Mastropasqua L, Carpineto P, Ciancaglini M, Falconio G
Institute of Ophthalmology, University 'G. D'Annunzio', Chieti, Italy.
Ophthalmologica. 1998;212(5):318-21. doi: 10.1159/000027315.
The authors studied the intraocular pressure (IOP) changes after phacoemulsification with two different kinds of foldable silicone lens implantation using Healon GV as viscoelastic substance. One hundred patients undergoing cataract surgery were enrolled in this study. Inclusion criteria were: absence of ocular hypertension or glaucoma. Patients were randomly assigned to plate haptic (Silens PH, Domilens Chiron Vision, Lyon, France) or three-piece (CeeOntrade mark& ;920, Pharmacia spa, Milano, Italia) silicone intraocular lens (IOL) implantation. Following phacoemulsification and cortical aspiration, the capsular bag was reinflated with Healon GV. After foldable silicone IOL insertion residual Healon GV was removed from the anterior chamber. IOP was measured preoperatively and at 6, 24 h and 1 week postoperatively. Six hours postoperatively IOP was higher in the Silens PH group than in the CeeOn group (20. 85+/-5.42 vs. 18.88+/-2.95 mm Hg, p= 0.026). The difference was confirmed after 24 h (21.02+/-5.18 vs. 17.34+/-3.18 mm Hg, p < 0.01). Despite the medical treatment (acetazolamide 250 mg orally every 6 h), at the 24-hour control 2 eyes with plate haptic silicone lens showed IOP values higher than 30 mm Hg. Slitlamp examination showed in both eyes a shallowing of the anterior chamber together with the evidence of capsular bag hyperdistension and capsular block resulting from the occlusion of the circular anterior capsule opening by the plate haptic IOL. Residual Healon GV removal from the anterior chamber was performed. At 1-week control both eyes showed normalization of IOP. The use of a plate haptic silicone lens may be associated with a more consistent retention of Healon GV in the eye with trapping in the capsular bag. Retained viscoelastic may cause either trabecular meshwork blockage by viscoelastic substance or postoperative capsular bag hyperdistension, anteroplacement of the IOL optic and capsular block from occlusion of the circular anterior opening by the IOL optic.
作者使用Healon GV作为粘弹剂,研究了两种不同类型的可折叠硅胶人工晶状体植入超声乳化术后的眼压(IOP)变化。100例接受白内障手术的患者纳入本研究。纳入标准为:无高眼压或青光眼。患者被随机分配接受板式襻(Silens PH,法国里昂Domilens Chiron Vision公司)或三件式(CeeOntrade mark& ;920,意大利米兰Pharmacia spa公司)硅胶人工晶状体(IOL)植入。超声乳化和皮质吸出术后,用Healon GV使囊袋重新充盈。可折叠硅胶IOL植入后,从前房清除残留的Healon GV。术前及术后6小时、24小时和1周测量眼压。术后6小时,Silens PH组眼压高于CeeOn组(20.85±5.42 vs. 18.88±2.95 mmHg,p = 0.026)。24小时后差异得到证实(21.02±5.18 vs. 17.34±3.18 mmHg,p < 0.01)。尽管进行了药物治疗(每6小时口服250 mg乙酰唑胺),在24小时检查时,2例植入板式襻硅胶人工晶状体的患者眼压值高于30 mmHg。裂隙灯检查显示,两只眼睛前房变浅,同时有囊袋扩张和因板式襻IOL阻塞环形前囊开口导致的囊袋阻滞的证据。从前房清除了残留的Healon GV。在1周检查时,两只眼睛眼压均恢复正常。使用板式襻硅胶人工晶状体可能与Healon GV在眼内更持续的留存有关,导致其被困在囊袋中。留存的粘弹剂可能会导致小梁网被粘弹物质阻塞,或术后囊袋扩张、IOL光学部前移以及IOL光学部阻塞环形前开口导致囊袋阻滞。