This article is only available in the PDF format. Download the PDF to view the article, as well as its associated figures and tables.
To the Editor.
—Orcolon is a high-molecular-weight viscoelastic agent (purified polyacrylamide polymer) manufactured by Optical Radiation Corp (Azusa, Calif) for use in intraocular procedures. Two multicenter clinical trials in patients undergoing cataract surgery performed as part of the Food and Drug Administration approval process failed to detect any pattern of intraocular toxic effects. Nonetheless, we recently evaluated two patients who suffered postoperative complications that we believe may be secondary to the use of this substance.
Report of Cases.
—On April 22, 1991, a total of 12 patients underwent uneventful cataract surgery performed by the same surgeon (H.J.S.) at the same surgical facility. All patients underwent the same preoperative, intraoperative, and postoperative regimen. Intraoperative medications used consisted of balanced salt solution (Alcon) with 0.5 mL of epinephrine, 50 mg/mL vancomycin hydrochloride, and 40 mg/mL gentamicin sulfate, 0.01% carbachol (Miostat), and Orcolon in the anterior chamber; balanced salt solution (Alcon), tobramycin
Siegel MJ, Spiro HJ, Miller JA, Siegel LI. Secondary Glaucoma and Uveitis Associated With Orcolon. Arch Ophthalmol. 1991;109(11):1496-1497. doi:10.1001/archopht.1991.01080110030018