Sheikh Rafi, Memarzadeh Khashayar, Torbrand Christian, Blohmé Jonas, Malmsjö Malin
Lund University, Skane University Hospital, Department of Clinical Sciences Lund, Ophthalmology, Lund, Sweden.
Lund University, Skane University Hospital, Department of Clinical Sciences Lund, Urology, Lund, Sweden.
J Plast Reconstr Aesthet Surg. 2017 Mar;70(3):322-329. doi: 10.1016/j.bjps.2016.10.017. Epub 2016 Nov 11.
The present study aimed to examine hypoperfusion in response to epinephrine following the administration of a local anaesthetic. The concentration of epinephrine that causes maximal hypoperfusion, the spread of hypoperfusion in the tissue and the time to the stabilization of hypoperfusion were investigated.
Blood perfusion was monitored using laser Doppler velocimetry and laser speckle contrast imaging of random-pattern advancement flaps (1 × 4 cm) or intact skin on the pig flank. Epinephrine was either injected cumulatively (0.1, 1.0, 10 or 100 μg/ml) after injecting 20 mg/ml lidocaine, to determine the concentration response, or given as a single dose (12.5 μg/ml epinephrine+20 mg/ml lidocaine). Control experiments were performed with saline or lidocaine (without epinephrine).
Increasing concentrations of epinephrine resulted in a gradual decrease in skin perfusion, approaching a minimum after injecting 10 μg/ml. The area of hypoperfusion was 12 mm in radius, and the time from the injection to the stabilization of hypoperfusion was approximately 120 s. After the administration of 10 μg/ml epinephrine in flaps with small pedicle, 25% blood perfusion still remained.
Local anaesthetic with an epinephrine concentration of approximately 10 μg/ml appears to be adequate for vasoconstriction before surgery. Incisions were required to be delayed only for 2 min following local anaesthetic with epinephrine in pigs. The remaining 25% blood perfusion observed after the administration of epinephrine supports the use of epinephrine in flaps with a small pedicle. Obviously, these experimental findings must be clinically assessed before being considered for infiltration anaesthesia during plastic surgery procedures.
本研究旨在检测局部麻醉药给药后肾上腺素引起的组织灌注不足情况。研究了导致最大灌注不足的肾上腺素浓度、灌注不足在组织中的扩散范围以及灌注不足稳定所需的时间。
使用激光多普勒测速仪和激光散斑对比成像技术监测猪侧腹随机模式推进皮瓣(1×4厘米)或完整皮肤的血流灌注。在注射20毫克/毫升利多卡因后,累积注射肾上腺素(0.1、1.0、10或100微克/毫升)以确定浓度反应,或者给予单剂量(12.5微克/毫升肾上腺素+20毫克/毫升利多卡因)。用生理盐水或利多卡因(不含肾上腺素)进行对照实验。
肾上腺素浓度增加导致皮肤灌注逐渐减少,注射10微克/毫升后接近最低值。灌注不足区域的半径为12毫米,从注射到灌注不足稳定的时间约为120秒。在蒂部较小的皮瓣中注射10微克/毫升肾上腺素后,仍有25%的血流灌注。
肾上腺素浓度约为10微克/毫升的局部麻醉药似乎足以在手术前进行血管收缩。在猪身上,使用含肾上腺素的局部麻醉药后,只需延迟2分钟即可进行切口。注射肾上腺素后观察到的剩余25%血流灌注支持在蒂部较小的皮瓣中使用肾上腺素。显然,这些实验结果在被考虑用于整形手术的浸润麻醉之前必须进行临床评估。