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PubMed1991

Precision in automated refraction.

Forty-six eyes were examined with automated refraction with the Nidek 1000-AR autorefractometer to determine how large variation there was in readings of each patient, under dry conditions (without cycloplegia) and in atropine and cyclopentolate cycloplegia. Likewise, the differences between methods of cycloplegia were analysed with regard to sphere, cylinder power, and axis. Overall the variation in each set of measurements was greatest for the spherical component, and a larger variation was found in the youngest age group. Variation in cylinder power and axis was small. Cycloplegics had a significant influence on the spherical component of automated refraction, and a mean difference of 0.76D was found between atropine and dry readings, and 0.23D between atropine and cyclopentolate readings. The differences between cycloplegic and dry readings in cylinder power and axis were insignificant. A regression model relating spherical power of dry and cyclopentolate automated refraction was developed, and the predictive power of this equation was tested.

Accommodation, Ocular↗
PubMed2004

Refraction and keratometry in 40 week old premature (corrected age) and term infants.

AIM: To compare refraction and keratometry readings between premature and term babies at 40 weeks' postconceptional age (PCA), and the possible effect of birth weight (BW) and gestational age (GA) on ocular parameters. METHODS: 33 preterm babies hospitalised in the neonatal unit between January and March 2002 were matched with 33 term babies born within the same period and hospitalised in the same unit. The preterm group underwent funduscopy at 4-5 weeks after delivery. Ophthalmic examination at 40 weeks' PCA included cycloplegic retinoscopy, funduscopy, and keratometric measurements. Mean and standard deviation of refraction, astigmatic power (plus cylinder), axis of astigmatism, and keratometric reading were calculated and compared between groups and correlated with BW and GA in the premature babies. RESULTS: Retinopathy of prematurity (ROP) stage 1 or 2 was noted in 88% of the premature babies on the first funduscopy examination, but only in 36% by the corrected age of 40 weeks. Statistically significant between groups differences were found for cycloplegic refraction (p = 0.02 for both eyes) and keratometry (p = 0.001 for both eyes). GA and BW had no impact on the refractive and keratometric findings in the preterm babies. CONCLUSIONS: Babies with mild ROP at the corrected age of 40 weeks have mild hypermetropia compared to the moderate hypermetropia found in term babies (a difference of 50%), and they have higher and steeper keratometric values. The greater corneal curvature may contribute to the development of myopia. Ophthalmologists and parents need to be aware of the possibility of visual dysfunction already very early in life even in relatively older premature infants.

Astigmatism↗
PubMed1979

Refraction of 1-year-old children after cycloplegia with 1% cyclopentolate: comparison with findings after atropinisation.

Cyclopentolate 1% is significantly less effective than atropine 1% at producing cycloplegia in 1-year-old children. If cycloplegic refraction is to be used for investigation or screening children for visual defects during the sensitive period, the more prolonged and profound cycloplegia following atropine could potentially have a disastrous effect on the development of vision. Cyclopentolate 1% would have to be used, and allowance made for its inadequacy as a cycloplegic.

Atropine↗
PubMed1996

Clinical evaluation of the Allergan Humphrey 500 autorefractor and the Nidek AR-1000 autorefractor.

AIMS/BACKGROUND: The intentions of this study were to estimate agreement between two different autorefractors and standard subjective refraction techniques and to evaluate the clinical implications of relying on the autorefractor measurements. METHODS: Subjective refraction was carried out on 448 cycloplegic eyes and compared with cycloplegic readings with the Allergan Humphrey 500 autorefractor (448 eyes) and the Nidek AR-1000 autorefractor (160 eyes). Each refraction was followed by clinical visual acuity measurement. The study population comprised 224 healthy students, 107 men and 117 women, with a mean age of 20.6 (SD 1.1) years. RESULTS: Both the Nidek and Humphrey autorefractors measured more negative or less positive refractive values compared with subjective refraction and these biases were statistically significant (Humphrey right eye -0.23 D, p = 0.0001, left eye -0.20 D, p = 0.0001), (Nidek right eye -0.13 D, p = 0.0001, left eye -0.11 D, p = 0.0002). Comparing the results of autorefraction with subjective refraction, the Nidek was better than the Humphrey autorefractor in several ways: a smaller mean difference, better agreement between spherical equivalent values, narrower limits of agreements, and better visual acuity obtained with the autorefraction. On the other hand, the Humphrey autorefractor agreed better with subjective refraction concerning cylinder axis. CONCLUSION: The results show that both autorefractors represent a valuable complement to subjective refraction, but cannot be used as a replacement.

