCT values of cCL and timeCL (p = 0.315, r = −0.125). CCT values of gPK did not correlate with timePK (p = 0.738, r = 0.054).ConclusionsThe data reported here indicate that in the same statistical model among CCT values of cNHE, cIOL and gPK only long-term soft contact lenses (CL) wearer have significantly lower CCT measurements.     

Scleral contact lens management of bilateral exposure and neurotrophic keratopathy

We report an interesting case of therapeutic scleral lens management of bilateral exposure and neurotrophic keratopathy resulting from bilateral cranial nerve (CN) palsies including V, VI and VII, which caused lagophthalmos and anaesthetic corneas. Subsequent development of severe exposure keratitis with vascularisation and keratinisation of the inferior cornea was previously treated with intensive ocular lubrication, botulinum toxin injections to the upper eyelid levator muscle, temporary tarsorrhophies, bilateral amniotic membrane grafts, punctal plugs, lid taping, gold eyelid weights and soft bandage contact lenses. Corneal integrity was re-established but visual acuity remained significantly compromised by corneal vascularisation, scarring and keratin deposits. Visions on presentation to the contact lens department were R 1.90 log MAR, L 1.86 log MAR. Therapeutic, high Dk, non-fenestrated, saline filled, scleral lenses were fitted. Daily wear of these lenses have protected and hydrated the cornea, enabling corneal surface recovery whilst retaining visual and social function. The visual acuities 6 months post-scleral fitting with lenses in situ are R 0.90 log MAR and L log MAR 0.70.     

Correlation of Back Optic Zone Radius measurement of rigid contact lenses with radiuscope and keratometer

PurposeTo investigate the accuracy of Back Optic Zone Radius (BOZR, base curve) measurements with manual keratometer for spherical polymethylmethacrylate (PMMA) lenses.Methods100 spherical PMMA contact lenses were selected randomly from the trial sets. One investigator measured the BOZR with radiuscope. The second investigator measured the BOZR with keratometer. The two investigators were masked to each other's readings. As the keratometer is designed to measure a convex corneal surface, the BOZR readings are less than actual radii. A correction factor of 0.025 was used to have corrected keratometers readings.ResultsThere was a high correlation between the BOZR measurement with radiuscope and the uncorrected (Pearson's correlation coefficient, r = 0.99) and corrected (r = 0.99) measurements with keratometer. The mean difference between BOZR measurement with radiuscope and the uncorrected and corrected measurements with keratometer were 0.003 mm (p = 0.62) and ?0.024 mm (p < 0.001) respectively. The 95% limits of agreement for the BOZR measurements with radiuscope and the uncorrected and corrected measurements with keratometer were ?0.11 to 0.11 mm and ?0.14 to 0.09 mm respectively.ConclusionWe found that the uncorrected BOZR measurements with keratometer were similar to the BOZR measurements with radiuscope. With unavailability of radiuscope in majority of contact lens practice, keratometer can be used to measure the BOZR of contact lenses.     

A pilot study investigating the effect of extended contact lens wear on limbal and central corneal morphology

PurposeTo investigate the effect of long-term extended soft contact lens wear on limbal and central corneal cell morphology, and limbal architecture.MethodsEach participant attended a study visit involving in vivo confocal microscopy of central corneal and limbal epithelium. Scans were graded by five masked graders for three features: central epithelial irregularity, limbal epithelial irregularity and the prominence of palisades of Vogt. The variability of grades between different graders and the difference of grades between extended wearers and daily soft/non-contact lens wearers were assessed.ResultsNineteen participants (9 extended soft contact lens wearers and 10 daily soft/non-contact lens wearers) aged 31–65 years were enrolled in this study. Scans from 37 eyes were included in the analysis. Agreement between graders for each feature was moderate to good with inter class correlation >0.7. While there were no significant differences in central epithelial cell irregularity (p = 0.527) and the prominence of palisade of Vogt (p = 0.182) between extended or daily soft/non-contact lens wearers, limbal epithelial cell irregularity showed a trend with increased irregularity in extended soft contact lens wearers (p = 0.091).ConclusionsWhile no differences in limbal cell morphology and structure or central epithelial cell was found in this subjective grading study of extended wearers compared to daily soft/non-contact lens wearers, further studies using a larger sample size or a longitudinal study design are warranted.     

Peripheral myopization and visual performance with experimental rigid gas permeable and soft contact lens design

PurposeTo evaluate the performance of two experimental contact lenses (CL) designed to induce relative peripheral myopic defocus in myopic eyes.MethodsTen right eyes of 10 subjects were fitted with three different CL: a soft experimental lens (ExpSCL), a rigid gas permeable experimental lens (ExpRGP) and a standard RGP lens made of the same material (StdRGP). Central and peripheral refraction was measured using a Grand Seiko open-field autorefractometer across the central 60° of the horizontal visual field. Ocular aberrations were measured with a Hartman-Shack aberrometer, and monocular contrast sensitivity function (CSF) was measured with a VCTS6500 without and with the three contact lenses.ResultsBoth experimental lenses were able to increase significantly the relative peripheral myopic defocus up to −0.50 D in the nasal field and −1.00 D in the temporal field (p < 0.05). The ExpRGP induced a significantly higher myopic defocus in the temporal field compared to the ExpSCL. ExpSCL induced significantly lower levels of Spherical-like HOA than ExpRGP for the 5 mm pupil size (p < 0.05). Both experimental lenses kept CSF within normal limits without any statistically significant change from baseline (p > 0.05).ConclusionsRGP lens design seems to be more effective to induce a significant myopic change in the relative peripheral refractive error. Both lenses preserve a good visual performance. The worsened optical quality observed in ExpRGP was due to an increased coma-like and spherical-like HOA. However, no impact on the visual quality as measured by CSF was observed.     

