Comparison of conventional method of contact lens fitting and software based contact lens fitting with Medmont corneal topographer in eyes with corneal scar

PurposeTo compare conventional method of contact lens fitting with software based contact lens fitting using Medmont corneal topographer in eyes with nebular and macular corneal scars.MethodsFifteen participants who were diagnosed with nebular and macular scars were fitted with rigid gas permeable lenses using conventional method of contact lens fitting. During the lens dispensing visit, participants underwent Medmont corneal topography. Agreement between the two methods of contact lens fitting was studied.ResultsParameters of contact lenses which were concluded using conventional method was compared to that of software based fitting. Mean difference in base curve of contact lens between the two methods was 0.094 mm ± 0.147 mm (95% CI: +0.383 to −0.194). Mean difference in diameter of contact lens between the two methods was 0.16 mm ± 0.172 mm (95% CI: +0.497 to −0.177). Contact lens parameters that were achieved using two different methods of fitting showed good correlation. Correlation coefficients, as comparison of two methods in base curve and diameter were 0.96 (P < 0.05) and 0.94 (P < 0.05), respectively.ConclusionSoftware based contact lens fitting would be useful for contact lens practitioners to predict initial base curve of contact lens in corneal scars.     

The accuracy of Goldmann applanation tonometry over silicone hydrogel contact lenses in patients with glaucoma

PurposeTo investigate the accuracy of measuring intraocular pressure over a silicone hydrogel contact lens using Goldmann applanation tonometry in eyes with glaucoma.MethodsThis was a prospective, randomized study and enrolled 28 patients (28 right eyes) with primary open angle glaucoma. Intraocular pressure was taken with and without a silicone hydrogel contact lens (−0.50 D), in situ (using Goldmann applanation tonometry), in a randomized order of measurements. Statistical analysis was performed using paired t-test and Bland–Altman plot.ResultsThe mean difference (± standard deviation) found between intraocular pressure measurement without (mean 16.7 ± 3.2 mmHg) and with (mean 17.3 ± 3.0 mmHg) contact lens was found to be −0.57 ± 2.3 mmHg (95% confidence interval, −1.5 to 0.3). No significant statistical difference was found between the two groups with paired t-test (p = 0.19). The Bland Altman plot showed some evidence of increasing variability of differences between two measures of intraocular pressure, with increasing intraocular pressure. The 95% limits of agreement of the Bland Altman plot were unacceptably large (−5 mmHg to 3.9 mmHg).ConclusionAgreement between Goldmann applanation tonometry with and without contact lenses seems to be poor in patients with glaucoma, especially for high intraocular pressure.     

Kerasoft IC compared to Rose-K in the management of corneal ectasias

PurposeTo determine the efficacy of the KeraSoft^® IC (KIC) (Ultravision International Limited, Bedfordshire, UK), a silicone hydrogel contact lens, for the optical management of non-surgical corneal ectasias and to compare it with the Rose-K 2 RGP contact lens.MethodsIn a retrospective study ninety-four eyes fitted with KIC (group A) were compared with seventy-seven eyes fitted with Rose-K^® RGP lenses as a control group. Ocular diagnoses, corneal curvature by topography, refraction, best spectacle-corrected visual acuity (BSCVA), and age at time of fitting were noted. Outcome data included average daily wearing time, contact lens complications, visual acuity with the lens (BCLCVA), power of the lenses and length of follow-up.ResultsDifferences in either BCLCVA or wearing time could not be statistically established (p = 0.63, p = 0.15) between both groups. More biomicroscopic complications were found in the RGP group, basically corneal staining (P < 0.0001). In the KIC group, BCLCVA was statistically similar between types of ectasia (p = 0.19) as well as in mild and moderate keratoconus (p = 0.45).ConclusionsKIC is a good alternative for the optical management of irregular corneal astigmatism in non surgical corneal ectasias such as keratoconus and pellucid marginal degeneration.     

