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.     

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.     

Predicting success with silicone-hydrogel contact lenses in new wearers

Purposeto evaluate changes in tear metrics and ocular signs induced by six months of silicone-hydrogel contact lens wear and the difference in baseline characteristics between those who successfully continued in contact lens wear compared to those that did not.MethodsNon-invasive Keratograph, Tearscope and fluorescein tear break-up times (TBUTs), tear meniscus height, bulbar and limbal hyperaemia, lid-parallel conjunctival folds (LIPCOF), phenol red thread, fluorescein and lissamine-green staining, and lid wiper epitheliopathy were measured on 60 new contact lens wearers fitted with monthly silicone-hydrogels (average age 36 ± 14 years, 40 females). Symptoms were evaluated by the Ocular Surface Disease Index (OSDI). After six months full time contact lens wear the above metrics were re-measured on those patients still in contact lens wear (n = 33). The initial measurements were also compared between the group still wearing lenses after six months and those who had ceased lens wear (n = 27).ResultsThere were significant changes in tear meniscus height (p = 0.031), bulbar hyperaemia (p = 0.011), fluorescein TBUT (p = 0.027), corneal (p = 0.007) and conjunctival (p = 0.009) staining, LIPCOF (p = 0.011) and lid wiper epitheliopathy (p = 0.002) after six months of silicone-hydrogel wear. Successful wearers had a higher non-invasive (17.0 ± 8.2 s vs 12.0 ± 5.6 s; p = 0.001) and fluorescein (10.7 ± 6.4 s vs 7.5 ± 4.7 s; p = 0.001) TBUT than drop-outs, although OSDI (cut-off 4.2) was also a strong predictor of success.ConclusionSilicone-hydrogel lenses induced significant changes in the tear film and ocular surface as well as lid margin staining. Wettability of the ocular surface is the main factor affecting contact lens drop-out.     

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.     

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.     

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.     

Comparison of corneal hysteresis and corneal resistance factor after small incision lenticule extraction and femtosecond laser-assisted LASIK: A prospective fellow eye study

PurposeTo compare corneal hysteresis (CH) and corneal resistance factor (CRF) between eyes treated with small incision lenticule extraction (SMILE) and femtosecond laser-assisted laser in situ keratomileusis (femto-LASIK).SettingBeyoğlu Eye Training and Research Hospital.DesignProspective comparative case series.MethodsSixty eyes from 30 patients with bilateral myopia or myopic astigmatism were studied. Inclusion criteria were spherical equivalent of subjective manifest refraction (SE) <10 diopters (D) and a difference ≤0.50 D between the SEs of both eyes. One eye of each patient was treated with SMILE, and the fellow eye underwent femto-LASIK. Randomization was performed using a sealed envelope system. The main outcome measures were CH and CRF measured preoperatively and postoperatively (1 and 6 months).ResultsPreoperative SE was similar in both groups (p = 0.852). CH and CRF values were reduced postoperatively in both groups compared to their corresponding preoperative values (p < 0.001). At the 6-month follow-up visit, the mean CH values in the SMILE and femto-LASIK groups were 8.95 ± 1.47 and 9.02 ± 1.27, respectively (p = 0.852), and the mean CRF values were 7.77 ± 1.37 and 8.07 ± 1.26, respectively (p = 0.380).ConclusionCH and CRF decreased after SMILE. There were no differences between SMILE and femto-LASIK treatments in postoperative CH or CRF values.     

