Research article

Clinical relevance of heparin-PF4 complex antibody in DVT after total joint replacement

Takafumi Torigoshi¹ , Satoru Motokawa¹ , Yumi Maeda² , Kazushige Maeda¹ , Takeshi Hiura¹ , Gou Takayama¹ , Kenji Taguchi¹ , Hiroyuki Shindo³ and Kiyoshi Migita²

¹Department of Orthopedics Surgery and Department of Rheumatology, NHO Nagasaki Medical Center, Nagasaki, Japan

²Clinical Research Center, NHO Nagasaki Medical Center, Kubara 2-1001-1, Omura, 856-8652, Japan

³Department of Orthopedics Surgery, Nagasaki University School of Medicine Sakamoto 1-7-1, Nagasaki, 852-8501, Japan

author email corresponding author email

BMC Musculoskeletal Disorders 2009, 10:42doi:10.1186/1471-2474-10-42

Published:	28 April 2009

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 post-operative 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.