Thromb Haemost 2003; 90(01): 71-76
DOI: 10.1055/s-0037-1613601
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Impact of pre-treatment INR level on the effect of intravenous low dose vitamin K in patients with excessive anticoagulation

Aharon Lubetsky
1   Department of Medicine, Anticoagulation Clinic, Division of Clinical Pharmacology, Tel Aviv University, Tel-Aviv, Israel
,
Yigal Shasha
1   Department of Medicine, Anticoagulation Clinic, Division of Clinical Pharmacology, Tel Aviv University, Tel-Aviv, Israel
,
David Olchovsky
1   Department of Medicine, Anticoagulation Clinic, Division of Clinical Pharmacology, Tel Aviv University, Tel-Aviv, Israel
,
Ronen Loebstein
1   Department of Medicine, Anticoagulation Clinic, Division of Clinical Pharmacology, Tel Aviv University, Tel-Aviv, Israel
,
Hillel Halkin
1   Department of Medicine, Anticoagulation Clinic, Division of Clinical Pharmacology, Tel Aviv University, Tel-Aviv, Israel
,
David Ezra
1   Department of Medicine, Anticoagulation Clinic, Division of Clinical Pharmacology, Tel Aviv University, Tel-Aviv, Israel
› Author Affiliations
Further Information

Publication History

Received 22 January 2003

Accepted after revision 08 April 2003

Publication Date:
07 December 2017 (online)

Summary

Administration of vitamin K is the common mode of treatment in excessively anticoagulated patients. However, patient’s response to vitamin K varies, depending on the vitamin K dose and the route of administration. Another potential source of variation is the pre-treatment INR which has not been accounted for in most previous studies. In the present study the effect of baseline INR on the response to a single dose of intravenous vitamin K (0.5 mg) was studied in 95 episodes of excessively anticoagulated patients (n = 76).

In 67 episodes of moderately excessive baseline INR (6-10) mean INR declined from 8.0 ± 1.2 to 2.6 ± 0.9 at 24 hours, 59/67 (88%) responding within the first 12 hours and not requiring a second dose. In contrast, in 28 episodes with highly excessive baseline INR (> 10) response was slower; mean INR declining from 13.6 ± 2.7 to 4.0 ± 2.1 at 24 hours. In 14/28 of these episodes, patients failed to respond to vitamin K in the first 12 hours and required a second vitamin K dose.

We conclude that INR at presentation affects the response to vitamin K and that this INR value should be considered in determining appropriate vitamin K doses.

 
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