Peripheral refractive changes associated with myopia progression

Purpose.: To evaluate the changes in peripheral refraction profiles associated with myopia progression and treatment modalities used in the Cambridge Anti-Myopia Study. Methods.: One hundred and seventy-seven myopes in the age range of 14 to 22 years were enrolled in the study. The mean spherical equivalent refractive error was −3.12 ± 1.87 diopters (D) and the refractive error of each participant was corrected with contact lenses. The participants were randomly assigned to one of four treatment groups, which included: altered spherical aberration and vision training, altered spherical aberration only, vision training only, and control. Peripheral refractive error was measured using an open field autorefractor in the central 60° of the retina in 10° steps. The refractive error was measured using cycloplegic autorefraction. Two-year refractive progression data and initial peripheral refraction measurements were available in 113 participants. Measurements of peripheral refraction and cycloplegic refraction were obtained at three visits over 2 years in 12-month intervals for 92 participants. Results.: All subjects showed a relative peripheral hyperopia, especially in the nasal retina. A limited magnitude of myopia progression of −0.34 ± 0.36 D over 2 years was found in each of the four groups on average. There were no significant differences in the rate of progression between any of the treatment groups (P > 0.05). Initial peripheral J45 astigmatic refractive error at 20° and 30° in the nasal retina was weakly correlated with progression of myopia over 2 years (r = −0.27, P = 0.004 and r = −0.20, P = 0.040, respectively; n = 113). The change in spherical equivalent peripheral refractive error at 30° nasal retina over time was also significantly correlated with progression of myopia especially at 24 months (r = −0.24, P = 0.017, n = 92). Conclusions.: Relative peripheral hyperopia is associated with myopia. Myopia progression may be weakly linked to changes in the peripheral refraction profiles in the nasal retina. However, a causative link between peripheral refractive error and myopia progression could not be established

The Cambridge Anti-myopia Study: variables associated with myopia progression

Purpose: To identify variables associated with myopia progression and to identify any interaction between accommodative function, myopia progression, age, and treatment effect in the Cambridge Anti-Myopia Study. Methods: Contact lenses were used to improve static accommodation by altering ocular spherical aberration, and vision training was performed to improve dynamic accommodation. One hundred forty-two subjects, aged 14–21 years, were recruited who had a minimum of −0.75D of myopia. Subjects were assigned to contact lens treatment only, vision training only, contact lens treatment and vision training, or control group. Spherical aberration, lag of accommodation, accommodative convergence/accommodation (AC/A) ratio, accommodative facility, ocular biometry, and refractive error were measured at regular intervals throughout the 2-year trial. Results: Ninety-five subjects completed the 24-month trial period. There was no significant difference in myopia progression between the four treatment groups at 24 months. Age, lag of accommodation, and AC/A ratio were significantly associated with myopia progression. There was a significant treatment effect at 12 months in the contact lens treatment group in younger subjects, based on a median split, aged under 16.9 years (p = 0.005). This treatment effect was not maintained over the second year of the trial. Younger subjects experienced a greater reduction in lag of accommodation with the treatment contact lens at 3 months (p = 0.03), compared to older contact lens treatment and control groups. There was no interaction between AC/A ratio and contact lens treatment effect. Conclusions: Age, lag of accommodation, and AC/A ratio were significantly associated with myopia progression. Although there was no significant treatment effect at 24 months, an interaction between age and contact lens treatment suggests younger subjects may be more amenable, at least in the short term, to alteration of the visual system using optical treatments

Visual Performance and the Use of Colored Filters in Children Who Are Deaf

Purpose. To assess visual performance and the effects of color overlays on reading in children who were deaf and children who could hear. Methods. Thirty-one children who were deaf (mean [±SD] age, 14 [±1.99] years) and 39 children who could hear (mean [±SD] age, 13.58 [±3.09] years) underwent an optometric examination with specific emphasis on near vision. Participants chose an overlay with color optimal for clarity and comfort and completed the Wilkins Rate of Reading Test both with and without an overlay of this color. Nineteen of the participants who were deaf were retested a year later with a modified rate of reading test that used only words that can readily be signed. This modified rate of reading test was repeated 1 week after its first administration. Results. Participants who were deaf had greater ametropia (p = 0.003), a more distant near point of convergence (p = 0.002), and reduced amplitude of accommodation (p < 0.001) compared with normal-hearing participants. All the children who were deaf chose a color overlay, with 45% choosing a yellow overlay, which increased the rate of reading by 18%. Only 66% of the participants who could hear chose an overlay, and it had no effect on reading speed. With the modified reading test, 7 of 19 (37%) again chose yellow. These participants showed a 9% increase in reading speed with the yellow overlay, which was repeatable 1 week later. The remainder showed no increase in rate of reading with their chosen overlay. Conclusions. An eye examination of children who are deaf needs to include a comprehensive assessment of near visual function so that deficiencies of amplitude of accommodation, near point convergence, and ametropia can be treated. A yellow overlay improved reading speed in the participants who were deaf, whereas other colors did not, a finding at variance with earlier work on hearing populations

Aberration control and vision training as an effective means of improving accommodation in individuals with myopia

