Redistribution of the corneal epithelium after overnight wear of orthokeratology contact lenses for myopia reduction

BackgroundTo investigate changes in the corneal thickness profile in juvenile myopia after overnight wear of orthokeratology lenses (OK).MethodsA total of 53 juveniles (53 right eyes) successfully wore OK between January 2016 and July 2017 and they were reviewed one day, one week and one month after first wearing it. Epithelial and corneal data were obtained by optical coherence tomography (OCT). Changes in uncorrected visual acuity, refractive error, corneal refractive power, and epithelial and corneal thickness were analyzed before and after wear of OK.ResultsThe corneal epithelium was reshaped after 1 day of OK; the myopia degree was reduced, and uncorrected visual acuity reached 0 logMAR at 1 week. The central (2 mm) average epithelial thickness was 52.04 ± 2.35 μm, 49.25 ± 2.67 μm, 45.91 ± 2.80 μm, and 47.53 ± 3.44 μm before and after 1 day, 1 week, and 1 month of OK, respectively (t = 4.497, 9.741, and 7.340, respectively, P<0.001). The central epithelium was thinnest at 1 week, when the average thinning of 6.13 ± 1.67 μm accounted for approximately 11.78 % ± 3.21 % of the total epithelium thickness at baseline. The epithelial thickness of the reverse curve zone was 51.83 ± 2.49 μm, 57.62 ± 3.01 μm, 59.43 ± 3.19 μm, and 60.22 ± 2.75 μm before and after 1 day, 1 week, and 1 month of OK, respectively, showing a significant increase over time (t=-4.752, -6.208, and -6.848, respectively, P < 0.001).ConclusionIn the early stage of OK, the corneal epithelium was redistributed very quickly. The central epithelium became thin, while the epithelium of the reverse curve zone correspondingly thickened. Effectively reduced the refractive power of the cornea equivalent to the effect of adding a concave spectacle lens, which ensures uncorrected vision after removal of the lenses.     

Corneal epithelial thickness and corneal curvature changes during the day: The effects of daily disposable contact lens wear

PurposeTo evaluate the changes in corneal epithelial thickness and corneal anterior and posterior curvatures during the day, and the effect of wearing daily disposable soft contact lenses.MethodsThirty-two healthy volunteers were enrolled in a randomized crossover study. At the baseline visit, corneal and epithelial thickness maps (OCT; Optovue, Inc., Fremont, CA, USA) and keratometric measurements (Pentacam, Oculus, GmbH, Germany) were performed in the morning and in the afternoon (8 hours after). Then, each subject was fitted with the following brands of daily disposable contact lenses in random order: Dailies Total 1 (Delefilcon A), Dailies Aqua Comfort (Nelfilcon A), TruEye (Narafilcon A) and Biotrue Oneday (Nesofilcon A) on different days. All fitted lenses had a power of −3.00 diopters (D). Measurements were repeated before putting the contact lens on and after an-eight-hour contact lens wear.ResultsWith no lens wear, the anterior topographic indices showed significant steepening [Kflat: p < 0.0001; Ksteep: p < 0.0001 and maximum keratometry value (Kmax): p = 0.04] and the corneal thickness significantly decreased in the central and temporal portion of the cornea in the afternoon. There were no significant changes in the posterior topographical indices and corneal epithelial thickness. With contact lens wear, no significant change occurred in the corneal and epithelial thickness, and the anterior and posterior curvatures during the day (all p values >0.05). There was no statistically significant difference in the epithelial thickness among the groups wearing different contact lens types (p > 0.05).ConclusionsAnterior corneal topographic indices steepen depending on the natural diurnal variations. Daily wear of soft contact lenses appears to mask this steepening. The corneal epithelial thickness is not affected by daily disposable soft contact lenses.     

Contact lens care in keratoconus.

