Plain English Summary
Background and study aims
In critically ill patients it is important to closely monitor aspects of blood flow (haemodynamic parameters) such as amount of blood flow, the blood pressure, the heart output. The technique used to measure this is known as transpulmonary thermodilution and pulse contour analysis. The measurements can be performed using a tube attached to sensory equipment inserted into a large blood vessel (central venous catheter). Precise and reliable measurements are important. At the present time there are two devices which are routinely using transpulmonary thermodilution and pulse contour analysis to determine extended haemodynamic parameters: PiCCO and EV1000 monitoring systems. The aim of this study is to compare the PiCCO and EV1000 for neck vein (jugular) and leg vein (femoral) measurements.
Who can participate?
Patients aged 18 years or above who are being treated in the intensive care unit.
What does the study involve?
In this study EV1000 will be replaced by PiCCO device or vice-versa. During the exchange of these monitoring systems, measurements will be performed using the jugular and femoral central venous catheter to allow the comparison of both haemodynamic monitoring systems.
What are the possible benefits and risks of participating?
The measurements during the exchange from one to another monitoring system guarantee the reliability of determined parameters and its usefulness for further therapeutic management. As both systems are clinically approved and routinely used, there is no additional risk by the devices.
The decision for exchange of arterial or central venous/shaldon catheter will be made irrespective of the study according to local standards. The most common complication of replacement of arterial or central venous line are vascular-, pulmonary-, cardiac-complications, catheter dysfunction or infection.
Where is the study run from?
Klinik und Poliklinik für Innere Medizin II am Klinikum rechts der Isar, Technische Universität München, Germany
When is the study starting and how long is it expected to run for?
January 2017 to March 2017
Who is funding the study?
Klinik und Poliklinik für Innere Medizin II am Klinikum rechts der Isar, Technische Universität München, Germany
Who is the main contact?
Dr Alexander Herner
alexander.herner@mri.tum.de
Prof. Wolfgang Huber
wolfgang.huber@mri.tum.de
The usefulness of transpulmonary thermodilution (TPTD) for the measurement of extended hemodynamic parameters (e.g. cardiac index (CI), global end-diastolic volume index (GEDVI), extra vascular lung water index (EVLWI), pulmonary vascular permeability index (PVPI) and global ejection fraction (GEF)) has been demonstrated in a number of studies. Usually TPTD is performed by indicator injection via the jugular or subclavian vein. However, under certain circumstances, superior vena cava access is not feasible. In these cases, femoral access can be used for measurement. Femoral Indicator bolus injections using PiCCO®-device have demonstrated significant overestimation particularly of GEDVI due to the additional volume of the inferior vena cava. This overestimation was corrected by formula and integrated in the newest algorithm used by PiCCO®-device. Recently, in addition to the PiCCO® device, another commercially available device for TPTD has been introduced, EV1000/VolumeView® which uses similar methodologies and algorithms as the PiCCO® device. However, there are no systematic data on the impact of femoral indicator injection for the EV-1000® device
Therefore, we compared the agreement of hemodynamic parameters sequentially derived by femoral as well as jugular indicator injection using the EV-1000® and the PiCCO® device in patients equipped with both jugular and femoral venous access.
Study website
Contact information
Type
Scientific
Contact name
Dr Alexander Herner
ORCID ID
http://orcid.org/0000-0003-3905-9280
Contact details
Klinikum rechts der Isar
II. Medizinische Klinik
Ismaningerstrasse 22
München
81675
Germany
+49 (0)8941409334
alexander.herner@mir.tum.de
Type
Scientific
Contact name
Prof Wolfgang Huber
ORCID ID
Contact details
Klinikum rechts der Isar
II. Medizinische Klinik
Ismaningerstrasse 22
München
81675
Germany
+49 (0)8941402214
wolfgang.huber@mri.tum.de
Additional identifiers
EudraCT/CTIS number
Nil known
IRAS number
ClinicalTrials.gov number
Nil known
Protocol/serial number
EV-1000
Study information
Scientific title
Comparison of global end-diastolic volume index derived from jugular and femoral indicator injection in patients equipped with both a PiCCO-2 and an EV-1000-device
Acronym
Study hypothesis
Are parameters derived by PiCCO and EV-1000-device comparable?
