Clinical trials and observations: Reducing the hospital burden of heparin-induced thrombocytopenia: Impact of an avoid-heparin program

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Abstract

Heparin-induced thrombocytopenia (HIT) is an adverse drug reaction occurring in up to 5% of patients exposed to unfractionated heparin (UFH). We examined the impact of a hospital-wide strategy for avoiding heparin on the incidence of HIT, HIT with thrombosis (HITT), and HIT-related costs. The Avoid-Heparin Initiative, implemented at a tertiary care hospital in Toronto, Ontario, Canada, since 2006, involved replacing UFH with lowmolecularweight heparin (LMWH) for prophylactic and therapeutic indications. Consecutive cases with suspected HIT from 2003 through 2012 were reviewed. Rates of suspected HIT, adjudicated HIT, and HITT, along with HIT-related expenditures were compared in the pre-intervention (2003-2005) and the avoid-heparin (2007-2012) phases. The annual rate of suspected HIT decreased 42%, from 85.5 per 10 000 admissions in the pre-intervention phase to 49.0 per 10 000 admissions in the avoidheparin phase (P

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McGowan, K. E., Makari, J., Diamantouros, A., Bucci, C., Rempel, P., Selby, R., & Geerts, W. (2016). Clinical trials and observations: Reducing the hospital burden of heparin-induced thrombocytopenia: Impact of an avoid-heparin program. Blood, 127(16), 1954–1959. https://doi.org/10.1182/blood-2015-07-660001

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