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ABSTRACT: PURPOSE: To develop a new schematic scheme for efficiently recording the key parameters of gas permeable contact lens (GP) fits based on current consensus. METHODS: Over 100 established GP fitters and educators met to discuss the parameters proposed in educational material for evaluating GP fit and concluded on the key parameters that should be recorded. The accuracy and variability of evaluating the fluorescein pattern of GP fit was determined by having 35 experienced contact lens practitioners from across the world, grading 5 images of a range of fits and the topographer simulation of the same fits, in random, order using the proposed scheme. The accuracy of the grading was compared to objective image analysis of the fluorescein intensity of the same images. RESULTS: The key information to record to adequately describe the fit of an GP was agreed as: the manufacturer, brand and lens parameters; settling time; comfort on a 5 point scale; centration; movement on blink on a ±2 scale; and the Primary Fluorescein Pattern in the central, mid-peripheral and edge regions of the lens averaged along the horizontal and vertical lens axes, on a ±2 scale. On average 50-60% of practitioners selected the median grade when subjectively rating fluorescein intensity and this was correlated to objective quantification (r=0.602, p<0.001). Objective grading suggesting horizontal median fluorescein intensity was generally symmetrical, as was the vertical meridian, but this was not the case for subjective grading. Simulated fluorescein patterns were subjectively and objectively graded as being less intense than real photographs (p<0.01). CONCLUSION: GP fit recording can be standardised and simplified to enhance GP practice.
Contact lens & anterior eye: the journal of the British Contact Lens Association 03/2013;
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ABSTRACT: BackgroundThe repeatability and interchangeability of imaging devices measuring central corneal thickness (CCT) and anterior chamber
depth (ACD) are important in the assessment of patients considering refractive surgery. The purpose of this study was to investigate
the agreement of CCT and ACD measurements using three imaging technologies in healthy eyes and in eyes after phakic intraocular
lens implantation (pIOL).
MethodsIn this comparative study, CCT and ACD were measured using anterior segment optical coherence tomography (AS-OCT), Orbscan
II, and Pentacam in 33 healthy volunteers (66 eyes) and 22 patients (42 eyes) after pIOL implantation. Intraobserver repeatability
was evaluated for all three devices in the healthy volunteer group.
ResultsPairwise comparison of CCT measurements showed significant differences between all devices (P < 0.001), except for the AS-OCT and Orbscan II in the healthy volunteer group (P = 0.422) and the Orbscan II and Pentacam in the pIOL group (P = 0.214). ACD measurements demonstrated significant differences between all pairwise comparisons in both groups (P ≤ 0.001). Intraobserver reliability was high for CCT and ACD measurements in the healthy volunteer group, with coefficients
of variation ranging from 0.6% to 1.2% and 0.4% to 0.5% respectively.
ConclusionsCCT and ACD measurements using AS-OCT, Orbscan II, and Pentacam demonstrated high intraobserver reliability. However, these
devices should not be used interchangeably for measurements of CCT and ACD in healthy subject and patients after pIOL implantation.
Albrecht von Graæes Archiv für Ophthalmologie 04/2012; 247(8):1139-1146. · 2.17 Impact Factor
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ABSTRACT: Raman spectroscopy holds potential for the assessment of intraocular pharmacokinetics. Raman spectra of ocular drugs were acquired, to determine the drug-specific Raman signature. The ability of the Raman technique to quantify drug concentrations was also investigated.
The experimental setup was based on a High Performance Raman Module 2500 Raman module, designed for 180° "backscatter" signal detection in the wavenumber range of 400-1,800 cm(-1). Excitation source was a diode laser emitting a beam with a wavelength of 785 nm and a power of 10 mW. Laser light was focused in the sample with a long-working-distance microscope objective (25×/0.50). Samples were measured in quartz cuvettes in 10 sequential measurements, with exposure time 30 s. The total number of measured drugs was 49. To determine whether signal intensity and drug concentration correlate, 2 drugs were diluted in water and measured with 120 s exposure time at different concentrations.
