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Michael D Twa

Publications and source records attributed to Michael D Twa.

13 recordsLinked to original sources

A prospective randomized clinical trial of laser in situ keratomileusis with two different lasers.

PURPOSE: To compare optical quality, visual function, corneal shape, ocular wavefront aberrations, and patient-reported symptoms and satisfaction after laser in situ keratomileusis (LASIK) with two different excimer lasers. DESIGN: Prospective randomized clinical trial. METHODS: In an institutional practice setting, 60 eyes of 30 patients with low to moderate myopia were randomized to receive LASIK in one eye with the Technolas 217A; the other eye was treated with the VISX S3. Patients were followed for 6 months after surgery. The primary outcome measure was best spectacle-corrected visual acuity. RESULTS: At 6 months, the mean best-spectacle corrected high contrast visual acuity was similar between the two treatment groups: mean difference (95% confidence interval) was -0.01 logarithm of minimal angle of resolution (logMAR) (-0.03 to +0.01 logMAR). Uncorrected visual acuity differences were also not significant. The difference in residual spherical equivalent subjective refractive error between treatment groups was -0.15 diopter (-0.34 to +0.05 diopter). Spherical aberration increased in both groups after treatment, and the change in root mean square (RMS) ocular wavefront error was greater in the VISX group by +0.07 microm (+0.03 to +0.11 microm). After LASIK, corneal curvature was steeper in the midperipheral region among VISX-treated eyes by +1.39 diopters (+2.06 to +0.72 diopters). There were no patient-reported differences in satisfaction between eyes. CONCLUSIONS: There were no significant differences in visual acuity or refractive outcomes attributed to either laser under any of the conditions measured. There was also no significant difference in patient-reported symptoms, satisfaction with treatment, or eye preference associated with either laser. Additional study is needed to establish the importance of differences in higher-order optical aberrations and corneal shape that we observed in these two treatment groups.

Adult↗

Response of the posterior corneal surface to laser in situ keratomileusis for myopia.

PURPOSE: To describe the response of the posterior corneal surface in laser in situ keratomileusis (LASIK) and determine whether residual stromal bed thickness or treatment magnitude is predictive of the posterior corneal surface elevation after uneventful LASIK. SETTING: A private hospital-based refractive surgery practice, Hong Kong SAR, China. METHODS: Orbscan I (Bausch & Lomb) videokeratography examinations were performed on 1124 patients before and 6 months after LASIK for myopia (mean -6.81 diopters [D] +/- 2.52 [SD]; range -0.88 to -14.50 D). The best-fit sphere (BFS) over the central 9.0 mm region of the posterior corneal surface before and after treatment was compared. The location and magnitude of the 1.0 mm diameter region of highest elevation above the BFS for the central 4.0 mm diameter zone were calculated before and after treatment and compared using a paired t test. Stepwise regression was used to model the best predictors of the posterior radius of the BFS and the central elevation of the corneal surface above the BFS before and after treatment. RESULTS: The mean radius of curvature of the posterior surface BFS decreased 0.10 mm after LASIK, from 6.31 to 6.21 mm (P<.001). Elevation above this BFS was increased 10 microm within a 1.00 mm diameter region of interest, and this was correlated with postoperative corneal thickness, inferotemporal decentration of the highest point, residual myopia, and steeper central posterior radius of curvature. CONCLUSIONS: No eye was diagnosed with corneal ectasia at the time of the 6-month postoperative visit. After LASIK, there was a decreased radius of curvature for the BFS of the posterior corneal surface, with the highest elevation point located paracentrally. These findings are similar to the anterior corneal surface changes observed in corneal ectasia after LASIK but smaller in magnitude.

Adolescent↗

Repeatability of autorefraction and axial length measurements after laser in situ keratomileusis.

