Harvey Martyn, Cave Grant, Lahner Daniel, Desmet Jan, Prince Gaynor, Hopgood Gary
Department of Emergency Medicine, Waikato Hospital, Pembroke Street, Hamilton 3204, New Zealand.
Crit Care Res Pract. 2011;2011:361737. doi: 10.1155/2011/361737. Epub 2011 Mar 31.
Background and objective. Beta-blocker overdose may result in intractable cardiovascular collapse despite conventional antidotal treatments. High dose insulin/glucose (ING), and more recently intravenous lipid emulsion (ILE), have been proposed as potentially beneficial therapies in beta blocker intoxication. We compare efficacy of the novel antidotes ING, with ILE, in a rabbit model of combined enteric/intravenous propranolol toxicity. Methods. Sedated, mechanically ventilated and invasively monitored New Zealand White rabbits underwent mini-laparotomy and enterostomy formation with 40 mg/kg propranolol instilled into the proximal small bowel. At 30 minutes propranolol infusion was commenced at 4 mg/kg/hr and continued to a target mean arterial pressure (MAP) of 50% baseline MAP. Animals were resuscitated with insulin at 3 U/kg plus 0.5 g/kg glucose (ING group), or 10 mL/kg 20% Intralipid (ILE group). Results. Rate pressure product (RPP; RPP = heart rate × mean arterial pressure) was greatest in the ING group at 60 minutes (P < .05). A trend toward greater heart rate was observed in the ING group (P = .06). No difference was observed in survival between groups (4/5 ING versus 2/5 ILE; P = .524). Conclusions. High dose insulin resulted in greater rate pressure product compared with lipid emulsion in this rabbit model of severe enteric/intravenous propranolol toxicity.
背景与目的。尽管采用了传统解毒治疗方法,β受体阻滞剂过量仍可能导致难治性心血管衰竭。高剂量胰岛素/葡萄糖(ING)以及最近的静脉注射脂质乳剂(ILE)已被提议作为β受体阻滞剂中毒可能有益的治疗方法。我们在兔肠内/静脉联合给予普萘洛尔毒性模型中比较新型解毒剂ING与ILE的疗效。方法。对新西兰白兔进行镇静、机械通气和有创监测,行小剖腹术并形成肠造口,将40mg/kg普萘洛尔注入近端小肠。30分钟后,以4mg/kg/小时的速度开始输注普萘洛尔,并持续至目标平均动脉压(MAP)为基线MAP的50%。动物分别用3U/kg胰岛素加0.5g/kg葡萄糖(ING组)或10mL/kg 20%英脱利匹特(ILE组)进行复苏。结果。ING组在60分钟时速率压力乘积(RPP;RPP = 心率×平均动脉压)最大(P < 0.05)。ING组观察到心率有升高趋势(P = 0.06)。两组之间的生存率无差异(ING组4/5,ILE组2/5;P = 0.524)。结论。在这个严重肠内/静脉普萘洛尔毒性兔模型中,与脂质乳剂相比,高剂量胰岛素导致更大的速率压力乘积。