Objective and subjective visual performance of multifocal contact lenses: Pilot study

PurposeThe aim of the present study was to compare the objective and subjective visual performance of three different soft multifocal contact lenses.Methods10 subjects (habitual soft contact lens wearers) between the ages of 40 and 45 years participated in the study. Three different multifocal silicone hydrogel contact lenses (Acuvue Oasys, Air Optix and Biofinity) were fit within the same visit. All the lenses were fit according to the manufacturers’ recommendation using the respective fitting guide. Visual performance tests included low and high contrast distance and near visual acuity, contrast sensitivity, range of clear vision and through-focus curve. Objective visual performance tests included measurement of open field accommodative response at different defocus levels and optical aberrations at different viewing distances.ResultsAccommodative response was not significantly different between the three types of multifocal contact lenses at each of the accommodative stimulus levels (p > 0.05). Accommodative lag increased for higher stimulus levels for all 3 types of contact lenses. Ocular aberrations were not significantly different between these 3 contact lens designs at each of the different viewing distances (p > 0.05). In addition, optical aberrations did not significantly differ between different viewing distances for any of these lenses (p > 0.05). ANOVA revealed no significant difference in high and low contrast distance visual acuity as well as near visual acuity and contrast sensitivity function between the 3 multifocal contact lenses and spectacles (p > 0.05).ConclusionsThere was no statistically significant difference in accommodative response, optical aberrations or visual performance between the 3 multifocal contact lenses in early presbyopes.     

Efficacy of two silicone-hydrogel contact lenses for bandage use after photorefractive keratectomy

PurposeTo evaluate the efficacy of two silicone hydrogel (SiH) contact lenses, approved for continuous wear for one week, following photorefractive keratectomy (PRK).MethodsForty seven myopic patients (94 eyes) undergone bilateral PRK were enrolled in this prospective, double-masked, comparative study. One eye of each patient was fitted with a Lotrafilcon B lens (Ciba Vision, Duluth, US; 30-day recommended replacement) whereas the fellow eye was fitted with an Asmofilcon A lens (Menicon, Nagoya, Japan; 14-day recommended replacement). Epithelial defect size was assessed using slit lamp biomicroscopy on the day of surgery and at days 1–4 post-operatively. Uncorrected and best-corrected visual acuity and retinal straylight (C-Quant, Oculus Optigerate, Germany) were evaluated pre-operatively and one month post-operatively.ResultsAverage epithelial defect size for Asmofilcon A and Lotrafilcon B was 25.5 ± 11.0 mm² vs. 27.1 ± 9.9 mm² at day 1 (p = 0.007) and 6.3 ± 7.0 mm² vs. 9.2 ± 9.5 mm² at day 2 (p = 0.012) post-operatively. Re-epithelialization at day 3 was completed in 87.2% of the eyes fitted with Asmofilcon A lenses, compared to 74.5% with Lotrafilcon B lenses (p = 0.012). At the 3rd post-operative day 29.8% of re-epithelialized eyes showed irregular suture with Lotrafilcon B, compared to 12.8% eyes with Asmofilcon A lenses (p < 0.001). Finally, no statistically significant differences were found post-operatively between the two lenses retinal straylight (p = 0.98) and best-corrected visual acuity (p = 0.68).ConclusionsSiH lenses can be used as an effective bandage after PRK due to the limited time requested for achieving complete corneal re-epithelialization. Faster and smoother epithelial healing is provided with Asmofilcon A over Lotrafilcon B lenses.     

Utility of a semi-scleral contact lens design in the management of the irregular cornea

ObjectivesTo evaluate the utility of the Rose K2 XL semi-scleral contact lens (Menicon Co. Ltd., Nagoya, Japan) in the management of the irregular cornea.MethodsTwenty-seven subjects (34 eyes) with irregular corneas referred for contact lens fitting were evaluated. A diagnostic trial set was used in the fitting process. Once the trial lens was considered optimal, a final lens was ordered from the manufacturer with the necessary changes in power, edge lift and diameter. We analyzed visual acuity, number of lenses ordered and patients’ ability to wear and handle lenses.ResultsTwenty-three subjects (30 eyes) were fitted with the Rose K2 XL lens. Four subjects (4 eyes) decided not to conclude the fitting process for different reasons. Average logMAR visual acuity without correction and with the lens was 0.82 and 0.09, respectively (p < 0.001). An average of 1.4 ordered lenses (range 1–3) were necessary to achieve the optimal fit. Nineteen eyes (63%) were fitted with the first lens ordered. Three subjects (13%) had problems with lens handling, and three subjects (4 eyes) abandoned the wear of the lenses after three months due to discomfort (3 eyes) and unsatisfactory visual acuity (1 eye), respectively. Follow-up ranged from 6 to 9 months.ConclusionRose K2 XL semi-scleral contact lens provides good visual acuity and comfort in patients with irregular corneas.