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Published on: July 25, 2025
Repeat episodes of severe muscle rigidity in a child receiving sevoflurane
Ira Todd Cohen1, Richard Kaplan
1Department of Anesthesiology, Children's National Medical Center, Washington, DC 20010, USA. icohen@cnmc.org
Abstract:
We report on a patient who developed two episodes of severe muscle rigidity, increased endtidal CO2 and increased creatine phosphate kinase associated with sevoflurane anesthesia. Dysrhythmias and hyperthermia were not observed and dantrolene was not administered. Genetic testing for the 17 known mutations associated with malignant hyperthermia (MH) was negative. Although we cannot rule out MH or other neuromuscular diseases we suggest that this rare event may be a direct effect of sevoflurane.
Insights
Severe muscle rigidity and elevated creatine kinase occurred in a patient during sevoflurane anesthesia. This rare event, not linked to malignant hyperthermia (MH), suggests a potential direct effect of sevoflurane.
Area of Science:
- Anesthesiology
- Pharmacology
- Neuromuscular Disorders
Background:
- Sevoflurane is a widely used inhalation anesthetic.
- Malignant hyperthermia (MH) is a rare, life-threatening pharmacogenetic disorder of skeletal muscle.
Observation:
- A patient experienced two episodes of severe muscle rigidity, increased end-tidal CO2, and elevated creatine phosphokinase.
- The patient did not exhibit dysrhythmias or hyperthermia.
- Dantrolene administration was not required.
Findings:
- Genetic testing for known malignant hyperthermia (MH) mutations was negative.
- The clinical presentation suggests a possible adverse reaction to sevoflurane.
- The absence of typical MH signs and negative genetic results warrant further investigation.
Implications:
- This case highlights a potential, rare adverse effect of sevoflurane not consistent with malignant hyperthermia (MH).
- Further research is needed to elucidate the mechanism of sevoflurane-induced muscle rigidity.
- Clinicians should consider sevoflurane as a potential cause for similar episodes in patients without MH susceptibility.
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