Bacterial vaginosis: comparative effectiveness of treatments with 5-nitroimidazole derivatives

I. G. Kutsenko, I. O. Borovikov, E. I. Kravtsova, S. K. Batmen, A. S. Magay, O. I. Borovikova, V. A. Avakimyan, A. A. Andreeva
{"title":"Bacterial vaginosis: comparative effectiveness of treatments with 5-nitroimidazole derivatives","authors":"I. G. Kutsenko, I. O. Borovikov, E. I. Kravtsova, S. K. Batmen, A. S. Magay, O. I. Borovikova, V. A. Avakimyan, A. A. Andreeva","doi":"10.32364/2618-8430-2023-6-2-78-87","DOIUrl":null,"url":null,"abstract":"Aim: to perform a comparative analysis of clinical and microbiological efficacy and compliance to treatment with 5-nitroimidazole derivatives in patients with bacterial vaginosis (BV). Patients and Methods: this prospective open randomized study included 96 patients diagnosed with BV. The patients were divided into two groups: group 1 (n=48) received antimicrobials — oral secnidazole 2000 mg in a single dose (decontamination therapy) and vaginally administered L. casei rhamnosus Doderleini for 14 days to restore the vaginal flora (contamination therapy); group 2 (n=48) received oral metronidazole 500 mg twice daily for 7 days (decontamination therapy) and vaginally administered L. casei rhamnosus Doderleini for 14 days (contamination therapy). Clinical efficacy was evaluated one and six months after the end of therapy. The treatment efficacy criteria included the absence of specific patient's complaints, clinical and laboratory findings (pH; Nugent score), and PCR results. The compliance to treatment was assessed using clinical and psychological tests (the Morisky-Green Scale and the Modified Medication Compliance Scale). The assessment of safety profile was based on the analysis of adverse events (AE). Results: one month after the end of treatment all patients had a statistically significant (p<0.05) reduction in the prevalence of BV symptoms (unpleasant vaginal odor, pathological vaginal discharge, itching, dyspareunia, dysuria events) as compared to those at the baseline. At month 1 after the end of treatment, subgroup analysis did not demonstrate a significant difference. Six months after the end of treatment the proportion of the group 1 patients who had pathological vaginal discharge with specific odor increased to 16.7%, while in the group 2 patients it reduced to 8.3% (p<0.05). Microbiological assessment (PCR) of the combination therapy in two groups of patients with BV demonstrated a high antibacterial efficacy of 5-nitroimidazole derivatives during the first month of follow-up. The patients were considered fully compliant if they scored 4 on the Morisky — Green Scale and scored 30 on the Modified Medication Compliance Scale of V.M. Bekhterev National Medical Research Center for Psychiatry and Neurology. The percentage of full compliance was 76.2±2.8% in the group 1 patients and 93.75±3.25% in the group 2 patients. Conclusion: a high comparative clinical and microbiological effectiveness of treatments with 5-nitroimidazole derivatives (metronidazole and secnidazole) with further vaginal colonization with lactobacilli was demonstrated in patients with bacterial vaginosis. Full medication compliance was higher in patients receiving secnidazole for BV treatment. KEYWORDS: bacterial vaginosis, vaginal microbiota, vaginal discharge, 5-nitroimidazole derivatives, metronidazole, secnidazole, compliance. FOR CITATION: Kutsenko I.G., Borovikov I.O., Kravtsova E.I. et al. Bacterial vaginosis: comparative effectiveness of treatments with 5-nitroimidazole derivatives. Russian Journal of Woman and Child Health. 2023;6(2):78–87 (in Russ.). DOI: 10.32364/2618-8430-2023- 6-2-78-87.","PeriodicalId":34075,"journal":{"name":"RMZh Mat'' i ditia","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RMZh Mat'' i ditia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32364/2618-8430-2023-6-2-78-87","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Aim: to perform a comparative analysis of clinical and microbiological efficacy and compliance to treatment with 5-nitroimidazole derivatives in patients with bacterial vaginosis (BV). Patients and Methods: this prospective open randomized study included 96 patients diagnosed with BV. The patients were divided into two groups: group 1 (n=48) received antimicrobials — oral secnidazole 2000 mg in a single dose (decontamination therapy) and