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The effect of cumulative energy in repeated subliminal transscleral cyclophotocoagulation: a retrospective study

Abstract

Background

The long-term safety and efficacy of repeated applications of subliminal transscleral cyclophotocoagulation (SL-TSCPC) with a focus on cumulative energy was evaluated in glaucoma patients.

Methods

In this retrospective, multicentric study the data of a total of 82 eyes with various causes of glaucoma that were treated with a single or multiple applications of SL-TSCPC were collected. Treatments were performed under general or local anesthesia with an 810 nm diode laser. Power was 2000 mW; duty cycle, 31.3%; total treatment duration, 80–320 s; equaling a total energy of 50–200 J per treatment session. Fifty-five eyes (55 patients) presented for all follow-ups, and these eyes were selected for further statistical analysis. The mean age was 60.0 ± 17.1 years, and 22 (40%) of the patients were female. Intraocular pressure (IOP) and dependence on further glaucoma medication were evaluated at 12 months following the initial treatment.

Results

Eyes underwent 1 or 2 consecutive SL-TSCPC treatments. Median (min–max) baseline IOP of 34 (13–69) decreased to 21.5 (7–61), 22 (8–68), 20 (9–68), and 19.5 (3–60) mmHg at the 1, 3, 6, and 12-month postoperative timepoints respectively. The mean (± SD) IOP decrease at 12 months was 26 ± 27%, 39 ± 32%, and 49 ± 33% in the low (below 120 J, n = 18), medium (120–200 J, n = 24), and high (above 200 J, n = 13) cumulative energy groups respectively. At the 12-month timepoint, oral carbonic anhydrase use was discontinued in ¾ of the cases.

Conclusions

It was found that the repeated application of SL-TSCPC safely and efficiently decreases IOP in a Caucasian population with heterogenous causes of glaucoma, eyes with silicone oil responded to a greater extent. Inclusion of cumulative energy scales may contribute to better addressing repeated procedures in a standardized fashion.

Peer Review reports

Background

Current glaucoma treatment modalities aim to reduce the intraocular pressure (IOP) [1,2,3] by increasing the outflow of the aqueous and/or decreasing its production. The classical therapeutic regimen usually consists of topical medication [4] or selective laser trabeculoplasty (SLT) [5] as first-line options. Second-line options should the conservative first-line approaches fail to reduce IOP to the target level [6], include oral carbonic anhydrase inhibitor (CAI) treatment [7] and invasive surgical techniques, such as trabeculectomy [8] and the implantation of drainage devices [9, 10]. Cyclodestructive procedures have been considered as a last step in controlling IOP, as these procedures are often associated with severe adverse events [11, 12]. With the advent of subliminal transscleral cyclophotocoagulation (SL-TSCPC), the incidence of complications appear to be lower compared to continuous wave transscleral cyclophotocoagulation (CW-TSCPC), making it a plausible choice for patients in whom other surgical options would be less feasible [13]. The efficacy and the safety of SL-TSCPC treatment in primary open-angle glaucoma (POAG) [14,15,16] seem to be favourable, and the results in secondary glaucoma cases have also been promising [17, 18]. The delivered treatment energy shows large variations in power, duration, and duty cycle [19,20,21,22,23]. Sweep velocity and the resulting fluence are also paramount factors to be considered, as higher fluence is associated with greater efficacy [24]. According to the hypothetical search for ideal parameters by Sanchez et al., the target energy should be approximately 150 J [25]. While Lim et al., who have investigated repeated SL-TSCPC procedures and have introduced the concept of cumulative energy, postulated higher values of 150–200 J [26].

Expert consensus guidelines were published [24, 27] after the examined treatment period and during the data processing period of this study, and these guidelines recommend a total energy of 125.2 J. Alongside the importance of fluence, we would also advocate that cumulative energy, as proposed by Lim, should be included when designing future studies regarding the safety and efficacy of SL-TSCPC treatment.

In this work, we investigated the clinical response to SL-TSCPC treatment in various types of IOP rise.

Methods

Data collection

A retrospective, multicentric analysis of 82 eyes of 82 Caucasian patients undergoing SL-TSCPC between 2019 and 2021 at three regional ophthalmology centers (University of Szeged, Szeged, Hungary, Péterfy Hospital, Budapest, Hungary, and Erzsébet Teaching Hospital, Sopron, Hungary) was performed (Table 1). The Ethics Committee of the University of Szeged approved the data acquisition with the participation of the ancillary sites (protocol number: SLTSCPCRET-001; file number: 34/2022SZTE RKEB). The study was conducted in accordance with the Tenets of the Declaration of Helsinki. Baseline characteristics, including the type of glaucoma (Table 2), the age and sex of the patient, as well as visual acuity (VA), IOP, topical and oral antiglaucoma medication were noted. Furthermore, the following interventional parameters were collected: anesthesia, laser machine used, marking method of the treatment area, energy, duty cycle, duration, postoperative care regimen. Follow-up visit times were defined at postoperative months 1, 3, 6 and 12. At each follow-up, VA, IOP, topical and oral antiglaucoma medication and adverse event data were registered for further analysis.

