Spinal or Intravenous Dexmedetomidine for Spinal Anesthesia with Chloroprocaine in Ambulatory Knee Arthroscopies: A Double-Blind Randomized Trial.

IF 1.5 Q3 ANESTHESIOLOGY Local and Regional Anesthesia Pub Date : 2021-11-20 eCollection Date: 2021-01-01 DOI:10.2147/LRA.S324876
Margaretha B Breebaart, Lies Saerens, Jordi Branders, Sari Casaer, Luc Sermeus, Patrick Van Houwe
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Abstract

Purpose: Chloroprocaine provides spinal anesthesia for day-case surgery lasting up to 40 minutes. Intravenous and spinal dexmedetomidine can prolong spinal anesthesia, but no data are available for the combination with chloroprocaine. This double-blind randomized controlled trial compares chloroprocaine with spinal or intravenous dexmedetomidine regarding block characteristics, micturition, and discharge times.

Patients and methods: After ethical approval and informed consent, 135 patients scheduled for knee arthroscopy were randomized to receive either 40mg spinal chloroprocaine (Chloro-group), 40mg chloroprocaine with 5 mcg spinal dexmedetomidine (Spinal Dex-group) or 40mg chloroprocaine with 0.5 mcg/kg IV dexmedetomidine (IV DEXgroup). Block characteristics, hemodynamic variables and the use of analgesics were registered. Voiding and discharge times were noted. A scoring system was used for micturition problems and sedation. Transient neurological symptoms (TNS) and other late side effects were evaluated after one week.

Results: Demographic data were similar between groups. Block onset times and intensity of motor block were comparable between groups. The time to L2 and Bromage 1 regression was prolonged in the SpinalDEx-group by approximately 30 minutes compared to the other groups (p < 0.01). First voiding as well as discharge from the hospital was prolonged in the Spinal Dex-group by approximately 40 minutes p < 0.01. There was no significant difference between groups regarding treatment of hypotension, sedation, micturition problems or the use of postoperative analgesics (P > 0.8). One patient experienced TNS.

Conclusion: Intrathecal but not intravenous (0.5 mcg/kg) dexmedetomidine can prolong chloroprocaine (40mg) spinal anesthesia when surgery is expected to last over 40 minutes. Despite a similar incidence of adverse effects, this also led to a postponed hospital discharge time.

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脊髓或静脉注射右美托咪定与氯丙卡因用于膝关节置换术的脊髓麻醉:一项双盲随机试验。
目的:氯普鲁卡因为日间手术提供长达40分钟的脊髓麻醉。静脉注射和脊髓注射右美托咪定可延长脊髓麻醉时间,但与氯普鲁卡因联用没有相关数据。这项双盲随机对照试验比较氯普鲁卡因与脊髓或静脉注射右美托咪定在阻滞特征、排尿和排泄时间方面的差异。患者和方法:经伦理批准和知情同意后,135例膝关节镜患者随机接受40mg氯普鲁卡因(氯组)、40mg氯普鲁卡因加5mcg右美托咪定(脊髓右美托咪定组)或40mg氯普鲁卡因加0.5 mcg/kg静脉右美托咪定(静脉右美托咪定组)治疗。记录阻滞特征、血流动力学变量和镇痛药的使用。记录排尿和出院时间。排尿问题和镇静使用评分系统。一周后评估短暂性神经症状(TNS)和其他晚期副作用。结果:组间人口学数据相似。两组间阻滞发作时间和运动阻滞强度具有可比性。与其他组相比,spinaldex组的L2和Bromage 1回归时间延长了约30分钟(p < 0.01)。Spinal dex组首次排尿和出院时间延长约40分钟,p < 0.01。两组患者在低血压、镇静、排尿问题及术后镇痛药使用方面差异无统计学意义(P > 0.8)。一名患者经历了TNS。结论:当手术时间超过40分钟时,鞘内注射右美托咪定可延长氯普鲁卡因(40mg)脊髓麻醉时间,但静脉注射(0.5 mcg/kg)无效。尽管不良反应发生率相似,但这也导致了出院时间的推迟。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
12
审稿时长
16 weeks
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