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1.
Rev. bras. oftalmol ; 82: e0043, 2023. tab, graf
Article in English | LILACS | ID: biblio-1507881

ABSTRACT

ABSTRACT LASIK is a refractive surgical procedure in which a corneal flap is created to expose the corneal stromal bed. Preoperative estimation of corneal flap thickness is necessary to calculate the percentage tissue altered in LASIK, an important quantitative risk factor for ectasia. The objective of this study was to assess flap thickness and calculate percentage tissue altered to check if unexpectedly thicker flaps and higher percentage tissue altered could pose as risk factors of ectasia. Four subjects (eight eyes) were submitted to mechanical LASIK in 2009 and 2010. Pre and postoperative clinical and tomographic data were reviewed. Mean preoperative estimated percentage tissue altered was 39.18±1.31%, which was borderline for increased ectasia risk when considering the limit of 40%. However, when considering the postoperatively measured flap thickness, the actual mean percentage tissue altered turned out to be 45.17 ± 4.13%, which was significantly higher than predicted preoperatively (p=0.002). Unexpectedly higher postoperative percentage tissue altered may be responsible for corneal ectasia after mechanical LASIK.


RESUMO A LASIK é um procedimento cirúrgico refrativo, no qual um retalho corneano é criado para expor o leito estromal corneano. A estimativa pré-operatória da espessura do retalho corneano é necessária para calcular o percentual de tecido alterado no LASIK, um importante fator de risco quantitativo para ectasia. O objetivo deste estudo foi avaliar a espessura do retalho e calcular o percentual de tecido alterado para verificar se retalhos inesperadamente mais espessos e percentuais de tecido alterado mais altos poderiam representar fatores de risco de ectasia. Quatro indivíduos (oito olhos) foram submetidos à LASIK mecânica em 2009 e 2010. Dados clínicos e tomográficos pré e pós-operatórios foram revisados. A média de percentual de tecido alterado pré-operatória estimada foi de 39,18±1,31%, limítrofe para risco aumentado de ectasia quando considerado o limite de 40%. No entanto, ao considerar a espessura do retalho medida no pós-operatório, o percentual de tecido alterado médio real foi de 45,17±4,13%, ou seja, significativamente maior do que o previsto no pré-operatório (p=0,002). O percentual de tecido alterado pós-operatóriao inesperadamente mais alto pode ser responsável pela ectasia da córnea após LASIK mecânico.


Subject(s)
Humans , Male , Female , Adult , Postoperative Complications , Surgical Flaps/pathology , Keratomileusis, Laser In Situ/adverse effects , Keratomileusis, Laser In Situ/methods , Dilatation, Pathologic/etiology , Lasers, Excimer/adverse effects , Refractive Errors , Cornea/surgery , Cornea/pathology , Corneal Topography/methods , Tomography, Optical Coherence , Dilatation, Pathologic/diagnosis , Refractive Surgical Procedures/methods , Lasers, Excimer/therapeutic use
3.
Rev. bras. oftalmol ; 79(2): 91-94, Mar.-Apr. 2020. graf
Article in Portuguese | LILACS | ID: biblio-1137941

ABSTRACT

Resumo Objetivos: Avaliar a satisfação dos pacientes submetidos à cirurgia de Presbilasik central e determinar a prevalência de sintomas relatados após a cirurgia. Métodos: Este é um estudo descritivo, observacional, transversal, com dados obtidos de pacientes submetidos previamente ao PresbiLASIK. Resultados: A amostra consistiu de 45 pacientes, com média de idade de 57,7 (±7,19) anos. A nota média atribuída para a satisfação visual com o procedimento foi 8.9 (±1.0). A qualidade visual após a cirurgia foi classificada como igual ou melhor que a esperada por 84,5% dos pacientes e 31% apresentaram sintomas noturnos, como halos e raios de cometa. Conclusão: A qualidade de visão após o procedimento de PresbiLASIK foi altamente satisfatória para os pacientes. Fator determinante dessa satisfação é o processo de manejo das expectativas pré-operatórias dos pacientes, informando das possibilidades terapêuticas disponíveis, e, no caso da escolha cirúrgica, acerca das vantagens e limitações.


Abstract Objectives: Toassess the satisfaction of patients undergoing central Presbilasik surgery and to determine the age of patients who undergo PresbiLASIK and the prevalence of symptoms reported after surgery. Methods: This is a descriptive, observational, cross-sectional study with data collected from patients previously submitted to PresbiLASIK. Results: The sample consisted of 45 patients, with a mean age of 57.7 (±7,19) years. The average score attributed to visual satisfaction with the procedure was 8.9 (±1.0). Visual quality after surgery was classified as equal to or better than expected by 84.5% of the patients and 31% complained of nocturnal symptoms such as halos and comet rays. Conclusion: The quality of vision after the PresbiLASIK procedure was highly satisfactory for the patients. A determining factor for this satisfaction is the process of managing patients' preoperative expectations, informing them about the therapeutic possibilities available, and, in the case of surgical choice, about its advantages and limitations.


Subject(s)
Humans , Middle Aged , Presbyopia/surgery , Presbyopia/epidemiology , Patient Satisfaction , Keratomileusis, Laser In Situ/methods , Epidemiology, Descriptive , Cross-Sectional Studies , Evaluation Studies as Topic , Observational Study
4.
Arq. bras. oftalmol ; Arq. bras. oftalmol;83(1): 76-81, Jan.-Feb. 2020. tab, graf
Article in English | LILACS | ID: biblio-1088947

ABSTRACT

ABSTRACT The point of centration for refractive surgery is a theme of great importance that generates considerable discussion among specialists and surgeons in the field. Notably, any changes in light can alter the size of the pupil, and the visual axis of the fixation line to the fovea is unique in each patient. A variety of options have been described in the literature with respect to centration in refractive surgery, and the results differ among these methods. No consensus has been established regarding the ideal refractive surgery technique for evaluation of centration in each patient that will yield a satisfactory surgical result.


