Vahedpoor Zahra, Abastabar Mahdi, Sehat Mojtaba, Talebian Parisa, Felfelian Fini Tayebeh, Dastanpour Zahra, Haghani Iman, Chelongarian Ramtin, Nazeri Mehdi
Autoimmune Diseases Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Invasive Fungi Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Curr Med Mycol. 2021 Sep;7(3):36-43. doi: 10.18502/cmm.7.3.7803.
Vulvovaginal candidiasis is considered the second most prevalent gynecologic infection among women and one of the main reasons for referring to a gynecologist. During recent decades, probiotic usage has been defined as one of the therapeutic regimens for vaginal candidiasis management, but these findings were controversial. The current study was conducted to determine the effect of fluconazole plus vaginal and oral probiotics supplementation on clinical and mycological improvement of vaginal candidiasis concomitant with antifungal susceptibility of species to fluconazole.
This double-blind, randomized, placebo-controlled trial was conducted on 76 women with vaginal candidiasis admitted to Naghavi and Imam Reza Gynecology Clinics in Kashan, Central Iran, from July 2017 to March 2020. Patients were diagnosed according to vaginal candidiasis symptoms and positive culture for species. The patients were divided into two groups; one of them received fluconazole plus vaginal and oral probiotics, while the other one received fluconazole with placebo. The clinical and mycological findings were recorded before and after the treatment. In vitro, the fluconazole susceptibility test was determined by the microdilution method according to the Clinical and Laboratory Standards Institute (M27-A3) for the baseline isolates.
Based on the findings, 35 days after the intervention, a significant reduction was reported in vaginal candidiasis symptoms in the probiotics supplementation group. Although probiotics supplementation therapy was a better mycological cure, compared to the fluconazole with the placebo group, this difference was not significant (68.4% vs. 46.9%, =0.184). Exclusion of resistant and susceptible dose-dependent strain in the regression model demonstrated a significant reduction in positive culture probiotics in the supplementation group.
Oral and vaginal supplementation with probiotics for 4 weeks played a significant role in the elimination of vaginal candidiasis symptoms. Adjustment of clinical and mycological responses with drug resistance patterns of patients could open a promising horizon for probiotics consumption as a complementary treatment.
外阴阴道念珠菌病被认为是女性中第二常见的妇科感染,也是转诊至妇科医生的主要原因之一。在最近几十年中,益生菌的使用已被定义为阴道念珠菌病治疗方案之一,但这些结果存在争议。本研究旨在确定氟康唑联合阴道和口服益生菌补充剂对阴道念珠菌病临床和真菌学改善的影响,以及念珠菌属对氟康唑的抗真菌药敏情况。
本双盲、随机、安慰剂对照试验于2017年7月至2020年3月在伊朗中部卡尚的纳哈维妇产科诊所和伊玛目礼萨妇产科诊所对76例阴道念珠菌病女性患者进行。患者根据阴道念珠菌病症状和念珠菌属阳性培养结果进行诊断。患者分为两组;一组接受氟康唑联合阴道和口服益生菌,另一组接受氟康唑加安慰剂。在治疗前后记录临床和真菌学结果。体外,根据临床和实验室标准协会(M27 - A3)的微量稀释法对基线分离株进行氟康唑药敏试验。
基于研究结果,干预35天后,益生菌补充剂组阴道念珠菌病症状显著减轻。虽然与氟康唑加安慰剂组相比,益生菌补充疗法在真菌学治愈方面更好,但这种差异不显著(68.4%对46.9%,P = 0.184)。回归模型中排除耐药和剂量依赖性敏感菌株后,补充剂组阳性培养的益生菌显著减少。
口服和阴道补充益生菌4周对消除阴道念珠菌病症状起显著作用。根据患者的耐药模式调整临床和真菌学反应,可能为益生菌作为辅助治疗的应用开辟一个有前景的方向。