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BACKGROUND: To evaluate the optical performance and safety of a new multifocal lens with a novel optical design featuring two additional foci (or intensifiers) in patients with cataract and presbyopia. METHODS: In this single-center, non-randomized prospective observational study, 31 patients underwent implantation of the new multifocal IOL between March 2020 and November 2021 at a tertiary clinical center in Buenos Aires and Ramos Mejia, Argentina. Postoperative examinations with emphasis on uncorrected and corrected visual acuity at distance and near and at two different intermediate distances (80 cm and 60 cm) were performed during the 3 postoperative months. RESULTS: Of the 31 patients who underwent implantation of the new IOL, 30 underwent bilateral surgery (61 eyes in total). At 3 months, all 61 eyes had an uncorrected distance visual acuity (UCDVA) of at least 0.15 logMAR; 57 eyes (93%) had an uncorrected distance visual acuity (UCDVA) of 0.1 logMAR and 27 eyes (44%) had an UCDVA of 0.0 logMAR. At 80 cm, 60 eyes (98%) had an uncorrected intermediate visual acuity (UCIVA) of at least 0.1 log MAR and 48 eyes (79%) had an UCIVA of 0.0 logMAR. CONCLUSION: The new multifocal IOL with a novel optical concept (5 foci) showed a wide range of visual acuity especially at intermediate and near distances in patients undergoing cataract surgery. Uncorrected visual acuity was excellent at all tested distances, monocularly and binocularly, spectacle independence and patient satisfaction were high.

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ABSTRACT Objective To evaluate intraocular lens power calculation and postoperative refractive errors in patients with high myopia undergoing cataract surgery, comparing predicted target refraction and actual postoperative refraction measured 30 days after surgery with SRK/T formula. Methods This retrospective analysis comprised 39 eyes of 31 patients undergoing cataract surgery through phacoemulsification with in-the-bag IOL implantation. Axial length was measured by partial coherence interferometry or immersion ultrasound biometry, with measurements greater than 26 mm and preoperative myopia greater than -6.0 D Manifest refraction was performed at the 1-month postoperative visit, and the spherical equivalent was analyzed. Results After analysis of 39 eyes of 31 patients undergoing cataract surgery with a mean axial length of 30.4 (standard deviation of 2.2) mm, the mean preoperative refractive spherical equivalent was -15.6 (standard deviation of 7.6) D, ranging from -24.0 to -13.4 D. At 30 days postoperatively, the mean spherical equivalent was -0.35 (standard deviation of 1.1) D, ranging from -2.4 to 2.50 D. Conclusion We encountered a correlation between the absolute refractive error and the dioptric power of the intraocular lens. Against expectations, in our study, ultrasound biometry yielded better results than the optical biometer device, probably due to the small number of patients undergoing optical biometry, suggesting that well-performed immersion biometry can still produce satisfactory results.

RESUMO Objetivo Avaliar os cálculos de potência da lente intraocular e os erros refrativos pós-operatórios em pacientes com alta miopia submetidos à cirurgia de catarata, comparando a refração-alvo prevista e a refração pós-operatória real medida 30 dias após a cirurgia com a fórmula SRK/T. Métodos Esta análise retrospectiva incluiu 39 olhos de 31 pacientes com cirurgia de catarata de facoemulsificação não complicada com implantação de lente intraocular na bolsa. Os comprimentos axiais foram medidos por biometria de coerência óptica ou ultrassônica (imersão), com medidas de axial length (AL) maiores que 26 mm em pacientes com miopia maior que -6.0 D. A refração manifesta foi realizada na consulta pós-operatória de 1 mês, e o equivalente esférico foi analisado. Resultados Após análise de 39 olhos de 31 pacientes submetidos à cirurgia de catarata com AL médio de 30,4 (desvio-padrão de 2,2) mm, o equivalente esférico refrativo médio pré-operatório foi de -15,6 (desvio-padrão de 7,6) D, variando de -24,0 a -13,4 D. Aos 30 dias de pós-operatório, o equivalente esférico médio foi de -0,35 (desvio-padrão de 1,1) D, variando de -2,4 a 2,50 D. Conclusão Encontramos uma correlação entre o erro refrativo absoluto e o poder dióptrico da lente intraocular. Contrariando as expectativas, em nosso estudo, a biometria ultrassônica apresentou melhores resultados que o biômetro óptico, provavelmente devido ao pequeno número de pacientes submetidos à biometria óptica, sugerindo que a biometria de imersão bem executada ainda pode produzir resultados satisfatórios.

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PURPOSE: To evaluate residual refractive astigmatism using the Panacea and enVista toric calculators, compared to the gold-standard Barrett toric calculator. DESIGN: A retrospective and comparative study was conducted in one center. METHODS: We reviewed the medical records of all patients with a diagnosis of senile cataracts and regular corneal astigmatism, without previous corneal or intraocular surgery, who underwent phacoemulsification with implantation of a toric intraocular lens, who had pre- and postoperative corneal topography, biometry, and refraction measurements. RESULTS: The frequency of preoperative astigmatism according to the axis was 70 (84%) eyes showing with-the-rule (WTR) astigmatism, 9 (14%) eyes with against-the-rule (ATR) astigmatism, and 1 (2%) eye with oblique astigmatism. Regarding astigmatism prediction errors, there were statistically significant differences between the enVista and Panacea calculators (median of 0.39, 0.18, and 0.52 for Barrett, enVista, and Panacea, respectively). The residual astigmatism prediction error centroid was similar for the Barrett and enVista toric calculators, and both were lower compared to the Panacea calculator (x-component p < 0.001). CONCLUSIONS: The enVista toric calculator incorporating the Emmetropia Verifying Optical (EVO) toric calculator provides similar results to the gold-standard Barrett calculator.