Progression of keratoconus in patients wearing pancorneal toric edge rigid gas-permeable contact lenses

PurposeTo investigate the rate of progression of keratoconus in patients wearing pancorneal toric edge rigid gas-permeable contact lenses (pancorneal RGP-CL) compared to non-pancorneal RGP-CL. We also evaluated alterations in anterior chamber parameters with the progression of keratoconus and investigated the location of the cone in eyes with keratoconus.MethodsThe current study was a retrospective study including patients with clinically evident keratoconus from the outpatient clinic from the Department of Ophthalmology of the Erasmus Medical Center, Rotterdam, the Netherlands. Medical history and contact lens characteristics were documented. All participants underwent ophthalmic examination including corneal topography. Corneal topography was repeated at one of the consecutive visits of the patient. Patients were divided into two groups: those wearing pancorneal RGP-CL and those wearing other contact lens types. As a measure of progression of keratoconus differences in corneal topography parameters between both groups were compared.ResultsA total of 82 patients were included of which 42 had follow-up (mean 17.8 months) data. We found a significant difference in progression between eyes fitted with and without pancorneal RGP-CL (K-flat: p = 0.09, K-steep: p = 0.02, K-mean: p = 0.02, and K-minimum: p = 0.04). Compared with eyes fitted without pancorneal RGP-CL no significant difference in K-values was found for eyes fitted with pancorneal RGP-CL during follow-up. Furthermore, a significant decrease in anterior chamber volume (p < 0.001) and corneal volume (p = 0.008) was found during follow-up. In 86.6% the location of the cone was located infero-temporal.ConclusionsPancorneal RGP-CL have a better effect on stabilizing progression of keratoconus than non-pancorneal RGP-CL. The finding of an infero-temporal location of the cone in keratoconic corneas may improve results of contact lens fitting and surgical management.     

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.     

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.     

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.     

Which soft contact lens power is better for piggyback fitting in keratoconus?

PurposeTo evaluate the impact of differente soft contact lens power in the anterior corneal curvature and regularity in subjects with keratoconus.MethodsNineteen subjects (30 eyes) with keratoconus were included in the study. Six corneal topographies were taken with Pentacam Eye System over the naked eye and successively with soft lens (Senofilcon A) powers of −3.00, −1.50, 0.00, +1.50 and +3.00 D. Corneal measurements of mean central keratometry (MCK), maximum tangential curvature (TK), maximum front elevation (MFE) and eccentricity (Ecc) at 6 and 8 mm diameters as well as anterior corneal surface high order aberrations (i.e. total RMS, spherical- and coma-like and secondary astigmatism) were evaluated.ResultsNegative- and plano-powered soft lenses flattened (p < 0.05 in all cases), whereas positive-powered lenses did not induce any significant changes (p > 0.05 in all cases) in MCK in comparison to the naked eye. The TK power decreased with negative lenses (p < 0.05 in both cases) and increased with +3.00 D lenses (p = 0.03) in comparison to the naked eye. No statistically significant differences were found in MFE with any soft lens power in comparison to the naked eye (p > 0.05 in all cases). Corneal eccentricity increased at 8 mm diameter for all lens powers (p < 0.05 in all cases). No statistically differences were found in HOA RMS and spherical-like aberration (both p > 0.05). Statistically differences were found in coma-like and secondary astigmatism (both p < 0.05).ConclusionNegative-powered soft contact lenses provide a flatter anterior surface in comparison to positive-powered lenses in subjects with keratoconus and thus they might be more suitable for piggyback contact lens fitting.     

Predicting initial base curve of the rigid contact lenses according to Javal keratometry findings in patients with keratoconus

PurposeTo find an appropriate correlation between the base curve (BC) of rigid gas permeable (RGP) contact lenses and manual keratometry findings in Iranian patients with keratoconus (KCN) in order to simplify the fitting process, reduce the time, and lower the costs.MethodThis retrospective study was done in 121 eyes of 69 patients with KCN fitted with a specific trial set of RGP contact lenses over a 7-year period. The specifications of the final lens parameters included power, total diameter (1), and BC, the first two of which were fixed in all of the lenses in the trial set while BC was changed in 0.1-mm steps. Javal keratometer was used to measure keratometric values. The final fit assessment was performed based on the standard criterion of "three-point touch".ResultSingle and multiple linear correlations were done and the result was the following equation: BC = 2.455 (constant of the final multiple regression model) + 0.280 (steep keratometry) + 0.368 (flat keratometry) + 0.047 (corneal astigmatism)ConclusionThe advantages of this study include simplifying the RGP fitting process, reducing the examination time, lowering the costs, enhancing the confidence of the examiners and patients, easier lens fitting in remote places where more advanced devices are not accessible.     

