Non-invasive cardiac index monitoring in women undergoing laparoscopic procedure under general anaesthesia Surgery
Conditions
Interventions
During the preparation for anaesthesia, two distinct measures of cardiac index will be extracted. Firstly, a small neck sensor will be placed in proximity to the external jugular vein and then a pulse
Sponsors
University Hospital of Geneva
Eligibility
Sex/Gender
Female
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. 18 years old or older 2. Undergoing general anaesthesia for a planned gynaecological laparoscopic procedure that is expected to last more than 60 minutes (combined anaesthesia and surgical time) 3. Can understand and read French 4. American Society of Anesthesiologists (ASA) 1-3 status
Exclusion criteria
Exclusion criteria: 1. Body mass index (BMI) >35 kg/m² 2. Any condition limiting the use of VenArt CO (according to the user manual, e.g. very restricted neck anatomy, abnormalities in peripheral saturations, known allergy to adhesive products [skin sensor], central vein stenosis, Reynaud's disease, severe COPD) 3. Any condition limiting the feasibility of TTE 4. Unplanned surgery (emergency) 5. Aortic regurgitation 6. Laparoscopie vNOTES procedure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cardiac index values from the VenArt® CO device and transthoracic echocardiography measured simultaneously | — |
Secondary
| Measure | Time frame |
|---|---|
| Cardiac index over time during the intraoperative course between the VenArt® CO device and transthoracic echocardiography. CO measures will be recorded at five different timepoints: before induction of general anaesthesia, after induction, before surgery, after pneumoperitoneum and finally after reduction of pneumoperitoneum and table tilt). | — |
Countries
Switzerland
Contacts
Public ContactCatherine Paschoud
Outcome results
None listed