PURPOSE: To assess the repeatability and agreement of refractive error measurements and the repeatability of axial length (AL) measurements in patients after laser in situ keratomileusis (LASIK). SETTING: The Ohio State University College of Optometry, Columbus, Ohio, USA. METHODS: Subjective refraction, autorefraction measurements with the Grand Seiko and Humphrey autorefractors, and AL measurements with the IOLMaster were completed for 40 previously myopic LASIK patients under noncycloplegic and cycloplegic conditions on 2 separate occasions. RESULTS: The mean difference between visits for axial length measurements was 0.008 mm +/- 0.04 (SD). The between visits repeatability for all refractive error measurements were <0.75 diopter (D). The mean difference between the subjective refraction and the Humphrey autorefractor for spherical equivalent was statistically significant under noncycloplegic conditions (-0.90 D, P<.0001) and cycloplegic conditions (-2.05 D, P<.0001). The mean difference between subjective refraction and Grand Seiko autorefraction measurements was not significant under noncycloplegic conditions (+0.05 D, 95% limits of agreement [LoA]=-0.99, 1.09; P=.52) conditions but was statistically significant, but not clinically relevant, under cycloplegic conditions (+0.17 D, 95% LoA=-0.73, 1.07; P=.03). CONCLUSIONS: Refractive error measurements after LASIK using the Grand Seiko autorefractor are reliable and agree well with subjective refraction measurements.

Adult↗

Sensitivity of the National Eye Institute Refractive Error Quality of Life instrument to refractive surgery outcomes.

PURPOSE: To evaluate scores from the National Eye Institute Refractive Error Quality of Life instrument (NEI-RQL) relative to refractive surgery outcomes in myopic patients. SETTING: Large institutional ophthalmic practices. METHODS: Patients seeking refractive surgery (n = 59) self-administered the NEI-RQL before and 6 months after surgery; the comparison group of myopes and emmetropes (n = 72) not seeking refractive surgery also completed the NEI-RQL. Myopic patients seeking refractive surgery had bilateral, same-day laser in situ keratomileusis (LASIK) treatment. Regression analyses were conducted to compare survey scores in the LASIK treatment group before surgery with those in the myopic sample who were not seeking refractive surgery and to compare the survey scores in the post-LASIK treatment group (surgical emmetropes) to those in the naturally emmetropic group. Logistic regression was used to determine NEI-RQL subscales that were related to myopic patients seeking refractive surgery and myopic patients not seeking refractive surgery. RESULTS: Myopes seeking LASIK reported greater expectations for vision improvement (P < .0001), greater activity limitations (P < .0001), suboptimal correction (P = .04), worse appearance (P < .0001), and lower satisfaction (P < .0001) than myopes not seeking refractive surgery. Logistic regression showed that worse self-perceived appearance (odds ratio 20.71), more dissatisfaction with current correction (odds ratio 8.28), and higher expectations for "optimal" correction (odds ratio 6.41) were independently associated with myopes seeking LASIK, while better perceived "clarity of vision" (odds ratio = 0.20) was associated with myopes not seeking surgery. Overall, surgical emmetropes were similar to natural emmetropes in terms of refractive-error-specific quality of life (clarity of vision, near vision, far vision, diurnal fluctuations) and clinical measures of visual function, yet they reported significantly better appearance (P = .02) and greater satisfaction (P < .0001) than natural emmetropes. CONCLUSION: The NEI-RQL demonstrated vision-related quality-of-life differences when comparing patient samples associated with refractive surgery.

Adult↗

Automated decision tree classification of corneal shape.

PURPOSE: The volume and complexity of data produced during videokeratography examinations present a challenge of interpretation. As a consequence, results are often analyzed qualitatively by subjective pattern recognition or reduced to comparisons of summary indices. We describe the application of decision tree induction, an automated machine learning classification method, to discriminate between normal and keratoconic corneal shapes in an objective and quantitative way. We then compared this method with other known classification methods. METHODS: The corneal surface was modeled with a seventh-order Zernike polynomial for 132 normal eyes of 92 subjects and 112 eyes of 71 subjects diagnosed with keratoconus. A decision tree classifier was induced using the C4.5 algorithm, and its classification performance was compared with the modified Rabinowitz-McDonnell index, Schwiegerling's Z3 index (Z3), Keratoconus Prediction Index (KPI), KISA%, and Cone Location and Magnitude Index using recommended classification thresholds for each method. We also evaluated the area under the receiver operator characteristic (ROC) curve for each classification method. RESULTS: Our decision tree classifier performed equal to or better than the other classifiers tested: accuracy was 92% and the area under the ROC curve was 0.97. Our decision tree classifier reduced the information needed to distinguish between normal and keratoconus eyes using four of 36 Zernike polynomial coefficients. The four surface features selected as classification attributes by the decision tree method were inferior elevation, greater sagittal depth, oblique toricity, and trefoil. CONCLUSION: Automated decision tree classification of corneal shape through Zernike polynomials is an accurate quantitative method of classification that is interpretable and can be generated from any instrument platform capable of raw elevation data output. This method of pattern classification is extendable to other classification problems.