RESUMO O ponto de centralização da cirurgia refrativa é tema de grande importância e gera muita discussão entre especialistas e cirurgiões da área. Afinal, qualquer alteração na luz pode alterar o tamanho da pupila, além disso, o eixo visual da linha de fixação para a fóvea é particular em cada paciente. Existem opções para centralização em cirurgia refrativa com resultados diferentes na literatura. Ainda não há consenso sobre a melhor técnica em cirurgia refrativa que avalie cada caso específico visando um resultado cirúrgico final satisfatório.


Subject(s)
Humans , Pupil/physiology , Cornea/surgery , Keratomileusis, Laser In Situ/methods , Lasers, Excimer , Refraction, Ocular , Cornea/pathology , Fixation, Ocular
5.
Egyptian Journal of Hospital Medicine [The]. 2018; 71 (2): 2470-2476
in English | IMEMR | ID: emr-192485

ABSTRACT

Background: laser in situ keratomileusis [LASIK] has become the most widely used form of refractive surgery. The objective of this surgical technique was to modify the anterior corneal shape by ablating tissue from the stroma by means of the excimer laser after creating a hinged corneal flap. By this way, we were able to change the refractive status of the patient and provided better unaided vision. Continuous improvements in the original technique made the surgical procedure safer, more accurate and repeatable. These progressions are due to the development of novel technologies that are responsible for new surgical instrumentation, which makes the surgical procedure easier for the surgeon and better excimer laser ablation algorithms, which increase the optical quality of the ablation and thus the safety of the vision correction procedure


Aim of work: the aim of this study was to compare between Q value based ablation and topography-guided LASIK as regards safety, visual acuity, contrast sensitivity and high order aberration HOAs [spherical, coma and trefoil]


Patients and methods: this study was conducted on 60 eyes of 30 patients, thirty eyes of them underwent topography guided LASIK and the other 30 underwent Q value based ablation. Preoperative CDVA [corrected distant visual acuity] was done. Postoperative UDVA and CDVA were measured. Postoperative high order aberrations were measured 3 months postoperatively


Results: our results showed that there was no statistically significant difference between both groups as regards UDVA, spherical equivalent, high order aberrations and Strehl ratio point spread function


Conclusion: topographic guided ablation and Q value based groups provided essentially equivalent outcomes after myopic LASIK, with statistically insignificant difference between both profiles, although both laser profiles have been found to be effective, safe and predictable


Recommendations: we recommended doing more research regarding this study with larger number of cases and doing further investigations


Subject(s)
Humans , Keratomileusis, Laser In Situ/methods , Refractive Surgical Procedures , Corneal Topography
6.
Rev. bras. oftalmol ; 76(4): 190-193, July-Aug. 2017. graf
Article in Portuguese | LILACS | ID: biblio-899078

ABSTRACT

Resumo Objetivo: Monovisão é um conceito que descreve a correção propositadamente desigual da visão de em um olho para longe e outro olho para perto, sendo utilizada principalmente para correção da presbiopia. O objetivo principal foi avaliar a satisfação dos pacientes com a cirurgia refrativa de monovisão avançada. Os objetivos secundários foram avaliar a necessidade de uso de óculos após a cirurgia, e analise do perfil dos participantes. Métodos: Foi realizado um estudo transversal observacional de série de casos baseado na revisão de prontuários de participantes submetidos a cirurgia refrativa de monovisão em uma clínica oftalmológica privada. A população estudada foi do tipo não-probabilistica com n de 50 participantes. A amostragem foi por conveniência, sendo selecionados os prontuários dos últimos 50 participantes que retornaram para consulta de revisão após a cirurgia refrativa realizada até novembro de 2016. Resultados: Foram analisados 50 prontuários. Quando questionados sobre a satisfação com o procedimento, a nota média atribuída foi 9,4 ± 0,6 dentro de uma escala de 0 a 10. Sobre a necessidade do uso de óculos após o procedimento, 92% dos pacientes referiram não necessitar. Os demais 8% que referiram utilizar eventualmente óculos para perto eram hipermetropes antes da cirurgia Conclusão: Concluímos que o índice de satisfação com a cirurgia de monovisão na amostra estudada foi alto e a maioria dos participantes referiu não necessitar de óculos após o procedimento. A amostra foi composta majoritariamente por mulheres com média de idade de 52 anos, hipermetropes, que realizaram a cirurgia em ambos os olhos. Nossa amostra foi distinta de outros estudos devido ao fato de incluirmos maior parte de participantes hipermetropes.


Abstract Objective: Monovision is a concept that describes the purposely unequal correction of vision from one eye to the other and eye to eye, and is mainly used to correct presbyopia. The main objective was to evaluate patients' satisfaction with advanced monovision refractive surgery. The secondary objectives were to evaluate the need for glasses after surgery, and to analyze the profile of the participants. Methods: A cross-sectional observational study of a series of cases was carried out based on the review of medical records of participants submitted to refractive surgery of monovision in a private ophthalmologic clinic. The population studied was of the non-probabilistic type with n of 50 participants. Sampling was for convenience, and the medical records of the last 50 participants who returned for revision consultation after refractive surgery performed until November 2016 were selected. Results: Fifty patients were analyzed. When questioned about satisfaction with the procedure, the mean score assigned was 9.4 ± 0.6 on a scale of 0 to 10. Regarding the need for glasses after the procedure, 92% of the patients reported not needing it. Conclusion: We concluded that the satisfaction index with monovision surgery in the sample studied was high and most of the participants reported that they did not require glasses after the procedure. The sample consisted mainly of women with mean age of 52 years, hypermetropes, who underwent surgery in both eyes. Our sample was different from other studies due to the fact that we included most participants with hypermetropes.