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Objetivo: Caracterizar los resultados refractivos del implante de una lente intraocular plegable de cámara posterior suturada al iris en la afaquia sin o con inadecuado soporte capsular. Métodos: Se realizó un estudio descriptivo, prospectivo y longitudinal, en el que se incluyeron 30 pacientes (30 ojos) seguidos por un período de un año de septiembre de 2019 a septiembre de 2021, después del implante de una lente intraocular de cámara posterior suturada al iris en la afaquia. Se les realizó examen oftalmológico completo y se evaluaron variables como mejor agudeza visual sin corrección, con corrección, resultados refractivos, presión intraocular, astigmatismo inducido, densidad celular y complicaciones. Resultados: La mejor agudeza visual sin corrección en el preoperatorio fue del 93,3 por ciento (<0,1) y con corrección de 0,66, al año del posoperatorio fue de 0,493/0,890, respectivamente. La presión intraocular preoperatoria fue de 20,7 mmHg, y al año 19,7 mmHg. La densidad celular en el preoperatorio fue de 1755,7 cél/mm2 y al año fue de 1363,8 cél/mm2, y en los pacientes bien corregidos al mes del posoperatorio fue de 73,4 por ciento y al año de 70 por ciento. El astigmatismo inducido en el posoperatorio al año fue de -0,51 D. Conclusiones: La agudeza visual sin corrección y con corrección mejoran después del implante de una lente intraocular plegable de cámara posterior suturada al iris en la afaquia sin o con inadecuado soporte capsular. Predominan los pacientes bien corregidos, sin cambios en la presión intraocular y la complicación más frecuente fue el edema corneal(AU)

Objective: To characterize the refractive outcomes of implanting a posterior chamber foldable intraocular lens sutured to the iris in aphakia without or with inadequate capsular support. Methods: A descriptive, prospective and longitudinal study was carried out, including 30 patients (30 eyes) followed up for a period of one year, from September 2019 to September 2021, after being implanted a posterior chamber intraocular lens sutured to the iris in aphakia. Complete ophthalmologic examination was performed and variables were assessed, such as best visual acuity without correction, with correction, refractive results, intraocular pressure, induced astigmatism, cell density and complications. Results: The best visual acuity without correction in the preoperative period was 93.3 % (<0.1) and 0.66 with correction; while one-year postoperative visual acuity was 0.493 and 0.890, respectively. Preoperative intraocular pressure was 20.7 mmHg, while it was 19.7 mmHg at one year. Preoperatively cell density was 1755.7 cells/mm2, and it was 1363.8 cells/mm2 at one year it; while in well-corrected patients, it was 73.4 percent at one month postoperatively and 70 percent at one year. Postoperative induced astigmatism at one year was -0.51 D. Conclusions: Both uncorrected and corrected visual acuity improve after implantation of a posterior chamber foldable intraocular lens sutured to the iris in aphakia without or with inadequate capsular support. Well-corrected patients predominate, with no change in intraocular pressure, while the most frequent complication was corneal edema(AU)

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Objetivo: Caracterizar resultados visuales del implante de lente intraocular plegable de cámara posterior suturada al iris en la afaquia traumática de pacientes pediátricos. Métodos: Se realizó un estudio preexperimental, prospectivo, longitudinal con 17 niños, con seguimiento de un año. Se les realizó examen oftalmológico completo y se evaluaron variables como edad, sexo, lateralidad, mejor agudeza visual sin corrección, con corrección, resultados refractivos, presión intraocular, y complicaciones. Resultados: La edad promedio fue de 13,2 años, masculinos fueron el 64,7 por ciento. La mejor agudeza visual sin corrección en el preoperatorio fue del 47,1 por ciento <0,1 y con corrección de 0,7, al año del posoperatorio fue de 0,43/0,78, respectivamente. La presión intraocular preoperatoria fue de 14,1 mm Hg, y al año 14,71 mm Hg. La densidad celular en el preoperatorio fue de 2559.76 células/mm2 y al año de 2475,88 células/mm2. La hexagonalidad preoperatorio fue del 53,12 por ciento y al año del 56,94 por ciento. El cilindro preoperatorio -1,35 D y el 23,5 por ciento presentó astigmatismo inducido al año del posoperatorio. Conclusiones: La aplicación del implante de lente intraocular plegable de cámara posterior suturada al iris en la afaquia traumática de pacientes pediátricos logra mejorar su agudeza visual y la complicación más frecuente fue el edema corneal(AU)

Objective: To characterize visual outcomes of iris-sutured posterior chamber foldable intraocular lens implantation in traumatic aphakia in pediatric patients. Methods: A pre-experimental, prospective, longitudinal, pre-experimental study was performed with 17 children, with a one-year follow-up. A complete ophthalmologic examination was performed and variables such as age, sex, laterality, best visual acuity without correction, with correction, refractive results, intraocular pressure and complications were evaluated. Results: The average age was 13.2 years, 64.7 percent were male. The best visual acuity without correction preoperatively was 47.1 percent <0.1 and with correction 0.7, one year postoperative visual acuity was 0.43/0.78, respectively. Preoperative intraocular pressure was 14.1 mm Hg, and at one year 14.71 mm Hg. Cell density preoperatively was 2559.76 cells/mm2 and at one year 2475.88 cells/mm2. The preoperative hexagonality was 53.12 percent and at one year 56.94 percent. Preoperative cylinder -1.35 D and 23.5 percent presented induced astigmatism at one year postoperatively. Conclusions: The application of posterior chamber foldable intraocular lens implant sutured to the iris in traumatic aphakia in pediatric patients achieves improved visual acuity and the most frequent complication was corneal edema(AU)