vaginally administered L. casei rhamnosus Doderleini for 14 days to restore the vaginal flora (contamination therapy); group 2 (n=48) received oral metronidazole 500 mg twice daily for 7 days (decontamination therapy) and vaginally administered L. casei rhamnosus Doderleini for 14 days (contamination therapy). Clinical efficacy was evaluated one and six months after the end of therapy. The treatment efficacy criteria included the absence of specific patient's complaints, clinical and laboratory findings (pH; Nugent score), and PCR results. The compliance to treatment was assessed using clinical and psychological tests (the Morisky-Green Scale and the Modified Medication Compliance Scale). The assessment of safety profile was based on the analysis of adverse events (AE). Results: one month after the end of treatment all patients had a statistically significant (p<0.05) reduction in the prevalence of BV symptoms (unpleasant vaginal odor, pathological vaginal discharge, itching, dyspareunia, dysuria events) as compared to those at the baseline. At month 1 after the end of treatment, subgroup analysis did not demonstrate a significant difference. Six months after the end of treatment the proportion of the group 1 patients who had pathological vaginal discharge with specific odor increased to 16.7%, while in the group 2 patients it reduced to 8.3% (p<0.05). Microbiological assessment (PCR) of the combination therapy in two groups of patients with BV demonstrated a high antibacterial efficacy of 5-nitroimidazole derivatives during the first month of follow-up. The patients were considered fully compliant if they scored 4 on the Morisky — Green Scale and scored 30 on the Modified Medication Compliance Scale of V.M. Bekhterev National Medical Research Center for Psychiatry and Neurology. The percentage of full compliance was 76.2±2.8% in the group 1 patients and 93.75±3.25% in the group 2 patients. Conclusion: a high comparative clinical and microbiological effectiveness of treatments with 5-nitroimidazole derivatives (metronidazole and secnidazole) with further vaginal colonization with lactobacilli was demonstrated in patients with bacterial vaginosis. Full medication compliance was higher in patients receiving secnidazole for BV treatment. KEYWORDS: bacterial vaginosis, vaginal microbiota, vaginal discharge, 5-nitroimidazole derivatives, metronidazole, secnidazole, compliance. FOR CITATION: Kutsenko I.G., Borovikov I.O., Kravtsova E.I. et al. Bacterial vaginosis: comparative effectiveness of treatments with 5-nitroimidazole derivatives. Russian Journal of Woman and Child Health. 2023;6(2):78–87 (in Russ.). DOI: 10.32364/2618-8430-2023- 6-2-78-87.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
细菌性阴道病:5-硝基咪唑衍生物治疗的比较疗效
目的:比较分析5-硝基咪唑衍生物治疗细菌性阴道病(BV)的临床、微生物学疗效及依从性。患者和方法:本前瞻性开放随机研究纳入96例诊断为BV的患者。将患者分为两组:第一组(48例)给予单剂量塞克硝唑2000 mg(去污治疗)和阴道给予鼠李糖干酪乳杆菌14天(污染治疗)以恢复阴道菌群;2组(48例)口服甲硝唑500 mg,每日2次,连续7天(去污治疗),阴道给予鼠李糖干酪乳杆菌14天(污染治疗)。在治疗结束后1个月和6个月评估临床疗效。治疗疗效标准包括无特定患者主诉、临床和实验室检查结果(pH值;Nugent评分),以及PCR结果。采用临床和心理测试(Morisky-Green量表和改良药物依从性量表)评估治疗依从性。安全性评估以不良事件(AE)分析为基础。结果:治疗结束一个月后,与基线相比,所有患者BV症状(阴道异味、病理性阴道分泌物、瘙痒、性交困难、排尿困难事件)的发生率均有统计学意义(p<0.05)降低。治疗结束后第1个月,亚组分析无显著差异。治疗结束6个月后,1组患者病理性阴道分泌物有特殊气味的比例上升至16.7%,而2组患者下降至8.3% (p<0.05)。随访第1个月,两组BV患者联合用药的微生物学评价(PCR)显示,5-硝基咪唑衍生物具有较高的抗菌效果。如果患者在Morisky - Green量表中得分为4分,在V.M. Bekhterev国家精神病学和神经病学医学研究中心的修改药物依从性量表中得分为30分,则认为患者完全依从。1组患者完全依从率为76.2±2.8%,2组为93.75±3.25%。结论:5-硝基咪唑衍生物(甲硝唑和塞克硝唑)治疗细菌性阴道病患者具有较高的临床和微生物学比较疗效,乳酸菌进一步在阴道定植。接受塞克硝唑治疗BV的患者完全服药依从性较高。关键词:细菌性阴道病,阴道微生物群,阴道分泌物,5-硝基咪唑衍生物,甲硝唑,塞克硝唑,依从性。引证:Kutsenko i.g., Borovikov i.o., Kravtsova E.I.等。细菌性阴道病:5-硝基咪唑衍生物治疗的比较疗效。俄罗斯妇女与儿童健康杂志。2023;6(2):78-87。Doi: 10.32364/2618-8430-2023- 6-2-78-87。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
0.60
自引率
0.00%
发文量
14
审稿时长
12 weeks
期刊最新文献
Monitoring the puerperium microbiota is a necessary condition for diagnosing newborn infections in the early neonatal period Abnormal placentation: modern views on etiology, pathogenesis and diagnosis Gynecological aspects of sexual dysfunction in the postmenopausal women Identifying the source of peritoneal carcinomatosis by molecular biological method (a clinical case) The assessment of bone strength based on the results of ultrasound densitometry in infants born after in vitro fertilization (IVF) weighing less than 1500 g
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1