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Literatur-Nr.: 16 Optometty (2006) 77, 446-449 Standort: SILOrdner II Silicone oiL emulsification vitreoretinal surgery in the anterior chamber after Dennis J. Light, 0.0. Department of Veterans Affairs, Eastern Colorado Health Care System Eye Clinic, Pueblo, Colorado . • KEYWORDS Abstract Silicone oil; Endotamponade; Retinal detachmen~; Keratopathy; Glaucoma; Cataract BACKGROUND: The use of &iliconeoil as an endotamponade for the treatment of complicated retinaI detachment is common, hut lang-term complications can oceur if the oil is not removed later. This artic1e documents a case of emulsified silicone oil migration into the anterior chamber after vitreoretinaI surgery and provides a diseussion and review of comrnon anterior segment eomplieations trom this condition. CASE REPORT: A 59-year-old man reported to the eye clinic complaining of a "growth •• over bis right eye that had increased in size over the last month. Stit tamp examination found a "reverse pseudohypopyon" iri the right eye, which was actuaIly emutsified silicone oil that had migrated from the posterior ehamber after a previous retinal detachrnent repair. Tbe patient was referred for surgical removal of this oily obstruetion. Although surgical treatment was delayed for 18 months, his vision improved and bis intraocular pressure was lowered through surgieal and medical management. CONCLUSIONS: The use of silicone oil as an endotamponade in cases of complex retina! detachment has become common, but it also may lead to postoperative complications if it is not surgically removed Iater. This case highlights possible complications from the migration of emuIsified silicone oil into the anterior chamber and illustrates the importance of follow-up care for every ophthalmie surgical procedure. Optometry 2006;77:446-449 The use of silicone oil in complex vitreoretinal was first introduced in 1962.1 Its injection into the cavity.to serve as an endotamponade has become a technique and, when combined with vitreoretinal surgery vitreous standard surgery, has been used sÜccessfully in the repair of proliferative vitreoretinopathy, prolifera,tive diabetic retinopathy, giant retinal tears, and ocular trauma. 2 . Silicone oll has been known to emu1sify and migrate into various locations within the globe.3 Because this can lead to long-term cornplications, such as cornea! decompensation, cataract, and glau- Correspondingauthor: Dennis J. Light, O.D., Departmentof Veterans Affairs,Eastern Colorado Henlth Care SystemEye Clinic, 4112 Outlook B1vd.,Pueblo, Colorado 81008. E-mail: [email protected] coma, it should endotamponade.4 be removed after adequate duration of (ase report A 59-year-old man reported to the eye clinic complaining of a "growth" over bis right eye that had increased in size over the last month according to his wife's observation. He denied any asthenopia but reported that he "had very little vision" in this eye and that Hit might have gotten a little worse:' His medical history included a '3S-year history of type 2 diabetes mellitus for which he had taken insulin for the last 15 years. His last Ale 1529-1839/06/$ -see front matter © 2006 American Optometrie Association All rights reserved. doi:lO.l 016/j.optm.2006.04.l19 hemoglobin test, a measure of the Oenni" J. Light ClinicaL Ca,,, 447 iness Figure 1 A "reverse pseudohypopyon" lets in the superior anterior of emulsified silicone oil drop· chamber. --""!1lilunt 01' glycnsylated h~moglobin in the blilod and a good esrim;1lOr pI' htH\- \IcH the diabetes has been managed over the pr~~\'ious 3 rnonlhs. \las 8.Y{;. He also had hypertension. rhcumatniJ arthritis. hypcrlipidemia. duonie lower back pain. kidncy stones. gallbladder disea~c. and depression. His medications inc!uued insulin ntlvolin. rosiglitazone maleate. and metarürmin HeL für his diabetes; Iisinopril. cyclobenl.aprine HeL hydrocblorothiazide. and metoprolol für his ~. hypertension; gemtlbr~nil for his hyperlipidemia: and amitrypliline Hel. for his depression. He reported no allergies. His ocular hhtory was somcwhat sketchy but included previous "laser treatments for diabetö in bOlh eyes" and a retinal detad111lCl1l repair 01' his right cye ! yeur previously. His uncorrccted visua! <lcuitics were 1/160 in the right eye (O.D.) amI 20170 2 in the !en eye (O.5.t Manifest refraclion was unable 10 improve the vision in his right eye whiie his !efl eye was best conected to 20/60' 2. Pupils were 4mm and wund but with minimal reactiol1s in both eves (OU). A , .:rade ! + right relative afferent pupillary defect was present. Billmicroscopy showed clear amI quiet conjlloctival tissues OU. The cornea was clear wilhollt ederna or endothebaI strimions OU. In thc right eye. there was a globule of silicone oil oceupying 40o/c of the superior anterio! chamber that would O)ove sJightly with head tilt to either shoulder (see Figure 1 ). Thc globulctilled the entire superior anterior chamber and contacted the corneal endothelium amI the amerior iris. 11 was composed 01' multiple, smalf, semiopaque, nil droplets thm gave a "rock candy" appearance 10 the globule. Gonioscopy llndings showed the angle open to the ciliary body inferiorly 0.0.. but there was