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Physostigmine and anaesthesia emergence delirium in preschool children: a randomized blinded trial
W Funk1, H Hollnberger, J Geroldinger
1Department of Anaesthesia and Intensive Care Medicine, Klinikum St Marien, Amberg, Germany. funk.wolfgang@klinikum-amberg.de
Insights
Physostigmine did not significantly reduce emergence agitation in preschool children. While not a routine treatment, it may offer therapeutic options when administered carefully to avoid side effects like nausea and vomiting.
Area of Science:
- Anesthesiology
- Pediatric Medicine
- Pharmacology
Background:
- Severe emergence agitation is common in preschool children post-anesthesia.
- Symptoms resemble central anticholinergic syndrome.
- Physostigmine, a cholinesterase-inhibitor, was investigated for efficacy.
Purpose of the Study:
- To assess physostigmine's effectiveness in treating emergence agitation in children.
- To identify adverse effects associated with physostigmine use.
- To evaluate physostigmine as a treatment for post-anesthetic delirium.
Main Methods:
- 211 children (1-5 years) were anesthetized with sevoflurane.
- Multimodal pain therapy was administered.
- Severely agitated children received physostigmine (30 mcg/kg) or placebo in a double-blind, randomized trial.
- Agitation was assessed using a 5-step score.
Main Results:
- 19% of children experienced severe delirium.
- Physostigmine showed no statistically significant reduction in severe agitation at 5 minutes compared to placebo.
- Postoperative nausea and vomiting increased significantly in the physostigmine group (45% vs. 15%).
Conclusions:
- The study does not support the routine use of physostigmine for emergence agitation.
- Physostigmine may be a therapeutic option if administered slowly with prophylaxis for nausea and vomiting.
- Emergence agitation may be linked to anticholinergic effects.
Background:
A significant proportion of preschool children experiences severe emergence agitation after anaesthesia. The symptoms of disorientation, restlessness, inconsolable crying and thrashing resemble an acute psychosis similar to an agitated central anticholinergic syndrome. The primary aim of this randomized controlled study was to assess the efficiency of the cholinesterase-inhibitor physostigmine in these children and to identify adverse effects.
Methods:
We anaesthetized 211 children (1-5 yr) with sevoflurane after midazolam premedication for varying operative procedures. Multimodal intraoperative and prophylactic pain therapy combined alfentanil, piritramide, diclofenac and regional/local bupivacaine. A 5-step score assessed emergence agitation. Severely agitated children were treated immediately with physostigmine (30 mug kg-1) or placebo in a randomized, double-blind fashion. The primary variable was the agitation score after 5 min.
Results:
Severe delirium occurred in 19% of all children. Five minutes following injection, severe agitation was still present in 10 out of 20 patients treated with physostigmine and 16/20 with placebo. This difference did not reach statistical significance (P = 0.1). Rescue therapy with intravenous propofol was given after 15 min of severe agitation to four children following physostigmine and nine following placebo (non-significant). An increased rate of postoperative nausea and vomiting (45% vs. 15%, P < 0.05) was the only adverse effect observed.
Conclusions:
Severe emergence agitation might be related to a central anticholinergic syndrome as diagnosed empirically with a successful treatment with physostigmine. However, the results of this study do not support its routine use. The substance may augment the therapeutic options if injected slowly and after suitable prophylaxis to avoid postoperative nausea and vomiting.
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