Hennig A, Pradhan D, Evans J R, Johnson G J, Foster A
Lahan Eye Hospital, Nepal.
Ophthalmologe. 1998 Jul;95(7):504-6. doi: 10.1007/s003470050306.
There are estimated to be 20 million people blinded by cataracts, 80-90% of whom live in rural areas of developing countries where expert surgical resources are scarce. The majority of all cataract operations are still intracapsular extractions (ICCE). Aphakic correction using spectacles is problematical in developing countries. This study was undertaken to evaluate the safety of multiflex open loop anterior chamber intraocular lenses (AC IOLs).
A total of 2000 people attending Lahan Eye Hospital, South-east Nepal, with bilateral cataract were randomly allocated to receive in their first eye either ICCE with AC IOL (AC IOL group) or ICCE with aphakic correction (control group). All operations were performed by two ophthalmologists using a standardized technology and 4.5 x operating loupe magnification. Functional and best corrected vision was recorded. The primary outcome measure was poor vision after surgery, which was defined as a visual acuity of less than 6/60 at 1 year follow-up (WHO definition for severe visual impairment and blindness).
The median time needed to perform ICCE was 4.1 min and to perform ICCE with AC IOL 6 min. Of all study patients 91% were examined after 1 year. Five percent of the AC IOL group and 5.4% of the control group had a functional visual acuity of less than 6/60. Causes of reduced vision in the AC IOL group versus the control group were: correctable refractive error (22 vs 29), uveitis/secondary glaucoma (13 vs 2), endophthalmitis (4 vs 7), pre-existing eye diseases (4 vs 5), retinal detachment (0 vs 4), and corneal decompensation (0 vs 1). Of the control group, 24 patients were found to be functionally blind in the operated eye (vision < 3/60) because they did not wear their aphakic spectacles. Normal vision (WHO definition: > or = 6/18) was achieved best corrected in 89.9% of the AC IOL group and 93.2% of the control group. Analysis of additional long-term follow-ups (2-5 years post-operatively) has not yet been completed.
This study provides evidence that in developing countries well-manufactured multiflex open loop AC IOLs can be implanted safely by experienced ophthalmologists after routine ICCE, avoiding the disadvantages of aphakic spectacle correction.
据估计,有2000万人因白内障而失明,其中80 - 90%生活在发展中国家的农村地区,这些地区缺乏专业的手术资源。所有白内障手术中,大部分仍为囊内摘除术(ICCE)。在发展中国家,使用眼镜进行无晶状体眼矫正存在问题。本研究旨在评估多柔性开环前房型人工晶状体(AC IOL)的安全性。
共有2000名就诊于尼泊尔东南部拉汉眼科医院的双侧白内障患者被随机分配,其第一眼接受ICCE联合AC IOL(AC IOL组)或ICCE联合无晶状体眼矫正(对照组)。所有手术均由两名眼科医生采用标准化技术并在4.5倍手术放大镜放大下进行。记录功能和最佳矫正视力。主要结局指标为术后视力差,定义为随访1年时视力低于6/60(世界卫生组织对严重视力损害和失明的定义)。
进行ICCE所需的中位时间为4.1分钟,进行ICCE联合AC IOL所需时间为6分钟。所有研究患者中,91%在1年后接受了检查。AC IOL组5%的患者和对照组5.4%的患者功能视力低于6/60。AC IOL组与对照组视力下降的原因分别为:可矫正屈光不正(22例对29例)、葡萄膜炎/继发性青光眼(13例对2例)、眼内炎(4例对7例)、既往眼部疾病(4例对5例)、视网膜脱离(0例对4例)以及角膜失代偿(0例对1例)。在对照组中,发现24例患者手术眼功能失明(视力<3/60),原因是他们未佩戴无晶状体眼镜。AC IOL组89.9%的患者和对照组93.2%的患者在最佳矫正后达到正常视力(世界卫生组织定义:≥6/18)。额外长期随访(术后2 - 5年)的分析尚未完成。
本研究提供了证据表明,在发展中国家,经验丰富的眼科医生在常规ICCE后可安全植入制造精良的多柔性开环AC IOL,避免了无晶状体眼镜矫正的缺点。