Resultados del mundo real de la ciclofotocoagulación con láser micropulsado en una población latinoamericana y análisis de los factores asociados con la tasa de éxito / Real-world outcomes of micropulse cyclophotocoagulation in a Latin American population and analysis of the factors associated with the success rate

Objetivo Reportar los resultados de la ciclofotocoagulación transescleral con láser micropulsado en una población latinoamericana con glaucoma refractario en un entorno del «mundo real» y evaluar los factores asociados con éxito a un año de seguimiento. Materiales y métodos Estudio multicéntrico, retrospectivo. Se revisaron los expedientes de pacientes sometidos a ciclofotocoagulación transescleral con láser micropulsado entre septiembre de 2017 y octubre de 2018. El éxito del tratamiento se definió como una presión intraocular de 5 a 21mmHg o una reducción de la presión intraocular del 20% de la basal, con o sin tratamiento médico adicional para glaucoma. Resultados Se incluyeron 83 ojos de 83 pacientes, con un seguimiento promedio de 10,1 ±3,1meses. La presión intraocular y el número de medicamentos para glaucoma disminuyeron significativamente en todas las visitas postoperatorias de una media de 21,9 ±7,6mmHg con 3,8 medicamentos a 13,1 ±3,5mmHg con 2,8 medicamentos a 12meses de seguimiento. La presión intraocular media disminuyó un 40,1% de la basal a los 12meses. La tasa de éxito acumulada fue del 54,5% (IC del 95%: 44-67%) a 12meses de seguimiento. Identificamos una presión intraocular basal más alta como predictor independiente significativo del éxito del tratamiento (p=0,03). Las complicaciones tardías incluyeron 1ojo con edema corneal, 1ojo con inflamación prolongada en cámara anterior y edema macular quístico y 9ojos (11%) con pérdida visual de 2líneas de Snellen o más. Conclusiones La ciclofotocoagulación transescleral con láser micropulsado es un tratamiento eficaz y seguro para pacientes latinoamericanos y puede proporcionar reducciones de la presión intraocular y del número de medicamentos con una sola aplicación a un año de seguimiento. La presión intraocular basal alta fue el predictor más significativo del éxito del tratamiento (AU)

Objective To report the outcomes of micropulse cyclophotocoagulation in a Latin American population with refractory glaucoma in a «real-world» setting and to evaluate the factors associated with success after a one-year follow-up. Materials and methods Retrospective, multicenter study. The medical records of patients who underwent micropulse cyclophotocoagulation between September 2017 and October 2018 were reviewed. Treatment success was defined as an intraocular pressure of 5-21mmHg or a 20% intraocular pressure reduction with or without additional glaucoma medical therapy. Results Eighty-three eyes from 83 patients were included, with a mean follow-up of 10.1 ±3.1months. The intraocular pressure and number of glaucoma medications significantly decreased at all postoperative visits from a mean of 21.9 ±7.6mmHg on 3.8 medications to 13.1 ±3.5mmHg on 2.8 medications at the 12-month follow-up. The mean intraocular pressure decreased 40.1% from baseline at 12months. The cumulative success rate was 54.5% (95% CI: 44%-67%) at 12-month follow-up. We identified a higher baseline intraocular pressure as a significant independent predictor of treatment success (P=.03). Late complications included 1eye with corneal edema, 1eye with prolonged anterior chamber inflammation and cystoid macular edema and 9eyes (11%) with visual loss of 2Snellen lines or more. Conclusions Micropulse cyclophotocoagulation is an effective and safe treatment for Latin American patients and can provide intraocular pressure and medication reductions with a single treatment after a one-year follow-up. A high baseline intraocular pressure was the most significant predictor of treatment success (AU)

Real-world outcomes of micropulse cyclophotocoagulation in a Latin American population and analysis of the factors associated with the success rate.

