Many venous access devices (VADs) are routinely flushed with small doses of heparinized saline (2 to 3 cc, 100 units/cc). In larger intravenous doses, heparin causes immune-mediated thrombocytopenia in 1 to 3 percent of patients and leads to heparin-related antibodies in approximately 5 to 50 percent of patients. The risk of heparin-induced thrombocytopenia from daily VAS flushed, as reflected in the appearance of heparin-related antibodies, is not known. The purpose of this study is to estimate this risk by testing for heparin-induced antibodies in serum samples. Presence of heparin-induced antibodies will be evaluated in 120 subjects before VAD insertion and approximately 4 and 8 weeks later. The protocol was amended to include catheters in place for less than 24 hours. Summary of Findings: In 49 subjects who received daily heparin flushes, none devel-oped heparin-induced thrombocytopenia. However, mild heparin sensitization occurred in approximately one-third of subjects, with one additional subject developing more sig-nificant sensitization. The findings of this study are in press in the journal Supportive Care in Cancer.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL001128-03
Application #
6289430
Study Section
Nursing Research Study Section (NURS)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code