Use of Midodrine for Intraoperative Hemostasis in Cutaneous and Percutaneous Surgery

Joanna Dong , Naiem T. Issa , Michael Kaiser , Simonetta I. Gaumond , Michael Solis , Joel Gil , Robert S. Kirsner , Stephen C. Davis , Joaquin J. Jimenez
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Abstract

Owing to the increasingly high volume of cutaneous and percutaneous procedures performed annually, the demand for local anesthesia has steadily risen. The gold-standard formulations for local anesthesia contain epinephrine at a concentration of 1:100,000 added to lidocaine to aid in hemostasis. Epinephrine, an α-agonist, also exhibits off-target β-adrenergic effects that carry risk of adverse events with these injections. Furthermore, the ongoing global shortage of epinephrine highlights the need for a safer and viable alternative. Midodrine, a targeted a1-adrenergic receptor agonist, is utilized as a vasopressor to induce arterial and venous vasoconstriction. We developed a formulation of 2% lidocaine combined with 1:2,000,000 epinephrine and 50 μM midodrine (midodrine/lidocaine/epinephrine formulation), hypothesizing that this combination would exhibit synergism on hemostasis. In a porcine model of blood loss after punch biopsies, our formulation was compared with 2% lidocaine; 2% lidocaine with 1:100,000 epinephrine; 2% lidocaine with 1:2,000,000 epinephrine; and 2% lidocaine with 50 μM midodrine. Our results indicate that 2% lidocaine with 1:100,000 epinephrine and our midodrine/lidocaine/epinephrine formulation were statistically comparable, with both significantly reducing bleeding when compared with the 2% lidocaine (P < .05). The 2% lidocaine with midodrine alone also showed additional promise as an effective hemostatic formulation. Thus, combination of low-concentration epinephrine and midodrine with lidocaine may exhibit synergistic hemostatic effect in cutaneous surgical settings while reducing potential off-target effects of either vasoconstrictor alone at higher concentrations as adjunct monotherapies.
Midodrine在皮、经皮手术中止血的应用
由于每年越来越多的皮肤和经皮手术,对局部麻醉的需求稳步上升。局部麻醉的金标准配方含有1:10万浓度的肾上腺素,加入利多卡因以帮助止血。肾上腺素,一种α-激动剂,也表现出脱靶β-肾上腺素能作用,这些注射有不良事件的风险。此外,持续的全球肾上腺素短缺突出了需要一种更安全可行的替代品。Midodrine是一种靶向a1-肾上腺素能受体激动剂,被用作血管加压剂来诱导动脉和静脉血管收缩。我们开发了一种2%利多卡因联合1:20 000 000肾上腺素和50 μM米多卡因的配方(米多卡因/利多卡因/肾上腺素配方),假设这种组合在止血方面具有协同作用。在穿孔活检后失血的猪模型中,我们的配方与2%利多卡因进行比较;2%利多卡因配1:10万肾上腺素;2%利多卡因加1:20 000肾上腺素;2%利多卡因加50 μM米多宁。我们的研究结果表明,2%利多卡因加1:10万肾上腺素和我们的米多卡因/利多卡因/肾上腺素配方在统计学上具有可比性,与2%利多卡因(P <;. 05)。2%利多卡因与单独的米多卡因也显示出作为有效止血制剂的额外希望。因此,低浓度的肾上腺素、米多卡因与利多卡因联合使用可能在皮肤手术环境中表现出协同止血作用,同时减少单独使用高浓度血管收缩剂作为辅助单药治疗的潜在脱靶效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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