The Influence of Postoperative Analgesia on Systemic Inflammatory Response and POCD After Femoral Fractures Surgery
Postoperative Cognitive Dysfunction
About this trial
This is an interventional treatment trial for Postoperative Cognitive Dysfunction focused on measuring postoperative analgesia, postoperative cognitive disfunction
Eligibility Criteria
Inclusion Criteria:
- patients age 65 and over
- fracture of the proximal femur
- preoperative assessment American Society of Anesthesiologists(ASA) score I - ASA III
- a written consent of the patient to participate in research
Exclusion Criteria:
- patient non-compliance
- ASA status IV and IV above
- patients younger than 65 years
- dementia, Parkinson's disease, cerebrovascular accident history; simultaneous head injuries,the use of opioids and benzodiazepines longer than a month before the surgery; alcoholism; serious liver disease (class C according to Child-Pugh's classification); severe kidney disease that require dialysis
- result of MMSE test (Mini-Mental State Examination) under 17
- the existence of any contraindications for the implementation of regional anesthesia and one or other form of post-operative analgesia.
Sites / Locations
- Clinical Hospital Centre Osijek
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
morphine
levobupivacaine
The patient-controlled intravenous analgesia with morphine (basal flow of 0.5-2 mg / h, bolus dose of 0.5 mg, lockout interval of 20 minutes, hour limit of 3 doses), which will be carried out 72 hours after the surgery
Upon completion of the operation for a period of 72 hours will be implemented continuous epidural local anesthetic through the Patient Controlled Analgesia (PCA) pump (Levobupivacaine 0.125%, basal flow of 6 ml / hour, a bolus dose of 2 ml, lockout interval of 20 minutes, hour limit of 3 doses).