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Introducción: El síndrome de uveítis-glaucoma-hifema (UGH) es una complicación infrecuente de las cirugías de catarata, debido a un roce mecánico ejercido por una lente intraocular (LIO) sobre el iris. Caso clínico: Un varón de 64 años, con antecedente de cirugía de catarata, presenta disminución de la agudeza visual y dolor en el ojo derecho. En el examen oftalmológico, se evidenciaron signos de uveítis anterior, presión intraocular (PIO) elevada, microhifema y una LIO de una pieza plegable en sulcus que provocaba un roce mecánico con la cara posterior del iris. El tratamiento médico fue insuficiente, por lo que se realizó una cirugía de explante de LIO de una pieza plegable y se reemplazó por una LIO de tres piezas plegables. La evolución posoperatoria fue favorable. Conclusión: Se debe sospechar de esta complicación, en pacientes con antecedente de cirugía de catarata, especialmente en casos en los cuales la LIO es de una pieza y ha sido implantada fuera del saco capsular.

Introduction: Uveitis-glaucoma-hyphema syndrome (UGH) is a rare complication of cataract surgery, due to mechanical chafing exerted by an intraocular lens (IOL) on the iris. Clinical case: A 64-year-old man with a history of cataract surgery, who presented decreased visual acuity and pain in the right eye. The ophthalmological examination revealed signs of anterior uveitis, elevated intraocular pressure (IOP), microhyphema, and a single-piece foldable IOL in the sulcus that caused a mechanical chafing with the posterior face of the iris. The medical treatment was insufficient; for this reason, a folding simple-piece IOL explant surgery was performed and replaced by a three-piece IOL. Postoperative evolution was favorable. Conclusion: Should be suspected this complication in patients with a history of cataract surgery, especially in cases in which the IOL is in single-piece and has been implanted outside the capsular bag.

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ABSTRACT Purpose: To evaluate primary intraocular lens implantation in the treatment of children's aphakia in the Brazilian public health system and compare the outcomes among different age groups. Methods: Children aged 0-12 years old with unilateral or bilateral congenital/developmental cataracts and underwent primary intraocular lens implantation were included. Results: A total of 108 eyes from 68 children were evaluated, and the children were divided into four age groups (<7 months [mo]; 7 mo-2 years old [y/o]; 2-5 y/o, and >5 y/o) were evaluated. Nineteen eyes (17.59%) presented visual axis opacification as a postoperative complication, which was more frequently observed in the <7 mo age group (37.93%). The difference was significant between the <7 mo and >5 y/o age groups (p=0.002). Visual axis opacification was divided into two categories: pupillary membrane and lens cell proliferation. Eight eyes presented pupillary membrane, whereas 14 showed lens cell proliferation. Out of eight eyes with pupillary membrane, seven occurred in the <7 mo age group. The difference between the <7 mo age group and the 2-5 y/o or >5 y/o age group was significant (p=0.01). Lens cell proliferation was more frequent in the <7 mo and 2-5 y/o age groups, but the difference was significant only between the < 7 mo age group and >5 y/o age group (p=0.040). Glaucoma and glaucoma suspect cases were not observed during the follow-up period. Conclusions: The main complication found in the study was visual axis opacification, which had a higher incidence in children operated on or before the age of 7 months.

RESUMO Objetivo: Avaliar o implante de lente intraocular primária para tratamento da afacia pediátrica no Sistema Único de Saúde (SUS) e comparar os resultados em diferentes faixas etárias. Métodos: Foram incluídas crianças com catarata congênita e do desenvolvimento unilateral ou bilateral de 0-12 anos de idade e submetidas a implante de lente intraocular primária. Resultados: Cento e oito olhos de 68 crianças divididas em quatro grupos de idade (<7m; 7m-2a; 2-5a e > 5a) foram avaliados. Dezenove olhos (17,59%) apresentaram opacificação do eixo visual como complicação pós-operatória. Essa complicação foi mais frequente na faixa etária <7 meses (37,93%). A diferença foi significativa entre os grupos de idade <7 meses e > 5 anos (p=0,002). A opacificação do eixo visual foi dividida em duas categorias: membrana pupilar e proliferação de células do cristalino. Oito olhos apresentaram membrana pupilar e 14 proliferação de células do cristalino. Dos oito olhos com membrana pupilar, sete ocorreram na faixa etária <7 meses. A diferença entre o grupo de idade <7 meses e os grupos de 2-5 anos e > 5 anos foi significativa (p=0,01). A proliferação de células do cristalino foi mais frequente nos grupos de idade <7 meses e 2-5 anos, mas significativa apenas quando comparados o grupo de idade <7 meses com o grupo> 5 anos de idade (p=0,040). Glaucoma e suspeitos de glaucoma não foram observados durante o acompanhamento. Conclusões: A principal complicação encontrada no estudo foi a opacificação do eixo visual. Sua incidência foi maior em crianças operadas antes dos 7 meses de idade.

