AIMS To evaluate the effect of trans scleral cyclophotocoagulation (TSCPC) on intraocular pressure (IOP) in the eyes retaining intravitreal silicone oil with medically uncontrolled secondary glaucoma following intravitreal silicone oil injection.
METHODS Medical records of 11 eyes of 11 patients who underwent TSCPC for medically uncontrolled glaucoma without pupillary block following intravitreal silicone oil injection for complicated retinal detachment were reviewed retrospectively. In all cases, intravitreal silicone oil was not removed for fear of retinal redetachment. Diode laser contact TSCPC was performed at a power of 1.5–2.5 W, for a duration of 2 seconds, and with 20–27 applications. IOP, number of glaucoma medications, and success rate were evaluated.
RESULTS After a mean follow up period of 52.5 (SD 8.2) (range 42–68) weeks, the mean pretreatment level of IOP, 43.0 (14.4) (26–67) mmHg, had fallen to 14.5 (4.3) (7–20) mm Hg (p=0.003). The number of glaucoma medications was reduced from 2.6 (0.8) to 0.6 (1.0) (p= 0.005). Qualified success was achieved in nine eyes (81.8%) and complete success in six (54.5%). After TSCPC, patients’ retinal status had not changed.
CONCLUSION Patients with medically uncontrolled glaucoma secondary to intravitreal silicone oil injection can be treated with TSCPC in spite of the retained intravitreal silicone oil.
- silicone oil
- diode laser trans-scleral cyclophotocoagulation
- intraocular pressure
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The injection of intravitreal silicone oil for the management of complicated retinal detachment can be associated with elevated intraocular pressure (IOP). When secondary glaucoma is resistant to medical treatment, removal of this oil is the treatment of choice. Owing to complications such as redetachment of the retina or hypotony,1 a physician may, however, be reluctant to follow this course of action.
In intractable glaucoma cases, trans-scleral cyclophotocoagulation (TSCPC) has recently been shown to effectively reduce IOP2-4 in silicone oil induced glaucoma. The efficacy of this treatment in the eye retaining intravitreal silicone oil has not yet been reported, however. We retrospectively reviewed the course of postoperative IOP in patients who underwent TSCPC for medically uncontrolled secondary glaucoma following intravitreal silicone oil injection for complicated retinal detachment.
Subjects and methods
Between 1 April 1996 and 31 July 1997, surgery for the management of medically uncontrolled glaucoma secondary to intravitreal silicone oil injection was performed at Seoul National University Hospital on 11 eyes of 11 consecutive patients who had given their informed consent.
Medically uncontrolled glaucoma was defined as occurring (1) when IOP was equal to or higher than 25 mm Hg, in spite of the use of two or more antiglaucoma medications, and (2) when eyeball pain, headache, or a sign of corneal oedema presented as a secondary symptom. Patients with severe ocular pain or severe corneal decompensation due to increased IOP underwent TSCPC, even though they had no light perception. Patients with advanced glaucoma intolerant of antiglaucoma medications (for example, oral acetazolamide in patients with severe diabetic nephropathy) in an attempt to reduce or stop medications were also included in this study. Eyes with pupillary block were not treated by TSCPC.5 Eyes with a diagnosis of glaucoma antedating silicone oil injection, or with a history of filtering, implant, or cyclodestructive surgery did not undergo TSCPC.
Of the 11 patients who underwent TSCPC, nine were men and two were women; their mean age was 46.9 (SD 9.2) (range 29–63) years. The mean follow up period was 52.5 (8.2) (42–68) weeks.
At the time of silicone oil injection, three patients (cases 1, 7, 10) presented with combined rhegmatogenous and tractional retinal detachment associated with high risk proliferative diabetic retinopathy, one patient (case 3) presented with traumatic retinal detachment, three patients (cases 2, 5, 8) presented with proliferative vitreoretinopathy6 with aphakic or pseudophakic retinal detachment after cataract extraction or clear lens extraction, and four patients (cases 4, 6, 9, 11) presented with severe proliferative vitreoretinopathy6 with rhegmatogenous retinal detachment (Table 1). The mean number of operations before TSCPC was 3.4 (SD 1.1) (range 2–5). Seven patients (cases 1, 2, 5, 8, 9, 10, 11) had corneal subepithelial oedema and two (cases 3, 7) had stromal oedema secondary to high IOP. Two eyes (cases 3, 9) showed total peripheral anterior synechiae, with a patent inferior iridectomy site without pupillary block. In seven patients (cases 2, 3, 4, 5, 6, 9, 11), emulsified silicone oil was seen in the anterior chamber. All patients were aphakic or pseudophakic after surgery; all in the former category underwent inferior iridectomy at the time of silicone oil injection. In all of two pseudophakic eyes without previous inferior iridectomy, the pupillary block component did not contribute to the IOP elevation.