An active ingredient-specific Raman signature was detected in 4 glaucoma drugs, 6 mydriatics, 5 antibiotics, 4 anesthetics, 3 anti-inflammatory drugs, 2 types of artificial tears, and 5 other drugs. In 20 drugs, no specific Raman signature was detected. Linear correlation of drug concentration with signal intensity was high (R(2)≥0.94).
Using low laser powers, Raman signatures for 29 commonly used ocular drugs were detected. Correlation of drug concentration with signal intensity is high, which is essential for monitoring drug concentration in ocular media. The presented results encourage the use of Raman spectroscopy to acquire detailed information on the pharmacokinetics of these ocular drugs.
Journal of ocular pharmacology and therapeutics: the official journal of the Association for Ocular Pharmacology and Therapeutics 07/2011; 27(5):445-51. · 1.46 Impact Factor
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ABSTRACT: To analyze the symptoms, etiology, and treatment of patient dissatisfaction after multifocal intraocular lens (IOL) implantation.
Department of Ophthalmology, Maastricht University Medical Center, The Netherlands.
Case series.
In this retrospective chart review, the main outcome measures were type of complaints, uncorrected and corrected distance visual acuities, uncorrected and distance-corrected near visual acuities, refractive state, pupil diameter and wavefront aberrometry measurements, and type of treatment.
Seventy-six eyes of 49 patients were included. Blurred vision (with or without photic phenomenon) was reported in 72 eyes (94.7%) and photic phenomena (with or without blurred vision) in 29 eyes (38.2%). Both symptoms were present in 25 eyes (32.9%). Residual ametropia and astigmatism, posterior capsule opacification, and a large pupil were the 3 most significant etiologies. Sixty-four eyes (84.2%) were amenable to therapy, with refractive surgery, spectacles, and laser capsulotomy the most frequent treatment modalities. Intraocular lens exchange was performed in 3 cases (4.0%).
The cause of dissatisfaction after implantation of a multifocal IOL can be identified and effective treatment measures taken in most cases.
Journal of cataract and refractive surgery 03/2011; 37(5):859-65. · 2.75 Impact Factor
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ABSTRACT: To evaluate visual outcomes and patient satisfaction after implantation of an aspheric apodized diffractive intraocular lens (IOL) or a spherical apodized diffractive IOL in cataract surgery.
Maastricht University Medical Center, The Netherlands.
Nonrandomized clinical trial.
This prospective nonrandomized study with a 6-month follow-up compared the results of cataract surgery with implantation of an aspheric AcrySof ReSTOR SN6AD3 IOL and a spherical AcrySof ReSTOR SN60D3 IOL. Main outcome measures were uncorrected (UDVA) and corrected (CDVA) distance visual acuities, uncorrected (UNVA) and distance-corrected (DCNVA) near visual acuities, straylight levels, incidence of glare and halos, and contrast sensitivity levels.
The mean UDVA was 0.14 ± 0.15 logMAR in the aspheric group (47 eyes) and 0.14 logMAR ± 0.17 (SD) in the spherical group (45 eyes) and the mean CDVA, -0.01 ± 0.06 logMAR and 0.02 ± 0.10 logMAR, respectively. The mean UNVA was Jaeger (J) 1 in 83.0% of patients in the aspheric group and 55.5% of patients in the spherical IOL group (P = .003). The DCNVA was J1 in 95.7% and 71.1%, respectively (P = .001). There were no significant differences between the 2 groups in contrast sensitivity levels, intraocular straylight levels, incidence of night-vision symptoms, or subjective rating of vision.
Patients with the aspheric multifocal IOL had significantly better near vision than patients with the multifocal spherical IOL. The UDVA, CDVA, intraocular straylight, night-vision symptoms, and contrast sensitivity were similar between the 2 groups.