Subject(s)
Humans , Male , Female , Middle Aged , Presbyopia/surgery , Vision, Monocular , Patient Satisfaction , Refractive Surgical Procedures/methods , Presbyopia/diagnosis , Refraction, Ocular , Refractive Errors , Cross-Sectional Studies , Corneal Topography/instrumentation , Keratomileusis, Laser In Situ/methods , Eyeglasses , Lasers, Excimer/therapeutic use , Observational Study , Hyperopia/surgery
7.
Arq. bras. oftalmol ; Arq. bras. oftalmol;80(1): 52-56, Jan.-Feb. 2017. tab, graf
Article in English | LILACS | ID: biblio-838776

ABSTRACT

ABSTRACT We describe a case of late-onset remarkable depigmentation of a small aperture corneal inlay implanted for presbyopia compensation. The patient was a participant in a clinical trial designed to evaluate the safety and efficacy of the AcuFocusTM ACU-10R160, which is a 10 µm-thick polyimide film tinted with an organic dye. Inlay implantation occurred under mechanical microkeratome Lasik flaps set for a depth of 120 µm. The patient returned to the clinic 11 years after surgery and reported loss of near-vision acuity. Clinical examination showed the complete absence of pigments in the device and the total loss of the initial effect on near vision, despite normal distance vision. Manifest refraction remained stable during the follow-up period. Scheimpflug images characterized the loss of the small aperture effect on incoming light. Confocal analysis revealed small hyper-reflective round images on the endothelium and no signs of inflammation.


RESUMO Descrevemos um caso de importante despigmentação de início tardio de implante corneano de pequena abertura implantada para compensação de presbiopia. O paciente foi um dos participantes de ensaio clínico destinado a avaliar a segurança e eficácia do AcuFocusTM ACU-10R160, uma película de poliimida de 10 microns de espessura, tingida com um corante orgânico. A implantação ocorreu sob um flap de Lasik criado por microcerátomo mecânico ajustado para profundidade de 120 µm. O caso aqui descrito foi avaliado 11 anos após a cirurgia, relatando diminuição de acuidade de visão para perto. O exame clínico mostrou ausência total de pigmentos no dispositivo e perda total do efeito inicial na visão de perto, apesar da visão normal para distância. A refração manifesta permaneceu estável durante o período de seguimento. As imagens de Scheimpflug caracterizaram a perda do efeito da abertura pequena na luz entrante. A análise de microscopia confocal revelou pequenas imagens hiper-reflexivas redondas sobre o endotélio, sem sinais de inflamação.


Subject(s)
Humans , Female , Aged , Presbyopia/surgery , Prostheses and Implants , Corneal Stroma/surgery , Prosthesis Implantation/instrumentation , Keratomileusis, Laser In Situ/instrumentation , Refraction, Ocular , Surgical Flaps , Visual Acuity , Prosthesis Implantation/methods , Keratomileusis, Laser In Situ/methods
8.
Rev. bras. oftalmol ; 75(4): 333-335, July-Aug. 2016. graf
Article in Portuguese | LILACS | ID: lil-794865

ABSTRACT

RESUMO O DSAEK (Descemet stripping automated endotelial Keratoplasty) é um dos procedimentos de escolha para tratamento das doenças que acometem o endotélio corneano. Apesar do sucesso terapêutico, o procedimento pode induzir uma hipermetropia residual. Em média a refração se estabiliza em um perído que varia de 6 a 12 meses após o transplante. O objetivo desse relato é descrever a evolução dessa opção terapêutica utilizada em um paciente de 54 anos portador de Distrofia de Fuchs. O paciente foi submetido ao transplante de córnea (DSAEK) e a remoção do cristalino no mesmo tempo cirúrgico o que resultou em hipermetropia residual. Após 3 anos de acompanhamento apresentava-se com a melhor visão corrigida de 20/20 (Snellen) no olho operado com uma refração de +3,25 -1,00 (5º). Optou-se por realização de LASIK (Laser assisted in situ Keratomileusis) hipermetrópico, obtendo um resultado visual satisfatório.


ABSTRACT DSAEK (Descemet stripping automated endothelial keratoplasty) is one of the options for corneal endothelium disease, which in some patients can result in a residual hyperopia after the procedure. Usually 6 to 12 months after corneal transplantation refraction is already stable. This report describes a therapeutic option used in a 54 years old patient with Fuchs' endothelial dystrophy submitted to cataract and corneal transplant that resulted in residual hyperopia, three years after the procedure the best corrected vision was 20/20 with a refraction of +3.25 -1.00 (5 º) treated with Hyperopic - LASIK (Laser-assisted In Situ Keratomileusis) with satisfactory visual result.


Subject(s)
Humans , Male , Middle Aged , Keratomileusis, Laser In Situ/methods , Descemet Stripping Endothelial Keratoplasty/adverse effects , Hyperopia/surgery , Hyperopia/etiology , Fuchs' Endothelial Dystrophy/surgery , Phacoemulsification/methods , Lens Implantation, Intraocular/methods , Tomography, Optical Coherence , Descemet Stripping Endothelial Keratoplasty/methods , Hyperopia/diagnosis
9.
Rev. cuba. med. mil ; 44(4): 379-388, oct.-dic. 2015. tab
Article in Spanish | LILACS, CUMED | ID: lil-777055

ABSTRACT

INTRODUCCIÓN: la queratomielusis es un procedimiento quirúrgico de valor en el tratamiento de las ametropías. OBJETIVO: determinar los resultados de la queratomileusis "in situ" asistida por láser de excímeros (LASIK) en la corrección del astigmatismo miópico. MÉTODOS: se realizó un estudio retrospectivo de 73 pacientes con astigmatismo miópico, operados con la técnica LASIK durante el año 2013 en el Hospital Militar "Dr. Carlos J. Finlay". Las variables fueron: edad, sexo, agudeza visual con corrección pre y postoperatorias, equivalente esférico, complicaciones trans-operatorias, postoperatorias inmediatas y tardías. Para el procesamiento de la información se utilizó programa SPSS. RESULTADOS: se mantuvo la agudeza visual previa corregida y no se detectaron complicaciones graves o irreversibles. Se observaron cambios significativos en las variables estudiadas con tendencia a la emetropía para un 92,3 %. CONCLUSIÓN: LASIK es una técnica segura y útil para la corrección del astigmatismo miópico, que permite mejorar la agudeza visual.


