Department of Ophthalmology, The New York Eye and Ear Infirmary, New York, 10003, USA.
Am J Ophthalmol. 2012 May;153(5):949-957.e1. doi: 10.1016/j.ajo.2011.10.004. Epub 2012 Jan 20.
To investigate the clinical features, risk factors, and treatment outcomes following immunologic graft rejection in eyes that have undergone Descemet stripping automated endothelial keratoplasty (DSAEK).
Retrospective case review.
The charts for 353 DSAEK procedures performed at a single clinical practice at the New York Eye and Ear Infirmary from August 2006 to November 2010 were reviewed. Cases with at least 3 months follow-up were included. Outcome measures included rates of graft rejection, clinical findings, treatment outcomes, and risk factor analysis.
Thirty of 353 DSAEKs developed graft rejection (8.5%). Kaplan-Meier rate of rejection was 6.0% at 1 year (n = 175), 14.0% at 2 years (n = 79), and 22.0% at 3 years (n = 39). Rejection episodes occurred between 0.8 and 34 months. Clinical findings included anterior chamber cells, keratic precipitates, endothelial rejection line, and host-donor interface vascularization. Risk factors for development of graft rejection were cessation of postoperative steroid (hazard ratio 5.49, P < .0001) and black race (hazard ratio 2.71, P = .02). Recipient age, sex, surgical indication, glaucoma, postoperative steroid response, corneal neovascularization or peripheral anterior synechiae, graft size, prior keratoplasty in fellow eye, and concurrent or subsequent procedures were not associated with graft rejection. Twenty-two out of 30 rejection episodes (73.3%) resolved with steroid treatment.
Graft rejection is an important complication following DSAEK. In contrast to penetrating keratoplasty, rejection following DSAEK is almost exclusively endothelial. Among risk factors traditionally associated with graft rejection, cessation of topical steroids was most significant. Prompt recognition and treatment of DSAEK rejection can lead to favorable outcomes.
研究接受 Descemet 撕囊自动内皮角膜移植术(DSAEK)后的免疫性移植物排斥反应的临床特征、危险因素和治疗结果。
回顾性病例研究。
回顾了 2006 年 8 月至 2010 年 11 月在纽约眼耳医院单一临床实践中进行的 353 例 DSAEK 手术的图表。纳入至少有 3 个月随访的病例。观察指标包括移植物排斥率、临床发现、治疗结果和危险因素分析。
353 例 DSAEK 中有 30 例(8.5%)发生移植物排斥。Kaplan-Meier 排斥率在 1 年(n=175)时为 6.0%,在 2 年(n=79)时为 14.0%,在 3 年(n=39)时为 22.0%。排斥发作发生在 0.8 至 34 个月之间。临床发现包括前房细胞、角膜后沉着物、内皮排斥线和宿主-供体界面血管化。发生移植物排斥的危险因素包括术后停止使用皮质类固醇(危险比 5.49,P<0.0001)和黑种人(危险比 2.71,P=0.02)。受者年龄、性别、手术适应证、青光眼、术后皮质类固醇反应、角膜新生血管或周边前粘连、移植物大小、对侧眼的先前角膜移植以及同时或随后的手术与移植物排斥无关。30 例排斥发作中的 22 例(73.3%)经皮质类固醇治疗后得到缓解。
移植物排斥是 DSAEK 后的一个重要并发症。与穿透性角膜移植术不同,DSAEK 后排斥几乎完全是内皮性的。在与移植物排斥相关的传统危险因素中,停止局部皮质类固醇治疗是最重要的。及时识别和治疗 DSAEK 排斥反应可获得良好的结果。