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

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

Conjunctival UV autofluorescence – Prevalence and risk factors

PurposeAutofluorescence of ultraviolet (UV) light has been shown to occur in localised areas of the bulbar conjunctiva, which map to active cellular changes due to UV and environmental exposure. This study examined the presence of conjunctival UV autofluorescence in eye care practitioners (ECPs) across Europe and the Middle East and its associated risk factors.MethodImages were captured of 307 ECPs right eyes in the Czech Republic, Germany, Greece, Kuwait, Netherlands, Sweden, Switzerland, United Arab Emirates and the United Kingdom using a Nikon D100 camera and dual flash units through UV filters. UV autofluorescence was outlined using ImageJ software and the nasal and temporal area quantified. Subjects were required to complete a questionnaire on their demographics and lifestyle including general exposure to UV and refractive correction.ResultsAverage age of the subjects was 38.5 ± 12.2 years (range 19–68) and 39.7% were male. Sixty-two percent of eyes had some conjunctival damage as indicated by UV autofluorescence. The average area of damage was higher (p = 0.005) nasally (2.95 ± 4.52 mm²) than temporally (2.19 ± 4.17 mm²). The area of UV damage was not related to age (r = 0.03, p = 0.674), gender (p = 0.194), self-reported sun exposure lifestyle (p > 0.05), geographical location (p = 0174), sunglasses use (p > 0.05) or UV-blocking contact lens use (p > 0.05), although it was higher in those wearing contact lenses with minimal UV-blocking and no spectacles (p = 0.015). The area of UV damage was also less nasally in those who wore contact lenses and spectacles compared to those with no refractive correction use (p = 0.011 nasal; p = 0.958 temporal).ConclusionUV conjunctival damage is common even in Europe, Kuwait and UAE, and among ECPs. The area of damage appears to be linked with the use of refractive correction, with greater damage nasally than temporally which may be explained by the peripheral light focusing effect.     

Corneal changes following short-term miniscleral contact lens wear

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

Comparison of visual acuity and higher-order aberrations after femtosecond lenticule extraction and small-incision lenticule extraction

PurposeTo compare postoperative visual acuity and higher-order aberrations (HOAs) after femtosecond lenticule extraction (FLEX) and after small-incision lenticule extraction (SMILE).MethodsMedical records of refractive lenticule extraction patients were retrospectively reviewed. Twenty patients were treated with FLEX. A comparable group of 20 SMILE patients were retrospectively identified. Only one eye of each patient was randomly chosen for the study. Visual acuity, subjective manifest refraction and corneal topography before and 6 months after the surgery were analyzed for both groups. Total HOAs, spherical aberrations, coma and trefoil were calculated from topography data over the 4- and 6-mm-diameter central corneal zone.ResultsThe mean preoperative SE was −4.03 ± 1.61 in the SMILE group and −4.46 ± 1.61 in the FLEX group. One year after surgery, the mean SE was −0.33 ± 0.25 in the SMILE group and −0.31 ± 0.41 in the FLEX group (p = 0.86). In the SMILE group a greater number of eyes were within ±0.50 D of the target refraction (95% versus 75%); however, the difference was not statistically significant (p = 0.18). Furthermore, 80% of FLEX eyes and 95% of SMILE eyes had an uncorrected distance visual acuity of 20/25 or better (p = 0.34). Total HOAs, spherical aberration, coma and trefoil increased postoperatively in both groups. However, there was no statistically significant difference between the groups preoperatively and postoperatively.ConclusionFLEX and SMILE result in comparable refractive results. In addition, corneal aberrations induced by different techniques of lenticule extraction seemed similar to each other.     

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 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.     

Evaluating the effect of splitting cylindrical power on improving patient tolerance to toric lens misalignment

PurposeEvaluating the impact of splitting toric power on patient tolerance to misorientation such as with intraocular lens rotation.SettingUniversity vision clinic.MethodsHealthy, non astigmats had +1.50D astigmatism induced with spectacle lenses at 90°, 135°, 180° and +3.00D at 90°. Two correcting cylindrical lenses of the opposite sign and half the power each were subsequently added to the trial frame misaligned by 0°, 5° or 10° in a random order and misorientated from the initial axis in a clockwise direction by up to 15° in 5° steps. A second group of adapted astigmats with between 1.00 and 3.00DC had their astigmatism corrected with two toric spectacle lenses of half the power separated by 0°, 5° or 10° and misorientated from the initial axis in both directions by up to 15° in 5° steps. Distance, high contrast visual acuity was measured using a computerised test chart at each lens misalignment and misorientation.ResultsMisorientation of the split toric lenses caused a statistically significant drop in visual acuity (F = 70.341; p < 0.001). Comparatively better acuities were observed around 180°, as anticipated (F = 3.775; p = 0.035). Misaligning the split toric power produced no benefit in visual acuity retention with axis misorientation when subjects had astigmatism induced with a low (F = 2.190, p = 0.129) or high cylinder (F = 0.491, p = 0.617) or in the adapted astigmats (F = 0.120, p = 0.887).ConclusionMisalignment of toric lens power split across the front and back lens surfaces had no beneficial effect on distance visual acuity, but also no negative effect.     

