Remove 2024 Remove Circulation Remove Pharmacology
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Correction to: Pharmacological Management of Cardiac Arrhythmias in the Fetal and Neonatal Periods: A Scientific Statement From the American Heart Association

Circulation

Circulation, Volume 149, Issue 12 , Page e996-e996, March 19, 2024.

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Abstract 4146046: A Chemical Language Model for the Design of De Novo Molecules Targeting the Inhibition of TLR3

Circulation

Circulation, Volume 150, Issue Suppl_1 , Page A4146046-A4146046, November 12, 2024. However, there are currently no pharmacological treatments for CAVD, and the discovery of de novo molecules targeting a specific protein is a time-intensive and financially demanding process.

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Bivalirudin in Extracorporeal Membrane Oxygenation

Journal of Cardiovascular Pharmacology

Heparin, the most utilized anticoagulant, carries concerns for heparin-induced thrombocytopenia and possible resistance given its dependence on co-factors and circulating proteins to exert its pharmacologic effect. Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

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Abstract 4137905: The association between prehospital epinephrine administration and short-term outcomes in patients with shockable out-of-hospital cardiac arrest and extracorporeal cardiopulmonary resuscitation: a propensity matched analysis

Circulation

Circulation, Volume 150, Issue Suppl_1 , Page A4137905-A4137905, November 12, 2024. Background:In out-of-hospital cardiac arrest (OHCA) patients with an initial shockable rhythm, epinephrine increases the likelihood of return of spontaneous circulation (ROSC), but its effect on neurological outcome remains uncertain.

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Abstract 4117657: Targeting GPR39 for Hypoxia-induced Pulmonary Hypertension in Mice

Circulation

Circulation, Volume 150, Issue Suppl_1 , Page A4117657-A4117657, November 12, 2024. Pharmacological inhibition of GPR39 may open new frontiers in the treatment of PAH. Background:Primary pulmonary arterial hypertension (PAH) is a disease affecting young subjects. It has very poor prognosis and optimal treatment is not available.

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Lowering Atherosclerotic Cardiovascular Disease Events by Treating Residual Inflammatory Risk

DAIC

Inflammation driven by signaling cytokines, circulating immune cells, adhesion molecules, and oxidized low-density lipoprotein cholesterol (LDL-C) leads to atherosclerotic plaque development, plaque progression, and eventual rupture.14,15 2019 Sep 10;140(11):e649-e650] [published correction appears in Circulation. Circulation.

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Abstract 4145490: Direct Oral Anticoagulants versus Low Molecular Weight Heparins for Prevention of VTE in Active Malignancy: Insights from a Pooled Analysis of RCTs

Circulation

Circulation, Volume 150, Issue Suppl_1 , Page A4145490-A4145490, November 12, 2024. Background:Cancer is well known to cause a pro-thrombotic state, however, the pharmacologic therapy for prevention of Venous Thromboembolism (VTE) remains under contention.