Table 1 Demographic information
Table 2 Distribution of Glaucoma Types

Criteria for success were defined as 20% or greater reduction in IOP (criterion A), 25% or greater reduction in IOP (criterion B), and 30% or greater reduction in IOP from baseline (criterion C), with or without topical glaucoma medications at follow-up as published by Tekeli et al. [19] Target IOP values at or under 18, 15, and 12 mmHg were defined as a secondary outcome measure, also based on the same publication [19].

Complete failure was defined as IOP lower than 6 mmHg with hypotony maculopathy (criterion 1), loss of three or more Snellen lines or loss of light perception (criterion 2), or surgical failure when additional glaucoma surgical intervention to control the IOP was needed, or discontinuation of oral CAI was not possible (criterion 3), as published by Jun Yong Chow et al. [28] and modified to this study so that criterion 3 excluded repeated SL-TSCPC or other non-invasive lasers, such as SLT.

SL-TSCPC procedures

Treatments were performed under general or local (retrobulbar, peribulbar or sub-Tenon’s block) anesthesia with either the Supra 810 or the Vitra 810 systems (n = 77) and the Subcyclo probe (Quantel Medical, Rockwall, TX, USA) or the Cyclo G6 Laser System (n = 5) with the original MicroPulse P3 probe (IRIDEX Corporation, Mountain View, CA). Power and duty cycle were constant at 2000 mW and 31.3%, respectively. The treatment area was defined with the aid of transillumination; eyes not suitable for visualizing the ciliary body band were marked 3 millimeters posterior to the limbus, with 3 and 9 clock hours omitted in all cases. Total treatment duration ranged from 80 to 320 s, equaling a total energy of 50 to 200 J per treatment session, delivered via a slow continuous sweeping motion.

Two subgroups were formed based on the number of total SL-TSCPC sessions: the first subgroup participated in a single session, the other subgroup consisted of eyes that received one additional treatment during the follow-up period. Cumulative energy was calculated in eyes undergoing repeated treatment sessions. The follow-up time commenced from the first session of the study period.

Statistical analysis

IOP data is expressed as median (minimum–maximum), and other data is expressed as mean ± standard deviation (SD). The homoscedasticity of each variable was confirmed using Bartlett’s test, and the normality of their distribution was confirmed using the Shapiro-Wilk test. Statistical analysis was performed in R (Vienna, Austria), using RStudio (PBC, Boston). Cumulative success and failure in all 82 eyes were evaluated using Kaplan–Meier survival analysis and log-rank test. Further statistical analysis was performed on the 55 eyes that completed the 12-month follow-up. Changes in IOP throughout the follow-up period were treated as repeated measurements and were analysed using ANOVA followed by Bonferroni-corrected t-tests. When calculating the required IOP decrease (%) to fulfil criteria, the required percentages were calculated for each patient, and these percentages are presented as mean ± SD. The decrease in oral CAI use and subgroup analyses for silicone oil eyes were evaluated using Fisher’s exact test. Other possible explanatory variables were also analysed using Fisher’s exact test and logistic regression analysis. Statistical significance was assumed when the p-value was < 0.05.

Results

A total number of 104 SL-TSCPC treatments on 82 eyes were reviewed: 82, 76, 66 and 55 eyes had 1, 3, 6 and 12 months of follow-up respectively.

Kaplan–Meier survival analysis performed on 82 eyed showed at least 25% success in all eyes for all success criteria. Repeated treatment showed statistically significant additional benefit (Fig. 1).

A substantial portion of the 82 eyes presented with secondary glaucoma induced by silicone oil (n = 31) A variety of other etiologies accounted for the remaining cases (Table 3).

Fig. 1
figure 1

Kaplan–Meier survival analysis based on success criterion A, 20% or greater reduction in IOP (A); criterion B, 25% or greater reduction in IOP (B); and criterion C, 30% or greater reduction in IOP (C); and failure criteria 1-3; p-values calculated using log-rank test

Table 3 Prior History of Ocular Procedures

Mean age at treatment was 60.0 ± 17.1 years. The male to female ratio was 22:33, and the right to left eye distribution was 26:29.

Of the 55 eyes that completed the 12-month follow up 37 (67%) underwent one, while 18 (33%) received two consecutive SL-TSCPC treatments depending on the clinical response and on the amount of IOP decrease. Thus, cumulative energy delivered throughout the sessions was calculated for each eye and the following thresholds were defined: under 120 J (mean delivered energy: 96.5 ± 10.9 J), 120–200 J (mean delivered energy: 186.4 ± 25.4 J) and above 200 J (mean delivered energy: 291.8 ± 65.3 J) as low (n = 18, 33%), medium (n = 24, 44%) and high (n = 13, 23%) cumulative energy groups respectively.

The postoperative treatment regimen consisted of dexamethasone, NSAIDs, cyclopentolate, and atropine in various combinations. Only 1 of the 55 eyes did not receive anti-inflammatory therapy.

VA was recorded on Kettesy’s chart, which is a decimal chart similar to Snellen’s ranging from 0.1 to 1.0 values, read from 5 m. Visual acuities below this were converted as follows; 0.08, 0.06, 0.04, 0.02 for counting fingers from 4, 3, 2 and 1 m respectively. Hand movement and light perception were given 0.001 and 0.0001 values respectively. No light perception equaled 0.

