玻璃体切除及经巩膜固定黑膈人工晶状体治疗外伤性无虹膜。

W. Omulecki, A. Synder
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引用次数: 25

摘要

背景与目的严重眼外伤后发生的部分或完全无虹膜是一个治疗难题。膜片人工晶状体是一种用于矫正无虹膜的人工晶状体,但在创伤性病例中植入这种晶状体的安全性和有效性尚未得到很好的确定,因为报道很少,研究的病例也很少。患者与方法6例患者,男4例,女2例,平均年龄44岁,采用玻璃体切割术和经巩膜固定黑隔膜人工晶状体治疗外伤性无虹膜。全无虹膜3眼,部分无虹膜3眼。4眼无晶状体,2眼晶状体严重半脱位。2例合并玻璃体出血,1例合并细菌性眼内炎。随访时间4 ~ 39个月(平均23个月)。结果5例患者最佳矫正视力改善,1例保持不变。所有病例均达到良好的视力(20/20 - 20/40),所有晶状体中心良好。无严重并发症。6例患者中有3例术前和术后需要局部青光眼药物治疗,以达到良好的眼压控制。结论玻璃体切除联合巩膜固定黑膈人工晶体植入术治疗外伤性无虹膜是安全的。非常好的功能结果和缺乏严重的并发症是令人鼓舞的。为了支持我们的观点,需要更多的病例和更长的随访研究。
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Pars plana vitrectomy and transscleral fixation of black diaphragm intraocular lens for the management of traumatic aniridia.
BACKGROUND AND OBJECTIVES Partial or complete aniridia occurring after severe ocular trauma is a difficult therapeutic problem. Diaphragm intraocular lenses were developed for the correction of aniridia, but the safety and efficacy of implanting such lenses are not well established in traumatic cases because of very few reports, and the small number of cases studied. PATIENTS AND METHODS Six patients, 4 men and 2 women with a mean age of 44 years, were treated for traumatic aniridia using pars plana vitrectomy and transscleral fixation of a black diaphragm intraocular lens. Total aniridia was observed in 3 eyes and partial aniridia in 3 eyes. Four eyes were aphakic and severe lens subluxation was seen in 2 eyes. Vitreous hemorrhage coexisted in 2 patients and bacterial endophthalmitis was present in 1 patient. Follow-up time ranged between 4 and 39 months (mean, 23 months). RESULTS Best-corrected visual acuity improved in 5 patients and 1 remained unchanged. Good visual acuity (20/20 - 20/40) was achieved in all cases and all lenses were well-centered. No severe complications were noted. Three of 6 patients required glaucoma topical medications pre- and postoperatively achieving good intraocular pressure control. CONCLUSION The management of traumatic aniridia using pars plana vitrectomy and implantation of scleral fixation black diaphragm intraocular lenses seem to be safe. Very good functional results and lack of severe complications are encouraging. Additional cases with a longer follow-up study are necessary to support our opinion.
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