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Purpose: To compare best-corrected visual acuity (BCVA) before and after implantable collamer lens (ICL) surgery in patients with low, moderate and high myopia. Methods: A single-centre, prospective, registry-based study involving patients with myopia who received ICLs between October 2018 and August 2020. The study population was divided into three groups of subjects with low (from 0 to -6 D), moderate (-6 to -10 D) and high myopia (more than -10 D). We analysed uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), spherical equivalent (SE), differences between BCVA pre- and 1-month postoperative, and line gain in BCVA 1 month after surgery. Results: A total of 770 eyes belonging to 473 patients were surgically intervened during the study period, of which 692 eyes completed 1 month of postoperative follow-up and were included in the study population. At 1-month follow-up, 478 eyes (69%) achieved a BCVA of 20/20, 599 (87%) obtained 20/25 or better, and 663 (96%) had a BCVA of 20/40 or better. We identified a significant improvement in BCVA (baseline 0.15±0.2 logMAR vs follow-up 0.07±0.2 logMAR, p<0.0001) and a significant reduction in SE (baseline -9.23±4.1 D, vs follow-up -0.21±0.8 D, p<0.0001), with a significant relationship between preoperative SE and line gain (r = -0.46, p<0.0001). We identified a significantly higher line gain among eyes with higher degrees of myopia (low myopia 0.22±0.69 lines compared to moderate myopia 0.56±1.1 lines and high myopia 1.51±1.9 lines, p<0.0001). Notably, 99.6% of eyes with a high grade of myopia achieved improvement to a low degree (less than -6 D) at follow-up. The safety and efficacy indexes were 0.083±0.1 and -0.001±0.1, respectively. Conclusion: In this large patient cohort, ICL surgery was related to a significant line gain in BCVA, particularly among eyes with higher degrees of myopia.

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AIM: To evaluate whether the Visian Implantable Collamer Lens with a central port (V4c ICL®; STAAR Surgical, Switzerland) affects the retinal nerve fibre layer (RNFL), macula and optic nerve head (ONH) measurements obtained by optical coherence tomography (OCT), and Heidelberg Retina Tomography (HRT). METHODS: This prospective study included myopic patients undergoing V4c ICL® implantation. RNFL thickness, macular thickness, ganglion cell analysis (GCA) and ONH main parameters were evaluated with RTVue OCT (Optovue Inc., USA) and Cirrus-HD OCT (Carl Zeiss Meditec, USA). ONH variables were also analysed with HRT-3 (Heidelberg Engineering, Germany). All measurements were performed before and 1 week and 12 months after the surgery. RESULTS: 31 eyes of 31 patients (mean age 30.1 ± 5.5 years) were included. Comparing with preoperative values, no significant differences in average RNFL thickness were found with RTVue, while a slight increase (4.3 µm) was detected with Cirrus-HD (85.2 ± 10.3 µm, preoperatively) at 1-week postoperatively (89.5 ± 8.3 µm; p < 0.05). Those changes were not observed at the last follow-up visit (86.6 ± 8.6 µm; p = 0.41). Cirrus-HD detected that macular thickness was slightly higher 1 week after surgery, compared with the preoperative examination (3.4% increase; p = 0.04). That difference remained stable at the 12-month postoperative visit (p = 0.01). GCA showed no changes. The ONH analysis with Cirrus-HD determined that rim area (p = 0.03) as well as disc area (p = 0.04) significantly increased. HRT-3 found no significant changes affecting those variables. CONCLUSIONS: The implantation of V4c ICL® did not induce a clinically significant impact on the results of the RNFL/ONH analysis with OCT and HRT.

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PURPOSE: To evaluate the stability and the refractive error of the different intraocular lens (IOL) after cataract surgery. METHOD: Retrospective, observational and single-center study. Patients diagnosed with cataract and myopia who underwent a phacoemulsification surgery with intraocular lens placement without complications were included. All patients underwent a complete ophthalmological examination, ultrasound biomicroscopy was performed at 2 weeks, 1 and 3 months after surgery. Descriptive statistics were performed using measures of central tendency and comparative analyzes. A value of p < 0.05 was considered significant. RESULTS: Thirty-one subjects with a diagnosis of axial myopia and senile cataract were included, 20 women (64.5%) and 11 men (35.5%), with a mean age was 62.8 ± 13.14 years. The IOL displacement were not different for the upper, lower, temporal and nasal quadrants; however, we observed a tendency to inclination to the temporal sector (p = 0.054) between the first and third postoperative month. Therefore, the were no significant differences in spherical equivalent between groups postoperatively. CONCLUSIONS: The inclination of the IOL did not change over time after surgery, the changes were similar with the different three types of IOL.