OBJETIVE: to determinate the results of Excímer laser assisted "in situ" keratomileusis (LASIK)in the correction of myopic astigmatism. METHODS: a descriptive, retrospective study of the results was performed after surgery LASIK in 73 patients with myopic astigmatism. The variables were: age, sex, pre and postoperative visual acuity without correction, spherical equivalent, intraoperative complications, postoperative immediate and late complications. Significant changes were observed in all the variables studied tending to emmetropia and 92.3 %. RESULTS: with the use of this surgical technique the corrected previous visual acuity remained and not serious or irreversible complications were detected. CONCLUSIONS: Lasik is a safe and useful technique for the correction of myopic astigmatism that improves visual acuity.


Subject(s)
Humans , Astigmatism/surgery , Electronic Data Processing/statistics & numerical data , Visual Acuity , Keratomileusis, Laser In Situ/methods , Emmetropia , Retrospective Studies
10.
Rev. bras. oftalmol ; 73(5): 273-278, Sep-Oct/2014. tab, graf
Article in Portuguese | LILACS | ID: lil-741903

ABSTRACT

Objetivo: Analisar a secreção lacrimal, coloração da superfície ocular e estabilidade do filme lacrimal em indivíduos submetidos à cirurgia de PRK e LASIK com laser de femtossegundo (femto LASIK). Métodos: Vinte olhos de 10 pacientes submetidos à técnica de Femto LASIK e 11 olhos de 6 pacientes submetidos à técnica de PRK foram estudados de forma prospectiva, longitudinal e intervencionista. Tempo de rotura do filme lacrimal (TRFL), teste de Schirmer basal e coloração da superfície ocular com lissamina verde foram analisados no pré-operatório (pré), no 15º e no 30º dia pós-operatório (15º pós e 30º pós, respectivamente). Resultados: Agrupando todos os olhos, observou-se que o TRFL reduziu-se de forma estatisticamente significante no 15º pós em relação ao valor pré-operatório (p=0,025), mantendo-se reduzido no 30º pós (p= 0,001); não houve diferença estatisticamente significativa entre o 15º pós e o 30º pós (p=0,219). No teste da lissamina verde, houve aumento significativo desse escore, no 15º pós em relação ao período pré-operatório (p=0,021), havendo, posteriormente, redução no 30º pós (p=0,010). No teste de Schirmer basal, não foi detectada mudança estatisticamente significante ao longo dos três momentos (p=0,107). Comparando-se os testes TRFL, lissamina verde ou Schirmer basal, nos dois grupos estudados (PRK e LASIK), não houve diferença estatisticamente significante em nenhum dos três momentos (pré, 15º pós e 30º pós). Conclusão: Evidenciou-se alteração do filme lacrimal nos pacientes submetidos à cirurgia refrativa, quando foram utilizados os testes de TRFL e lissamina verde. Nas duas técnicas empregadas, não houve diferença estatisticamente significante de alteração do filme lacrimal, quando comparadas entre si (PRK e LASIK). .


Purpose: To evaluate tear film stability, ocular surface staining and tear secretion in patients undergoing PRK and femtosecond laser LASIK. Methods: Twenty eyes of 10 patients submitted to femtosecond laser LASIK and 11 eyes of the 6 patients submitted do PRK underwent tear film break-up time (TBUT), Schirmer’s basal and lissamine green staining measurements pre and postoperatively on days 15 (PO 15) and 30 (PO 30). Results: When grouping all eyes TBUT was reduced on PO 15 (p=0.025) and on PO 30 (p=0.001) compared to preoperative values. No difference was found between PO 15 and PO 30 (p=0.219). Compared to preoperative measurements, lissamine green test demonstrated a significant increase in score on PO 15 (p=0.021) and a significant reduction on PO 30 (p=0.010), when both groups were analyzed together (all 42 eyes). No changes in Schirmer’s basal test were detected in all 3 time periods (p=0.107). TBUT, lissamine green and Schirmer’s basal measurements were no different in all 3 time periods when both groups (PRK and femtosecond laser LASIK) were compared. Conclusion: TBUT and lissamine green measurements were altered after refractive surgery regardless the technique (PRK or femtosecond laser LASIK). When comparing one technique to the other, no difference was found in all measurements. .


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Tears/metabolism , Dry Eye Syndromes/diagnosis , Dry Eye Syndromes/etiology , Photorefractive Keratectomy/adverse effects , Keratomileusis, Laser In Situ/adverse effects , Lacrimal Apparatus/metabolism , Osmolar Concentration , Postoperative Complications , Staining and Labeling/methods , Surface Tension , Prospective Studies , Longitudinal Studies , Photorefractive Keratectomy/methods , Fluorescein/administration & dosage , Keratomileusis, Laser In Situ/methods , Lasers, Excimer/therapeutic use , Fluorescent Dyes/administration & dosage , Lissamine Green Dyes/administration & dosage
11.
Arq. bras. oftalmol ; Arq. bras. oftalmol;77(3): 159-163, May-Jun/2014. tab, graf
Article in English | LILACS | ID: lil-723831

