T-IL-Co-ReCa: Anesthetic Technique on Immune Response in Colorectal Cancer
Study Details
Study Description
Brief Summary
Knowing the fact that the anesthetic substances can alter the immune response during the surgery, the purpose of the study is to evaluate the influence of two general anesthetic techniques - inhalation vs. total intravenous anesthesia on the immune response in patient with colorectal surgery for neoplastic disease, evaluated by the plasma level of the interleukins 6 and 10(IL6, IL10).
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Introduction
Several factors are contributing to perioperative immunosuppression such as: surgery itself, general anesthesia. In vivo and in vitro studies have shown that anesthesia itself may alter the immune response either by direct effect on immune cells (such as natural killer and T helper) ) or indirectly by the influence of anesthetic substances on pro (IL-1, IL-6, tumor necrosis factor alpha ) and anti-inflammatory ( IL-4, IL-10) cytokines release.
The study aims to evaluate the influence of two general anesthetic techniques inhalation versus total intravenous anesthesia- target controlled infusion (TIVA-TCI) on the immune response in patient with colorectal surgery for neoplastic disease, evaluated by the plasma level of the interleukins IL6, IL10.
Study group:
- patients admitted to the Surgical Clinic of the Regional Institute of Gastroenterology and Hepatology Prof Dr Octavian Fodor, undergoing open surgery for colorectal cancer (right/left colectomy, colorectal resection).
After obtaining written informed consent 70 ASA physical status I-III patients scheduled for colorectal cancer resection are randomly allocated to 2 groups of study by computer randomization:
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group I, TIVA-TCI (n=35 patient) receive total intravenous-target controlled infusion anesthesia with propofol and remifentanil
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group II (ISOFLURANE) (n=35 patients) receive inhalatory anesthesia with isoflurane and remifentanil
Methods:
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Premedication with midazolam 7.5 mg orally 30 min before surgery in all patients.
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On arrival in the operating room a venous cannula is inserted and a blood sample for interleukin measurement is performed. This cannula is designated for fluid administration during anesthesia and for blood sampling for subsequent interleukin measurements. A second cannula is inserted for the administration of anesthetic substances.
In group I (TIVA-TCI):
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anesthesia is induced with a target-controlled infusion (TCI) of propofol with an initial target plasma concentration (Cp) of 4 micrograms/ml (modified Marsh model)( Base Primea™, Fresenius, France), adjusted in steps 0.2 micrograms/ml to maintain the BIS values between 40-55 during surgery.
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propofol infusion stops at the end of surgery before the last 2 stitches.
In group II (ISOFLURANE):
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anesthesia is induced with propofol bolus 1,5-2 mg/kg.
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maintenance of anesthesia is achieved with isoflurane 1-1.5 MAC in order to maintain the BIS value between the values of 40-55.
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isoflurane administration cease before the last 2 stitches.
In both groups:
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remifentanil TCI mode (Minto model) (Base Primea™, Fresenius, France) is used for analgesia, with an initial Cp of remifentanil set at 4 ng/ml at induction, and a Cp between 3-8 ng/mL during maintenance(increments of 0.5 ng/ml) depending on the painful moments of surgery and the patient's analgesic needs assessed by changes in heart rate, blood pressure (more than 20% of the previous value of induction), sweating, tearing.
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remifentanil infusion ceases after suturing the wound.
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muscle relaxation is achieved with atracurium, 0.5-0.6 mg/kg at induction, and further maintained on top up doses as needed. At the end of surgery the residual neuromuscular blockade is reversed with atropine 0.02mg/kg and neostigmine 0.0 5mg/kg.
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the lungs are ventilated with an air/oxygen mixture.
Postoperative analgesia:
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morphine patient controlled analgesia(PCA ) with boluses of 1 mg to 5 min interval to maintain the VAS ˂ 4 on 10-point visual analogue scale (VAS). The first dose of morphine 0.1 mg/kg is administered 40 minutes before completing the surgery.
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in addition to morphine, is given paracetamol intravenous, 1g every 8 hours. The first dose of paracetamol is administered intra-operatively before the end of surgery.
Monitoring:
- Intraoperative:
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ASA basic monitoring: continuous monitoring ECG, heart rate (HR), arterial blood pressure (BP), pulse oximetry (SpO2), CO2 concentration in expired gases (Et CO2), concentration of isoflurane in exhaled gases (Et Iso), minimum alveolar concentration (MAC) of isoflurane, and core temperature.
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depth of anesthesia - bispectral index (BIS) (BIS Vista -Aspect Medical System, USA).
Systolic, diastolic blood pressure and HR are recorded every minute at induction time and every 5 minutes after endotracheal intubation, until the end of surgery.
Hypotension (defined as a decrease of mean arterial blood pressure by over 20% of baseline values) is treated with higher rate of infusion solutions and intravenous boluses of ephedrine 5 mg.
Inadequate anesthesia (hypertension, tachycardia, lacrimation, sweating) is treated by adjusting the remifentanil infusion as previously mentioned.
- Postoperative:
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opioid analgesic requirement in the first 24 hours
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pain score on the visual analog scale (VAS 0-10)in the first 24 hour
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incidence of postoperative nausea and vomiting episodes requiring the administration of antiemetic drug (metoclopramide 20 mg or ondansetron 4 mg)
Blood sampling to determine interleukins IL6 , IL10 plasma levels are drawn at the following moments:
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T0- before the induction of anesthesia (venous cannula insertion time)
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T1- after induction but before starting surgery:
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in group I (TIVA -TCI) when the plasma concentration of propofol is 3-3.5 micrograms/ml
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in group II (ISOFLURANE) when concentration of isoflurane in exhaled air (Et Isoflurane) is between 0.3-0.5%
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T2, T3 - at 2 and 24 hours after surgery
The collected blood samples are centrifuged at 2500 rpm / min for 10 minutes and the resulting plasma is stored at -70 ° C until the interleukins assay is performed.
