Clinical Outcomes of MicroPulse Transscleral Laser Therapy with the Revised P3 Delivery Device.

Aim: To evaluate the success and safety of MicroPulse transscleral laser therapy (TLT) on intraocular pressure (IOP) reduction in adults with uncontrolled glaucoma using different total treatment durations, sweep velocities, and a number of sweeps utilizing the revised MicroPulse P3 delivery device. Materials and methods: A single-center Institutional Review Board (IRB) approved multiple cohort studies of MicroPulse TLT with the revised MicroPulse P3 delivery device, which was conducted in 61 eyes from 40 adults with uncontrolled glaucoma. Eyes that received 50-second (GI, GII, and GIII) and 60-second (GIV, GV, and GVI) treatment applications between May and October 2020 were reviewed. Each hemisphere received a total of five, four, or three sweeps. The patient's IOP and glaucoma medications were monitored over 12 months follow-up. Qualified success was defined as an IOP of ≤21 mm Hg and/or reduction of ≥20% from baseline at 12 months, with no secondary glaucoma reinterventions. Complete success was defined as meeting the above criteria with no increase in glaucoma medications at 12 months. All eyes requiring a glaucoma surgical intervention were considered a failure. Results: Qualified success was achieved in 83.6% of eyes, while complete success was achieved in 75.4% of eyes. In eyes receiving 50-second applications of five, four, or three sweeps (GI, GII, and GIII), 70, 90, and 91% achieved qualified success, respectively; in eyes receiving 60-second applications of five, four, or three sweeps (GIV, GV, and GVI), 78, 82, and 90% achieved qualified success, respectively. Within each subgroup, mean IOP reductions ranged from 32.8 to 49.4% and were statistically significant (p < 0.008). The failure rate was 16.4%, and at least one eye failed in each subgroup. Conclusions: MicroPulse TLT with the revised MicroPulse P3 delivery device and relatively low total energy levels is safe and effective at lowering IOP. Efficacy appears to increase with longer treatment durations and slower sweep velocities, but statistical differences between age and clinical differences between baseline IOP measurements limit comparison between subgroups. Clinical significance: There is a lack of literature evaluating the safety and IOP-lowering success of the revised MicroPulse P3 delivery device using different total treatment durations, sweep velocities, and number of sweeps. How to cite this article: Checo LA, Dorairaj S, Wagner IV, et al. Clinical Outcomes of MicroPulse Transscleral Laser Therapy with the Revised P3 Delivery Device. J Curr Glaucoma Pract 2024;18(1):10-15.

Success rate in micropulse diode laser treatment with regard to lens status, refractive errors, and glaucoma subtypes.

PURPOSE: To evaluate the efficacy of micropulse transscleral cyclophotocoagulation (MP-TSCPC) considering different characteristics: glaucoma subtypes and lens status. METHODS: A retrospective case-series study was designed to evaluate intraocular pressure (IOP), and the number of IOP-lowering medications, used by glaucoma patients treated with MP-TSCPC between 2016 and 2019. Cases had a follow-up period of 12 months. Achieving an IOP reduction higher than 20%, or the decrease of at least one IOP-lowering medication, was considered a successful outcome. The same population was analyzed by classifying them in two groups as: glaucoma subtypes and lens status. The baseline spherical equivalent (SE) was also calculated for considering association with the achieved IOP. RESULTS: A total of 86 eyes were included. In most cases, IOP and IOP-lowering medications were decreased with a statistically significant difference (p < 0.0001), and all of them had a successful outcome. The percentage of IOP drop oscillated between 25.9% (open-angle glaucoma sub-group) and 37.5% (pseudoexfoliative glaucoma sub-group), 12 months after surgery. The difference between the groups was not statistically significant (p 0.20 and 0.32 for glaucoma subtypes and lens status, respectively). The Pearson's coefficient obtained was low for the SE and IOP association, at the 12 -month postoperative mark (- 0.009; p < 0.001). CONCLUSIONS: The MP-TSCPC treatment was successful in decreasing IOP and IOP-lowering medications, in different glaucoma subtypes. Differences between groups (glaucoma subtypes, phakic and pseudophakic eyes) were not statistically significant. No association was found between the SE and the IOP achieved value after MS-TSCPC treatment.

Combined Technique for the Application of Micropulse Cyclophotocoagulation in Patients with Uncontrolled Glaucoma: Cyclo Mix.

PURPOSE: To describe the outcomes of a combined technique (Cyclo Mix) in uncontrolled glaucoma cases. MATERIALS AND METHODS: Retrospective study. The Supra 810 nm subliminal laser (Quantel Medical, Cournon d'Auvergne, France) was used. A combined technique was performed using the subliminal mode (Subcyclo) in one hemifield (power of 2,000 mW, a duty cycle of 35%, and 80-150 seconds), and the continuous wave mode (Thermo Cyclo) on the other hemifield (power of 1,000 mW, exposure time of 2 seconds per spot). The primary endpoint was the probability of surgical failure. Mean intraocular pressure (IOP) change, best-corrected visual acuity (BCVA), number of glaucoma eye drops, and complications at 6 months postoperatively were secondary outcomes. RESULTS: Twenty-three eyes from 13 patients were included. Mean age was 61.4 ± 16.7 (range: 18-78 years), and 69% were female, with a baseline IOP of 20.3 ± 5.9 (range: 13-38 mm Hg). The cumulative probability of failure was 18 and 22% on days 90 and 180, respectively. Mean IOP reduction was -25.6 ± 20.9% at 6 months. The number of glaucoma eye drops was reduced to 1.2 ± 1 (p = 0.0024) at 6 months. No statistically significant change in the mean BCVA compared with baseline at 6 months was found (p = 0.84), and no severe complications were reported. CONCLUSION: Cyclo Mix seems to be a safe therapy that effectively reduces the IOP and glaucoma medications in eyes with uncontrolled open-angle glaucoma for up to 6 months. HOW TO CITE THIS ARTICLE: Waldo L-G, Julio H-Q, Jennifer C-V, et al . Combined Technique for the Application of Micropulse Cyclophotocoagulation in Patients with Uncontrolled Glaucoma: Cyclo Mix. J Curr Glaucoma Pract 2020;14(3):93-97.

