Cornea and Anterior Segment Services, L V Prasad Eye Institute, Hyderabad, Telangana, India.
Ramayamma International Eye Bank, LV Prasad Eye Institute, Hyderabad, Telangana, India.
Indian J Ophthalmol. 2024 Sep 1;72(9):1254-1260. doi: 10.4103/IJO.IJO_3106_23. Epub 2024 Aug 23.
To report the clinical profile and donor characteristics of post-optical keratoplasty adverse events notified at an eye bank.
Between January 2013 and December 2022, 37,041 donor corneas were utilized for keratoplasty, of which 16,531 were used for penetrating keratoplasty (PK), 12,171 for endothelial keratoplasty (EK), and 1356 for anterior lamellar keratoplasty (ALK). EK included 10,956 Descemet stripping automated endothelial keratoplasty (DSAEK) and 1215 Descemet membrane endothelial keratoplasty (DMEK). The adverse events reported within the first 6 weeks of optical keratoplasty were analyzed for donor-related parameters.
A total of 41 (0.11%) recipients had post-keratoplasty infections. Of these, 33 occurred after EK (29 after DSAEK, and four after DMEK), two after ALK, and six after PK. The clinical presentation was keratitis alone in 16 eyes and associated with endophthalmitis in 25 eyes. The organisms isolated were gram-negative bacteria in 26 eyes, fungus in eight eyes, gram-positive bacteria in four eyes, mixed infection in five eyes, and microbiology inconclusive in seven eyes. The majority (78%) of the gram-negative infections were due to multidrug-resistant organisms. Most (88%) donor corneas were harvested from hospital premises. The most common cause of donor mortality was trauma. The median duration of presentation from surgery was 4.46 (range: 1-30) days. The death to preservation time was 4.18 (1.5-7.65) hours. The death to utilization time was 3 (2-4.7) days.
The overall risk of infectious adverse events after keratoplasty was 0.11%, ranging from 0.08% to 0.36%. Most (80.4%) of the adverse events occurred after EK. The majority (78.9%) of the adverse events were of bacterial etiology, of which gram-negative infections (68.4%) were the most common. The trends and microbiological spectrum of organisms associated with infections should be thoroughly documented in eye banks to gain insights and formulate guidelines on the management of adverse events.
报告一家眼库通报的光学角膜移植术后不良事件的临床特征和供体特征。
2013 年 1 月至 2022 年 12 月期间,共有 37041 枚供体角膜用于角膜移植,其中 16531 枚用于穿透性角膜移植术(PK),12171 枚用于内皮角膜移植术(EK),1356 枚用于前板层角膜移植术(ALK)。EK 包括 10956 例去上皮自动内皮角膜移植术(DSAEK)和 1215 例去内皮膜内皮角膜移植术(DMEK)。分析光学角膜移植术后 6 周内报告的不良事件与供体相关参数的关系。
共有 41 名(0.11%)受者发生移植后感染。其中,33 例发生在 EK 后(29 例发生在 DSAEK 后,4 例发生在 DMEK 后),2 例发生在 ALK 后,6 例发生在 PK 后。临床表现为单纯角膜炎 16 只眼,合并眼内炎 25 只眼。分离出的病原体包括革兰氏阴性菌 26 只眼,真菌 8 只眼,革兰氏阳性菌 4 只眼,混合感染 5 只眼,7 只眼微生物学结果不确定。大多数(78%)革兰氏阴性菌感染是由多药耐药菌引起的。大多数(88%)供体角膜来自医院场地。供体死亡的最常见原因是创伤。从手术到出现症状的中位时间为 4.46 天(范围:1-30 天)。从死亡到保存时间为 4.18 小时(1.5-7.65 小时)。从死亡到使用时间为 3 天(2-4.7 天)。
角膜移植术后发生感染性不良事件的总体风险为 0.11%,范围为 0.08%至 0.36%。大多数(80.4%)不良事件发生在 EK 后。大多数(78.9%)不良事件为细菌性病因,其中革兰氏阴性菌感染(68.4%)最为常见。眼库应详细记录与感染相关的病原体的趋势和微生物谱,以深入了解并制定不良事件管理指南。