ABSTRACT

Purpose: To assess the reliability and reproducibility of static cyclotorsion correction (SCC) measurements made using the Schwind Amaris Excimer laser in patients undergoing LASIK or PRK, and compare the outcomes of treating astigmatism with and without SCC. Methods: Eighty eyes of 40 patients were included in this study. All eyes underwent 2 or 3 sets of five measurements: before and after speculum placement, and after flap-lift (in LASIK cases). We assessed the reproducibility, accuracy, and the percentage of "no catch" measurements. The astigmatism was calculated pre-and 3-months-postoperatively by vector analysis. Results: The mean age of the patients was 23.67 ± 4.19 years. Preoperative spherical equivalent and astigmatism were -2.56 ± 2.86 D and +1.36 ± 0.98 D, respectively. The mean measurement time was 15.1 seconds per measurement. The percentages of "no catch" were: 63.8%, 14.9%, and 26.9%; pre-speculum, post-speculum, and post flap-lift, respectively. Cyclotorsion of ≥±2º was seen in 41.25% and 66% of the cases before and after the flap-lift, respectively. Significant cyclotorsion (≥±5º) was seen in 12.50% and 18% of the eyes pre and post flap-lift. The mean astigmatism dropped from +1.53 D@1º to +0.34D@3º when SCC was used and from +1.86D@1º to +0.23D@7º when SCC was not used. No statistical difference was noticed between the groups (p>0.05) in the postoperative residual astigmatism. A postoperative astigmatism of ≥1 D was seen in 10% and 20% of eyes with and without SCC, respectively (p<0.01). Conclusion: Although not always feasible, the SCC measurement is a simple and useful tool. Postoperative astigmatism showed less variability when SCC was used. .


Objetivo: Avaliar a confiabilidade e reprodutibilidade da correção da medida de ciclotorção estática (SCC), realizada com o excimer laser Schwind Amaris em pacientes submetidos a LASIK ou PRK, e comparar os resultados do tratamento de astigmatismo com e sem SCC. Método: Oitenta olhos (40 pacientes). Todos os olhos foram submetidos a 2 ou 3 séries de 5 medições: antes e após a colocação do espéculo, e depois do levantamento do flap (nos casos de LASIK). Foram avaliadas a reprodutibilidade, a precisão e a porcentagem de medições "não obtidas". O astigmatismo foi avaliado no pré-operatório e aos 3 meses de pós-operatório, por meio de análise vetorial. Resultados: A idade foi 23,67 ± 4,19 anos. O equivalente esférico e o astigmatismo pré-operatórios foram -2,56 ± 2,86 D, e 1,36 ± 0,98 D, respectivamente. O tempo de medição médio foi 15,1 segundos por medição; as porcentagens de medidas "não obtidas" foram: 63,8%, 14,9% e 26,9%; pré, pós-espéculo, e pós-levantamento do flap, respectivamente. Ciclotorção ≥±2º foi observada em 41,25% e 66 % dos casos pré e pós-levantamento do flap. Ciclotorção significativa (≥±5º) foi observada em 12,50% e 18% pré e pós-levantamento do flap. A média do astigmatismo diminuiu de 1,53D @ 1º para 0,34D @ 3º quando SCC foi usado e de 1,86D @ 1º a 0,23D @7º quando SCC não foi usado. O astigmatismo residual pós-operatório não foi estatisticamente diferente entre os grupos (p>0,05). O astigmatismo pós-operatório ≥1D foi observado em 10% e 20 % dos olhos com e sem SCC, respectivamente (p<0,01). Conclusão: A medição do SCC é fácil e útil, apesar de nem sempre ...


Subject(s)
Adult , Female , Humans , Male , Young Adult , Astigmatism/physiopathology , Astigmatism/surgery , Keratomileusis, Laser In Situ/methods , Lasers, Excimer/therapeutic use , Torsion Abnormality/physiopathology , Torsion Abnormality/surgery , Cornea/surgery , Lasers, Excimer , Patient Positioning , Prospective Studies , Reproducibility of Results , Surgical Flaps , Time Factors , Treatment Outcome , Visual Acuity
12.
Article in English | WPRIM | ID: wpr-76250

ABSTRACT

PURPOSE: To determine effectiveness of laser-assisted in situ keratomileusis (LASIK) in the treatment of astigmatism following penetrating keratoplasty (PK). METHODS: We performed a retrospective review of medical records of patients who underwent LASIK following PK and had over 1 year of follow-up data. RESULTS: Twenty-six patients (26 pairs of eyes) underwent LASIK following PK. Mean age of the patients at the time of LASIK was 40.7 years (range, 26 to 72 years). Following LASIK, the mean cylinder was reduced by 2.4 diopters and mean reduction of cylinder after LASIK was 65.4% from the preoperative values at the last follow-up visit. Uncorrected visual acuity became 20 / 50 or better in 69.2% of the eyes after LASIK. Best-corrected visual acuity became 20 / 50 or better in 73.1% of the eyes after LASIK. All of them were intolerable to contact lenses before LASIK. After LASIK, 6 pairs (23.1%) did not need to use contact lenses and 18 pairs (69.2%) were tolerable to using contact lenses or spectacles. There were no significant endothelial cell density changes 12 months after LASIK (p = 0.239). CONCLUSIONS: LASIK is effective in the treatment of astigmatism following PK and increases contact lens and spectacle tolerance.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Astigmatism/etiology , Contact Lenses/statistics & numerical data , Corneal Topography , Keratomileusis, Laser In Situ/methods , Keratoplasty, Penetrating/adverse effects , Lasers, Excimer/therapeutic use , Refraction, Ocular/physiology , Retrospective Studies , Vision, Binocular/physiology , Visual Acuity/physiology
13.
Article in English | WPRIM | ID: wpr-147473

