Auffarth G U, Wesendahl T A, Brown S J, Apple D J
Department of Ophthalmology, Storm Eye Institute, Medical University of South Carolina, Charleston 29425.
Ophthalmology. 1994 Dec;101(12):1913-22. doi: 10.1016/s0161-6420(94)31083-9.
The authors pose the question as to whether there are any anterior chamber intraocular lenses (AC IOLs) acceptable for clinical use in the 1990s.
Data on the incidence and types of complications of 4104 AC IOLs that were submitted to the Center for IOL Research from 1982 to 1993 were retrieved from the laboratory database and analyzed using cumulative frequency calculations and the chi-square test. Normalized explantation rates were related to implantation rates that were derived from market-share analysis.
Of 4104 explanted IOLs, 50% were closed-loop designs (n = 2095/4104); 26% (1100/4104) were miscellaneous, older designs; and 22% (919/4104) were open-loop lenses. The most important complications were corneal pathology (2065/4104) and inflammation (1370/4104). Closed-loop designs were responsible for almost 80% of corneal pathology, with an increasing complication rate with ongoing implant duration (P < 0.0001). Open-loop AC IOLs showed, in relation to their normalized rate of implantation, a significantly lower rate of complications and explantations (P < 0.01).
Complication rates of flexible, open-loop AC IOLs are much lower than previously assumed. They should be distinguished clearly from most older AC IOL designs. Consideration of these lenses as an alternative to sutured posterior chamber IOLs for secondary or exchange implantation may be warranted for selected clinical indications. They also could provide an alternative to the aphakic spectacle rehabilitation program in developing countries, which will have a positive impact on the overwhelming backlog of patients with cataract in the underprivileged world.
作者提出一个问题,即20世纪90年代是否存在任何可用于临床的前房型人工晶状体(AC IOL)。
从实验室数据库中检索1982年至1993年提交至人工晶状体研究中心的4104枚AC IOL的并发症发生率及类型数据,并使用累积频率计算和卡方检验进行分析。标准化取出率与通过市场份额分析得出的植入率相关。
在4104枚取出的人工晶状体中,50%为闭环设计(n = 2095/4104);26%(1100/4104)为其他较旧设计;22%(919/4104)为开环晶状体。最重要的并发症是角膜病变(2065/4104)和炎症(1370/4104)。闭环设计导致了近80%的角膜病变,且随着植入时间的延长并发症发生率增加(P < 0.0001)。与标准化植入率相关,开环AC IOL的并发症和取出率显著较低(P < 0.01)。
可弯曲的开环AC IOL的并发症发生率远低于先前的假设。应将它们与大多数较旧的AC IOL设计明确区分开来。对于某些特定的临床适应证,考虑将这些晶状体作为二期或置换植入的缝合后房型人工晶状体的替代方案可能是合理的。它们还可为发展中国家的无晶状体眼镜康复计划提供替代方案,这将对贫困地区大量积压的白内障患者产生积极影响。