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The incidence of masseter muscle rigidity after succinylcholine in infants and children
V A Lazzell1, A S Carr, J Lerman
1Department of Anaesthesia, Hospital for Sick Children, University of Toronto, Ontario, Canada.
Insights
The anesthetic induction sequence impacts masseter muscle rigidity (MMR) in children. Sodium thiopentone (STP) followed by succinylcholine (Sch) showed no MMR cases, unlike halothane-based anesthesia.
Area of Science:
- Anesthesiology
- Pediatric Anesthesia
- Pharmacology
Background:
- Masseter muscle rigidity (MMR) is a rare complication during anesthesia.
- The influence of anesthetic induction sequence on MMR incidence requires clarification.
Purpose of the Study:
- To investigate the relationship between anesthetic induction sequence and the incidence of masseter muscle rigidity in pediatric patients.
Main Methods:
- Prospective study of 5,641 infants and children undergoing anesthesia for tracheal intubation.
- Comparison of three induction sequences: intravenous sodium thiopentone (STP) alone, halothane alone, or halothane followed by STP.
- Muscle relaxation facilitated by succinylcholine (Sch) or non-depolarizing agents; MMR episodes were recorded.
Main Results:
- No cases of MMR occurred when STP was followed by Sch.
- MMR incidence was 0.9% after halothane and Sch, and 0.4% after halothane, STP, and Sch.
- STP induction resulted in a significantly lower MMR incidence compared to halothane-based inductions (P < 0.025).
Conclusions:
- The anesthetic induction sequence significantly affects the incidence of masseter muscle rigidity in children.
- Using sodium thiopentone prior to succinylcholine may reduce the risk of MMR.
- Further research into the mechanisms of MMR and its association with specific anesthetic agents is warranted.
Abstract:
To determine whether the incidence of masseter muscle rigidity is affected by the anaesthetic induction sequence, we prospectively studied for ten months the anaesthetic course in 5,641 infants and children who received muscle relaxation to facilitate tracheal intubation. The anaesthetic induction sequence consisted of intravenous sodium thiopentone (STP) 5 mg.kg-1 alone, halothane induction alone 1-4%, or halothane followed by STP. Inhalational inductions with halothane included nitrous oxide and oxygen. Tracheal intubation was facilitated by either intravenous succinylcholine (Sch) at least 1.5 mg.kg-1 or by a non-depolarizing muscle relaxant. The induction sequence and all episodes of MMR were recorded. Ninety percent of the patients received Sch and 10% received a non-depolarising agent. Of those who received Sch, 88% (5,064 patients) were anaesthetised with STP and 12% (607 patients) were anaesthetised with halothane alone or halothane followed by STP. Masseter muscle rigidity was defined clinically by the transient inability to distract the mandible from the maxilla such that the mouth could not be opened or could only be opened with force. No children anaesthetised with STP followed by Sch developed MMR. One child (0.9%) developed MMR after halothane and Sch and two developed MMR after halothane, STP and Sch (0.4%). The incidence of MMR after Sch was less with STP than with halothane alone or with halothane and STP (P < 0.025). The peak CPK values in the three children who developed MMR were 17,580 IU.L-1 after halothane and Sch, and 7,280 IU.-1 and 3,273 IU.-1 after halothane, STP and Sch. There was no evidence of MH reactions in these patients.(ABSTRACT TRUNCATED AT 250 WORDS)
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