César Lipener

Prevalence and causes of visual impairment in low-middle income school children in Sao Paulo, Brazil.

PURPOSE Assess prevalence and causes of vision impairment among low-middle income school children in São Paulo. METHODS Cluster sampling was used to obtain a random sample of children ages 11 to 14 years from public schools (grades 5-8) in three districts from June to November 2005. The examination included visual acuity testing, ocular motility, and examination of the external eye, anterior segment, and media. Cycloplegic refraction and fundus examination were performed in children with uncorrected visual acuity 20/40 or worse in either eye. A principal cause of visual impairment was determined for eyes with uncorrected visual acuity of 20/40 or worse. RESULTS A total of 2825 children were enumerated and 2441 (86.4%) were examined. The prevalence of uncorrected, presenting, and best-corrected visual acuity 20/40 or worse in the better eye was 4.82%, 2.67%, and 0.41%, respectively. Spectacles were used by 144 (5.9%) children. Refractive error was a cause in 76.8% of children with visual impairment in one or both eyes; amblyopia, 11.4%; retinal disorders, 5.9%; other causes, 2.7%; and unexplained causes, 7.7%. Myopic visual impairment (spherical equivalent -0.50 D in one or both eyes) was not associated with age or grade level, but female sex was marginally significant (P = 0.070). Hyperopic visual impairment (+2.00 D or more) was not associated with age, grade level, or sex. CONCLUSIONS The prevalence of reduced vision in low-middle income urban São Paulo school children was low, most of it because of uncorrected refractive error. Cost-effective strategies are needed to address this easily treated cause of vision impairment.

A randomized clinical comparison of OPTI-FREE EXPRESS and ReNu MultiPLUS multipurpose lens care solutions

ObjectiveTo evaluate subjective symptoms and clinical signs of tolerability and comfort in silicone and non-silicone hydrogel contact lens (CL) wearers using two different multipurpose solution (MPS) CL care regimens.MethodsThis was a randomized, double-masked, contralateral, crossover, multicenter (n=9) study. One hundred and eleven subjects were enrolled in the study, and were randomly assigned either silicone hydrogel CLs or non-silicone hydrogel CLs. Before wear, the CLs were randomly conditioned for at least 10 hours in a multipurpose disinfection solution (MPDS) preserved with either: Regimen 1-polyquaternium-1 0.001% and myristamidopropyl dimethylamine 0.0005% (POLYQUAD® and ALDOX®, respectively; OPTIFREE EXPRESS® MPDS, Alcon Laboratories, Inc., Fort Worth, TX, USA); or Regimen 2-multipurpose solution preserved with polyhexamethylene biguanide 0.0001% (PHMB, ReNu MultiPLUS® MPS, Bausch & Lomb, Rochester, NY, USA). The study had two in-office visits, 1 week apart. Subjects wore assigned CLs for approximately 4 hours at each visit. At each visit, subjects’ eyes were examined before CL insertion and at 2 hours and 4 hours after insertion. Corneal staining type and area, conjunctival staining, conjunctival injection, subjective symptoms (tolerability), and comfort were evaluated.ResultsOne hundred and five subjects (210 eyes) completed the study. The total corneal staining score of area and type were statistically significantly less in Regimen 1 than in Regimen 2 (P<0.000001). The area of conjunctival staining was statistically significantly less in Regimen 1 than in Regimen 2 (P=0.03). No clinically significant hyperemia was observed for either regimen. Both tolerability (P=0.02) and patient preference (P=0.05) were in favor of Regimen 1.ConclusionsStatistically significant clinical differences were evident between the two CL care regimens when used with silicone and non-silicone hydrogel CLs. OPTI-FREE EXPRESS MPDS users showed less corneal and conjunctival staining and reported greater comfort and tolerability to the CL/solution combination than ReNu MultiPLUS MPS users.

