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Prilocaine hydrochloride 2 hyperbaric solution for intrathecal injection: a clinical review

机译:盐酸普洛卡因2%高压溶液鞘内注射的临床评价

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摘要

Prilocaine is a local anesthetic characterized by intermediate potency and duration and fast onset of action. As hyperbaric formulation of 5% solution, it was introduced and has been successfully used for spinal anesthesia since 1960. A new formulation of 2% plain and hyperbaric solution is currently available in Europe. Because of its lower incidence of transient neurological symptoms, prilocaine is suggested as substitute to lidocaine and mepivacaine in spinal anesthesia for ambulatory surgery, as well as a suitable alternative to low doses of long-acting local anesthetics. The National Library of Medicine database, the Excerpta Medica database, the Cochrane Database of Systematic Reviews, and the Cochrane Central Register of Controlled Trials database, were searched for the period 1970 to September 2016, with the aim to identify studies evaluating the intrathecal use of 2% prilocaine. A total of 13 randomized clinical trials (RCTs), 1 observational study, 2 dose finding, and 4 systematic reviews has been used for this review. The studies evaluated showed that 2% hyperbaric prilocaine due to a favorable anesthetic and safety profile is an alternative drug to lidocaine and mepivacaine for spinal anesthesia of intermediate or short duration. In comparison with plain solutions, hyperbaricity remarkably accelerates the onset and offset times of intrathecal 2% prilocaine. Literature suggests a dose ranging between 40 and 60 mg of prilocaine for lower extremities and lower abdominal procedures lasting up to 90 min, whereas a dose ranging from 10 to 30 mg is appropriate for perineal surgery. Readiness for discharge occurs in ~4 h from spinal administration.
机译:Prilocaine是一种局部麻醉药,其特征是中等效力和持续时间,起效快。作为5%溶液的高压制剂,自1960年以来,它已被引入并成功用于脊柱麻醉。欧洲目前有2%的纯净和高压溶液的新制剂。由于普利卡因在短暂性神经系统症状中的发生率较低,因此建议在脊柱麻醉中代替利多卡因和甲哌卡因进行非卧床手术,以及低剂量长效局麻药的合适替代品。在1970年至2016年9月期间,搜索了国家医学图书馆数据库,Excerpta Medica数据库,Cochrane系统评价数据库和Cochrane对照试验中央注册数据库,目的是确定评估鞘内注射使用的研究。 2%丙胺卡因。总共13项随机临床试验(RCT),1项观察性研究,2项剂量寻找和4项系统评价已用于本评价。评估的研究表明,由于麻醉和安全性良好,2%的高压丙胺卡因可替代利多卡因和甲哌卡因,用于中度或短时间的脊柱麻醉。与普通溶液相比,高压灭菌显着加快了鞘内2%丙胺卡因的发作和抵消时间。文献表明,对于下肢和下腹部手术,丙胺卡因的剂量范围为40至60 mg,持续时间长达90分钟,而会阴手术的剂量范围为10至30 mg。脊柱给药后约4小时即可出院。

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