Journal of cataract and refractive surgery 11/2010; 36(11):1897-904. · 2.75 Impact Factor
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ABSTRACT: To compare total ocular aberrations and corneal aberrations identified with four different aberrometers and to determine the repeatability and interobserver variability.
In this prospective comparative study, 23 healthy subjects underwent bilateral examination with four aberrometers: the Irx3 (Hartmann-Shack; Imagine Eyes, Orsay, France), Keratron (Hartmann-Shack; Optikon, Rome Italy), iTrace (ray-tracing; Tracey Technologies, Houston, TX), and OPD-Scan (Automated Retinoscopy; Nidek, Gamagori, Japan). Six images per eye were obtained. Second-, third- and fourth-order spherical aberrations were exported for 5.0-mm pupils.
Significant differences in measurements were found for several total ocular aberrations (defocus [2,0], astigmatism [2,2], trefoil [3,-3], trefoil [3,3], and spherical aberration [4,0]) and corneal aberrations (defocus [2,0] and astigmatism [2,2]). The Irx3 showed the highest repeatability in measuring total ocular aberrations, followed by the Keratron, OPD-Scan, and iTrace. The repeatability of the corneal aberration measurements was highest for the iTrace, followed by the Keratron and OPD-Scan. The OPD-Scan showed a lower interobserver variability, compared with the Irx3, Keratron, and iTrace.
Total ocular and corneal aberrations are not comparable when measured with different aberrometers. Hartmann-Shack aberrometers showed the best repeatability for total ocular aberrations and iTrace for corneal aberrations. It would be worthwhile in the future to evaluate aberrometers in patients with more aberrant eyes.
Investigative ophthalmology & visual science 11/2010; 52(3):1302-11. · 3.43 Impact Factor
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ABSTRACT: To study the reproducibility and variability of iridocorneal angle (ICA) measurements by using anterior segment optical coherence tomography (AS-OCT) by expert and nonexpert observers.
Twenty-three healthy volunteers (nonexperts with a basic knowledge of ophthalmology) acquired five consecutive AS-OCT images in the enhanced anterior segment single mode in the 180° to 0° meridian of the right eyes of their peers. Two experts and the 23 nonexperts analyzed the images. The ICA software tool was used to determine the angle opening distance (AOD) and the trabecular iris surface area (TISA) at 500 and 750 μm. A random intercept model was fitted to evaluate the variability of acquiring an image. For both the experts and the nonexperts, inter- and intraobserver variability of analyzing an AS-OCT image was determined with the coefficient of variation (CV). Reproducibility was qualified by using the intraclass correlation coefficient (ICC).
There was no statistically significant difference in the variability of acquiring an image. The range of intraobserver variability in image analysis was from 9.4% to 12.5% in the experts and from 4.2% to 17.4% in the nonexperts. Interobserver variability was 10.7% in the experts and 10.2% in the nonexperts. The reproducibility was high, 0.875 and 0.942 in the experts and 0.906 in the nonexperts.
The overall reproducibility of the ICA measurements with the AS-OCT is good in open angles. Inter- and intraobserver variability showed similar mean values of reproducibility between the experts and nonexperts. The wide range of intraobserver variation in the nonexperts suggests that this group should undergo extensive instruction before routinely analyzing AS-OCT images.
Investigative ophthalmology & visual science 09/2010; 52(5):2095-9. · 3.43 Impact Factor
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ABSTRACT: Anterior segment optical coherence tomography (AS-OCT) is an important new noncontact imaging technology that uses a 1310 nm super luminescent diode. It can be used to assess anterior chamber biometry, corneal thickness, lens thickness, and angle configuration; to visualize pathological processes; to evaluate postsurgical anatomy and posttraumatic eyes; and to image phakic intraocular lenses and intracorneal ring segments. Because it is a noncontact technique, it can also be used intraoperatively, which could be useful during trabeculectomy and after deep anterior lamellar keratoplasty to detect abnormalities in the cornea and interface. A disadvantage of AS-OCT is its inability to penetrate the iris pigment epithelium, which makes it impossible to evaluate the structures behind the iris. The most frequently used devices are time-domain AS-OCT, but new Fourier-domain OCT devices, which have faster image acquisition and higher resolution, are currently under investigation. FINANCIAL DISCLOSURE: No author has a financial or proprietary interest in any material or method mentioned.
