Abstract
Background: IV lipid emulsions contain vitamin K in substantial quantities and in 1989, we therefore stopped supplying vitamin K1 to patients receiving home parenteral nutrition (HPN). Methods: Nine patients (group I) receiving HPN before 1989 (10 mg IV vitamin K1 supplementation weekly until 1989, which was discontinued thereafter) and six patients with an initial low plasma vitamin K1 concentration (related to their malabsorption) (group II) receiving HPN after 1989 were studied. Pro-thrombin time (PT), plasma vitamin K1 concentration, and vitamin K 1 content in lipid emulsions were measured throughout the period of HPN. Results: All lipid emulsions, except for Eurolip 20% and Clinoleic 20% (Baxter SA, Maurepas, France) contained vitamin K1, with concentration ranges from 179 ± 39 to 353 ± 78 ng/L. Group I patients had an initial high plasma vitamin K1 concentration due to the vitamin K1 supplementation. After this supplementation was discontinued, plasma vitamin K1 decreased and remained in normal ranges with a normal PT. Throughout the HPN period after 1989, patients received 255 ± 104 μg of vitamin K1 weekly through lipid emulsions. The PT and plasma vitamin K 1 concentrations in group II patients were restored by lipid emulsions, which contained 418 ± 143 μg/wk of vitamin K1. Conclusions: In patients receiving IV lipids (except for Eurolip and Clinoleic), a normal vitamin K1 status can be maintained during long-term HPN without vitamin K1 supplementation. However, vitamin K supplementation cannot be abandoned until the vitamin K content of emulsions is standardized by manufacturers. A weekly supply of 250 to 400 μg of vitamin K1 is enough to maintain and even restore a normal vitamin K1 status in HPN. (Journal of Parenteral and Enteral Nutrition
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