Corneal biomechanical properties: Precision and influence on tonometry

PurposeTo assess the precision and reproducibility of the corneal biomechanical parameters, and their relationships with the intraocular pressure (IOP) measured with the Goldmann tonometer and a noncontact tonometer.MethodsReadings for biomechanical properties and for IOP measured with the Goldmann and noncontact tonometers, were taken on one randomly selected eye of 106 normal subjects, on each one of two measurement sessions. Measurements with the ocular response analyzer (ORA) and the noncontact tonometer were randomized, followed by the measurement of central corneal thickness and with the Goldmann tonometer.ResultsRepeatability coefficients for CCT, corneal hysteresis (CH) and corneal resistance factor (CRF) in Session 1 were ±0.01 μm, ±3.05 mmHg and ±2.62 mmHg, respectively. The mean CCT, CH, CRF, Goldmann and noncontact tonometry did not vary significantly between sessions. Reproducibility coefficients for CCT, CH and CRF were ±0.02 μm, ±2.19 mmHg and ±1.97 mmHg, respectively. Univariate regression analysis showed that CCT, CH and CRF significantly (P < 0.0001) correlated with the IOP measured with the Goldmann and noncontact tonometers (and with the differences between tonometers) in Session 1. There were no significant correlations with the differences between tonometers in Session 2. Multivariate analysis revealed a minimal effect of CCT on Goldmann measurements but a significant effect on those of the noncontact tonometer.ConclusionsMeasurement of the biomechanical properties of the cornea, using the ORA, are repeatable and reproducible, affect Goldmann tonometry less than noncontact tonometry, and have a minimal influence on the difference in measured intraocular pressure between tonometers.     

The relationship between measurement method and corneal structure on apparent intraocular pressure in glaucoma and ocular hypertension

PurposeTo analyse the relationship between measured intraocular pressure (IOP) and central corneal thickness (CCT), corneal hysteresis (CH) and corneal resistance factor (CRF) in ocular hypertension (OHT), primary open-angle (POAG) and normal tension glaucoma (NTG) eyes using multiple tonometry devices.MethodsRight eyes of patients diagnosed with OHT (n = 47), normal tension glaucoma (n = 17) and POAG (n = 50) were assessed. IOP was measured in random order with four devices: Goldmann applanation tonometry (GAT); Pascal^® dynamic contour tonometer (DCT); Reichert^® ocular response analyser (ORA); and Tono-Pen^® XL. CCT was then measured using a hand-held ultrasonic pachymeter. CH and CRF were derived from the air pressure to corneal reflectance relationship of the ORA data.ResultsCompared to the GAT, the Tonopen and ORA Goldmann equivalent (IOPg) and corneal compensated (IOPcc) measured higher IOP readings (F = 19.351, p < 0.001), particularly in NTG (F = 12.604, p < 0.001). DCT was closest to Goldmann IOP and had the lowest variance. CCT was significantly different (F = 8.305, p < 0.001) between the 3 conditions as was CH (F = 6.854, p = 0.002) and CRF (F = 19.653, p < 0.001). IOPcc measures were not affected by CCT. The DCT was generally not affected by corneal biomechanical factors.ConclusionThis study suggests that as the true pressure of the eye cannot be determined non-invasively, measurements from any tonometer should be interpreted with care, particularly when alterations in the corneal tissue are suspected.     

Topographic and biomechanical evaluation of cornea in patients with ichthyosis vulgaris

PurposeTo compare the topographic and biomechanical properties of corneas in eyes of patients with ichthyosis vulgaris (IV) and eyes of healthy individuals.MethodsThirty healthy individuals (control group) and 30 patients with IV (study group) were enrolled in this prospective study. Topographic measurements, including keratometry values, irregularity, and surface asymmetry index in the right eye of each participant were obtained using Scheimpflug camera with a Placido disc topographer (Sirius). Corneal hysteresis (CH), corneal resistance factor (CRF), corneal-compensated intraocular pressure (IOPcc) and Goldman-related intraocular pressure (IOPg) were measured using the Reichert Ocular Response Analyzer (ORA). Central corneal thickness (CCT) was also measured with ultrasonic pachymetry and the Sirius corneal topography system.ResultsTopographic parameters were not significantly different between both groups (p > 0.05). Although mean CH was not significantly different between the groups, the CRF was significantly lower in patients with IV (p = 0.249 and p = 0.005, respectively). The CCT was significantly lower in patients with IV compared to healthy controls (p < 0.001). The IOPg and IOPcc were significantly lower in the patients with ichthyosis than in healthy controls (p = 0.001 and p = 0.004, respectively).ConclusionsThe study demonstrated that while the eyes of patients with IV had corneal topographic findings and corneal hysteresis similar to those of healthy controls, some of corneal biomechanical properties such CRF and CCT and IOP values such as IOPg and IOPcc were significantly lower in patients with IV. These results should be taken into account when planning a corneal refractive surgery and glaucoma screening for patients with IV.     

