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Correlation between intraocular pressure reduction and anterior chamber aqueous flare after micropulse transscleral cyclophotocoagulation
BMC Ophthalmology volume 21, Article number: 266 (2021)
Micropulse transscleral cyclophotocoagulation (MP-CPC) is a technique that has been approved in recent years to treat glaucoma. MP-CPC causes anterior chamber inflammation; a relationship with reduced intraocular pressure (IOP) has not been reported. Therefore, we analyzed the correlation between IOP and anterior chamber aqueous flare after MP-CPC.
This retrospective study included 37 eyes of 37 patients who underwent MP-CPC between November 2018 and October 2020. IOP and flare values were measured at 1, 4, and 12 weeks after MP-CPC. Correlations were assessed between the percentage IOP reduction and flare elevation by calculating Spearman’s rank correlation coefficient.
The percentage IOP reduction at 1 week after surgery was correlated with the flare elevation at 1 week after surgery (ρ = 0.47, P = 0.006). The percentage IOP reduction at 12 weeks after surgery was correlated with the flare elevation at 4 weeks after surgery (ρ = 0.53, P = 0.006).
A short-term correlation was implied between reduced IOP and flare elevation after MP-CPC.
Glaucoma is the leading cause of blindness worldwide. The damage to the optic nerve and visual field caused by glaucoma is progressive and irreversible . The only reliable evidence-based treatment for glaucoma is the lowering of intraocular pressure (IOP). Treatment options include medical, laser, and surgical therapies [2, 3]. Traditionally used continuous-wave transscleral cyclophotocoagulation (CW-CPC) is an effective method to lower IOP, but patients can develop serious complications, such as phthisis bulbi [4, 5]. Micropulse transscleral cyclophotocoagulation (MP-CPC) was approved by the US Food and Drug Administration in 2015 as a glaucoma treatment technique. MP-CPC is presumed to be a safe procedure as a result of minimizing thermal coagulation of adjacent tissues and repeating the on/off laser irradiation cycle in microseconds. However, the mechanism of lowering IOP has not been fully explained [4, 5]. MP-CPC causes anterior chamber inflammation; however, a relationship with reduced IOP has not been reported [4,5,6].
The numbers of cells and the intensity of the flare, reflecting protein concentrations, increase when inflammation occurs in the anterior chamber [7, 8]. A laser flare meter has been developed in Japan to quantitate aqueous flare and cells in the anterior chamber, and the measured values are highly correlated with the numbers of anterior chamber cells and the aqueous flare observed by slit-lamp [7, 8]. Aqueous flare indicates an increase in aqueous humor protein concentrations. When the blood-ocular barriers are disrupted due to inflammation, serum protein leaks into the aqueous humor, and aqueous flare increases . A laser flare meter projects a laser beam into the anterior chamber, and aqueous flare is measured using a photomultiplier to detect scattering of the laser beam by protein in the aqueous humor [7, 8]. These findings motivated us to analyze the correlation between reduced IOP and elevated aqueous flare measured by a laser flare meter after MP-CPC. To the best of our knowledge, this is the first report investigating the relationship between IOP and aqueous flare after MP-CPC. If there were a correlation between inflammation and IOP reduction, it would help elucidate the mechanism of lowering IOP by MP-CPC for the prediction of postoperative IOP.