Cornea↗

Estimation of pupil size by digital photography.

PURPOSE: To evaluate a digital photography method of pupil size estimation over a broad range of illumination conditions and to compare this method with common clinical techniques. SETTING: College of Optometry, Ohio State University, Columbus, Ohio, USA. METHODS: Two examiners measured the pupil diameter in 45 right eyes at 3 illumination levels: <0.63 lux (dark), 5 lux (dim), and 1000 lux (bright). Estimation by infrared video recording, the reference standard, was compared with measurements by digital photography, ruler, semicircular templates, and the Colvard pupillometer. Masked graders measured pupil size from infrared video recordings and digital photographs. RESULTS: The repeatability of the measurement method determined by the mean intraclass correlation coefficients was highest for video recording across conditions (0.86-0.97), followed by digital photography (0.76-0.94), Colvard pupillometry (0.63-0.82), ruler (0.71-0.85), and templates (0.70-0.83). An analysis of variance showed a significant difference in pupil size by method (P<.001). All methods except digital photography estimated smaller pupil sizes under dark and dim illumination than infrared video measurements (all P<.01). Under bright illumination, the ruler measurements were significantly smaller (-0.15 mm) and the Colvard pupillometer measurements were greater (+0.30 mm) than the reference (P<.01). The 95% limits of agreement (LoA) between examiners were smallest for video measurements at all light levels. The remaining measures ranked from best to worst by 95% LoA were digital photography, Colvard pupillometry, ruler, and templates. CONCLUSIONS: Estimation of pupil size by digital photography was more repeatable and accurate than estimates by common clinical techniques over a wide range of illumination. Although not as quick as other methods, digital photography is relatively inexpensive, permits lasting documentation, and allows independent grading suitable for clinical research purposes.

Adult↗

Morphologic characteristics of lamellar channel deposits in the human eye: a case report.

OBJECTIVE: To report the histologic characteristics of lamellar channel deposits after polymethyl methacrylate intrastromal corneal ring segments in a human eye. METHODS: A 34-year-old man previously diagnosed with keratoconus received photorefractive keratectomy in his left eye that exacerbated his corneal ectasia. To delay or possibly prevent corneal transplant, the patient elected to have intrastromal corneal segments implanted in the left eye. One year later the patient underwent corneal transplant. Before transplant, lamellar channel deposits were noted on clinical microscopic examination of the left eye. We performed histologic evaluation to assess changes to the patient's excised corneal tissue and to further characterize the observed lamellar channel deposits. RESULTS: Lamellar channel deposits in humans are histologically similar to our previous descriptions of deposits in rabbits. These deposits primarily consist of intracellular lipid accumulations that stain positively with oil red O and filipin but not periodic acid Schiff reaction. Immunohistochemistry of cells located in the deposit region stained positively with vimentin, suggesting that these cells were keratocytes. Stains for cytokeratins 3 and 12 and for CD68 were both negative, indicating that epithelial cells and macrophages were not present in the deposit region. CONCLUSION: Lamellar channel deposits are a common clinical finding after intrastromal corneal implants. This case provides further evidence to support our hypothesis that lamellar channel deposits in humans are a tissue response to corneal implants that consist of intracellular lipid accumulations. We use this case to propose a theoretical construct for the observation of stromal lipid accumulation in response to corneal injury.

Adult↗

Characteristics of corneal ectasia after LASIK for myopia.

