Comparison of Clinical Outcomes: Bivalirudin With Transfemoral Access Versus Heparin With Transradial Access in Patients With ST segment Elevation Myocardial Infarction.


Journal

Critical pathways in cardiology
ISSN: 1535-2811
Titre abrégé: Crit Pathw Cardiol
Pays: United States
ID NLM: 101165286

Informations de publication

Date de publication:
09 2019
Historique:
entrez: 27 7 2019
pubmed: 28 7 2019
medline: 7 7 2020
Statut: ppublish

Résumé

The best combination of access site and anticoagulant used during primary percutaneous coronary intervention (PCI) in patients presenting with ST segment elevation myocardial infarction is not known. We conducted a retrospective cohort study of all patients >18 years of age who underwent primary PCI in 2 large regional ST segment elevation myocardial infarction centers in Massachusetts between 2012 and 2014. The cohort was divided into 3 groups: bival/fem, hep/rad, or off-protocol, based on anticoagulation and access used. We used multiple logistic regression model to compare major cardiovascular events-major adverse cardiovascular events (MACE) and bleeding complications between the 2 on-protocol groups (bival/fem and hep/rad). Of the 1074 patients in this study, there were 443 (41%), 501 (47%), and 130 (12%) patients in bival/fem, hep/rad, and off-protocol groups, respectively. There were significantly higher number of cardiogenic shock patients in the bival/fem compared to the hep/rad group (6.5% vs. 3.0%, P < 0.001). There was a trend toward reduced MACE in the hep/rad group compared to bival/fem (2.8 % vs. 5.1%, P = 0.068). When cardiogenic shock patients are excluded, there is no significant difference in mortality rates (bival/fem: 2.7% vs. hep/rad: 1.0%, P = 0.07) or bleeding complications between the groups (hep/rad: 4.5% vs. bival/fem: 2.1%, P = 0.06). In patients undergoing primary PCI, there was a trend toward reduced inpatient MACE with the use of heparin and radial access compared with bivalirudin with femoral access. In patients without cardiogenic shock, there is no significant difference in mortality or bleeding rates between the 2 groups.

Identifiants

pubmed: 31348072
doi: 10.1097/HPC.0000000000000182
pii: 00132577-201909000-00004
doi:

Substances chimiques

Antithrombins 0
Fibrinolytic Agents 0
Hirudins 0
Peptide Fragments 0
Recombinant Proteins 0
Heparin 9005-49-6
bivalirudin TN9BEX005G

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

130-134

Auteurs

Jaya Mallidi (J)

From the Division of Cardiology, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

John Ulahannan (J)

From the Division of Cardiology, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

Vinod K Chaubey (VK)

From the Division of Cardiology, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

Auras R Atreya (AR)

From the Division of Cardiology, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

Muhammad T Shakoor (MT)

From the Division of Cardiology, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

Daniel Fisher (D)

Division of Cardiology, Department of Internal Medicine, University of Massachusetts Memorial Medical Center, University of Massachusetts Medical School, Worcester, MA.

Jane Garb (J)

Division of Biostatistics, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

Amir Lotfi (A)

From the Division of Cardiology, Department of Internal Medicine, Baystate Medical Center, Springfield, MA.

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Classifications MeSH