Scleral contact lenses for visual rehabilitation after penetrating keratoplasty: Long term outcomes

PurposeTo evaluate the success rate of highly gas permeable scleral contact lenses (SCL) for visual rehabilitation after penetrating keratoplasty (PK), over a period of up to 9 years.MethodsA total database of 31 consecutive patient fitted with SCL between January 2004 and December 2009 was retrospectively reviewed. Demographic data, etiology prior to lens fitting, visual outcomes, follow up time and complications were analyzed.ResultsAll eyes were fitted due to inadequate spectacle-corrected vision after successful penetrating keratoplasty or failure of other contact lens modalities. Out of 31 patients fitted, 28 (33 eyes) continue to wear SCL for periods between 0.5 and 8.8 years. The mean duration of follow-up after contact lens fitting was 5.2 ± 2.2 years. The mean age of corneal graft was 17.6 ± 11.4 years (range 4.3–42), and the mean interval between PK and initial contact lens fitting was 12.2 ± 10.7 years (range 0.7–36.0). The average steepest keratometry of our cohort was 55.0 ± 7.5 diopter (D) and the refractive astigmatism was 8.0 ± 4.4 D. The mean contact lens corrected visual acuity (BCVAcl) was 0.78 ± 0.25 (range 0.3–1.2). Twenty-three (82%) patients achieved a functional vision of 0.5 or more.During the studied period, ten (30.0%) eyes presented at least one graft rejection episode and two eyes (6%) had an episode of microbial keratitis. Corneal transplants of 20 years or more show a higher rate of refits due to ectasia recurrence.ConclusionsScleral lenses should be considered as lens of choice in eyes with complex corneal geometry, as besides visual rehabilitation, their use may delay or prevent further surgical involvement.     

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.     

Lens parameter changes under in vitro and ex vivo conditions and their effect on the conjunctiva

PurposeTo quantify changes in contact lens parameters induced by lens wear and determine whether these changes are associated with contact lens-induced conjunctival staining (CLICS).MethodsIn vitro: Lens diameter, sag, edge shape, base curve of six contact lens brands (balafilcon, comfilcon, etafilcon, lotrafilcon B, omafilcon and senofilcon) measured at 21 °C and 35 °C (eye temperature). Ex vivo: Diameter of lenses collected from a prospective, randomised, contra-lateral, cross-over clinical trial from 36 subjects wearing all lens types for 1 week daily wear, measured in 35 °C PBS after removal. Ocular surface was examined for lens-induced conjunctival staining by masked examiner.ResultsIn vitro: Changes in diameter and base curve outside ISO tolerance were found with etafilcon A and omafilcon A. Ex vivo: Comfilcon A and etafilcon A had greatest shrinkage in diameter (0.18 mm) and base curve (0.11 mm steeper) with temperature increase from 21 °C to 35 °C. Senofilcon A, lotrafilcon B and balafilcon A maintained most stable parameters between 21 °C and 35 °C. Changes in diameter and base curve from lens wear were not correlated with CLICS (p > 0.49). Multivariate analysis showed significantly greater levels of lens induced staining were associated with lens modulus (p < 0.001) and knife (p < 0.001) and chisel (p < 0.001) edge shapes.ConclusionsParameter changes induced by lens wear were associated with increasing temperature, but these changes in lens diameter and base curve did not induce CLICS. Modulus and edge shape were associated with increased CLICS. The susceptibility of etafilcon A and omafilcon A lenses to parameter changes might be related to their high water content.     

