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比较肥胖患者按理想体重与按总体重给药时的阿曲库铵的效果。

Comparative evaluation of atracurium dosed on ideal body weight vs. total body weight in morbidly obese patients.

机构信息

Departments of Anaesthesiology and Intensive Care, Clinical Pharmacy and Surgery, St Antonius Hospital, Koekoekslaan 1, Nieuwegein, The Netherlands.

出版信息

Br J Clin Pharmacol. 2011 Jan;71(1):34-40. doi: 10.1111/j.1365-2125.2010.03803.x.

Abstract

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT

Different conflicting reports have been published for the use of atracurium in morbidly obese patients. Dosing of atracurium based on lean body mass, total body weight, and total body weight with a dose reduction for every 10 kg more than 70 kg have been proposed.

WHAT THIS STUDY ADDS

The current prospective randomized double-blind study compares atracurium 0.5 mg kg(-1) ideal body weight vs. 0.5 mg kg(-1) total body weight when used as a muscle relaxant in morbidly obese patients undergoing bariatric surgery. Based on our results in patients with body weights varying from 112 to 260 kg, we have concluded that atracurium 0.5 mg kg(-1) ideal body weight results in a predictable profile of muscle relaxation allowing for adequate intubation conditions and recovery of muscle strength within 60 min with lack of need for antagonism. A dose-dependent prolongation of action is shown when dosing is based on total body weight.

AIMS

This double-blind randomized study evaluated atracurium dosing based on ideal body weight vs. total body weight for muscle relaxation in morbidly obese patients undergoing bariatric surgery.

METHODS

Twenty patients (body weight 112-260 kg, BMI 38-79 kg m(-2) ) were randomized to receive atracurium 0.5 mg kg(-1) ideal body weight vs. 0.5 mg kg(-1) total body weight. Primary endpoint was neuromuscular blockade using train-of-four ratios (TOF ratios) and secondary endpoints were intubation conditions and need for antagonism with neostigmine.

RESULTS

In the ideal body weight group, times to recovery of TOF ratio from 0 to 5%, 50% and 75% were significantly shorter [TOF ratio from 0 to 5%: mean difference 30 min (95% CI 23, 39 min)] and with lower variability compared with the total body weight group. In the total body weight group there was a significant correlation between atracurium dose and time to a TOF ratio of 5% (r= 0.82, P < 0.001), which was absent in the ideal body weight group (r= 0.24). In both groups, intubation conditions were good while 70% of the patients in the total body weight group needed neostigmine at the end of surgery compared with 0% in the ideal body weight group.

CONCLUSION

In morbid obesity (112-260 kg), atracurium 0.5 mg kg(-1) ideal body weight results in a predictable profile of muscle relaxation allowing for adequate intubation conditions and recovery of muscle strength to a TOF ratio >90% within 60 min with lack of need for antagonism. A dose-dependent prolongation of action is shown when dosing is based on total body weight.

摘要

关于这个主题已经有不同的相互矛盾的报告发表。有人提出,根据去极化肌松药的瘦体重、总体重和总体重给药,对于病态肥胖患者,每超过 70 公斤体重应减少剂量。

本研究新增内容

目前这项前瞻性随机双盲研究比较了肥胖患者接受减重手术时,使用 0.5mg/kg 理想体重的阿曲库铵与 0.5mg/kg 总体重的阿曲库铵作为肌松药的效果。根据体重 112-260kg 的患者的结果,我们得出结论,0.5mg/kg 理想体重的阿曲库铵可产生可预测的肌肉松弛作用,可实现充分的插管条件,并在 60 分钟内恢复肌力,无需拮抗。当基于总体重给药时,会出现剂量依赖性的作用延长。

目的

本双盲随机研究评估了基于病态肥胖患者接受减重手术时的理想体重和总体重来给予阿曲库铵以实现肌肉松弛的效果。

方法

20 名患者(体重 112-260kg,BMI 38-79kg/m2)被随机分为接受 0.5mg/kg 理想体重的阿曲库铵或 0.5mg/kg 总体重的阿曲库铵。主要终点是使用四个成串刺激(TOF 比值)评估神经肌肉阻滞,次要终点是插管条件和新斯的明拮抗的需要。

结果

在理想体重组中,从 0 恢复到 5%、50%和 75%的 TOF 比值的时间明显更短[从 0 到 5%的 TOF 比值:平均差异 30 分钟(95%CI 23,39 分钟)],且变异性更低,与总体重组相比。在总体重组中,阿曲库铵剂量与 TOF 比值为 5%的时间之间存在显著相关性(r=0.82,P<0.001),而在理想体重组中则不存在(r=0.24)。在两组中,插管条件良好,而总体重组 70%的患者在手术结束时需要新斯的明,而理想体重组则无此需要。

结论

在病态肥胖(112-260kg)中,0.5mg/kg 理想体重的阿曲库铵可产生可预测的肌肉松弛作用,可实现充分的插管条件,并在 60 分钟内恢复肌力至 TOF 比值>90%,且无需拮抗。当基于总体重给药时,会出现剂量依赖性的作用延长。

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