no view through the globule 10 the superior angle. His irides were normal, w1lh no rubcoslS 01' indotomy present in either eye. Grade 3+ l111clear sclerosis O.D. and grade 1 + nlldear sclerosis O.S. were prescnt. lntn.lOClllar pressures by Gold· mann applan::.llion tonometry wert' 18 mmHg O.D. and 13 rnmHg O.S. at ]0:02 AM. DiJared fundus examinariofl fj nJings were remarkabJe for dense vitreous debris and hall' 0.0. Because 01' the cloud- 01' the media. a limiled view ur the fundus was available O.D .. and unfortunately. fine retinal detail could not be viewed. A red reflex was presenr in aH quadrants. B-scan ultrasonography. although indicalcd in cases in which the retina cannol be visualized cleady to help determine the presence or absence of retina I detachment. was not performed owing to unavailability 01' the instrument. There was 360-degree panretinal pholocoagulation 0.5. with flbrous vascular scarring temporal to thc rnacula. This patient had emuJsified silicone oil in the anterior chamber 01' the right eye after retinal detachment repair ! year previously. He was referred to a vÜreoretinal specialist for evaluation and surgical rem ova] of the emulsified silicone oil. The decision to remove the emulsiflcd silicone oi! sllrgically was based on the patiem's des ire to improve his cosmetic appearance (remove "thc grO\vth"), improve the reduction of visual acuity, decrease tbe elevated intraocular presslIre. rcmove the prescnee of comeal touch. and remove thc catamc!. Unforlunately, this patient had unstablc angina associared with poofly controlled hypel1cnsion causing him ro canee! his surgical procedure. He returned for eare I year later. and a! thm time his vision had dccreased to light perception 0.0..and his imraocular prcssure had risen to 28 mmHg 0.0. He was prescribed O.2o/c brimonidine tartrate twiee a day O.D., which lowered the intraocuJar pressure to 18 mmHg O.D. His SUHrcrv was delaved again after he suffered a transient ischemic aHack .that warranted flIrther cardiac and '-..' "' ..J •••• carotid artery evaluations. Six months later, however. he underwent successfuJ surgicaJ removal of the silicone oil 0.0. with phacoemulsification and posterior charnber intraocular lens implantation. One day postoperative]y, vision had improved to 4/1600.0. although there was considerable comeal edema Iikely from endothelial cell los5 and dysfunction from the silicone oil contact. His intraocular pressure was 13 mmHg 0.0. Fundus examination tindings showed extensive panretinaJ photocoaglliation with areas of fibrosis. auenuated vessels. ghost (sclerotic) vesseIs. and moderate optic nerve pa]]or 0.0. believed to have resulted from previous diabetic optic neuropathy. At his 6-monrh postoperative visit, vision had improved to 20/] 50 0.0. The comea O.D. continued to show mild edema without endothelial striation. The posterior eh amber intraocular lens implant O.D. was centered and elear. The intraocular pressure was 16 mmHg O.D. on O.2'k brimonidinc tartrate bid. Discussion Silicone oil often is placed in the vitreoretinal cavily as an aid in the repair of proliferative vitreoretinopathy, prolifcrative cliabetic rctinopathy, reCllrrent retinal dClachmenh. giant retinal tears. macular hole. viral retinitis. and lTaumatic retinal injuries. 5 Ir has a densily lower than water and Illuch greater surface tensions. making it an dfective intraocubr 448 tamponade. When injected into the vitreal cavity, its buoyancy mechanically pushes the retina back into its proper anatomie position, while its surface tension helps keep it there. This also keeps vitreal fluid from entering through a retinal break into the subretinal space, thus allowing for a strong chorioretinal adhesion to take place.6 The use of silicone oll as a tamponade has a few advantages compared with long-lasting gases used for similar purposes. Unlike the gas-filled eye, which leaves the patient with no useful vision, silicone oil is transparent (it does not mix with intraocular fluids or blood) and perrnits the patient to see after proper refraction.7 The use of silicone oil eliminates the need for facedown positioning during healing, and it allows for high altitude and air travel (gas expands at higher altitudes). Perhaps its biggest advantage is that it does not dissolve, allowing for longer-acting tamponade in the repair of very complicated retinal detachments.8 This permanence of silicbne oil in ocular tissue has c;sociated risks. Over time, silicone oil bas a tendency to •.