학술논문

Clinical relevance of heparin-PF4 complex antibody in DVT after total joint replacement.
Document Type
Article
Source
BMC Musculoskeletal Disorders. 2009, Vol. 10, Special section p1-7. 7p. 4 Charts, 3 Graphs.
Subject
*VEIN diseases
*THROMBOSIS
*HEPARIN
*THERAPEUTIC use of immunoglobulins
*MUSCULOSKELETAL system diseases
Language
ISSN
1471-2474
Abstract
Background: Antibodies to the heparin-platelet factor-4 (HPF-4) complex (HIT antibodies) have been observed in patients with heparin-induced thrombocytopenia (HIT). These antibodies are thought to be involved in thrombosis through activation of platelet/endothelial cells. This prospective study was conducted to determine the incidence of post-operative HIT antibodies to assess the associated risk of deep vein thrombosis (DVT) in patients undergoing total knee arthroplasty (TKA) or total hip arthroplasty (THA). Methods: We studied 104 patients who underwent unilateral primary TKA (n = 44) and primary THA (n = 60) with short-duration prophylaxis (1-2 days of a fixed dose of unfractionated heparin). HIT antibodies were assayed using a sandwich-type ELISA before the operation and after heparin treatment (post-operative day 7). Results: In the clinical outcome, the incidence of symptomatic DVT was 15.4% (16/104, TKA; 10, THA 6) and pulmonary embolism (PE) was not observed. The total seroconversion rate of HIT antibodies at post-operative day 7 was 34.6% (36/104). Among 36 seroconverted patients, 11 (30.6%) developed symptomatic DVT and 5 out of 68 of the non-seroconverted patients (7.4%) developed symptomatic DVT. The incidence for DVT was significantly higher in the seroconverted patients compared with that of the non-seroconverted patients (odds ratio 5.5, 95%CI: 1.7-17.6 p = 0.0028). Furthermore, in the patients with symptomatic DVT, the titer of HIT antibodies at postoperative day 7 was significantly higher compared with those without symptomatic DVT. Conclusion: Our data therefore suggest that seroconversion for HIT antibodies generated by heparin is associated with a risk of DVT in patients undergoing total joint replacement. [ABSTRACT FROM AUTHOR]