Journal of cataract and refractive surgery 07/2010; 36(7):1213-29. · 2.75 Impact Factor
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ABSTRACT: Evaluation of the reproducibility of the Lenstar LS 900 non-contact biometer, and a comparison with the Visante anterior-segment optical coherence tomography (AS-OCT) and the IOLMaster.
Central corneal thickness (CCT), anterior chamber depth (ACD), lens thickness (LT), keratometry (K) values, corneal diameter (CD) and axial length (AL) were obtained in 38 healthy volunteers (76 eyes) to determine the reproducibility of the Lenstar. CCT, ACD, CD, K values and AL measurements measured with the Lenstar were compared with the AS-OCT and IOLMaster. Intraocular lens (IOL) power calculations were done to study the significance of the difference between AL measurements.
The reproducibility of the Lenstar was better than 0.9% for CCT, ACD, LT, K values and AL measurements. Although all correlations were highly significant (p<0.001), all comparisons showed a significant difference, except for the comparison of CD measurements using the Lenstar and IOLMaster (p = 0.175). The differences in IOL power calculations for an AL of 20, 25 and 30 mm with a mean difference between Lenstar and IOLMaster AL measurements of 0.03 mm, were 0.13 D, 0.10 D and 0.08 D, respectively.
The reproducibility of the Lenstar was excellent. Small but significant differences exist between the Lenstar, Visante OCT and the IOLMaster. Therefore, measurements of the Lenstar, AS-OCT and IOLMaster are not interchangeable. Despite the significant difference between AL measurements, there is no clinically significant difference in the IOL power calculation results.
The British journal of ophthalmology 08/2009; 94(1):106-10. · 2.92 Impact Factor
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ABSTRACT: To elucidate the physiological characteristics of eyes implanted with iris-fixated anterior chamber phakic intraocular lenses (pIOLs), which are increasingly being used for the correction of higher myopic and hyperopic refractive errors.
In a case series of 20 patients (39 eyes), the position of the pIOL to the natural lens and the cornea was evaluated under photopic (135 lux) and low mesopic (< 1 lux) circumstances with anterior segment optical coherence tomography.
The distance between the pIOL and the natural lens decreased, and congruently, the distance from the pIOL to the corneal endothelium increased under low mesopic circumstances.
The distance between the pIOL and the corneal endothelium increases when the pupil dilates under dark circumstances, contributing to the already excellent safety data available on pIOL implantation.
Journal of refractive surgery (Thorofare, N.J.: 1995) 04/2009; 25(4):394-6. · 2.54 Impact Factor
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Albrecht von Graæes Archiv für Ophthalmologie 04/2009; · 2.17 Impact Factor
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ABSTRACT: Purpose: Refractive error (RE) is suggested to cause not only visual impairment, but also functional problems such as aspecific health complaints and lower levels of school achievement. During the last few decades the prevalence of myopia has increased worldwide, especially in Asia. We investigated the prevalence of habitual RE and anisometropia in a Dutch population of children and employees.Methods: In a cross-sectional study, RE in both eyes of 520 children (aged 11–13 years) and 444 hospital employees (aged 17–60 years) were measured using an autorefractometer. The measurements were performed without using a cycloplegium. Pearson’s correlation coefficient (r) was used to analyse correlations between the right and left eyes. Chi-square tests were used to test the differences between subgroups according to gender and age.Results: In schoolchildren 28% of right eyes were myopic (> 0.50 D) and 8% hyperopic (> 0.50 D). Pearson’s r between right and left eyes for spherical equivalent power (SEP) was 0.93. The mean cylinder deviation in right eyes was 0.26 D (range 0.00–4.50 D). Anisometropia > 1.00 D was present in 4.6% of children; 22% of children were not optimally (> 0.50 D) corrected. In hospital employees, 30% of right eyes were myopic (> 0.50 D) and 10% hyperopic (> 0.50 D). Pearson’s r between right and left eyes for SEP was 0.53. The mean cylinder deviation in right eyes was 0.35 D (range 0.00–5.75 D). Anisometropia > 1.00 D was present in 25% of employees. Anisometropia was more frequently present in employees aged 40–60 years, than in those aged 17–39 years (30% versus 18%; p = 0.02, Cramer’s V = 0.15).Conclusions: Refractive errors are common in children aged 11–13 years and in working adults aged 17–60 years. Distributions of sphere and cylinder deviations are similar for Dutch schoolchildren and hospital employees. Surprisingly, anisometropia proved to be more prevalent with age. In children many eyes are not optimally corrected. Increased attention should be paid to uncorrected and miscorrected REs.
