TAVR-Highflow: High Flow Nasal Oxygen Cannula in Transcatheter Aortic Valve Replacement: Complications and Biomarkers
Study Details
Study Description
Brief Summary
Background Transcatheter aortic valve replacement is a risky procedure, performed in patients that can also be considered at risk of developing complications. The use of HFNO could be justified in this context and could improve the results and safety of these procedures. The use of HFNO during sedation for TAVR could increase oxygen content and minimise hypercapnia, which occurs frequently. This may have 2 potential benefits: one in terms of facilitating the patient's tolerance to anaesthetic sedation; and the other to optimise oxygen delivery to organs such as the brain, kidneys, and myocardium.
Primary aim The number of oxygen desaturation episodes. An oxygen desaturation episode is defined as any episode of Sp02 <93% for more than 10 seconds.
Method A single-center prospective randomised controlled clinical trial with 132 individuals comparing the use of High Flow Nasal oxygen (intervention group) with the conventional standard of care oxygenation with nasal cannula standard oxygenation (control group) of patients undergoing sedation for transfemoral TAVR. The randomisation process will be carried out with a 1:1 assignment, using the RedCap Clínic tool for this purpose. Both groups will be treated at the same centre and by the same interventional cardiology and anaesthesia team. Sedation regime will be based on Target controlled infusion (TCI) with propofol and remifentanil. Local anaesthesia will be infiltrated by interventional cardiologist prior obtaining femoral vascular access. 50 L/min with 0.6% FiO2 will be administered through a high-flow nasal cannula in the intervention group. In the control group, oxygen therapy will also be administered in all cases, using the usual procedure: oxygen therapy through a conventional nasal cannula and at a flow of 5 L/min.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Intervention In the intervention group, 50 L/min with 0.6 FiO2 will be administered through a high-flow nasal cannula. |
Device: High flow nasal oxygen
Use of High-flow nasal oxygen at 60% 50 L/min.
|
| No Intervention: Control In the control group, oxygen therapy will also be administered in all cases, using the usual procedure: oxygen therapy through a conventional nasal cannula and at a flow of 5 L/min |
Outcome Measures
Primary Outcome Measures
- The number of oxygen desaturation episodes. [up to 24 hours]
An oxygen desaturation episode is defined as any episode of Sp02 <93% more than 10 seconds
Secondary Outcome Measures
- Hypoxia [At placing the arterial catheter moment (baseline), and 45 minutes after the start of sedation]
PO2
- Hipercapnia [At placing the arterial catheter moment (baseline), and 45 minutes after the start of sedation]
PaCO2
- Trends in plasmatic enolase neurospecific [the day before the procedure (baseline), 45 minutes, and 8 hours after the start of sedation.]
Study of plasmatic biomarkers of ischaemic damage in brain with Enolase neurospecific
- Trends in plasmatic Biomarkers of kidney injury [the day before the procedure (baseline), 45 minutes, and 8 hours after the start of sedation.]
Study of plasmatic biomarkers of ischaemic damage in kidney with creatinine
- Trends in plasmatic Biomarkers of myocardial injury [the day before the procedure (baseline), 45 minutes, and 8 hours after the start of sedation.]
Study of plasmatic biomarkers of ischaemic damage in myocardium with troponin and pro-BNP
- Respiratory depression [During the TAVI procedure]
Number of respiratory depression episodes requiring manual ventilation.
Eligibility Criteria
Criteria
Inclusion Criteria:
- All patients >18 years of age undergoing transfemoral TAVR procedure under local anaesthesia and sedation consenting to participate in the study
Exclusion Criteria:
- <18 years and/or refusal to give informed consent for participation General anaesthesia required to perform complex cases of TAVR
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Hospital Clinic of Barcelona
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HCB/2022/1095