PURPOSE: To quantify the complexity involved in fitting contact lenses on the eyes of patients with keratoconus. METHODS: The contact lens care of one randomly selected eye each of 38 keratoconus patients was retrospectively analyzed and compared to that of 38 gender and age matched controls. We evaluated the number of diagnostic contact lenses used to establish the initial contact lens order, number of ordered rigid gas permeable (RGP) contact lenses needed to complete the fit, number of office visits during the initial 4 months of care, best spectacle and RGP contact lenses corrected Log MAR visual acuities, complications encountered, and whether or not the patient was successful in contact lens wear. RESULTS: Keratoconic eyes statistically used more diagnostic lenses, more ordered lenses, and more office visits than did normal eyes. Visual acuities improved from an average of 20/40 with spectacles to an average of 20/20 by use of RGP contact lenses in keratoconic eyes. Visions were corrected to 20/20 with both spectacles and contact lenses in control eyes. Sixty nine percent (69%) of keratoconic eyes and 95% of controls were successful in contact lens wear. CONCLUSIONS: Contact lens care of keratoconic eyes is more challenging than care of normal eyes because of the need for more diagnostic and ordered contact lenses and the use of more professional time. Keratoconic eyes may suffer more complications than normals during contact lens care, but this does not affect the success rates, and such patients benefit from enhanced visual acuity with RGP contact lenses compared to that achieved with spectacles.     

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.     

Clinical observations of the effect of orthokeratology in children with myopic anisometropia

PurposeTo evaluate the clinical effect of orthokeratology in controlling myopia and treating anisometropia among children with myopic anisometropia.MethodsA total of 108 myopic anisometropic children aged 8–16 years old who wore orthokeratology lenses in both eyes were enrolled in this study and followed up for over 1 year. The more severely myopic eye of each patient was assigned to the more myopic group (108 eyes), with a mean spherical equivalent refraction of −4.25 (−5.00, −3.38) D; the opposite eye of each patient was assigned to the less myopic group (108 eyes), with a refraction of −2.75 (−3.63, −1.88) D. This study observed and analyzed changes in ocular parameters after orthokeratology (Wilcoxon signed-rank test).ResultsIn children who wore orthokeratology lenses for approximately 1 year, the level of anisometropia significantly dropped from 1.38 (1.13, 1.75) D to 1.25 (1.13, 1.75) D (P = .005). The difference between the axial lengths of the two eyes significantly dropped from 0.54 (0.37, 0.74) mm to 0.46 (0.28, 0.67) mm (P< .0001).ConclusionsOrthokeratology seemed to be more effective at delaying the progression of myopia in the more myopic eyes than in the less myopic eyes of myopic anisometropic children. Orthokeratology lenses are suitable for anisometropic children, although the effectiveness of orthokeratology against anisometropia requires additional follow-up time for further observation and study.     

Changes in aniseikonia of an axial anisometrope at various stages of orthokeratology lens wear

PurposeTo report a case of reduced aniseikonia in a myopic axial anisometrope during orthokeratology (OK) lens wear.Case reportA 19-year-old female university student with myopic anisometropia presented for an OK lens fitting consultation. At baseline, perceptual interocular image size difference or aniseikonia of 1.45% was found, with a smaller image seen by the right eye compared to the left eye. The patient was fitted with a pair of OK lenses and interocular image size differences, subjective refraction and corneal topography were measured after 7, 14 and 47 days of overnight lens wear. Hyperopic shifts in central refraction and corresponding flattening of the central cornea was measured during OK treatment. Aniseikonia reduced after OK wear with the most significant change measured from baseline to day 7. Aniseikonia recorded after 7, 14 and 47 nights of lens wear was 0.05%, 0.35% and 0.85%, respectively. Although minimum differences in refractive error between eyes was reached after 47 days of OK, aniseikonia was greater than that measured after 7 and 14 days of OK.ConclusionThis case report demonstrates reduction in aniseikonia with OK lens wear in a myopic patient with axial anisometropia, although this effect was not sustained beyond 1 week of lens wear. As the impact of corneal curvature changes on aniseikonia is not well understood, future studies on the impact of OK on aniseikonia and associated asthenopia is required.     

Refractive and corneal responses of young myopic children to short-term orthokeratology treatment with different compression factors

PurposeTo evaluate changes in refractive and corneal responses in myopic children wearing orthokeratology (ortho-k) lenses with conventional compression factor (CCF, 0.75 D) and increased compression factor (ICF, 1.75 D).MethodsThis was a double-blind self-controlled study. Subjects were randomly fitted with CCF in one eye and ICF in the fellow eye. Weekly monitoring of refraction, visual acuity (VA), external ocular health, and corneal responses were performed over one month of lens wear and after discontinuation of lens wear until stabilization was achieved.ResultsTwenty-five subjects, aged 9.4 ± 1.0 years, completed one-month lens wear, of whom 23 completed the washout period. The first fit success rates for CCF and ICF were 93% and 96%, respectively. Myopia, unaided VA, central corneal thickness, anterior corneal curvatures (K), apical power (AP), and corneal resistance factor (CRF) all changed significantly during the study period (P < 0.003). Between-eye difference was significant only for myopia reduction (P = 0.001). About 4% and 8% of ICF and CCF eyes were under-corrected. The attempted target was achieved in about 80% of CCF and 60% of ICF eyes at week 4. At the end of the washout period (3 weeks), myopia, K, and AP were significantly different compared to baseline (P < 0.001).ConclusionIncreasing the compression factor did not affect the first fit success rate and external ocular health, but did allow faster correction of refractive error within one month of lens wear. Further investigation is warranted to investigate the long-term effects of ICF on myopia control compared to CCF.     

