Yoon Jin Sook, Lew Helen, Kim Sung Joo, Lee Sang Yeul
Department of Ophthalmology, Institute of Vision Research, Yonsei University College of Medicine, Seoul, Korea.
Ophthalmology. 2008 Mar;115(3):566-572.e2. doi: 10.1016/j.ophtha.2007.06.014. Epub 2007 Sep 14.
To document the long-term experience with hydroxyapatite (HA) orbital implants (Bio-Eye) and analyze the factors influencing implant exposure, including surgical type, procedural modification, use of different wrapping materials and peg materials.
Retrospective observational case series.
Eight hundred two eyes from 802 patients who underwent anophthalmic socket surgery (eviscerations, enucleations, secondary implant placements) using HA implants, performed by one surgeon between May 1990 and December 2005.
All patients' clinical records were reviewed. Baseline age, cause of anophthalmic surgery, surgical type, size of HA implant, wrapping material, and peg system were recorded.
Postoperative complications, especially implant exposure, were recorded separately before and after pegging, and compared according to type of surgery, wrapping material, and peg system.
The main cause of anophthalmic surgery was trauma (73%). A variety of wrapping materials have been used, including Tutoplast-dura, Vicryl mesh, autogenous sclera, and polyester-urethane. Implant exposure occurred in 17 patients (2.1%) before pegging and 14 (4.0%) after pegging. The exposure rate was significantly higher in eyes eviscerated without (7.2%) than with (1.1%) keratectomy (P = 0.018), but did not differ according to type of surgery (P = 0.710). When distributed according to 5-year periods, the exposure rate was higher from 1990 to 1994 (4.7%) than in later periods (P = 0.004). In patients who underwent enucleation or secondary implantation, there was no difference in exposure rate between Tutoplast-dura- and Vicryl mesh-wrapped implants (P = 0.235). Among the 353 patients (44.0%) who underwent pegging, those who received titanium-pegged implants had a significantly lower incidence of peg extrusion (5.2%), major discharge (5.2%), and pyogenic granuloma (9.1%) than those with nonsleeved polymethyl methacrylate and sleeved polycarbonate peg materials (P<0.05).
Exposures associated with HA orbital implants decreased with the improvement of surgical technique over time and have been managed successfully, both before and after pegging. The incidence of peg-related complications have decreased since the introduction of the titanium peg system.
记录羟基磷灰石(HA)眼眶植入物(Bio-Eye)的长期使用经验,并分析影响植入物暴露的因素,包括手术类型、手术操作改进、不同包裹材料和栓钉材料的使用情况。
回顾性观察病例系列。
1990年5月至2005年12月期间,由一名外科医生对802例患者的802只眼进行了无眼球眼眶手术(眼球内容剜除术、眼球摘除术、二期植入手术),使用HA植入物。
查阅所有患者的临床记录。记录基线年龄、无眼球手术的原因、手术类型、HA植入物大小、包裹材料和栓钉系统。
分别记录栓钉植入前后的术后并发症,尤其是植入物暴露情况,并根据手术类型、包裹材料和栓钉系统进行比较。
无眼球手术的主要原因是外伤(73%)。使用了多种包裹材料,包括Tutoplast硬脑膜、薇乔网片、自体巩膜和聚酯-聚氨酯。栓钉植入前,17例患者(2.1%)发生植入物暴露;栓钉植入后,14例患者(4.0%)发生暴露。未行角膜切除术的眼球内容剜除术患者的暴露率(7.2%)显著高于行角膜切除术的患者(1.1%)(P = 0.018),但根据手术类型不同,暴露率无差异(P = 0.710)。按5年时间段分布,1990年至1994年的暴露率(4.7%)高于后期(P = 0.004)。在接受眼球摘除术或二期植入术的患者中,Tutoplast硬脑膜包裹的植入物和薇乔网片包裹的植入物的暴露率无差异(P = 0.235)。在353例(44.0%)接受栓钉植入的患者中,接受钛栓钉植入物的患者的栓钉挤出、大量分泌物和化脓性肉芽肿的发生率(分别为5.2%、5.2%和9.1%)显著低于使用无套管聚甲基丙烯酸甲酯和有套管聚碳酸酯栓钉材料的患者(P<0.05)。
随着时间的推移,与HA眼眶植入物相关的暴露情况随着手术技术的改进而减少,并且在栓钉植入前后均得到了成功处理。自引入钛栓钉系统以来,与栓钉相关的并发症发生率有所下降。