OBJETIVO: Evaluar la estabilidad y el desplazamiento de diferentes lentes intraoculares (LIO) a los 3 meses y los cambios refractivos asociados después de la facoemulsificación. MÉTODO: Estudio retrospectivo, observacional y unicéntrico. Se revisaron expedientes de pacientes sometidos a cirugía de facoemulsificación con colocación de LIO. Se realizó un examen oftalmológico completo, ultrabiomicroscopía a las 2 semanas, 1 y 3 meses después de la cirugía. Se realizó estadística descriptiva y análisis comparativos. Se tomó como diferencia significativa un valor de p < 0.05. RESULTADOS: Se incluyeron 31 ojos con diagnóstico de miopía y catarata senil, 20 mujeres (64.5%) y 11 hombres (35.5%), con una edad media de 62.8 ± 13.14 años. En cuanto al desplazamiento de la LIO, no se observaron diferencias significativas para los cuadrantes superior, inferior, temporal y nasal. Se observa una tendencia hacia temporal (p = 0.054) entre el primer y el tercer mes posoperatorios. El equivalente esférico tampoco mostró diferencias. CONCLUSIONES: El desplazamiento de la LIO no cambió con el tiempo después de la facoemulsificación. Los cambios fueron similares con los tres diferentes tipos de LIO y al compararlos proporcionan estabilidad refractiva en pacientes miopes.

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Objetivo: Determinar la relación de los planos anatómicos del cristalino con la posición real de la lente intraocular en pacientes con diagnóstico de catarata atendidos en el Centro de Microcirugía Ocular del Instituto Cubano de Oftalmología durante el período de enero del 2018 a enero 2021. Métodos: Se realizó un estudio observacional, descriptivo, prospectivo longitudinal en 89 ojos de 67 pacientes operados de catarata con implante de lente intraocular (LIO) por técnica de facoemulsificación. Se empleó para el cálculo del poder de la lente el IOL Master 700 y la fórmula de SRK/T. Se utilizó la imagen de OCT ofrecida por el IOL Máster 700 para determinar el plano ecuatorial y plano central del cristalino, así como la posición real de la lente intraocular. Resultados: Predominó el grupo de edad entre 60 - 79 años, el sexo femenino representó el 53 por ciento. Los ojos tamaño promedio y las medidas biométricas oculares en valores promedios estándar fueron los más representativos. El plano ecuatorial mostró menos diferencia con la posición real de la lente intraocular en comparación con la diferencia evidenciada entre el plano central y la posición real de la lente. La adecuada posición del lente intraocular calculado en la bolsa capsular independiente a la longitud axial, permitió obtener un resultado refractivo en correspondencia al esperado previo a la cirugía. Conclusión: Los parámetros anatómicos del cristalino (plano ecuatorial, plano central) constituyen variables importantes a tener en cuenta para el desarrollo y perfeccionamiento de las fórmulas para el cálculo del lente intraocular(AU)

Purpose: To determine the relationship of the anatomical planes of the crystalline lens with the actual position of the intraocular lens in patients with a diagnosis of cataract seen at the Ocular Microsurgery Center of the Cuban Institute of Ophthalmology during the period January 2018 and January 2021. Methods: An observational, descriptive, prospective longitudinal study was performed in 89 eyes of 67 patients operated on for cataract with intraocular lens implantation (IOL) by phacoemulsification technique. The IOL Master 700 and the SRK/T formula were used to calculate lens power. The OCT image provided by the IOL Master 700 was used to determine the equatorial plane and central plane of the crystalline lens, as well as the actual position of the intraocular lens. Results: The age group 60-79 years was predominant, female gender represented 53 percent. Average eye size and ocular biometric measurements in standard average values were the most representative. The equatorial plane showed less difference with the actual intraocular lens position compared to the difference evidenced between the central plane and the actual lens position. The adequate position of the intraocular lens calculated in the capsular bag independent to the axial length, allowed to obtain a refractive result in correspondence to the one expected before surgery. Conclusion: The anatomical parameters of the crystalline lens (equatorial plane, central plane) are important variables to be taken into account for the development and improvement of the formulas for the calculation of the intraocular lens(AU)

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BACKGROUND: Cataract surgery with multifocal IOLs could give patients good vision and great satisfaction, at the same time generating high expectations; therefore, its precise indication is essential if we are to reach our goal. The use of optical coherence tomography may be a valuable tool in the screening of macular diseases, which often cannot be detected in routine clinical examinations. This study evaluates the benefit of including spectral domain optical coherence tomography (SD-OCT) in routine preoperative cataract surgery protocols for better case selection in multifocal IOLs. METHODS: Observational and retrospective clinical study that includes patients with an indication for multifocal IOL implantation who underwent retinal fundus exam and SD-OCT examination between 2018 and 2019. The clinical examination with ophthalmoscopy and SD-OCT imaging results were evaluated to observe their influence on the final choice of the lens implanted lens in cataract surgery. RESULTS: 405 eyes from 207 patients with multifocal IOL indication were included. It was found that 220 (54.2%) of all indicated multifocal or trifocal IOLs were in fact implanted. The most important reason for not implanting the indicated IOL was financial, in 116 (59.46%) eyes. The second cause were retinal abnormalities detected by SD-OCT, 63 eyes (15.6%). Those abnormalities included dry age-related macular degeneration (AMD) (50.7%), neovascular AMD (3.1%), vitreomacular adhesion (11.1%), diabetic macular edema (3.1%), epiretinal membrane (ERM) (25.3%) and other macular abnormalities (6.3%). Of the 63 eyes with an abnormal SD-OCT result, 44 (69.8%) were also identified by fundus examination. Nineteen (30.2%) eyes had abnormalities detected only by SD-OCT imaging with a normal clinical exam. CONCLUSIONS: Routine use of SD-OCT imaging may help diagnose pre-existing macular pathologies not identified by clinical exam, helping both physicians and patients choose the ideal IOL individually and has the potential to prevent unsatisfactory functional results.