PURPOSE: There are numerous reports of corneal ectasia after laser in situ keratomileusis (LASIK) for myopia without a consistent definition of this condition or a definitive etiology. We conducted a retrospective analysis of published case reports to describe common characteristics of this postoperative event and compared them with findings from a group of successful LASIK patients. METHODS: A MEDLINE search for "LASIK" and "ectasia" yielded 21 relevant articles published before May 2003 (n = 86 eyes, 59 patients). A comparison group (n = 103 eyes, 63 patients) was selected from a clinic-based sample of successful LASIK patients with 12 months of follow-up after treatment. Descriptive statistics are reported as median and interquartile range. Comparisons were performed using the Wilcoxon rank sum, Wilcoxon signed rank, and chi-square tests. RESULTS: Time to diagnosis of ectasia after LASIK was 13 months (6 to 20 months). Residual myopia in the ectasia group was -3.69 D (-6.00 to -2.13 D) and was significantly greater than the comparison group, -0.38 D (-0.75 to 0.00 D), P < 0.001. After surgery, eyes with ectasia had increased corneal toricity 2.87 D (2.00 to 4.9 D) with increased oblique astigmatism 1.3 D (0.23 to 2.89 D) relative to eyes in the comparison group 0.00 D (0.00 to 0.08 D), and a loss of 2 lines (-0.5 to -6 lines) of best spectacle-corrected visual acuity (all P < 0.001). Thirty-five percent of reported cases resulted in subsequent corneal transplantation. CONCLUSIONS: Preoperative characteristics of corneal ectasia include worse visual acuity, less corneal thickness, greater residual myopia, and greater corneal toricity than nonectatic eyes. Treatment factors associated with corneal ectasia after LASIK are greater stromal ablation and less residual stromal bed thickness. Postoperative characteristics of corneal ectasia are myopic refractive error with increased astigmatism, worse spectacle-corrected visual acuity, increased corneal toricity with topographic abnormality, and progressive corneal thinning.

Adult↗

Correction of astigmatism with short arc-length intrastromal corneal ring segments: preliminary results.

OBJECTIVE: To evaluate the refractive effect of 130 degrees short arc length intrastromal corneal ring segments (ICRS) designed to correct myopia concurrent with astigmatism. DESIGN: Prospective, nonrandomized, comparative (self-controlled) trial. PARTICIPANTS: Ten eyes of 6 patients from one surgical center with manifest refraction spherical equivalent between -1.00 and -6.00 diopters (D), manifest cylinder correction between 1.00 and 6.00 D, and best spectacle-corrected visual acuity of 20/20 or better. INTERVENTION: The patients were assigned to receive 1 of 6 ICRS thicknesses, ranging from 0.25 to 0.50 mm by 0.05 mm increments, with an arc length of 130 degrees. MAIN OUTCOME MEASURES: Vector analysis of astigmatic correction. Efficacy was assessed by uncorrected visual acuity and by deviation of postoperative spherical and cylindrical refractive error from predicted correction. Safety was assessed by maintenance or loss of preoperative best spectacle-corrected visual acuity. Measurements were made before surgery and after surgery at days 1 and 7 and months 1, 2, 3, and 6. RESULTS: At 6 months, uncorrected visual acuity was 20/20 or better in 80% of eyes (8/10) and 20/40 or better in all eyes. Eight of 10 eyes (80%) were within +/-0.25 D of plano spherical equivalent manifest refraction. There was no loss of best spectacle-corrected visual acuity, and 6 of 10 eyes (60%) gained a line. Reduction of keratometric cylinder by ICRS thickness was statistically significant (P = 0.039). CONCLUSIONS: Preliminary results of visual and refractive performance after correction of compound myopic astigmatism using short arc length ICRS are promising.

Adult↗

Histologic evaluation of corneal stroma in rabbits after intrastromal corneal ring implantation.

PURPOSE: Previous refractive corneal implants have produced histologic changes characteristic of nonspecific lipid keratopathy. Intacs intrastromal corneal ring segments are polymethylmethacrylate (PMMA) corneal inserts approved for the correction of low myopia by the U.S. Food and Drug Administration. The purpose of this study was to describe histologic changes associated with these corneal implants in rabbit eyes. METHODS: Two 150-degree PMMA arc segments, 0.30 mm thick, were surgically implanted through a single radial incision at two-thirds stromal depth in the mid-peripheral cornea of five New Zealand white rabbits. We collected corneas 6 months after implantation that were prepared for light and electron microscopy. We analyzed tissue with oil red O, filipin, and periodic acid-Schiff (PAS) staining. Additional studies with energy-dispersive x-ray analysis and autofluorescent microscopy were conducted. RESULTS: In all samples, we observed new collagen formation with lamellar organization adjacent to the implant and increased keratocyte density. Intracellular accumulations of osmophilic and saturated lipid material corresponded to stromal opacification visible by slit-lamp microscopy. These same regions were autofluorescent and stained positively with oil red O, and filipin but negatively with PAS. Granular lipid inclusions characteristic of lipofuscinosis were absent on transmission electron microscopy. Energy-dispersive x-ray analysis demonstrated elevated levels of calcium compared with adjacent tissue. CONCLUSION: Tissue response to these corneal inserts includes keratocyte activation, intracellular lipid accumulation, and new collagen formation. Our histologic findings suggest that these deposit formations are not lipofuscin accumulations.

