Prabhasawat P, Tesavibul N, Komolsuradej W
Department of Ophthalmology, Faculty of Medicine, Siriraj Hospital Mahidol University, Bangkok, Thailand.
Br J Ophthalmol. 2001 Dec;85(12):1455-63. doi: 10.1136/bjo.85.12.1455.
To evaluate the efficacy of amniotic membrane transplantation (AMT) in persistent corneal epithelial defect with or without stromal thinning and corneal perforation.
28 patients (28 eyes) with persistent corneal epithelial defect unresponsive to medical treatment were given preserved human amniotic membrane transplants. The patients were divided into three groups: group A, persistent corneal epithelial defect 10 eyes; group B, epithelial defect with stromal thinning 13 eyes; and group C, corneal perforation five eyes. AMT was performed using one layer in group A and multilayers in group B and C. The causes of persistent epithelial defect were neurotrophic keratopathy (24 eyes), limbal deficiency (six eyes), exposure keratopathy (four eyes), and Mooren's ulcer (one eye).
Success was noted in 82.1% (23/28 eyes) in all groups, with 80% (8/10 eyes), 84.6% (11/13 eyes), and 80% (4/5 eyes) in groups A, B, and C respectively, with a mean follow up of 10.9 months (1-30 months). The mean epithelialisation time after AMT was 2.1 weeks. The healing times of groups B and C are also significantly shorter than group A (p=0.017 and 0.018, respectively). Corneal stromal thickness was significantly increased in all cases in groups B and C (p=0.006). Those with corneal perforation in group C were completely healed by multilayer AMT. There was no difference in the epithelialisation time between successful cases treated by a single operation (17 eyes) or repeated operation (six eyes). Vision improved in 18.9% (8/28 eyes) and worsened as a result of cataract formation in 2.3% (1/28 eyes). Failure was noted in 17.9% (5/28 eyes), because of corneal infection (two eyes), neurotrophic keratopathy with and without limbal deficiency (two eyes), and intractable corneal perforation (one eye). No patient developed major immediate postoperative complications or graft rejection.
Amniotic membrane can successfully treat refractory corneal epithelial defect by promoting epithelial healing and thus prevent corneal perforation. It can be used as a treatment for corneal perforation by restoring corneal stromal thickness so that emergency penetrating keratoplasty can be avoided.
评估羊膜移植术(AMT)治疗伴有或不伴有基质变薄及角膜穿孔的持续性角膜上皮缺损的疗效。
对28例(28眼)药物治疗无效的持续性角膜上皮缺损患者进行保存人羊膜移植。患者分为三组:A组,持续性角膜上皮缺损10眼;B组,上皮缺损伴基质变薄13眼;C组,角膜穿孔5眼。A组采用单层羊膜移植,B组和C组采用多层羊膜移植。持续性上皮缺损的病因包括神经营养性角膜病变(24眼)、角膜缘缺陷(6眼)、暴露性角膜病变(4眼)和蚕蚀性角膜溃疡(1眼)。
所有组的成功率为82.1%(23/28眼),A组、B组和C组分别为80%(8/10眼)、84.6%(11/13眼)和80%(4/5眼),平均随访10.9个月(1 - 30个月)。羊膜移植术后平均上皮化时间为2.1周。B组和C组的愈合时间也明显短于A组(分别为p = 0.017和0.018)。B组和C组所有病例的角膜基质厚度均显著增加(p = 0.006)。C组角膜穿孔患者通过多层羊膜移植完全愈合。单次手术(17眼)或重复手术(6眼)治疗成功的病例上皮化时间无差异。视力提高的占18.9%(8/28眼),因白内障形成视力恶化的占2.3%(1/28眼)。失败率为17.9%(5/28眼),原因包括角膜感染(2眼)、伴有或不伴有角膜缘缺陷的神经营养性角膜病变(2眼)和难治性角膜穿孔(1眼)。无患者发生严重的术后即刻并发症或移植排斥反应。
羊膜可通过促进上皮愈合成功治疗难治性角膜上皮缺损,从而预防角膜穿孔。它可用于通过恢复角膜基质厚度治疗角膜穿孔,从而避免紧急穿透性角膜移植术。