The Effect of Different End-tidal Carbon-dioxide Levels on Cerebral CO2 Vasoreactivity and the Stiffness of Systemic Arteries During Propofol Anesthesia
Information source: University of Debrecen
ClinicalTrials.gov processed this data on August 20, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Propofol-anaesthesia Via Target-controlled Infusion
Intervention: Partial pressure of CO2 at the end of an exhaled breath (Procedure); Propofol (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: University of Debrecen Official(s) and/or principal investigator(s): Csilla Molnár, MD, PhD, Principal Investigator, Affiliation: University of Debrecen Medical and Health Science Center Department of Anesthesiology and Intensive Care 4032-Debrecen, Nagyerdei krt 98. Hungary Tel/fax: +36-52-255-347
Overall contact: Csilla Molnár, MD, PhD, Phone: +36-30-299-8097, Email: csmolnar@med.unideb.hu
Summary
Purpose:
The purpose of this study is to examine the effect of different carbon-dioxide
concentrations on cerebral CO2 sensitivity and the resistance and stiffness of systemic
arteries during anesthesia with target-controlled infusion anesthesia using intravenous
propofol. Propofol is a widely and commonly used intravenous anaesthetic, that is mainly
used for the induction of general anesthesia and the maintenance of total intravenous
anaesthesia (TIVA).
Changes in the velocity of cerebral blood flow and arterial stiffness due to the different
exhaled carbon-dioxide concentrations will allow us to conclude how propofol affects these
parameters during the course of the narcosis.
Instruments:
An ultrasound device called transcranial doppler (TCD) is used to measure the velocity of
blood flow within a main artery located inside the skull.
A tonometry device named SphygmoCor is used to assess the pressure wave proceeding in the
radial artery, from which the stiffness of the systemic vessels can be concluded.
Measurements:
- Examinations with the ultrasound and tonometry devices are carried out once before the
operation, three times during the intervention, with different exhaled CO2 values and once
after the operation is completed.
Hypothesis:
- Propofol alters cerebral carbon-dioxide sensitivity and the stiffness of systemic arteries
during TCI anaesthesia.
Clinical Details
Official title: The Effect of Different End-tidal Carbon-dioxide Levels on Cerebral CO2 Vasoreactivity and the Stiffness of Systemic Arteries During Propofol Anesthesia
Study design: Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
Primary outcome: Blood flow velocity in the middle cerebral artery
Secondary outcome: Arterial wall stiffness of the radial arteryChanges in the central systolic and diastolic blood pressure
Detailed description:
Study protocol:
- The study is conducted in four stages: in the first stage, measurements are performed
preoperatively in awake patients. Patients are placed in supine position and mean arterial
blood pressure (MAP), heart rate, oxygen saturation are measured. The transcranial doppler
(TCD) probe is fixed in place by applying a headband to maintain a constant angle of
insonation. Mean blood flow velocity (MBFV) and pulsatility index (PI) in the middle
cerebral artery (MCA) are obtained. MCA is insonated through the right temporal window by
using pulsed 2 megahertz TCD ultrasound probe. Identification of the MCA is confirmed by
using standard criteria, at a depth of 45-55 mm. Cerebral CO2 vasoreactivity is calculated
as the percentage change in MBFV or PI for mmHg change in end-tidal CO2 (ETCO2).
SphygmoCor is placed on the left radial artery to obtain data about the central aortic blood
pressure, augmentation pressure (AP) and augmentation index normalised to a 75 beat per
minute heart rate (Alx75). From the derived aortic pulse, calculations can be made, using
the area under the systolic and diastolic part of the curve, to determine the heart's ratio
of oxygen supply and demand, it is called the subendocardial viability ratio (SEVR).
As part of the premedication each patient receives 100 mg diclofenac per os 30 minutes and
500 ml Lactated-Ringer infusion 60 minutes prior to the operation.
Anesthesia is induced and maintained with target-controlled infusion anesthesia (TCI) using
intravenous propofol at 4 mcg/ml constant plasma concentration. Analgesia is provided by
using 2 ug/kg sufentanyl bolus dose at the time of induction. Afterwards 0. 6 mg/kg
rocuronium is given for muscle paralysis and subsequently patients were intubated with a
suitable intratracheal tube. After induction of anaesthesia, the patients are placed on a
mechanical ventilation system, using a volume-controlled setting with an air and oxygen
mixture set to 0. 4 fraction of inspired oxygen (FiO2) , the fresh gas flow rate to 2 l/min.
.
Differences in the depth of anesthesia could influence cerebral activity, thereby cerebral
metabolism and blood flow. Bispectral index is placed onto every patient in order to assure
constant depth of anaesthesia during the intervention.
The second series of TCD and SphygmoCor measurements are performed 20 minutes after the
respiratory rate is set to maintain end-tidal CO2 at 40 mmHg in order to allow sufficient
time for equilibrium to be reached and the effect of drugs used for the induction of
anesthesia to be terminated. Subsequently the examinations are repeated twice again at 35
and 30 mmHg ETCO2. The measurements were carried out 5-5 minutes after adjusting the minute
ventilation to reach target ETCO2 values.
Statistical methods:
- Comparisons between the preoperative and three intraoperative stages of the study are made
using repeated measures ANOVA with the Bonferroni post hoc correction. The relationship
between MBFV, PI and ETCO2 is assessed using linear regression, while the connection between
SEVR, pulse and Alx75 is calculated with bivariate correlation.
Eligibility
Minimum age: 18 Years.
Maximum age: 50 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Above the age 18
- American Society of Anesthesiologists (ASA) physical classification I. or II.
- Patients undergoing elective varicotomy, inguinal hernioplasty or breast surgery in
general anesthesia
Exclusion Criteria:
- Patients with cerebral, cardiac or systemic vascular disorders (hypertension,
diabetes)
- Patients receiving medication that affects the blood vessels (antihypertensive,
antidiabetic, antiarrhythmic medications)
Locations and Contacts
Csilla Molnár, MD, PhD, Phone: +36-30-299-8097, Email: csmolnar@med.unideb.hu
University of Debrecen Medical and Health Science Center Department of Anesthesiology and Intensive Care, Debrecen 4032, Hungary; Recruiting Erzsébet Igbonu-Nagy, Phone: +36-20-399-1551, Email: nagyboske@yahoo.com Marianna Juhász, MD, Principal Investigator Levente Molnár, MD, Sub-Investigator
Additional Information
Starting date: January 2014
Last updated: July 25, 2014
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