British Journal of Anaesthesia, 2002, Vol. 89, No. 5 702-706
© 2002 The Board of Management and Trustees of the British Journal of Anaesthesia
Clinical Investigations |
Spinal anaesthesia: comparison of plain ropivacaine 5 mg ml1 with bupivacaine 5 mg ml1 for major orthopaedic surgery
1 Department of Anaesthetics and Intensive Care Medicine, The Queens University of Belfast, Whitla Medical Building, 97 Lisburn Road, Belfast BT9 7BL, UK. 2 Department of Anaesthetics, Musgrave Park Hospital, Stockmans Lane, Belfast, UK. 3 AstraZeneca R&D, Sodertalje, Sweden*Corresponding author
Background. Ropivacaine provides effective spinal anaesthesia for total hip arthroplasty. This study was designed to compare the efficacy and safety of plain ropivacaine with plain bupivacaine for spinal anaesthesia in patients undergoing total hip arthroplasty.
Methods. Sixty-six patients, ASA I or II, were randomized to receive an intrathecal injection of one of two local anaesthetic solutions. Group R (n=32) received 3.5 ml of ropivacaine 5 mg ml1 (17.5 mg). Group B (n=34) received 3.5 ml of bupivacaine 5 mg ml1 (17.5 mg). The onset and duration of sensory block at dermatome level T10, maximum upper and lower spread of sensory block and the onset, intensity and duration of motor block were recorded, as were safety data.
Results. Onset of motor and sensory block was rapid with no significant differences between the two groups. The median time of onset of sensory block at the T10 dermatome was 2 min (range 25 min) in Group R and 2 min in Group B (range 29 min). The median duration of sensory block at the T10 dermatome was 3.0 h (range 1.54.6 h) in Group R and 3.5 h (2.75.2 h) in Group B (P<0.0001). The median duration of complete motor block (modified Bromage Scale 3) was significantly shorter in the ropivacaine group compared with the bupivacaine group (2.1 vs 3.9 h, P<0.001).
Conclusions. Intrathecal administration of either 17.5 mg plain ropivacaine or 17.5 mg plain bupivacaine was well tolerated and an adequate block for total hip arthroplasty was achieved in all patients. A more rapid postoperative recovery of sensory and motor function was seen in Group R compared with Group B.
Br J Anaesth 2002; 89: 7026
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