Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| CSEM Centre Suisse d'Electronique et de Microtechnique SA - Recherche et Developpement | INDUSTRY |
Not provided
Not provided
Not provided
Not provided
To assess whether changes in electrical impedance - measured using an electrical impedance tomography (EIT) chest belt - can be used to derive changes in pulmonary artery pressure (PAP) in critically ill patients when compared to invasive gold-standard PAP measured using pulmonary artery catheter (PAC).
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| All Study Participants |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Electrical impedance tomography | Device | In addition to routine critical care with a pulmonary artery catheter already in place (PAC), an electrical impedance tomography (EIT) belt will be placed in patients enrolled in this study. Data will be analyzed offline and clinical trajectory and/or decisions will not be impacted by this additional monitoring. EIT is a non-invasive, safe, and radiation-free medical imaging modality. |
| Measure | Description | Time Frame |
|---|---|---|
| Mean difference between EIT-derived and PAC-measured changes in pulmonary artery pressure | The primary outcome is the difference - expressed as mean and standard deviation (SD) - between changes in EIT-derived pulmonary artery pressure (ΔPAP_EIT), derived from changes in the pulmonary pulse arrival time, and changes in pulmonary artery catheter-based pulmonary artery pressure (ΔPAP_PAC). This will be measured over recording periods of up to 48 hours. | Up to 48 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Data acceptance rate | Data acceptance rate, i.e., the percentage of total recording duration during which lung EIT signals show pulmonary pressure morphology and thus allow to estimate EIT-derived PAP values. | Up to 48 hours |
| Concordance rate (%) of directional changes in pulmonary artery pressure between EIT and PAC measurements (Trending ability) |
Not provided
Inclusion criteria:
Exclusion criteria:
Not provided
Not provided
Not provided
For this study the investigators plan to enroll 28 patients with complete datasets for evaluation of PAP derived by PAC and EIT for a minimum duration of 4 hours in the ICU at Inselspital (Bern) with clinical decision to monitor PAP using a PAC.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Kaspar F Bachmann, MD | Contact | +41 31 632 21 11 | kaspar.bachmann@faculty.unibe.ch |
| Name | Affiliation | Role |
|---|---|---|
| Kaspar F Bachmann, MD | Department of Intensive Care Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland | Principal Investigator |
| Carmen A Pfortmueller, MD | Department of Intensive Care Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Inselspital Bern, Universitätsklinik für Intensivmedizin | Recruiting | Bern | 3010 | Switzerland |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
The trending ability will be assessed using four quadrant plot analysis to calculate the concordance rate between EIT-derived and PAC-measured pulmonary artery pressure changes. The concordance rate is defined as the percentage of data points in which both methods agree on the direction of change (increase or decrease) in pulmonary artery pressure. |
| Up to 48 hours |
| Accuracy and trending ability of EIT-derived cardiac output compared to PAC measurements | The difference between EIT-derived cardiac output (CO_EIT) and pulmonary artery catheter-based cardiac output (CO_PAC) will be calculated. This will be expressed as mean difference ± standard deviation in L/min. The ability of EIT to track changes in cardiac output over time will be evaluated by comparing directional changes in CO_EIT with corresponding changes in CO_PAC. This will be reported as the percentage of concordant directional changes between the two methods. | Up to 48 hours |
| Agreement between EIT-derived and ventilator-measured respiratory parameters | This outcome assesses the ability of EIT to measure key respiratory parameters compared to the mechanical ventilator measurements. The difference between EIT-derived tidal volume and ventilator-measured tidal volume as well as the difference between EIT-derived respiratory rate and ventilator-measured respiratory rate will be calculated and expressed as mean difference ± standard deviation. Other ventilation-related parameters: Additional parameters such as end-expiratory lung volume changes or regional ventilation distribution may also be assessed, depending on the capabilities of the EIT system and the available ventilator data. | Up to 48 hours |
| Study Director |
| ID | Term |
|---|---|
| D065627 | Familial Primary Pulmonary Hypertension |
| ID | Term |
|---|---|
| D006976 | Hypertension, Pulmonary |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
Not provided
Not provided