Bergmanson J P, Söderberg P G, Estrada P
Institute for Contact Lens Research, College of Optometry, University of Houston, TX.
Acta Ophthalmol (Copenh). 1987 Aug;65(4):417-23. doi: 10.1111/j.1755-3768.1987.tb07017.x.
Eighty-two hydrogel extended wear contact lenses (EWCL) from four brands were tested for overall quality and variations in specified parameters. Two of the EWCL brands were approved by the United States Food and Drug Administration (FDA) for wear by the public, while two of the brands were uninvestigated. In addition, the packaging solution was examined for osmolarity and pH. All brands were delivered with solutions that had estimated means of pH and osmolarity departing from what may be considered ideal physiologically. The EWCLs all had a consistent power and an acceptable thickness reproducibility. One of the FDA approved brands, demonstrated diameter variations of a magnitude that may produce an unpredictability in the lens fit. Several lenses of one brand suffered from edge quality deficiencies. Although the FDA clinical trial is designed to control the clinical performance of contact lenses prior to the market entry, the results of the present investigation indicate that an authority independent of the manufacturer should regularly sample the lens quality. It is for this purpose imperative that standards for contact lenses are established.
对来自四个品牌的82片水凝胶长戴型隐形眼镜(EWCL)进行了整体质量和特定参数变化的测试。其中两个EWCL品牌已获得美国食品药品监督管理局(FDA)批准可供公众佩戴,而另外两个品牌未经调查。此外,还对包装溶液的渗透压和pH值进行了检测。所有品牌所配备溶液的pH值和渗透压估计均值均偏离生理理想值。EWCL的屈光度均一致,厚度重复性也可接受。其中一个获FDA批准的品牌显示出一定程度的直径变化,这可能会导致镜片佩戴的不可预测性。某一品牌的几片镜片存在边缘质量缺陷。尽管FDA临床试验旨在在隐形眼镜上市前控制其临床性能,但本次调查结果表明,应由独立于制造商的机构定期对镜片质量进行抽样检测。因此,制定隐形眼镜标准势在必行。