Key result
Oral intravenous phytonadione matches tablets for achieving 24-hour INR reversal.
Why the study?
The intravenous formulation of phytonadione given orally has not been directly evaluated compared to commercially available phytonadione tablets for warfarin-related coagulopathy reversal.
Observational (n=200)
May support oral IV phytonadione solution as tablet alternative when needed; leaves open confirmation in prospective trials.
Introduction The cost of phytonadione tablets has increased markedly and is significantly higher than the intravenous formulation. The intravenous formulation given orally is a potential alternative but has not been directly evaluated in comparison to the commercially available tablet. The objective of this study was to evaluate the efficacy of phytonadione intravenous solution given orally compared to commercially available phytonadione tablets for reversal of coagulopathy related to warfarin.Methods We conducted a retrospective, observational study of adult patients who received phytonadione tablets and the IV formulation orally for warfarin-related coagulopathy. The international normalized ratio (INR) was measured before and after phytonadione administration. The primary outcome was INR <1.5 at 24 h after phytonadione administration.Results From January 1, 2015 to August 1, 2018 a total of 200 patients were identified. In total, 58% (n = 116) patients received IV phytonadione solution given orally and 42% (n = 84) patients received the tablets. The primary outcome of INR <1.5 at 24 h was not significantly different between groups (p = 0.321).Discussion The IV phytonadione solution given by mouth and the tablet formulation performed similarly.
No takes yet. Share an insight, caveat, or question.
Rice et al. (2021) conducted an observational in Warfarin-related coagulopathy (n=200). Intravenous phytonadione solution given orally vs. Phytonadione tablets was evaluated on INR <1.5 at 24 h after phytonadione administration (p=0.321). Intravenous phytonadione solution given orally performed similarly to the tablet formulation for achieving an INR <1.5 at 24 hours (p = 0.321).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: