Literature DB >> 19729904

Etanercept clearance during an in vitro model of continuous venovenous hemofiltration.

Geoffrey M Fleming1, Noha N Salama, Saada K Eid, Kenneth R Cooke, Bruce A Mueller.   

Abstract

BACKGROUND/AIMS: Etanercept is a tumor necrosis factor-alpha antagonist used in inflammation-mediated conditions. Continuous venovenous hemofiltration (CVVH) has also been used in patients with inflammatory conditions. This study evaluated etanercept clearance using an in vitro CVVH model.
METHODS: Etanercept clearance was assessed in vitro in bovine blood at 1-3 mg/l final serum concentration, and urea control at 750 mg/l. CVVH was performed using polyacrylonitrile, polysulfone, and polymethylmethacrylate filters at 3 l/h ultrafiltrate and 200 ml/min blood flow rates. Transmembrane clearance was estimated using sieving coefficient calculations, and adsorptive removal rate was approximated using a mass balance calculation.
RESULTS: Urea sieving coefficient remained constant (1.04 +/- 0.01). Ultrafiltrate etanercept concentrations were undetectable (sieving coefficient < 0.02) and transmembrane and adsorptive clearances were negligible.
CONCLUSION: Etanercept is not cleared appreciably by transmembrane or adsorptive mechanisms in CVVH using polyacrylonitrile, polysulfone, or polymethylmethacrylate hemofilters. Copyright 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19729904      PMCID: PMC2914439          DOI: 10.1159/000232936

Source DB:  PubMed          Journal:  Blood Purif        ISSN: 0253-5068            Impact factor:   2.614


  25 in total

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4.  Trace element removal during in vitro and in vivo continuous haemodialysis.

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7.  Daptomycin clearance during modeled continuous renal replacement therapy.

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Review 8.  Importance of increased ultrafiltration volume and impact on mortality: sepsis and cytokine story and the role of continuous veno-venous haemofiltration.

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Review 9.  New concepts in anti-tumor necrosis factor therapy for inflammatory bowel disease.

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Review 10.  Pharmacokinetics and antimicrobial dosing adjustment in critically ill patients during continuous renal replacement therapy.

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