The mean overall follow up period between intravitreal silicone oil injection and TSCPC was 77.6 (SD 59.6) (range 1.2–164) weeks. Glaucoma was diagnosed, on average, 17.6 (21.6) weeks (1 day to 60 weeks) after silicone oil injection. TSCPC was performed 60.0 (49.6) weeks (4 days to 136 weeks) after the diagnosis of glaucoma.
Average baseline IOP was 43.0 (14.4) (26–67) mm Hg, and preoperative visual acuity ranged from 20/200 to no light perception. The patients had been taking two to five glaucoma medications, with an average of 2.6 (0.8). Two of the patients (cases 7, 10) had rubeosis iridis without any new vessels at the anterior chamber angle. In all eyes the retina at the macula was flat, while in three an inferior shallow elevation of the retina was seen. Owing to possible complications such as retinal detachment and phthisis, surgeons were—in all cases—reluctant to remove silicone oil.
TSCPC was performed after retrobulbar injection of 2–4 ml of 2% lignocaine. A semiconductor diode laser system (Oculight SLx, Iris Medical Instruments, Mountain View, CA, USA) was used; its maximum power output was 2.5 W, and maximum duration 9.9 seconds. A 600 μm diameter laser delivery quartz fibreoptic (G-probe, Iris Medical Instruments, Mountain View, CA, USA), its planar polished end protruding 0.7 mm from a handpiece and fabricated in a shape which encouraged accurate fibreoptic location, was centred 1.2 mm behind the surgical limbus and oriented parallel to the visual axis. Twenty to 27 laser applications, each of 2 seconds’ duration, were delivered to all four quadrants of the circumference of the ciliary body, except for case 1. In case 1, the first case among the 11 cases, 14 laser applications were performed saving the temporal portion of the ciliary body because of relatively low pretreatment IOP. Starting from 1.75 W, power was increased by 0.25 W up to 2.5 W if there was no tissue disruption reaction (a “pop” or “snap” from within the eye) during the two subsequent applications. If a “pop” sound occurred during more than one laser application, power was further reduced by 0.25–1.5 W and treatment was completed at this wattage.2 3 Mean total energy delivered was calculated from the following equation: mean power (W) × 2.0 (seconds) × number of applications. It ranged from 56.0–114.8 J with the average, 88.0 (SD 20.0) J.
Following TSCPC, medication comprised 1% prednisolone eye drops four times a day, 1% atropine eye drops twice a day, and 0.3% ofloxacin ophthalmic ointment twice a day. IOP was monitored at 1 hour, 1 day, and 1, 2, 4, 8, 12, 20, 28 weeks after the procedure. Ofloxacin 0.3% ointment was used for 2 weeks and topical steroid and atropine for 2 months. Antiglaucoma medications were tapered according to measured IOP. Topical antibiotics were prescribed routinely for the prophylaxis of conjunctival infection due to any possible clinical or subclinical conjunctival burn.3 7
Follow up included determination of best corrected vision, IOP measurements with a Goldmann applanation tonometer, and slit lamp biomicroscopic and ocular fundus examinations.
Retreatment was performed after 8 weeks of follow up when the IOP was above 30 mm Hg with at least two measurements 4 weeks apart in spite of maximum tolerable medical treatment.
In our series, we defined complete success as a final IOP equal to or lower than 21 mm Hg without glaucoma medication, and qualified success as final IOP equal to or lower than 21 mm Hg regardless of medication. Hypotony was defined as IOP lower than 5 mm Hg on two examinations at least 4 weeks apart, and if this condition was found, the procedure was classified as a failure. Loss of light perception was also classified as a failure.
Using Wilcoxon’s signed rank test, pre- and post-TSCPC IOP and the number of medications were statistically compared. A p value less than 0.05 was considered significant.
Overall changes in IOP following TSCPC are shown as a scattergram (Fig 1). During the last follow up, IOP of all 11 eyes was found to be less than before treatment. Pressure in all eyes (100%) was under 21 mm Hg 24 and 25 weeks, respectively, after they were first treated, two of these (cases 5, 8) required additional TSCPC.
After a mean follow up period of 52.5 (8.2) (42–68) weeks, mean pretreatment IOP, 43.0 (14.4) (26–67) mmHg had fallen significantly to 14.5 (4.3) (7–20) mm Hg (p=0.003, Wilcoxon’s signed rank test) (Table2).
IOP change according to follow up time is shown in Figure 2. Mean IOP 24 hours after treatment was 17.5 (5.4) mm Hg; the individual IOP reduction ranged from 55 to −1 mm Hg from baseline IOP. Only one eye was 1 mm Hg above baseline at 24 hours. If mean IOP had fallen to within the normal range within 24 hours of TSCPC, this was maintained until the last follow up.
