Single-Dose fluconazole versus standard 2-week therapy for Oropharyngeal Candidiasis in HIV-infected patients: a randomized, Double-Blind, Double-Dummy Trial
| dc.contributor.author | Moshi, Mainen J. | |
| dc.date.accessioned | 2023-08-11T08:58:55Z | |
| dc.date.available | 2023-08-11T08:58:55Z | |
| dc.date.issued | 2008-11-15 | |
| dc.description.abstract | Background. Oropharyngeal candidiasis is the most common opportunistic infection affecting patients with human immunodeficiency virus (HIV) infection. Because of convenience, cost, and reluctance to complicate antiretroviral treatment regimens, single-dose fluconazole may be a favorable regimen for treatment of moderate to severe oropharyngeal candidiasis. We conducted a prospective, randomized, double-blind, placebo-controlled trial to compare the clinical and mycological responses, relapse rates, and safety of a single 750-mg dose and a 14-day course of treatment with fluconazole. Methods. A total of 220 HIV-infected patients with clinical and mycological evidence of oropharyngeal candidiasis were randomly assigned in a 1:1 ratio to receive either a 750-mg single dose of orally administered fluconazole (110 patients) or 150 mg of orally administered fluconazole once per day for 2 weeks (110 patients). The primary efficacy analysis was based on clinical and mycological responses at the end of treatment. Secondary parameters were safety and relapse rate. Results. Single-dose fluconazole was equivalent to a 14-day course of fluconazole in achieving clinical and mycological cure, with clinical cure rates of 94.5% and 95.5%, respectively (odds ratio, 0.825; 95% confidence interval, 0.244–2.789; P=.99), and mycological cure rates of 84.5% and 75.5%, respectively (odds ratio, 1.780; 95% confidence interval, 0.906–3.496; P=.129). Drug-related adverse events were uncommon and were not different between the treatment groups. Conclusion. A single dose of 750 mg of fluconazole was safe, well tolerated, and as effective as the standard 14-day fluconazole therapy in patients with HIV infection and acquired immunodeficiency syndrome who had oropharyngeal candidiasis coinfection. | en_US |
| dc.identifier.citation | Hamza, O.J., Matee, M.I., Brüggemann, R.J., Moshi, M.J., Simon, E.N., Mugusi, F., Mikx, F.H., van der Lee, H.A., Verweij, P.E. and van der Ven, A.J., 2008. Single-dose fluconazole versus standard 2-week therapy for oropharyngeal candidiasis in HIV-infected patients: a randomized, double-blind, double-dummy trial. Clinical infectious diseases, 47(10), pp.1270-1276. | en_US |
| dc.identifier.other | https://doi.org/10.1086/592578 | |
| dc.identifier.uri | http://hdl.handle.net/123456789/1104 | |
| dc.language.iso | en | en_US |
| dc.publisher | Clinical infectious diseases | en_US |
| dc.subject | HIV | en_US |
| dc.subject | Fluconozole | en_US |
| dc.subject | Safety | en_US |
| dc.title | Single-Dose fluconazole versus standard 2-week therapy for Oropharyngeal Candidiasis in HIV-infected patients: a randomized, Double-Blind, Double-Dummy Trial | en_US |
| dc.type | Article | en_US |