CONTINUOUS EPIDURAL INFUSION OF ROPIVACAINE FOR THE PREVENTION OF POSTOPERATIVE PAIN AFTER MAJOR ORTHOPEDIC-SURGERY - A DOSE-FINDING STUDY

Purpose: A dose-finding study to investigate the use of epidural infus ions of ropivacaine for postoperative analgesia following orthopaedic surgery. Methods: This was a randomized, double-blind study. Surgery w as performed using a combination of a lumbar epidural block utilizing ropivacaine 0.5% and a standardized general anaesthetic. Postoperative ly, an epidural infusion of the study solution (saline, ropivacaine 0. 1%, 0.2% or 0.3%) was started at the rate of 10 ml . hr(-1) and contin ued for 21 hr after arrival in the PACU. Analgesia was supplemented wi th PCA morphine (dose = 1.0 mg, lock-out = 5 min). Results: Forty-four patients completed the study. The ropivacaine 0.1%, 0.2%, 0.3% groups required less morphine over the 21 hr than the saline group (P < 0.01 ). The VAS pain scores were also lower in the three ropivacaine groups (P < 0.001). The ropivacaine groups maintained sensory anaesthesia to pinprick when compared with saline (P < 0.05). The motor block in the 0.3% group was significantly higher than the saline group at all time s (P < 0.05), and higher than the 0.1% group at eight hours (P < 0.01) , while the 0.2% group had higher Bromage scores than saline at 4 and 21 hr (P < 0.05). Conclusions: The use of continuous epidural infusion s of ropi vacaine 0.1%, 0.2% and 0.3% at 10 ml . hr(-1) improved posto perative pain relief and decreased PCA morphine requirements in patien ts undergoing major orthopaedic surgery. The 0.1% and 0.2% concentrati ons produced similar sensory anaesthesia with less motor blockade than the 0.3% concentration.