Critical Care Group - Portex Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK.
Arch Dis Child. 2012 Feb;97(2):139-44. doi: 10.1136/adc.2010.210518. Epub 2011 May 28.
Bradycardia occurs during the intubation of some critically ill children as a result of vagal stimulation due to hypoxia and/or laryngeal stimulation; such 'stable' bradycardia is accompanied by selective vasoconstriction. Some induction drugs also induce bradycardia which may be accompanied by vasodilatation which is also a feature of certain pathologies, which influence the progression to 'unstable' bradycardia, which does not respond to re-oxygenation and a pause in laryngoscopy. Preintubation atropine diminishes the overall incidence of stable bradycardia during routine anaesthesia. However, clinical studies of critical care intubation show that atropine does not prevent all episodes of bradycardia and specifically cannot affect vasodilatation. As such, there is insufficient evidence to support a recommendation for the indiscriminate use of atropine for intubation during critical care illness, including simple neonatal respiratory distress. Atropine is appropriate during septic or late stage hypovolaemic shock where abnormal vasomotor tone and bradycardia may potentially set up a negative feedback loop of cardiac hypo-oxygenation and hypoperfusion and during premedication when using suxamethonium.
在一些危重病儿童的插管过程中,由于缺氧和/或喉部刺激引起的迷走神经刺激会导致心动过缓;这种“稳定”的心动过缓伴随着选择性血管收缩。一些诱导药物也会引起心动过缓,可能伴有血管扩张,这也是某些病理特征之一,会影响到“不稳定”心动过缓的进展,这种心动过缓对再给氧和暂停喉镜检查没有反应。插管前给予阿托品可降低常规麻醉期间稳定心动过缓的总发生率。然而,危重病患者插管的临床研究表明,阿托品并不能预防所有心动过缓发作,特别是不能影响血管扩张。因此,没有足够的证据支持在包括单纯新生儿呼吸窘迫在内的危重病期间,对阿托品进行插管的无差别使用。在感染性休克或晚期低血容量性休克期间,由于异常的血管运动张力和心动过缓可能会形成心脏缺氧和灌注不足的负反馈循环,以及在使用琥珀胆碱进行预给药时,阿托品是合适的。