Micropulse Transscleral Cyclophotocoagulation: A Hypothesis for the Ideal Parameters.

MicroPulse transscleral cyclophotocoagulation (IRIDEX Corp., Mountain View, CA) is a novel technique that uses repetitive micropulses of active diode laser (On cycles) interspersed with resting intervals (Off cycles). It has been proposed that the OFF cycles allow thermal dissipation and, therefore, reduce collateral damage. The literature suggests that Micropulse has a better safety profile compared to traditional continuous-wave cyclophotocoagulation. However, because it is a relatively new technique, there are no clear guidelines stating the ideal laser parameters that would allow the best balance between high and sustained effectiveness with minimal side effects. This research reviewed the literature to approximate ideal parameters for single-session treatment. To simplify the comparison between studies, this study used Joules (J) as a way to standardize the energy levels employed. The reviewed clinical publications allowed reduction of these parameters to a range between 112 and 150 J of total energy, which allows a moderate IOP lowering effect of around 30% with few/no complications. An additional narrowing of the parameters was achieved after analyzing recently published experimental data. These data suggest a different mechanism of action for the Micropulse, similar to that of the pilocarpine. This effect was maximum at 150 J. Since clinical studies show few or no complications, even at those energy levels, it could be hypothesized that the ideal parameters can be located at a point closer to 150 J. This data also leads to the concept of dosimetry; the capacity to dose mTSCPC treatment based on desired IOP lowering effect and risk exposure. Further prospective studies are needed to test the proposed evidence-based hypothesis.

Ciclofotocoagulación transescleral con sonda Nidek vs. G-Probe en el glaucoma absoluto doloroso / Transscleral cyclophotocoagulation with Nidek probe vs. G-Probe in painful absolute glaucoma

Objetivo: comparar los resultados del tratamiento, mediante ciclofotocoagulación transescleral con láser diodo utilizando sonda Nidek y sonda G-Probe, a ojos con glaucoma absoluto doloroso de pacientes atendidos en el Servicio de Glaucoma del Instituto Cubano de Oftalmología Ramón Pando Ferrer durante un año. Métodos: se realizó un estudio comparativo-prospectivo a 50 ojos distribuidos aleatoriamente en dos grupos: 25 ojos sometidos al procedimiento con sonda Nidek y 25 ojos tratados con sonda G-Probe. Se analizaron y compararon las variables presión intraocular, dolor, medicamentos hipotensores utilizados, así como complicaciones posoperatorias antes y después de aplicado el tratamiento. Resultados: los 50 ojos antes del tratamiento eran hipertensos; tres meses después los valores de la presión intraocular eran considerados normales para ambos grupos de estudio. Se mostró una variación estadísticamente significativa (p= 0,0000) respectivamente. Todos los pacientes referían dolor ocular previo. En ambos grupos se redujo satisfactoriamente el componente doloroso y se obtuvieron resultados similares. Se redujo significativamente el número de medicamentos hipotensores, y la mayor parte de los ojos no requirió más terapia farmacológica después de los tres meses. El número de complicaciones asociadas fue discretamente superior en los ojos tratados con sonda Nidek. La uveítis y los picos hipertensivos en el posoperatorio inmediato fue lo más destacado con el uso de ambas sondas. Conclusiones: la ciclofotocoagulación transescleral con láser diodo reduce las cifras de presión intraocular y el componente doloroso con ambas sondas satisfactoriamente. La mayoría de los ojos tratados no requiere terapia farmacológica hipotensora después de 3 meses de realizada. El procedimiento ciclodestructivo es seguro y causa un número discreto de complicaciones con el uso de ambas sondas(AU)

Objective: compare the results of treatment with diode laser transscleral cyclophotocoagulation using Nidek probe and G-probe for eyes with painful absolute glaucoma of patients cared for at the Glaucoma Service of Ramón Pando Ferrer Cuban Institute of Ophthalmology during one year. Methods: a prospective comparative study was conducted of 50 eyes randomly distributed in two groups: 25 treated with Nidek probe and 25 with G-Probe. The following variables were analyzed and compared: intraocular pressure, pain, hypotensive drugs used, and postoperative complications before and after application of the treatment. Results: before treatment, the 50 eyes were hypertensive, whereas three months later intraocular pressure values were considered to be normal in both study groups. A statistically significant variation was found (p= 0.0000). All the patients stated having had ocular pain previously. The two groups showed a satisfactory reduction in pain, with similar results between them. The number of hypotensive drugs was significantly reduced, and most eyes did not require any more drug therapy after three months. The number of associated complications was slightly higher in the eyes treated with Nidek probe. Uveitis and hypertensive peaks in the immediate postoperative period were the most outstanding events with the use of both probes. Conclusions: diode laser transscleral cyclophotocoagulation satisfactorily reduces intraocular pressure values and pain with the use of both probes. Most of the eyes treated do not require hypotensive drug therapy after 3 months. The cyclodestructive procedure is safe, causing a slight number of complications with the use of both probes(AU)