首页> 美国卫生研究院文献>Journal of Clinical Medicine >The Effectiveness of 0.6 Povidone Iodine Eye Drops in Reducing the Conjunctival Bacterial Load and Needle Contamination in Patients Undergoing Anti-VEGF Intravitreal Injection: A Prospective Randomized Study
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The Effectiveness of 0.6 Povidone Iodine Eye Drops in Reducing the Conjunctival Bacterial Load and Needle Contamination in Patients Undergoing Anti-VEGF Intravitreal Injection: A Prospective Randomized Study

机译:0.6%聚维酮碘滴眼液降低抗玻璃体腔内注射患者结膜细菌负荷和针头污染的有效性:一项前瞻性随机研究

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摘要

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 (p < 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 (p = 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.
机译:本研究的目的是评估在玻璃体内注射抗血管内皮生长因子的患者中,使用不含防腐剂的0.6%聚维酮碘滴眼液作为围手术期预防性治疗降低结膜细菌负荷和针头污染率的功效。入组患者被随机分为研究组(0.6%聚维酮碘,注射前三天预防性治疗)或对照组(安慰剂,三天预防性治疗)。两组在预防性治疗前后均获得结膜拭子。玻璃体内注射以无菌方式进行。收集注射针和对照针用于微生物培养。分析了研究组和对照组分别来自254只和253只眼的数据。预防性使用聚维酮碘后,结膜拭子培养的细菌生长显着低于基线和安慰剂预防(p <0.001),表明在研究组中,细菌生长的根除率为82%。在研究组中,没有注射针显示出细菌污染,而在对照组中,有六个注射针是培养阳性的(p = 0.015)。没有记录到严重的眼和非眼不良事件。 0.6%的聚维酮碘溶液被证明可有效减少结膜细菌负荷和针头污染的风险。

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