Median baseline IOP (34 (13–69) mmHg) decreased statistically significantly at 1 month (21.5 (7–61) mmHg) postoperatively and maintained a significant decrease through the 3-month (22 (8–68) mmHg) and the 6-month timepoints (20 (9–68) mmHg), all the way to the 12-month endpoint (19.5 (3, 4, 5, 60) mmHg; p < 0.001).

Success based on criteria A, B and C, with no failure criteria fulfilled, at 12 months were met in 27 (49%), 25 (45%), and 24 (44%) out of 55 eyes respectively. When secondary success endpoints were evaluated, eyes under or at 18 mmHg, under or at 15 mmHg and under or at 12 mmHg were 14 (25%), 8 (15%), and 6 (11%) respectively out of 55. (Fig. 2) Neither cumulative energy group did significantly outperform any other at each decrease threshold.

Fig. 2
figure 2

Scatterplot of pre-and postoperative IOP values; dashed line represents the limit below which IOP decrease was achieved, full diagonal lines represent 20%, 25%, and 30% decrease respectively, horizontal lines represent postoperative IOP values of 18, 15, 12, and 6 mmHg respectively

The mean decrease of IOP at 12 months was 26 ± 28%, 39 ± 32%, and 49 ± 33% in the low, medium and high cumulative energy groups respectively, with no statistically significant difference between the groups (ANOVA p = 0.17; Fig. 3). Median IOP at 12 months in the corresponding energy groups was 22 (6–42), 19 (5–60), 18 (3–48).

Fig. 3
figure 3

Changes in IOP at 12 months in the low, medium, and high cumulative energy groups

One eye (2%) with hypotony maculopathy (criterion 1), 17 eyes (31%) with a marked decrease in VA (criterion 2), and 6 eyes (11%) with surgical failure (criterion 3) were identified as treatment failures at 12 months. There was no statistically significant difference in the occurrence of failures between cumulative energy groups.

VA improved in 9 eyes (16%), decreased by 3 or more lines in 17 eyes (31%), and remained relatively stable in 29 eyes (53%). The magnitude of IOP decrease at 12 months was not correlated with VA loss of 3 or more lines decimal (failure criterion 2). Progression to no light perception (NLP) occurred in 5 patients during the 12-month follow-up. Preoperative VA was of hand motion or light perception in 4 of the 5 patients and 1 patient had 0.6 decimal vision that was lost after retinal detachment. Possible causes of decrease in VA, including baseline VA, baseline IOP, decrease in IOP, number of treatments, and cumulative energy were also evaluated using logistic regression. None of these variables were in interaction with the decrease in VA (Table 4).

Table 4 Changes in VA at 12 months after the first treatment

In the studied cohort, amaurosis fugax occurred in 1 patient, 3 patients presented with IOP under 6 mmHg after the procedure, and 2 of them retained preoperative VA with no maculopathy. Cystoid macular edema developed in 1 patient, age-related macular degeneration developed in 1 patient, diabetic retinopathy developed in 1 patient, central retinal vein occlusion (CRVO) developed in 1 patient, retinal detachment was seen in 1 patient, uveitis developed in 2 patients, and Meibomian gland dysfunction occurred in 1 patient.

There was a slight but not significant change recorded in the number of topical IOP lowering medications used at baseline and postoperative 12 months both in the number of bottles (1.7 ± 0.7 to 1.5 ± 0.5) and in the number of active ingredients (2.9 ± 1.0 to 2.5 ± 1.3). On the other hand, oral CAI use at postoperative 12 months had been successfully discontinued in 18 of the 24 patients previously in need of acetazolamide therapy (75% decrease, p < 0.01; Fig. 4).

Fig. 4
figure 4

Changes in glaucoma medications from baseline to postoperative 12 months (CAI, carbonic anhydrase inhibitor); * – p < 0.05, Fisher’s exact test

The IOP decrease at 12 months in eyes with silicone oil (–43 ± 29%) was more pronounced compared to the rest of eyes (–33 ± 33%; p = 0.21). Criterion A success was also more common in eyes with silicone oil (Table 5, p = 0.03). These eyes had an odds ratio of 3.65 to reach 20% of IOP reduction compared to eyes with no silicone oil. No statistically significant difference was found between eyes with and without silicone oil regarding retreatments (p = 0.46) or the incidence of VA decrease (p = 1.00). Success in eyes with silicone oil was achieved with seemingly lower energy levels (162.8 ± 77.4 J) compared to non-silicone oil eyes (181.1 ± 58.9 J; p = 0.52).

Table 5 Criterion A success (–20% IOP) in eyes with and without silicone oil

The following categoric variables were further evaluated using Fischer’s exact test: previous cataract surgery, prior glaucoma surgery, baseline oral CAI use, and sex; none of the variables were found to be associated with higher criterion A success (p = 0.36, p = 1.00, p = 0.42, and 1.00, respectively). Logistic regression was used to quantify the relative effect of the following continuous variables: cumulative energy, number of topical compounds at baseline, baseline IOP, baseline VA, and patient age. None of the variables were found to be associated with higher criterion A success (p = 0.33, p = 0.27, p = 0.64, p = 0.32, and p = 0.68).