ABSTRACT

PURPOSE: To investigate the effect of macrophage migration inhibitory factor (MIF) on corneal sensitivity after laser in situ keratomileusis (LASIK) surgery. METHODS: New Zealand white rabbits were used in this study. A hinged corneal flap (160-microm thick) was created with a microkeratome, and -3.0 diopter excimer laser ablation was performed. Expressions of MIF mRNA in the corneal epithelial cells and surrounding inflammatory cells were analyzed using reverse transcription polymerase chain reaction at 48 hours after LASIK. After LASIK surgery, the rabbits were topically given either 1) a balanced salt solution (BSS), 2) MIF (100 ng/mL) alone, or 3) a combination of nerve growth factor (NGF, 100 ug/mL), neurotrophine-3 (NT-3, 100 ng/mL), interleukin-6 (IL-6, 5 ng/mL), and leukemia inhibitory factor (LIF, 5 ng/mL) four times a day for three days. Preoperative and postoperative corneal sensitivity at two weeks and at 10 weeks were assessed using the Cochet-Bonnet esthesiometer. RESULTS: Expression of MIF mRNA was 2.5-fold upregulated in the corneal epithelium and 1.5-fold upregulated in the surrounding inflammatory cells as compared with the control eyes. Preoperative baseline corneal sensitivity was 40.56 +/- 2.36 mm. At two weeks after LASIK, corneal sensitivity was 9.17 +/- 5.57 mm in the BSS treated group, 21.92 +/- 2.44 mm in the MIF treated group, and 22.42 +/- 1.59 mm in the neuronal growth factors-treated group (MIF vs. BSS, p < 0.0001; neuronal growth factors vs. BSS, p < 0.0001; MIF vs. neuronal growth factors, p = 0.815). At 10 weeks after LASIK, corneal sensitivity was 15.00 +/- 9.65, 35.00 +/- 5.48, and 29.58 +/- 4.31 mm respectively (MIF vs. BSS, p = 0.0001; neuronal growth factors vs. BSS, p = 0.002; MIF vs. neuronal growth factors, p = 0.192). Treatment with MIF alone could achieve as much of an effect on recovery of corneal sensation as treatment with combination of NGF, NT-3, IL-6, and LIF. CONCLUSIONS: Topically administered MIF plays a significant role in the early recovery of corneal sensitivity after LASIK in the experimental animal model.


Subject(s)
Animals , Female , Humans , Rabbits , Epithelium, Corneal/drug effects , Interleukin-6/pharmacology , Keratomileusis, Laser In Situ/methods , Leukemia Inhibitory Factor/pharmacology , Macrophage Migration-Inhibitory Factors/genetics , Models, Animal , Nerve Growth Factor/pharmacology , Nerve Regeneration/drug effects , Neurotrophin 3/pharmacology , RNA, Messenger/metabolism , Recovery of Function/drug effects , Sensation/drug effects
14.
Arq. bras. oftalmol ; Arq. bras. oftalmol;76(6): 335-338, nov.-dez. 2013. graf, tab
Article in Portuguese | LILACS | ID: lil-701281

ABSTRACT

OBJETIVO: Avaliar comparativamente os resultados cirúrgicos, na técnica LASIK, realizando com laser de femtosegundo e microcerátomo mecânico. MÉTODOS: Estudo clínico, prospectivo, comparativo, randomizado e mascarado de 32 olhos (16 pacientes). Cada paciente foi submetido a diferentes técnicas para o LASIK, em um dos olhos foi utilizado o microcerátomo HansatomeTM Bausch & Lomb (grupo microcerátomo) e no outro foi utilizado femtosegundo FEMTO LDV TM Ziemer (grupo femtosegundo). A triagem ocorreu no setor de Cirurgia Refrativa do Hospital de Olhos do Paraná entre 07/2010 e 09/2010. Os critérios de inclusão foram miopia menor que 6,00 D, astigmatismo menor que 3,00 D, menor que 5,00 D de hipermetropia, refração estável, diâmetro corneano menor que 11 mm, descontinuação de lente de contato sete dias antes da avaliação pré-operatória, acuidade visual de no mínimo 20/20 em ambos os olhos. As variáveis analisadas no pré-operatório entre os grupos, femtosegundo e microcerátomo foram: acuidade visual sem correção e com correção, equivalente esférico, aberrações totais de alta ordem, acuidade visual de baixo contraste, preferência do paciente e complicações. RESULTADOS: Todas as variáveis estudadas foram similares nos dois grupos. CONCLUSÃO: Não foi possível observar neste estudo, diferenças significativas entre os grupos analisados.


PURPOSE: To assess LASIK flaps made by femtosecond laser and mechanical microkeratome. METHODS: Clinical, prospective, randomized, masked study of 32 eyes (16 patients). Both eyes of all patients were operated, each patient underwent different techniques for lasik. Microkeratome HansatomeTMBausch & Lomb (group microkeratome) was used in one eye and femtosecond laser Femto LDVTMZiemer (group femtosecond) was used for the fellow eye. Patients were selected from the Refractive Surgery service of the Eye Hospital of Paraná between July 2010 and September 2010. Inclusion criteria were myopia less than 6.00 D, astigmatism less than 3.00 D, hyperopia less than 5.00 D, stable refraction over one year, corneal diameter smaller than 11 mm, discontinuation of contact lenses seven days before the preoperative evaluation, corrected visual acuity of at least 20/20. Eyes were randomly allocated for each technique. The studied variables were: visual acuity with and without correction, residual refractive error, high order aberrations, low contrast visual acuity, complications and subjective patient preference. RESULTS: All studied variables were similar between the two groups. CONCLUSION: We could not demonstrate any difference between the studied groups.