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.     

Optical quality and intraocular scattering assessed with a double-pass system in eyes with contact lens induced corneal swelling

PurposeTo evaluate the impact of contact lens (CL)-induced corneal swelling on the optical quality of the eye by means of the double-pass technique.MethodsMeasurements of 6 healthy subjects were obtained in 5 visits over 1 week, at baseline and after sleeping with 4 different CLs of +0.50 D, +2.00 D, +5.00 D and +8.00 D (Acuvue2), randomly fitted on 4 different days. The control eye wore no CL. Corneal pachymetry and optical quality of the eye (OQAS, Visiometrics) were measured once at baseline and at three interval times in the follow-up visits: immediately after CL removal, and 1 and 2 h after CL removal. Optical quality was evaluated by means of the Strehl ratio and OQAS values at 100%, 20% and 9% contrasts. Intraocular scattering was evaluated with the objective scatter index (OSI).ResultsMean overnight swelling was 5.98 ± 4.29% in CL-eyes versus 0.30 ± 0.78% in control eyes (p < 0.01). Corneal swelling was maximal immediately after CL removal and decreased with time (p < 0.01). A significant worsening in all optical quality parameters and a significant increase of the OSI were found in eyes with corneal swelling (p < 0.05). Two hours after CL removal there were no statistically significant differences (p > 0.05) between CL-eyes and control eyes in any of the measured parameters.ConclusionsCorneal swelling has a significant impact on the optical quality of the eye and on intraocular scattering as assessed with the double-pass technique.     

The influence of lens power and center thickness on the intraocular pressure measured through soft lenses: a comparison of two noncontact tonometers

PurposeTo quantify the influence of soft contact lens power and thickness on the intraocular pressure (IOP).MethodsThirty-nine young, healthy adult volunteers completed this study. One eye of each subject was randomly assigned either a +6D or a ?6D high water content daily disposable lens. The other eye was fitted with the second lens. Triplicate measurements of IOP were taken before, during, and after contact lens wear. Each time, IOP was assessed in a randomized order with two noncontact tonometers. The lenses were swapped between eyes during a second session of measurements, one week later.ResultsIn the first session with the +6D lenses, the average IOPs (±SDs) before, with the lenses fitted, and after the lenses were removed, were: 14.3 ± 2.9 mmHg, 17.0 ± 3.3 mmHg and 13.9 ± 3.1 mmHg, respectively, for the CT80 and 13.6 ± 3.1 mmHg, 17.1 ± 4.5 mmHg and 13.3 ± 2.9 mmHg, respectively, for the PT100. The corresponding values for the first session with the ?6D lenses were: 14.3 ± 3.1 mmHg, 13.1 ± 3.1 mmHg and 14.1 ± 3.3 mmHg, respectively, for the CT80 and 13.6 ± 3.2 mmHg, 13.0 ± 3.0 mmHg and 13.6 ± 3.2 mmHg, respectively, for the PT100. IOP significantly (P < 0.05) increased (+ΔIOP = 2.7 ± 0.4 mmHg with the CT80 in the first session) with the +6D lenses, but decreased (P < 0.05) when the ?6D lenses were fitted (?ΔIOP = 0.6 ± 0.2 mmHg with the PT100 in the first session). The soft contact lens-induced changes were consistent between sessions but varied between tonometers.ConclusionsThe measurement of IOP through soft contact lenses resulted in consistent, statistically significant differences in IOP, which were not uniform across tonometers and which did not appear to be solely related to the central thickness of the soft contact lenses.     

