Schoenwald P K, Whalley D G, Schluchter M D, Gottlieb A, Ryckman J V, Bedocs N M
Cleveland Clinic Foundation, Department of General Anesthesiology, OH 44195, USA.
Anesth Analg. 1995 May;80(5):864-8. doi: 10.1097/00000539-199505000-00002.
The study was designed to investigate the hemodynamic responses to intravenous (IV) injections of various epidural test doses in vascular surgical patients to determine whether previously established criteria in healthier populations were valid in this inherently sicker population. A double-blind, prospective randomized study was performed on 50 patients, not receiving beta-adrenergic antagonists, presenting for vascular surgery and requiring an arterial line. Patients were randomly assigned to receive a 3-mL injection of one of five solutions, either saline (Group 1), lidocaine 45 mg (Group 2), lidocaine 45 mg and epinephrine 5 micrograms (Group 3), lidocaine 45 mg and epinephrine 10 micrograms (Group 4), or lidocaine 45 mg and epinephrine 15 micrograms (Group 5). After injection, a blinded observer recorded arterial blood pressure and heart rate (HR) every 15 s for 3 min. The changes in HR, systolic (SBP), mean (MBP), and diastolic (DBP) blood pressure as well as time to maximum change were analyzed both within and between groups. Only Group 5 had significant within-group changes for all hemodynamic variables measured. Only in the comparison between Groups 1 and 5 and between Groups 2 and 5 were there significant changes in both HR and SBP. The mean increase in HR and SBP within Group 5 was 17.0 +/- 5.9 bpm and 31.0 +/- 10.5 mm Hg, respectively. No differences were found between groups for time to maximum change for HR and SBP which for Group 5 were 64.5 +/- 37.4 s and 90.0 +/- 56.7 s, respectively. To achieve 100% sensitivity and specificity for HR increase, the criterion established was > or = 9 bpm.(ABSTRACT TRUNCATED AT 250 WORDS)
该研究旨在调查血管外科患者静脉注射不同硬膜外试验剂量后的血流动力学反应,以确定先前在健康人群中确立的标准在这类本就病情较重的人群中是否仍然有效。对50例未使用β - 肾上腺素能拮抗剂、拟行血管手术且需要动脉置管的患者进行了一项双盲、前瞻性随机研究。患者被随机分配接受3毫升五种溶液之一的注射,分别为生理盐水(第1组)、利多卡因45毫克(第2组)、利多卡因45毫克加肾上腺素5微克(第3组)、利多卡因45毫克加肾上腺素10微克(第4组)或利多卡因45毫克加肾上腺素15微克(第5组)。注射后,一名不知情的观察者每15秒记录一次动脉血压和心率(HR),持续3分钟。分析了组内和组间心率、收缩压(SBP)、平均压(MBP)和舒张压(DBP)的变化以及达到最大变化的时间。仅第5组所有测量的血流动力学变量在组内有显著变化。仅在第1组和第5组以及第2组和第5组的比较中,心率和收缩压均有显著变化。第5组心率和收缩压的平均增加值分别为17.0±5.9次/分和31.0±10.5毫米汞柱。第5组心率和收缩压达到最大变化的时间分别为64.5±37.4秒和90.0±56.7秒,组间未发现差异。为使心率增加的敏感性和特异性达到100%,确立的标准为≥9次/分。(摘要截断于250字)