Animals↗

Refractive change in response to acute hyperbaric stress in refractive surgery patients.

PURPOSE: To determine whether acute hyperbaric stress affects visual acuity or refractive power after keratorefractive surgery. SETTING: Clinical multiplace hyperbaric chamber and ophthalmology clinic, University of California, San Diego, California, USA. METHODS: This prospective convenience sample study included 3 groups: 3 patients who had had bilateral myopic radial keratotomy (RK); 2 who had had bilateral myopic laser in situ keratomileusis (LASIK); and 4 control subjects who had no previous corneal refractive surgery or ocular pathology but had a myopic refractive error (-1.25 to -8.38 diopters [D]) similar to that in the treated patients before refractive surgery. One additional patient had had unilateral LASIK only and was included in the LASIK and control groups. Best spectacle-corrected visual acuity (BSCVA), manifest spherocylindrical refractive error, and intraocular pressure were measured at baseline, at 4 atmospheres absolute (atm abs), and on return to ambient pressure. Corneal pachymetry and keratometry were measured at baseline and on return to ambient pressure. RESULTS: The mean BSCVA changed from 0.06 logMAR (20/25 Snellen equivalent) at baseline to 0.10 logMAR (20/25) at 4 atm abs in the RK group and from 0.00 logMAR (20/20) to -0.06 logMAR (20/15) in the LASIK group; it did not change in the control group. The mean refractive error changed from 0.25 D at baseline to 0.50 D at 4 atm abs in the RK group, from -0.90 to -1.02 D in the LASIK group, and from -4.58 to -4.53 D in the control group. CONCLUSIONS: Acute hyperbaric stress did not appear to alter refractive power after corneal surgery.

Adult↗

Twenty-four-hour pattern of intraocular pressure in young adults with moderate to severe myopia.

PURPOSE: To characterize the 24-hour change of intraocular pressure (IOP) in young adults with moderate to severe myopia. METHODS: Nineteen young adults, ages 18 to 25 years, with moderate to severe myopia (myopia group) and 17 age-matched volunteers with emmetropia or mild myopia (control group) were housed for 1 day in a sleep laboratory. An 8-hour accustomed sleep period was assigned to each volunteer. Twelve measurements of IOP, axial length, blood pressure, and heart rate were taken at 2-hour intervals. In the wake period, blood pressure and heart rate were measured after a 5-minute bed rest. Axial length and IOP were measured in supine volunteers. Volunteers then sat for 5 minutes, after which IOP was measured. In the sleep period, measurements were taken in supine volunteers in bed. RESULTS: In both the myopia and control groups, the average supine IOP in the sleep period was higher than the average sitting IOP in the wake period. However, the magnitude of this IOP elevation at night was significantly less in the myopia group. In the sleep period, IOP was less in the myopia group than in the control group. When only the 24-hour supine IOP data were considered, the trough occurred at 1:30 AM, and the peak occurred around noon in the myopia group. In the control group, the trough was at 9:30 PM, and the peak at 5:30 AM. Least-square cosine fits showed 24-hour rhythms of supine IOP in both groups, but their phase timings were different. Axial length remained unchanged throughout the day and night in both groups. There was no difference in the 24-hour rhythms of mean blood pressure and heart rate between the two groups. CONCLUSIONS: Considering habitual body positions, IOP increases at night in young adults with moderate to severe myopia, but the magnitude of the increase is significantly less than that in the age-matched control subjects. There is a 24-hour rhythm of supine IOP in the myopic group, but the phase timing is different from that in the control subjects. These variations of IOP in young adults with moderate to severe myopia are not related to changes in cardiovascular parameters.

Adolescent↗