OBJECTIVE: To report the outcomes of micropulse cyclophotocoagulation in a Latin American population with refractory glaucoma in a "real-world" setting and to evaluate the factors associated with success after a one-year follow-up. MATERIALS AND METHODS: Retrospective, multicenter study. The medical records of patients who underwent micropulse cyclophotocoagulation between September 2017 and October 2018 were reviewed. Treatment success was defined as an intraocular pressure of 5 to 21 mmHg or a 20% intraocular pressure reduction with or without additional glaucoma medical therapy. RESULTS: Eighty-three eyes from 83 patients were included, with a mean follow-up of 10.1 ± 3.1 months. The intraocular pressure and number of glaucoma medications significantly decreased at all postoperative visits from a mean of 21.9 ± 7.6 mmHg on 3.8 medications to 13.1 ± 3.5 mmHg on 2.8 medications at the 12-month follow-up. The mean intraocular pressure decreased 40.1% from baseline at 12 months. The cumulative success rate was 54.5% (95% CI, 44-67%) at 12-month follow-up. We identified a higher baseline intraocular pressure as a significant independent predictor of treatment success (p = 0.03). Late complications included 1 eye with corneal edema, 1 eye with prolonged anterior chamber inflammation and cystoid macular edema and 9 eyes (11%) with visual loss of 2 Snellen lines or more. CONCLUSIONS: Micropulse cyclophotocoagulation is an effective and safe treatment for Latin American patients and can provide intraocular pressure and medication reductions with a single treatment after a one-year follow-up. A high baseline intraocular pressure was the most significant predictor of treatment success.

Outcomes of trabeculectomy with polyvinylpyrrolidone collagen versus mitomycin in primary open angle glaucoma. 36-month follow-up. / Colágeno polivinilpirrolidona versus mitomicina C en trabeculectomía en pacientes con glaucoma primario de ángulo abierto. Seguimiento a 36 meses.

PURPOSE: Describe and compare the effects of intraoperative application of Polyvinylpyrrolidone Collagen (PVP) versus Mitomycin C (MMC) on the pattern of change in mean IOP reduction and mean number of medications over 36-months follow-up in patients with primary open angle glaucoma (POAG) undergoing trabeculectomy. METHODS: Prospective, randomized, comparative study. Twenty-six eyes of 26 patients with POAG and no previous incisional glaucoma surgery underwent trabeculectomy and were randomized to PVP or MMC and completed a 36-month follow-up. Main outcome measures were IOP and number of glaucoma medications. Multivariate longitudinal analysis was performed by fitting a linear trend model adjusting for baseline response for the IOP outcome and a log-linear regression model with within-subject associations for the number of hypotensive medications outcome. Sensitivity analysis was performed to assess lower and higher order polynomial trends over time in IOP. RESULTS: The univariate analysis revealed that the mean IOP reduction from baseline to 36 months was 7.62mmHg (3.05; 12.18) in the MMC group and 8.15mmHg (-0.64; 16.95) in the PVP group. Mean percentage IOP reduction from baseline was 37.09% (15.93; 58.17) and 36.08% (5.16; 67.20) in the PVP group. Mean change in number of medications from baseline to 36 months was -0.92 medications (-3.38; +1.54) for the MMC group and -1 medication (-3.12; +1.12) for the PVP group. Both groups had a statistically significant decline in mean IOP over the follow-up period (p<0.001) but there was no discernible difference between the two exposure groups in the rate of change in IOP (p=0.5975). Sensitivity analysis showed that a linear trend model is adequate to describe the IOP reduction over the follow-up period. Both groups had a statistically significant change in the number of hypotensive medications used between baseline and month 36 (p<0.05) but there was no discernible difference between exposure groups (p=0.2917). Both the PVP and MMC groups showed an initial reduction in number of medications until month 12 and a relatively linear increase towards month 36. A longer follow-up may be warranted to reveal differences in the number of medications between the two exposure groups. Postoperative complications were less frequent in the PVP group. CONCLUSIONS: The use of PVP during trabeculectomy achieves and maintains a statistically significant IOP reduction from baseline to 36 months and decreases the number of glaucoma medications. Secondary outcome measures showed a lower incidence of adverse events in the PVP group.

