Fong I W
Department of Medicine, St Michael's Hospital, University of Toronto, Ontario, Canada.
Genitourin Med. 1992 Dec;68(6):374-7. doi: 10.1136/sti.68.6.374.
To determine the comparative efficacy of oral itraconazole versus intravaginal clotrimazole in suppressing recurrent episodes of vulvovaginal candidiasis.
Prospective randomised open study of women with recurrent vulvovaginal candidiasis. Clinical and microbiological assessments were made monthly for 12 months.
Women's Clinic of a University teaching hospital.
Forty-four otherwise healthy, non-pregnant women, with at least four proven episodes of candida vaginitis in the last year were enrolled into the study.
After an acute episode of candida vaginitis, 22 women received oral itraconazole 200 mg daily for five days, then 200 mg twice weekly for six months; and 22 women received intra-vaginal clotrimazole 200 mg ovules daily for five days, then 200 mg twice weekly for six months.
Symptomatic recurrent clinical vulvovaginal candidiasis during the first six months of suppressive therapy was the major endpoint. A secondary endpoint was recurrent candida vaginitis within six months after completion of therapy.
Six patients did not complete the study, one in the itraconazole group and five in the clotrimazole group. Of the evaluable patients, seven of 21 patients (33.3%) in the itraconazole group versus none (0%) of 17 patients on clotrimazole were failures on suppressive therapy, p = 0.02. Following discontinuation of suppressive therapy, recurrences of candida vaginitis were similar, 10 (47.6%) of patients on itraconazole (95% confidence interval (CI) 27-67%), versus 11 (64%) patients on clotrimazole (CI 41-87%), p = 0.15.
Intermittent suppressive therapy with clotrimazole was more effective than itraconazole in preventing recurrent candida vaginitis, provided patients adhered to the regimen. Recurrence of vaginitis was common with both regimens after stopping suppressive therapy.
确定口服伊曲康唑与阴道用克霉唑在抑制复发性外阴阴道念珠菌病发作方面的相对疗效。
对复发性外阴阴道念珠菌病女性进行前瞻性随机开放研究。连续12个月每月进行临床和微生物学评估。
某大学教学医院的妇科门诊。
44名健康、非妊娠女性,过去一年中至少有4次经证实的念珠菌性阴道炎发作,纳入本研究。
念珠菌性阴道炎急性发作后,22名女性每日口服伊曲康唑200mg,连服5天,然后每周两次,每次200mg,共6个月;22名女性每日阴道内使用克霉唑200mg栓剂,连服5天,然后每周两次,每次200mg,共6个月。
抑制治疗前6个月内有症状的复发性临床外阴阴道念珠菌病为主要终点。次要终点是治疗结束后6个月内复发性念珠菌性阴道炎。
6名患者未完成研究,伊曲康唑组1名,克霉唑组5名。在可评估的患者中,伊曲康唑组21名患者中有7名(33.3%)抑制治疗失败,而克霉唑组17名患者中无一例(0%)失败,p = 0.02。停止抑制治疗后,念珠菌性阴道炎的复发情况相似,伊曲康唑组10名患者(47.6%)(95%置信区间(CI)27 - 67%),克霉唑组11名患者(64%)(CI 41 - 87%),p = 0.15。
克霉唑间歇抑制治疗在预防复发性念珠菌性阴道炎方面比伊曲康唑更有效,前提是患者坚持治疗方案。停止抑制治疗后,两种治疗方案的阴道炎复发都很常见。