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0.5%左旋布比卡因与0.5%布比卡因用于球周麻醉的有效性和安全性比较

Efficacy and safety of 0.5% levobupivacaine versus 0.5% bupivacaine for peribulbar anesthesia.

作者信息

Pacella Elena, Pacella Fernanda, Troisi Fabiana, Dell'edera Domenico, Tuchetti Paolo, Lenzi Tommaso, Collini Saul

机构信息

Department of Sense Organs, Faculty of Medicine and Dentistry, Rome, Italy.

出版信息

Clin Ophthalmol. 2013;7:927-32. doi: 10.2147/OPTH.S43553. Epub 2013 May 21.

Abstract

BACKGROUND

This randomized double-blind study examined the use of a new anesthetic agent, levobupivacaine 0.5%, which is the S(-)-enantiomer of a racemic mixture of bupivacaine, for peribulbar anesthesia and compared it with racemic bupivacaine 0.5% alone or in combination with hyaluronidase 10 IU/mL.

METHODS

A total of 160 patients undergoing ophthalmic surgery were randomized into four groups (n = 40 each) to receive inferotemporal peribulbar injection of levobupivacaine 0.5% (group L), racemic bupivacaine 0.5% (group B), levobupivacaine + hyaluronidase 10 IU/mL (group LH), or racemic bupivacaine + hyaluronidase 10 IU/mL (group BH) by two anesthetists and two ophthalmologists in a ratio of 25% each. Ocular akinesia and orbicularis oculi function were evaluated using a three-point scale; a value < 5 points was considered as requiring surgery, and movements were re-evaluated the day following surgery to confirm regression of the block.

RESULTS

The time to onset (12 ± 2.6 minutes versus 13 ± 2.8 minutes) and duration of anesthesia (185 ± 33.2 minutes versus 188 ± 35.7 minutes) were similar between groups L and B. Complete akinesia (score 0) was obtained more frequently when hyaluronidase was used in addition to the anesthetic, with occurrences of 72.5% versus 57.5% in group LH versus L, respectively, and 67.5% versus 45% in group BH versus B. Moderate hypotension (<30% of baseline) was observed in four patients (10%) in group L, two (5.0%) in group B, one (2.5%) in group LH, and three (7.5%) in group BH. The time to onset was significantly different between groups L and BH, B and BH, and LH and BH, and the duration of anesthesia differed significantly between groups B and LH, B and BH, and L and LH. The akinesia score differed significantly between groups L and LH and between groups B and LH (P = 0.043 and P = 0.018, respectively), and the number of patients with a score of 0 differed significantly between groups B and LH and between groups B and BH (P = 0.004 and P = 0.017, respectively).

CONCLUSION

Levobupivacaine is a long-lasting local anesthetic with limited cardiotoxicity and neurotoxicity, and may be considered the landmark for vitreoretinal surgery in elderly patients.

摘要

背景

本随机双盲研究考察了一种新型麻醉剂0.5%左旋布比卡因(布比卡因消旋混合物的S(-)-对映体)用于球周麻醉的情况,并将其与单独使用的0.5%消旋布比卡因或与10 IU/mL透明质酸酶联合使用的情况进行比较。

方法

总共160例接受眼科手术的患者被随机分为四组(每组n = 40),由两名麻醉师和两名眼科医生以每组25%的比例进行颞下球周注射,分别接受0.5%左旋布比卡因(L组)、0.5%消旋布比卡因(B组)、左旋布比卡因+10 IU/mL透明质酸酶(LH组)或消旋布比卡因+10 IU/mL透明质酸酶(BH组)。使用三点量表评估眼球运动不能和眼轮匝肌功能;<5分被认为需要手术,并在术后第二天重新评估运动情况以确认阻滞消退。

结果

L组和B组之间的起效时间(12±2.6分钟对13±2.8分钟)和麻醉持续时间(185±33.2分钟对188±35.7分钟)相似。当在麻醉剂中添加透明质酸酶时,更频繁地获得完全运动不能(0分),LH组和L组分别为72.5%对57.5%,BH组和B组分别为67.5%对45%。L组有4例患者(10%)、B组有2例患者(5.0%)、LH组有1例患者(2.5%)、BH组有3例患者(7.5%)出现中度低血压(<基线的30%)。L组和BH组、B组和BH组以及LH组和BH组之间的起效时间有显著差异,B组和LH组、B组和BH组以及L组和LH组之间的麻醉持续时间有显著差异。L组和LH组之间以及B组和LH组之间的运动不能评分有显著差异(分别为P = 0.043和P = 0.018),B组和LH组之间以及B组和BH组之间得0分的患者数量有显著差异(分别为P = 0.004和P = 0.017)。

结论

左旋布比卡因是一种长效局部麻醉剂,心脏毒性和神经毒性有限,可被视为老年患者玻璃体视网膜手术的标杆。

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