Mc. Kappersklunne et al., HEPARIN-INDUCED THROMBOCYTOPENIA AND THROMBOSIS - A PROSPECTIVE ANALYSIS OF THE INCIDENCE IN PATIENTS WITH HEART AND CEREBROVASCULAR DISEASES, British Journal of Haematology, 96(3), 1997, pp. 442-446
Heparin-induced thrombocytopenia and/or thrombosis (HITT) are serious
complications of heparin treatment. The incidence, as previously repor
ted, varies widely and, in consequence, is not precisely known. Moreov
er, most reports only concern clinically defined heparin-induced throm
bocytopenia. Therefore we carried out a prospective study of the incid
ence of serologically confirmed HITT. All patients admitted to the Dep
artments of Cardiology and Neurology of our institution with an indica
tion for treatment with therapeutic-dose intravenous unfractionated he
parin were enrolled in the study. The patients were examined daily for
the occurrence of thromboembolic complications. Regular platelet coun
ts and tests for the presence of heparin-dependent antibodies were car
ried out using two different tests: a quantitative platelet factor 4/c
ount from normal values of > 120 x 10(9)/l to < 60 x 10(9)/l or to < 1
00 x 10(9)/l if there was a rapid fall of >50% of starting value or >3
0% with concomitant acute thrombosis. The observed incidence of HITT w
as 1/358 patients (0.3%, 95% confidence limits 0.01-1.5%). However, El
isa PF4/hep specific IgG antibodies were demonstrated in nine (2.5%) a
nd IgM antibodies in seven (2.0%) of 358 patients. 30/358 patients (8.
4%) had platelet activating antibodies in the HIPAA. We conclude that
the incidence of serologically confirmed HITT in this study is very lo
w (0.3%) in patients with cardiac and neurologic diseases treated with
intravenous unfractionated heparin. The frequency of heparin-dependen
t antibodies without concomitant occurrence of thrombocytopenia is muc
h higher.