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Hypotension Prediction Index in Postoperative Surgical Patients — HPI-PACU  

Surgery Clinical Trial

Official title:
Hypotension Prediction Index in Postoperative Surgical Patients in the Post-anesthetic Recovery Room - a Feasibility Study

Clinical Trial Summary

PACU-HPI study evaluates the use of a hemodynamic monitor in the post-anesthetic recovery room on patients undergoing colorectal, hepatobiliary, and vascular surgery, to determine the feasibility of recruiting this surgical population.

Clinical Trial Description

Postoperative vascular complications, including myocardial infarction (MI), myocardial injury after noncardiac surgery (MINS), stroke, and death occur in up to 18% of surgical patients.1 Hypotension is a frequent occurrence in the postoperative period and can increase the risk of postoperative vascular complications.2 Therefore, accurate prediction of postoperative hypotension can identify patients at risk for postoperative vascular complications who would benefit from early intervention. The investigators propose a feasibility study to determine the accuracy of the hypotension prediction index (HPI) parameter of the HemoSphere monitor and Acumen IQ sensor (Edwards Lifesciences, Irvine, CA) to predict postoperative hypotension in surgical patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05335174
Study type Observational
Source Sir Mortimer B. Davis - Jewish General Hospital
Contact Stephen Yang, MD, MSc
Phone (514) 340-8222
Email stephen.yang@mail.mcgill.ca
Status Recruiting
Phase
Start date April 1, 2022
Completion date March 1, 2024
View Details
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