Manassero Alberto, Fanelli Andrea
Department of Emergency and Critical Care, Anesthesia and Intensive Care Unit, S. Croce e Carle Hospital, Cuneo.
Department of Medical and Surgical Sciences, Anesthesia and Intensive Care Unit, Policlinico S. Orsola-Malpighi, Bologna, Italy.
Local Reg Anesth. 2017 Mar 31;10:15-24. doi: 10.2147/LRA.S112756. eCollection 2017.
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.
丙胺卡因是一种局部麻醉剂,其特点是麻醉效能和持续时间中等,起效快。作为5%溶液的高压制剂,自1960年以来已被引入并成功用于脊髓麻醉。目前欧洲有2%普通溶液和高压溶液的新制剂。由于其短暂性神经症状的发生率较低,丙胺卡因被建议作为门诊手术脊髓麻醉中利多卡因和甲哌卡因的替代品,以及低剂量长效局部麻醉剂的合适替代品。检索了美国国立医学图书馆数据库、医学文摘数据库、Cochrane系统评价数据库和Cochrane对照试验中心注册数据库1970年至2016年9月期间的资料,目的是确定评估鞘内使用2%丙胺卡因的研究。本综述共使用了13项随机临床试验(RCT)、1项观察性研究、2项剂量探索研究和4项系统评价。评估的研究表明,2%高压丙胺卡因具有良好的麻醉和安全性,是利多卡因和甲哌卡因用于中短期脊髓麻醉的替代药物。与普通溶液相比,高压可显著加快鞘内注射2%丙胺卡因的起效和消退时间。文献表明,对于持续时间长达90分钟的下肢和下腹部手术,丙胺卡因的剂量范围为40至60毫克,而对于会阴手术,10至30毫克的剂量是合适的。脊髓给药后约4小时即可出院。