Estudio comparativo de la seguridad y eficacia entre el dispositivo valvular de Ahmed modelo M4 (polietileno poroso de alta densidad) y el modelo S2 (polipropileno) en pacientes con diagnóstico de glaucoma neovascular / Comparative study of the safety and efficacy of the Ahmed glaucoma valve model M4 (high density porous polyethylene) and the model S2 (polypropylene) in patients with neovascular glaucoma

OBJETIVO: El objetivo de este estudio fue evaluar de forma prospectiva la seguridad y eficacia del dispositivo valvulado de Ahmed modelo M4 (sistema valvular convencional en plato de polietileno poroso de alta densidad, Medpor) comparado con el modelo S2 (plato de polipropileno). MÉTODO: Se formaron 2 grupos de pacientes con glaucoma neovascular. Un grupo en el que se implantó el dispositivo M4 y el grupo en el que se implantó el dispositivo S2. En ambos grupos (M4 y S2) se incluyó a pacientes mestizos mexicanos. Dichos pacientes fueron intervenidos quirúrgicamente, utilizando la técnica convencional consistente en la fijación escleral del cuerpo valvular en el cuadrante temporal superior a 8mm del limbo y realizando un túnel subepiescleral para colocar el tubo del dispositivo dentro de la cámara anterior, de acuerdo con la técnica descrita por nuestro grupo en forma previa. Después de un año de seguimiento los resultados fueron evaluados tomando en cuenta la reducción de la presión intraocular (PIO), los cambios en la agudeza visual, el uso de hipotensores oculares complementarios y las complicaciones aparecidas, así como las características demográficas de cada grupo. En el caso del modelo M4, los procedimientos quirúrgicos fueron realizados por el mismo cirujano (FGC). Los pacientes en los que se implantó el modelo S2 fueron operados por diversos cirujanos, incluyendo a FGC, del Servicio de Glaucoma del Hospital Dr. Luis Sánchez Bulnes de la Asociación para Evitar la Ceguera en México (APEC). RESULTADOS: En cada uno de los 2 grupos se operaron 21 ojos de 21 pacientes con diagnóstico de glaucoma neovascular, conformando los 42 ojos incluidos en este estudio. La PIO promedio en el preoperatorio fue de 43,5mmHg (±11,8) para el grupo de M4 y de 42,24mmHg (±12,84) para el grupo de S2. Después de un año de seguimiento, la PIO reportada fue 18,9mmHg (±9,7) para el grupo de M4 y 16,38mmHg (±9,76) para el grupo de S2. CONCLUSIONES: Creemos que es necesario efectuar un mayor número de estudios a largo plazo con un número mayor de pacientes, para poder evaluar la ayuda de esta cubierta porosa en el control tensional de los pacientes con el diagnóstico de GNV

OBJECTIVE: To prospectively evaluate the safety and efficacy of the Ahmed glaucoma valve model M4 (High density porous polyethylene plate; Medpor) compared with the model S2 (polypropylene plate). METHOD: Mexican patients with neovascular glaucoma were randomly included for each group (M4 and S2). They were operated on using conventional techniques and creating a sub-episcleral tunnel to place the valve tube in the anterior chamber. After one year of follow-up, the results were evaluated with respect to a post-operative reduction in pressure, changes in visual acuity, the need for drugs, and complications, as well as the demographic characteristics of each group. Each operation using the M4 valve was performed by a single surgeon (FGC). Those operated on using the S2 model had their surgery performed by the staff surgeons at the Glaucoma Department of the Mexican Association to Prevent Blindness (APEC). RESULTS: Each group (M4 and S2) contained 21 eyes of 21 Mexican patients with a diagnosis of neovascular glaucoma, leading to a total of 42 patients undergoing surgery. The mean preoperative intraocular pressure (IOP) was 43.5 (±11.8), and 42.24 (±12.84) mmHg for the M4 and S2 groups, respectively. After one year of follow-up, the IOP reported was 18.9 (±9.7) mmHg for the final 18 patients in the M4 group, and 16.38 (±9.76) mmHg for the 21 patients in the S2 group. DISCUSSION: The design of a drainage valve device such as that of Ahmed has characteristics such as moderate control of IOP, thanks to the valve component in the immediate post-operative period, which makes them safer than other non-valve devices. This avoids an excess of flat chambers and the presence of low IOPs, which can lead to bleeding in the early post-operative period due to the weak desmosomal junctions of the newly formed vessels, with the advantage of maintaining suitable control of IOP from the first day after surgery. CONCLUSION: Further studies with longer follow-up with a larger number of patients are needed to evaluate the effectiveness of this porous coating in the control of neovascular glaucoma