Visual performance after overnight orthokeratology.

PURPOSE: To investigate visual performance after overnight orthokeratology in terms of changes from baseline values, regression of the orthokeratology effect over time, and evaluation of the best-corrected vision after treatment. In particular, to evaluate any residual visual deficits over the duration of a day due to the abnormal corneal topography induced by orthokeratology treatment. METHOD: One eye of each of six subjects was fitted with custom designed BE orthokeratology lenses (Capricornia, Brisbane, Australia), with the fellow eye acting as a control. Unaided vision, subjective sphero-cylindrical refraction, high contrast high luminance visual acuity, low contrast high luminance visual acuity, high contrast low luminance visual acuity and letter contrast sensitivity were measured at baseline and after one night (Day 1) and eight nights (Day 8) of lens wear. Except for baseline, data were collected after overnight lens wear immediately after lens removal, and again 3, 6 and 9h after lens removal. At each time point throughout the day, the visual performance measures were evaluated with the initial refraction of the day (the 0h refraction) and also using the optimum subjective refraction at each measurement time. This method was used to evaluate the practical visual performance to be expected after orthokeratology treatment and the residual visual deficits arising from any induced corneal changes after correction of defocus. RESULTS: As expected, orthokeratology lens wear significantly changed unaided vision and refraction from baseline. However, it did not significantly affect visual acuity in different contrast conditions, or contrast sensitivity. The spherical component of refraction was the only parameter to exhibit regression over each day (p=0.021), with more stability demonstrated on Day 8 than Day 1 (p=0.012). There were no statistically significant changes of best-corrected acuity from baseline in the differing contrast and luminance conditions. CONCLUSION: Apart from the predicted improvements in unaided vision and reduction of the myopic refractive error, orthokeratology treatment was not found to significantly change any other aspects of visual acuity and contrast sensitivity. All visual performance measures exhibited stability over a 9-h period. Spherical refractive error changed significantly on Day 1 but became stable after a week of treatment. These results indicate that the corneal topography changes induced by orthokeratology do not induce changes in aberrations that are large enough to significantly diminish visual performance.     

Soft contact lens extended wear affects corneal epithelial permeability: hypoxic or mechanical etiology?

Contact lens extended wear increases the permeability of epithelium to sodium fluorescein (P(dc)). The exact mechanism is not known. However, changes in P(dc) likely result from either corneal hypoxia or mechanical trauma, or both. We explored the effects of one-night continuous wear with either high- or low-Dk/t soft lenses on P(dc). The results show that corneal epithelial barrier function decreases significantly with both lens groups. We also observed that Asian eyes had higher P(dc) after overnight wear compared to non-Asian and that for both Asian and non-Asian eyes, the elimination of corneal hypoxia did not prevent changes in epithelial permeability.     

Corneal foreign body injury during overnight orthokeratology lens wear: A case report

PURPOSE: A case of asymptomatic corneal foreign body injury during orthokeratology lens wear is reported. CASE REPORT: An 8-year-old Chinese female myopic child with 21 months of overnight orthokeratology lens wear experienced a corneal foreign body injury without symptoms. The foreign body was removed and the eye treated with prophylactic antibiotic and ocular lubricant. Orthokeratology treatment was resumed 4 weeks after initial detection and management and a small residual corneal scar remained. DISCUSSION: The mechanisms, differential diagnoses, management and role of neural sensitivity in corneal foreign body injury during orthokeratology lens wear are discussed. Clinicians should be aware that subtle corneal insult may be without symptoms during prolonged overnight orthokeratology lens wear.     