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Objetivo: Determinar los resultados refractivos con las fórmulas Holladay 2 y Barret Universal 2 a partir del cálculo de la lente intraocular en pacientes operados de catarata. Métodos: Se realizó un estudio descriptivo prospectivo y longitudinal con 60 ojos de 50 pacientes operados de catarata mediante la técnica de facoemulsificación. Se empleó para el cálculo de la lente el IOL Master 700 y el Pentacam AXL con la fórmula Holladay 2 y Barret Universal 2, respectivamente. Resultados: Predominó el sexo femenino y el grupo etario mayor de 60 años. Los ojos mayores de 26 mm mostraron la mayor diferencia entre el poder dióptrico de la lente intraocular que se implantó según Holladay y en menores de 22 mm según Barret Universal. Ambos grupos presentaron una disminución del equivalente esférico, siendo superior a 7 y 5 dioptrías en ojos mayores de 26 mm en el posoperatorio de ambas fórmulas. Posterior a la cirugía se observó una mejoría en la agudeza visual sin corrección y corregida de más de 4 líneas en la cartilla de Snellen, independiente de la longitud axial, para ambos grupos en estudio. Sin cambios significativos en el cilindro queratométrico. En el 70,0 por ciento de los casos, el resultado refractivo final estuvo en rango de la emetropía para el grupo Holladay 2 y el 66,7 por ciento para el grupo Barret Universal 2. Conclusiones: Ambas fórmulas resultan útiles para el cálculo de la lente intraocular en todos los rangos de longitud axial(AU)

Objective: To determine refractive outcomes with the Holladay 2 and Barret Universal 2 formulas from intraocular lens calculation in cataract surgery patients. Methods: A prospective and longitudinal descriptive study was performed with 60 eyes of 50 patients who underwent cataract surgery by phacoemulsification. The IOL Master 700 and Pentacam AXL with the Holladay 2 and Barret Universal 2 formula, respectively, were used to calculate the lens. Results: Female gender and age group older than 60 years predominated. Eyes larger than 26 mm showed the greatest difference between the dioptric power of the intraocular lens implanted according to Holladay and those smaller than 22 mm according to Barret Universal. Both groups presented a decrease of the spherical equivalent, being higher than 7 and 5 diopters in eyes larger than 26 mm postoperatively in both formulas. Postoperatively, there was an improvement in uncorrected and corrected visual acuity of more than 4 lines in the Snellen chart, independent of axial length, for both groups under study. No significant changes in keratometric cylinder. In 70.0 percent of the cases, the final refractive result was in the emmetropia range for the Holladay 2 group and 66.7 percent for the Barret Universal 2 group. Conclusions: Both formulas are useful for the calculation of the intraocular lens in all axial length ranges(AU)

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Purpose: To evaluate the safety, visual performance, and patient satisfaction of a new presbyopic pseudophakic intraocular lens (IOL). Methods: A prospective non-randomized case-series study was performed in Buenos Aires, Argentina. Patients included in the study underwent a programmed Femtosecond laser assisted cataract surgery (FLACS), performed between October and December 2020, with a 6-month follow-up period. The Intensity (Hanita Lenses) IOL was bilaterally implanted. Spherical equivalent (SE) refraction, uncorrected distance and near visual acuity (UDVA/UNVA), defocus curve, endothelial cell density (ECD), central corneal thickness (CCT), and a satisfaction questionnaire were evaluated. Results: A total of 56 patients (112 eyes), aged 65 ± 6.12 years were included. The mean ± SD of preoperative SE was 1.85 ± 2.24 D (range; -4.50 to 4.75), which had decreased 6 months after surgery to -0.08 ±0.32 D (range; -0.75 to 0.63). No eyes experienced a loss of lines of vision, and 94% obtained SE values between ± 0.50 D. Defocus curve for different additions was 0.03 LogMAR (logarithm of the minimum angle of resolution) for -3.0 D, -0.005 LogMAR for -1.5 D, and -0.07 LogMAR for 0 D. The ECD, CCT remained stable (P: 0.09 and 0.58, respectively) and all patients achieved their preoperative expectations, with a 6-month follow-up period. Conclusion: Patients who underwent a safe bilateral implantation with Intensity IOL achieved a high degree of spectacle independence and satisfaction, 6 months after surgery.

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Objetivo: Optimizar las constantes utilizadas por las fórmulas SRK/T, SRK/T2, Holladay 1 y Hoffer Q para cinco modelos de lentes intraoculares (LIO), implantados durante la cirugía de catarata en el Instituto Cubano de Oftalmología (enero/2006-octubre/2019). Método: Se estudiaron retrospectivamente 47341 pacientes. Las constantes se optimizaron ajustando a cero el error de predicción promedio (EPm) y obteniendo el valor que arrojó el máximo número de ojos con error de predicción absoluto -EP- ≤; 0,25, tanto para la biometría ultrasónica como para la óptica. La eficacia de las constantes optimizadas se verificó mediante el análisis de los errores absolutos medio y mediano (EAM/EAMed) más bajos y el porcentaje de ojos en un intervalo determinado de error de predicción en función del valor de las constantes. También se analizaron el índice de rendimiento de la fórmula de Haigis y un nuevo índice introducido. Resultados: Las constantes optimizadas fueron significativamente diferentes de los valores del fabricante. Los valores obtenidos para EPm = 0 fueron diferentes a los mínimos de EAM y EAMed. El porcentaje de ojos con -EP- ≤ 0,25 y 0,50 D difirió cuando los criterios de optimización fueron diferentes. SRK/T y SRK/T2 mostraron los mejores rendimientos, según ambos índices. Conclusiones: Las constantes optimizadas mejoran los resultados postoperatorios para cada combinación LIO-fórmula. Diferentes criterios de optimización conducen a diferentes resultados. El EAM, el EAMed y el porcentaje de ojos con -EP- ≤; 0,50 D son parámetros válidos para comprobar el rendimiento de las fórmulas, hasta disponer de un índice único, fiable y consensuado(AU)

