Yousef Gamal T, Elsayed Khalid M
Department of Anesthesia and Intensive Care, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Anesth Essays Res. 2013 May-Aug;7(2):194-9. doi: 10.4103/0259-1162.118957.
In spite of being the preferred induction agent for LMA insertion, propofol has many undesirable side effects including dose-related cardiorespiratory depression and local pain at injection site. Ketofol as a novel induction agent has been introduced recently with comparable efficacy and improved hemodynamic control.
To investigate ketofol as a suitable induction agent alternative to propofol for insertion of LMA in children considering insertion conditions, hemodynamic stability, local pain at injection site, and recovery.
In this randomized, double-blind study, 100 children were randomly assigned into two groups of 50 patients each in which induction was performed with either propofol or ketofol. Providers were given one 20 ml syringe [represent either 2 mg/kg of propofol (P group) or 0.75 mg/kg of ketamine and 1.5 mg/kg of propofol (KP group)] and one 10 ml syringe for rescue if needed [represent 1 mg/kg of propofol (P group) or 0.25 mg/kg of ketamine and 0.5 mg/kg of propofol (KP group)]. After monitoring with bispectral index (BIS), general anesthesia was induced by infusion with a syringe perfuser at a constant rate of 250 ml/h with either of the two agents till the BIS values decreased to 40. Mean arterial pressure (MAP), heart rate (HR) were measured every 30 seconds up to 5 minutes after LMA placement. The time till BIS values decreased to 40 was measured. All children were evaluated for incidence of apnea, pain on injection, jaw relaxation, conditions for LMA insertion, and complications such as muscle rigidity, hallucinations, and excessive secretions.
Induction time (time to reach BIS of 40) was faster in the KP group (150 ± 23.5 seconds) than in the P group (205 ± 37.4 seconds). The incidence of injection pain was significantly lower in the KP group (10%) than in the P group (80%). Excellent jaw relaxation and full mouth opening were higher in the KP group [45 patients (90%)] than in the P group [38 patients (76%)]. Excellent LMA insertion conditions were observed in 45 patients (90%) in the KP group and 38 patients (76%) in the P group. The KP group showed preserved hemodynamic stability (mean blood pressure, heart rate) with less incidence and duration of apnea compared to the P group.
ketofol is a safe and effective alternative induction agent for LMA insertion in children with rapid onset of action and lower incidence of injection pain. It provided better LMA insertion conditions, improved hemodynamic stability with less prolonged apnea when compared with propofol.
尽管丙泊酚是喉罩置入术的首选诱导药物,但它有许多不良副作用,包括剂量相关的心肺抑制和注射部位局部疼痛。氯胺酮复合丙泊酚作为一种新型诱导药物,最近已被引入,其疗效相当且血流动力学控制有所改善。
考虑到置入条件、血流动力学稳定性、注射部位局部疼痛和恢复情况,研究氯胺酮复合丙泊酚作为丙泊酚的合适替代诱导药物用于儿童喉罩置入术。
在这项随机、双盲研究中,100名儿童被随机分为两组,每组50例,分别用丙泊酚或氯胺酮复合丙泊酚进行诱导。给麻醉医生一支20毫升注射器[分别代表2毫克/千克丙泊酚(P组)或0.75毫克/千克氯胺酮和1.5毫克/千克丙泊酚(KP组)],以及一支10毫升注射器以备需要时抢救用[分别代表1毫克/千克丙泊酚(P组)或0.25毫克/千克氯胺酮和0.5毫克/千克丙泊酚(KP组)]。用脑电双频指数(BIS)进行监测后,用注射器灌注器以250毫升/小时的恒定速率输注两种药物中的一种诱导全身麻醉,直至BIS值降至40。在置入喉罩后5分钟内,每30秒测量一次平均动脉压(MAP)、心率(HR)。测量BIS值降至40所需的时间。评估所有儿童的呼吸暂停发生率、注射疼痛、下颌松弛情况、喉罩置入条件以及诸如肌肉强直、幻觉和分泌物过多等并发症。
KP组(150±23.5秒)的诱导时间(达到BIS值40的时间)比P组(205±37.4秒)更快。KP组的注射疼痛发生率(10%)显著低于P组(80%)。KP组[45例(90%)]的下颌松弛良好和张口充分的比例高于P组[38例(76%)]。KP组45例(90%)和P组38例(76%)观察到喉罩置入条件良好。与P组相比,KP组血流动力学稳定性(平均血压、心率)得以维持,呼吸暂停的发生率和持续时间更低。
氯胺酮复合丙泊酚是一种安全有效的儿童喉罩置入术替代诱导药物,起效迅速,注射疼痛发生率较低。与丙泊酚相比,它提供了更好的喉罩置入条件,改善了血流动力学稳定性,且呼吸暂停时间缩短。