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Conscious Sedation for Transcatheter Aortic Valve Implantation

Not Applicable
Recruiting
Conditions
Postoperative Delirium
Satisfaction
Adverse Event
Death
Renal Function Disorder
Interventions
Drug: Continuous infusion of propofol
Registration Number
NCT05462938
Lead Sponsor
University of Ioannina
Brief Summary

Aortic valve stenosis is the heart valve disease with the highest prevalence among the elderly, and may lead to heart failure. Until recently, the only definitive treatment was surgical replacement (SAVR). However, the increased risk associated with the surgical procedure excluded patients with multiple co-morbidities. As the population is aging and more and more patients may present with aortic stenosis, the need of a less invasive approach has emerged. Transcatheter Aortic Valve Replacement (TAVR) offered an alternative therapy for these high risk patients. This new method has seen worldwide acceptance, has been proven very beneficial for these patients, and therefore its indications have been expanded to intermediate risk patients, as well. Until recently, general anesthesia was the primary anesthetic technique for TAVR, but conscious sedation or monitored anesthesia care (MAC) is gaining more and more popularity lately. Our knowledge regarding the comparison between general anesthesia and MAC in TAVR procedures is derived mainly from observational studies and few randomized trials. MAC seems to be associated with less inotropic drug usage, shorter procedural times, shorter intensive care unit (ICU) and hospital length of stay. However, according to published data, there were no differences in 30-day mortality and complications between these two techniques.

Even less are known about the most suitable anesthetic agent for MAC during TAVR. Many drugs have been used, with propofol and dexmedetomidine being the most popular. However, there are only few comparative studies and their results are not conclusive.

This study compares MAC under propofol and MAC under dexmedetomidine for TAVR in order to examine which method of conscious sedation comes with more beneficial postoperative outcomes for the patients.

Detailed Description

Aortic valve stenosis is the most common heart valve disease among the elderly, and eventually may lead to heart failure. Its surgical replacement (SAVR) was the only definitive treatment, but this operation is considered to be of increased risk for morbidity and mortality. Also, there is a growing number of elderly with severe co-morbidities, who are considered as high risk patients, that cannot undergo such an operation. Transcatheter Aortic Valve Replacement (TAVR) offered an alternative method of treatment for these patients. Furthermore, its indications were expanded to intermediate risk patients due to its advantages over SAVR.

At first, general anesthesia was the most popular anesthetic method for TAVR. However, conscious sedation and Monitored Anesthesia Care (MAC) have emerged as advantageous alternatives, in terms of inotropic drug usage, procedural times, intensive care unit (ICU) and hospital length of stay. However, few data exist about the anesthetic agents that are most suitable for TAVR under MAC, with propofol and dexmedetomidine being the most popular of them.

This is a prospective comparative study of propofol versus dexmedetomidine used for MAC in TAVR procedures. The patients will be randomly allocated into two groups and will be sedated by continuous infusion of either propofol or dexmedetomidine during the TAVR procedure. These two groups will be assessed for the overall quality of the sedation method, the clinical outcomes, the adverse events and the duration of hospitalization. At the preoperative evaluation, detailed patients' medical history will be taken, their comorbidities, physique, heart echocardiography measurements, level of frailty, renal function and neurocognitive level will be assessed and recorded and, finally, signed consent will be obtained.

During the procedure, the depth of sedation will be monitored with the use of Patient State Index (PSI) and the fluctuation of arterial pressure, heart rate, and oxygen saturation, the administration of vasoactive agents and fluids, apnea episodes and diuresis will be also recorded. By the end of the procedure, the volume and type of contrast agent used, the type of the implanted valve and the duration of both the sedation and the operation will be documented. Throughout their hospitalization, adverse events, renal function and neurocognitive level will be recorded, along with the occurrence of postoperative delirium. After patients' discharge, their duration of hospitalization, both in cardiac intensive care unit and cardiology clinic will be recorded. Follow up of the patients will be completed after thirty days. All-cause mortality will be assessed at this point and there will be a detailed recording of any adverse events and/or re-hospitalization along with long-term assessment of renal and cognitive function.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Patients scheduled for TAVR
Exclusion Criteria
  • Emergency operation
  • Pre-existing neurocognitive dysfunction (Mini Mental State Examination score <23)
  • Inability to cooparate - communicate
  • End Stage Renal Disease
  • Allergy to any of the administrated drugs
  • No consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Propofol groupContinuous infusion of propofolContinuous infusion of propofol
Dexmedetomidine groupContinuous infusion of dexmedetomidineContinuous infusion of dexmedetomidine
Primary Outcome Measures
NameTimeMethod
Change of serum creatinine from baselineUp to 30 days

Assessment of renal function by serial measurements of serum creatinine (mg/dL) at four different time points (at baseline, at 24 hours, at 48 hours and at 30 days postoperatively).

