Lysakowski C, Suppan L, Czarnetzki C, Tassonyi E, Tramèr M R
Division of Anaesthesiology, University Hospitals of Geneva, Geneva, Switzerland.
Acta Anaesthesiol Scand. 2007 Aug;51(7):848-57. doi: 10.1111/j.1399-6576.2007.01367.x.
Propofol-rocuronium is thought to be superior to thiopental-rocuronium for rapid sequence intubation (RSI). The role of the intubation model per se has never been investigated.
Randomized comparisons of rocuronium with succinylcholine for true RSI (administration of muscle relaxant immediately after the hypnotic, intubation within 60 s) or modified RSI (delay between administration of the hypnotic and the muscle relaxant, intubation within 60 s) were sought. Good or excellent intubation conditions were expressed as relative risks (RR) with 95% confidence intervals (CI).
Twelve trials (1,471 patients) used a true RSI. With propofol for induction, RR for good or excellent intubation conditions with conventional rocuronium doses (0.6-0.7 mg/kg) was 0.95 (95%CI, 0.90-1.00), with high doses (0.9-1.2 mg/kg) was 0.96 (0.92-1.01) compared with succinylcholine. With thiopental for induction, RR with conventional rocuronium doses was 0.69 (0.61-0.78) and with high doses was 0.99 (0.95-1.03). Nine trials (340 patients) used a modified RSI. With propofol for induction, RR with conventional rocuronium doses was 0.98 (0.91-1.06); data on high rocuronium doses were lacking. With thiopental for induction, RR with conventional rocuronium doses was 0.97 (0.92-1.02) and with high doses was 1.0. There was no evidence that concomitantly used opioids or the dose of the induction agent had an impact on intubation conditions, independent of the intubation model.
The efficacy of rocuronium for RSI is influenced by both, the induction agent and the intubation model. To test the clinical usefulness of alternatives to succinylcholine for RSI, a true RSI model should be used.
在快速顺序诱导插管(RSI)方面,丙泊酚 - 罗库溴铵被认为优于硫喷妥钠 - 罗库溴铵。但插管模型本身的作用从未被研究过。
对罗库溴铵与琥珀酰胆碱用于真正的RSI(催眠药给药后立即给予肌肉松弛剂,60秒内插管)或改良RSI(催眠药与肌肉松弛剂给药之间有延迟,60秒内插管)进行随机比较。良好或优秀的插管条件以相对危险度(RR)及95%置信区间(CI)表示。
12项试验(1471例患者)采用真正的RSI。以丙泊酚诱导时,与琥珀酰胆碱相比,常规罗库溴铵剂量(0.6 - 0.7mg/kg)时良好或优秀插管条件的RR为0.95(95%CI,0.90 - 1.00),高剂量(0.9 - 1.2mg/kg)时为0.96(0.92 - 1.01)。以硫喷妥钠诱导时,常规罗库溴铵剂量时RR为0.69(0.61 - 0.78),高剂量时为0.99(0.95 - 1.03)。9项试验(340例患者)采用改良RSI。以丙泊酚诱导时,常规罗库溴铵剂量时RR为0.98(0.91 - 1.06);缺乏罗库溴铵高剂量的数据。以硫喷妥钠诱导时,常规罗库溴铵剂量时RR为0.97(0.92 - 1.02),高剂量时为1.0。没有证据表明同时使用的阿片类药物或诱导剂剂量对插管条件有影响,与插管模型无关。
罗库溴铵用于RSI的疗效受诱导剂和插管模型两者影响。为测试琥珀酰胆碱替代药物用于RSI的临床实用性,应采用真正的RSI模型。