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首页> 外文期刊>Journal of cataract and refractive surgery >Inhibition of posterior capsule opacification with an immunotoxin specific for lens epithelial cells: 24 month clinical results.
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Inhibition of posterior capsule opacification with an immunotoxin specific for lens epithelial cells: 24 month clinical results.

机译:用晶状体上皮细胞特异的免疫毒素抑制后囊混浊:24个月的临床结果。

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PURPOSE: To assess the safety and effectiveness of an immunotoxin, MDX-RA, designed to inhibit posterior capsule opacification (PCO). SETTING: Eleven private practices in the United States. METHODS: This study comprised 63 eyes of 63 patients having extracapsular cataract extraction by phacoemulsification; these patients were enrolled in a Phase I/II clinical investigation of the immunotoxin MDX-RA. At the close of surgery, 21 patients were treated with placebo, 23 patients with 50 units of the immunotoxin, and 19 patients with 175 units of the immunotoxin as an aqueous solution. The patients were monitored for 24 months after primary cataract surgery using external eye and slitlamp examinations, visual acuity assessment, ophthalmoscopy, pachymetry, tonometry, endothelial cell counts, and lens capsule photography. Posterior capsule opacification, recorded on lens capsule photographs, was graded independently by a committee of 3 cataract surgeons. The incidence of neodymium:YAG (Nd:YAG) capsulotomy was projected from the opacification results. RESULTS: The immunotoxin, at the 50 unit dose, was well tolerated and effective in inhibiting PCO. At the 175 unit dose, there was a trend toward increased postoperative inflammation that was transient with no residua. From 6 to 24 months postoperatively, the 50 unit dose significantly inhibited PCO compared with the placebo (P < .05). This significant reduction in PCO translated into a significantly lower projected need for Nd:YAG capsulotomy in the 50 unit than the placebo group (P < .004). About 60% in the placebo group and 4% in the 50 unit group were projected to need an Nd:YAG capsulotomy by 3 years postoperatively. CONCLUSION: The immunotoxin was well tolerated and was effective in reducing PCO for up to 24 months after cataract surgery. Although these preliminary results are encouraging, a larger study is underway to determine whether the reduction in PCO by the immunotoxin decreases the need for Nd:YAG capsulotomy.
机译:目的:评估旨在抑制后囊混浊(PCO)的免疫毒素MDX-RA的安全性和有效性。地点:美国的11个私人诊所。方法:本研究包括63例通过超声乳化白内障摘除白内障囊外摘除术的63只眼;这些患者参加了免疫毒素MDX-RA的I / II期临床研究。在手术结束时,使用安慰剂治疗21例患者,使用50单位免疫毒素治疗23例患者,使用175单位免疫毒素治疗19例患者。在原发性白内障手术后,使用外眼和裂隙灯检查,视力评估,检眼镜,测厚仪,眼压计,内皮细胞计数和晶状体囊摄影对患者进行24个月的监测。由3名白内障外科医生组成的委员会对晶状体囊照片中记录的后囊混浊进行了独立分级。从遮光结果可以预测钕:YAG(Nd:YAG)切囊术的发生率。结果:50单位剂量的免疫毒素具有良好的耐受性,可有效抑制PCO。剂量为175单位时,术后炎症呈增加趋势,该现象是暂时性的,无残留。术后6至24个月,与安慰剂相比,50单位剂量可显着抑制PCO(P <.05)。 PCO的显着降低意味着与安慰剂组相比,50单位的Nd:YAG囊切开术的预计需求显着降低(P <.004)。预计到术后3年,安慰剂组中约60%的患者和50单位组中的4%的患者需要进行Nd:YAG囊切开术。结论:白内障手术后24个月内免疫毒素耐受性良好,可有效降低PCO。尽管这些初步结果令人鼓舞,但正在进行一项更大的研究,以确定免疫毒素对PCO的降低是否会减少Nd:YAG囊切开术的需要。

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