POLECAT: Perioperative Delta Renin Concentration (POLECAT)

We want to measure the amount of a hormone called renin in people's bodies before and after they have major abdominal surgery. We want to see if changes in renin levels are connected to problems with blood flow, unstable blood pressure, and kidney damage after surgery.

Study Overview

• Status: Not yet recruiting
• Conditions: Acute Kidney Injury; Post Operative Vasoplegic Syndrome

Detailed Description

The renin-angiotensin system (RAS) plays a key role in haemodynamic stability, vascular tone and electrolyte homeostasis. It is recognised that this system is dysfunctional during critical illness. It remains unknown as to whether significant dysfunction of RAS is found in patients who have undergone major abdominal surgery - however over 50% of these patients often require blood pressure support post-operatively, with nearly half of these patients having unexplained drops in blood pressure.

Renin represents an attractive biomarker that could be implicated in post operative vasoplegia and post operative AKI and as such elevated renin concentrations could be used to identify high-risk patients for cardiovascular instability and AKI who would benefit from timely intervention that could improve their outcomes, this would include the use of selective vasopressor agents such as angiotensin II which has been shown to confer a benefit in patients with underlying dysregulation of the RAS.

If we show that higher differences in renin concentrations are associated with a greater incidence of vasoplegia then we can design a subsequent clinical trial with a different treatment in those who have a higher change in renin. Such a trial is currently recruiting in Germany for patients with higher changes in renin due to cardiac surgery.

The primary aim is to assess whether there is an association between higher differences in renin concentrations (a protein that can be measured in your blood) and haemodynamic instability manifest as vasoplegia (patients exhibiting low blood pressure) in patients undergoing major abdominal surgery requiring post-operative admission to ICU.

• Study Type: Observational
• Enrollment (Estimated): 405

Contacts and Locations

• Study Contact: Name: Naomi Boyer, MBBS; Phone Number: 01483571122; Email: n.boyer@nhs.net
• Study Contact Backup: Name: Syeda Fizza Haider, MBBS; Phone Number: 01483571122; Email: syeda.haider1@nhs.net

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

Planned and unplanned emergency general surgical procedures. All surgical patients who have an intensive care bed booked, will be screened.

To sample patients we will approach all patients who are booked to come to the ICU post operatively.

Description

Inclusion Criteria:

• Age ≥18 years
• All patients having abdominopelvic surgery (planned or unplanned) needing ICU admission where arterial line or central line will been placed
• Able to provide consent, or personal/professional agreement

Exclusion Criteria:

• Patient < 18 years old at time of screening
• Patients already receiving vasopressor support pre-operatively
• Receiving palliative care at the time of recruitment or expected to die within next 24 hours
• Those on kidney replacement therapy (KRT) or end stage kidney disease (ESKD)
• Patient or consultee unable to communicate in verbal and written English
• Patients held in an institution by legal or official order
• Patients with severe mental health disorders that might impair their capacity

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
• The difference between pre and post-operative levels of circulating renin, and association with vasoplegia.	2 years

Secondary Outcome Measures

Outcome Measure	Time Frame
• Determine overall burden of vasopressor use post operatively.	2 years
• Incidence of post-operative AKI in this cohort of patients	2 years
• Trends of renin post-operatively following major abdominal surgery.	2 years
• Associations between changes in renin and AKI.	2 years
• Associations between type of surgery and incidence of post operative instability and renin measurements, with specific emphasis on patients with emergency surgery with peritonitis.	2 years
• Association between regular medications that alter the RAS-axis and changes in renin	2 years

Collaborators and Investigators

• Sponsor: Royal Surrey County Hospital NHS Foundation Trust
• Collaborators: European Society of Intensive Care Medicine
• Investigators: Principal Investigator: Lui Forni, Professor of Intensive Care Medicine, Royal Surrey Hospital

Study record dates

Study Major Dates

• Study Start (Estimated): July 1, 2023
• Primary Completion (Estimated): July 1, 2025
• Study Completion (Estimated): July 1, 2025

Study Registration Dates

• First Submitted: July 4, 2023
• First Submitted That Met QC Criteria: July 4, 2023
• First Posted (Actual): July 12, 2023

Study Record Updates

• Last Update Posted (Actual): July 12, 2023
• Last Update Submitted That Met QC Criteria: July 4, 2023
• Last Verified: July 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Cardiovascular Diseases; Vascular Diseases; Kidney Diseases; Urologic Diseases; Postoperative Complications; Renal Insufficiency; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Male Urogenital Diseases; Acute Kidney Injury; Vasoplegia
• Other Study ID Numbers: 319836

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No