BCLA CLEAR - Effect of contact lens materials and designs on the anatomy and physiology of the eye

This paper outlines changes to the ocular surface caused by contact lenses and their degree of clinical significance. Substantial research and development to improve oxygen permeability of rigid and soft contact lenses has meant that in many countries the issues caused by hypoxia to the ocular surface have largely been negated. The ability of contact lenses to change the axial growth characteristics of the globe is being utilised to help reduce the myopia pandemic and several studies and meta-analyses have shown that wearing orthokeratology lenses or soft multifocal contact lenses can reduce axial length growth (and hence myopia).However, effects on blinking, ptosis, the function of Meibomian glands, fluorescein and lissamine green staining of the conjunctiva and cornea, production of lid-parallel conjunctival folds and lid wiper epitheliopathy have received less research attention. Contact lens wear produces a subclinical inflammatory response manifested by increases in the number of dendritiform cells in the conjunctiva, cornea and limbus. Papillary conjunctivitis is also a complication of all types of contact lenses. Changes to wear schedule (daily disposable from overnight wear) or lens materials (hydrogel from SiHy) can reduce papillary conjunctivitis, but the effect of such changes on dendritic cell migration needs further study. These changes may be associated with decreased comfort but confirmatory studies are needed. Contact lenses can affect the sensitivity of the ocular surface to mechanical stimulation, but whether these changes affect comfort requires further investigation.In conclusion, there have been changes to lens materials, design and wear schedules over the past 20+ years that have improved their safety and seen the development of lenses that can reduce the myopia development. However, several changes to the ocular surface still occur and warrant further research effort in order to optimise the lens wearing experience.     

Changes in corneal thickness,corneal volume,and densitometry after long-term orthokeratology wear

PurposeTo investigate changes in the corneal volume, corneal densitometry and pachymetry of young myopes wearing over-night orthokeratology (OK) contact lenses.MethodsThe medical records of 28 right eyes of young myopes wearing OK between 2013 and 2018 were reviewed retrospectively. The baseline refractive error, best corrected visual acuities at baseline and uncorrected visual acuity at the most recent visit were recorded. Corneal volume of the central 10 mm cornea; densitometry at central, nasal and temporal cornea; and pachymetry along the horizontal and vertical meridians were collected from the Pentacam® HR at baseline, after one night of lens wear, and at the latest visit.ResultsThe mean age of subjects was 12.03 ± 3.80 years at the time of OK lens fitting and wore OK overnight for a mean duration of 666 days (range 206–1736 days). The baseline spherical equivalent refractive error was ?3.03 ± 1.56 D (range ?1.00 to ?6.00 D). The corneal volume increased significantly after OK wear (p = 0.001). Corneal densitometry increased after OK wear, but the change did not reach statistical significance (p = 0.113). Pachymetry in the central cornea did not change significantly across all visits (p > 0.05) but increased significantly in the mid-peripheral regions of the cornea. Baseline refractive error was not found to be correlated with the changes in corneal volume, corneal densitometry, or pachymetry.ConclusionThe increase in corneal volume and densitometry and no significant change in the central corneal thickness may indicate the presence of corneal oedema from long-term OK wear. The baseline refraction was not correlated with the changes in corneal volume, densitometry or pachymetry.     

Case series: Extended wear of rigid gas permeable scleral contact lenses for the treatment of persistent corneal epithelial defects

ObjectivesTo report the successful treatment of persistent corneal epithelial defects that failed to respond to alternative treatment methods using extended wear of three different rigid gas-permeable scleral lenses.MethodsEight eyes of eight patients with persistent corneal epithelial defects were treated with Blanchard Onefit 2.0 Scleral lens, BostonSight Scleral lens, and BostonSight PROSE device and were observed for defect resolution and improvement in best-corrected visual acuity over the duration of treatment.ResultsAll eyes observed complete re-epithelialization with a mean time of 11.1 ± 5.5 days. At the conclusion of the treatment, visual acuity improved in all but one patient. No complications were observed during treatment.ConclusionsScleral lenses provide the corneal epithelium with hydration, oxygen permeation, and protection from mechanical forces; thereby facilitating healing of persistent corneal epithelial defects. This case series demonstrates the successful use of continuous wear scleral lenses in a number of patients for the treatment of persistent epithelial defects refractory to other interventions.     

