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      Cost-Consequence Analysis of Using Cangrelor in High Angiographic Risk Percutaneous Coronary Intervention Patients: A US Hospital Perspective

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          Abstract

          Objectives

          The objective of this study was to evaluate a US hospital’s cost implications and outcomes of cangrelor use in percutaneous coronary intervention (PCI) patients with two or more angiographic high-risk features (HRFs), including avoidance of oral P2Y 12 inhibitor pretreatment in patients requiring cardiac surgery. Intravenous cangrelor provides direct, immediate onset and rapid-offset P2Y 12 inhibition, which may reduce the necessity for oral P2Y 12 pretreatment.

          Methods

          A decision analytic model was developed, estimating the annual impact over 3 years of cangrelor availability. Ischemic and bleeding events (48 h) from randomized clinical trial data were extrapolated to 30 days. Event costs were from the CHAMPION PHOENIX Economics substudy. Rates of coronary artery disease (CAD) presentation, PCI, oral P2Y 12 pretreatment, and inpatient hospitalization costs were from published literature and clinical experts. Scenario analyses evaluated the impact of cangrelor availability on potential reduced P2Y 12 pretreatment rates by 50–100%. Drug costs were 2019 wholesale acquisition costs and, where necessary, all costs were adjusted to 2019 dollars.

          Results

          In a hospital treating 1000 CAD PCI inpatients annually, increasing cangrelor use from 11 to 32% resulted in a reduction in 48-h ischemic events/year by 5.7%, while bleeding events increased by 2.9%. Total costs of $1,135,472 declined 12.8%, with a 50% reduction in P2Y 12 pretreatment or 30% with no pretreatment. Savings were driven by a decrease in ischemic events, decrease in glycoprotein IIb/IIIa inhibitor use, and less need for and shorter oral P2Y 12 inhibitor washout period for surgery patients.

          Conclusion

          Use of cangrelor in patients with two or more angiographic HRFs may improve outcomes and lower hospital budgets, mainly from avoiding surgery delays necessitated by oral P2Y 12 inhibitor pretreatment.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s40256-021-00491-9.

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          Most cited references27

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          2017 ESC Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation

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            2018 ESC/EACTS Guidelines on myocardial revascularization

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              OUP accepted manuscript

              (2020)
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                Author and article information

                Contributors
                Ivar.Jensen@precisionvh.com
                Journal
                Am J Cardiovasc Drugs
                Am J Cardiovasc Drugs
                American Journal of Cardiovascular Drugs
                Springer International Publishing (Cham )
                1175-3277
                1179-187X
                31 July 2021
                31 July 2021
                2022
                : 22
                : 1
                : 93-104
                Affiliations
                [1 ]Precision Health Economics, 133 Federal Street, 10th floor, Boston, MA 02110 USA
                [2 ]GRID grid.266859.6, ISNI 0000 0000 8598 2218, University of North Carolina at Charlotte, College of Health and Human Services, ; Charlotte, NC USA
                [3 ]GRID grid.470366.0, ISNI 0000 0004 0408 8724, Chiesi, Inc., ; Cary, NC USA
                [4 ]Elysis, Carlisle, MA USA
                [5 ]Department of Medicine, Stanford Center for Clinical Research, Stanford, CA USA
                [6 ]GRID grid.239395.7, ISNI 0000 0000 9011 8547, Division of Cardiology, , Beth Israel Deaconess Medical Center, ; Boston, MA USA
                [7 ]Université de Paris, Assistance Publique-Hôpitaux de Paris, Hôpital Bichat, INSERM U-1148, Paris, France
                [8 ]GRID grid.59734.3c, ISNI 0000 0001 0670 2351, The Zena and Michael A. Wiener Cardiovascular Institute, , Icahn School of Medicine at Mount Sinai, and the Cardiovascular Research Foundation, ; New York, NY USA
                [9 ]GRID grid.62560.37, ISNI 0000 0004 0378 8294, Brigham and Women’s Hospital Heart and Vascular Center, and Harvard Medical School, ; Boston, MA USA
                Author information
                http://orcid.org/0000-0002-0524-2709
                Article
                491
                10.1007/s40256-021-00491-9
                8748330
                34331235
                19753ae7-5444-4846-8e88-2444f97e2cf4
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 7 July 2021
                Funding
                Funded by: The manuscript was funded by Chiesi, Inc
                Categories
                Original Research Article
                Custom metadata
                © Springer Nature Switzerland AG 2022

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