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Influence of the "Hypotension Probability Index" on Intraoperative and Postoperative Hypotension in ENT- and OM-Surgery

Primary Purpose

Hypotension, ENT Disease, Acute Kidney Injury

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Hypotension probability index (HPI)
Sponsored by
University of Giessen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypotension focused on measuring Hypotension, tumor of the oropharynx, tumor of the nasopharynx, creatinine

Eligibility Criteria

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

Inclusion Criteria:

  • extensive surgery in the head and neck area
  • Age ≥ 18 years

Exclusion Criteria:

  • Participation in another interventional study
  • Pregnancy and nursing mothers
  • Surgery without controlled ventilation
  • Contraindication to invasive arterial pressure measurement
  • Renal insufficiency KDIGO stage ≥ 3
  • Congenital coagulation disorder

Sites / Locations

  • University Clinic GiessenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control Arm

Intervention Arm

Arm Description

blinded HPI monitoring

HPI monitoring to predict hypotension

Outcomes

Primary Outcome Measures

number (n) of intraoperative and postoperative hypotension
MAP below 65 mmHg for more than one minute in ventilated patients

Secondary Outcome Measures

Applied volume in ml
Amount of applied infusion volume (crystalloids, colloids, blood products and blood) in ml
Changes of catecholamine management
Dosage of vasopressors and inotropes (in μg)
Duration of surgery
cut-seam time
Fluid balance
blood loss and urin output in ml
Hospital length of stay
Duration of stay in hospital

Full Information

First Posted
October 14, 2019
Last Updated
October 28, 2021
Sponsor
University of Giessen
Collaborators
Edwards Lifesciences
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1. Study Identification

Unique Protocol Identification Number
NCT04151264
Brief Title
Influence of the "Hypotension Probability Index" on Intraoperative and Postoperative Hypotension in ENT- and OM-Surgery
Official Title
Influence of the "Hypotension Probability Index" on the Number and Duration of Intraoperative and Postoperative Hypotension During Extended Surgical Procedures in ENT- and OM-Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 30, 2020 (Actual)
Primary Completion Date
September 1, 2022 (Anticipated)
Study Completion Date
December 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Giessen
Collaborators
Edwards Lifesciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the project is to investigate whether the use of the HPI can reduce the number and duration of intra- and postoperative hypotension in ventilated patients during and two hours after extensive surgery in the head and neck area compared to the established monitoring.
Detailed Description
Blood pressure monitoring displays a crucial part of anesthetic management. An intraoperative hypotension (IOH) is an unwanted complication that can occur during an anaesthetization or during the following duration of the surgery. Causes for this can be vasodilatation (e.g. due to medication), loss of blood volume (e.g. bleeding) or lack of inotropy (reduced left ventricular function, e.g. due to medication). The main high-risk factors for intraoperative hypotension are age of the patient, pre-existing diseases (especially ASA 3 and higher), the duration of surgery, the urgency of the surgery (emergency surgery), antihypertensive long-term medication as well as combined anaesthesia (regional and general anaesthesia). According to the examined collective, the definition of IOH and the level of training of the performing doctor we can monitor IOH in up to 100% of patients (depending on the data collection). Monk et al. show that the one-year mortality of patients undergoing surgery was elevated to 3.6% for every minute the systolic pressure was less than 80mmHg. Also, the risk of mortality was 1.4 higher if the MAP decreased <55mmHg. The consequence of IOH can be a critical reduction of the oxygen supply in the organs. Therefore, organs with low tolerance for hypoxia or a high necessity for oxygen are prone to hypotension induced complications. Those include ischemic stroke or myocardial ischemia (especially in patients with preexisting anemia), mostly happening to older or critical ill patients. The extensive surgeries in ENT- and OM surgery are usually due to tumor diseases. The incidence for hypopharynx carcinoma is between 2-3/10.000 cases each year with an increasing tendency. The peak of this disease is in the 5.-6. decade of life. Causes for this are chronic noxae like alcohol and cigarettes. Numbers show, that the percentage of malignant tumors in the oral cavity and the pharynx in Germany in 2012 were at 3.7% with men and 1.6% with women in the entirety of incidence of malignant tumors. Especially these tumors require a radical resection also in the initial state of the disease which comes along with a long duration of surgery. The operative interventions include a radical resection of the tumor, neck dissection and if necessary a skin flap depending on the state of the tumor, TNM classification and status of lymph nodes. Complications that can occur with these types of surgery are (secondary) bleeding, stenosis, dyspnea, oedema of the mucosa, subcutaneous emphysema, dysphagia and aspiration. Because of the surgical treatment these patients require a postoperative sedation and ventilation. This enables the protection of the respiratory system when patients are at high risk for intra- or postoperative secondary bleeding and/or swelling. Also, the sedation will help not to imperil the success of the intervention (e.g. through coughing, pressure or choking). The Hypotension Prediction Index (HPI) was developed by Edwards Lifesciences (Irvine, California, USA) and is certified in the US and Europe. As part of the Edwards Acumen Decision Support software suite, the HPI is based on the minimal invasive FloTrac IQ sensor. The HPI indicates the probability of an occurring hypotensive event. The software was developed using 20,000 cases of past patient events. If the upper limit of hypotension is reached, the software will alert the responsible physician. The main outcome criteria are the numbers (n) and duration in minutes (t [min]) of intraoperative and postoperative hypotension. These are defined as MAP below 65 mmHg for more than one minute in ventilated patients with and without the use of HPI. The secondary objective criteria are the following: Assumed reason for hypotension Amount of applied infusion volume (crystalloids, colloids, blood products and blood) Type and dose of applied vasopressors Type and dose of applied inotropic agents Acute Kidney Injury Risk Score