No statistically significant difference was found between the two groups based on surgical treatment area, 3 mm posterior to the limbus (n = 34, 62%) versus transillumination (n = 21, 38%), in terms of mean IOP decrease, and fulfilment of success or failure criteria.

Discussion

In this heterogeneous cohort of mainly secondary glaucoma patients with a high baseline IOP uncontrollable by prior therapy, the SL-TSCPC procedure offered a non-invasive, relatively safe method for an additional 26–49% decrease of IOP that could be observed from the first postoperative month all the way to the endpoint at 12 months. This effect is approximately equivalent to adding an extra topical medication or a fixed combination to the treatment regimen. While the number of glaucoma drops used could not be decreased significantly, the procedure enabled a large proportion of the patients to discontinue oral IOP lowering medication.

Despite the favourable success in achieving up to 30% of IOP reduction, the target IOP values of 18, 15, and 12 mmHg defined as secondary outcome measures were met in a smaller number of eyes. However, this may be attributable to the relatively high baseline IOP values, as in order to completely fulfil these outcome measures, the required IOP decrease was calculated to be −45 ± 22%,

–54 ± 18% and −63 ± 15% on average in all energy groups.

Similarly to the findings of Zbiba [17], the subgroup analysis of silicone oil induced IOP elevations showed decrease of more than 43%, even though silicone oil removal was not performed prior to or during the procedure. No underlying correlation was uncovered that can be added to the current existing hypothesis that the absence of vitreous gel promotes the posterior movement of the ciliary body during the laser procedure [17].

Failure seems to be independent of the cumulative energy within the thresholds defined in this study. Prolonged hypotony with additional complications, such as maculopathy, following SL-TSCPC is typically not encountered [28,29,30] or is resolved without sequale [14, 19] but should still be considered a valid risk (2–7%) as presented in this and other studies [21, 26]. Deterioration of VA (failure criterion 2) was observed in one third of patients. Large variation across publications exists from no VA loss [20] or low incidence [30] up to similarly high failure ratios [23, 26] Whether this can be solemnly attributed to disease progression, treatment related or non-related adverse events, or the combination of the former is not yet evident. The retrospective nature of our study did not allow for further differentiation between causes in this patient cohort with already severely compromised visual functions. Neovascular glaucoma and silicone oil induced glaucoma already pose a higher risk of vison loss [31, 32].

Review of the current literature shows that the criteria of success varies on a broad scale from IOP reduction of at least 20% [17, 18, 20, 23, 26, 28, 29, 33,34,35,36,37,38,39], IOP reduction of at least 30% [40,41,42,43], the variations of specific IOP and percentage limits [13, 19, 21, 25, 44], all the way to the most stringent criteria by Tekeli and Soussi [30, 45]. In our study, the fulfilment of these criteria shows the discrepancy between the high proportion of patients with an IOP reduction of more than 30% (65%) versus the percentage of low target IOPs achieved (13%) with this method alone. The large difference between Tekeli’s success ratio for their original criteria A, B and C of 67%, 53%, and 42% respectively compared to the equivalent of our combined primary and secondary endpoints of 35%, 18%, and 13% might be attributable to varying glaucoma subtypes, such as POAG vs. secondary glaucoma, and pre-treatment IOPs. Our results better resemble those of Soussi with 35%, 27%, and 11% despite dissimilar baseline characteristics. It should also be noted that both studies and our current cohort are in the fluence range [24] of ≤ 52.4 J/cm2, which might limit the overall IOP decreasing potential as well, compared to studies reporting SL-TSCPC efficacy with higher fluence values.

The preferred method of the authors was delivering 150 J of energy per session to the treatment area marked with transillumination with the power set at 2.0 Watts, the duty cycle at 31.3%, and treatment time at 120 s per hemisphere with a sweep velocity/hemisphere of 20 s/sweep, with 3 and 9 o’clock hours omitted. Repeated procedure was warranted if a minimum of 20% decrease was not seen or target IOP was not reached. Expert consensus guidelines published during the data acquisition and processing of this study recommended power of 2.5 Watts, duty cycle of 31.3% and treatment time of 80 s per hemisphere with a sweep velocity/hemisphere of 20 s/sweep [24, 27]. The calculated total energy, dwell times, and fluence of this study are 150 J, 0.63 s, and 51.89 J/cm2. The recommendation in the guideline for the same variables is 125.2 J, 0.63 s, and 64.86 J/cm2 respectively.

Fluence is greatly determined by surgical technique. Even in the presence of fixed power and duty cycle settings, substantial variability in delivered energy can arise from a number of confounding factors including surgeon experience, patient anatomy, identification of treatment area, aiming, real-time sweep velocity. Although aided by the periodic beeping of the SL-TSCPC machine or any other chronometer, actual dwell times are subject to unaccounted deviations from predefined protocol.

High-quality randomised clinical trials aim at recruiting patients with well-outlined inclusion and exclusion criteria, homogeneous glaucoma types, preferably no prior (or one specific) surgical procedures to ensure clarity of data. Our mixed retrospective cohort rather illustrates a real-life scenario, where multiple comorbidities, treatments, and large variations in baseline characteristics introduce uncertainty in the identification of explanatory variables.

