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Estimated Oxygen Extraction Versus Dynamic Parameters for Perioperative Hemodynamic Optimization

Primary Purpose

Perioperative/Postoperative Complications, Morality

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Dynamic parameters of fluid responsiveness protocol
Estimated oxygen extraction protocol
Sponsored by
Università Politecnica delle Marche
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Perioperative/Postoperative Complications focused on measuring Peri-operative goal-directed therapy, Hemodynamic optimization, Postoperative complications, Mortality

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients undergoing general anesthesia and mechanical ventilation for elective major open abdominal surgery (gastrointestinal, urologic, gynecologic and vascular surgery)
  • expected duration of surgical procedure higher than 120 minutes
  • ASA II-III-IV
  • planned postoperative ICU/HDU admission

Exclusion Criteria:

  • <18 years old
  • pregnancy
  • arrhythmia
  • arterial curve alteration (resonance, damping) not solvable
  • palliative surgical procedures
  • denial of consent

Sites / Locations

  • AOU Ospedali Riuniti Ancona

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Estimated Oxygen Extraction

Dynamic Parameters

Arm Description

Outcomes

Primary Outcome Measures

Complications rate
Evaluate the difference of postoperative complications rate between the two groups

Secondary Outcome Measures

Fluid administered
Evaluate the difference of total amount of fluids administered during the perioperative period between the two groups
Fluid balance
Evaluate the difference of fluid balance (difference between fluid administered and fluid loss) during postoperative period between the two groups
Vasopressor/inopropic drugs
Evaluate the difference in needs of vasopressor/inotropic drugs (reporting mean dosage used) between the two groups
Hospital length of stay
Evaluate the difference of total number of days of hospital stay between the two groups
Mortality at day 28
Evaluate the difference of mortality rate at day 28 between the two groups

Full Information

First Posted
June 11, 2019
Last Updated
March 23, 2020
Sponsor
Università Politecnica delle Marche
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1. Study Identification

Unique Protocol Identification Number
NCT04053595
Brief Title
Estimated Oxygen Extraction Versus Dynamic Parameters for Perioperative Hemodynamic Optimization
Official Title
Estimated Oxygen Extraction Versus Dynamic Parameters for Perioperative Hemodynamic Optimization of Patients Undergoing Non-cardiac Surgery: a Non-inferiority Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 2020 (Anticipated)
Primary Completion Date
June 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Università Politecnica delle Marche

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The aim of the study is to evaluate the complications rate of high risk patients undergoing non-cardiac surgery that receive two different protocols of hemodynamic optimization. A group of patients receive a protocol based on dynamic parameters of fluid responsiveness; the other group of patients receive a protocol based of the optimization of oxygen extraction. The hypothesis is that a perioperative hemodynamic optimization protocol based on oxygen extraction is not inferior to a protocol based on dynamic parameters of fluid responsiveness considering the complication rate developed postoperatively.
Detailed Description
Any surgical intervention is a trauma for the organism and a stress response is activated to cope the external insult. This stress response is responsible of an increase in oxygen consumption. If patient is not able to overcome the deficit in oxygen consumption (VO2) during the first hours postoperatively, he/she will go toward complications (in case of delay to meet metabolic demand) or death (in case of persistent VO2 deficit). Therefore, several protocols have been developed to optimise haemodynamic parameters with the aim to reduce tissue hypoperfusion coming from maldistribution or inadequate perfusion and meet the increased metabolic need as soon as possible. Every patient that probably will not be able to face the surgical stress himself might benefit from modulation of haemodynamic parameters. Actually, goal directed therapy (GDT) is able to improve survival only in high-risk surgical patients. Instead, the reduction of complications rate has been shown also in intermediate-risk population. Originally, hemodynamic optimisation protocols were developed to reach supranormal value for cardiac output (CO), oxygen delivery (DO2) and VO2. Based on the concept that oxygen extraction rate (O2ER) reflects the balance between DO2 and VO2, a GDT protocol based on O2ER estimation (O2ERe) calculated as (SaO2-ScvO2)/SaO2 has been proposed showing a significantly lower number of organ failure postoperatively compared with control group. The major determinants of DO2 are cardiac output (CO), haemoglobin level (Hb) and arterial oxygen saturation (SaO2). An inadequate CO may be optimised using fluids as first line therapy and then inotropes. In mechanically ventilated patients, heart-lung interaction is useful to recognise in which portion of the Frank-Starling curve the heart of the patient is working and then if CO is able to rise after fluid administration aimed to increase preload. Several parameters based on mini-invasive monitor systems are available to assess fluid responsiveness such as pulse pressure variation (PPV) and stroke volume variation (SVV).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Perioperative/Postoperative Complications, Morality
Keywords
Peri-operative goal-directed therapy, Hemodynamic optimization, Postoperative complications, Mortality