Long-term Follow-up of Orthokeratology Corneal Reshaping Using Wavefront Aberrometry and Contrast Sensitivity

Purpose. To evaluate changes in ocular wavefront aberrations and contrast sensitivity during 1-year follow-up of overnight orthokeratology. Methods. Prospective study of 26 eyes that underwent orthokeratology with the BE lens design. Wavefront measurements were analyzed at baseline and after 1, 8, 30, 90, 180, and 365 nights of orthokeratology for a 6.5-mm pupil diameter. Contrast sensitivity 1 year after orthokeratology was compared to the baseline value under photopic conditions and mesopic conditions, with and without glare, in the spatial frequencies of 1.5, 3, 6, 12, and 18 cycles/degree. A P value of less than 0.05 was statistically significant. Results. Higher-order aberration root-mean-square (HOA-RMS) increased statistically significantly from 0.41 ± 0.12 &mgr;m to 1.04 ± 0.32 &mgr;m up to night 8. Defocus (Z4) decreased until night 8 and then stabilized. Astigmatism (Z3 + Z5) did not change. There was a sevenfold increase in spherical aberration (Z12) until night 8, which subsequently remained unchanged (P<0.001). Coma (Z7 + Z8) increased until night 90 and then stabilized (P<0.001). Other Zernike modes showed stability at night 1, with the exception of quadrafoil (Z14) (P=0.048). Mesopic contrast sensitivity, with and without glare, at 18 cycles/degree, decreased but failed to reach statistical significance (P=0.922 and P=0.827, respectively). Conclusions. Most optical aberrations stabilized within the first week after beginning orthokeratology with BE lens. There was not a statistically significant reduction in contrast sensitivity 1 year after treatment.

Adaptação de lente de contato gelatinosa especial para ceratocone

PURPOSE: To evaluate the fitting and use of a soft contact lens in keratoconic patients. METHODS: Retrospective study on 80 eyes of 66 patients, fitted with a special soft contact lens for keratoconus, at the Contact Lens Section of UNIFESP and private clinics. Keratoconus was classified according to degrees of disease severity by keratometric pattern. Age, gender, diagnosis, keratometry, visual acuity, spherical equivalent (SE), base curve and clinical indication were recorded. RESULTS: Of 66 patients (80 eyes) with keratoconus the mean age was 29 years, 51.5% were men and 48.5% women. According to the groups: 15.0% were incipient, 53.7% moderate, 26.3% advanced and 5.0% were severe. The majority of the eyes of patients using contact lenses (91.25%) achieved visual acuity better than 20/40. To 88 eyes 58% were tihed with lens with spherical power (mean -5.45 diopters) and 41% with spherocylinder power (from -0.5 to -5.00 cylindrical diopters). The most frequent base curve was 7.6 in 61% of the eyes. The main reasons for this special lens fitting were due to reduced tolerance and poor fitting pattern achieved with other lenses. CONCLUSION: The special soft contact lens is useful in fitting difficult keratoconic patients by offering comfort and improving visual rehabilitation that may allow more patients to postpone the need for corneal transplant.

The use of ocular anatomical measurements using a rotating Scheimpflug camera to assist in the Esclera® scleral contact lens fitting process

PURPOSE To test for associations between Pentacam(®) derived topography variables and to evaluate the predictive power of those variables in relation to scleral contact lens (SCL) fit. SETTING Department of Ophthalmology and Visual Sciences, Federal University of São Paulo, São Paulo-SP, Brazil. DESIGN Prospective observational non-randomised, non-comparative study. METHODS Forty-seven patients (63 eyes) were indicated for the use of Esclera(®) SCL. All patients underwent Scheimpflug imaging before the initial SCL evaluation. The following parameters were measured by Pentacam: corneal elevations, thickness, density, and anterior chamber depth (ACD). Correlations between the SCL parameters and the Pentacam measurements were analysed with Pearsons correlation coefficients. A simple linear regression model was created for each lens parameter using the most-correlated Pentacam variable. RESULTS In the total group, the results show correlations between the SCL parameters and the corneal astigmatism, ACD and pentacam-measured corneal height (Hm), with p<0.001 each. In addition, an inverse correlation between the lens sagittal depth (LSD) and the anterior radii minimum was shown (p<0.001). In the keratoconus group, the results show correlations between the SCL parameters and ACD and Hm (p<0.001, each). An inverse correlation between the LSD and the total thickness corneal density average was also observed (p=0.003). CONCLUSION There was a positive correlation between the LSD and ACD, even as LD and ACD in the keratoconus group. Thus, these results suggest that certain Pentacam measurements can be good predictors of the most appropriate Esclera lens to be fitted in keratoconus patients.

Stability of wavefront aberrations during the daytime after 6 months of overnight orthokeratology corneal reshaping.

