Smiddy W E, Mady M, Anagnoste S
Department of Ophthalmology, University of Miami School of Medicine, Bascom Palmer Eye Institute, Miami, Florida, USA.
Am J Ophthalmol. 2001 Jun;131(6):748-50. doi: 10.1016/s0002-9394(01)00835-2.
To report the results of placing a foldable acrylic intraocular lens through a clear cornea incision in eyes undergoing pars plana vitrectomy.
This interventional case series is a retrospective report of 15 eyes of 15 consecutive patients undergoing foldable (acrylic) intraocular lens insertion in conjunction with pars plana vitrectomy in a single academic institution. Outcome measures included visual acuity and complications.
The intraocular lens was successfully implanted and retained in position in all 15 cases. The intraocular lens did not pose difficulty in examining the fundus or cause any vitreoretinal complications. With mean follow-up of 4.5 months (range, 1--10 months), final median postoperative visual acuity range was 20/200 (range, 20/40--2/200) and consistent with the level of vitreoretinal disease.
Acrylic intraocular lenses may be safely implanted in conjunction with pars plana vitrectomy in selected cases.
报告在接受玻璃体切除术的眼中通过透明角膜切口植入可折叠丙烯酸人工晶状体的结果。
本干预性病例系列是对一家学术机构中15例连续患者的15只眼睛进行回顾性报告，这些患者在接受玻璃体切除术的同时植入了可折叠（丙烯酸）人工晶状体。观察指标包括视力和并发症。
所有15例患者的人工晶状体均成功植入并保持在位。人工晶状体在检查眼底时未造成困难，也未引起任何玻璃体视网膜并发症。平均随访4.5个月（范围1 - 10个月），术后最终中位视力范围为20/200（范围20/40 - 2/200），与玻璃体视网膜疾病的程度一致。
在特定病例中，丙烯酸人工晶状体可与玻璃体切除术联合安全植入。
