{"title":"Onset and duration of intradermal mixtures of bupivacaine and lidocaine with epinephrine.","authors":"James B Collins, Juhee Song, Raman C Mahabir","doi":"10.1177/229255031302100112","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/objective: </strong>Bupivacaine and lidocaine are often used concurrently, in theory, to combine the more rapid onset of lidocaine and the longer duration of bupivacaine. The purpose of this study was to evaluate this concept.</p><p><strong>Methods: </strong>Twenty-five subjects were enrolled in a double-blinded, randomized block design study to evaluate the onset and duration of four different mixtures of lidocaine and bupivacaine with epinephrine. The study was designed to achieve 80% power to detect an effect size of 0.37 at 5% overall significance. The four mixtures tested were: 0.25% bupivacaine with epinephrine (1:200,000); 1% lidocaine with epinephrine (1:100,000); 0.125% bupivacaine and 0.5% lidocaine with epinephrine (1:150,000); and 0.25% bupivacaine and 1% lidocaine with epinephrine (1:150,000). Four intradermal injections were made in the volar forearms of each participant. Time to effect and duration were measured by sensation of a sharp skin prick.</p><p><strong>Results: </strong>Mean time to onset ranged from 12 s to 29 s without statistical significance across all tested solutions (P=0.891). Mean duration of effect ranged from 6 h 38 min to 7 h 25 min with a statistically significant difference across the tested solutions (P=0.036).</p><p><strong>Conclusions: </strong>No statistical benefit was measured when comparing lidocaine with epinephrine, bupivacaine with epinephrine, and mixtures of these local anesthetics with regard to onset of action. While a statistical difference was observed in duration of effect, the clinical benefit measured was narrow.</p>","PeriodicalId":0,"journal":{"name":"","volume":"21 1","pages":"51-3"},"PeriodicalIF":0.0,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/229255031302100112","citationCount":"28","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/229255031302100112","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 28
Abstract
Background/objective: Bupivacaine and lidocaine are often used concurrently, in theory, to combine the more rapid onset of lidocaine and the longer duration of bupivacaine. The purpose of this study was to evaluate this concept.
Methods: Twenty-five subjects were enrolled in a double-blinded, randomized block design study to evaluate the onset and duration of four different mixtures of lidocaine and bupivacaine with epinephrine. The study was designed to achieve 80% power to detect an effect size of 0.37 at 5% overall significance. The four mixtures tested were: 0.25% bupivacaine with epinephrine (1:200,000); 1% lidocaine with epinephrine (1:100,000); 0.125% bupivacaine and 0.5% lidocaine with epinephrine (1:150,000); and 0.25% bupivacaine and 1% lidocaine with epinephrine (1:150,000). Four intradermal injections were made in the volar forearms of each participant. Time to effect and duration were measured by sensation of a sharp skin prick.
Results: Mean time to onset ranged from 12 s to 29 s without statistical significance across all tested solutions (P=0.891). Mean duration of effect ranged from 6 h 38 min to 7 h 25 min with a statistically significant difference across the tested solutions (P=0.036).
Conclusions: No statistical benefit was measured when comparing lidocaine with epinephrine, bupivacaine with epinephrine, and mixtures of these local anesthetics with regard to onset of action. While a statistical difference was observed in duration of effect, the clinical benefit measured was narrow.
背景/目的:理论上,布比卡因和利多卡因常同时使用,利多卡因起效快,布比卡因持续时间长。本研究的目的是评估这一概念。方法:25名受试者参加了一项双盲、随机区组设计研究,以评估四种不同的利多卡因、布比卡因与肾上腺素的混合物的起效和持续时间。该研究被设计为达到80%的检测能力,在5%的总体显著性下检测0.37的效应量。四种试验混合物分别为:0.25%布比卡因与肾上腺素(1:20万);1%利多卡因加肾上腺素(1:10万);0.125%布比卡因、0.5%利多卡因加肾上腺素(1:15万);0.25%布比卡因和1%利多卡因加肾上腺素(1:15万)。在每个参与者的掌侧前臂进行了四次皮内注射。通过皮肤刺痛的感觉来测量作用时间和持续时间。结果:各溶液的平均发病时间为12 ~ 29 s,差异无统计学意义(P=0.891)。平均作用持续时间为6 h 38 min至7 h 25 min,不同溶液间差异有统计学意义(P=0.036)。结论:比较利多卡因与肾上腺素、布比卡因与肾上腺素以及这些局部麻醉剂的混合物在起效方面没有统计学上的益处。虽然在效果持续时间上观察到统计学差异,但所测量的临床获益很窄。