ImPortance of Arterial Measurement Sites (IPAMS) on Intraoperative Hemodynamic Management
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Brachial line guided hemodynamic management, Radial line guided hemodynamic management, Radial line catheterization, Brachial line catheterization.
- Who it may be relevant to
- Registry conditions: Perioperative Care, Hemodynamics, Monitoring Blood Pressure, Arterial Lines. Basic parameters: 18 years — 90 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Importance of Arterial Measurement Sites on Intraoperative Hemodynamic Management of Major Abdominal Surgeries and Artificial Intelligence-based Prediction of Arterial Gradient Using Peripheral Radial Pressure Waveform Analysis
Overview
The goal of this clinical trial is to demonstrate the importance of arterial pressure measurement sites during major abdominal surgeries. This randomized controlled trial will compare arterial pressure measurements obtained from radial artery catheterization (the current standard method of monitoring) with those obtained from brachial artery catheterization (a more accurate reflection of central arterial pressure). At the end of the study, we are looking to answer the following questions: 1. Does arterial pressure measurement sites influence the amount of vasopressors that is administered during major abdominal surgeries? 2. What are the instances where there is a difference between peripheral (radial catheter) and central (brachial catheter) monitoring and what are the risk factors leading to the appearance of this radial-brachial pressure gradient? 3. With the data collected, can artificial intelligence based analysis help predict the reliability of a radial monitoring and help guide clinicians on choosing a peripheral versus central arterial pressure monitoring site? All adult participants who are scheduled for elective major abdominal surgeries and meeting our inclusion criteria will be approached and included if they consent. Participants will be randomized 1:1 in the intervention group and the standard of care group. In the intervention group, the brachial arterial line will be used intraoperatively to guide vasopressor and fluid administration. A radial line will also be installed to measure the radial arterial pressure simultaneously, but will not be used to guide hemodynamic management. In the standard of care group, both lines will be installed just like in the intervention group, however, it is the radial arterial line that will guide fluid and vasopressor administration. In both groups, the anesthesia protocol will be standardized and the anesthesiologist will be blinded to the arterial pressure measurement site.
Interventions
- Behavioral Brachial line guided hemodynamic management
Anesthesiologists in charge of the patients will guide their hemodynamic management based on the monitoring of brachial/humeral arterial line, instead of the most frequently used radial line. - Behavioral Radial line guided hemodynamic management
The anesthesiologist will guide their hemodynamic management on the classically used radial arterial line. - Device Radial line catheterization
An arterial line will be inserted in the radial artery of the patient. - Device Brachial line catheterization
An arterial line will be inserted in the brachial artery of the patient.
Primary outcome measures
- Time-weighted average administration of noradrenaline [Time frame: Intraoperative administration]
Secondary outcome measures (12)
- Total amount of noradrenaline administered [Time frame: Intraoperative administration]
- Total time of hypotension [Time frame: Intraoperative]
- Occurrence and depth of radial-to-brachial gradient [Time frame: Intraoperative]
- Dose of other inotropes and vasopressors [Time frame: Intraoperative administration]
- Fluid balance [Time frame: Intraoperative administration]
- Urine output [Time frame: Intraoperative]
- Total consumption of opioids [Time frame: Intraoperative]
- Total consumption of hypnotic drug [Time frame: Intraoperative]
- Cumulative duration of burst suppression and low BIS values [Time frame: Intraoperative]
- Troponin and Creatinine lab measurements [Time frame: Post-anesthesia care unit and post-operative day 1,3 and 7]
- Clavien-Dindo Score [Time frame: Post-operative day 1,3 and 7]
- Composite occurence of postoperative complications [Time frame: Post-operative day 1,3 and 7]
Eligibility criteria
Inclusion criteria
- Patients between 18 and 90 years of age;
- Major abdominal surgery via laparoscopy or laparotomy under general anesthesia - with or without concomitant use of regional or neuraxial anesthesia;
- Expected anesthesia time of more than 120 minutes.
Exclusion criteria
- Known peripheral severe vascular disease with subclavian artery stenosis,
- Significant arterial gradient between arms with preoperative non-invasive bloop pressure measurements (>25 mm Hg of systolic blood pressure or 10 mm Hg of mean arterial pressure);
- Inability or contraindications to insert arterial line on either arm (arteriovenous fistula, surgical sterility);
- Known allergies, intolerance, other medical conditions that precludes the use of prescribed general anesthesia protocol for this trial;
- Inability to communicate in French or English.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Triple blind
- Primary purpose
- Treatment
Study locations
Canada · 1 center
- Maisonneuve-Rosemont Hospital — Montreal
Publications
- Wijnberge M, Geerts BF, Hol L, Lemmers N, Mulder MP, Berge P, Schenk J, Terwindt LE, Hollmann MW, Vlaar AP, Veelo DP. Effect of a Machine Learning-Derived Early Warning System for Intraoperative Hypotension vs Standard Care on Depth and Duration of Intraoperative Hypotension During Elective Noncardiac Surgery: The HYPE Randomized Clinical Trial. JAMA. 2020 Mar 17;323(11):1052-1060. doi: 10.1001/ja PMID 32065827
- Futier E, Lefrant JY, Guinot PG, Godet T, Lorne E, Cuvillon P, Bertran S, Leone M, Pastene B, Piriou V, Molliex S, Albanese J, Julia JM, Tavernier B, Imhoff E, Bazin JE, Constantin JM, Pereira B, Jaber S; INPRESS Study Group. Effect of Individualized vs Standard Blood Pressure Management Strategies on Postoperative Organ Dysfunction Among High-Risk Patients Undergoing Major Surgery: A Randomized C PMID 28973220
- Galluccio ST, Chapman MJ, Finnis ME. Femoral-radial arterial pressure gradients in critically ill patients. Crit Care Resusc. 2009 Mar;11(1):34-8. PMID 19281442
- Ahuja S, Mascha EJ, Yang D, Maheshwari K, Cohen B, Khanna AK, Ruetzler K, Turan A, Sessler DI. Associations of Intraoperative Radial Arterial Systolic, Diastolic, Mean, and Pulse Pressures with Myocardial and Acute Kidney Injury after Noncardiac Surgery: A Retrospective Cohort Analysis. Anesthesiology. 2020 Feb;132(2):291-306. doi: 10.1097/ALN.0000000000003048. PMID 31939844
- Renaud-Roy E, Stockle PA, Maximos S, Brulotte V, Sideris L, Dube P, Drolet P, Tanoubi I, Issa R, Verdonck O, Fortier LP, Richebe P. Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli. Can J Anaesth. 2019 Sep;66(9):1049-1061. doi: 10.1007/s12630-019-01372-1. Epub 2019 Apr 17. PMID 30997633
- Tang Y, Zhu C, Liu J, Wang A, Duan K, Li B, Yuan H, Zhang H, Yao M, Ouyang W. Association of Intraoperative Hypotension with Acute Kidney Injury after Noncardiac Surgery in Patients Younger than 60 Years Old. Kidney Blood Press Res. 2019;44(2):211-221. doi: 10.1159/000498990. Epub 2019 Mar 29. PMID 30928979
Identifiers
NCT: NCT06982001 · 2023-3299