Subcutaneous Heparin Compared with Continuous Intravenous Heparin Administration in the Initial Treatment of Deep Vein Thrombosis

A Meta-analysis

Abstract

Objective: To quantitatively assess the efficacy and safety of published randomized trials comparing subcutaneous heparin with continuous intravenous heparin for the initial treatment of deep vein thrombosis.

Data Identification: Studies published between January 1966 and April 1991 were identified through computer searches of the MEDLINE database and through reviews of the Science Citation Index, Current Contents, proceedings and abstract books, and references cited in the identified articles. Complete manuscripts were obtained from the authors if only abstracts were available.

Study Selection: Eight clinical trials were identified that compared subcutaneous with intravenous heparin administration in patients with venographically confirmed deep vein thrombosis.

Data Extraction: Each study was independently analyzed for the percentage distribution of thrombosis, the method of outcome measurement, and the heparin dose. The methodologic strength of each study was assessed using predefined standards for the proper evaluation of a therapeutic intervention with particular emphasis on the type of patient allocation and objective measurements.

Results of Data Analysis: The overall relative risk for efficacy (defined as prevention of extension and recurrence of venous thromboembolism) of subcutaneous compared with intravenous heparin treatment was 0.62 (95% Cl, 0.39 to 0.98), whereas for safety (defined as major hemorrhage) it was 0.79 (Cl, 0.42 to 1.48).

Conclusions: The results of our meta-analysis indicated that heparin administered subcutaneously twice daily in the initial treatment of deep vein thrombosis is more effective and at least as safe as continuous intravenous heparin administration. Administration of heparin subcutaneously may simplify patient treatment and could facilitate home treatment.

Article and Author Information

  • From the Academic Medical Center, Amsterdam, The Netherlands; and the Instituto di Semeiotica Medica, Perugia, Italy. For current author addresses, see end of text.

  • Grant Support: By the Educational Erasmus Program (ICP 89-NL-0101) and a Fellowship from the Royal Netherlands Academy of Arts and Sciences to Dr. Büller.

  • Requests for Reprints: Daan W. Hommes, MD, Academic Medical Center, F4-139, Meibergdreef 9, 1105 AZ, Amsterdam (ZO), The Netherlands.

  • Current Author Addresses: Drs. Hommes, Büller, and ten Cate: Center for Haemostasis, Thrombosis, Atherosclerosis and Inflammation Research, Academic Medical Center, F4-139, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

    Ms. Bura and Ms. Mazzolai: University Center of Thrombosis and Haemostasis, Istituto di Semeiotica Medica, 06100 Perugia, Italy.

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