During the last follow up four eyes (36.4%) (cases 2, 7, 8, 11) needed an average of 1.75 (1.3) antiglaucoma medications; seven (63.6%) needed no medication. The number of antiglaucoma medications significantly decreased from 2.6 (0.8) at baseline to 0.6 (1.0) during the last follow up (p= 0.005, Wilcoxon’s signed rank test). In nine patients, best corrected visual acuity did not change, but in two it deteriorated; in one (case 2), this was from counting finger to no light perception, and in the other (case 10), from hand movements to no light perception (Table 2).
Eyeball pain, headache, and corneal oedema were not found during the last follow up, and no eye showed hypotony, hypopyon, band keratopathy, or change in the status of the retina.
In case 5 IOP was well controlled without glaucoma medication on the 15th day after the second treatment. Four months later, the silicone oil was removed because it was disturbing the visual axis; afterwards, the retina remained flat, IOP was well controlled, and there was no hypotony.
Qualified success, defined as a final IOP equal to or lower than 21 mm Hg regardless of glaucoma medication without visual loss or hypotony, was achieved in nine eyes (81.8%), and complete success, defined as a final IOP equal to or lower than 21 mm Hg without glaucoma medication, in six eyes (54.5%).
In cases where complicated retinal detachments has occurred, the use of intravitreal silicone oil injection has shown encouraging results. However, late complications may preclude a satisfactory long term outcome; one of the most common of these is elevated IOP, with an incidence of between 6% and 48%.8-13
Although removing silicone oil is the current standard primary surgical management for such cases, there are many theories about the role of silicone oil in IOP elevation. Laroche et al 14 noted normal IOPs even when silicone globules were present in the angle. Burk et al 15 reported that the mechanism of IOP change did not appear to be directly related to the presence of silicone, but rather to the preoperative status of the eye and other aspects of vitreoretinal surgery; the most common pressure inducing factors appeared to be preoperative compromise of aqueous outflow facility, including peripheral anterior synechiae and chronic structural alterations in the trabecular meshwork compounded by early postoperative insults, such as haemorrhage and inflammation. De Corralet al 16 suggested that rubeosis iridis, erythroclasis, haemolysis, mechanical causes (haemorrhage or silicone oil bubbles), inflammation, phacolysis, steroid responder, and pupillary block were possible causes of increased IOP after vitrectomy and intravitreal silicone oil injection. Moreover, removal of intraocular silicone oil in the setting of emulsification and postoperative glaucoma may not necessarily result in IOP reduction. Moisseiev et al 17 reported that in 91% of the glaucomatous eyes, removal of the emulsified oil did not affect IOP.
The high incidence of retinal detachment after silicone oil removal deters a physician from removing this silicone oil for lowering IOP. Retinal redetachment has been reported up in to 33% of patients1 10 and Casswell and Gregor1reported it as the most common major complication after the removal of oil. Retinal redetachment in diabetic eyes could be more serious because it is frequently associated with intractable rubeosis iridis.10
Except for silicone oil removal, glaucoma surgery has rarely been attempted in oil filled eyes with uncontrolled postoperative IOP.11 12 Because traditional filtering surgery is technically difficult owing to conjunctival scarring resulting from the multiple retinal surgery, artificial drainage devices or cyclodestructive procedures may be the most appropriate means of lowering medically uncontrollable IOPs associated with intravitreal silicone oil. In seven eyes with uncontrolled glaucoma secondary to silicone oil injection Nguyen et al 12 attempted glaucoma procedures, sometimes combined with silicone oil removal. Molteno implantations were performed in five of these eyes, with a success rate of 60% (3/5). Modified Schocket procedure, performed in one eye, was a qualified failure and Nd:YAG trans-scleral cyclophotocoagulation performed in another was a complete success.
Bloom et al 4 have presented successful results of diode laser trans-scleral cyclophotocoagulation from 36 eyes with silicone oil induced glaucoma, but there was no mention of whether they performed TSCPC in the eyes with silicone oil or the eyes with silicone oil removed.
In the present study, the IOP of all the patients (100%) was lowered below 20 mm Hg after treatment, and all patients were relieved of ocular pain and corneal oedema which were the causes of treatment in some patients. In lowering IOP, the success rate was 100%, but it was reduced to 81.8% because two of the patients (cases 2, 10) lost light perception after the treatment. In case 2, poorly controlled IOP for 14 months before the treatment caused the total cupping of disc and the remaining visual field of the central island disappeared immediately after the treatment. In case 10, the cause of visual loss was thought to be haemophthalmos secondary to the aggravation of proliferative diabetic retinopathy. Hypotony or sympathetic ophthalmia, which is the potential complication of cyclodestructive procedures, did not occur in the present study.
In conclusion, it can be stated that semiconductor diode laser appears to be a promising method for the treatment of medically uncontrolled glaucoma secondary to intravitreal silicone oil injection.
Supported by a grant no 02-97-328 from the Seoul National University Hospital Research Fund.
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