Ethics approval(s)
Approved 28/06/2012, Ethikkommission; Fakultät für Medizin; Technische Universität München (Ismaninger Straße 22, 81675, München, Germany; +49 4140-7737; ethikkommission@mri.tum.de), ref: 5384/12
Study design
Prospective observational study
Primary study design
Observational
Secondary study design
Cohort study
Study setting(s)
Hospital
Study type
Diagnostic
Patient information sheet
Not available in web format, please use the contact details below to request a patient information sheet
Condition
Critically ill patients with the need for extended hemodynamic monitoring
Intervention
First, only patients already equipped with a central venous catheter/dialysis catheter and PiCCO or EV-1000 monitoring system will be enrolled in this study.
Second, the treating physician (not involved in the study) performs the change of the CVC and the arterial line in patients with pre-existing and continuous need for advanced haemodynamic (transpulmonary thermodilution)-monitoring. This decision will be made irrespective of the study according to local standards. During the change of catheters, measurements with PiCCO- and EV-1000-device will be performed. A measurement consists of a triplicate injection of indicator (15 ml ice cold 0,9% saline solution). Duration of the measurement is around 15 minutes. There is no other intervention or follow up.
Intervention type
Device
Pharmaceutical study type(s)
Phase
Not Applicable
Drug/device/biological/vaccine name(s)
PiCCO® device
EV-1000® device
Primary outcome measure
Global end-diastolic volume (index) measured using PiCCO and EV1000
Secondary outcome measures
Measured using PiCCO and EV1000
1. Cardiac output/index
2. Cardiac function index
3. Global ejection fraction
4. Extravascular lung water index
5. Pulmonary vascular permeability index
6. Central venous pressure
7. Systolic volume variation
8. Pulse pressure variation
Overall study start date
01/08/2016
Overall study end date
31/03/2017
Reason abandoned (if study stopped)
Eligibility
Participant inclusion criteria
1. Patients treated on the intensive care unit
2. Critically ill patients
3. Patients with the need of a change of CVC and arterial line in patients with pre-existing and continuing need for TPTD-monitoring
4. Hemodynamic stable patients without vasopressors or with a constant vasopressor-dosage
Participant type(s)
Patient
Age group
Adult
Sex
Both
Target number of participants
10
Total final enrolment
10
Participant exclusion criteria
1. Pregnant
2. Younger than 18 years old
Recruitment start date
25/01/2017
Recruitment end date
31/03/2017
Locations
Countries of recruitment
Germany
Study participating centre
Klinikum rechts der Isar, Technische Universität München
Ismaningerstraße 22
Germany
81675
Germany
Sponsor information
Organisation
Klinikum der Universität München
Sponsor details
Klinik und Poliklinik für Innere Medizin II
Klinikum rechts der Isar
Technischen Universität München
Ismaningerstrasse 22
München
81675
Germany
+49 (0)89 4140-2251
direktion.med2@mri.tum.de
Sponsor type
Hospital/treatment centre
Website
http://www.frauenklinik.med.tum.de/
ROR
Funders
Funder type
Hospital/treatment centre
Funder name
Technische Universität München
Alternative name(s)
Technical University of Munich, TUM
Funding Body Type
government organisation
Funding Body Subtype
Universities (academic only)
Location
Germany
Results and Publications
Publication and dissemination plan
Planned publication in a peer reviewed journal.
Intention to publish date
31/12/2019
Individual participant data (IPD) sharing plan
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request
IPD sharing plan summary
Available on request
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | 27/11/2020 | 17/01/2023 | Yes | No |