All investigations adhered to the tenets of the Declaration of Helsinki. This study was approved by the Ethics Committee of Kumamoto University. Research information was disclosed to the patients on our website, and the freedom to refuse research use was guaranteed. This retrospective study included consecutive patients with refractory glaucoma who underwent MP-CPC between November 2018 and October 2020 at Kumamoto University Hospital. We excluded the cases in which aqueous flare could not be measured due to poor corneal transparency or poor fixation. We also excluded the case in which additional surgery was performed within 4 weeks. The aqueous flare values of all eyes were measured before and after surgery. MP-CPC was performed using a CYCLO G6™ micropulse P3 probe (IRIDEX, Mountain View, CA, USA) according to the manufacturer’s instructions. Briefly, the machine was preset to a power of 2,000 mW and a duty cycle of 31.3 %. After sub-Tenon’s anesthesia, the MP-CPC probe was applied by continuous sliding for 10–20 s per one-way, 80 s in total per hemisphere, avoiding the filtering bleb and the glaucoma drainage device (all cases were Baerveldt glaucoma implant). After the surgery, 1.5 % levofloxacin eye drops and 0.1 % fluorometholone eye drops were used for 1 week. However, in patients with excess postoperative inflammation, the fluorometholone eye drops were continued for more than 1 week or switched to betamethasone until the inflammation subsided. Patients who underwent additional surgery for reasons such as poor IOP reduction were excluded from the analysis after that time point. The IOP and aqueous flare values were measured preoperatively and at 1, 4, and 12 weeks after surgery. Most IOP readings were measured via Goldman applanation tonometry (GAT). The IOP in two eyes were measured using iCare rebound tonometry (Icare Finland Oy, Helsinki, Finland), because the IOP in these eyes could not be measured by GAT. The aqueous flare values were measured using an FM-700 laser flare meter (KOWA Co., Nagoya, Japan). Visual acuity was measured in the form of decimal visual acuity with the Landolt chart and converted into the logarithm of the minimum angle of resolution (LogMAR) scale, where counting fingers (CF), hand motion (HM), light perception (LP), and no light perception (NLP) were assigned values of 2.1, 2.4, 2.7, and 3.0, respectively . The visual field of patients with good fixation were examined using a Humphrey Field Analyzer (Carl Zeiss Meditec, Dublin, CA, USA). The anterior segment was evaluated using slit-lamp biomicroscopy, and the posterior segment was evaluated using indirect ophthalmoscopy and spectral-domain optical coherence tomography (SD-OCT). History of smoking was queried on the questionnaire. Surgical success was defined as an attained IOP reading between 5 and 21 mmHg and > 20 % IOP reduction at 12 weeks after MP-CPC, compared with the baseline without the addition of other IOP reduction therapies. Correlations between the percentage IOP reduction [(preoperative IOP − postoperative IOP) / preoperative IOP] and elevated aqueous flare (postoperative flare − preoperative flare) were estimated by calculating Spearman’s rank correlation coefficient. A P-value < 0.05 was considered significant.
Thirty-seven eyes of 37 patients were enrolled in this study. The mean age ± standard deviation (SD) was 70.6 ± 14.4 years, and 20 patients (54.1 %) were male. Sixteen eyes (43.2 %) had exfoliation glaucoma (EXG), nine eyes (24.3 %) had primary open-angle glaucoma (POAG), eight eyes (21.6 %) had uveitic glaucoma (UG), and four eyes (10.8 %) had neovascular glaucoma (NVG) (Table 1). In all, 28 eyes (75.7 %) had a history of cataract surgery, 13 (35.1 %) received trabeculectomy, (5 [13.5 %] of which also underwent Baerveldt tube shunt surgery), 7 (18.9 %) received vitrectomy, 12 (32.4 %) received trabeculotomy, 1 (2.7 %) had CW-CPC, and 8 (21.6 %) had MP-CPC.
The time course of IOP and the aqueous flare value in all cases are shown in Fig. 1. The mean IOPs ± SD were 14.5 ± 10.5, 19.0 ± 7.5, and 19.0 ± 8.4 mmHg at 1, 4, and 12 weeks after surgery, respectively. The corresponding aqueous flare values were 218.4 ± 165.4, 134.9 ± 103.6, and 97.0 ± 102.2 photon counts/ms, respectively. The mean success rate was 43.2 % at 12 weeks after surgery. By glaucoma type, the mean success rates of EXG, POAG, UG, and NVG group were 43.8 %, 33.3 %, 62.5 %, and 25.0 %, respectively. Complications were observed in 11patients: 5 (13.5 %) had prolonged anterior chamber inflammation that persisted for more than 4 weeks, 1 of whom also had macular edema (2.7 %); 5 (13.5 %) developed hypotony (IOP < 4 mmHg); and 1 (2.7 %) had hypotony maculopathy. Additional treatments were performed in 11 patients, 7 underwent MP-CPC, 1 received Baerveldt tube shunt surgery, 1 had selective laser trabeculoplasty (SLT), 1 had sub-Tenon injection of triamcinolone acetonide for macular edema, and 1 underwent cataract surgery. Details for each glaucoma type are shown in Table 2.