Acta ophthalmologica 03/2009; 87(5):538 - 543. · 2.44 Impact Factor
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ABSTRACT: Refractive error (RE) is suggested to cause not only visual impairment, but also functional problems such as aspecific health complaints and lower levels of school achievement. During the last few decades the prevalence of myopia has increased worldwide, especially in Asia. We investigated the prevalence of habitual RE and anisometropia in a Dutch population of children and employees.
In a cross-sectional study, RE in both eyes of 520 children (aged 11-13 years) and 444 hospital employees (aged 17-60 years) were measured using an autorefractometer. The measurements were performed without using a cycloplegium. Pearson's correlation coefficient (r) was used to analyse correlations between the right and left eyes. Chi-square tests were used to test the differences between subgroups according to gender and age.
In schoolchildren 28% of right eyes were myopic (> 0.50 D) and 8% hyperopic (> 0.50 D). Pearson's r between right and left eyes for spherical equivalent power (SEP) was 0.93. The mean cylinder deviation in right eyes was 0.26 D (range 0.00-4.50 D). Anisometropia > 1.00 D was present in 4.6% of children; 22% of children were not optimally (> 0.50 D) corrected. In hospital employees, 30% of right eyes were myopic (> 0.50 D) and 10% hyperopic (> 0.50 D). Pearson's r between right and left eyes for SEP was 0.53. The mean cylinder deviation in right eyes was 0.35 D (range 0.00-5.75 D). Anisometropia > 1.00 D was present in 25% of employees. Anisometropia was more frequently present in employees aged 40-60 years, than in those aged 17-39 years (30% versus 18%; p = 0.02, Cramer's V = 0.15).
Refractive errors are common in children aged 11-13 years and in working adults aged 17-60 years. Distributions of sphere and cylinder deviations are similar for Dutch schoolchildren and hospital employees. Surprisingly, anisometropia proved to be more prevalent with age. In children many eyes are not optimally corrected. Increased attention should be paid to uncorrected and miscorrected REs.
Acta ophthalmologica 03/2009; 87(5):538-43. · 2.44 Impact Factor
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ABSTRACT: This study evaluates the relationship between bulbar hyperemia, conjunctival staining, lens comfort and 3- and 9-o'clock corneal staining in rigid gas permeable (GP) contact lens wear.
The study involved 55 GP contact lens wearers (with and without 3- and 9-o'clock staining) and 26 non-lens wearers. Corneal staining was graded based on a specially designed image grading scale developed at the University of Maastricht. The Efron grading scale was used to grade bulbar hyperemia and conjunctival staining. Ocular comfort and lens comfort were analyzed using a visual analogue scale (VAS) and a questionnaire to differentiate symptomatic from asymptomatic subjects.
Bulbar hyperemia showed a significant but low correlation with corneal staining, and eyes with conjunctival staining showed more corneal staining than eyes without conjunctival staining. No correlation was found between staining in the nasal and temporal regions of the cornea in subjects with substantial 3- and 9-o'clock staining. No correlation was found between VAS comfort scores and corneal staining. In those subjects with substantial 3- and 9-o'clock staining, symptomatic subjects showed more corneal staining than asymptomatic subjects.