Purpose.: To test the efficacy of a novel dual treatment for improving accommodative accuracy and dynamics in young persons with myopia. Methods.: Ninety-three young persons with myopia (mean spherical equivalent, −3.0 ± 1.8 D; age 16.8 ± 2.1 years; spherical aberration +0.06 ± 0.04 μm) participated in the study. Custom-designed soft contact lenses were used to alter ocular SA to −0.10 μm to improve accommodative accuracy and reduce any lag of accommodation. A vision training regimen was performed for 18 minutes per day for up to 6 weeks to improve speed of dynamic accommodation. Control groups had contact lenses with no added SA and/or no exercises. To avoid any effects of natural levels of negative aberration on the results of the study, all participants who had negative SA were excluded. Results.: The treatment contact lenses produced a significant reduction in lag of accommodation (P < 0.05) at all proximal viewing distances measured. The vision training measurement and treatment resulted in a significant increase in distance facility rate for all groups compared with their own baselines (P < 0.05). Near facility rate improved in the vision training treatment group only compared with its baseline (P < 0.05). Both positive and negative response times for distant viewing were significantly shorter in all groups after training compared with their baseline values (P < 0.05). At near, the positive response times were decreased significantly (P < 0.05) in both groups, whereas the negative response times decreased significantly only in the vision training treatment group. Conclusions.: After 3 months, the dual treatments (altering SA and vision training) used in the study were effective in modifying accommodation. The static accommodative response to targets at proximal distances was increased by the altered SA contact lenses and rates of dynamic accommodation improved with vision training

Effect of positive and negative defocus on contrast sensitivity in myopes and non-myopes

This study investigated the effect of lens induced defocus on the contrast sensitivity function in myopes and non-myopes. Contrast sensitivity for up to 20 spatial frequencies ranging from 1 to 20 c/deg was measured with vertical sine wave gratings under cycloplegia at different levels of positive and negative defocus in myopes and non-myopes. In non-myopes the reduction in contrast sensitivity increased in a systematic fashion as the amount of defocus increased. This reduction was similar for positive and negative lenses of the same power (p=0.474). Myopes showed a contrast sensitivity loss that was significantly greater with positive defocus compared to negative defocus (p=0.001). The magnitude of the contrast sensitivity loss was also dependent on the spatial frequency tested for both positive and negative defocus. There was significantly greater contrast sensitivity loss in non-myopes than in myopes at low-medium spatial frequencies (1–8 c/deg) with negative defocus. Latent accommodation was ruled out as a contributor to this difference in myopes and non-myopes. In another experiment, ocular aberrations were measured under cycloplegia using a Shack–Hartmann aberrometer. Modulation transfer functions were calculated using the second order term for defocus as well as the fourth order Zernike term for spherical aberration. The theoretical maximal contrast sensitivity based on aberration data predicted the measured asymmetry in contrast sensitivity to positive and negative defocus that was observed in myopic subjects. The observed asymmetry in contrast sensitivity with positive and negative defocus in myopes may be linked to the altered accommodative response observed in this group

Effect of transcatheter aortic valve implantation vs surgical aortic valve replacement on all-cause mortality in patients with aortic stenosis

Importance: Transcatheter aortic valve implantation (TAVI) is a less invasive alternative to surgical aortic valve replacement and is the treatment of choice for patients at high operative risk. The role of TAVI in patients at lower risk is unclear. Objective: To determine whether TAVI is noninferior to surgery in patients at moderately increased operative risk. Design, Setting, and Participants: In this randomized clinical trial conducted at 34 UK centers, 913 patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk due to age or comorbidity were enrolled between April 2014 and April 2018 and followed up through April 2019. Interventions: TAVI using any valve with a CE mark (indicating conformity of the valve with all legal and safety requirements for sale throughout the European Economic Area) and any access route (n = 458) or surgical aortic valve replacement (surgery; n = 455). Main Outcomes and Measures: The primary outcome was all-cause mortality at 1 year. The primary hypothesis was that TAVI was noninferior to surgery, with a noninferiority margin of 5% for the upper limit of the 1-sided 97.5% CI for the absolute between-group difference in mortality. There were 36 secondary outcomes (30 reported herein), including duration of hospital stay, major bleeding events, vascular complications, conduction disturbance requiring pacemaker implantation, and aortic regurgitation. Results: Among 913 patients randomized (median age, 81 years [IQR, 78 to 84 years]; 424 [46%] were female; median Society of Thoracic Surgeons mortality risk score, 2.6% [IQR, 2.0% to 3.4%]), 912 (99.9%) completed follow-up and were included in the noninferiority analysis. At 1 year, there were 21 deaths (4.6%) in the TAVI group and 30 deaths (6.6%) in the surgery group, with an adjusted absolute risk difference of −2.0% (1-sided 97.5% CI, −∞ to 1.2%; P &lt; .001 for noninferiority). Of 30 prespecified secondary outcomes reported herein, 24 showed no significant difference at 1 year. TAVI was associated with significantly shorter postprocedural hospitalization (median of 3 days [IQR, 2 to 5 days] vs 8 days [IQR, 6 to 13 days] in the surgery group). At 1 year, there were significantly fewer major bleeding events after TAVI compared with surgery (7.2% vs 20.2%, respectively; adjusted hazard ratio [HR], 0.33 [95% CI, 0.24 to 0.45]) but significantly more vascular complications (10.3% vs 2.4%; adjusted HR, 4.42 [95% CI, 2.54 to 7.71]), conduction disturbances requiring pacemaker implantation (14.2% vs 7.3%; adjusted HR, 2.05 [95% CI, 1.43 to 2.94]), and mild (38.3% vs 11.7%) or moderate (2.3% vs 0.6%) aortic regurgitation (adjusted odds ratio for mild, moderate, or severe [no instance of severe reported] aortic regurgitation combined vs none, 4.89 [95% CI, 3.08 to 7.75]). Conclusions and Relevance: Among patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk, TAVI was noninferior to surgery with respect to all-cause mortality at 1 year. Trial Registration: isrctn.com Identifier: ISRCTN57819173