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Paul S. Pagel

Researcher at Veterans Health Administration

Publications -  474
Citations -  13788

Paul S. Pagel is an academic researcher from Veterans Health Administration. The author has contributed to research in topics: Isoflurane & Hemodynamics. The author has an hindex of 68, co-authored 457 publications receiving 12999 citations. Previous affiliations of Paul S. Pagel include United States Department of Veterans Affairs & Marquette University.

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Isoflurane mimics ischemic preconditioning via activation of K(ATP) channels: reduction of myocardial infarct size with an acute memory phase.

TL;DR: Isoflurane directly preconditions myocardium against infarction via activation of KATP channels in the absence of hemodynamic effects and exhibits acute memory of preconditioning in vivo.
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Intraoperative ketamine for prevention of postoperative delirium or pain after major surgery in older adults: an international, multicentre, double-blind, randomised clinical trial.

TL;DR: The administration of a single subanaesthetic dose of ketamine to older adults during major surgery did not show evidence of reducing postoperative delirium, pain, or opioid consumption, and might cause harm by inducing negative experiences.
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Mechanisms of cardioprotection by volatile anesthetics.

TL;DR: The experimental and clinical findings documenting the phenomenon of volatile anesthetic preconditioning against ischemic injury of myocardium are evaluated and several endogenous signal transduction pathways, acting through the adenosine triphosphate–sensitive potassium (KATP) channel and involving the generation of reactive oxygen species (ROS), have been implicated in mediating the antiischemic actions of volatileAnesthetics.
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Isoflurane Protects against Myocardial Infarction during Early Reperfusion by Activation of Phosphatidylinositol-3-Kinase Signal Transduction: Evidence for Anesthetic-induced Postconditioning in Rabbits

TL;DR: Isoflurane acts during early reperfusion after prolonged ischemia to salvage myocardium from infarction and reduces the threshold of ischemic postconditioning by activating PI3K.
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Levosimendan, a new positive inotropic drug, decreases myocardial infarct size via activation of K(ATP) channels.

TL;DR: Levosimendan exerts cardioprotective effects via activation of KATP channels at a dose that simultaneously enhances myocardial contractility and may be advantageous in patients requiring inotropic support who are also at risk ofMyocardial ischemia.