Abstract
Pseudophakic intraocular lenses (IOLs) are likely the most implanted devices in the world and can be used in earlier stages of life (e.g., pediatric implantation). Therefore, they are expected to remain in the intraocular environment for many decades and be biocompatible. This chapter reviews designs and materials currently used in the manufacture of IOLs, as well as their pathophysiology. According to the site of fixation, IOLs are described as anterior or posterior chamber lenses. They can also be described as manufactured in one piece (the entire IOL is manufactured from the same material), or multipiece. Biocompatibility of IOL materials is usually assessed in terms of uveal biocompatibility, related to the inflammatory foreign-body reaction of the eye against the implant, as well as in terms of capsular biocompatibility, determined by the relationship of the IOL with remaining lens epithelial cells (LECs) within the capsular bag. Interaction of residual LECs with IOLs may lead to different degrees of anterior capsule opacification, interlenticular opacification (between piggyback IOLs), posterior capsule opacification, and LEC ongrowth. IOLs are expected to remain transparent throughout the life span of the patient. However, different classes of IOL materials may adversely interact with specific conditions leading to IOL optic opacification. An overview of the different causes of IOL opacification according to the IOL material is also included in this chapter.
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Werner, L. (2022). Design, Material, Insertion, and Pathophysiology of IOLs. In: Albert, D.M., Miller, J.W., Azar, D.T., Young, L.H. (eds) Albert and Jakobiec's Principles and Practice of Ophthalmology. Springer, Cham. https://doi.org/10.1007/978-3-030-42634-7_192
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DOI: https://doi.org/10.1007/978-3-030-42634-7_192
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