Practitioners are advised to evaluate both the nasal and temporal regions of the cornea when assessing 3- and 9-o'clock staining, and they should be hesitant to rely on the amount of bulbar hyperemia for the prediction of the severity of 3- and 9-o'clock staining. Assessment of conjunctival staining could potentially be a useful tool in clinical practice to identify patients at risk of developing 3- and 9-o'clock staining. The lack of correlation between corneal staining and lens comfort stresses the need for regular contact lens check-ups in GP lens wearers. It appears that the simple registration of the presence or absence of ocular symptoms is a better predictor of 3- and 9-o'clock staining than using VAS comfort scores.
Optometry and vision science: official publication of the American Academy of Optometry 02/2009; 86(3):260-5. · 1.53 Impact Factor
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ABSTRACT: To analyze the position of iris-fixated phakic intraocular lenses (pIOLs) using anterior segment optical coherence tomography (AS-OCT) and evaluate the effect of anterior chamber morphometrics on endothelial cell changes.
Department of Ophthalmology, Academic Hospital Maastricht, The Netherlands.
In this cross-sectional study, AS-OCT was used to measure the distances from the center and the edges of the pIOL to the corneal endothelium in 242 eyes with various models of myopic pIOLs. Endothelial cell measurements were performed preoperatively and at each follow-up examination.
The mean follow-up was 34.1 months+/-24.7 (SD) (range 3 months to 7 years). The mean distance between the edge of the pIOL and the endothelium was 1.37+/-0.22 mm. Although this distance was smaller than the safety value of 1.50 mm in 68.6% of the eyes, no eye developed corneal decompensation. There was a significant endothelial cell density (ECD) loss of 1.28%+/-8.46%, 3.25%+/-8.24%, and 5.02%+/-10.40% at 2 years, 5 years, and 7 years, respectively. Linear mixed-model analysis predicted a yearly ECD loss of 0.98% for a mean edge distance of 1.37 mm, 0.15% for an edge distance of 1.59 mm (mean plus 1 SD), and 1.80% for an edge distance of 1.15 mm (mean minus 1 SD).
A shorter distance between the edge of the pIOL and the endothelium was significantly associated with higher ECD loss. For safety reasons, the postoperative examination should include long-term evaluation of the anterior chamber morphometrics in addition to ECD counts.
Journal of Cataract [?] Refractive Surgery 01/2009; 34(12):2110-8. · 2.26 Impact Factor
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ABSTRACT: To report the long-term performance of the AcrySof ReSTOR SA60D3 intraocular lens (IOL) after cataract surgery.
University Hospital Maastricht, Maastricht, The Netherlands.
This prospective clinical trial comprised 44 eyes (22 consecutive patients) having cataract surgery with implantation of the ReSTOR IOL. Monocular and binocular uncorrected distance visual acuity, best corrected distance visual acuity, uncorrected near visual acuity, best distance-corrected near visual acuity, spectacle dependence, undesired visual symptoms, patient satisfaction, and incidence of posterior capsule opacification were analyzed 6 months and 3 years postoperatively.
The mean uncorrected distance acuity (logMAR) was 0.046 +/- 0.099 at 6 months and 0.115 +/- 0.173 at 3 years and the mean best corrected distance acuity, -0.040 +/- 0.075 and -0.018 +/- 0.093, respectively. Binocular uncorrected and best-corrected near acuities (logMAR) were 0.009 +/- 0.029 at 6 months and 0.014 +/- 0.035 at 3 years. All patients achieved a binocular uncorrected and best distance-corrected near acuity of 20/25 or better at 6 months and 3 years. On a quality-of-life questionnaire, patients reported good distance, intermediate, and near acuity without complaints of severe glare or halos. Complete spectacle independence for distance and near acuity was achieved by 83.7% and 81.9% of patients, respectively, at 6 months and 85.0% and 75.0% of patients, respectively, at 3 years. Four eyes (9.1%) required neodymium:YAG capsulotomy.