The time course and nature of corneal oedema during sealed miniscleral contact lens wear

PurposeTo examine the magnitude and time course of central epithelial, stromal and total corneal thickness changes during sealed miniscleral contact lens wear and the influence of initial central corneal clearance upon these thickness changes.MethodsHigh-resolution OCT images were captured over an 8 h period of miniscleral contact lens wear (using a rotationally symmetric 16.5 mm diameter lens) in 15 young, healthy participants with normal corneae. Corneal thickness data were derived from OCT images using semi-automated image processing techniques over the central 4 mm.ResultsChanges in stromal and total corneal thickness followed a similar pattern throughout lens wear with oedema first detected 15 min after lens insertion (0.47 ± 0.09% increase in stromal and total corneal thickness, both p < 0.01) which peaked after 90 min of lens wear (1.36 ± 0.24% increase in stromal and 1.18 ± 0.20% increase in total corneal thickness, both p < 0.01) and gradually decreased thereafter. Epithelial thickness increased slightly during the first 30 min of lens wear (0.56 ± 0.30% increase, p > 0.05), then rapidly decreased reaching a minimum thickness 480 min after lens insertion (2.38 ± 0.70% decrease, p < 0.05). The maximum total corneal oedema, maximum stromal oedema, and maximum epithelial thinning were not associated with the initial central corneal clearance or the extent of lens settling over the 8 h period (all p > 0.05). Greater initial central corneal clearance resulted in less oxygen concentration reaching the cornea (∼2% less) based on previously published data, which manifested as ∼0.5% more central corneal oedema.ConclusionsScleral lens induced corneal oedema is stromal in nature. On average, central stromal and total corneal thickness increased rapidly following lens insertion and peaked after 90 min, while central epithelial thickness gradually decreased throughout lens wear consistent with natural diurnal variation. A greater initial central corneal clearance resulted in reduced oxygen delivery to the cornea, which had minimal short-term impact upon healthy eyes, however, minimising central corneal clearance may be important in eyes with reduced endothelial cell function to minimise hypoxic stress.     

Applanation tonometry in silicone hydrogel contact lens wearers

INTRODUCTION: Previous studies have investigated intraocular pressure (IOP) measurements through conventional soft (hydrogel) therapeutic contact lenses, and have found that an accurate IOP can be recorded in normal eyes, and in eyes with abnormal anterior segments. The IOP measurement through soft contact lenses may be affected by the water content and centre thickness of the lens. Silicone hydrogel contact lenses are now being used as therapeutic contact lenses due to their high oxygen permeability. The purpose of this study is to investigate if IOP can be accurately measured in a subject wearing a silicone hydrogel contact lens. METHODS: In a cohort study, the IOP was measured with a Goldmann applanation tonometer without a contact lens and then repeated with a hydrogel contact lens in situ. RESULTS: The IOP of 20 eyes of 10 volunteers with no ocular pathology was measured. The mean difference (+/-S.D.) found between IOP measurement with (mean 15.55+/-1.70 mmHg) and without (mean 16.05+/-1.90 mmHg) contact lens was found to be -0.5+/-0.89 mmHg. Statistical analysis was performed which revealed a correlation coefficient of 0.89. No significant statistical difference was found between the two groups with paired t-test (p=0.19). CONCLUSION: Accurate measurement of IOP by applanation tonometry can be achieved through a silicone hydrogel contact lens.     

Parameter stability of soft contact lenses made from different materials.

The parameters of soft contact lenses may alter during wear. A series of clinical and laboratory experiments were conducted in order to examine the parameter stability of eight soft contact lenses manufactured from different materials. The following materials (and nominal water contents) were used: HEMA/VP 40%, HEMA/VP 55%, HEMA/VP 70%, VP/MMA 55%, VP/MMA 70%, HEMA 40%, HEMA/MAA 55% and HEMA/MAA 70% (HEMA: 2-hydroxy-ethyl methacrylate, VP: vinyl pyrrolidone, MMA: methyl methacrylate, MAA: methacrylic acid). Two lenses from each of the eight soft contact lens groups were used in experiments concerning the parameter stability. Six subjects were fitted with lenses for 1 day. Verification of back optic zone radius, total diameter, back vertex power, centre thickness and water content was undertaken at 20 degrees C. In vitro measurements of water content, oxygen transmissibility, total diameter and back optic zone radius were taken at 35 degrees C before lens fitting and after 6h of lens wear. Distortion, discolouration and lens quality were assessed before and after lens wear. When the temperature was raised from 20 to 35 degrees C, a significant reduction in lens water content for all the lens types was observed, as well as a significant reduction in total lens diameter for the majority of the lens types. Water content, oxygen transmissibility, total diameter and back optic zone radius of all the lens types reduced, following a 6h open eye wearing period. For the majority of the lens types, these changes were found to be statistically significant. Distortion, discolouration and quality of the lenses remained unchanged throughout the study with the exception of the HEMA/MAA 70% lens. Correlating a number of parameters generated in this study, gave the following conclusions. High water content materials exhibit a low relative change in oxygen transmissibility following a 6h wear period. Soft contact lens dehydration leads to a decrease in oxygen transmissibility and total diameter, following a 6h wear period. These results will assist practitioners in predicting the alterations that occur in soft contact lens parameters and oxygen performance as a result of lens wear.     