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypotension, ENT Disease, Acute Kidney Injury, Anesthesia
Keywords
Hypotension, tumor of the oropharynx, tumor of the nasopharynx, creatinine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized two arm study with two groups.
Masking
Participant
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Arm
Arm Type
No Intervention
Arm Description
blinded HPI monitoring
Arm Title
Intervention Arm
Arm Type
Active Comparator
Arm Description
HPI monitoring to predict hypotension
Intervention Type
Device
Intervention Name(s)
Hypotension probability index (HPI)
Intervention Description
The intervention group is managed with the HPI parameter to detect and possibly prevent hypotension during anaesthesia.
Primary Outcome Measure Information:
Title
number (n) of intraoperative and postoperative hypotension
Description
MAP below 65 mmHg for more than one minute in ventilated patients
Time Frame
until 4 hours after the end of surgery
Secondary Outcome Measure Information:
Title
Applied volume in ml
Description
Amount of applied infusion volume (crystalloids, colloids, blood products and blood) in ml
Time Frame
until 4 hours after the end of surgery
Title
Changes of catecholamine management
Description
Dosage of vasopressors and inotropes (in μg)
Time Frame
until 4 hours after the end of surgery
Title
Duration of surgery
Description
cut-seam time
Time Frame
up to 24 hours
Title
Fluid balance
Description
blood loss and urin output in ml
Time Frame
until 4 hours after the end of surgery
Title
Hospital length of stay
Description
Duration of stay in hospital
Time Frame
up to 18 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: extensive surgery in the head and neck area Age ≥ 18 years Exclusion Criteria: Participation in another interventional study Pregnancy and nursing mothers Surgery without controlled ventilation Contraindication to invasive arterial pressure measurement Renal insufficiency KDIGO stage ≥ 3 Congenital coagulation disorder
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Sander, Prof.
Phone
004964198544401
Email
michael.sander@chiru.med.uni-giessen.de
First Name & Middle Initial & Last Name or Official Title & Degree
Christian Koch, MD
Phone
004964198544401
Email
christian.koch@chiru.med.uni-giessen.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Sander, Prof.
Organizational Affiliation
UKGM Giessen
Official's Role
Study Director
Facility Information:
Facility Name
University Clinic Giessen
City
Gießen
State/Province
Hessen
ZIP/Postal Code
35392
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael Sander, Prof.
Phone
004964198544401
Email
michael.sander@chiru.med.uni-giessen.de

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19934864
Citation
Bijker JB, van Klei WA, Vergouwe Y, Eleveld DJ, van Wolfswinkel L, Moons KG, Kalkman CJ. Intraoperative hypotension and 1-year mortality after noncardiac surgery. Anesthesiology. 2009 Dec;111(6):1217-26. doi: 10.1097/ALN.0b013e3181c14930.
Results Reference
background
PubMed Identifier
15616043
Citation
Monk TG, Saini V, Weldon BC, Sigl JC. Anesthetic management and one-year mortality after noncardiac surgery. Anesth Analg. 2005 Jan;100(1):4-10. doi: 10.1213/01.ANE.0000147519.82841.5E.
Results Reference
background
PubMed Identifier
22277949
Citation
Bijker JB, Persoon S, Peelen LM, Moons KG, Kalkman CJ, Kappelle LJ, van Klei WA. Intraoperative hypotension and perioperative ischemic stroke after general surgery: a nested case-control study. Anesthesiology. 2012 Mar;116(3):658-64. doi: 10.1097/ALN.0b013e3182472320.
Results Reference
background
Links:
URL
https://www.krebsdaten.de/Krebs/DE/Home/homepage_node.html
Description
German Cancer Record
URL
https://www.edwards.com/de/devices/Hemodynamic-Monitoring/FloTrac
Description
Edwards Information

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Influence of the "Hypotension Probability Index" on Intraoperative and Postoperative Hypotension in ENT- and OM-Surgery

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