Salim Sarwat, Du Haiming, Boonyaleephan Sumalee, Wan Jim
University of Tennessee Health Science Center, Memphis, TN, USA.
Clin Ophthalmol. 2012;6:955-62. doi: 10.2147/OPTH.S32282. Epub 2012 Jun 22.
To compare the surgical outcomes of the Ex-PRESS glaucoma filtration device in African American and white glaucoma patients.
Retrospective comparative case series.
This was a comparative case series of 36 eyes of 36 African Americans and 43 eyes of 43 whites that underwent placement of the Ex-PRESS glaucoma filtration device under a partial-thickness scleral flap for uncontrolled glaucoma. All eyes received intraoperative mitomycin C. The primary outcome measures were intraocular pressure (IOP), number of postoperative glaucoma medications, and surgical success. Surgical success was defined as IOP between 5 and 18 mm Hg, with or without glaucoma medications, without further glaucoma surgery, or loss of light perception vision.
Average follow-up was 31.9 ± 9.8 (range, 14.6-47) months for African Americans and 30.7 ± 8.6 (range, 14.3-47) months for whites. At 33 months, surgical success was 80.0% in the African American group and 83.3% in the white group (P = 1.00). Reasons for surgical failure included increased IOP (3 eyes, 3.8%), persistent hypotony with maculopathy (1 eye, 1.3%), and further surgery (4 eyes, 5.06%). Compared with preoperative values, the mean postoperative IOP and number of glaucoma medications were significantly reduced in both groups, and no statistical difference was observed between the two groups at 33 months. Postoperative complications were similar in the two groups.
Similar surgical outcomes were observed in African American and white glaucoma patients after implantation of the Ex-PRESS glaucoma filtration device. This latest modification of glaucoma filtration surgery may be a better surgical option for African Americans given its potential advantages of no tissue removal, predictable outcomes related to consistent lumen size and controlled flow, fewer postoperative complications, and overall reduced inflammation.
比较Ex-PRESS青光眼引流装置在非裔美国人和白人青光眼患者中的手术效果。
回顾性比较病例系列。
这是一个比较病例系列,纳入36例非裔美国人的36只眼和43例白人的43只眼,这些患者因青光眼控制不佳接受了在部分厚度巩膜瓣下植入Ex-PRESS青光眼引流装置的手术。所有患者术中均使用丝裂霉素C。主要观察指标为眼压(IOP)、术后青光眼药物使用数量及手术成功率。手术成功定义为眼压在5至18 mmHg之间(无论是否使用青光眼药物),无需进一步青光眼手术,或无光感丧失。
非裔美国人的平均随访时间为31.9±9.8(范围14.6 - 47)个月,白人为30.7±8.6(范围14.3 - 47)个月。在33个月时,非裔美国人群的手术成功率为80.0%,白人群为83.3%(P = 1.00)。手术失败的原因包括眼压升高(3只眼,3.8%)、持续性低眼压伴黄斑病变(1只眼,1.3%)和进一步手术(4只眼,5.06%)。与术前值相比,两组术后平均眼压和青光眼药物使用数量均显著降低,且在33个月时两组间未观察到统计学差异。两组术后并发症相似。
非裔美国人和白人青光眼患者植入Ex-PRESS青光眼引流装置后观察到相似的手术效果。鉴于其无组织切除、因管腔大小一致和流量可控而具有可预测的结果、术后并发症较少以及整体炎症减轻等潜在优势,这种青光眼滤过手术的最新改良术式可能是非裔美国人更好的手术选择。