Abstract | INTRODUCTION: MATERIALS/METHODS: 187 patients started on pDTI for presumed HIT were assessed in two time periods before (period 1, n=88 patients) and after the introduction of an IgG-specific assay (period 2, n=99 patients). RESULTS: Patients in period 2 were treated with pDTI therapy for a median of 5 days less (p<0.0001) however the incidence of Grade III and IV bleeding episodes was not different. Bleeding was observed to occur early during the hospital course at a median of 2-3 days after initiation of the pDTI. The average pDTI drug acquisition cost was markedly decreased in period 2 when compared to period 1 (p<0.0001). CONCLUSIONS: Implementation of the IgG class HIT EIA resulted in a decrease in the number of days on a pDTI and a decrease in the average pDTI acquisition cost per patient without an observed change in serious bleeding events.
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Authors | John L Reagan, Randall R Ingham 2nd, Samir Dalia, James N Butera, Joseph D Sweeney |
Journal | Thrombosis research
(Thromb Res)
Vol. 134
Issue 1
Pg. 90-2
(Jul 2014)
ISSN: 1879-2472 [Electronic] United States |
PMID | 24830900
(Publication Type: Journal Article)
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Copyright | Copyright © 2014 Elsevier Ltd. All rights reserved. |
Chemical References |
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Topics |
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Cohort Studies
- Female
- Heparin
(adverse effects)
- Humans
- Immunoglobulin G
(analysis)
- Male
- Middle Aged
- Retrospective Studies
- Thrombocytopenia
(chemically induced, diagnosis)
- Young Adult
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