Pastor

J. Pastor, J. M. Zarco, M. J. Nozal, A. Pampliega, P. Marinero
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Abstract

Silicone oil is a vitreous substitute used in complicated retinal detachments. The main indications for its use are moderate and advanced proliferative vitreoretinopathy (PVR), proliferative diabetic retinopathy (PDR) with tractional retinal detachment, and giant retinal tears (1). But the intraocular injection of silicone oil can cause various complications, such as wide variations in intraocular pressure (IOP) (hypotony and hypertony), band keratopathy and corneal alterations, emulsification, and preretinal reproliferation (PR) (1). Chemically, silicone oils are linear synthetic polymers (polydimethylsiloxanes) composed of different chains. Most silicone oils used worldwide have varying amounts of low-molecular-weight components (LMWC) due in part to the fact that there are no clear regulations on the degree of purification of the oils used in surgery (the so called medical grade). LMWC are believed to cause ocular toxicity (2-4). However, to the best of our knowledge, few studies have been conducted to prove this in humans. In the present retrospective study, we compared the use of a highly purified and a less purified silicone oil (both medical grade) in a consecutive series of 98 human eyes and assessed the incidence of complications in both groups. ABSTRACT: Purpose. To compare the ocular toxicity caused by the use of highly purified silicone oil to less purified silicone oil in humans. Methods. Fifty-six eyes received 2,000 centistokes (cs) purified silicone oil (group 1) and 42 eyes received 2,000 cs fractionated (highly purified) silicone oil (group 2) after pars plana vitrectormy. Follow-up ranged from 6 to 48 months. Results. Six months after injection, the following complications were found in groups 1 and 2, respectively: ocular hypotension (<13mmHg), 39.3% and 31%, sustained ocular hypertension (>23mmHg), 19.6% and 19%; acute hypertensive peaks (>30mmHg), 23.2% and 11.9%; corneal alterations, 19.6% and 14.3%; emulsification, 1.8% and 2.4%; silicone oil cloudiness, 28.6% and 0%; preretinal reproliferation, 14.3% and 4.8% and total or partial retinal reattachment, 78.6% and 90.5%. Conclusions. Highly purified silicone oil was better tolerated than the less purified oil and caused fewer complications. Poorly purified silicone oils should be avoided in clinical practice. (Eur J Ophthalmol 1998; 8: 179-83)
牧师
硅油是一种用于复杂视网膜脱离的玻璃体替代品。其主要适应症为中晚期增殖性玻璃体视网膜病变(PVR)、伴牵引性视网膜脱离的增殖性糖尿病性视网膜病变(PDR)和巨大的视网膜撕裂(1)。但眼内注射硅油可引起各种并发症,如眼压(IOP)变化大(低眼压和高眼压)、带性角膜病变和角膜改变、乳化和视网膜前再增殖(PR)(1)。硅油是由不同链组成的线性合成聚合物(聚二甲基硅氧烷)。世界上使用的大多数硅油都含有不同数量的低分子量成分(LMWC),部分原因是没有明确的规定用于手术(所谓的医疗级)的油的净化程度。LMWC被认为会引起眼毒性(2-4)。然而,据我们所知,很少有研究在人类身上证明这一点。在本回顾性研究中,我们比较了在连续98只人眼中使用高纯度硅油和低纯度硅油(均为医用级),并评估了两组并发症的发生率。文摘:目的。比较使用高纯度硅油和使用低纯度硅油对人体造成的眼部毒性。方法。玻璃体切割术后56只眼接受2000厘米(cm)纯硅油治疗(1组),42只眼接受2000厘米(cm)高纯度硅油治疗(2组)。随访6 ~ 48个月。结果。注射后6个月,1组和2组的并发症发生率分别为:低血压(23mmHg),分别为19.6%和19%;急性高血压峰值(>30mmHg),分别为23.2%和11.9%;角膜改变分别为19.6%和14.3%;乳化,1.8%和2.4%;硅油浑浊度分别为28.6%和0%;视网膜前再增殖,分别为14.3%和4.8%,视网膜全部或部分再植,分别为78.6%和90.5%。结论。高纯度硅油比低纯度硅油耐受性好,并发症少。临床应避免使用纯度较低的硅油。(欧洲眼科杂志1998;8: 179 - 83)
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