Mora-Galván Jessica A, Escobar-Ponce Luis F, Olguín-Ortega Andrea, Villeda-Gabriel Graciela, Figueroa-Damián Ricardo, Rendón-Molina Alejandro
Department of Gynecology, National Institute of Perinatology, Mexico City, MEX.
Department of Infectology and Immunology, National Institute of Perinatology, Mexico City, MEX.
Cureus. 2024 Nov 13;16(11):e73609. doi: 10.7759/cureus.73609. eCollection 2024 Nov.
Objective To evaluate the sterilization efficacy of hysteroscopy instruments using ultraviolet C (UV-C) light at a wavelength of 259 nm in the Endoscopic Diagnostic Center of the National Institute of Perinatology. Methods Consecutive patients undergoing office hysteroscopy via the Bettochi vaginoscopy technique were included, excluding those with conditions such as viable intrauterine pregnancy or acute pelvic infection. Samples were collected from six designated sites of the hysteroscope, including the inner sheath, internal holes of the inner sheath, lens, graspers, scissors, and outer sheath. Initially, samples were taken after the first sterilization using a LAOKEN LK/MJG-150 Plasma Sterilizer (Chengdu, China). Next, samples were collected after the routine use of the hysteroscope in the office setting to confirm contamination. Subsequently, a new set of samples were taken after a 20-minute UV-C sterilization cycle with the EsteriUV device. Results The initial sterilization achieved a 96.73% sterilization rate, with ten samples testing positive for -negative. Post-hysteroscopy, contamination increased significantly. Afterward, UV-C sterilization achieved a 96.08% sterilization rate, with 11 samples positive for -negative and one for (p=0.66). No clinical infections were reported in any patient within one-month post-procedure. Conclusion UV-C light is a viable alternative for hysteroscopy instrument sterilization, demonstrating comparable efficacy to conventional methods. Further studies are recommended to optimize UV-C parameters for enhanced sterilization efficiency.
目的 评估在国家围产医学研究所内镜诊断中心使用波长为259nm的紫外线C(UV-C)光对宫腔镜器械的灭菌效果。方法 纳入通过贝托奇阴道镜技术接受门诊宫腔镜检查的连续患者,排除有宫内活胎妊娠或急性盆腔感染等情况的患者。从宫腔镜的六个指定部位采集样本,包括内鞘、内鞘内孔、透镜、抓钳、剪刀和外鞘。最初,在使用LAOKEN LK/MJG-150等离子灭菌器(中国成都)首次灭菌后采集样本。接下来,在门诊环境中常规使用宫腔镜后采集样本以确认污染情况。随后,使用EsteriUV设备进行20分钟的UV-C灭菌循环后采集一组新的样本。结果 初次灭菌的灭菌率达到96.73%,有10个样本检测为阴性。宫腔镜检查后,污染显著增加。之后,UV-C灭菌的灭菌率达到96.08%,有11个样本检测为阴性而1个为阳性(p=0.66)。在术后一个月内,没有任何患者报告临床感染。结论 UV-C光对于宫腔镜器械灭菌是一种可行的替代方法,其效果与传统方法相当。建议进一步研究以优化UV-C参数以提高灭菌效率。