Abstract
Nonselective inhibition of cyclooxygenase (COX) by nonsteroidal anti-inflammatory drugs frequently induces renal failure in decompensated cirrhosis. Studies in experimental cirrhosis suggest that selective inhibitors of the inducible isoform COX-2 do not adversely affect renal function. However, very limited information is available on the effects of these compounds on renal function in human cirrhosis. This investigation consists of a double-blind, randomized, placebo-controlled trial aimed at comparing the effects of the selective COX-2 inhibitor celecoxib (200 mg every 12 hours for a total of 5 doses) on platelet and renal function and the renal response to furosemide (40 mg intravenously) with those of naproxen (500 mg every 12 hours for a total of 5 doses) and placebo in 28 patients with cirrhosis and ascites. A significant reduction (P < .05). In conclusion, our results indicate that short-term administration of celecoxib does not impair platelet and renal function and the response to diuretics in decompensated cirrhosis. Further studies are needed to evaluate the long-term safety of this drug in cirrhosis. Copyright © 2005 by the American Association for the Study of Liver Diseases.
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CITATION STYLE
Clària, J., Kent, J. D., López-Parra, M., Escolar, G., Ruiz-del-Arbol, L., Ginès, P., … Arroyo, V. (2005). Effects of celecoxib and naproxen on renal function in nonazotemic patients with cirrhosis and ascites. Hepatology, 41(3), 579–587. https://doi.org/10.1002/hep.20595
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