Reibaldi Michele, Avitabile Teresio, Bandello Francesco, Longo Antonio, Bonfiglio Vincenza, Russo Andrea, Castellino Niccolò, Rejdak Robert, Nowomiejska Katarzyna, Toro Mario, Furino Claudio, Cillino Salvatore, Fiore Tito, Cagini Carlo, Grassi Patrizia, Musumeci Rosario, Cocuzza Clementina Elvezia, Martinelli Marianna, Fallico Matteo
Department of Ophthalmology, University of Catania, 95123 Catania, Italy.
Department of Ophthalmology, University Vita Salute Hospital San Raffaele, 20132 Milano, Italy.
J Clin Med. 2019 Jul 13;8(7):1031. doi: 10.3390/jcm8071031.
The study purpose was to assess the efficacy of a preservative-free 0.6% povidone iodine eye drops as perioperative prophylactic treatment for reducing conjunctival bacterial load and the rate of needle contamination in patients undergoing intravitreal anti-vascular endothelial growth factor injection. Enrolled patients were randomized to either the study group (0.6% povidone iodine, three day-prophylactic treatment before the injection) or to the control group (placebo, three day-prophylactic treatment). Conjunctival swabs were obtained before and after the prophylactic treatment in both groups. Intravitreal injections were performed in a sterile fashion. The injection needle and a control needle were collected for microbiological culture. Data from 254 and 253 eyes in the study group and control group, respectively, were analyzed. Bacterial growth from conjunctival swab cultures was significantly lower after 0.6% povidone iodine prophylaxis compared to baseline and to placebo prophylaxis ( < 0.001), showing an 82% eradication rate in the study group. No injection needle showed bacterial contamination in the study group, whereas six needles were culture-positive in the control group ( = 0.015). No serious ocular and non-ocular adverse events were recorded. The 0.6% povidone iodine solution proved an effective treatment in reducing conjunctival bacterial load and risk of needle contamination.
本研究旨在评估不含防腐剂的0.6%聚维酮碘滴眼液作为围手术期预防性治疗,在接受玻璃体内抗血管内皮生长因子注射的患者中降低结膜细菌载量和针头污染率的疗效。纳入的患者被随机分为研究组(0.6%聚维酮碘,注射前进行为期三天的预防性治疗)或对照组(安慰剂,为期三天的预防性治疗)。两组在预防性治疗前后均采集结膜拭子。玻璃体内注射以无菌方式进行。收集注射针和对照针进行微生物培养。分别对研究组和对照组的254只眼和253只眼的数据进行分析。与基线和安慰剂预防相比,0.6%聚维酮碘预防后结膜拭子培养的细菌生长显著降低(<0.001),研究组的根除率为82%。研究组中没有注射针显示细菌污染,而对照组中有六根针培养呈阳性(=0.015)。未记录到严重的眼部和非眼部不良事件。0.6%聚维酮碘溶液被证明是一种有效的治疗方法,可降低结膜细菌载量和针头污染风险。