Still, limited data are available on the relationship between the cumulative energy, the safety, and the efficacy of repeated procedures. A number of studies include a variable number of repeated SL-TSCPC treatments and cumulative energy values ranging from as low as 56.31 J [20] to as high as 800 J [21] (Table 6). The highest reported number of repeated interventions was four. One study by Lim [26] specifically focuses on the cumulative energy with up to three repeated sessions in an Asian population, and seems to find a maximal effect in the in the 150–199.9 J range. In our retrospective study we were not able to reproduce such maximal effect with the investigated cumulative energy thresholds, as our results showed increasing efficacy with dose. All but one eye in the high energy group exhibited IOP decrease (Fig. 3). We were able to show that repeated procedures did indeed provide additional benefit without substantial increase in risk (Fig. 1C).

Table 6 Overview of reports with calculated cumulative energy values

The guidelines [24, 27] provide a useful collection of evidence-based consensus mainly on the MicroPulse (IRIDEX) machine. On the other hand, data regarding the safety and the efficacy of the Supra 810 and Vitra 810 (Quantel Medical) machines are scarce [37, 39, 50, 51]. Our results suggest that similar outcomes can be achieved with the Quantel machines, also broadening treatment options.

Among the aforementioned confounders, the greatest limitation of this study is the high percentage of dropout and data loss during the 12-month follow-up period. This is largely attributable to the study being conducted during the COVID pandemic, and to the consequent lockdown and transfer of medical personnel to COVID care facilities.

Conclusions

Our findings suggest that repeated SL-TSCPC procedures provide additional IOP lowering effect in the Caucasian population, similar to the Asian cohort described by Lim. Eyes with silicone oil seemed to respond to a greater extent over the period of this study. This study supports the inclusion of cumulative energy scales alongside treatment energy and fluence to better address the safety and the effectiveness of repeated procedures in a standardized fashion.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CRVO:

Central retinal vein occlusion

CW-TSCPC:

Continuous wave transscleral cyclophotocoagulation

IOP:

Intraocular pressure

LP:

Light perception

NLP:

No light perception

POAG:

Primary open-angle glaucoma

SD:

Standard deviation

SL-TSCPC:

Subliminal transscleral cyclophotocoagulation

SLT:

Selective laser trabeculoplasty

VA:

Visual acuity

References

  1. Kass MA, Heuer DK, Higginbotham EJ et al. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002;120(6):701–713; discussion 829–830 https://doi.org/10.1001/archopht.120.6.701.

    Article  PubMed  Google Scholar 

  2. Leske MC, Heijl A, Hussein M, et al. Factors for glaucoma progression and the effect of treatment: the early manifest glaucoma trial. Arch Ophthalmol. 2003;121(1):48–56. https://doi.org/10.1001/archopht.121.1.48.

    Article  PubMed  Google Scholar 

  3. The AGIS Investigators. The Advanced Glaucoma Intervention Study (AGIS): 7. The relationship between control of intraocular pressure and visual field deterioration.The AGIS Investigators. Am J Ophthalmol. 2000;130(4):429–40. https://doi.org/10.1016/s0002-9394(00)00538-9.

    Article  Google Scholar 

  4. Tanna AP, Rademaker AW, Stewart WC, Feldman RM. Meta-analysis of the efficacy and safety of alpha2-adrenergic agonists, beta-adrenergic antagonists, and topical carbonic anhydrase inhibitors with prostaglandin analogs. Arch Ophthalmol. 2010;128(7):825–33. https://doi.org/10.1001/archophthalmol.2010.131.

    Article  CAS  PubMed  Google Scholar 

  5. Gazzard G, Konstantakopoulou E, Garway-Heath D, et al. Laser in Glaucoma and ocular hypertension (LiGHT) trial: six-year results of primary selective laser trabeculoplasty versus Eye drops for the Treatment of Glaucoma and ocular hypertension. Ophthalmology. 2023;130(2):139–51. https://doi.org/10.1016/j.ophtha.2022.09.009.

    Article  PubMed  Google Scholar 

  6. Jampel HD. Target pressure in glaucoma therapy. J Glaucoma. 1997;6(2):133–8.

    Article  CAS  PubMed  Google Scholar 

  7. Berson FG, Epstein DL, Grant WM, Hutchinson BT, Dobbs PC. Acetazolamide dosage forms in the treatment of glaucoma. Arch Ophthalmol. 1980;98(6):1051–4. https://doi.org/10.1001/archopht.1980.01020031041005.

    Article  CAS  PubMed  Google Scholar 

  8. Lichter PR, Musch DC, Gillespie BW, et al. Interim clinical outcomes in the collaborative initial Glaucoma treatment study comparing initial treatment randomized to medications or surgery. Ophthalmology. 2001;108(11):1943–53. https://doi.org/10.1016/s0161-6420(01)00873-9.

