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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04803903
Other study ID # 11.15.2018
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 5, 2018
Est. completion date May 20, 2021

Study information

Verified date July 2021
Source Attikon Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study will investigate whether the use of Goal Directed Hemodynamic Therapy implemented with the HPI algorithm using a treatment algorithm will reduce the incidence of hypotension and improve treatment of hypotension.


Description:

The perioperative period is characterized by hemodynamic instability. Intraoperative hypotension (IOH) can be caused by anesthesia drugs, surgical manipulations, hypovolemia or inhibition of the sympathetic nervous system and impairment of baroreflex regulatory mechanisms. In a retrospective analysis performed at the Cleveland Clinic, the risk for acute kidney injury (AKI) and myocardial injury (MI) increased when mean arterial pressure (MAP) was less than 55 mmHg. Further, even short durations of intraoperative hypotension were associated with AKI and MI. Salmasi and coll analyzed whether associations based on relative thresholds were stronger than those based on absolute thresholds regarding blood pressure. They found that there were no clinically important interactions between preoperative blood pressures and the relationship between hypotension and ΜΙ or ΑΚΙ at intraoperative mean arterial blood pressures less than 65 mmHg. Absolute and relative thresholds had comparable ability to discriminate patients with ΜΙ or ΑΚΙ from those without it. The authors concluded that anesthetic management can thus be based on intraoperative pressures without regard to preoperative pressure. In a retrospective cohort study Sun and coll conclude that an increased risk of postoperative stage I AKI occurs when intraoperative MAP was less than 60 mmHg for more than 20 min and less than 55 mmHg for more than 10 min. Hence it is fundamental for the management of any hemodynamically unstable patient the rapid assessment of the factors that determine the cardiovascular collapse, followed by prompt treatment and, ultimately, reversal of the responsible process. Recently a Hypotension Probability Indicator (HPI) algorithm has been developed from Edwards Lifesciences using continuous invasively-measured arterial waveforms to predict hypotension with high accuracy minutes before blood pressure actually decreases. The HPI algorithm can be integrated with a goal-directed hemodynamic treatment (GDHT) to achieve hemodynamic optimization by increasing global blood flow and prevent organ failure. We developed a treatment protocol implementing HPI with GDHT that can be used in general anesthesia patients to guide clinical practice.


Recruitment information / eligibility

Status Completed
Enrollment 99
Est. completion date May 20, 2021
Est. primary completion date March 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Aged 18 years or older - Planned to receive general anaesthesia > 2h - Planned to receive an arterial line during surgery - Aim for MAP of = 65 mmHg during surgery - Being able to give written informed consent prior to surgery Exclusion Criteria: - Aim for MAP other than 65 mmHg at discretion treating physician - Significant hypotension before surgery defined as a MAP <65 - Right- or left sided cardiac failure (e.g. LVEF<35%) - Known cardiac shunts (significant) - Known aortic stenosis (severe) - Severe cardiac arrhythmias including atrial fibrillation - Requiring dialysis - Liver surgery with Pringle maneuver - Vascular surgery with clamping of the aorta

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Flotraq Sensor with EV1000 incorporating the HPI algorithm
The HPI algorithm is only available on the EV1000, Hemosphere and Flotrac monitoring systems and requires the use of a Flotrac sensor connected to an arterial line (Edwards Lifesciences Corp., Irvine, CA, USA). The Flotrac sensor has a splitter which enables the splitting of the arterial blood pressure signal to facilitate a blood pressure signal on both the anesthesia machine monitor (standard care) and the HemoSphere monitor (study). In the intervention arm we asked the anesthesiologist and anesthesia nurse to use the study treatment flowchart . If the HPI alarm goes off, which entails both a sound and a flickering light, we ask the anesthesiologist to act upon this alarm immedietaly. Use of the study treatment flowchart ensures that the anesthesiologist has to think about the underlying cause. The HemoSphere/EV1000 with HPI software has a second screen with variables that provide information about the underlying cause of the predicted hypotension.

Locations

Country Name City State
Greece Attikon University Hospital Athens Attika

Sponsors (1)

Lead Sponsor Collaborator
Attikon Hospital

Country where clinical trial is conducted

Greece, 

References & Publications (3)

Salmasi V, Maheshwari K, Yang D, Mascha EJ, Singh A, Sessler DI, Kurz A. Relationship between Intraoperative Hypotension, Defined by Either Reduction from Baseline or Absolute Thresholds, and Acute Kidney and Myocardial Injury after Noncardiac Surgery: A Retrospective Cohort Analysis. Anesthesiology. 2017 Jan;126(1):47-65. — View Citation

Sun LY, Wijeysundera DN, Tait GA, Beattie WS. Association of intraoperative hypotension with acute kidney injury after elective noncardiac surgery. Anesthesiology. 2015 Sep;123(3):515-23. doi: 10.1097/ALN.0000000000000765. — View Citation

Walsh M, Devereaux PJ, Garg AX, Kurz A, Turan A, Rodseth RN, Cywinski J, Thabane L, Sessler DI. Relationship between intraoperative mean arterial pressure and clinical outcomes after noncardiac surgery: toward an empirical definition of hypotension. Anesthesiology. 2013 Sep;119(3):507-15. doi: 10.1097/ALN.0b013e3182a10e26. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary TWA hypotension (measured with Flotrac sensor) Time weighted average spent in hypotension, defined as MAP <65mmHg for =1min intraoperative, starting 15 minutes after induction
Secondary Incidence of hypotension (measured with Flotrac sensor) Incidence of hypotension, defined as MAP <65mmHg for =1min intraoperative, starting 15 minutes after induction
Secondary Time spent in hypotension (measured with Flotrac sensor) Time spent in hypotension, in minutes, defined as MAP <65mmHg for =1min intraoperative, starting 15 minutes after induction
Secondary Treatment choice (drugs/fluids) Medication used to prevent/treat hypotension. A study member is present at the OR to make notes intraoperative, starting 15 minutes after induction
Secondary Treatment dose (drugs/fluids) Dose of medication used to prevent/treat hypotension. A study member is present at the OR to make notes intraoperative, starting 15 minutes after induction
Secondary Time to treatment (drugs/fluids) time to treatment of hypotension, defined as MAP <65mmHg for =1min. intraoperative, starting 15 minutes after induction
Secondary Diagnostic guidance protocol deviations Diagnostic guidance protocol deviations, a study member is present at the OR to make notes of any protocol deviations. intraoperative, starting 15 minutes after induction
Secondary Postoperative Morbidity Incidence of complications: cardiac, pulmonary, renal postoperative, up to 30 days after surgery or until discharge from the hospital
Secondary Postoperative Creatinine levels Measurement if creatinine levels postoperatively postoperative, up to 30 days after surgery or until discharge from the hospital
Secondary Mortality Incidence of mortality 30 days after surgery postoperative, up to 30 days after surgery
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