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ARTICLE

The Weight-based Heparin Dosing Nomogram Compared with a "Standard Care" Nomogram

A Randomized Controlled Trial

right arrow Robert A. Raschke; Brendan M. Reilly; James R. Guidry; Joseph R. Fontana; and Sandhya Srinivas

1 November 1993 | Volume 119 Issue 9 | Pages 874-881

Objective: To determine whether an intravenous heparin dosing nomogram based on body weight achieves therapeutic anticoagulation more rapidly than a "standard care" nomogram.

Design: Randomized controlled trial.

Setting: Two community teaching hospitals in Phoenix, Arizona, and Rochester, New York.

Participants: One hundred fifteen patients requiring intravenous heparin treatment for venous or arterial thromboembolism or for unstable angina.

Intervention: Patients were randomized to the weight-based nomogram (starting dose, 80 units/kg body weight bolus, 18 units/kg per hour infusion) or the standard care nomogram (starting dose, 5000-unit bolus, 1000 units per hour infusion). Activated partial thromboplastin time (APT) values were monitored every 6 hours, and heparin dose adjustments were determined by the nomograms.

Measurements: Activated partial thromboplastin times were measured using a widely generalizable laboratory method. The primary outcomes were the time to exceed the therapeutic threshold (APT > 1.5 times the control) and the time to achieve therapeutic range (APT, 1.5 to 2.3 times the control). Bleeding complications and recurrent thromboembolism were also compared.

Results: Kaplan-Meier curves for the primary outcomes favored the weight-based nomogram (P < 0.001 for both). In the weight-based heparin group, 60 of 62 patients (97%) exceeded the therapeutic threshold within 24 hours, compared with 37 of 48 (77%) in the standard care group (P < 0.002). Only one major bleeding complication occurred (in a standard care patient). Recurrent thromboembolism was more frequent in the standard care group; relative risk, 5.0 (95% CI, 1.1 to 21.9).

Conclusions: The weight-based heparin nomogram is widely generalizable and has proved to be effective, safe, and superior to one based on standard practice.

Author and Article Information
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From Good Samaritan Regional Medical Center, Phoenix, Arizona; the University of Rochester School of Medicine, Rochester, New York; St. Mary's Hospital, Rochester, New York.
Requests for Reprints: Robert A. Raschke, MD, Department of Medicine, Good Samaritan Regional Medical Center, 1111 E. McDowell Road, Phoenix, AZ 85006.
Acknowledgments: The authors thank Drs. Alvin Mushlin, Barbara Weber, and Michael Wagner for their review of the manuscript and Dr. Philip C. Comp and Toppy Nelson for performing anti-factor Xa assays.
Grant Support: By The Palms Clinic, Phoenix, Arizona.


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