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
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Central venous pressure (CVP) is characterized by a low-frequency pleural-dependent as well as a high-frequency cardiac pulsatile component. The aim of the study is to compare the low-frequency component of CVP with the esophageal pressure (Pes), as surrogate of pleural pressure, to estimate trans-pulmonary pressure (PL).
The investigators will enroll mechanically ventilated patients admitted to the intensive care unit with the diagnosis of respiratory failure monitored with a dedicated nasogastric catheter and a central venous catheter for measuring Pes and CVP, respectively. Electrocardiogram trace, Pes, CVP and airway pressure (Paw) will be recorded at the end of inspiratory and expiratory pauses. The CVP waveforms will be analyzed off-line using a dedicated low-pass digital filter to obtain the low-frequency component of CVP (filtered CVP, fCVP). Paw, Pes and fCVP will be used to calculate PL using transpulmonary driving pressure formula (PL-Pes and PL-fCVP, respectively). The PL values obtained with fCVP and Pes will be compared to assess the correlation of the two methods.
Not provided
Not provided
Not provided
Not provided
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Transpulmonary pressure | Correlation and agreement between the transpulmonary pressure obtained from esophageal balloon catheter and central venous catheter | Within 72 hours from the starting of mechanical ventilation |
| Measure | Description | Time Frame |
|---|---|---|
| Transpulmonary pressure in subgroups of patients | Agreement between trans pulmonary pressure obtained with the two methods in subgroup of patients such as those with acute respiratory distress syndrome or obesity | Within 72 hours from the starting of mechanical ventilation |
| Transpulmonary pressure in patients at risk for ventilator-induced-lung-injury |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Patients admitted to ICU treated with mechanical ventilation.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Federico Franchi, MD | University of Siena, Depatment of Medical Biotechnology | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Azienda Ospedaliera Universitaria Senese | Siena | 53100 | Italy |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D012128 | Respiratory Distress Syndrome |
| ID | Term |
|---|---|
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D012120 | Respiration Disorders |
Not provided
Not provided
Not provided
Not provided
Not provided
Comparison of the transpulmonary pressure obtained with the two methods in patients at risk for ventilator-induced-lung-injury |
| Within 72 hours from the starting of mechanical ventilation |