Skip to content

Hypotension Prediction Index in Postoperative Surgical Patients

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05335174
Acronym
HPI-PACU
Enrollment
30
Registered
2022-04-19
Start date
2022-04-01
Completion date
2027-03-01
Last updated
2025-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgery

Brief 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.

Detailed 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.

Interventions

DEVICEDevice: HemoSphere monitor and Acumen IQ sensor.

Patients will be placed on this monitor for the duration of study in the PACU. Followed by 30-day phone call to record cardiovascular complications.

Sponsors

Sir Mortimer B. Davis - Jewish General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patient ≥45 years old 2. Will undergo open colorectal, hepatobiliary, or vascular surgery; 3. Is expected to have an arterial cannula inserted intraoperatively; 4. Has an anticipated stay in PACU for at least 2 hours; 5. Able to provide written informed consent

Exclusion criteria

1. Planned admission to ICU; 2. Refusal to participate; 3. Previously enrolled in the study

Design outcomes

Primary

MeasureTime frameDescription
Incidence of intraoperative hypotensionin 12 monthsDescribe the incidence of hypotension defined as MAP \<65 intraoperatively.
Incidence of postoperative hypotensionin 12 monthsDescribe the incidence of postoperative hypotension defined as MAP \<65 in the PACU
Hemodynamic changes with treatment of hypotensionin 12 monthsDescribed the changes in cardiac index with each medical treatment of a hypotensive episode.

Secondary

MeasureTime frameDescription
Sensitivity and Specificity of HPIin 12 monthsSensitivity and Specificity of HPI compared to a hypotensive events in the postoperative setting
Cardiovascular outcomesin 12 monthsNumber of patients with Mortality, MI, MINS, acute pulmonary edema, stroke, pulmonary embolism, deep vein thrombosis

Countries

Canada

Contacts

Primary ContactStephen Yang, MD, MSc
stephen.yang@mail.mcgill.ca(514) 340-8222
Backup ContactMirana Rakotoarivony
mirana.rakotoarivony@affiliate.mcgill.ca

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026