Sensory block duration after spinal anaesthesia supplemented with intravenous dexamethasone: a randomised controlled double-blinded trial

医学 麻醉 地塞米松 布比卡因 恶心 呕吐 生理盐水 外科 内科学
作者
Alexis Bikfalvi,Gregory Hofmann,Ahmed Bashawyah,Jean‐Benoît Rossel,Erin Gonvers,Éric Albrecht
出处
期刊:BJA: British Journal of Anaesthesia [Elsevier]
卷期号:130 (6): 780-785 被引量:1
标识
DOI:10.1016/j.bja.2023.02.027
摘要

Background Intravenous dexamethasone prolongs duration of analgesia or sensory block after injection of local anaesthetics close to peripheral nerves by an average of 8 h. Uncertainty remains on the potential increase in the duration of sensory block after spinal anaesthesia. The objective of this randomised controlled double-blinded trial was to investigate whether dexamethasone i.v. prolongs the sensory block of spinal anaesthesia with bupivacaine when compared with a control group. Methods Of 50 patients undergoing lower limb osteoarticular surgery under spinal anaesthesia with isobaric bupivacaine 15 mg i.t. with morphine 100 μg i.t. were randomised to receive either dexamethasone 0.15 mg kg−1 i.v. or normal saline 3 ml i.v. The primary outcome was duration of sensory block defined as the time elapsed between injection of the local anaesthetic in the intrathecal space and the regression of sensory block by two dermatomes compared with the highest dermatome blocked. Secondary outcomes included intravenous morphine consumption, pain scores at rest and on movement, postoperative nausea and vomiting, and blood glucose at 2, 24, and 48 h. Results Median duration of sensory block was 135 (105–225) min in the dexamethasone group and 158 (135–240 min) in the control group (P=0.19). Patients in the dexamethasone group received less morphine at 24 h, had significantly less postoperative nausea and vomiting at 2 h and 24 h, and had increased blood glucose at 24 h. Other secondary outcomes were similar between groups. Conclusion Intravenous dexamethasone did not prolong the sensory block of spinal anaesthesia with isobaric bupivacaine. However, it reduced morphine consumption and rate of postoperative nausea and vomiting at 24 h, at the expense of an increased blood glucose. Clinical trial registration NCT03527576 (Clinicaltrials.gov).
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