Abstract
Purpose
To report a case of iris epithelium detachment following Nd:YAG laser capsulotomy.
Observations
We describe the case of an 81 year old woman who developed hyphema and detachment of the iris epithelium following standard Nd:YAG laser capsulotomy. The detachment was readily visualized using anterior segment OCT. The hyphema was managed with topical atropine and steroids. The detachment itself was left untreated.
Conclusions and importance
No persisting subjective complaints or effect on visual function were noted. To our knowledge, this complication represents a novel observation .
1
Introduction
Posterior capsule opacification (PCO) is a common delayed complication of cataract surgery with opacification of the posterior capsule due to migration and proliferation of lens epithelial cells. Incidences ranging up to about 50% have been described and depend on patient-related factors as well as surgical technique and intraocular lens (IOL) design. Neodymium:Yttrium–Aluminum-Garnet (Nd:YAG) laser capsulotomy as treatment for PCO was introduced by Daniele Aron-Rosa in 1979. In general, the procedure is safe and effective, but a number of complications involving the posterior and anterior segment have been observed. , IOL damage, transient inflammation, or elevation of intraocular pressure (IOP) are relatively common. Severe complications are rare and include cystoid macular edema, IOL luxation, and aqueous misdirection or pupillary block with subsequent glaucomatous damage to the optic nerve head.
We report a further rare complication of Nd:YAG laser capsulotomy with detachment of the iris epithelium and associated hyphema.
2
Case report
An 81 year old woman with a medical history of arterial hypertension, atrial fibrillation, hypercholesterolemia, and gout managed appropriately including anticoagulant therapy with warfarin was referred for Neodymium:Yttrium–Aluminum-Garnet (Nd:YAG) laser capsulotomy in the right eye. Bilateral cataract surgery with implantation of TECNIS one-piece IOLs (ZCB00) had been performed five years earlier. Surgery had been uncomplicated without iris manipulation and the postoperative course was unremarkable with only mild and transient inflammation. Subsequent Nd:YAG laser capsulotomy in the left eye two years earlier had been uncomplicated. Laser retinopexy for a retinal tear had been performed in the right eye twelve years before cataract surgery. Visual acuity for the right eye was 12/20 before treatment and slit-lamp examination was unremarkable except moderate posterior capsule opacification. The procedure was performed by one of our consultants with the use of 21 applications totaling 35.7 mJ in a cruciate pattern and no immediate complications were observed.
The days following capsulotomy she experienced an increasing number of floaters and developed ocular discomfort, which led to evaluation in our emergency clinic. She presented with hand movements for the right eye. IOP was elevated to 25 mmHg and increased following dilatation to 42 mmHg. Slit-lamp examination revealed a moderate hyphema that partly obscured deeper ocular structures. Ultrasound B-scan demonstrated retinal apposition. Blood pressure was normal 101/67 mmHg. INR was moderately elevated to 3.8, which lead to temporary cessation of anti-coagulant therapy. The hyphema was managed with topical steroids and atropine. The increase in IOP was managed with the topical anti-hypertensives apraclonidine, brinzolamide, and timolol.
The hyphema had almost resolved at follow-up four days later. The IOL was found in situ, but conspicuous transillumination defects of the iris were noticed ( Fig. 1 A). Surprisingly, following dilatation the iris epithelium with an attached blood clot was observed in the pupillary space ( Fig. 1 B). Fundoscopy was unremarkable. Anterior segment optical coherence tomography (AS-OCT) readily revealed the detached posterior epithelium involving the central part of its temporal half ( Fig. 2 ). Ultrasound biomicroscopy did not show additional anterior segment pathology.
