Key result
Full-dose UFH, prolonged exposure, and comorbidities are linked to increased HIT risk in inpatients.
Observational (n=25,653)
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Heparin-induced thrombocytopenia (HIT) is an unpredictable reaction to heparin characterized by thrombocytopenia and increased risk of life-threatening venous and/or arterial thrombosis. Data are lacking regarding additional risk factors that may be associated with the development of HIT. This study aimed to identify the risk factors that may be associated with HIT in medical inpatients receiving heparin. Twenty five thousand six hundred and fifty-three patients admitted to the medicine service who received heparin product were reviewed retrospectively. The diagnosis of HIT was confirmed if the platelet count dropped >50% from baseline and there was a positive laboratory HIT assay. Fifty-five cases of in-hospital HIT were observed. Multivariate analysis identified the administration of full anticoagulation dose with unfractionated heparin or exposure to heparin products for more than 5 d with an increased risk of HIT. Moreover, patients who were on haemodialysis, carried a diagnosis of autoimmune disease, gout or heart failure were also at increased risk. The results suggest that when using heparin products in these patient cohorts, increased surveillance for HIT is necessary.
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Kato et al. (2011) conducted an observational in Heparin-induced thrombocytopenia (HIT) (n=25,653). Heparin products (including full-dose unfractionated heparin or exposure >5 days) and clinical risk factors (haemodialysis, autoimmune disease, gout, heart failure) vs. Medical inpatients receiving heparin without these risk factors was evaluated on In-hospital heparin-induced thrombocytopenia (platelet count drop >50% from baseline and positive laboratory HIT assay). Full-dose unfractionated heparin, heparin exposure >5 days, haemodialysis, autoimmune disease, gout, and heart failure were associated with increased HIT risk (55 cases among 25,653 inpatients).
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