Department of Clinical, Surgical, Diagnostic and Paediatric Sciences, University of Pavia, Pavia, Italy; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Department of Clinical, Surgical, Diagnostic and Paediatric Sciences, University of Pavia, Pavia, Italy; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Eur J Obstet Gynecol Reprod Biol. 2024 Nov;302:310-316. doi: 10.1016/j.ejogrb.2024.09.040. Epub 2024 Sep 27.
Several topical and oral drugs are available for maintenance therapy of recurrent vulvovaginal candidiasis (RVVC)(≥ 3 episodes of symptomatic Candida infection per year). The study aimed to assess the risk of early (24 weeks) and late (48-52 weeks) clinical and mycological recurrences associated with oral/topical pharmacological maintenance therapy of RVVC.
Search strategy: PubMed, EMBASE, Cochrane Library, OVID and clinical trials registers,from inception until January 2024.
Blinded and unblinded randomized studies of pharmacological prevention of RVVC recurrences during active treatment and after discontinuation of therapy.
Risk of bias, indirectness, imprecision, heterogeneity and incoherence of the network were evaluated by a semi-automated software.Bayesian network meta-analysis was used to evaluate effects of interventions on outcomes,league table and ranking of effects.
The network included 17 studies with 2304 women for early and 2179 for late recurrences. During active treatment weekly oral oteseconazole (OR = 0.05,95 %CI = 0.02-0.12, moderate confidence),weekly oral fluconazole/itraconazole (OR = 0.12,95 %CI = 0.052-0.35,moderate confidence) and weekly topical clotrimazole (OR = 0.087,95 %CI = 0.018-0.48,moderate confidence) were associated with a significant reduction in RVVC recurrence risk compared to placebo/untreated subjects.Weekly use of fluconazole/itraconazole (OR = 0.44,95 %CI = 0.24-0.80,moderate confidence) and monthly topical treatment (OR = 0.34,95 %CI = 0.18-0.66,moderate confidence) maintained efficacy after discontinuation of therapy (48-52 weeks). Weekly oteseconazole was significantly more effective in reducing the occurrence of late clinical (OR = 0.065,95 %CI = 0.036-0.11,moderate confidence) and mycological (OR = 0.073,95 %CI = 0.044-0.12,moderate confidence) RVVC recurrences than all other types of treatment tested.
Weekly maintenance therapy with oral fluconazole/itraconazole,oteseconazole, or topical clotrimazole was equally effective in preventing early RVVC recurrence.After therapy discontinuation, oteseconazole outperformed all other oral or topical regimens, lowering RVVC clinical and mycological recurrence rates by more than 90%.
有几种局部和口服药物可用于复发性外阴阴道念珠菌病(RVVC)(每年≥3 次有症状的念珠菌感染)的维持治疗。本研究旨在评估口服/局部药物治疗 RVVC 复发的早期(24 周)和晚期(48-52 周)临床和真菌学复发的风险。
检索策略:PubMed、EMBASE、Cochrane 图书馆、OVID 和临床试验登记处,从成立到 2024 年 1 月。
在活性治疗期间和停药后预防 RVVC 复发的药理学预防的盲法和非盲法随机研究。
使用半自动软件评估偏倚、间接性、不精确性、异质性和网络的不连贯性。贝叶斯网状荟萃分析用于评估干预措施对结局的影响、效果等级表和效果排名。
该网络包括 17 项研究,共纳入 2304 名女性用于早期复发,2179 名女性用于晚期复发。在活性治疗期间,每周口服奥昔康唑(OR=0.05,95%CI=0.02-0.12,中度置信度)、每周口服氟康唑/伊曲康唑(OR=0.12,95%CI=0.052-0.35,中度置信度)和每周局部应用克霉唑(OR=0.087,95%CI=0.018-0.48,中度置信度)与安慰剂/未治疗组相比,RVVC 复发风险显著降低。氟康唑/伊曲康唑(OR=0.44,95%CI=0.24-0.80,中度置信度)和每月局部治疗(OR=0.34,95%CI=0.18-0.66,中度置信度)在停药后(48-52 周)仍能保持疗效。每周奥昔康唑在降低晚期临床(OR=0.065,95%CI=0.036-0.11,中度置信度)和真菌学(OR=0.073,95%CI=0.044-0.12,中度置信度)RVVC 复发方面明显优于其他所有测试的治疗类型。
每周口服氟康唑/伊曲康唑、奥昔康唑或局部克霉唑维持治疗在预防早期 RVVC 复发方面同样有效。停药后,奥昔康唑优于所有其他口服或局部方案,将 RVVC 临床和真菌学复发率降低 90%以上。