Guest guest Posted March 25, 2008 Report Share Posted March 25, 2008 Study: Voriconazole eye drop formulation may be effective for treating fungal keratitis OSN SuperSite - Thorofare,NJ* http://www.osnsupersite.com/view.asp?rID=27241 A formulation of voriconazole eye drops appears effective, well- tolerated and capable of reaching adequate aqueous humor levels for treating refractory fungal keratitis, according to a prospective study by researchers in Australia, published in the March issue of Archives of Ophthalmology. " This preparation is likely to have a valuable role in the therapeutic management of Candida and Aspergillus keratitis. It is substantially more affordable than oral therapy and has less potential to cause systemic adverse effects, " the authors said. Mervyn Ferdinands, MBBS(Hons), and colleagues randomly assigned 10 patients with refractory fungal keratitis to receive a 1% solution of Vfend (voriconazole, Pfizer) in one of two dosing regimens before performing routine anterior segment surgery. Specifically, the researchers administered a 1% solution of voriconazole, preserved with 0.01% benzalkonium chloride, to five patients every 6 hours for 3 days and to five patients in 4 hourly preoperative doses. During the anterior segment procedure, the surgeons used a 30-gauge needle attached to a syringe to aspirate 0.1 mL to 0.2 mL of aqueous humor through a paracentesis site before infusing irrigation solution. Aqueous humor samples were then refrigerated at 4°C, and the researchers used validated high-performance liquid chromatography to determine voriconazole levels. The mean voriconazole concentration after hourly dosing before surgery was 1.9 µg/mL. The mean voriconazole concentration after a single dosing preoperatively every 6 hours was 0.94 µg/mL. The mean sampling times after the last administration of eye drops were 1.1 hours after hourly dosing and 2.1 hours after a single dosing every 6 hours, according to the study. The surgeons administered a total of 80 eye drops, with each patient receiving between 2 mg and 6 mg, or " about 1% to 3% of the usual daily oral dose, " the authors noted. " Five participants reported no adverse reaction, three reported one instance of stinging, one reported two instances of stinging, and one reported sneezing and coughing after the initial dose, " they added. Quote Link to comment Share on other sites More sharing options...
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