Evaluation of Closed-loop TIVA Propofol, Sufentanil and Ketamine Guided by BIS Monitor

Acute Cholecystitis Clinical Trial

Official title: Evaluation of Closed-loop Titration of the Intravenous Anesthetic Propofol, Sufentanil and Ketamine Guided by BIS Monitor

Status Completed

Clinical Trial Summary

The purpose of this study is to compare a closed-loop intravenous anesthetic using Bispectral Index as a feedback loop and a controller based on reinforcement learning to titrate dose and intravenous anesthetic that is manually controlled or a standard volatile anesthetic agent titrated by the anesthesiologist to determine improvement in the following parameters as compared to controls: time to discharge from the Post Anesthesia Care Unit, post-operative nausea and vomiting, pain scores and sedation scores.

Clinical Trial Description

Recent efforts have focused on the development of new software systems that are able to directly titrate anesthesia based on activity of the brain (EEG) as a feedback mechanism . Brain activity is used to measure the effect of anesthetic medications (anesthetic "depth"), which can vary from person to person despite being given the same amount of medication. There is a potential for new systems to considerably improve anesthetic control by using methods that are able to adapt to the constant input of brain activity. The purpose of this study is to compare a closed -loop intravenous anesthetic (TIVA) using BIS (Bispectral Index) as a feedback loop and a controller based on reinforcement learning to titrate dose and TIVA that is manually controlled or a standard volatile anesthetic agent titrated by the anesthesiologist.

Propofol is the most frequently applied hypnotic-anesthetic IV drug during anesthesia. In "open-loop" controlled propofol administration during anesthesia, initial dosing guidelines are based on the typical subject, without taking into account the large inter-individual variability. To manage this variability, most clinicians will start by giving a standard dose, observes the therapeutic effect and will adapt the dose regimen. Although, "open-loop" drug administration is clinically "standard-of-care", the efficiency of this decision process highly depends on the expertise of the clinician, is very time consuming and might result in a suboptimal therapy.

The study will be using patient with acute cholecystitis scheduled for laparoscopic cholecystectomy surgery and the inclusion/exclusion criteria is described in the appropriate sections. Potential subjects will be identified prior to their surgery based on meeting the inclusion/exclusion criteria. The subject will be approached in the inpatient unit or pre-operative holding area, a private area where curtains can be drawn to maintain privacy. This is a place where patients are routinely examined and consented prior to surgery.. The subject will be informed that participation or a lack of participation in the study does not influence their treatment in any way. The subject will be informed that if they give consent for participation in the study that they may withdraw consent at any time before performance of the study. This withdrawal of consent may be given to the investigator in oral or written form.

The Investigator will explain the study to the potential subject verbally, providing all pertinent information (purpose, procedures, risks, benefits, alternatives to participation, etc.), and allow the potential subject ample opportunity to ask questions. Following this verbal explanation, the potential subject will be provided with a written consent form and given at least one hour to consider whether or not to participate in the research. After allowing the potential subject time to read the consent form, an Investigator listed on the consent form will meet with the potential subject and answer any additional questions she/he may have.

The subject will have been pre randomized to a study arm (Permuted block randomisation via computer generated numbers) and will not be informed which study arm. The three study arms are RL-TIVA (experimental), Manual TIVA, and INH-Sevo.

Premedication and Induction: Premedication with up to 0.05mg/kg IV midazolam

Prior to arrival in the operating room, a peripheral intravenous line will be inserted in a large forearm vein in all patients and 500 ml of saline will be infused. This is required to administer drugs and fluids during anesthesia and is routinely done in all patients. On arrival in the operating room, vital signs (heart rate, non-invasive blood pressure, blood oxygen saturation and end-tidal CO2) will be measured in all patients (standard of care during anesthesia). The RL-TIVA group will also have a non-traumatic, commercially available unilateral BIS electrode applied at the patient's forehead. This EEG sensor will be connected to the BIS (Covidien, Mansfield, MA, USA) monitor to calculate the BIS.

All patients will undergo a standard IV induction using:

1mg/kg 1% lidocaine up to maximum of 100mg 100mcg fentanyl 2mg/kg propofol up to maximum of 200mg 0.6mg/kg rocuronium

Patients will be randomly allocated to standard volatile based anesthesia or BIS-guided intravenous anesthesia administration. The protocol for each of the study arms is as follows:

-RL-TIVA: Propofol, ketamine and sufentanil (PKS) administration will be done via a three way stop cock connected directly to the IV catheter to minimize dead space volume. PKS solution will contain total of 50ml. Propofol 10mg/ml, Ketamine 1mg/ml (will be omitted in subsequent preparations after first 50ml), Sufentanil 0.25 mcg-ml. Drug will be administered using a Harvard 33 syringe pump (The Harvard 33 Syringe pump has been used in human trials in prior study at Stanford that is pending publication). This pump will be connected via a RS 232 interface to the study computer running RL (reinforcement learning) control software. This software platform collects real time vital signs and BIS values and steer the target controlled infusion pumps and the closed-loop controllers.

Baseline vital signs, including BIS will be recorded for 2 minutes. During induction until 5 minutes after intubation, NIBP will be measured every minute. Thereafter, NIBP will be measured at least every 3 minutes until the end of the case. The start of the baseline measures will be considered as the "START CASE" moment.