Long-term changes in straylight induced by corneal refractive therapy: A pilot study

PurposeTo assess long-term intraocular straylight changes induced by corneal refractive therapy (CRT) and to determine whether these changes persist after cessation of CRT lens wear.MethodsA single-center, prospective, longitudinal study was performed in 22 subjects (group 1) undergoing overnight corneal refractive therapy for 1 year. Ten right eyes of 10 subjects (group 2) with emmetropia served as controls. In each subject, high contrast visual acuity (HCVA), manifest refraction and intraocular straylight were determined at several time points during treatment and 1 month after discontinuing treatment. Straylight was measured using the van den Berg straylight meter (third generation). EDTRS charts (logMAR units) were used to assess HCVA. For both groups, only data for the right eyes were analyzed.ResultsStraylight (mean ± standard deviation) significantly fell from baseline (0.98 ± 0.13) to values recorded after 1 month (0.88 ± 0.13, p = 0.011), 3 months (0.88 ± 0.13, p = 0.004), 6 months (0.88 ± 0.13, p = 0.000) and 12 months (0.76 ± 0.12, p = 0.003) of treatment. One month after discontinuing CRT lens wear, straylight was still significantly lower than baseline (0.89 ± 0.13, p = 0.003). No correlations were observed between intraocular straylight and HCVA.ConclusionsGood refractive outcomes and reductions in straylight were observed in response to corneal refractive therapy for myopia. The reduction in straylight observed after discontinuing CRT warrents further investigation.     

Evaluation of the ocular tolerance of a novel eyelid-warming device used for meibomian gland dysfunction

PurposeObstructive meibomian gland dysfunction (MGD) frequently induces a chronic complaint with various symptoms related to dry eye and discomfort. Previous research indicates a pivotal role for heat therapy for melting the meibum as part of any successful management plan, but delivery of constant temperature during treatment is vital. This study evaluated the performance of a novel device designed to deliver controlled, latent, moist heat to the eyelids and surrounding area.MethodsThe signs, symptoms and ocular temperature of 25 normal subjects (M8, F17; age 29.2 ± 5.7 years) were recorded before and after a 10 min application of the Blephasteam^® device. Ocular temperature (non-invasive ocular thermography; A40 Flir, UK), tear film stability (NIBUT), intra-ocular pressure (IOP), and ocular surface staining and hyperaemia were recorded. Results were checked for normality and compared using paired t-tests.ResultsTemperatures in both eyelids were significantly greater after device application (upper +1.7 ± 0.9 °C; lower +2.1 ± 0.7 °C, p < 0.0005). Bulbar conjunctival hyperaemia significantly decreased after treatment (p < 0.005), but limbal and palpebral hyperaemia remained similar (p = 0.33 and p = 0.11, respectively). Ocular surface staining (p = 0.74) and tear film stability (p = 0.12) were unchanged in this normal cohort, and there was no significant change in IOP (13.8 ± 2.0 mmHg vs 12.9 ± 2.2 mmHg; p = 0.092).ConclusionsThe Blephasteam^® device provides effective levels of warming that would be sufficient to melt meibum, and no adverse ocular responses were recorded in this cohort, indicating that this is a safe device. Interestingly, even in this normal cohort, ocular surface redness appears less after treatment.     

Evaluation of anterior chamber angle under dark and light conditions in angle closure glaucoma: An anterior segment OCT study

AimTo evaluate changes of nasal and temporal anterior chamber angle (ACA) in subjects with angle closure glaucoma using Spectralis AS-OCT (SAS-OCT) under dark and light conditions.MethodsBased on dark-room gonioscopy, 24 subjects with open angles and 86 with narrow angles participated in this study. The nasal and temporal angle opening distance at 500 μm anterior to the scleral spur (AOD500), nasal and temporal ACA were measured using SAS-OCT in light and dark conditions.ResultIn 2 groups, ACA and AOD500 in nasal and temporal quadrants were significantly greater in light compared to dark (all with p = 0.000). The AOD500 and ACA were significantly higher in nasal than temporal in measured conditions for 2 groups except the ACA and AOD500 of normal group measured in light. The difference between nasal and temporal in dark (29.07 ± 65.71 μm for AOD500 and 5.7 ± 4.07° for ACA) was greater than light (24.86 ± 79.85 μm for AOD500 and 2.09 ± 7.21° for ACA) condition. But the difference was only significant for ACA (p = 0.000). The correlation analysis showed a negative correlation between AOD500 and pupil diameter in temporal and nasal quadrants (both with p = 0.000). While temporal AOD500 difference correlated with spherical equivalent, temporal and asal gonioscopy, nasal AOD correlated with IOP, temporal and nasal gonioscopy.ConclusionsClinically important changes in ACA structure could be detected with SAS-OCT in nasal and temporal quadrants under different illumination intensity. The results could help in improvement of examination condition for better and more accurate assessment of individuals with angle closure glaucoma.     

