Elsevier

Ophthalmology

Volume 108, Issue 11, November 2001, Pages 1986-1991
Ophthalmology

Cyclodiode photocoagulation for refractory glaucoma after penetrating keratoplasty1,

Presented in part at the Oxford Ophthalmological Congress, Oxford, England, July 1998.
https://doi.org/10.1016/S0161-6420(01)00767-9Get rights and content

Abstract

Objective

This study analyzes the results of intraocular pressure (IOP) reduction by contact diode cycloablation (cyclodiode) in cases of refractory glaucoma after penetrating keratoplasty.

Design

Retrospective noncomparative, interventional case series.

Participants

Twenty-eight eyes in 28 patients attending the Moorfields Eye Hospital.

Intervention

Cyclodiode (40 applications × 1.5 W × 1.5 seconds over 270–300°) was used to control the IOP in refractory glaucoma after penetrating keratoplasty.

Main outcome measures

Postoperative IOP, graft status, visual acuity, and number of antiglaucoma medications were recorded after cyclodiode treatment.

Results

Cyclodiode resulted in a reduction of IOP from a median of 33 mmHg (interquartile range [28, 40.5]) to a median of 15 mmHg (interquartile range [12, 20.5]). Most patients had a significant lowering in IOP with a median reduction of 16 mmHg (interquartile range [12, 25]; P < 0.0001). IOPs of 6 to 21 mmHg were achieved in 22 patients (79%). Sixteen patients (57%) required more than one treatment with cyclodiode to control the IOP, with three patients (11%) requiring three treatments and two patients (7%) requiring four treatments. Visual acuity improved (> two Snellen lines of acuity) in three patients (11%) and remained the same (± one Snellen line) in 17 patients (61%). The mean number of antiglaucoma medications before cycloablation was 2.6 and was 1.8 after treatment (P < 0.001). Of the 19 patients (68%) with originally clear grafts, three grafts (16%) developed opacification. One patient (4%), with a history of nanophthalmos and recurrent uveal effusion, had delayed hypotony (IOP < 6 mmHg) occurring 46 months after the diode treatment. All patients had at least 6 months follow-up.

Conclusions

These patients have often undergone multiple previous complicated ocular interventions and are often not suitable for filtration surgery. Reduction of IOP with maintenance of visual acuity and a good safety profile was achieved in most patients in this study but may require multiple treatments. We propose cyclodiode as an effective treatment for many patients in the management of refractory glaucoma after penetrating keratoplasty.

Section snippets

Patients and methods

Consecutive patients under one surgeon (PTK) who underwent contact cyclodiode for refractory glaucoma after penetrating keratoplasty at Moorfields Eye Hospital between 1996 and 1998 had their case notes reviewed. Ethics committee approval was not required for this study. Information was collected on age, gender, date of penetrating keratoplasty, reason for penetrating keratoplasty, IOP, visual acuity, lens status, previous surgery, number of treatments necessary, time from penetrating

Results

Twenty-eight eyes of 28 patients (18 male, 10 female) were treated with cyclodiode for refractory glaucoma after complicated penetrating keratoplasty (Table 1). Median age was 60.5 years (range, 9–90). Twenty-four patients (86%) were Caucasian, one patient (4%; patient 21) was African Caribbean, and three patients (11%; patients 5, 12, and 23) were Asian. In six patients (21%), the eye undergoing treatment was the only effective eye for vision. All patients had at least 6 months follow-up, with

Discussion

The incidence of glaucoma after penetrating keratoplasty varies between studies depending on techniques and patient population, with recent studies indicating an incidence of 11% to 18%.10, 11, 12 In the short term, it can be caused by angle compression, inflammation, pupil-block, steroid response, hemorrhage, and pigment dispersion.2 In the longer term, glaucoma is due to chronic angle closure from the formation of peripheral anterior synechiae, steroids, and chronic inflammation. Associated

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This work has been undertaken by the authors who receive support in part from the NHS Executive, London, England and from the International Glaucoma Association, London, England. The views expressed in this publication are those of the authors and not necessarily of the NHS Executive.

1

The authors have no propriety interest in any of the materials used in this study.

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