IV anesthetic administration will start using the closed-loop system by setting the BIS target at 45.

When required, optimization of the patients' positioning, disinfection and draping will ensue. When ready, surgery will start.

During surgery, anesthesia will be maintained by propofol-ketamine-sufentanil via closed-loop at a BIS target of 45.

• Manual TIVA: Manually titrated IV anesthetics are routinely done in the operating room as an alternative to inhalational anesthetics. Propofol, ketamine and sufentanil (PKS) administration will be done via a three way stop cock connected directly to the IV catheter to minimize dead space volume. PKS solution will contain total of 50ml. Propofol 10mg/ml, Ketamine 1mg/ml (will be omitted in subsequent preparations after first 50ml), Sufentanil 0.25 mcg-ml. Drug will be administered using an Alaris infusion pump titrated by the anesthesiologist based on blood pressure and heart-rate as is traditionally done and is standard of care with intravenous anesthetics.

• INH-Sevo: After the patient is intubated Sevoflurane will be started and titrated to between 0.8 and 1.5 MAC by the anesthesiologist. At end of surgery, as defined by placement of surgical dressing, volatile anesthetic will be discontinued.

Wake up protocol will be the same for all three arms. Normocapnia will be maintained during recovery by mechanical ventilation till spontaneous breathing is resumed. No decrease in the Minute Ventilation is allowed during recovery. Moment of return of spontaneous breathing will be recorded. Once spontaneous breathing is returned, patients will be asked by their name to open their mouth. A positive response will be recorded and the trachea will be extubated. Thereafter, patients will be transferred to the PACU. The parameters listed in the appropriate section will be evaluated.

Data Collection: Subject data will be kept in 3 specific locations. A hard copy print out will be maintained in a folder that will contain the eligibility criteria, consent form, and source document. This will be stored in a locked file cabinet with limited access to the PI and Co-Investigators. The electronic data will be stored on an encrypted flash drive kept in the locked file cabinet and will be backed up on a secure encrypted Network folder that only the PI and Co-Investigators will have authorization to access.

Statistical Analysis: A power analysis of the previously reported Stanford human volunteer study data was performed in order to estimate appropriate sample sizes. To estimate "worst-case" conditions, the measured parameter demonstrating greatest variation, MDPE, was selected. Assuming comparison with a two-sample, two-tailed t-test and a p-value of 0.05, a single-group sample size of 25 produced statistical power values of ~1.0. Given this size, we can detect a 10% difference in MDPE under standard deviations of up to 7 and still maintain power values > 0.85; thus, we selected n=25 for each of the three study groups, yielding a total sample size of 75. We acknowledge that this sample size might prove to be over-powered; however, intraoperative study is known to be challenging. For example, all of the measured variables should not be expected to demonstrate normal distributions (a critical assumption in the above power analysis), and we anticipate limited occurrence of confounding influences, such as protocol deviations and interruptions in data collection. Given the vagaries of intraoperative study, the chosen sample size of 75 patients seems reasonable.

Descriptive statistics Categorical data:, sex, age, weight, height, induction times, times to accurate control (time to reach target, overshoot in BIS), % of time for accurate control and hemodynamic stability, recovery times, nausea, vomiting, sedation score, pain score, and drug concentrations. Closed-loop control performance data (see below).

Continuous variables: BIS, heart rate, blood pressure, saturation, EtCO2 Univariate analysis, Student's t-test or Mann-Whitney U-test will be used will be used to compare numerical data and performance parameters.

Chi-squared will be used to analyse qualitative data. RMANOVA will be used to analyze the continuous data.

Safety: An anesthesiologist or resident will be present for the entire duration of the anesthetic as is standard of care. If at any time there is hardware or software failure, the infusion can be disconnected and conventional volatile anesthetic can be rapidly instituted. LIMITS OF THE CLOSED-LOOP (safety) : In the closed-loop control software, safety limits have been installed.

Procedure for Analysis and Interpretation of the Safety Data: The monitoring entity will be Benjamin Wallisch, MD. He will oversee the research participant's safety, monitor for unanticipated problems involving risks to participants or others, and assure that such events are reported to the IRB. Integrity and appropriate handling (confidentiality) of the following data will be monitored: Demographic and morphometrics data, vital signs, bispectral (BIS) index values, infusion pump flow rate, and recording of occurrence and severity of drug side effects. Monitoring will occur after every study patient is enrolled. Should unexpected adverse events occur. All effort will be made to identify the source causing the event. Source identification may mandate the temporary halting of the study as well as protocol adjustments (e.g. reduction of drug doses). Serious adverse events will be reported by Benjamin Wallisch, MD within 2 business days. Serious adverse events will be brought to the attention of the IRB within 24 hours.

Deviations to the study protocol or adverse events will be addressed by the IRB protocol. A log will be kept of Adverse events and Protocol Deviation kept on the encrypted flash drive and backed up on the encrypted network drive. The reporting of events will be as above stated.

An annual progress report will be submitted to the IRB for review. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

• Acute Cholecystitis
• Cholecystitis
• Cholecystitis, Acute
• Chronic Cholecystitis

• NCT number: NCT01942356
• Study type: Interventional
• Source: The University of Texas Health Science Center at San Antonio
• Status: Completed
• Phase: N/A
• Start date: September 2013
• Completion date: August 2014