The use of the Ocular Response Analyser to determine corneal hysteresis in eyes before and after excimer laser refractive surgery

Purpose

To compare corneal biomechanical parameters and two measures of intraocular pressure (IOP) in eyes before and after excimer laser refractive surgery, with the Ocular Response Analyser (ORA).

Materials and methods

Eighty normal eyes of 41 patients undergoing excimer laser refractive surgery in Birmingham, U.K. were recruited into three groups: Laser Assisted-Epithelial Keratomileusis (LASEK) (Myopes), Laser Assisted in Situ Keratomileusis (LASIK) (myopes) and LASIK (hyperopes). The preop and 3 months postop Goldmann correlated IOP (IOPg), corneal compensated IOP (IOPcc), corneal hysteresis (CH), and corneal resistance factor (CRF) were measured by the ORA. Central corneal thickness (CCT) was measured using ultrasonic pachymeter. The differences of the changes in IOPg, IOPcc, CH, CRF and CCT between the three groups were estimated. A General Linear Model was selected to investigate the influence of gender, age, initial conditions (CH, CRF, CCT, IOPcc and IOPg) and changes in CCT on the measured IOP.

Results

The differences between the mean IOPg, CH and CRF after refractive surgery were statistically significant for all three groups. The hyperopic LASIK group had a significantly smaller change compared to the other groups (which had no statistical significance). The preop IOPg, preop CH and gender were significant predictors of the changes in measured pressure and biomechanical parameters after surgery in the myopic groups only.

Conclusion

CH and CRF were found to decrease after both myopic and hyperopic refractive surgery. CH and CRF measurement may prove important tools to clarify the role of corneal biomechanics for refractive surgery.     

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.     

Ocular residual astigmatism and topographic disparity vector indexes in normal healthy eyes

PurposeTo define a range of normality for the vectorial parameters Ocular Residual Astigmatism (ORA) and topography disparity (TD) and to evaluate their relationship with visual, refractive, anterior and posterior corneal curvature, pachymetric and corneal volume data in normal healthy eyes.MethodsThis study comprised a total of 101 consecutive normal healthy eyes of 101 patients ranging in age from 15 to 64 years old. In all cases, a complete corneal analysis was performed using a Scheimpflug photography-based topography system (Pentacam system Oculus Optikgeräte GmbH). Anterior corneal topographic data were imported from the Pentacam system to the iASSORT software (ASSORT Pty. Ltd.), which allowed the calculation of the ocular residual astigmatism (ORA) and topography disparity (TD). Linear regression analysis was used for obtaining a linear expression relating ORA and posterior corneal astigmatism (PCA).ResultsMean magnitude of ORA was 0.79 D (SD: 0.43), with a normality range from 0 to 1.63 D. 90 eyes (89.1%) showed against-the-rule ORA. A weak although statistically significant correlation was found between the magnitudes of posterior corneal astigmatism and ORA (r = 0.34, p < 0.01). Regression analysis showed the presence of a linear relationship between these two variables, although with a very limited predictability (R²: 0.08). Mean magnitude of TD was 0.89 D (SD: 0.50), with a normality range from 0 to 1.87 D.ConclusionThe magnitude of the vector parameters ORA and TD is lower than 1.9 D in the healthy human eye.     

Lens-care-solution-induced alterations in dynamic interfacial properties of human tear-lipid films

PurposeTo evaluate the influence of lens care solutions (LCS) on interfacial dynamics and rheological properties of human tear-lipid films.MethodsTear lipids were extracted from Schirmer strips collected from 6 healthy subjects. Sessile bubble tensiometry was used to study interfacial properties at 22 °C. Lipids were deposited on an air bubble immersed into electrolytes solution to form 90 ± 20 nm films. Lipid films were subjected to expansion-compression cycles for dynamic interfacial properties and to step-strain relaxations for assessments of rheological properties. LCS (BioTrue [BT], PureMoist [PM], Revitalens [RL], ClearCare [CC]) were injected into optical chamber and equilibrated for 2 h without or with lipid films. Dynamic interfacial properties of films were measured. Then electrolyte solution was pumped through chamber and properties of films were re-evaluated.ResultsEquilibrium surface tension (EST), elasticity modulus (E), and relaxation times (τ) of tear lipids were 22 ± 2.1 mN/m, 10.7–14.8 mN/m, and 80–150 s, respectively. EST for LCS was 45.3 ± 0.8 for CC, 40.3 ± 0.8 for BT, 33.4 ± 1.0 for PM, and 30.1 ± 0.8 mN/m for RL. E for LCS varied within 0.5–6.7 mN/m, and τ varied from 49 to 68 ± 5 s. For mixed lipids + LCS films, EST remained unchanged whereas E and τ were reduced for all LCS types. Exposure to PM and RL noticeably altered the shape of lipid-film iso-cycles. These changes persisted after LCS washout.ConclusionsSome components of LCS bind irreversibly to lipid films and make them less viscous and less elastic. These findings suggest the possibility of tear-film destabilization upon LCS exposure.     