If intraoperatively is revealed local extension of colorectal cancer (tumor invades adjacent organs) or distant metastasis the patient is excluded from the study.
Data collection is done longitudinally prospective, for each patient the following variable are registered:
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quantitative: - weight, plasmatic or brain concentration of the anesthetics used in TIVA-TCI mode, BIS value, plasmatic concentration of the interleukins on 4 intra- and post-operatory moments, the duration of the surgery and anesthesia, number of episodes of nausea and vomiting, opioid analgesic requirement.
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qualitative: ASA score, sex, post-operatory pain score (VAS) Collected data are introduced in a database using the Excel Office programme.
The statistical analysis will be performed using the SPSS 16.0 software (SPSS Inc Chicago, IL, USA). Quantitative variables will be expressed as mean ± SD, and qualitative variables as absolute and relative frequencies. Given multiple measurements at different time intervals, area under curve (AUC) is calculated for each IL and the results will be compared between groups.A p less 0.05 will be considered significant.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Group 1 - TIVA-TCI include 35 patients with colorectal cancer undergoing surgery anaesthesia is induced and maintained with total intravenous target-controlled infusion ( TIVA-TCI) of propofol and remifentanil. for propofol initial target plasma concentration (Cp) is set to 4 micrograms/ml (modified Marsh model)( Base Primea™, Fresenius, France) and then adjusted in steps 0.2 micrograms/ml to maintain the BIS values between 40-55 during surgery. for Remifentanil initial Cp is set at induction at 4 ng/ml and then the Cp is maintained between 3-8 ng/mL(increments of 0.5 ng/ml in case of inadequate anesthesia). intervention:blood sampling for IL measurement |
Other: blood sampling for IL measurement
Blood sampling to determine interleukins IL6 , IL10 plasma levels are drawn at the following moments:
T0- before the induction of anesthesia (venous cannula insertion time)
T1- after induction but before starting surgery
In the group I (TIVA -TCI) when the plasma concentration of propofol is 3-3.5 ng/ml
In group II (ISOFLURANE) when concentration of isoflurane in exhaled air (Et Isoflurane) is between 0.3-0.5%
T2, T3- at 2 and 24 hours after surgery
|
| Group II- ISOFLURANE include 35 patients with colorectal cancer undergoing surgery anesthesia is induced with propofol bolus 1,5-2 mg/kg and remifentanil TCI mode (Minto model) (Base Primea™, Fresenius, France) with an initial Cp 4 ng/ml maintenance of anesthesia is achieved with isoflurane 1-1.5 MAC in order to maintain the BIS value between the values of 40-55 and remifentanil TCI with Cp between 3-8 ng/mL (increments of 0.5 ng/ml in case of inadequate anesthesia) intervention:blood sampling for IL measurement |
Other: blood sampling for IL measurement
Blood sampling to determine interleukins IL6 , IL10 plasma levels are drawn at the following moments:
T0- before the induction of anesthesia (venous cannula insertion time)
T1- after induction but before starting surgery
In the group I (TIVA -TCI) when the plasma concentration of propofol is 3-3.5 ng/ml
In group II (ISOFLURANE) when concentration of isoflurane in exhaled air (Et Isoflurane) is between 0.3-0.5%
T2, T3- at 2 and 24 hours after surgery
|
Outcome Measures
Primary Outcome Measures
- measurement of interleukins IL6 and IL 10 plasmatic level [-before anesthesia induction (T0 time)]
-once the intravenous cannula is inserted
- measurement of interleukins IL6, IL10 plasmatic level [after anesthesia induction but before surgical incision (T1)]
in group I (TIVA-TCI) when plasma concentration of propofol is 3-3.5 micrograms/ml in group II (ISOFLURANE) when concentration of isoflurane in exhaled gases (Et iso) is between 0.3-0.5 %
- measurement of interleukins IL6 and IL10 plasmatic level [2 hours postoperatively (T2)]
- measurement of interleukins IL6 and IL 10 plasmatic level [24 hours postoperatively (T3)]
Secondary Outcome Measures
- total opioid analgesic dose (mg) [for the first 24 hours postoperatively]
Other Outcome Measures
- Pain score on the visual analog scale (VAS 0-10) [for the first 24 hour postoperatively]
at 15, 30 minutes post surgery 6, 12, 18, 24 hours postoperatively
- incidence of postoperative nausea and vomiting episodes requiring antiemetic medication [for the 24 hours postoperatively]
- total opioid dose of remifentanil (mg ) used during surgery [an average 3 hours]
total dose (mg) of remifentanil administered in TCI mode during surgery
Eligibility Criteria
Criteria
Inclusion Criteria:
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patients over 18 years with ASA physical status I-III.
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colorectal cancer patients with no sign of local invasion (adjacent organs) and distant metastasis revealed by imaging studies
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surgery performed by the same surgical team
Exclusion Criteria:
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ASA physical status IV patients
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hepatic and renal impairment
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diabetes or other endocrine disorders
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obesity (BMI 30 kg/m2)
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immune disorders or immunosuppressive therapy
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steroid treatment in the last 6 months
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asthma
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Medicine and Pharmacy Iuliu Hatieganu; Regional Institute of Gastroenterology and Hepatology Prof Dr Octavian Fodor | Cluj Napoca | Romania | 400162 |
Sponsors and Collaborators
- Iuliu Hatieganu University of Medicine and Pharmacy
Investigators
- Principal Investigator: Simona C Margarit, lecturer, University of Medicine and Pharmacy Iuliu Hatieganu
Study Documents (Full-Text)
None provided.More Information
Publications
- TICC