Objective: To optimize the constants used by the SRK/T, SRK/T2, Holladay 1 and Hoffer Q formulas for five intraocular lens (IOL) models implanted during cataract surgery at the Cuban Institute of Ophthalmology (January/2006-October/2019). Methods: 47341 patients were retrospectively studied. The constants were optimized by adjusting the average prediction error (EPm) to zero and obtaining the value that showed the maximum number of eyes with absolute prediction error -EP- ≤ 0.25, for both ultrasonic and optical biometry. The effectiveness of the optimized constants was verified by analyzing the lowest average and median absolute errors (EAM/EAMed) and the percentage of eyes in a given range of prediction error as a function of the value of the constants. The Haigis formula performance index and a newly introduced index were also analyzed. Results: The optimized constants were significantly different from the manufacturer's values. The values obtained for EPm = 0 were different from the EAM and EAMed minima. The percentage of eyes with -EP- ≤ 0.25 and 0.50 D differed when the optimization criteria were different. SRK/T and SRK/T2 showed the best performances, according to both indexes. Conclusions: Optimized constants improve postoperative outcomes for each IOL-formula combination. Different optimization criteria lead to different results. The EAM, the EAMed and the percentage of eyes with -EP- ≤ 0.50 D are valid parameters to check the performance of the formulas, until a single, reliable and consensual index is available(AU)

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We report three cases of refractory chronic endophthalmitis after cataract surgery presenting to a referral center, and with repeated negative cultures. Initial treatment consisted of intravitreal and systemic antibiotics, with partial improvement. After subsequent worsening, pars plana vitrectomy, intraocular lens explantation and en bloc capsulectomy were performed. Histopathological examination revealed multiple filamentous fungal structures, sequestered between anterior/posterior lens capsule in all cases. Chronic postoperative fungal endophthalmitis may manifest with negative cultures possibly associated with sequestration of the microorganism into the capsular bag. Careful histopathological examination of lens capsule in these cases may be essential for a definite diagnosis.

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PURPOSE: To analyse the distribution of the difference between both eyes in the calculation of the dioptric power of the intraocular lens in a series of 7994 patients and the biometric variables that determine it. METHODS: The data of patients between 3 and 99 years old, residents of the city of Guayaquil and neighbouring sites, who received ocular biometry by partial optical coherence interferometry between 2004 and 2020 were reviewed. Ocular biometrics, including axial length (AL), anterior chamber depth (ACD), and the mean corneal dioptre power (CD), were measured by partial coherence interferometry. Refraction without or with cycloplegia was recorded in spherical equivalent (SE). The Haigis formula from the IOL Master instrument was used to calculate the dioptric power of the intraocular lens in both eyes. RESULTS: Data from the bilateral optical biometry of 7994 patients were analysed. The mean and standard deviation of AL, CD, ACD and dioptre power of the IOL were 23.66 ±â€¯1.25, 43.70 ±â€¯1.49, 3.34 ±â€¯0.40 and +20.46 ±â€¯3.84, respectively. 2538 (31.7%) patients had equal dioptre power of the IOL between both eyes. 3243 (40.6%) patients had a 0.50 D difference; 1162 (14.5%), 1.0 D; 425 (5.3%), 1.5 D. 626 patients (7.8%) had a difference in IOL dioptre of 2 D or more, with a maximum of 24 D. The asymmetry of AL between OU was ≥0.4 mm in 10.49%, while that of CD reached ≥1 D in 1.9%. CONCLUSIONS: 92.16% of patients had a difference within 1.5 D between both eyes in the calculation of the dioptre power of the intraocular lens. In case an eye is programmed in which it is impossible to perform a reliable biometry, either due to trauma or due to white or brunescent cataract, the calculation of the intraocular lens could be done taking as a reference the biometry of the contralateral eye.

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PURPOSE: To assess visual results (including the Lapid-Kushlin defocus coefficient), and satisfaction, following the implantation of PanOptix® a trifocal intraocular lens. METHODS: Observational, retrospective cohort study. 130 eyes of 65 subjects with bilateral implantation were included. Binocular uncorrected visual acuities [distance (Binocular UDVA), intermediate (Binocular UIVA) and near (Binocular UNVA)] were measured. Also, the manifest refraction, binocular defocus curve and binocular contrast sensitivity were determined. The Lapid-Kushlin defocus coefficient, a new single numerical parameter based on the area under the curve of the defocus curve, was calculated. The validated Spanish CATQUEST-9SF satisfaction survey was applied. RESULTS: Postoperative visual acuity ranges were: binocular UDVA 0.18 to 0.0 LogMAR, binocular UIVA 0.30 to 0.0 LogMAR and Binocular UNVA 0.18 to 0.0 LogMAR. The levels of contrast sensitivity both in bright light conditions (with and without glare) and low light conditions with glare, remained within the limits of normality. Under scotopic conditions without glare values below normality were found at lower spatial frequencies. The binocular defocus curve showed a plateau without a clearly evident peak. The Lapid-Kushlin defocus coefficient was 0.199. Two patients (3.1%) needed glasses after the procedure for near and intermediate vision. No patient manifested great visual difficulties or was dissatisfied with the results. CONCLUSIONS: The trifocal platform showed very good results in this series of patients. 96.9% of the patients achieved independence of the glasses and expressed a high degree of satisfaction. The Lapid-Kushlin defocus coefficient was better than those calculated from literature, for other multifocal intraocular lenses.