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.     

Changes in central corneal thickness values after instillation of oxybuprocaine hydrochloride 0.4%

PurposeTo assess the variation in central corneal thickness (CCT) following the instillation of oxybuprocaine hydrochloride (0.4%), in normal subjects.MethodsThis was a randomized, prospective study of CCT measurements (before and after the instillation of topical anaesthesia) obtained with the Topcon SP-3000P noncontact specular microscope, in 60 eyes of thirty subjects. The subjects’ mean age was 20 ± 1 years (mean ± SD). In each subject, one eye was treated with one drop of oxybuprocaine hydrochloride (HCl) and the fellow eye with one drop of normal saline (control). The SP-3000P CCT readings were first obtained before instillation (baseline) and monitored every 30 s after instillation of each eye drop for a period of 10 min.ResultsThe mean baseline CCT for oxybuprocaine was 526 ± 23 μm. Ten minutes after, it was 526 ± 24 μm. In the control, the mean CCT was 526 ± 27 μm, 10 min after it was 526 ± 28 μm. The mean variation in CCT measurement was ?0.7 ± 3.1 (5.5 to ?6.8 μm, 95% CI) for oxybuprocaine and ?0.6 ± 4.1 μm (7.5 and ?8.6 μm, 95% CI) for the fellow eyes (P > 0.05). There was no significant variation among the 20 CCT columns for either oxybuprocaine or the control group (P > 0.05 for both).ConclusionsOne drop of topical oxybuprocaine 0.4% did not cause a significant change in CCT at up to 10 min following instillation. However, higher differences were observed at 2.30 min and 4.30 min after instillation.     

The impact of short-term fenestrated scleral lens wear on intraocular pressure

PurposeTo examine the influence of short-term fenestrated scleral lens wear on intraocular pressure (IOP) in healthy eyes.MethodsIOP was measured before, during, and after a brief period (1–2 min) of fenestrated, scleral lens wear, using a rebound tonometer, in fifty, young healthy adults (mean age 23 ± 4 years) with normal corneas.ResultsImmediately following lens insertion, 48 of the 50 (96 %) of participants displayed an increase in IOP (mean ± SD increase in these participants of 3.8 ± 2.0 mmHg). Immediately following lens removal, 50 % of participants displayed a reduction in IOP, equal to or lower than, the pre-insertion IOP (-1.0 ± 0.8 mmHg lower than baseline). The remaining 50 % of participants displayed an IOP slightly greater than the pre-insertion IOP (1.6 ± 1.0 mmHg greater) after lens removal.ConclusionsShort-term fenestrated scleral lens wear resulted in a small, but statistically significant, increase in IOP in 96 % of young healthy participants (< 4 mmHg on average), which decreased to a level similar to pre-lens insertion IOP levels immediately following lens removal. Further research is required to determine if this measured change in IOP during scleral lens wear is artefactual, or an elevation in the true IOP.     

Effect of three different liposomal eye sprays on ocular comfort and tear film

PurposeTo evaluate the effect of three different liposomal eye sprays on ocular comfort and tear film stability.MethodsOptrexActiMist (AM, Optima-Pharma, Germany) was applied onto one, randomly selected eye of 80 subjects (female = 49; mean age = 49 years ± 18.6 SD) in a multi-centred, double-masked study. DryEyesMist (DEM, Boots) or TearMist (TM, Tesco) was applied onto the contralateral eye in randomized order. Over-all symptoms were investigated using the Ocular Surface Disease Index (OSDI). Ocular comfort (visual-analogue scale 0–100 [100 = perfect]) and non-invasive tear film stability (NIBUT) of each eye was evaluated before application (randomized order) and were again measured 10 min after application. Effects of products on ocular comfort and NIBUT were calculated as “factor” (=after-treatment/before-treatment). Differences between measurements were analysed by ANOVA repeated measurements and differences between groups by the dependent t-test (or the non-parametric equivalent).ResultsOSDI-scores (mean = 8.1 ± 9.0 SD), comfort (65 ± 24) and NIBUT (12 s ± 12.3) were statistically similar between centres (p > 0.400). Comfort and NIBUT were not different (p > 0.14) between product groups before application. Comfort and NIBUT improved significantly after application of AM (p < 0.001) but worsened with the comparing products (p < 0.058). Comfort improved by a mean factor of 1.5 (±0.82 SD) after application of AM but decreased after application of the comparing products (DEM: 0.9 ± 0.33; TM: 0.9 ± 0.34). Both factors were significantly better in AM (p < 0.027).ConclusionThe original liposomal eye-spray ‘OptrexActiMist’ significantly improved ocular comfort and tear film stability while ‘TearMist’ or ‘DryEyesMist’ worsened both criteria. The latter two products may not be clinically effective in the treatment of dry eye.     