Correlation between long-term use of rigid gas permeable contact lenses and endothelial morphometric changes in keratoconus patients

PurposeThis study was conducted to evaluate the effects of long-term use of rigid gas-permeable (RGP) contact lenses on corneal endothelium in keratoconus (KC) patients using non-contact specular microscopy. In addition, the correlation between wearing duration of RGP lenses (years & hours /d) and endothelial morphometric changes in KC patients was performed. This may provide more useful data for clinical application of RGP contact lens.Study designThis study was a prospective, observational, comparative, hospital based, nonrandomized, cross-sectional, and quantitative study.Subjects and methodsThe study included 40 eyes of non-wearer contact lens KC patients (group 1) and 38 KC eyes with a long history of Rose K2 RGP contact lens wearing (group 2). The corneal endothelial morphology such as endothelial cell density (ECD); coefficient of variation of cell area (CV); percentage of hexagonal cells (HEX); and central corneal thickness (CCT) were evaluated in all patients using SP3000P Specular Microscope.ResultsThe study included 40 eyes of non-wearer contact lens KC patients (20 mild KC eyes and 20 moderate KC eyes) and 38 KC eyes with a long history of RGP contact lens wearing (18 mild KC eyes and 20 moderate KC eyes). The mean duration of RGP lenses wearing was 5.67 ± 3.481 years & 12.11 ± 2.698 h/d in mild KC eyes and 7.15 ± 5.294 years &13.65 ± 2.889 h/d in moderate KC eyes. Wearing duration in hours in mild KC eyes showed a significant moderate negative correlation with ECD (r = ?0.529, p = 0.024) and a moderate positive correlation with CV (r = 0.565, p = 0.015). In addition, wearing duration in years in moderate KC eyes showed a significant moderate negative correlation with ECD (r = ?0.465, p = 0.039) and moderate positive correlation with CV (r = 0.627, p = 0.003). However, wearing duration in hours in moderate KC eyes showed a significant moderate negative correlation with HEX only (r = ?0.490, p = 0.028). This study reported significant corneal thinning in contact lens wearer KC eyes in contrast to non-wearer KC eyes.ConclusionThis study documented a significant correlation between a long-term use of Rose K2 RGP using the three-point touch and corneal endothelial morphometric changes in KC patients. In addition, the current study confirmed a significant corneal thinning in RGP contact lens wearer compared to non-contact lens wearer KC patients. Further studies are recommended to evaluate the association between different RGP lens materials with different oxygen permeability transmissibility; different lens design types; different fitting methods; the duration of contact lens wear and the endothelial morphometric changes in KC patients.     

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.     

Anterior segment characteristics of keratoconus eyes in a sample of Asian population

PurposeTo assess changes in anterior segment parameters of keratoconus eyes at different stages of the disease in a sample of the Asian population.MethodsFiles of 32 patients (48 eyes) diagnosed as clinical keratoconus were assessed and the following parameters noted: central corneal thickness (CCT), thinnest corneal thickness (TCT), location of thinnest pachymetry, anterior chamber depth (ACD) at the centre from posterior corneal surface, ACD at 1, 2 and 3 mm inferior-paracentral, ACD at thinnest pachymetry, anterior chamber volume (ACV) and anterior chamber angle (ACA). For analysis, keratoconus eyes were classified into 3 subgroups according to mean keratometry readings (mild: K ≤ 47.0 D, moderate: 47.0 < K < 52.0 D, and severe: K ≥ 52.0 D). Forty-five subjects (45 right eyes) were recruited as a control group. They underwent Pentacam tomographic evaluation. The same parameters were recorded for control subjects as in the keratoconus patients.ResultsEach keratoconus subgroup comprised of 16 eyes. CCT, TCT, ACD at centre, ACD at 1, 2 mm inferior-paracentral and ACD at thinnest pachymetry were statistically different between mild and severe keratoconus groups (P < 0.05). There were also significant differences between normal with each of the moderate and severe keratoconus groups (P < 0.05). Non-significant differences were found in ACV (P = 0.84) and ACA (P = 0.71) between all measured groups.ConclusionWith the exception of ACV and ACA, parameters that include CCT, TCT, ACD at centre, thinnest pachymetry and 1, 2 mm inferior-paracentral were significantly altered with progression of keratoconus. These findings may be useful in monitoring and management of keratoconus patients.     

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.     

