蓝光二极管治疗慢性外阴阴道炎:一系列病例。

Ana Cláudia Machado Pereira E Silva, Milena Bastos Brito, Mariana Robatto, Maria Clara Pavie, Andrea Q Villas Boas, Raiane Sousa, Patricia Lordelo
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引用次数: 1

摘要

目的:本初步研究旨在评价蓝光二极管(LED)治疗后慢性外阴阴道炎的特征性体征和症状。方法:对具有外阴阴道炎特征性体征和症状的妇女进行访谈,获取临床和社会人口学资料。她们回答了女性性功能指数(FSFI)和世界卫生组织生活质量(WHOQOL)简短问卷。怀疑诊断为外阴阴道炎的妇女由妇科医生进行临床检查,随后进行微生物学评估,氢氧化钾测试,阴道pH值评估,并收集阴道液进行肿瘤细胞学和真菌培养。研究参与者被要求在15天后返回,接受405纳米蓝光LED治疗,包括三次双周治疗。治疗完成28天后,患者返回进行临床再评估,并重新评估FSFI和whoqol - brief评分。结果:所有8名女性都报告了至少一种外阴阴道炎的特征性体征或症状的改善或治愈,其中5名女性的FSFI总分和whoqol - brief评分均有所改善。结论:蓝光LED治疗可改善或治愈外阴阴道炎、性功能和整体生活质量评分相关症状。临床试验注册:NCT03075046,注册日期为2017年3月9日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blue Light-Emitting Diode Therapy for Chronic Vulvovaginitis Symptoms: A Series of Cases.

Objective: This pilot study aimed to evaluate the characteristic signs and symptoms of chronic vulvovaginitis after blue light-emitting diode (LED) treatment. Methods: Women with characteristic signs and symptoms of vulvovaginitis were interviewed to obtain clinical and sociodemographic data. They answered the Female Sexual Function Index (FSFI) and the World Health Organization Quality of Life (WHOQOL)-bref questionnaires. Women with a suspected diagnosis of vulvovaginitis underwent clinical examination by a gynecologist, followed by microbiological evaluation, potassium hydroxide testing, vaginal pH assessment, and collection of vaginal fluid for oncotic cytology and fungal culture. The study participants were instructed to return after 15 days to undergo the 405 nm blue LED treatment, which consisted of three biweekly sessions. After 28 days of treatment completion, the patients returned for clinical re-evaluation and reassessment of the FSFI and WHOQOL-bref scores. Results: All eight women reported improvement or cure of at least one characteristic sign or symptom of vulvovaginitis, and five showed improvement in total FSFI and WHOQOL-bref scores. Conclusions: Treatment with blue LED may improve or cure symptoms associated with vulvovaginitis, sexual function, and the global quality of life score. Clinical Trial registration: NCT03075046 dated March 9, 2017.

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