Cataract surgery with the AcrySof ReSTOR SA60D3 IOL provided good, stable distance and near visual acuities over a 3-year follow-up, leading to low spectacle independence and high patient satisfaction.
Journal of Cataract [?] Refractive Surgery 10/2008; 34(9):1476-82. · 2.26 Impact Factor
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ABSTRACT: The primary goal of this study was to evaluate if there is a difference in frequency and in completeness of eyeblinks (type of eyeblink) in rigid gas permeable (GP) lens wearers experiencing 3- and 9-o'clock staining compared with GP lens wearers without substantial staining and nonlens wearers.
The study involved 26 nonlens wearers and 55 GP contact lens wearers, with and without 3- and 9-o'clock staining. Every eyeblink over a 5-min period was categorized as a complete eyeblink, incomplete eyeblink, or an eyeblink attempt. In addition, type of lens fit (interpalpebral vs. lid attachment), lens-to-cornea fit (flat vs. steep), spherical equivalent of the refraction, and corneal coverage (on-eye lens diameter) were analyzed.
No difference in overall eyeblink frequency was found between nonlens wearers (group I, n = 26), GP lens wearers with less than grade 1 corneal staining (group II, n = 25) and GP lens wearers with grade 1 or more corneal staining (group III, n = 30). Fewer complete eyeblinks, more incomplete eyeblinks and more eyeblink attempts were seen in group III than in group I or II (p < 0.01, p = 0.03, p < 0.01, respectively). Fewer complete eyeblinks and more eyeblink attempts (p < 0.01 for both) were found in interpalpebral lens fits than in lid attachment fits. Fewer complete eyeblinks (p = 0.02) and more incomplete eyeblinks (p = 0.03) were found with lenses rated as large or optimal in size than with lenses rated as small.
GP lens wearers experiencing 3- and 9-o'clock staining showed a different eyeblink frequency for individual types of eyeblinks, but not for overall eyeblinks. Fewer complete eyeblinks, more incomplete eyeblinks, and more eyeblink attempts were observed in GP wearers with 3- and 9-o'clock staining compared with wearers with minimal staining and nonwearers. In addition, some individual contact lens variables were associated with more incomplete eyeblinks.
Optometry and vision science: official publication of the American Academy of Optometry 09/2008; 85(9):E857-66. · 1.53 Impact Factor
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ABSTRACT: To compare a handheld and a digital pupillometer in determining pupil size in a population of refractive surgery candidates (group 1) and after implantation of an Artisan phakic intraocular lens (PIOL) for correction of myopia (group 2).
Pupil size was measured with the Colvard and Procyon pupillometers in 121 eyes in group 1 and 83 eyes in group 2. Pupil sizes measured with the Colvard device were compared with the scotopic, mesopic-low and mesopic-high measurements taken with the Procyon pupillometer in both groups. Analysis of comparison between pupil measurements was performed according to methods described by Bland and Altman.
The mean Colvard scotopic pupil diameter, scotopic, mesopic-low and mesopic-high Procyon pupil diameters were 5.86 +/- 0.81 mm, 6.42 +/- 0.88 mm, 5.55 +/- 0.95 mm and 4.21 +/- 0.73 mm in group 1 and 5.32 +/- 0.67 mm, 6.14 +/- 0.81 mm, 5.33 +/- 0.78 mm and 4.02 +/- 0.55 mm in group 2, respectively. The Colvard diameter compared most favourably with the Procyon mesopic-low diameter (group 2; p = 0.78).
Measurements of pupil diameter with the Colvard pupillometer correlated best with measurements taken by the Procyon pupillometer under standardized mesopic-low light conditions. We believe that digital binocular infrared pupillometry is advantageous for obtaining standardized measurements of pupil size.