Adolescent↗
PubMedDate not supplied

The problem of cycloplegia in the pediatric age group: a combination formula for refraction.

Cycloplegic refraction and indirect ophthalmoscopy are essential to evaluation of the pediatric patient. Unfortunately, along with this practice occur the attendant risks of toxicity and the unpleasantness of instillation. The literature that documents the development of cycloplegic agents is often contradictory regarding efficacy and side effects. It is presented for perspective. We have found that efficacy and discomfort are inseparable; however, as with efficacy and toxicity they are directly related to the concentration used. The case is therefore made to use each agent in its minimal effective concentration and thereby minimize both discomfort and toxicity. Our combination of 1.3% cyclogyl, .167% mydriacil, and 1.6% phenylephrine accomplishes effective cycloplegia for refraction and indirect ophthalmoscopy, has a rapid onset and short duration, works reliably in dark irides, is accomplished in a single encounter with the patient, and exhibits none of the side effects of the individual agents in our series.

Age Factors↗
PubMedDate not supplied

Refractive changes in children under general anesthesia.

Twenty-five pediatric patients were refracted without topical cycloplegic agents following induction of halothane anesthesia. Comparison of the intraoperative refraction with a preoperative, outpatient, cycloplegic refraction revealed a variable increase in myopia ranging from 0.25 to 5.50 diopters under general anesthesia. Several patients showed a significant asymmetry in myopic shift between fellow eyes, suggesting that a central accommodative mechanism may not be entirely responsible for the refractive changes observed.

Anesthesia, General↗
PubMedDate not supplied

Systemic effects of mydriatics in low weight infants.

Two-and-a-half percent phenylephrine eye drops were used in combination with 0.5% tropicamide for routine pupillary dilation in 10 low weight infants. Significant systolic blood pressure elevation was noted in eight of 10 infants. A matched control group dilated with cycloplegics alone did not show a significant rise in systolic blood pressure. The mean change in pupillary dilation in the study group was 3.9 mm compared with 3.1 mm in the control group. This difference is not statistically significant. We therefore recommend that cycloplegic agents alone be used for pupillary dilation in these high risk infants.

Blood Pressure↗
PubMedDate not supplied

Medical management of accommodative esotropia.

Cycloplegic drugs are the principal medications used in the diagnosis of accommodative esotropia. The same cycloplegics can be used as a "medical patch" in the treatment of amblyopia. Miotics may be as good as glasses in controlling accommodative esotropia but are almost never better. The response to miotics does not rule out the presence of accommodative esotropia. Miotics also may be used as a supplementary agent to glasses, bifocals, or surgery in the treatment of esotropia. The most widely used miotics today include phospholine iodide and DFP with iris cysts being the major local side effect in the eye with the use of miotics in children. Miotics and other drugs are valuable tools in the treatment of accommodative esotropia; however, the use must be correlated with other tools, including surgery, patching, glasses, and orthoptic exercises.

Accommodation, Ocular↗
PubMedDate not supplied

Atropine cycloplegia: how many instillations does one need?

Atropine is accepted generally as the most efficient cycloplegic agent. Although it is considered a relatively safe drug, toxic local and systemic side effects do occur. The recommended regimen for atropine cycloplegia has been 7 to 10 applications within 3 to 4 days. We compared the cycloplegic effect of four instillations of atropine drops to the effect of eight instillations. The results showed that the cycloplegia obtained after eight instillations was not greater than after four instillations.

Accommodation, Ocular↗
PubMed1998

Laser in situ keratomileusis for hyperopia and hyperopic astigmatism.

BACKGROUND: The correction of hyperopia by excimer laser remains challenging because the procedure is followed by regression and loss of effect. We evaluated excimer laser in situ keratomileusis (LASIK) to correct hyperopia and hyperopic astigmatism using the NIDEK scanning slit excimer laser and a modified nomogram. METHODS: The study included the first consecutive 58 eyes treated for hyperopia and hyperopic astigmatism by one surgeon. All eyes were operated at the Alexandria Eye Center, Alexandria, Egypt using the Nidek excimer laser and the Chiron automated corneal shaper. Astigmatic correction was done first by myopic ablation using a 5.0 mm ablation zone and a 5.5 mm transition zone, followed by narrow hyperopic ablation using a 5.5 to 7.5 mm zone. RESULTS: Mean preoperative cycloplegic spherical equivalent refraction was +3.75 D (range, +1.00 to +6.00 D). Mean preoperative astigmatism was 2.75 D (range 0 to 4.00 D). After hyperopic LASIK, all eyes had a reduction in their hyperopia, but regression occurred gradually until the last follow-up examination. At 6 months follow-up, the mean cycloplegic refraction was +2.25 D (range, 0 to +3.25 D). The postoperative astigmatism had a mean of 1.25 D (range 0 to 2.75 D). Four eyes had a reduction in the quality of vision due to a decentered ablation and a small ablation zone, but no other vision threatening complications were reported. CONCLUSION: LASIK to correct hyperopia and hyperopic astigmatism is safe, effective, and repeatable. Predictability and long-term stability needs improvement. A better ablation profile and modified algorithm need to be provided by excimer laser manufacturers.

