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Anesthesia and analgesia · Aug 2007
Randomized Controlled Trial Comparative StudySpinal ropivacaine for lower limb surgery: a dose response study.
- Ying Y Lee, Warwick D Ngan Kee, Hang K Chang, Chi L So, and Tony Gin.
- Department of Anaesthesiology, Kwong Wah Hospital, Shatin, Hong Kong, SAR, China. yyleekwh@yahoo.com
- Anesth. Analg. 2007 Aug 1;105(2):520-3.
BackgroundThe dose-response relationship for spinal ropivacaine in patients undergoing surgery of the lower extremity has not been fully determined.MethodsWe performed a prospective, randomized, double-blind study of 60 patients scheduled for lower limb surgery under combined spinal-epidural anesthesia. Patients were assigned to receive 1 of 5 doses of intrathecal ropivacaine: 2, 4, 7, 10, or 14 mg diluted to 2.8 mL with normal saline. A dose was considered successful if a sensory block to cold was achieved bilaterally at the T12 dermatome within 20 min and surgery proceeded without supplementation for at least 50 min.ResultsAnesthesia was successful in 0, 0, 42, 83, and 100% of the 2, 4, 7, 10, and 14 mg groups, respectively. The derived value for ED(50) was 7.6 mg (95% CI: 6.2-8.7 mg) and for ED(95) was 11.4 mg (95% CI: 9.7-18.3 mg). The cephalic level of sensory block and the degree of motor block increased with larger doses of ropivacaine.ConclusionThe ED(50) and ED(95) for spinal ropivacaine in lower limb surgery of 50 min duration or less were 7.6 and 11.4 mg, respectively. This provides a useful guide for clinicians to choose the optimal dose of spinal ropivacaine under different clinical situations.
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