Comparison of normal and keratoconic corneas by Galilei Dual-Scheimpflug Analyzer

Background and objectiveTo determine the efficacy of different Galilei Scheimpflug-Analyzer (GSA) parameters in discriminating between keratoconic and myopic eyes.Patients and methodsGSA measurements were obtained for 67 patients (67 eyes) with keratoconus and 151 patients (151 eyes) with myopia or myopic astigmatism. Several parameters, provided by the software or derived from the elevation maps, were evaluated and compared for the two groups.ResultsBetween the two groups, statistically significant differences were observed for all corneal parameters obtained by GSA (P < 0.001) except for the anterior chamber depth (P = 0.149). ROC analysis determined that posterior corneal elevation was the best predictive parameter (area under the curve: 0.99). The posterior corneal elevation, at a cut-off value of 18.5 μm, had 98.5% sensitivity and 98.3% specificity in discriminating keratoconus from myopic eyes.ConclusionElevation, pachymetric and keratometric parameters measured by the GSA, as well as the specific predictive GSA software parameters can effectively distinguish advanced keratoconus from myopic corneas. Also, keratoconus that is easily diagnosed by other means can be diagnosed easily by GSA software parameters.     

Fluid filled scleral contact lens in pediatric patients: challenges and outcome

PurposeTo study the indications and the challenges while fitting scleral contact lens (ScCL) filled with fluid prior to lens insertion in pediatric patients.MethodsWe retrospectively reviewed charts of patients of 16 years or less who received ScCL (PROSE – Prosthetic Replacement of the Ocular Surface Ecosystem, Boston Foundation for Sight, Needham Heights, MA, USA) that were filled with fluid (Normal saline) before lens insertion during July 2006 to April 2010. The main goal of ScCL fitting was to improve vision in patients having keratoconus (KC) and improve the ocular microenvironment in ocular surface disease (OSD). Visual acuity before and after lens wear was noted.ResultsFluid-filled ScCL were dispensed to 15 patients (20 eyes). The indications for ScCL fitting were KC (n = 3 eyes), Stevens Johnson syndrome (SJS, n = 13 eyes), radiation keratopathy (n = 1 eye), combined KC and SJS (n = 1 eye) and KC and vernal keratoconjunctivitis (VKC, n = 2 eyes). Mean age of the patients was 12.85 years. The average daily lens wear was 9 h. The vision improved by 2 lines or more in 85% and dropped by 2 lines or more in 45% eyes after 4 h of lens wear due to tear debris collection. None of the patients had any complications. Patients were self sufficient inserting and removing ScCL. Two patients had broken lenses during the follow-up.ConclusionsScCL are useful for pediatric patients who have OSD, irregular astigmatism or the two coexisting; KC combined with VKC or SJS, helping to maintain the health of the ocular surface and improves vision in these patients.     

Bitoric rigid gas permeable contact lenses in the optical management of penetrating keratoplasty

PurposeThe purpose of this study was to evaluate the complexity and effectiveness of fitting bitoric rigid gas permeable contact lenses (RGPCLs), compared to spherical RGPCLS, when used in the correction of high amounts of post-penetrating keratoplasty astigmatism.MethodsRecords of post-penetrating keratoplasty (PKP) patients being managed with bitoric RGPCLs were compared to controls (post-PKP patients managed with spherical RGPCLs). Factors that were analyzed included the number of diagnostic RGPCLs used to assess the initial fit, the number of RGPCLs ordered to finalize the fit and the number of total doctor visits to finalize the fit.ResultsFourteen eyes of 14 patients satisfied the study criteria. The average amount of total astigmatism in this study group was 10.0 D ± 5.0 compared to the control group which was 3.3 D ± 2.6. The number of diagnostic RGPCLs used for the study group was 1.2 ± 0.4 compared to 1.0 ± 0.0 for the control group. The mean number of contact lenses ordered to complete the fitting for the study group was 1.9 ± 0.7 compared to the control which was 2.1 ± 0.8. The study group presented for an average of 6.3 ± 1.6 visits whereas the control group presented for 4.9 ± 1.1 visits. Contact lens corrected acuity for the study group was 0.101 ± 0.11 (20/25) compared to the control group 0.08 ± 0.12 (20/24).ConclusionsThe complexity of fitting bitoric RGPCLs was found to be similar to fitting spherical RGPCLs on post-PKP eyes and the visual outcomes were not different.