Effect of Remifentanil on Postoperative Cognition Function in Patients Undergoing Major Abdominal Surgery
- Conditions
- Patients Undergoing Major Abdominal SurgeryPostoperative Confusion
- Interventions
- Registration Number
- NCT01627873
- Lead Sponsor
- Catholic University of the Sacred Heart
- Brief Summary
The purpose of this study is to investigate the effects of two different analgesic methods (Fentanyl vs Remifentanil) during major abdominal surgery on postoperative cognitive status of patients.
- Detailed Description
The purpose of this study is to investigate the effects of two different analgesic methods (Fentanyl vs Remifentanil) during major abdominal surgery on postoperative cognitive status of patients. In particular, whether there is a correlation between type of anesthesia and the appearance of postoperative cognitive disorder (POCD), including type of anesthesia and levels of pro and anti inflammatory cytokines and investigate whether there is an association between presence or absence of POCD and cytokines levels
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 622
- Age over 60 years
- Patients undergoing major abdominal surgery, in General Anesthesia
- ASA class status I-III
- History of allergy to drugs used in the study
- Mini-Mental State Examination (MMSE) value < 26
- Expected duration of anesthesia less than 1 hour and more than 4 hours
- Presence of a cognitive disorder severity of overt such as to prevent collaboration of the patient
- Presence of severe electrolyte disturbances or not controlled bool glucose levels
- History of pain or cerebral vascular disease on the basis of significant carotid or cerebral artery stenosis, to be verified by scanning eco-color doppler
- Habitual use of tranquillizers or other drugs affecting the central nervous system
- Difficulties in the management of the airways, such as to make the necessary changes in anesthesia technique
- Severe hypotension or hypertension or other vascular disorders, particularly thrombotic events or bleeding during surgery or in the perioperative period
- Bleeding that requires blood transfusion
- Medication needs higher or lower than that indicated in the protocol to ensure the depth of hypnosis, indicated by values of BIS targets
- Refusal by the patient
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Remifentanyl Remifentanil In group A induction of anesthesia will be performed with Propofol (2mg/kg), Cisatracurium (0.15mg/kg)and continous infusion of Remifentanil (0.15mcg/kg/min).Anesthesia will be maintained by Sevoflurane with oxygen (Fi=40%)and air, with a MAC value to maintain BIS between 40 and 60. Intraoperative analgesia will be obtained with Remifentanil 0.15-0.25mcg/kg/min. Additional boluses of Cisatracurium (0.02mcg/kg)will be administered as needed during surgery. At the beginning of closure of the peritoneum bolus of morphine (0.1mg/kg)and acetaminophen 1g will be administered. Propofol and remifentanil infusions will be interrupted at the end of wound closure. Fentanyl Fentanyl In group B anesthesia will be induced by Propofol (2mg/kg), Fentanyl (2mcg/kg)and Cisatracurium (0.15mg/kg). Anesthesia will be maintained by Sevoflurane, oxygen (Fi=40%) and air and boluses of Fentanyl (50mcg). additional boluses of Cisatracurium (0.02mg/kg)will be administered as needed during surgery. At the beginning of closure of the peritoneum acetaminophen 1g will be administered.
- Primary Outcome Measures
Name Time Method Rey verbal memory test of words before and after major abdominal surgery participants will be followed the day before and after surgery and for the duration of hospital stay, an expected average of 5 days In test of Rey to the subject is presented for 5 times the same list of 15 bisyllabic words or trisillabic common use of which he must recall as many as possible within 1 minute; after about 15 minutes the patient, meanwhile distracted by the test , must again try to remember the greatest number possible without a further reading. The maximum possible score of the first phase of the test is an expression of the ability of short term memory of the subject, the result of the test is repeated at a distance of 15 minutes is indicative of its storage capacity, to intermediate term.
Stroop Test before and after surgery participants will be followed the day before and after surgery and for the duration of hospital stay, an expected average of 5 days In the Stroop Test patient is instructed to read a random sequence of adjectives "green", "red", "blue" written in black font, then he refers the colour of a succession of circumferences filled of the three colors above in random order; finally, another random succession of three words "green", "red", "blue" written in three characters of the same colors, but not associated with corresponding adjective. Number of errors that the subject does in reading is an indication of its ability to attention
- Secondary Outcome Measures
Name Time Method Quantitative determination of serum pro and anti inflammatory cytokines before and after surgery participants will be followed the day before and after surgery and for the duration of hospital stay, an expected average of 5 days Blood samples will be made for the quantitative determination of serum cytokines IL-1β, IL-6, IL-8, TNF-α, IL-10 and IL-12. Determinations will be given by Multiplex Elisa method.
Trial Locations
- Locations (1)
Policlinico Universitario "A.Gemelli"
🇮🇹Rome, Italy