Long term results of Epi-LASIK and LASEK for myopia

PurposeTo evaluate the long term clinical and confocal results of mechanical (Epi-LASIK) versus alcohol-assisted laser epithelial keratomileusis (LASEK) for correction of myopia.SettingGazi University Medical School, Department of Ophthalmology, Ankara, Turkey.DesignRetrospective study.MethodsTwenty-two eyes treated with LASEK and twenty eyes treated with Epi-LASIK were evaluated with a mean follow-up duration of 45 months. Mechanical separation of the epithelium was performed with Lasitome epithelial separator, and alcohol-assisted separation with 25 s application of 18% alcohol. Laser ablation was performed with the ESIRIS laser. All patients were examined daily until epithelial closure; at 1, 3, 6, and 12 months; and every year subsequently. Main outcome measures were uncorrected visual acuity (UCVA), manifest refraction, haze, and gray scale value in confocal microscopy, efficacy and safety indexes.ResultsPreoperative myopic spherical equivalent refraction was −4.65 ± 1.74 D in the LASEK and −3.87 ± 1.30 D in the Epi-LASIK-treated eyes (p = 0.36). Of both LASEK and Epi-LASIK-treated eyes, 95% achieved 20/25 or better final UCVA. The grade of haze and mean gray scale value in confocal microscopy were similar in LASEK and Epi-LASIK-treated eyes at all postoperative periods. The efficacy index was 0.94 in LASEK group and 0.96 in Epi-LASIK group (p = 0.44). The safety index was 1.01 in LASEK group and 1.02 in Epi-LASIK group (p = 0.42).ConclusionsBoth LASEK and Epi-LASIK offer safe and effective correction of myopia in the long term.     

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.     

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.     

Phenolic profile and antioxidant activity of the Algerian ripe date palm fruit (Phoenix dactylifera)

The aim of this study was to determine the phenolic profile of seven different varieties of ripe date palm fruit (Phoenix dactylifera) from Algeria by LC–DAD–MS (ESI+), to investigate their respective antioxidant activities by the DPPH^· method and to estimate their phenolic content using the Folin–Ciocalteu method. The total phenolic content was in the range of 2.49 ± 0.01 to 8.36 ± 0.60 mg gallic acid equivalents (GAE) per 100 g fresh fruit. This fruit was shown to possess an antioxidant activity, giving values of antiradical efficient (AE) from 0.08 ± 0.00 to 0.22 ± 0.00. The phenolic contents and the antiradical efficiencies of the different varieties were highly correlated (R²=0.975). All the varieties were found to contain mainly p-coumaric, ferulic and sinapic acids and some cinnamic acid derivatives. Three different isomers of 5-o-caffeoylshikimic acid were detected. Different types of flavonoids were identified, mainly flavones, flavanones and flavonol glycosides.     

Overnight orthokeratology with two brands of reverse-geometry contact lenses

PurposeTo evaluate the refractive and corneal topographical changes of overnight orthokeratology in myopia with two brands of contact lenses.MethodsFourty-four eyes of 22 myopic patients with manifest refraction spherical equivalent (MRSE) of −1.00 to −5.00 D (cylinder ≤ −1.0) were fitted with either DreamLens (Hanita Lenses Investments, Hanita, Israel) (group A) or Rinehart–Reeves (R&R; Danker Laboratories, Sarasota, FL) (group B) reverse-geometry lenses. Each subject eye was evaluated in regards to the uncorrected and corrected distance visual acuities, manifest refraction, slit lamp biomicroscopy, and corneal topography at each follow-up examination.ResultsThe follow-up was 1 year. For groups A and B, the mean uncorrected distance visual acuity was −0.02 ± 0.10 log MAR (20/20) and −0.08 ± 0.12 log MAR (20/20) respectively at year-1 examination. The mean MRSE decreased from −2.70 ± 0.9 D to −0.50 ± 0.08 D in group A and −3.1 ± 1.1 to −0.62 ± 0.18 D in group B at week-1; and remained stable thereafter in each group. For both groups, starting with week-1, the mean anterior best-fit sphere (ABFS) was statistically significantly flatter from baseline. A high correlation was found between the change in apical corneal power (ACP) and MRSE (r₁ = 0.79, r₂ = 0.71), and there was a good correlation between the change in ABFS and MRSE (r₁ = 0.67, r₂ = 0.64) in both groups. No significant ocular adverse events were observed during study.ConclusionsBoth types of contact lenses safely and effectively decreased the myopic refractive error at 1 year follow-up. The refractive effect was mainly induced by the changes in the anterior corneal shape and the ACP.