    Article  CAS  PubMed  Google Scholar 

  9. Gedde SJ, Schiffman JC, Feuer WJ, et al. Treatment outcomes in the Tube Versus Trabeculectomy (TVT) study after five years of follow-up. Am J Ophthalmol. 2012;153(5):789–e8032. https://doi.org/10.1016/j.ajo.2011.10.026.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Christakis PG, Zhang D, Budenz DL, et al. Five-year pooled data analysis of the Ahmed Baerveldt Comparison Study and the Ahmed Versus Baerveldt Study. Am J Ophthalmol. 2017;176:118–26. https://doi.org/10.1016/j.ajo.2017.01.003.

    Article  PubMed  Google Scholar 

  11. Hennis HL, Stewart WC. Semiconductor diode laser transscleral cyclophotocoagulation in patients with glaucoma. Am J Ophthalmol. 1992;113(1):81–5. https://doi.org/10.1016/s0002-9394(14)75758-7.

    Article  CAS  PubMed  Google Scholar 

  12. Kosoko O, Gaasterland DE, Pollack IP, Enger CL. Long-term outcome of initial ciliary ablation with contact diode laser transscleral cyclophotocoagulation for severe glaucoma. The Diode laser ciliary ablation Study Group. Ophthalmology. 1996;103(8):1294–302. https://doi.org/10.1016/s0161-6420(96)30508-3.

    Article  CAS  PubMed  Google Scholar 

  13. Aquino MCD, Barton K, Tan AMWT, et al. Micropulse versus continuous wave transscleral diode cyclophotocoagulation in refractory glaucoma: a randomized exploratory study. Clin Exp Ophthalmol. 2015;43(1):40–6. https://doi.org/10.1111/ceo.12360.

    Article  PubMed  Google Scholar 

  14. Chang HL, Chao SC, Lee MT, Lin HY. Micropulse transscleral cyclophotocoagulation as primary surgical treatment for primary open angle glaucoma in Taiwan during the COVID-19 pandemic. Healthc (Basel). 2021;9(11):1563. https://doi.org/10.3390/healthcare9111563.

    Article  Google Scholar 

  15. Tong W, Shen TYT, Wong HC, Aquino MC, Chew P, Lim D. One-year outcomes of micropulse cyclophototherapy for primary open-angle glaucoma. J Glaucoma. 2021;30(10):911–20. https://doi.org/10.1097/IJG.0000000000001925.

    Article  PubMed  Google Scholar 

  16. Sarrafpour S, Saleh D, Ayoub S, Radcliffe NM. Micropulse transscleral cyclophotocoagulation: a look at long-term effectiveness and outcomes. Ophthalmol Glaucoma. 2019;2(3):167–71. https://doi.org/10.1016/j.ogla.2019.02.002.

    Article  PubMed  Google Scholar 

  17. Zbiba W, Sayadi S, Kharrat M, Daoued M. Efficacy and safety of Micropulse Transscleral Laser Therapy in Silicone Oil-induced Glaucoma. J Glaucoma. 2022;31(8):689–93. https://doi.org/10.1097/IJG.0000000000002051.

    Article  PubMed  Google Scholar 

  18. de Vries VA, Pals J, Poelman HJ, Rostamzad P, Wolfs RCW, Ramdas WD. Efficacy and safety of Micropulse Transscleral Cyclophotocoagulation. J Clin Med. 2022;11(12):3447. https://doi.org/10.3390/jcm11123447.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Tekeli O, Köse HC. Outcomes of micropulse transscleral cyclophotocoagulation in primary open-angle glaucoma, pseudoexfoliation glaucoma, and secondary glaucoma. Eur J Ophthalmol. 2021;31(3):1113–21. https://doi.org/10.1177/1120672120914231.

    Article  PubMed  Google Scholar 

  20. Vig N, Ameen S, Bloom P, et al. Micropulse transscleral cyclophotocoagulation: initial results using a reduced energy protocol in refractory glaucoma. Graefes Arch Clin Exp Ophthalmol. 2020;258(5):1073–9. https://doi.org/10.1007/s00417-020-04611-0.

    Article  PubMed  Google Scholar 

  21. Magacho L, Lima FE, Ávila MP. Double-session micropulse transscleral laser (CYCLO G6) for the treatment of glaucoma. Lasers Med Sci. 2020;35(7):1469–75. https://doi.org/10.1007/s10103-019-02922-1.

    Article  PubMed  Google Scholar 

  22. Emanuel ME, Grover DS, Fellman RL, et al. Micropulse Cyclophotocoagulation: initial results in refractory Glaucoma. J Glaucoma. 2017;26(8):726–9. https://doi.org/10.1097/IJG.0000000000000715.

    Article  PubMed  Google Scholar 

  23. Williams AL, Moster MR, Rahmatnejad K, et al. Clinical efficacy and Safety Profile of Micropulse Transscleral Cyclophotocoagulation in Refractory Glaucoma. J Glaucoma. 2018;27(5):445–9. https://doi.org/10.1097/IJG.0000000000000934.

    Article  PubMed  Google Scholar 

  24. Grippo TM, Sanchez FG, Stauffer J, Marcellino G. MicroPulse® transscleral laser therapy - fluence may explain variability in clinical outcomes: a literature review and analysis. Clin Ophthalmol. 2021;15:2411–9. https://doi.org/10.2147/OPTH.S313875.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Sanchez FG, Peirano-Bonomi JC, Grippo TM. Micropulse transscleral cyclophotocoagulation: a hypothesis for the Ideal parameters. Med Hypothesis Discov Innov Ophthalmol. 2018;7(3):94–100.