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Estimated Oxygen Extraction
Arm Type
Experimental
Arm Title
Dynamic Parameters
Arm Type
Active Comparator
Intervention Type
Diagnostic Test
Intervention Name(s)
Dynamic parameters of fluid responsiveness protocol
Intervention Description
Dynamic parameter of fluid responsiveness (pulse pressure variation/stroke volume variation) are used to optimize hemodynamics intraoperatively and during the first 6 hours postoperatively when appropriate. A cutoff of 12% is used to predict an increase of stroke volume >10% after fluid administration.
Intervention Type
Diagnostic Test
Intervention Name(s)
Estimated oxygen extraction protocol
Intervention Description
Oxygen extraction is estimated by the difference of arterial oxygen saturation and central venous oxygen saturation divided by arterial oxygen saturation. A cutoff of 27% is used as a marker of inadequate tissue perfusion requiring hemodynamic optimization.
Primary Outcome Measure Information:
Title
Complications rate
Description
Evaluate the difference of postoperative complications rate between the two groups
Time Frame
From date of randomization until the date of hospital discharge assessed up to 90 days
Secondary Outcome Measure Information:
Title
Fluid administered
Description
Evaluate the difference of total amount of fluids administered during the perioperative period between the two groups
Time Frame
Immediately after the surgery, 6 hours postoperatively and at the date of ICU/HDU discharge assessed up to 90 days
Title
Fluid balance
Description
Evaluate the difference of fluid balance (difference between fluid administered and fluid loss) during postoperative period between the two groups
Time Frame
Immediately after the surgery, 6 hours postoperatively and at the date of ICU/HDU discharge assessed up to 90 days
Title
Vasopressor/inopropic drugs
Description
Evaluate the difference in needs of vasopressor/inotropic drugs (reporting mean dosage used) between the two groups
Time Frame
Immediately after the, 6 hours postoperatively and at the date of ICU/HDU discharge assessed up to 90 days
Title
Hospital length of stay
Description
Evaluate the difference of total number of days of hospital stay between the two groups
Time Frame
From date of randomization until the date of hospital discharge or death from any cause assessed up to 90 days
Title
Mortality at day 28
Description
Evaluate the difference of mortality rate at day 28 between the two groups
Time Frame
Day 28 from randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients undergoing general anesthesia and mechanical ventilation for elective major open abdominal surgery (gastrointestinal, urologic, gynecologic and vascular surgery) expected duration of surgical procedure higher than 120 minutes ASA II-III-IV planned postoperative ICU/HDU admission Exclusion Criteria: <18 years old pregnancy arrhythmia arterial curve alteration (resonance, damping) not solvable palliative surgical procedures denial of consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Abele Donati, MD, PhD
Phone
+390715963858
Email
a.donati@univpm.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abele Donati, MD, PhD
Organizational Affiliation
Università Politecnica delle Marche
Official's Role
Principal Investigator
Facility Information:
Facility Name
AOU Ospedali Riuniti Ancona
City
Ancona
ZIP/Postal Code
60126
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
32305061
Citation
Carsetti A, Amici M, Bernacconi T, Brancaleoni P, Cerutti E, Chiarello M, Cingolani D, Cola L, Corsi D, Forlini G, Giampieri M, Iuorio S, Principi T, Tappata G, Tempesta M, Adrario E, Donati A. Estimated oxygen extraction versus dynamic parameters of fluid-responsiveness for perioperative hemodynamic optimization of patients undergoing non-cardiac surgery: a non-inferiority randomized controlled trial. BMC Anesthesiol. 2020 Apr 18;20(1):87. doi: 10.1186/s12871-020-01011-z.
Results Reference
derived

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Estimated Oxygen Extraction Versus Dynamic Parameters for Perioperative Hemodynamic Optimization

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