Terconazole Cream for Non-Candida albicans Fungal Vaginitis: Results of a Retrospective Analysis

• Published in: Infectious Diseases in Obstetrics and Gynecology Vol. 2000; no. 5-6; pp. 240 - 243
• Main Authors: Geetika Sood, Paul Nyirjesy, M. Velma Weitz, Ashwin Chatwani
• Format: Journal Article
• Language: English
• Published: Hindawi Limiteds 01-12-2000; Hindawi Limited
• Subjects: candidiasis; vaginitis; antifungal therapies
• ISSN: 1064-7449; 1098-0997
• DOI: 10.1155/S1064744900000351

Objective: Although it is FDA-approved for use in vulvovaginal candidiasis caused by non-Candida albicansspecies, terconazole cream has not been been studied in patients with these infections. We sought to assess the clinical and mycological efficacy of terconazole cream in women with non-C. albicans vaginitis. Methods: The records of patients who had received a 7-day course of terconazole cream for culture-proved non-C. albicans vaginitis were reviewed. Data with regard to patient demographics, clinical and mycologic response to therapy within 1 month of treatment, and outcome with other antifungal therapies were analyzed. Results: Twenty-eight patients received terconazole cream for non-C. albicans infections. Three patients did not return for follow-up. The median age was 45 years. Seven (28%) patients were nulliparous. The median duration of symptoms was 3 years. Nine patients (36%) had received terconazole within the 6 months prior to referral. Overall, there were 20 C. glabrata cases, 3 C. parapsilosis, and 2 C. lusitaniae. Fourteen (56%) patients achieved a mycologic cure; 11 (44%) noted a resolution of their symptoms. Prior terconazole use was not associated with treatment failure (P = 0.09). Ten failures received boric acid suppositories as subsequent treatment; a cure was effected in 4 (40%). Two of three patients (67%) were eventually cured with flucytosine cream. Five (20 %) patients remained uncured. Conclusions: Terconazole cream may be an appropriate first-line treatment for non C. albicans vaginitis, even in patients who have previously received the drug.