Adolescent↗
PubMedDate not supplied

Artisan phakic iris claw intraocular lens for high primary and secondary hyperopia.

PURPOSE: To evaluate the efficacy, predictability, and safety of the Artisan iris claw phakic intraocular lens for the correction of high primary and secondary hyperopia. METHODS: Fifty-seven eyes were divided into two groups: 29 eyes had primary hyperopia (mean refraction 6.06 +/- 1.26 D, and 28 eyes had secondary hyperopia, (mean refraction 5.88 +/- 1.88 D) induced or residual following a previous corneal refractive procedure. Consecutive implantation of the Artisan iris claw phakic intraocular lens was performed. Main outcome measures recorded were BSCVA, UCVA, refraction, and astigmatic change, intraocular inflammation, and endothelial cell loss. RESULTS: Primary hyperopic group: Preoperatively, mean UCVA was 0.4 +/- 0.7 and mean BSCVA was 0.2 +/- 0.6. After implantation, mean UCVA was 0.3 +/- 0.6 and BSCVA was 0.1 +/- 0.6. Mean cycloplegic residual spherical refractive error after surgery was 0.10 +/- 0.57 D (range -1 to +2 D). Mean surgically induced astigmatism was 1.48 +/- 0.89 D. Safety index was 1.11. Efficacy index was 0.83. Secondary hyperopic group: Preoperatively, mean UCVA was 0.5 +/- 0.7 and mean BSCVA was 0.2 +/- 0.6. Postoperatively, mean UCVA was 0.4 +/- 0.7 and mean BSCVA was 0.2 +/- 0.6. Mean cycloplegic residual spherical refractive error was 0.55 +/- 1.49 D. Mean surgically induced astigmatism was 1.85 +/- 1.19 D. Safety index was 1.05. Efficacy index was 0.7. Postoperative iridocyclitis was observed in one eye (3.4%) in the primary group and in three eyes (10.7%) in the secondary group. Overall corneal endothelial cell loss at 1 year of follow-up was 9.4%. CONCLUSION: The Artisan iris claw phakic intraocular lens was reasonably safe and predictable for correcting high hyperopia.

Adult↗
PubMedDate not supplied

LADARWave wavefront measurement in normal eyes.

PURPOSE: We evaluated the correlation of Alcon LADARWave wavefront measurements with clinical refraction and corneal topography. METHODS: In a retrospective, non-comparative case series, 60 eyes (30 patients) of healthy individuals evaluated by preoperative examination for refractive surgery were enrolled (manifest sphere, -11.00 to +4.50 D; manifest cylinder, 0 to -4.75 D; 45 eyes were myopic, 12 eyes were hyperopic, and 3 had mixed astigmatism). Correlation of manifest refraction, cycloplegic refraction, and topographic data with wavefront refraction and higher order aberration was assessed. Match percentage given by the wavefront was analyzed. This number represents how much of the wavefront refraction is due to sphere and cylinder (high percentage match) or is influenced by higher order aberration (low percentage match), in which case aberrometer refraction will not be close to phoropter refraction. Pearson's correlation coefficient was assessed for two continuous variables, adjusting for repeated measurements. RESULTS: The median match percentage was 91%. Mean values for all higher order aberration components in a 7.0-mm pupil were: coma = 0.35 +/- 0.29 microm, spherical aberrations = 0.36 +/- 0.31 microm, and other terms of higher order aberrations = 0.31 +/- 0.14 microm. Wavefront sphere, cylinder, and axis terms were highly correlated to manifest and cycloplegic measurements. The high match subgroup had a higher correlation coefficient than the low match subgroup for refraction. Topographic cylinder and axis were not strongly correlated to wavefront refraction, but manifest axis was significantly correlated to topographic axis. CONCLUSION: In 60 normal eyes, the Alcon LADARWave wavefront measurement was highly correlated with refraction, but less well with corneal topography.