    PubMed  PubMed Central  Google Scholar 

  26. Lim EJY, Aquino CM, Lun KWX, et al. Efficacy and safety of repeated micropulse transscleral diode cyclophotocoagulation in advanced glaucoma. J Glaucoma. 2021;30(7):566–74. https://doi.org/10.1097/IJG.0000000000001862.

    Article  PubMed  Google Scholar 

  27. Grippo TM, Töteberg-Harms M, Giovingo M, et al. Evidence-based consensus guidelines series for micropulse transscleral laser therapy - surgical technique, post-operative care, expected outcomes and retreatment/enhancements. Clin Ophthalmol. 2023;17:71–83. https://doi.org/10.2147/OPTH.S389198.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Chow JY, Wan Norliza WM, Bastion MC. Outcomes of Subliminal Transscleral Cyclophotocoagulation treatment in glaucoma. Med J Malaysia. 2021;76(2):236–40.

    CAS  PubMed  Google Scholar 

  29. Yelenskiy A, Gillette TB, Arosemena A, et al. Patient outcomes following Micropulse Transscleral Cyclophotocoagulation: intermediate-term results. J Glaucoma. 2018;27(10):920–5. https://doi.org/10.1097/IJG.0000000000001023.

    Article  PubMed  Google Scholar 

  30. Tekeli O, Köse HC. Comparative efficacy and safety of micropulse transscleral laser cyclophotocoagulation using different duration protocols in eyes with good visual acuity. Graefes Arch Clin Exp Ophthalmol. 2021;259(11):3359–69. https://doi.org/10.1007/s00417-021-05265-2.

    Article  PubMed  Google Scholar 

  31. Kingston EJ, Lusthaus JA. Two-year outcomes of patients presenting to Sydney Eye Hospital with neovascular glaucoma. Int Ophthalmol. 2023;13. https://doi.org/10.1007/s10792-023-02675-5. Published Online March.

  32. Nicolai M, Lassandro N, Franceschi A, et al. Intraocular pressure rise linked to silicone oil in retinal surgery: a review. Vis (Basel). 2020;4(3):36. https://doi.org/10.3390/vision4030036.

    Article  Google Scholar 

  33. de Crom RMPC, Slangen CGMM, Kujovic-Aleksov S, Webers CAB, Berendschot TTJM, Beckers HJM. Micropulse Trans-scleral cyclophotocoagulation in patients with Glaucoma: 1- and 2-Year treatment outcomes. J Glaucoma. 2020;29(9):794–8. https://doi.org/10.1097/IJG.0000000000001552.

    Article  PubMed  Google Scholar 

  34. Laruelle G, Pourjavan S, Janssens X, Marinescu-George C, Boustani G. Real-life experience of micropulse transscleral cyclophotocoagulation (MP-TSCPC) in advanced and uncontrolled cases of several glaucoma types: a multicentric retrospective study. Int Ophthalmol. 2021;41(10):3341–8. https://doi.org/10.1007/s10792-021-01896-w.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Kuchar S, Moster MR, Reamer CB, Waisbourd M. Treatment outcomes of micropulse transscleral cyclophotocoagulation in advanced glaucoma. Lasers Med Sci. 2016;31(2):393–6. https://doi.org/10.1007/s10103-015-1856-9.

    Article  PubMed  Google Scholar 

  36. Zaarour K, Abdelmassih Y, Arej N, Cherfan G, Tomey KF, Khoueir Z. Outcomes of Micropulse Transscleral Cyclophotocoagulation in uncontrolled Glaucoma patients. J Glaucoma. 2019;28(3):270–5. https://doi.org/10.1097/IJG.0000000000001174.

    Article  PubMed  Google Scholar 

  37. Benhatchi N, Bensmail D, Lachkar Y. Benefits of SubCyclo Laser Therapy guided by high-frequency Ultrasound Biomicroscopy in patients with refractory Glaucoma. J Glaucoma. 2019;28(6):535–9. https://doi.org/10.1097/IJG.0000000000001230.

    Article  PubMed  Google Scholar 

  38. Chen HSL, Yeh PH, Yeh CT, et al. Micropulse transscleral cyclophotocoagulation in a Taiwanese population: 2-year clinical outcomes and prognostic factors. Graefes Arch Clin Exp Ophthalmol. 2022;260(4):1265–73. https://doi.org/10.1007/s00417-021-05468-7.

    Article  CAS  PubMed  Google Scholar 

  39. Keilani C, Benhatchi N, Bensmail D, et al. Comparative effectiveness and tolerance of Subliminal Subthreshold Transscleral Cyclophotocoagulation with a duty factor of 25% Versus 31.3% for advanced Glaucoma. J Glaucoma. 2020;29(2):97–103. https://doi.org/10.1097/IJG.0000000000001409.

    Article  PubMed  Google Scholar 

  40. Preda MA, Karancsi OL, Munteanu M, Stanca HT. Clinical outcomes of micropulse transscleral cyclophotocoagulation in refractory glaucoma-18 months follow-up. Lasers Med Sci. 2020;35(7):1487–91. https://doi.org/10.1007/s10103-019-02934-x.

