Yang L L, Lambert S R, Lynn M J, Stulting R D
Emory Eye Center, Emory University, Atlanta, Georgia 30322, USA.
Ophthalmology. 1999 Apr;106(4):833-48. doi: 10.1016/S0161-6420(99)90175-6.
To determine the long-term results of corneal graft survival after penetrating keratoplasty for Peters anomaly and to identify risk factors for graft failure.
Noncontrolled interventional case series: a single-center retrospective review of a consecutive surgical series.
The records of all children 12 years of age or younger who underwent penetrating keratoplasty for Peters anomaly between January 1971 and December 1992 were reviewed. All study eyes had completed a minimum of 3 years of follow-up from the date of first keratoplasty and had undergone most of their corneal surgery at Emory University.
Characteristics of the recipient, the eye, the donor, and the surgical procedure were analyzed for their influence on survival of the first graft. Survival probabilities were estimated using the Kaplan-Meier method. Multivariate regression analysis was performed to estimate relative risks and adjusted survival probabilities.
Graft clarity.
One hundred forty-four penetrating keratoplasties were performed in 72 eyes of 47 patients. The median age at first keratoplasty was 4.4 months. The median follow-up was 11.1 years. Fifty-four percent of eyes received one graft, 18% received two grafts, and 28% received three or more grafts. The overall probability of maintaining a clear first graft was 56% at 6 months, 49% at 12 months, 44% at 3 years, and 35% at 10 years. The probability of second or subsequent grafts surviving for 3 years was less than 10%. Thirty-nine percent of eyes had a clear graft at the time of review; 36% of eyes had a clear first graft. Multivariate analysis identified disease severity, donor cornea size, coexisting central nervous system abnormalities, and quadrants of anterior synechiae as the strongest risk factors for graft failure. Supplemental multivariate analysis, restricted to observable preoperative variables, identified stromal vessels, total limbal opacification, and preoperative glaucoma as independent preoperative predictors of graft failure. Allograft rejection was the most frequently identified cause of graft failure. Major complications after keratoplasty were phthisis, retinal detachment, cataract, and glaucoma.
The overall long-term probability of maintaining a clear graft after initial penetrating keratoplasty for Peters anomaly is 35% +/- 0.06%, with subsequent grafts rarely surviving. Eyes with severe disease, larger donor corneas, coexisting central nervous system abnormalities, and anterior synechiae have significantly poorer outcomes than eyes without these factors. These data should be carefully considered before recommending corneal transplantation for Peters anomaly, particularly after previous graft failure.
确定彼得斯异常行穿透性角膜移植术后角膜植片存活的长期结果,并识别植片失败的危险因素。
非对照干预性病例系列:对连续手术系列进行单中心回顾性研究。
回顾了1971年1月至1992年12月期间所有12岁及以下因彼得斯异常接受穿透性角膜移植术的儿童的记录。所有研究眼自首次角膜移植之日起至少随访了3年,且大部分角膜手术在埃默里大学进行。
分析受者、患眼、供体及手术操作的特征对首次植片存活的影响。采用Kaplan-Meier法估计存活概率。进行多因素回归分析以估计相对风险和调整后的存活概率。
植片透明度。
47例患者的72只眼共进行了144次穿透性角膜移植术。首次角膜移植时的中位年龄为4.4个月。中位随访时间为11.1年。54%的眼接受了一次植片,18%接受了两次植片,28%接受了三次或更多次植片。首次植片保持透明的总体概率在6个月时为56%,12个月时为49%,3年时为44%,10年时为35%。第二次或后续植片存活3年的概率小于10%。在复查时,39%的眼植片透明;36%的眼首次植片透明。多因素分析确定疾病严重程度、供体角膜大小、并存的中枢神经系统异常以及前粘连象限是植片失败的最强危险因素。限于术前可观察变量的补充多因素分析确定基质血管、全角膜缘混浊和术前青光眼是植片失败的独立术前预测因素。同种异体植片排斥是最常见的植片失败原因。角膜移植术后的主要并发症为眼球痨、视网膜脱离、白内障和青光眼。
彼得斯异常初次穿透性角膜移植术后保持植片透明的总体长期概率为35%±0.06%,后续植片很少存活。患有严重疾病、供体角膜较大、并存中枢神经系统异常和有前粘连的眼,其预后明显比无这些因素的眼差。在推荐对彼得斯异常进行角膜移植时,尤其是在先前植片失败后,应仔细考虑这些数据。