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纽扣式人工角膜植入治疗高危角膜移植角膜盲多中心临床试验

[A multicenter clinical trial of collar-button type keratoprosthesis implantation for the treatment of corneal blindness in high-risk transplantation].

作者信息

Zhang T, Wang L L, Gu J J, Xu J J, Chen W, Huang Y F, Hong J X, Wang T, Li S X, Gao H, Wang J T, Shi W Y

机构信息

Eye Institute of Shandong First Medical University, Eye Hospital of Shandong First Medical University (Shandong Eye Hospital), State Key Laboratory Cultivation Base, Shandong Provincial Key Laboratory of Ophthalmology, School of Ophthalmology, Shandong First Medical University, Jinan 250021, China.

Ophthalmology Division of Chinese PLA General Hospital, Beijing 100853, China.

出版信息

Zhonghua Yan Ke Za Zhi. 2023 Apr 11;59(4):262-271. doi: 10.3760/cma.j.cn112142-20221103-00565.

Abstract

To evaluate the efficiency and safety of collar-button type keratoprosthesis (c-bKPro) implantation for corneal blindness in high-risk transplantation in China. It was a case series study. High-risk corneal blind patients who planned to undergo c-bKPro implantation were prospectively and continuously enrolled in the Eye Hospital of Shandong First Medical University, Ophthalmology Division of Chinese PLA General Hospital, Zhongshan Ophthalmic Center Department of Ophthalmology in Eye & ENT Hospital of Fudan University, and Eye Hospital of Wenzhou Medical University from July 2019 to January 2020. The cure for blindness and surgical success were assessed based on visual acuity (VA)≥0.05. The complications and keratoprosthesis retention rate were recorded to determine the safety of the surgery. Thirty-seven subjects (eyes) were included, of which 32 were male and 5 were female, aged 27 to 72 years old. The indications of c-bKPro implantation were corneal graft failure (21 eyes, 56.8%), chemical injury (8 eyes, 21.6%), thermal burn (5 eyes, 13.5%), unexplained corneal opacity (2 eyes, 5.4%), and corneal perforation (1 eye, 2.7%). Two patients withdrew from the clinical trial at 3 months postoperatively. Thirty-five patients were followed up for 6 months, and 31 were followed up for 12 months. The VA was ≥0.05 in 83.8% of eyes at 6 months and in 81.8% of eyes at 12 months. Among the 11 eyes diagnosed with concurrent glaucoma, 6 eyes achieved a VA of ≥0.05. At 12 months, the c-bKPro retention rate was 100%. The surgical complications included retroprosthetic membrane formation (5 eyes, 16.1%), persistent corneal epithelial defects (5 eyes, 16.1%), macular edema (4 eyes, 12.9%), new-onset glaucoma (4 eyes, 12.5%; including one eye withdrawn from the study at 3 months), sterile corneal melting (2 eyes, 6.5%), sterile vitritis (1 eye, 3.2%), and infectious keratitis (1 eye, 3.2%). C-bKPro implantation is an effective and safe option for treating corneal blindness in high-risk transplantation in China. Improved visual outcomes could be achieved in most cases, with a relatively low incidence of postoperative complications.

摘要

评估中国式领扣型人工角膜(c-bKPro)植入术治疗高危角膜移植导致的角膜盲的有效性和安全性。这是一项病例系列研究。2019年7月至2020年1月,前瞻性、连续性纳入计划接受c-bKPro植入术的高危角膜盲患者,这些患者来自山东第一医科大学附属眼科医院、中国人民解放军总医院眼科、复旦大学附属眼耳鼻喉科医院眼科中山眼科中心以及温州医科大学附属眼视光医院。根据视力(VA)≥0.05评估失明治愈情况和手术成功率。记录并发症和人工角膜留存率以确定手术安全性。共纳入37例受试者(眼),其中男性32例,女性5例,年龄27至72岁。c-bKPro植入术的适应证包括角膜移植失败(21眼,56.8%)、化学伤(8眼,21.6%)、热烧伤(5眼,13.5%)、不明原因角膜混浊(2眼,5.4%)以及角膜穿孔(1眼,2.7%)。2例患者术后3个月退出临床试验。35例患者随访6个月,31例患者随访12个月。6个月时83.8%的眼视力≥0.05,12个月时81.8%的眼视力≥0.05。在诊断为合并青光眼的11眼中,6眼视力达到≥0.05。12个月时,c-bKPro留存率为100%。手术并发症包括人工角膜后膜形成(5眼,16.1%)、持续性角膜上皮缺损(5眼,16.1%)、黄斑水肿(4眼,12.9%)、新发青光眼(4眼,12.5%;包括1例术后3个月退出研究的眼)、无菌性角膜溶解(2眼,6.5%)、无菌性葡萄膜炎(1眼,3.2%)以及感染性角膜炎(1眼,3.2%)。c-bKPro植入术是中国治疗高危角膜移植导致的角膜盲的一种有效且安全的选择。大多数病例可实现改善的视觉效果,术后并发症发生率相对较低。

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