Adult↗
PubMed1997

[A corneal topographic analysis of astigmatism after excimer laser photorefractive keratectomy].

OBJECTIVE: To identify the astigmatism changes after excimer laser photorefractive keratectomy (PRK) and the visual influence of astigmatism. METHODS: 109 myopic eyes followed up for more than 1 year were analyzed by using videokeratography, and their visual acuities were examined. Before the operation, the astigmatic errors with cycloplegic refractive examination were -1.00(-)-2.00 D. RESULTS: The position of astigmatism axis was basically consistent with that in corneal topography, but the astigmatism diopter was of some difference between the cycloplegic examination and topographic analysis. With-the-rule astigmatism was in 61% of the eyes, asymmetrical was 33% and against-the-rule was 6% in topographic analysis. Only was a little change in the position of astigmatism axis after PRK observed. Some changes of postoperative astigmatism diopter were seen in different periods. It was increased in the postoperative 10 days or 1 month, and afterwards it became gradually decreased and stable in 6 months to 1 year. The postoperative residual astigmatism was low in degree, that did not affect the visual acuity a great deal. The actual corrected diopter was within the anticipated corrected diopter range of +/- 1.00 D, accounting for 97%. CONCLUSION: By using spherical equivalent method of calculation in PRK, the refractive correction of the operation in cases with myopia and low degree of astigmatism (< -2.00 D) can be satisfactory.

Astigmatism↗
PubMed2000

Astigmatism and Amblyopia among Native American Children (AANAC): design and methods.

The overall goal of the AANAC study is to improve detection of astigmatism and prevention of amblyopia in populations with a high prevalence of astigmatism. To meet this goal, the study will evaluate four methods of screening for astigmatism in preschool children and will assess both the short-term and long-term benefits of early correction of astigmatism in improving acuity and preventing amblyopia. This paper presents an overview of the design and methodology of the AANAC study. Subjects are members of the Tohono O'Odham Nation, a Native American tribe with a high prevalence of astigmatism. Preschool-age children who attend Head Start are screened with four tools: the Marco Nidek KM-500 autokeratometer, the MTI photoscreener, the Nikon Retinomax K-Plus autorefractor, and the Lea Symbols acuity chart. Sensitivity and specificity for detection of significant astigmatism, as measured by a technique that uses both cycloplegic retinoscopy and cycloplegic autorefraction, is determined for each of the four screening tools. Presence of amblyopia is evaluated by measurement of best-corrected recognition acuity and acuity for orthogonal gratings. Spectacles are provided to all 3-year-old children with > or =2.00 diopters (D) of astigmatism and all 4- and 5-year-old children with > or =1.50 D of astigmatism. Persistence of amblyopia after glasses wearing is evaluated by follow-up measurement of best-corrected recognition acuity and acuity for orthogonal gratings, conducted 2-5 months after glasses are prescribed. Long-term effectiveness of early screening and glasses prescription is evaluated through measurement of recognition acuity in two groups of first-grade children: one group who participated in the Head Start program before the intensive vision screening program was initiated, and a second group who participated in the study's Head Start vision screening program.

Amblyopia↗
PubMed1975

The influence of tropicamide on intraocular pressure.

Elevation of intraocular pressure by many cycloplegic drugs has been reported to occur in eyes in which the filtration angle remained open during mydriasis. Tropicamide 1% is also capable of this phenomenon in patients with open angle glaucoma who are being medicated with pilocarpine. However, in normal eyes as well as those with untreated open angle glaucoma, this cycloplegic has a relatively small effect on intraocular pressure. It is postulated that this difference between the subject groups may be due to competitive inhibition of the miotic at the receptor site in those treated with pilocarpine. In 3 patients in whom the intraocular tension elevation was found to be quite marked, heavy pigments showers in the anterior chamber occurred which suggested an outflow obstructive phenomenon similar to that seen in "Pigmentary Glaucoma."

Amides↗
PubMed2001

Treatment of childhood myopia with atropine eyedrops and bifocal spectacles.