Subject(s)
Humans , Keratomileusis, Laser In Situ/methods , Lasers, Excimer/therapeutic use , Myopia/surgery , Surgical Flaps/surgery , Contrast Sensitivity , Cornea/surgery , Corneal Stroma/surgery , Keratomileusis, Laser In Situ/instrumentation , Postoperative Period , Prospective Studies , Statistics, Nonparametric , Time Factors , Treatment Outcome , Visual Acuity
15.
Arq. bras. oftalmol ; Arq. bras. oftalmol;76(5): 270-273, set.-out. 2013. ilus
Article in English | LILACS | ID: lil-690602

ABSTRACT

PURPOSE: The present study aimed to compare the postoperative contrast sensitivity functions between wavefront-guided LASIK eyes and their contralateral wavefront-guided PRK eyes. METHODS: The participants were 11 healthy subjects (mean age=32.4 ± 6.2 years) who had myopic astigmatism. The spatial contrast sensitivity functions were measured before and three times after the surgery. Psycho and a Cambridge graphic board (VSG 2/4) were used to measure luminance, red-green, and blue-yellow spatial contrast sensitivity functions (from 0.85 to 13.1 cycles/degree). Longitudinal analysis and comparison between surgeries were performed. RESULTS: There was no significant contrast sensitivity change during the one-year follow-up measurements neither for LASIK nor for PRK eyes. The comparison between procedures showed no differences at 12 months postoperative. CONCLUSIONS: The present data showed similar contrast sensitivities during one-year follow-up of wave-front guided refractive surgeries. Moreover, one year postoperative data showed no differences in the effects of either wavefront-guided LASIK or wavefront-guided PRK on the luminance and chromatic spatial contrast sensitivity functions.


OBJETIVO: A proposta do presente estudo é comparar funções de sensibilidade ao contraste obtidas após wavefront-LASIK e wavefront-PRK no olho contralateral. MÉTODOS: Os participantes foram 11 sujeitos saudáveis (idade média=32,4 ± 6,2 anos) com astigmatismo miópico. As funções de sensibilidade ao contraste espacial foram obtidas antes e três vezes após a cirurgia. O programa Psycho e uma placa gráfica da Cambridge Research Systems (VSG 2/4) permitiram gerar os estímulos com contraste espacial de luminância e cromático (verde-vermelho e azul-amarelo) de 0,85 até 13,1 ciclos/grau. Análises longitudinais e comparações entre as cirurgias foram realizadas. RESULTADOS: Não houve mudança significativa da sensibilidade ao contraste durante o primeiro ano após a cirurgia para o olho que recebeu o LASIK ou para o olho que recebeu o PRK. A comparação entre as cirurgias também foi semelhante no pós-operatório de um ano. CONCLUSÕES: Os resultados apresentados mostraram sensibilidade ao contraste semelhante durante o primeiro ano após a cirurgia refrativa com o wavefront. Além disso, no pós-operatório de um ano não houve diferença nas funções de sensibilidade ao contraste de luminância e cromático entre os olhos que receberam LASIK e os que receberam PRK.


Subject(s)
Adult , Female , Humans , Male , Astigmatism/surgery , Contrast Sensitivity/physiology , Keratomileusis, Laser In Situ/methods , Myopia/surgery , Photorefractive Keratectomy/methods , Light , Prospective Studies , Refractive Surgical Procedures/methods , Treatment Outcome
16.
Rev. bras. oftalmol ; 72(4): 219-222, jul.-ago. 2013. ilus
Article in Portuguese | LILACS | ID: lil-690255

ABSTRACT

Objetivo: Comparar as técnicas de PRK e Epi-LASIK com relação à recuperação visual e sintomatologia pós-operatória. Métodos: Série de casos intervencionista que incluiu 38 olhos de 19 pacientes com miopia até 5DE e astigmatismo até 1DC. Foram selecionados pacientes com erros refracionais semelhantes nos dois olhos, realizando-se, no mesmo tempo cirúrgico, PRK em um olho e Epi-LASIK no olho contralateral. Os pacientes foram acompanhados por um ano, avaliando-se a eficácia refracional e grau de desconforto pós-operatório. Resultados: Durante as primeiras 12 horas, 79,9% dos pacientes (p=0,0003) referiram dor mais intensa no olho operado com a técnica Epi-LASIK. Após 24 horas, 63,2% dos pacientes (p=0,012) ainda referiam mais dor neste olho e apenas 10,5% no olho contralateral. A acuidade visual não corrigida foi melhor nos olhos do grupo PRK no primeiro dia (p=0,034). Nos demais dias não houve diferença significativa entre os grupos. Houveopacidade corneana grau 0,5 (Fantes) em três olhos do grupo PRK e em dois no grupo Epi-LASIK. Conclusão: Ambos os grupos apresentaram resultado visual refracional satisfatório, porém o grupo Epi-LASIK apresentou maior desconforto no pós-operatório imediato.


Objective: Compare PRK and Epi-LASIK techniques regarding postoperative visual recovery and symptoms. Methods: Interventional case series study including 38 eyes of 19 patients with myopia up to 5DE and astigmatism up to 1DC. Study included patients with similar refractive errors to be submitted to PRK in one eye and Epi-LASIK in the fellow eye at the same time. Follow-up was 1 year and included refractive error analysis and postoperative discomfort. Results: During the first 12 hours after surgery, 79% (P=0,0003) of patients reported more pain and discomfort in the eye submitted to Epi-LASIK. Twenty-four hours after surgery 63,2% (P=0,012) of patients still referred more pain in the eye submitted to Epi-LASIK and only 10,5% in the contralateral eye. Uncorrected visual acuity was better on the PRK group at the 1th day (p=0.034). No difference was observed at the other postoperative days after surgery. Postoperative corneal haze 0,5 (Fantes) was observed in three eyes of the PRK group and in two days of the Epi-LASIK group. Conclusion: Both groups presented good visual refractive results, but the Epi-LASIK group presented more discomfort immediately after surgery.


Subject(s)
Humans , Male , Female , Young Adult , Astigmatism/surgery , Photorefractive Keratectomy/methods , Keratomileusis, Laser In Situ/methods , Eye Pain , Myopia/surgery , Treatment Outcome , Visual Acuity
17.
Arq. bras. oftalmol ; Arq. bras. oftalmol;76(3): 195-196, maio-jun. 2013. ilus
Article in English | LILACS | ID: lil-681856

ABSTRACT

Keratoconus has usually been described as bilateral but asymmetric disease. Corneal ectasia is one of the long-term complications of modern refractive surgery, especially those submitted to laser in situ keratomileusis (LASIK). We describe a patient with keratoconus in the right eye that was submitted to radial keratectomy (RK) in the left eye 19 years ago with no progression of the ectatic cornea and no complications related to the refractive surgery. Because unilateral keratoconus is rare, we believe that RK was performed on an already ectatic cornea (not clinically detected) or with fruste keratoconus. However, neither corneal ectasia progressed, nor ectasia was induced by RK in the fellow eye.


