Literature DB >> 15519009

Economic evaluation of bivalirudin with provisional glycoprotein IIB/IIIA inhibition versus heparin with routine glycoprotein IIB/IIIA inhibition for percutaneous coronary intervention: results from the REPLACE-2 trial.

David J Cohen1, A Michael Lincoff, Tara A Lavelle, Huei-Ling Chen, Ameet Bakhai, Ronna H Berezin, Daniel Jackman, Ian J Sarembock, Eric J Topol.   

Abstract

OBJECTIVES: The purpose of this study was to compare the cost of percutaneous coronary intervention (PCI) using bivalirudin with provisional platelet glycoprotein (GP) IIb/IIIa inhibition with that of heparin + routine GP IIb/IIIa inhibition.
BACKGROUND: Although GP IIb/IIIa inhibition has been shown to reduce ischemic complications in a broad range of patients undergoing PCI, many patients currently do not receive such therapy because of concerns about bleeding complications or cost. Recently, bivalirudin with provisional GP IIb/IIIa inhibition has been validated as an alternative to heparin + routine GP IIb/IIIa inhibition for patients undergoing PCI. However, the cost-effectiveness of this novel strategy is unknown.
METHODS: In the Randomized Evaluation in PCI Linking Angiomax to Reduced Clinical Events (REPLACE)-2 trial, 4,651 U.S. patients undergoing non-emergent PCI were randomized to receive bivalirudin with provisional GP IIb/IIIa (n = 2,319) versus heparin + routine GP IIb/IIIa (n = 2,332). Resource utilization data were collected prospectively through 30-day follow-up on all U.S. patients. Medical care costs were estimated using standard methods including bottom-up accounting (for procedural costs), the Medicare fee schedule (for physician services), hospital billing data (for 2,821 of 4,862 admissions), and regression-based approaches for the remaining hospitalizations.
RESULTS: Among the bivalirudin group, 7.7% required provisional GP IIb/IIIa. Thirty-day ischemic outcomes including death or myocardial infarction were similar for the bivalirudin and GP IIb/IIIa groups, but bivalirudin resulted in lower rates of major bleeding (2.8% vs. 4.5%, p = 0.002) and minor bleeding (15.1% vs. 28.1%, p < 0.001). Compared with routine GP IIb/IIIa, in-hospital and 30-day costs were reduced by $405 (95% confidence interval [CI] $37 to $773) and $374 (95% CI $61 to $688) per patient with bivalirudin (p < 0.001 for both). Regression modeling demonstrated that, in addition to the costs of the anticoagulants themselves, hospital savings were due primarily to reductions in major bleeding (cost savings = $107/patient), minor bleeding ($52/patient), and thrombocytopenia ($47/patient).
CONCLUSIONS: Compared with heparin + routine GP IIb/IIIa inhibition, bivalirudin + provisional GP IIb/IIIa inhibition resulted in similar acute ischemic events and cost savings of $375 to $400/patient depending on the analytic perspective.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15519009     DOI: 10.1016/j.jacc.2004.05.085

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  25 in total

Review 1.  Cost effectiveness of anticoagulation in acute coronary syndromes.

Authors:  Jaime Latour-Pérez; Eva de-Miguel-Balsa
Journal:  Pharmacoeconomics       Date:  2012-04       Impact factor: 4.981

Review 2.  Direct thrombin inhibitors in cardiovascular disease.

Authors:  Kyle A Arsenault; Jack Hirsh; Richard P Whitlock; John W Eikelboom
Journal:  Nat Rev Cardiol       Date:  2012-05-01       Impact factor: 32.419

3.  Adjunct bivalirudin dosing protocol for neuro-endovascular procedures.

Authors:  Alexandros L Georgiadis; Qaisar Shah; M Fareed K Suri; Adnan I Qureshi
Journal:  J Vasc Interv Neurol       Date:  2008-04

4.  Safety and tolerability of high-intensity anticoagulation with bivalirudin during neuroendovascular procedures.

Authors:  Ameer E Hassan; Muhammad Zeeshan Memon; Alexandros L Georgiadis; Gabriela Vazquez; M Fareed K Suri; Adnan I Qureshi
Journal:  Neurocrit Care       Date:  2011-08       Impact factor: 3.210

5.  The comparative efficacy of bivalirudin is markedly attenuated by use of radial access: insights from Blue Cross Blue Shield of Michigan Cardiovascular Consortium.

Authors:  Emily Perdoncin; Milan Seth; Simon Dixon; Louis Cannon; Akshay Khandelwal; Arthur Riba; Shukri David; David Wohns; Hitinder Gurm
Journal:  Eur Heart J       Date:  2015-09-15       Impact factor: 29.983

Review 6.  Bivalirudin: a review of its use in patients undergoing percutaneous coronary intervention.

Authors:  Marit D Moen; Gillian M Keating; Keri Wellington
Journal:  Drugs       Date:  2005       Impact factor: 9.546

Review 7.  Antiplatelet therapy in patients undergoing percutaneous coronary intervention: economic considerations.

Authors:  William S Weintraub; Leonid Mandel; Sandra A Weiss
Journal:  Pharmacoeconomics       Date:  2013-11       Impact factor: 4.981

Review 8.  Current periprocedural anticoagulation in transcatheter aortic valve replacement: could bivalirudin be an option? Rationale and design of the BRAVO 2/3 studies.

Authors:  Ziad Sergie; Thierry Lefèvre; Eric Van Belle; Socrates Kakoulides; Usman Baber; Efthymios N Deliargyris; Roxana Mehran; Eberhard Grube; Jochen Reinöhl; George D Dangas
Journal:  J Thromb Thrombolysis       Date:  2013-05       Impact factor: 2.300

Review 9.  A systematic review of the quality of economic models comparing thrombosis inhibitors in patients with acute coronary syndrome undergoing percutaneous coronary intervention.

Authors:  Maximilian H M Hatz; Reiner Leidl; Nichola A Yates; Björn Stollenwerk
Journal:  Pharmacoeconomics       Date:  2014-04       Impact factor: 4.981

10.  The Role of Glycoprotein IIb/IIIa Inhibitors- A Promise Not Kept?

Authors:  Edo Kaluski
Journal:  Curr Cardiol Rev       Date:  2008-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.