2010
DOI: 10.1177/0148607109337257
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Warfarin Bioavailability With Feeding Tubes and Enteral Formula

Abstract: Feeding-tube administration compromises the total amount of warfarin reaching patients. It appears, from this in vitro study, that the mechanism of the interaction of warfarin may be a result of direct binding to the feeding tube.

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Cited by 21 publications
(12 citation statements)
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“…Fluctuations in INR due to warfarin binding to the enteral feeding or to protein supplementation were avoided by holding the enteral feeding for 1 hour prior to and after administration of warfarin 2 and liquid protein supplementation was scheduled to be administered separately from the warfarin administration time by at least 2 hours. Recent data suggest potential binding of warfarin to enteral feeding tubes 16 . However, this interaction did not likely contribute to this interaction as the patient consistently received warfarin via a feeding tube throughout the observational period.…”
Section: Discussionmentioning
confidence: 96%
“…Fluctuations in INR due to warfarin binding to the enteral feeding or to protein supplementation were avoided by holding the enteral feeding for 1 hour prior to and after administration of warfarin 2 and liquid protein supplementation was scheduled to be administered separately from the warfarin administration time by at least 2 hours. Recent data suggest potential binding of warfarin to enteral feeding tubes 16 . However, this interaction did not likely contribute to this interaction as the patient consistently received warfarin via a feeding tube throughout the observational period.…”
Section: Discussionmentioning
confidence: 96%
“…There had a great variation of Ka with a higher RSE (43.7%, 129.4%, 74.6% for PK models of warfarin, R- warfarin, and S- warfarin) meaning an incredible consequence about absorption. The bioavailability of warfarin is more than 95% ( Mark et al, 2010 ; Juno et al, 2013 ), some reports had applied 100% bioavailability when developing models ( Maria et al, 2003 ; Hamberg et al, 2007 ; Steven et al, 2011 ). Moreover, there were few reports to evaluate the absorption of warfarin due to its high bioavailability.…”
Section: Discussionmentioning
confidence: 99%
“…Structural PK model was fit to plasma concentrations, and typical values of absorption rate constant (Ka), apparent volume of distribution (V/F), and oral clearance (CL/F) were calculated (where F denotes bioavailability). In this study, each individual parameter was expressed approximately as a coefficient of variation to be a log-normal distribution with the mean of population parameters according to results of previous researches ( Maria et al, 2003 ; Eunice et al, 2010 ; Mark et al, 2010 ; Juno et al, 2013 ).…”
Section: Methodsmentioning
confidence: 99%
“…However, based on physician orders for the same product at the same rate starting 4 days prior to initiation, as well as the lack of physician orders for a long duration of NPO time during warfarin administration, as detailed in Table 2, it is possible but not likely that changing rates of enteral feeds alone caused the decrease in INR. In addition, warfarin resistance has been associated with enteral tube feedings and is thought to be due to warfarin either binding to the protein component of enteral nutrition (EN) products in a pH‐dependent manner or directly binding to feeding tubes 31 , 32 . While this interaction may have been present in this patient, it is unlikely to have caused the decrease in his INR, since the decrease occurred on the 10th day of warfarin administration after several weeks of receiving EN.…”
Section: Discussionmentioning
confidence: 99%