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克霉唑 500mg 阴道栓与舍他康唑 300mg 治疗妊娠合并急性霉菌性阴道炎的随机、双盲对照研究

Sertaconazole 300 mg versus clotrimazole 500 mg vaginal suppository for treating pregnant women with acute vaginal candidiasis: a double-blinded, randomized trial.

机构信息

Unit of Infectious Diseases, Department of Obstetrics and Gynaecology, Faculty of Medicine Siriraj Hospital, Mahidol University, 2 Wanglang Road, Bangkok Noi, Bangkok, 10700, Thailand.

Division of Materno-Fetal Medicine, Department of Obstetrics and Gynaecology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

BMC Pregnancy Childbirth. 2024 Apr 4;24(1):235. doi: 10.1186/s12884-024-06440-z.

Abstract

BACKGROUND

Vaginal candidiasis (VC) commonly affects pregnant women. Traditionally, clotrimazole vaginal tablets (CLO) have been the cornerstone of management. However, sertaconazole ovules (SER) offer a novel topical antimycotic option. This double-blinded, randomized trial evaluated the efficacy of single-dose SER and CLO in treating acute VC during pregnancy.

METHODS

From June 2020 to May 2021, this trial recruited pregnant women aged ≥ 18 years with VC symptoms (abnormal vaginal discharge and/or vulvar/vaginal itching) confirmed by microscopy. Participants with ≥ 4 VC episodes in the prior year, immunocompromised status, or imidazole contraindications and those who were absent at the 2-week follow-up were excluded. Participants were randomized to receive either 300 mg SER or 500 mg CLO. Evaluations 2 weeks after the initial medication administration included clinical cure (self-reported resolution of all symptoms), microscopic cure (pseudohyphal absence), patient satisfaction, side effects, and time to clinical cure. Participants with persistent VC received weekly SER doses until delivery. Assessments of recurrence and pregnancy outcomes were done.

RESULTS

The analysis included 96 participants (48 per group, mean age 27.4 ± 7.4 years, gestational age at diagnosis 22.9 ± 6.4 weeks). Without statistical significance, SER achieved a higher clinical cure rate (62.5% vs 50%, p = 0.217; a mean difference of 12.5%, 95%CI: -17.5% to 42.5%; and a rate ratio of 1.25, 95%CI: 0.71 to 2.23) and a lower microscopic cure (47.9% vs. 62.5%, p = 0.151; a mean difference of -14.6%, 95%CI: -44.3% to 15.1%; and a rate ratio of 0.77, 95%CI: 0.43 to 1.37). The two groups had comparable times to clinical cure (SER: 3.1 ± 1.8 days, CLO: 3.4 ± 2.7 days; p = 0.848) and substantial satisfaction rates (SER: 66.7%, CLO: 60.4%; p = 0.753). No side effects were reported. Of 60 participants who gave birth at Siriraj Hospital, there were no significant differences in pregnancy outcomes. Repeated SER dosing eradicated symptoms and enhanced the microscopic cure rate. Recurrence was observed in four SER and two CLO participants within 1-2 months.

CONCLUSION

In the treatment of acute VC during pregnancy, 300 mg SER and 500 mg CLO exhibited comparable efficacy in terms of clinical and microscopic cure rates, satisfaction, side effects, time to clinical cure, recurrence rates, and pregnancy outcomes.

TRIAL REGISTRATION

TCTR20190308004 (registration date March 8, 2019).

摘要

背景

阴道念珠菌病(VC)常影响孕妇。传统上,克霉唑阴道片(CLO)一直是管理的基石。然而,酮康唑阴道栓(SER)提供了一种新的局部抗真菌选择。这项双盲、随机试验评估了单剂量 SER 和 CLO 在治疗妊娠期急性 VC 中的疗效。

方法

从 2020 年 6 月至 2021 年 5 月,该试验招募了年龄≥18 岁的有 VC 症状(异常阴道分泌物和/或外阴/阴道瘙痒)的孕妇,并通过显微镜检查确诊。排除了过去一年中有≥4 次 VC 发作、免疫功能低下或有咪唑类药物禁忌证且在 2 周随访时未出现的患者。参与者被随机分配接受 300mg SER 或 500mg CLO。初始用药 2 周后的评估包括临床治愈(自我报告所有症状缓解)、微观治愈(假丝酵母菌不存在)、患者满意度、副作用和临床治愈时间。持续存在 VC 的参与者每周接受 SER 剂量,直至分娩。对复发和妊娠结局进行评估。

结果

分析纳入了 96 名参与者(每组 48 名,平均年龄 27.4±7.4 岁,诊断时的妊娠龄为 22.9±6.4 周)。无统计学意义,SER 达到了更高的临床治愈率(62.5%比 50%,p=0.217;平均差异 12.5%,95%CI:-17.5%至 42.5%;和率比 1.25,95%CI:0.71 至 2.23)和更低的微观治愈率(47.9%比 62.5%,p=0.151;平均差异-14.6%,95%CI:-44.3%至 15.1%;和率比 0.77,95%CI:0.43 至 1.37)。两组的临床治愈时间(SER:3.1±1.8 天,CLO:3.4±2.7 天;p=0.848)和满意度(SER:66.7%,CLO:60.4%;p=0.753)相当。未报告副作用。在 60 名在诗里拉吉医院分娩的参与者中,妊娠结局无显著差异。重复使用 SER 可消除症状并提高微观治愈率。在 4 名 SER 和 2 名 CLO 参与者中,在 1-2 个月内观察到复发。

结论

在治疗妊娠期急性 VC 时,300mg SER 和 500mg CLO 在临床和微观治愈率、满意度、副作用、临床治愈时间、复发率和妊娠结局方面具有相当的疗效。

试验注册

TCTR20190308004(注册日期为 2019 年 3 月 8 日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/316a/10993551/02e6ae5b7ccd/12884_2024_6440_Fig1_HTML.jpg

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