Change of serum cystatin C from baselineUp to 30 days

Assessment of renal function by serial measurements of serum cystatin C (mg/l) at four different time points (at baseline, at 24 hours, at 48 hours and at 30 days postoperatively).

Change of glomerular filtration rate (GFR) from baseline using the Cockcoft-Gault equationUp to 30 days

Assessment of renal function by serial calculations of GFR (ml/min) at four different time points (at baseline, at 24 hours, at 48 hours and at 30 days postoperatively) using the Cockcoft-Gault equation.

Change of glomerular filtration rate (GFR) from baseline using the MDRD equationUp to 30 days

Assessment of renal function by serial calculations of GFR (ml/min) at four different time points (at baseline, at 24 hours, at 48 hours and at 30 days postoperatively) using the MDMR equation.

Postoperative dellirium48 hours

Recording of postoperative delirium using the Confusion Assessment Method (CAM) score.

Change of blood urea nitrogen (BUN) from baselineUp to 30 days

Assessment of renal function by serial measurements of BUN (mg/dL) at four different time points (at baseline, at 24 hours, at 48 hours and at 30 days postoperatively).

Secondary Outcome Measures
NameTimeMethod
Neurocognitive levelUp to 48 hours

Assessment of neurocognitive function of the patient with the use of the mini mental state examination (MMSE) score.

Vasoactive and inotropic agentsIntraoperatively

The usage of norepinephrine, epinephrine, phenylephrine, ephedrine, nitroglycerin, atropine, or other relevant agents will be recorded as the cumulative dosage of each administered during the procedure.

StrokeUp to 30 days

The occurrence of stroke after the procedure will be assessed as a binary outcome variable (yes/no).

Myocardial infractionUp to 30 days

The occurrence of myocardial infraction after the procedure will be assessed as a binary outcome variable (yes/no).

DeathUp to 30 days

The occurence of death

Acute heart failureUp to 30 days

The occurrence of acute heart failure after the procedure will be assessed as a binary outcome variable (yes/no).

Cardiologist satisfaction24 hours

The satisfaction of the interventional cardiologists performing the procedure will be assessed by the Likert satisfaction scale.

AwarenessUp to 30 days

Occurrence of intraoperative awareness of the patient will be assessed using the Michigan Awareness Classification Instrument.

Life threatening arrythmiasUp to 30 days

The occurrence of life threatening arrythmias after the procedure will be assessed as a binary outcome variable (yes/no).

RehospitalizationUp to 30 days

The occurrence of rehospitalization will be assessed as a binary outcome variable (yes/no).

Pain intensityUp to 48 hours

Pain intensity will be recorded using the numerical rating scale (NRS).

HeadacheUp to 48 hours

The occurrence of headache after the procedure will be assessed as a binary outcome variable (yes/no)

Nausea/vomitingUp to 48 hours

The occurrence of nausea/vomiting after the procedure will be assessed by a 5-point scale (0 to 4, with 4 indicating the worse outcome).

PruritusUp to 48 hours

The occurrence of pruritus after the procedure will be assessed by an 11-point scale (0 to 10, with 10 indicating the worse outcome).

HypoxemiaUp to 48 hours

The occurrence of hypoxemia after the procedure will be assessed by continuous monitoring of oxygen level (SpO2).

Duration of sedationIntraoperatively

The duration of sedation is defined as the time (minutes) from the start of the sedative agent administration to patient recovery (alert and able to communicate).

Procedural timeIntraoperatively

Procedural time is defined as the time (minutes) from the start of the procedure to last suture.

Rapid pacing timeIntraoperatively

Rapid pacing time is defined as the cumulative time (seconds) of rapid ventricular pacing performed during the procedure.

ICU length of stayPostoperatively and up to 30 days

The cumulative length of stay in the cardiac intensive care unit (days) after the procedure.

Length of stayPostoperatively and up to 30 days

The cumulative length of stay in the ward (days) after the procedure.

Patient satisfaction24 hours

Patient satisfaction will be assessed using the Likert satisfaction scale.

Trial Locations

Locations (1)

Univesity Hospital of Ioannina

🇬🇷

Ioannina, Epirus, Greece

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