O ceratocone é descrito como uma doença bilateral porém assimétrica e vários dados na literatura comprovam que a ectasia corneana é uma das complicações de longo prazo da cirurgia refrativa moderna, especialmente do laser in situ keratomileusis (LASIK). Nós descrevemos um caso de uma paciente com ceratocone no olho direito e que foi submetida à ceratotomia radial no olho esquerdo há 19 anos, desde então sem sinais de progressão da ectasia corneana nem de complicações relativas à cirurgia refrativa. Como o ceratocone unilateral é raro, acreditamos que a cirurgia refrativa tenha sido realizada num olho com ectasia corneana não detectada clinicamente ou com ceratocone frustro. Entretanto, a ectasia do olho direito não progrediu e também não houve sinais de ectasia no olho submetido à cirurgia refrativa nesse período de 19 anos de acompanhamento.


Subject(s)
Adult , Female , Humans , Keratoconus/surgery , Keratomileusis, Laser In Situ/methods , Keratotomy, Radial/methods , Corneal Topography , Disease Progression , Treatment Outcome
18.
Article in English | WPRIM | ID: wpr-143915

ABSTRACT

PURPOSE: The corneal change induced by refractive procedures influence both the postoperative refractive status and the ocular spherical aberration (SA). We evaluated changes in corneal SA after three types of surface ablation: phototherapeutic keratectomy (PTK), myopic photorefractive keratectomy (PRK), and myopic wavefront-guided laser epithelial keratomileusis (LASEK). METHODS: Twenty-six eyes (25 patients) were subjected to PTK 26 eyes (14 patients) to PRK, and 34 eyes (17 patients) to wavefront-guided LASEK. Corneal SA was measured with the iTrace in all patients both preoperatively and 6 months postoperatively. RESULTS: Six months after surgery, mean corneal SA was -0.173 +/- 0.171 micrometer in the PTK group, 0.672 +/- 0.200 micrometer in the PRK group, and 0.143 +/- 0.136 micrometer in the wavefront-guided LASEK group. The mean difference between the preoperative and postoperative corneal SA (DeltaSA) was -0.475 micrometer in the PTK group, 0.402 micrometer in the PRK group, and -0.143 micrometer in the wavefront-guided LASEK group. CONCLUSIONS: Surgically induced changes in corneal SA vary with procedure. The prediction of the pattern of SA change induced by various surface ablation procedures may be helpful for developing future surgical procedures.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Corneal Dystrophies, Hereditary/surgery , Corneal Wavefront Aberration/surgery , Follow-Up Studies , Keratomileusis, Laser In Situ/methods , Myopia/surgery , Photorefractive Keratectomy/methods , Prospective Studies , Treatment Outcome
19.
Article in English | WPRIM | ID: wpr-143922

ABSTRACT

PURPOSE: The corneal change induced by refractive procedures influence both the postoperative refractive status and the ocular spherical aberration (SA). We evaluated changes in corneal SA after three types of surface ablation: phototherapeutic keratectomy (PTK), myopic photorefractive keratectomy (PRK), and myopic wavefront-guided laser epithelial keratomileusis (LASEK). METHODS: Twenty-six eyes (25 patients) were subjected to PTK 26 eyes (14 patients) to PRK, and 34 eyes (17 patients) to wavefront-guided LASEK. Corneal SA was measured with the iTrace in all patients both preoperatively and 6 months postoperatively. RESULTS: Six months after surgery, mean corneal SA was -0.173 +/- 0.171 micrometer in the PTK group, 0.672 +/- 0.200 micrometer in the PRK group, and 0.143 +/- 0.136 micrometer in the wavefront-guided LASEK group. The mean difference between the preoperative and postoperative corneal SA (DeltaSA) was -0.475 micrometer in the PTK group, 0.402 micrometer in the PRK group, and -0.143 micrometer in the wavefront-guided LASEK group. CONCLUSIONS: Surgically induced changes in corneal SA vary with procedure. The prediction of the pattern of SA change induced by various surface ablation procedures may be helpful for developing future surgical procedures.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Corneal Dystrophies, Hereditary/surgery , Corneal Wavefront Aberration/surgery , Follow-Up Studies , Keratomileusis, Laser In Situ/methods , Myopia/surgery , Photorefractive Keratectomy/methods , Prospective Studies , Treatment Outcome
20.
Rev. cuba. oftalmol ; 25(2): 218-225, oct.-dic. 2012.
Article in Spanish | LILACS | ID: lil-657926

ABSTRACT

Métodos: se realizó un estudio comparativo y prospectivo en 64 pacientes de la consulta externa del Servicio de Cirugía Refractiva del Instituto Cubano de Oftalmología Ramón Pando Ferrer. Estos fueron distribuidos aleatoriamente en dos grupos iguales para ambas técnicas. Las variables estudiadas fueron agudeza visual sin corrección y mejor corregida, aberración y sensibilidad al contraste en condiciones fotópicas...


Methods: a comparative and prospective study was conducted in 64 patients who attended the refractive surgery outpatient service of Ramon Pando Ferrer Cuban Institute of Ophthalmology. They were randomly distributed in two groups for both procedures. Several variables were studied such as: uncorrected visual acuity, best corrected visual acuity, aberration and contrast sensitivity at photopic conditions...


Subject(s)
Humans , Male , Female , Refractive Surgical Procedures/methods , Keratomileusis, Laser In Situ/adverse effects , Keratomileusis, Laser In Situ/methods , Case-Control Studies , Prospective Studies
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