Efficacy of continuous wear PureVision contact lenses for therapeutic use.

PURPOSE: To evaluate the Bausch and Lomb PureVision contact lens as continuous wear contact lens for therapeutic and medical indications in a prospective open-ended non-randomized trial. METHODS: Patients who required therapeutic contact lens wear for various indications such as pain relief, corneal protection, persistent epithelial defects, corneal perforation and chemical burns were fitted with PureVision continuous wear contact lenses (balafilcon A, 36% water content). Success or failure of specific treatment indication was assessed in each case with evaluation of ocular and lens related complications. RESULTS: 30 eyes of 28 patients were fitted with PureVision continuous wear contact lenses. A successful fit was seen in 27 of 30 eyes with therapeutic success in 26 of 30 eyes. However, all patients reported symptomatic relief. Duration of lens use ranged from 3 days to 3 months. Dry eye was the most frequent cause of contact lens associated therapeutic failure. Complications included lens loss (two eyes), tight lens (one eye) and infective keratitis (two eyes). CONCLUSIONS: PureVision contact lenses were found to be safe and efficacious for continuous wear therapeutic use to a maximum of 90 days. The contact lens was also easier to handle by virtue of its resilient nature. There were no significant corneal complications of hypoxia, i.e. corneal oedema. Lens losses and deposits were minimal. The lens performance and fitting characteristics compares favorably with previous therapeutic lenses used by the investigators. This new lens may be considered as a safe and effective alternative for use as bandage contact lens.     

Orthokeratology for slowing myopic progression in a pair of identical twins

PurposeTo compare the axial length elongation and change in refractive errors in a pair of identical twins wearing orthokeratology (ortho-k) and single vision lenses (SVLs), respectively.Case reportIdentical Twin A and B, who were 8 years of age, with the same amount of near activities, were assigned to wear ortho-k and SVLs randomly and they were monitored for two years for myopic progression. Twin A and B were assigned to wear ortho-k and SVLs, respectively. Myopic progression was evaluated by the change in axial length and in refractive errors. A faster axial length elongation was observed in each eye of Twin B during the two-year study period. The overall change in axial length was 0.52 mm (OD) and 0.70 (OS) in Twin A and 0.77 mm (OD) and 0.82 mm (OS) in Twin B. In terms of cycloplegic refractive errors (SER), one month after ceasing lens wear (after completion of the two-year study), the increase (from baseline) were 11% (OD) and 48% (OS) in Twin A and 87% (OD) and 67% (OS) in Twin B.ConclusionsOrtho-k is more effective in controlling myopic progression in terms of axial elongation than wearing SVLs in this pair of identical twins.     

The 75th anniversary of the Tuohy corneal contact lens: A review

The aim of this review is to mark the 75th anniversary of the introduction of the original corneal contact lens of Tuohy in 1948.American documents in the public domain, such as census records and draft registration cards, were consulted in order to provide a more comprehensive biography of Kevin M Tuohy, inventor of the corneal contact lens, than those previously published.Perhaps due to a failure to consult original sources concerning the Tuohy corneal lens, some historical accounts have provided incomplete or incorrect information about its design and dimensions. The back surface specification of the bi-curve Tuohy lens in its standard diameter of 11.50 mm has been tabulated and edge lift and edge clearance values calculated. A colour photograph illustrates the fluorescein pattern of a Tuohy lens.Patients wearing Tuohy lenses were able to achieve a much longer wearing time compared to those wearing sealed scleral lenses since they eliminated corneal epithelial oedema, a frequent problem which necessitated removal of lenses after a few hours of wear due to cloudy vision. Only some of Tuohy lens wearers exhibited an adverse corneal response such as fluorescein staining after 12, or more, hours of wear.The clinical success of the Tuohy lens and the fact that its fitting procedure was simpler and quicker than that for scleral lenses encouraged optometrists to commence contact lens practice and to implement improvements in the design of the corneal lens.