Comparative study of the safety and efficacy of the Ahmed glaucoma valve model M4 (high density porous polyethylene) and the model S2 (polypropylene) in patients with neovascular glaucoma. / Estudio comparativo de la seguridad y eficacia entre el dispositivo valvular de Ahmed modelo M4 (polietileno poroso de alta densidad) y el modelo S2 (polipropileno) en pacientes con diagnóstico de glaucoma neovascular.

OBJECTIVE: To prospectively evaluate the safety and efficacy of the Ahmed glaucoma valve model M4 (High density porous polyethylene plate; Medpor) compared with the model S2 (polypropylene plate). METHOD: Mexican patients with neovascular glaucoma were randomly included for each group (M4 and S2). They were operated on using conventional techniques and creating a sub-episcleral tunnel to place the valve tube in the anterior chamber. After one year of follow-up, the results were evaluated with respect to a post-operative reduction in pressure, changes in visual acuity, the need for drugs, and complications, as well as the demographic characteristics of each group. Each operation using the M4 valve was performed by a single surgeon (FGC). Those operated on using the S2 model had their surgery performed by the staff surgeons at the Glaucoma Department of the Mexican Association to Prevent Blindness (APEC). RESULTS: Each group (M4 and S2) contained 21 eyes of 21 Mexican patients with a diagnosis of neovascular glaucoma, leading to a total of 42 patients undergoing surgery. The mean preoperative intraocular pressure (IOP) was 43.5 (±11.8), and 42.24 (±12.84) mmHg for the M4 and S2 groups, respectively. After one year of follow-up, the IOP reported was 18.9 (±9.7) mmHg for the final 18 patients in the M4 group, and 16.38 (±9.76) mmHg for the 21 patients in the S2 group. DISCUSSION: The design of a drainage valve device such as that of Ahmed has characteristics such as moderate control of IOP, thanks to the valve component in the immediate post-operative period, which makes them safer than other non-valve devices. This avoids an excess of flat chambers and the presence of low IOPs, which can lead to bleeding in the early post-operative period due to the weak desmosomal junctions of the newly formed vessels, with the advantage of maintaining suitable control of IOP from the first day after surgery. CONCLUSION: Further studies with longer follow-up with a larger number of patients are needed to evaluate the effectiveness of this porous coating in the control of neovascular glaucoma.

Comparison of Goldmann applanation and dynamic contour tonometry in a population of Mexican open-angle glaucoma patients.

To compare intraocular pressure (IOP) measurements obtained with Goldmann applanation (GAT) and dynamic contour tonometry (DCT) in a Mexican population. 40 glaucoma patients were included in this cross-sectional observational cohort study. IOP measurements were performed in the following order: DCT, ultrasonic pachymetry and GAT, with a 5-minute difference between each measurement, between 8 am and 2 pm. Only DCT measurements of good quality (Q ≤ 3) were accepted. GAT measurements were made three times with the same Goldmann tonometer, previously checked for calibration errors, and the mean was used for statistical purposes. The IOP (mean [standard deviation], 95 % confidence interval [CI]) measured with the Goldmann tonometer (13.2 [2.4], 12.4-14.0 mmHg) was significantly lower than that obtained with the DCT (18.4 [3.3], 17.0-19.2 mmHg), p < 0.0001. Pearson's correlation coefficients between CCT and IOP measured with GAT and DCT were (r = 0.24, 95 % CI = 0.07-0.52, p = 0.133) and (r = 0.13, 95 % CI = -0.19 to 0.43, p = 0.412), respectively. The concordance correlation coefficient between GAT and DCT was r c = 0.3, 95 % CI = 0.17-0.41). DCT seems to overestimate the IOP as compared to GAT. Additionally, although there was a good correlation between the IOP measurements assessed with either GAT or DCT, the agreement was poor.