Total knee arthroplasty (TKA) is one of the most common orthopedic surgical procedure and is associated with severe pain in the immediate postoperative period, thus limiting early recovery. Postoperative pain management requires multimodal analgesia, combining drugs and injection of a local anesthetic (LA). For optimal pain management, several peripheral nerve blocks should be associated. Thus, a recent study shows that the combination of IPACK, femoral triangle and obturator nerve blocks (ITO blocks) provides an effective pain control after TKA. The hypothesis of this study is that a quadruple nerve block combining femoral, sciatic, obturator and lateral femoral cutaneous nerve blocks (quadri-block) could improve analgesia after TKA. The main objective of this monocenter, prospective, randomized, open-label, controlled trial is to assess the effect of quadri-block on morphine consumption after TKA compared to ITO blocks.
In the pre-anaesthesia room, after the implementation of classical monitoring with an oxygen mask and a peripheral venous catheter, all patients will receive an antibioprophylaxis according to SFAR (French Society of Anesthesia \& Intensive Care Medecine) recommendations and injection of 10 mg of IV dexamethasone. The patients will be then randomized in 2 groups: * ITO group (usual technique): IPACK combined to femoral triangle and obturator nerve blocks * Quadriblock group (experimental technique): femoral, sciatic, obturator and lateral femoral cutaneous nerve blocks. An experienced anesthetist will perform ultrasound-guided blocks 30 minutes before surgery with ropivacaine 0.3%, total volume of 70 ml. In the operating room, general anesthesia will be induced by intravenous ketamine (0.4 mg/kg) and propofol (3 mg/kg). Anesthesia will be maintained with propofol. Postoperative analgesia protocol : * Multimodal analgesia will be instituted from the end of the surgery by the administration of paracetamol (1 g) and ketoprofen (100 mg). * In post-anesthesia care unit (PACU): oxynorm titration if VRS (pain score) \>3 according to the centre's usual care. * In ward: systematic per os analgesia with paracetamol (1 g, 4 times a day) and ibuprofen (400 mg, 3 times a day); oxynorm (10 mg, lockout interval: 4 h) if VRS (pain score) \>3.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Enrollment
90
25 milliliters of ropivacaine 0.3% will be injected between popliteal artery and femur.
25 milliliters of ropivacaine 0.3% will be injected on the lateral side of the femoral artery at the distal part of the femoral triangle.
20 milliliters of ropivacaine 0.3% will be injected between the adductor magnus and adductor brevis muscles and between the adductor brevis muscle the pectineus.
20 milliliters of ropivacaine 0.3% will be injected in supine position under the fascia iliaca lateral to the femoral artery.
25 milliliters of ropivacaine 0.3% will be injected in prone position in the subgluteal space by lateral approach.
5 milliliters of ropivacaine 0.3% will be injected laterally to the sartorius muscle.
Clinique Médipôle Garonne
Toulouse, Haute-Garonne, France
Postoperative analgesia, defined by the morphine consumption in the first 48 hours post-surgery.
Total amount of oxynorm (mg) administered during the first 48 hours post-surgery.
Time frame: 48 hours
Postoperative pain: Verbal Rating Scale (VRS)
Pain will be assessed every 6 hours using a Verbal Rating Scale (VRS) ranging from 0 to 10 (0=no pain, 10=worst possible pain).
Time frame: 48 hours
Oxynorm consumption in the first 24 hours post-surgery
Total amount of oxynorm (mg) administered during the first 24 hours post-surgery.
Time frame: 24 hours
Ability to walk
0: unable to get up; 1: able to get up but not to walk; 2: walk \<50 m; 3: walk \> 50 m
Time frame: 48 hours
Quadricep mobilization
0: paralysis; 1: paresis, 2: normal contraction
Time frame: 48 hours
Foot elevator muscle mobilization
0: paralysis; 1: paresis; 2: normal contraction
Time frame: 48 hours
Side effects of opioids
Collect side effects associated with oxynorm : nausea or vomiting, drowsiness, constipation, urinary retention, itching, disorientation.
Time frame: 48 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.