PURPOSE To evaluate the stability of wavefront aberrations during the daytime after 6 months of overnight orthokeratology corneal reshaping. METHODS A prospective study of 26 eyes using the Ultravision BE lens design during 6 months of overnight wear. Uncorrected visual acuity (UCVA), cycloplegic refraction, and wavefront aberrometry were measured at 8 AM (within 1 hour after awakening and removing lenses), 1 PM (5 to 6 hours after lens removal), and 6 PM (10 to 12 hours after lens removal). RESULTS There was no significant difference in UCVA between 8 AM, 1 PM, and 6 PM (P=.383). Spherical power from wavefront aberrometry showed significant regression from 8 AM to 1 PM (P<.001) and stabilized near zero diopters. Total root-mean-square (RMS) increased and higher order aberration RMS and defocus (Z4) decreased between 8 AM and 1 PM (P<.001) but did not change for the rest of the day (P>.001). There was no statistically significant change in astigmatism (Z3 and Z5) (P=.449) and coma (Z7 and Z8) (P=.145) between 8 AM, 1 PM, and 6 PM. Spherical aberration (Z12) showed regression throughout the day (P<.001). CONCLUSIONS After 6 months of overnight orthokeratology wear, some optical aberrations showed regression during the day. Despite no significant change in UCVA during 10 to 12 hours, there was a significant increase in defocus (Z4) within the first 5 hours after removing the orthokeratology lens and a decrease in spherical aberration (Z12) throughout the day.

Lente de contato de material híbrido em pacientes com ceratocone e astigmatismo miópico composto

PURPOSE To evaluate comfort and visual performance in relation to two different used contact lens types: hybrid material (HM) and rigid-gas-permeable (RGP), in patients with regular myopic astigmatism and with keratoconus. METHODS A randomized, double masked, prospective study of 22 patients with the diagnosis of myopic astigmatism (8 with myopic astigmatism and 14 with keratoconus) was conducted. Fifteen patients were female and 7 were male, and mean age was: 32.13 +/- 8.12 years. In one of the eyes a rigid-gas-permeable contact lens was adapted (DK 30), and in the other a hybrid material contact lens was adapted (DK 23). All patients were submitted to the following tests: measurement of comfort level by means of the analogical visual scale, tear break-up time, best corrected visual acuity with the Bailey-Lovie scale adapted for 4 meters, functional acuity contrast test (FACT) and wavefront analysis. RESULTS In relation to comfort, there was no association with the evaluated contact lens type (p=0.350). There was a variation in comfort level during the first 7 days. The visual acuity increased between the 7th and the 15th day of adaptation. Visual acuity stabilized right after this period. The visual acuity did not show differences in relation to the studied lens type. It was verified that there was no difference in the tear break-up time (p=0.989) in relation to the studied lenses type and there was a decrease in the tear break-up time (p=0.001) when we compared the measurement before the use of the lenses and 2 months after their use. There was no difference in contrast sensitivity in the used lens type and between each type and the use of glasses (p<0.047). High order aberrations decreased significantly when comparing patients with and without contact lenses, except for spherical and coma aberrations (p=0.394). CONCLUSION Comfort and visual performance when comparing hybrid material and rigid-gas-permeable contact lenses did not show any significant difference in the patients or when compared separately in regular myopic astigmatism and in keratoconus patients.

Comparação da função visual e do índice de qualidade de vida com uso de óculos ou de lente de contato progressiva

OBJETIVO: Comparar a funcao visual e a resposta dos pacientes ao indice de qualidade de vida quando estes sao corrigidos com oculos com lentes progressivas ou lente de contato progressiva. METODOS: Foram selecionados 35 pacientes presbitas, usuarios de oculos com acuidade visual igual, ou melhor, a logMAR zero (longe) e J1 (perto), para adaptarem a lente de contato Focus Progressive®. Foram comparadas medidas de acuidade visual para longe, perto e sensibilidade ao contraste com a lente de contato e com os oculos. Os resultados do questionario de avaliacao de qualidade de vida NEI VFQ-25 dos mesmos pacientes corrigidos com os oculos e com a lente de contato progressiva foram comparados, levando-se em consideracao o tipo de ametropia e a idade. RESULTADOS: A acuidade visual para longe, perto e a sensibilidade ao contraste foram significantemente piores com lente de contato progressiva do que com os oculos. As respostas do questionario nao diferiram quanto a forma de correcao quando se analisou o tipo de ametropia, entretanto foram significantemente piores com a lente de contato nos grupos miope e hipermetrope abaixo das suas respectivas medianas da idade e maiores no hipermetrope acima de sua mediana. CONCLUSAO: As funcoes visuais foram significantemente piores com a lente de contato e o tipo de ametropia nao influenciou nas respostas ao indice de qualidade de vida quanto a forma de correcao, mas sim, quanto a idade.