•mulsify and break into smaller oil droplets, which have a propensity to leak through very small openings.9 The droplets may egress surgical incision sites or rnigrate through anatomically compromised areas such as through broken zonules.10 Migration has been observed in phakic, aphakic, and pseudophakic eyes, and has been documented from eyelidJ1•12 to optic nerveY·J4 Emulsification of silicone oil to some degree has been reported to occur in 56% tO.1 00% of cases over aperiod of months· to years.3.10 Multiple factors may contribute to silicone oil emulsification, inc1uding the use oflow viscosity silicone oils (higher viscosity oils restriet mechanical emul sificati on),9 residual fluid in the vitreous cavity, and hemorrhage or leakage of other blood constituents from the breakdown of the blood-aqueous barrier after surgery.J5.J6 Anterior segment complications associated with the use of silicone oil include alterations of corneal structure or integrity,17 increased intraocular pres----'lre,18and development or progression of cataract.4 Silicone oil is toxic to the cornea. Specular microscopic studies have shown the main corneal complication to be endothelial cell darnage inc1uding decreased cell density, pleomorphism, and necrosis. If allowed to enter the anterior chamber, silicone oll will eventually lead to corneal endothelialcell damage, edema, or band keratopathy.19 Rates of keratopathy after silicone oil injection have been reported to range from 4.5% to 63%.2 As seen in this case report, corneal edema may riot always be present on initial presentation, even if there is significant corneal touch and presumed endothelial damage. Silicone oil in the anterior chamber may act as a physical barrier and interfere with corneal homeostasis.20 When the oi! is removed later damaged endothelium may allow for excess stromal hydration and lead to corneal edema. The prevalence of elevated intraocular press ure after silicone oil injection has been reported to range from 1.5% ~o.48%,21 Silicone oil in the vitreous cavity may push the ms or lens forward resulting in pupillary block or direct angle obstruction. Emulsified silicone oil also may fill the Optometry, Vol 77, No 9, September 2006 anterior chamber, infiltrate the trabecular meshwork, and decrease the aqueous outflow.22 Outflow in this case is affected initially through direct obstruction, aIthough histologie studies have shown that silicone damages the outftow pathway with a loss of cellularity and fibrosis. Foreign body granuloma containing macrophages laden with oil also may develop.22.23 Clinically significant increased intraocular pressure after silicone oil injection usually can be controlled by topical antiglaucoma medications and is reversible in most patients after oil removal.23 By preventing the anterior migration cf silicone oil from the vitreous cavity, the risk of damage to the cornea and development of elevated intraocular pressure can be re· duced?4 A prophylactic inferior peripheral iridotomy may be placed at the time of silicone injection. The buoyancy of the silicone oil coupled with the inferior placement of the iridotomy encourages a natural flow of aqueous from the posterior chamber into the anterior eh amber. This helps prevent pupillary block and indirectly limits the access and migration of silicone oil into the anterior chamber.25 Cataracts can develop in nearly all eyes in wh ich silicone oil remains in situ for a few months, and up to 60% of lenses that appear relative1y clear at the time of silicone oil removal will also develop a clinically significant cataraet after 2 years?6 Obstruction of normal metabolie exchange at the silicone-Iens interface results in cataract fonnationP Cataract formation may be delayed by the early removal of silicone oil,28but it is considered to be almost unavoidable. The reported incidence of alterations to the corneal structure or integrity, increased intraocular pressure, and cataract progression show a varied range of occurrence. This variation can be attributed to a number of factors including sampIe size, viscosity of silicone oi! used, the duration of silicone oil endotamponade, the presence of inferior iridotomy, and previous surgical history. Surgical removal of silicone oil significantly increases the likelihood of improved visual acuity and reduces the risk of keratopathy, secondary glaucoma, and cataract progression.4 The timing of silicone oil removal remains contcoversial,29.3obut in most cases, removal is recommended 2 to 3 months after surgery31 or as soon as a stable retinal situation is achieved. This can be difficult to assess. Clinical signs include a quieting of inflammation, a whitening of any epiretinal membrane formation, and, most important, a lack of change in the appearance or configuration of the retina.32 Contraindications for removal are unclear but include the presenee of profound hypotony,33 In any case, there is an increased risk of retinal detachment after oil removal. Most retinal redetachments occur within the first 3 months after removal of silicone oil. Six months after oiI removal, a retinal redetachment becomes unlikely. 34 Summary The use of silicone oil as an endotamponade in cases of complicated retina! detachment has become increasingly Dennis J. Light Clinical Care common, but it is has been associated with alterations to the corneal structure or integrity, increased intraoeular pressure, and cataraet progression. Surgical removal of the silicone oil reduces the risk of these eomplications and signifieantly increases the likelihood of improved visual aeuity. Removal is reeommended as soon as the tamponade effect is no longer needed. This case shows the importanee of follow-up care for every ophthalmie surgical procedure. The optometrist should be familiar with the technique and materials used during ophthalmie surgery and be aware ofthe clinical signs of potential eomplications. 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