BACKGROUND: Animal and human studies have suggested that muscarinic antagonists and bifocal spectacles may decrease the progression of myopia in children. The purpose of this study is to report the largest known series of patients treated simultaneously with bifocals and topical atropine. DESIGN: Retrospective, interventional, non-comparative case series. METHODS: 706 myopic children (296 boys and 410 girls, ages 6 to 16 years) were prescribed full cycloplegic spectacle corrections, with photochromic lenses and +2.25 diopter (D) reading adds in each eye. Both eyes were treated with atropine 1% drops once daily. OUTCOME MEASURES: Annual change in cycloplegic refractions of right eyes. Compliance with therapy was monitored by patient and parental report. RESULTS: 496 (70%) of the 706 patients reported full compliance with the treatment regimen, whereas the remaining 210 (30%) patients were partially compliant. The median interval of treatment was 3.62 years (range, 21 days-10.1 years). The mean rate of myopic progression was significantly less (P<0.001) in patients who were fully compliant with atropine therapy and bifocals (0.08 D/year) than in patients who were partially compliant with the treatment regimen (0.23 D/per year). No serious adverse effects were associated with atropine therapy. CONCLUSIONS: Full compliance with topical atropine therapy and bifocal spectacles was associated with decreased progression of myopia compared to partial compliance with treatment. For each of the treated groups, the mean rate of myopic progression was significantly less (P<0.05) than the mean annual rates of myopic progression published for the pediatric population.

Adolescent↗
PubMed2002

Baseline refractive and ocular component measures of children enrolled in the correction of myopia evaluation trial (COMET).

PURPOSE: To describe baseline refractive and ocular component measures in children with myopia enrolled in the Correction of Myopia Evaluation Trial (COMET). COMET is a multicenter, randomized clinical trial to evaluate whether progressive-addition lenses slow the progression of juvenile-onset myopia compared with single-vision lenses. METHODS: Four hundred sixty-nine children with myopia between -1.25 and -4.50 D spherical equivalent and without eye or systemic conditions known to affect refractive development were recruited from four geographically and ethnically diverse communities in the United States. Their ages were 6 to 11 years inclusive, and 52% were girls. The main outcome measure for the overall trial is progression of myopia determined by cycloplegic autorefraction after inducement of cycloplegia with 2 drops of 1% tropicamide. Axial length, the secondary outcome measure, was assessed by ultrasonography. The distance correction was determined by subjective methods before cycloplegia, with noncycloplegic autorefraction values as the starting point. RESULTS: Because data were similar in both eyes, they are reported for the right eye only. The mean spherical equivalent measured by cycloplegic autorefraction was -2.38 +/- 0.81 D. Young children had significantly less myopia than older children (P = 0.03), but the amount of myopia did not differ by gender or ethnicity. Mean axial dimensions were 4.0 +/- 0.2 mm (anterior chamber), 3.4 +/- 0.2 mm (lens), 16.8 +/- 0.7 mm (vitreous chamber), and 24.1 +/- 0.7 mm (axial length). Girls' eyes had significantly shorter axial length than boys' (P < 0.0001). Mean corneal radii were 7.73 +/- 0.25 mm (horizontal) and 7.59 +/- 0.24 mm (vertical). Ninety-five percent of the eyes had a ratio of axial length to corneal radius higher than 3.0. CONCLUSIONS: These baseline measures provide cross-sectional data on a large group of ethnically diverse children with myopia. Refractive and axial component dimensions are consistent with data in other studies showing that myopic eyes have longer vitreous chambers than emmetropic eyes. The measures reported herein will serve as a basis for examining changes that occur over a minimum of 3 years of follow-up of children enrolled in COMET.

Accommodation, Ocular↗
PubMed2001

[Value of the Bébé-Vision test in the screening of strabismus and anisometropic amblyopia in infants].

PURPOSE: To evaluate the accuracy of the Bébé-Vision test for detecting strabismic, ametropic and anisometropic amblyopia in childhood. METHODS: We screened 199 infants under 20 months of age. The screening consisted of a full orthoptic examination by a trained orthopist (cover test, fixation test), a forced choice preferential looking technique (Bébé-Vision test) prior to cycloplegia to test visual acuity, cycloplegic refraction by retinoscopy, and examination of the fundi. RESULTS: Fifteen infants were abnormal on orthoptic examination (clinical evidence of esotropia and/or limitation of abduction and/or amblyopia). The Bébé-Vision test demonstrated a significant interocular difference on the same side of the suspected amblyopic eye in 3 cases and on the opposite side in 3 cases, and no difference in 9 cases. The monocular Bébé-Vision test was abnormal in 51 cases and there was an abnormal cycloplegic refraction in 33 cases. Statistical analysis of these tests demonstrated a very low sensitivity (42%) and a good specificity (90%) for the Bébé-Vision test in detecting amblyopia related to refractive error. CONCLUSION: The Bébé-Vision test does not reliably reveal strabismic or anisometropic amblyopia and is not recommended as a screening test. Diagnosis should continue to be based mainly on the classical clinical methods.

Amblyopia↗