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阿托品在重症监护插管中的治疗价值。

The therapeutic value of atropine for critical care intubation.

作者信息

Jones Peter

机构信息

Réanimation Pédiatrique (PICU), AP-HP, Hôpital Robert Debré, Paris, France Critical Care Group, Respiratory Critical Care and Anaesthesia Section, Institute of Child Health, University College London, London, UK London School of Hygiene and Tropical Medicine, London, UK.

出版信息

Arch Dis Child. 2016 Jan;101(1):77-80. doi: 10.1136/archdischild-2014-308137. Epub 2015 Jul 21.

Abstract

Recent studies of atropine during critical care intubation (CCI) have revealed that neonates frequently experience bradycardia, are infrequently affected by ventricular arrhythmias and conduction disturbances and deaths have not been reported in a series of studies. The indiscriminate use of atropine is unlikely to alter the outcome during neonatal CCI other than reducing the frequency of sinus tachycardia. In contrast, older children experience a similar frequency of bradycardia to neonates and are more frequently affected by ventricular arrhythmias and conduction disturbances. Mortality during CCI is in the order of 0.5%. Atropine has a beneficial effect on arrhythmias and conduction disturbances and may reduce paediatric intensive care unit mortality. The use of atropine for children >1 month of age may positively influence outcomes beyond a reduction in the frequency of sinus bradycardia. There is indirect evidence that atropine should be used for intubation during sepsis. Atropine should be considered when using suxamethonium. The reliance on heart rate as the sole measure of haemodynamic function during CCI is no longer justifiable. Randomised trials of atropine for mortality during CCI in general intensive care unit populations are unlikely to happen. As such, future research should be focused on establishing of a gold standard for haemodynamic decompensation for CCI. Cardiac output or blood pressure are the most likely candidates. The 'lost beat score' requires development but has the potential to be developed to provide an estimation of risk of haemodynamic decompensation from ECG data in real time during CCI.

摘要

近期关于重症监护插管(CCI)期间使用阿托品的研究表明,新生儿在CCI期间经常出现心动过缓,很少受到室性心律失常和传导障碍的影响,并且在一系列研究中未报告死亡病例。在新生儿CCI期间,滥用阿托品除了降低窦性心动过速的发生率外,不太可能改变预后。相比之下,大龄儿童心动过缓的发生率与新生儿相似,且更常受到室性心律失常和传导障碍的影响。CCI期间的死亡率约为0.5%。阿托品对心律失常和传导障碍有有益作用,可能降低儿科重症监护病房的死亡率。对于1个月以上的儿童,使用阿托品可能会对预后产生积极影响,而不仅仅是降低窦性心动过缓的发生率。有间接证据表明,在脓毒症期间插管应使用阿托品。使用琥珀酰胆碱时应考虑阿托品。在CCI期间仅依靠心率作为血流动力学功能的唯一指标已不再合理。在普通重症监护病房人群中进行阿托品对CCI期间死亡率影响的随机试验不太可能开展。因此,未来的研究应侧重于建立CCI血流动力学失代偿的金标准。心输出量或血压最有可能成为候选指标。“漏搏评分”需要进一步发展,但有可能发展为在CCI期间根据心电图数据实时评估血流动力学失代偿风险。

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