Blankenship G W
Department of Ophthalmology, Penn State University College of Medicine, Hershey 17033.
Graefes Arch Clin Exp Ophthalmol. 1991;229(1):62-5. doi: 10.1007/BF00172263.
For evaluation of the efficacy and toxicity of dexamethasone phosphate after pars plana vitrectomy, 27 randomly selected eyes received 0.8 mg intravitreal dexamethasone phosphate and 30 control eyes did not receive this injection. No signs of dexamethasone phosphate toxicity were observed during 6 months of follow-up evaluations. Visual acuities of 20/40 or better were obtained in 26% of the dexamethasone-treated group and 33% of the control group, and those of 20/200 or better were obtained in 74% of the dexamethasone-treated eyes and 73% of the control eyes. Moderate anterior chamber flare or fibrin formation occurred in only 15% of the dexamethasone-treated eyes but in 27% of the control eyes one day after surgery. Lens changes occurred equally in both groups. None of the eyes in either group developed substantial intraocular proliferation or membranes following surgery.
为评估玻璃体切除术后磷酸地塞米松的疗效和毒性,随机选取27只眼接受0.8毫克玻璃体内注射磷酸地塞米松,30只对照眼未接受该注射。在6个月的随访评估期间未观察到磷酸地塞米松毒性迹象。地塞米松治疗组26%的患眼和对照组33%的患眼视力达到20/40或更好,地塞米松治疗眼74%和对照眼73%的患眼视力达到20/200或更好。术后一天,中度前房闪光或纤维蛋白形成仅发生在地塞米松治疗眼的15%,但发生在对照眼的27%。两组晶状体变化情况相同。两组均无患眼在术后出现大量眼内增殖或膜形成。