Flare elevation at 1 week after surgery was positively correlated with the percentage IOP reduction at 1 week after surgery (ρ = 0.47, P = 0.006; Fig. 2 A). In addition, flare elevation at 4 weeks after surgery was positively correlated with the percentage IOP reduction at 12 weeks after surgery (ρ = 0.53, P = 0.006; Fig. 2B). We also analyzed each type of glaucoma. Percentage IOP reduction tended to correlate with flare elevation in UG and NVG; however, the sample size was too small to reach any conclusions (Table 3).
The mean surgical success rate was 43.2 % at 12 weeks after surgery, lower than in previous studies [6, 10]. This may be due to the large number of refractory glaucoma patients with a history of glaucoma surgery in this study and different MP-CPC irradiation methods. A correlation was detected between flare elevation and the percentage IOP reduction at 1 week after surgery. However, no correlation was observed between flare elevation and the IOP reduction at 4 or 12 weeks. These results indicate that the degree of acute intraocular inflammation reflected the IOP reduction at the early stage after MP-CPC, but not at the later stage. MP-CPC may cause intraocular inflammation by coagulating the ciliary body at the early stage, thereby decreasing production of the aqueous humor at that time . However, some studies have reported that MP-CPC does not cause significant damage to the ciliary body because the 810-nm irradiation is emitted in on/off cycling mode to avoid ciliary body destruction. Therefore, there may be a mechanism of IOP reduction other than decreased aqueous humor production [12, 13]. An alternative explanation for the correlation would be increased aqueous outflow by proinflammatory cytokines induced by acute intraocular inflammation. For example, interleukin-1α, interleukin-8, and monocyte chemoattractant protein-1 (MCP-1) increase aqueous humor outflow [14,15,16]. In general, intraocular inflammation occurs time-dependently, while the reduction in IOP was maintained after MP-CPC. Thus, it would be reasonable to say that the degree of intraocular inflammation at that time did not reflect the reduction in IOP at the later stage.
Flare elevation at 4 weeks after surgery was correlated with the percentage IOP reduction at 12 weeks after surgery, indicating that the degree of inflammation at 4 weeks after surgery may predict IOP control in the future, to some extent. Additionally, the mechanism of IOP reduction by MP-CPC may differ between the acute and chronic stages. However, the actual mechanism remains unclear, so further studies are required. Analysis by glaucoma type showed that a correlation between IOP reduction and flare elevation may be more likely to be observed in UG and NVG. Given that UG and NVG usually have a strong inflammatory response to invasive treatment, it is speculated that a short-term increase in flare value reflects the degree of ciliary body destruction. In addition, UG and NVG tend to have higher levels of proinflammatory cytokines such as MCP-1, which increase aqueous humor outflow, and it is speculated that this may be related to the IOP reduction in the later stage [17, 18]. Further studies with a larger sample size are required.
The limitations of the present study are its retrospective design, small sample size, and short follow-up time after MP-CPC.
We observed a positive correlation between postoperative reduction in IOP and elevated aqueous flare after MP-CPC. This correlation is more likely to be seen in UG and NVG, which have higher levels of proinflammatory cytokines. Thus, our results suggest that anterior chamber inflammation is associated with IOP reduction by MP-CPC. These findings provide insight into the IOP-lowering mechanism of MP-CPC; however, further studies are required.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Continuous-wave transscleral cyclophotocoagulation
Micropulse transscleral cyclophotocoagulation
Goldman applanation tonometry
Logarithm of the minimum angle of resolution
No light perception
Spectral-domain optical coherence tomography
Primary open-angle glaucoma
Selective laser trabeculoplasty
Monocyte chemoattractant protein-1
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This study received no funding support.
Ethics approval and consent to participate
This study was conducted in accordance with the tenets of the Declaration of Helsinki and was approved by the Ethics Committee of Kumamoto University, Japan (Advanced No. 2370). The committee waived the need for written informed consent due to the retrospective design. Research information was disclosed to the patients on our website, and the freedom to refuse research use was guaranteed.
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Kimura, A., Nakashima, KI. & Inoue, T. Correlation between intraocular pressure reduction and anterior chamber aqueous flare after micropulse transscleral cyclophotocoagulation. BMC Ophthalmol 21, 266 (2021). https://doi.org/10.1186/s12886-021-02012-3
- Micropulse transscleral cyclophotocoagulation
- Intraocular pressure
- Aqueous flare