Fluconazole
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Fluconazole


Fluconazole is a synthetic antimycotic drug of the triazole class of compunds. The drug is sold under the brand name DiflucanĀ®. It is used orally and intravenously to treat yeast and other fungal infections. more...

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Mode of action

Fluconazole inhibits, much like the imidazole-antimycotics, the fungal P450-enzyme. The consequences are that Lanosterol can no longer be converted to Ergosterol. Ergosterol is an essential part of the fungal membrane and its deficit alters the permeability of the membrane and this eventually disrupts fungal growth. It acts fungistatic or fungizide depending on the susceptibility of the strain and the dose regime used. Fluconazole is theoretically capable of inhibiting demethylases in the human body, but this effect is not seem with therapeutic doses.

Susceptible fungi

Animal models (infection studies) showed that fluconazole is active against infections with strains of Candida, Cryptococcus, Aspergillus, Blastomyces, Coccidioides and Histoplasma. In vitro test systems are still inreliable.

Pharmacokinetic data

Following oral dosing, fluconazole is almost completely absorbed within two hours. The high bioavailability of over 90% is not significantly reduced by concomitant intake of meals and co-medication with H2-antagonists (e.g. cimetidine, ranitidine). Concentrations measured in urine, saliva, sputum and vaginal secrete are approximately equal to the plasma concentration measured following a wide dose range from 100 to 400 mg oral as a single dose. The half-life of fluconazole is approximately 30 hours and is increased in patients with impaired renal function.

Elimination and excretion

Fluconazol is renally eliminated and primarily (80%) excreted in the urine as unchanged drug.

Carcinogenicity

Male rats treated with 5 mg and 10 mg/kg weight respectively showed a higher incidence of hepatocelluar adenomas than expected. No data exists on human carcinogenity.

Uses

  • Infections with Candida in mouth and esophagus.
  • Recurrent vaginal infections, if local therapy is not sufficient.
  • Prophylaxis of infections with Candida in tumor patients receiving chemo- or radiotherapy.
  • Treatment of deep or recurrent fungal infection of the skin (dermatomycosis), if local treatment was not successful. The efficacy of fluconazole in the treatment of onchomycosis (fungal infection of the nails) has not been demonstrated.
  • Sepsis due to emergence of Candida in the blood (candidaemia).
  • Meningitis and prophylaxis of meningitis caused by cryptococcus in AIDS-Patients. In a subgroup of patients Fluconazole acts more slowly than amphotericin B alone or in combination with flucytosine. Nonetheless, response and curation rates were not significantly different.
  • Treatment of blastomycosis, histoplasmosis, coccidioidomycosis, sporotrichosis, and aspergillosis. Sometimes amphotericin B is the preferred agent.

Read more at Wikipedia.org


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Fluconazole is more effective for treating thrush in infants - Tips from Other Journals
From American Family Physician, 4/15/03 by Richard Sadovsky

Oral candidiasis (thrush) commonly occurs in healthy infants. Nystatin oral suspension is the usual treatment, but cure rates as low as 54 percent have been confirmed in clinical studies. Fluconazole, from the imidazole class of antifungals, has been found effective in treating thrush in immunocompromised children, but studies among otherwise healthy children have not been done. Goins and associates compared fluconazole and nystatin suspensions for treatment of thrush in infants using a prospective, unblinded, randomized clinical trial.

Infants from 1 to 12 months of age with clinical signs and positive microscopic confirmation of thrush who were otherwise healthy were randomly assigned to receive either nystatin suspension (1 mL four times daily to affected mucosa for 10 days) or fluconazole suspension (3 mg per kg orally once daily for seven days). Patients with a negative initial fungal culture were not included in the study.

On day 3, at the end of therapy (day 7 for the fluconazole group or day 10 for the nystatin group), and on day 28, patients were re-examined and follow-up cultures were performed. A clinical cure was considered the absence of any oral plaque at the end of therapy. A microbiologic cure was considered a negative fungal culture also obtained at this time. Clinical recurrence was defined as oral plaques confirmed to be fungal by microscopic examination on day 28.

Six of the 21 infants (28.6 percent) receiving nystatin were clinically cured after 10 days of treatment compared with all of the 15 infants (100 percent) receiving fluconazole for seven days. Microbiologic cure occurred in one of the 18 infants in the nystatin group (5.6 percent) who were cultured at the end of therapy compared with 11 of the 15 patients in the fluconazole group (73.3 percent). Recurrence rates could not be evaluated in the nystatin group because 15 of the 21 patients who failed nystatin therapy were switched to fluconazole. There were no complications of therapy in either group.

The authors conclude that administration of oral fluconazole, resulting in a high drug concentration in the oral mucosa and saliva, is significantly more effective than conventional nystatin suspension in the treatment of oral candidiasis in otherwise healthy infants. There were no adverse events noted with fluconazole use. Problems with the use of fluconazole include cost and the possibility of developing fluconazole-resistant strains of Candida albicans. Larger studies are needed to look at the cost efficiency of fluconazole treatment of thrush in infants.

COPYRIGHT 2003 American Academy of Family Physicians
COPYRIGHT 2003 Gale Group

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