    Article  PubMed  Google Scholar 

  41. Al Habash A, AlAhmadi AS. Outcome of MicroPulse® transscleral photocoagulation in different types of glaucoma. Clin Ophthalmol. 2019;13:2353–60. https://doi.org/10.2147/OPTH.S226554.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Tan AM, Chockalingam M, Aquino MC, Lim ZIL, See JLS, Chew PT. Micropulse transscleral diode laser cyclophotocoagulation in the treatment of refractory glaucoma. Clin Exp Ophthalmol. 2010;38(3):266–72. https://doi.org/10.1111/j.1442-9071.2010.02238.x.

    Article  PubMed  Google Scholar 

  43. ELGwaily AM, Khedr SA, Assaf AH, Latif MA, Elsayed HA, Latif AA. MicroPulse® transscleral laser therapy in the management of glaucoma patients. Arch Soc Esp Oftalmol (Engl Ed). 2021;96(12):640–8. https://doi.org/10.1016/j.oftale.2020.12.005.

    Article  CAS  PubMed  Google Scholar 

  44. Chamard C, Bachouchi A, Daien V, Villain M. Efficacy, Safety, and Retreatment Benefit of Micropulse Transscleral Cyclophotocoagulation in Glaucoma. J Glaucoma. 2021;30(9):781–8. https://doi.org/10.1097/IJG.0000000000001900.

    Article  PubMed  Google Scholar 

  45. Souissi S, Baudouin C, Labbé A, Hamard P. Micropulse transscleral cyclophotocoagulation using a standard protocol in patients with refractory glaucoma naive of cyclodestruction. Eur J Ophthalmol. 2021;31(1):112–9. https://doi.org/10.1177/1120672119877586.

    Article  PubMed  Google Scholar 

  46. Issiaka M, Zrikem K, Mchachi A, et al. Micropulse diode laser therapy in refractory glaucoma. Adv Ophthalmol Pract Res. 2023;3(1):23–8. https://doi.org/10.1016/j.aopr.2022.10.003.

    Article  PubMed  Google Scholar 

  47. Lee JH, Shi Y, Amoozgar B, et al. Outcome of Micropulse Laser Transscleral Cyclophotocoagulation on Pediatric Versus adult Glaucoma patients. J Glaucoma. 2017;26(10):936–9. https://doi.org/10.1097/IJG.0000000000000757.

    Article  PubMed  Google Scholar 

  48. Logioco C, Perrone LD, Caruso D, Albertazzi R, Valvecchia G, Zanutigh V. Assessment of efficacy and safety of micropulse diode laser treatment in glaucoma: one year follow-up. Arch Soc Esp Oftalmol (Engl Ed). 2020;95(7):327–33. https://doi.org/10.1016/j.oftal.2020.03.002.

    Article  CAS  PubMed  Google Scholar 

  49. Varikuti VNV, Shah P, Rai O, et al. Outcomes of micropulse transscleral cyclophotocoagulation in eyes with good central vision. J Glaucoma. 2019;28(10):901–5. https://doi.org/10.1097/IJG.0000000000001339.

    Article  PubMed  Google Scholar 

  50. Bresson Dumont H, Ballereau L, Lehoux A, Santiago PY. Diode laser in malignant Glaucoma treatment. J Fr Ophtalmol. 2006;29(Spec 2):73–7. https://doi.org/10.1016/s0181-5512(06)73962-6.

    Article  PubMed  Google Scholar 

  51. Waldo LG, Julio HQ, Jennifer CV, et al. Combined technique for the application of micropulse cyclophotocoagulation in patients with uncontrolled glaucoma: cyclo mix. J Curr Glaucoma Pract. 2020;14(3):93–7. https://doi.org/10.5005/jp-journals-10078-1289.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

Not applicable.

Funding

Open access funding provided by University of Szeged. No funding was received for the planning and execution of the study. Funding for open access publishing was provided by the University of Szeged Open Access Fund (grant ID: 6548).

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Contributions

Á.Sz.: conceptualised the study, performed laser procedures, collected data, wrote and edited the manuscript, T.A.-L.: analysed and visualised data, wrote and edited the manuscript, K.H.: collected data, I.Cs.: performed laser procedures, collected data, P.V.: performed laser procedures, E.T.-M.: provided clinical resources, critically reviewed the manuscript.

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Correspondence to Áron Szabó.

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The Ethics Committee of the University of Szeged approved the data acquisition with the participation of the ancillary sites (protocol number: SLTSCPCRET-001; file number: 34/2022SZTE RKEB). The need for informed consent to data acquisition and data processing has been waivered by the above ethics committee. The data reported in this work contains no personally identifiable information. The study was conducted in accordance with the Tenets of the Declaration of Helsinki.

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Szabó, Á., Árpádffy-Lovas, T., Hagyó, K. et al. The effect of cumulative energy in repeated subliminal transscleral cyclophotocoagulation: a retrospective study. BMC Ophthalmol 24, 233 (2024). https://doi.org/10.1186/s12886-024-03505-7

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