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Objetivo: Comparar la exactitud de las fórmulas SRK/T, Hoffer Q, Barrett Universal y HRBF en el cálculo del lente intraocular. Métodos: Se realizó un estudio descriptivo longitudinal prospectivo de 70 ojos de 70 pacientes operados de cirugía de catarata con implante de lente intraocular, de junio del año 2018 a junio del 2019, utilizando el IOL Master 700, en el Instituto Cubano de Oftalmología "Ramón Pando Ferrer". Se determinó la exactitud de cada fórmula respecto al error de predicción del equivalente esférico y se compararon entre sí. Resultados: Los pacientes entre 60 y 80 años constituyeron el 70,00 por ciento de los casos y el sexo femenino representó el 61,43 por ciento. Los ojos de tamaño medio representaron el 91,43 por ciento del total. No hubo diferencias en el error de predicción absoluto medio entre de las fórmulas analizadas para el rango total de longitudes axiales. La fórmula de Barrett tuvo el 65,71 por ciento de ojos con un error de predicción dentro de ± 0,50 D. El mayor porcentaje de ojos con un error mayor a 1 dioptría recayó sobre la Hoffer Q (10,00 por ciento). Conclusiones: El grupo etario más representado está entre 60 y 80 años y el sexo femenino es mayoritario. Predominan los ojos de tamaño medio y las mensuraciones biométricas dentro de los valores promedio estándar. Las fórmulas HRBF, SRK/T, Hoffer Q y Barrett predicen el resultado refractivo posoperatorio con una exactitud similar para el rango total de longitudes axiales. La fórmula de Barrett logra el mayor porcentaje de ojos con errores de predicción posoperatorios dentro del rango de la emetropía(AU)

Objective: Compare the accuracy of the formulas SRK/T, Hoffer Q, Barrett Universal and HRBF for intraocular lens calculation. Methods: A prospective longitudinal descriptive study was conducted of 70 eyes of 70 patients undergoing cataract surgery with intraocular lens implantation from June 2018 to June 2019 at Ramón Pando Ferrer Cuban Institute of Ophthalmology. In all cases IOL Master 700 was used for lens calculation. Determination of the accuracy of each formula in error prediction of the spherical equivalent was followed by a comparison of the formulas. Results: Patients aged 60-80 years were 70.00 percent of the cases; female sex represented 61.43 percent. Medium sized eyes were 91.43 percent of the total eyes examined. Mean absolute prediction error did not show any difference between the formulas analyzed for the total range of axial lengths. The Barrett formula spotted 65.71 percent of the eyes with a prediction error within ± 0.50 D. The highest percentage of eyes with an error greater than 1 diopter corresponded to the Hoffer Q formula (10.00 percent ). Conclusions: The best represented age group was 60-80 years; female sex prevailed. A predominance was found of medium size and biometric measurements within standard mean values. The formulas HRBF, SRK/T, Hoffer Q and Barrett predict the postoperative refractive result with similar accuracy throughout the total range of axial lengths. The Barrett formula achieves the highest percentage of eyes with postoperative prediction errors within the range of emmetropia(AU)

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El gran desarrollo de la cirugía de glaucoma mínimamente invasiva, conocida como MIGS, ha supuesto una alternativa eficaz en el tratamiento de esta enfermedad, y ha demostrado ser efectiva en la reducción de la presión intraocular. Presentamos a un paciente varón de 51 años con glaucoma en progresión, quien requería tratamiento médico máximo para el control de su enfermedad y en el que se realizó un triple procedimiento quirúrgico: cirugía de retirada de lente intraocular, facoemusificación e implante XEN®. La cirugía fue un éxito. Se consiguió el control tensional y se pudo prescindir completamente del uso de medicación hipotensora, lo que mejoró mucho la calidad de vida de nuestro paciente. La cirugía MIGS es una alternativa muy válida para el manejo del glaucoma. Cuenta con excelentes resultados, beneficios respecto a la cirugía clásica de glaucoma y un buen perfil de seguridad. En este caso clínico, presentamos el implante XEN® como una opción terapéutica útil en un paciente con glaucoma y valoramos sus indicaciones, beneficios y ventajas(AU)

Due to its great development, minimally invasive glaucoma surgery (MIGS) has become a useful alternative in the treatment of this condition, proving effective for intraocular pressure reduction. A case is presented of a male 51-year-old patient with glaucoma in progression who required maximum medical treatment to control his disease. The patient underwent a triple surgical procedure: intraocular lens removal surgery, phacoemulsification and XEN® implantation. The surgery was successful: pressure control was achieved and hypotensive medication was completely eliminated, with which the patient's quality of life improved considerably. MIGS is a very valid alternative in glaucoma management, due to its excellent results, benefits with respect to classic glaucoma surgery, and a good safety profile. The clinical case herein presented illustrates the use of XEN® implantation as a useful therapeutic option in a glaucoma patient, and reference is made to its indications, benefits and advantages(AU)

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