Small optical zones with aspheric profiles in laser refractive surgery for myopia: A surgical outcome and patient satisfaction study

PurposeTo assess the outcomes of small optical zone (OZ) ablations used in conjunction with large transition zones (TZ) and a highly aspheric treatment profile.MethodsInterventional case series of 39 consecutive patients with myopia or myopic astigmatism. Patient data included pre and postoperative refraction and visual acuities, laser treatment settings and pre and postoperative corneal topography as well as questionnaire responses about the use of glasses and the quality of vision postoperatively.ResultsThe mean preoperative spherical equivalent was −4.50 ± 2.11 dioptres (D) and the mean OZ and TZ diameters were 4.5 ± 0.5 mm and 8.1 ± 0.4 mm, respectively. The mean patient age was 40.7 ± 10.4 years. Manifest spherical refraction was within ±0.5 D in 87% of patients (±1.0 D in 99%) and cylindrical refraction within 0.5 D in 79% (≤1.0 D in 95%). The need to wear distance glasses postoperatively was associated with dissatisfaction with the quality of daytime vision (p = 0.05) and unhappiness with night vision was associated with symptoms of halos (p = 0.03) and starbursts (p = 0.02). The proportion of patients reporting symptoms of dysphotopsias included: ghosting 0%; glare 2%; halos 10%; and starbursts 15%. There was a significant difference in the measured mean effective OZ diameter (4.8 ± 0.3 mm) compared to the mean programmed OZ (4.5 ± 0.5 mm, p = 0.00).ConclusionsSmall ablation zones, when used in conjunction with a large diameter TZ, do not lead to a greater incidence of unwanted visual phenomena over that reported by many studies with larger OZs.     

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.     

Pain,wound healing and refractive comparison of mechanical and transepithelial debridement in photorefractive keratectomy for myopia: Results of 1 year follow-up

PurposeTo compare the efficacy, safety and postoperative pain of mechanical versus transepithelial photorefractive keratectomy (PRK) techniques.SettingCornea and refractive surgery subspecialty.DesignProspective clinical trial.MethodsThis prospective comparative study included 84 eyes of 42 patients with myopia who received mechanical PRK (m-PRK) in 1 eye and transepithelial PRK (t-PRK) in the contralateral eye. The mean patient age was 28.5 ± 6.3 years (range 20–46 years). Postoperative uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), manifest refractions, postoperative epithelial healing time, surgical time, postoperative pain rating and corneal haze were recorded.ResultsAt week 1, statistically the UDVA was significantly better in the t-PRK eyes; however, at 3 months, similar refractive stability was achieved in both groups. The mean spherical equivalent (SE) decreased from −2.44 ± 1.00 D (m-PRK eyes) and −2.88 ± 1.24 D (t-PRK eyes) at baseline to −0.19 ± 0.38 D and −0.30 ± 0.40 D, respectively, after 1 year. Surgical time was 98.6 ± 9.8 s in m-PRK eyes and 58.0 ± 6.4 s in t-PRK eyes. On postoperative days 1 and 3, using the global assessment rating, 81% of mPRK eyes that had pain, reported more pain than that reported for the tPRK eyes. In addition, m-PRK treated eyes demonstrated higher mean pain scores based on the 11-point numerical rating scale and Visual Analogue Scale (VAS). The mean time to complete epithelial healing was 2.19 ± 0.39 days (t-PRK) and 3.76 ± 0.43 days (m-PRK).Conclusiont-PRK for mild-to-moderate myopia was more comfortable than conventional m-PRK; patients had less pain, and faster healing time.