Ceratocone: fatores prognósticos

PURPOSE To study keratoconus disease carrier patients in an age range under the usual one and try to detect any factor which can influence in disease evolution and prognosis. METHODS Patients under 15 years old with a keratoconus diagnosis where analyzed. All of them answered a questionnaire, and were submitted to ocular examination and also computerized keratoscopy. These patients were divided into three groups and went through a contact lens test: 1) it was possible for this group to adapt to contact lenses; 2) a cornea transplant for this group was recommended; 3) for this group it was suggested that they use glasses. RESULTS Patients who had 20/40 or greater visual acuity usually did not progress to transplant in the studied period. On the other hand, patients who had 20/60 or less acuity, progress to a deep transplant very quickly. Other cases, related to a lower age range (10-15 years old) progressed to a transplant. We can observe that the cornea apex has a very unsteady location, which explains the different difficulty levels regarding adaptation to contact lenses. In all patients who had a superior out of place apex and values greater than 66 D adaptation was successful. In the central apex eyes the adaptation was easier. In the inferior apex eyes it was not possible to set a standard to indicate the person for surgery. In the eyes which were adapted to the contact lenses and whose curvature was smaller than 51.10 D there were fewer chances of evolution to a cornea transplant, on comparison with patients who had a curvature of 57.60 or even greater. CONCLUSION Patients who have curvatures greater than 57.40, acuity lower than 20/60 and are under 18 years old have more chances to evolve to a cornea transplant. When the keratocone apex is central the contact lens adaptation becomes easier.PURPOSE: To study keratoconus disease carrier patients in an age range under the usual one and try to detect any factor which can influence in disease evolution and prognosis. METHODS: Patients under 15 years old with a keratoconus diagnosis where analyzed. All of them answered a questionnaire, and were submitted to ocular examination and also computerized ceratoscopy. These patients were divided into three groups and went through a contact lens test: 1) it was possible for this group to adapt to contact lenses; 2) a cornea transplant for this group was recommended; 3) for this group it was suggested that they use glasses. RESULTS: Patients who had 20/40 or greater visual acuity usually did not progress to transplant in the studied period. On the other hand, patients who had 20/60 or less acuity, progress to a deep transplant very quickly. Other cases, related to a lower age range (10-15 years old) pregressed to a transplant. We can observe that the cornea apex has a very unsteady location, which explains the different difficulty levels regarding adaptation to contact lenses. In all patients who had a superior out of place apex and values greater than 66 D adaptation was successful. In the central apex eyes the adaptation was easier. In the inferior apex eyes it was not possible to set a standard to indicate the person for surgery. In the eyes which were adapted to the contact lenses and whose curvature was smaller than 51.10 D there were fewer chances of evolution to a cornea transplant, on comparison with patients who had a curvature of 57.60 or even greater. CONCLUSION: Patients who have curvatures greater than 57.40, acuity lower than 20/60 and are under 18 years old have more chances to evolve to a cornea transplant. When the ceratocone apex is central the contact lens adaptation becomes easier.

Adaptação de lentes de contato após cirurgia refrativa

PURPOSE: To evaluate the fitting and use of contact lens in patients submitted to refractive surgery. METHODS: This was a retrospective study in 53 patients submitted to refractive surgery who later started to use contact lens, from 1999 to 2003. The parameters were: previous ametropia, refractive surgery procedure, ametropia after surgery, postoperative spherical equivalent, postoperative keratometry, base curve of fitted contact lens, contact lens design, final visual acuity with spectacles after surgery, final visual acuity with contact lens, complications and the reason for stopping the use. The follow-up of patients ranged from 1 month to 84 months (average of 42,5 months). RESULTS: Of 53 evaluated patients, 19 patients had undergone LASIK (Laser Assisted in Situ Keratomileusis), 29 patients had undergone RK (radial keratotomy), 4 patients had undergone PRK (photorefractive keratectomy) and in one patient it was not possible to know which surgery was performed. 61.29% of the patients (57 eyes of a total of 93 eyes) were fitted with rigid gas-permeable lenses. There was an improvement of visual acuity in 60.21% of the cases (VA>20/40), with few complications. CONCLUSION: Due to the great number of performed refractive surgery, an increase in the number of patients unhappy with the postoperative result is expected, and for these patients, many times the use of contact lens is the best option. The fitting of contact lenses after refractive surgery demands knowledge, dedication and has good results principally regarding better visual acuity.