Acta Ophthalmologica Scandinavica 06/2007; 85(3):324-8. · 1.85 Impact Factor
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ABSTRACT: Refractive error (RE) is considered to be a possible cause for headaches. We aimed to gain insight into the relation between habitual RE (sphere and astigmatism) and headache complaints.
In a cross-sectional study the habitual refractive state of 487 children, aged between 11 and 13 years, was measured using an autorefractometer (Topcon, RM-8000B). Headache complaints were measured using a questionnaire. Data were analyzed using Pearson correlation coefficients, bivariate analysis, and multiple logistic regression analysis.
For right eyes we found 15% habitual myopia < -0.50 D and 12% habitual hyperopia > +0.50 D; habitual astigmatism > 0.25 D was found in 33% of children. Pearson R between right and left eyes was 0.76 for the spherical component and 0.42 for the cylindrical. In the total group of children 70% reported the occurrence of headache in the last year. These headaches were reported as "often or frequent" by 37% of children, "severe" by 15%, "with long duration" by 45%, and "with severe burden" by 27%. In the total sample we found various associations between gender, sphere/cylinder components of habitual RE, and headache complaints. Headache was reported more in girls than in boys. Of the total variance of headache complaints in girls, the sphere component of habitual RE explained 4% of frequency, 6% of intensity, 2% of duration, and 2% of amount of burden. Of the total variance of headache complaints in boys the cylinder component of habitual RE explained 3% of frequency, and 4% in amount of burden.
Habitual RE and headache complaints are relatively common conditions in schoolchildren aged between 11 and 13 years. Headache complaints showed a small but statistically significant association with the sphere component of habitual RE in girls and the cylinder component of habitual RE in boys. The associations found between habitual RE and headache complaints indicate that habitual RE might be a risk factor for headache in children.
Optometry and Vision Science 03/2007; 84(2):137-43. · 2.11 Impact Factor
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ABSTRACT: To compare pre- and postoperative horizontal and vertical pupil diameters after horizontal Artisan phakic intraocular lens (PIOL) (Ophtec BV, Groningen, The Netherlands) implantation for correction of myopia.
The pre- and postoperative scotopic pupil diameters measured by the Colvard pupillometer (Oasis Medical, Glendora, Calif) were compared in 71 eyes after Artisan PIOL implantation (Artisan Colvard group). Analysis of pupil shape (vertical vs horizontal diameter, V/H ratio) after horizontal Artisan PIOL implantation was performed with the Procyon pupillometer (Procyon Instruments Ltd, London, United Kingdom) in 121 eyes (Artisan Procyon group) under scotopic, mesopic-low, and mesopic-high conditions and compared to an age- and refraction-matched control group of 121 eyes of refractive surgery candidates (Procyon control group).
After horizontal Artisan PIOL implantation, the mean horizontal pupil diameter decreased from 6.231 +/- 0.70 mm preoperatively to 5.34 +/- 0.68 mm postoperatively in the Artisan Colvard group (P < .01). The mean horizontal scotopic diameter was 5.60 +/- 0.66 mm, the mesopic-low diameter was 4.94 +/- 0.71 mm, and the mesopic-high diameter was 3.98 +/- 0.54 mm for the Artisan Procyon group. The mean horizontal scotopic diameter was 6.29 +/- 0.91 mm, the mesopic-low diameter was 5.40 +/- 0.96 mm, and the mesopic-high diameter was 4.16 +/- 0.80 mm in the Procyon control group. A significant increase was noted in V/H ratio under scotopic, mesopic-low, and mesopic-high conditions from 1.02, 1.02, and 1.01, respectively, in the Procyon control group to 1.17, 1.12, and 1.06, respectively, in the Artisan Procyon group (P < .01).
Horizontal pupil size was significantly decreased after horizontal Artisan PIOL implantation and might be attributed to a mechanical restriction of the iris in the horizontal meridian.
Journal of refractive surgery (Thorofare, N.J.: 1995) 04/2006; 22(4):367-71. · 2.54 Impact Factor
