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Real-World Experience with Cangrelor as Adjuvant to Percutaneous Coronary Intervention: A Single-Centre Observational Study.

Authors :
Thim T
Jakobsen L
Jensen RV
Støttrup N
Eftekhari A
Grove EL
Larsen SB
Sørensen JT
Carstensen S
Amiri S
Veien KT
Christiansen EH
Terkelsen CJ
Maeng M
Kristensen SD
Source :
Cardiology research and practice [Cardiol Res Pract] 2023 Jun 16; Vol. 2023, pp. 3197512. Date of Electronic Publication: 2023 Jun 16 (Print Publication: 2023).
Publication Year :
2023

Abstract

Background: Reversible P2Y12 inhibition can be obtained with cangrelor administered intravenously. More experience with cangrelor use in acute PCI with unknown bleeding risk is needed.<br />Objectives: To describe real-world use of cangrelor including patient and procedure characteristics and patient outcomes.<br />Methods: We performed a single-centre, retrospective, and observational study including all patients treated with cangrelor in relation to percutaneous coronary intervention at Aarhus University Hospital during the years 2016, 2017, and 2018. We recorded procedure indication and priority, the indications for cangrelor use, and patient outcomes within the first 48 hours after initiation of cangrelor treatment.<br />Results: We treated 991 patients with cangrelor in the study period. Of these, 869 (87.7%) had an acute procedure priority. Among acute procedures, patients were mainly treated for STEMI ( n  = 723) and the remaining were treated for cardiac arrest and acute heart failure. Use of oral P2Y12 inhibitors prior to percutaneous coronary intervention was rare. Fatal bleeding events ( n  = 6) were only observed among patients undergoing acute procedures. Stent thrombosis was observed in two patients receiving acute treatment for STEMI. Thus, cangrelor can be used in relation to PCI under acute circumstances with advantages in terms of clinical management. The benefits and risks, in terms of patient outcomes, should ideally be assessed in randomized trials.<br />Competing Interests: Steen Dalby Kristensen has received fees from Idorsia for National Coordinator work. Erik Lerkevang Grove has received speaker honoraria or consultancy fees from Alexion Pharma, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Pfizer, MSD, MundiPharma, Portola Pharmaceuticals, and Lundbeck Pharma. He is an investigator in studies sponsored by AstraZeneca and has received unrestricted research grants from Boehringer Ingelheim. All other authors declare that they have no conflicts of interest.<br /> (Copyright © 2023 Troels Thim et al.)

Details

Language :
English
ISSN :
2090-8016
Volume :
2023
Database :
MEDLINE
Journal :
Cardiology research and practice
Publication Type :
Academic Journal
Accession number :
37361000
Full Text :
https://doi.org/10.1155/2023/3197512