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Anesthetic Hypersensitivity in a Case-Controlled Series of Patients With Mitochondrial Disease
Vincent C Hsieh1, Julie Niezgoda2, Margaret M Sedensky1
1From the Department of Anesthesiology and Perioperative Medicine, University of Washington and Seattle Children's Hospital, Seattle, Washington.
Insights
Children with complex I mitochondrial disease exhibit increased sensitivity to sevoflurane anesthesia. This hypersensitivity is less pronounced in other mitochondrial defects, highlighting the importance of targeted anesthetic care for these patients.
Area of Science:
- Anesthesiology
- Pediatrics
- Mitochondrial Medicine
Background:
- Children with mitochondrial disease require anesthesia for various procedures.
- Perioperative medications can impact mitochondrial function.
- Electron transport chain (ETC) defects may cause sevoflurane hypersensitivity in children.
Purpose of the Study:
- To investigate sevoflurane sensitivity in children with mitochondrial disease undergoing anesthesia for diagnostic muscle biopsies.
- To compare sevoflurane sensitivity across different mitochondrial ETC complex deficiencies.
Main Methods:
- A multicenter study involving 91 children (6 months to 16 years) undergoing diagnostic muscle biopsy.
- Anesthesia induced with inhaled sevoflurane, monitoring end-tidal (ET) sevoflurane for Bispectral Index (BIS) of 60.
- Comparison of sevoflurane sensitivity between patients with complex I defects and other groups.
Main Results:
- Patients with complex I defects required significantly lower ET sevoflurane concentrations (0.98%) to reach BIS 60 compared to complex II (1.95%), III (2.0%), IV (2.0%), and normal groups (2.2%).
- Correlation between complex I activity and ET sevoflurane concentration (BIS=60) showed a significant inverse relationship (Spearman's coefficient = 0.505, P < .001).
- Sevoflurane hypersensitivity was less pronounced during anesthetic maintenance than induction.
Conclusions:
- Children with complex I mitochondrial dysfunction demonstrate significant hypersensitivity to sevoflurane anesthesia.
- This hypersensitivity is specific to complex I defects and less common in other mitochondrial abnormalities or in non-diagnosed patients.
- Findings underscore the need for careful anesthetic management in pediatric patients with mitochondrial disease, particularly those with complex I defects.
Background:
Children with mitochondrial disease undergo anesthesia for a wide array of surgical procedures. However, multiple medications used for their perioperative care can affect mitochondrial function. Defects in function of the mitochondrial electron transport chain (ETC) can lead to a profound hypersensitivity to sevoflurane in children. We studied the sensitivities to sevoflurane, during mask induction and maintenance of general anesthesia, in children presenting for muscle biopsies for diagnosis of mitochondrial disease.
Methods:
In this multicenter study, 91 children, aged 6 months to 16 years, presented to the operating room for diagnostic muscle biopsy for presumptive mitochondrial disease. General anesthesia was induced by a slow increase of inhaled sevoflurane concentration. The primary end point, end-tidal (ET) sevoflurane necessary to achieve a bispectral index (BIS) of 60, was recorded. Secondary end points were maximal sevoflurane used to maintain a BIS between 40 and 60 during the case, and maximum and minimum heart rate and blood pressures. After induction, general anesthesia was maintained according to the preferences of the providers directing the cases. Primary data were analyzed comparing data from patients with complex I deficiencies to other groups using nonparametric statistics in SPSS v.27.
Results:
The median sevoflurane concentration to reach BIS of 60 during inductions (ET sevoflurane % [BIS = 60]) was significantly lower for patients with complex I defects (0.98%; 95% confidence interval [CI], 0.5-1.4) compared to complex II (1.95%; 95% CI, 1.2-2.7; P < .001), complex III (2.0%; 95% CI, 0.7-3.5; P < .001), complex IV (2.0%; 95% CI, 1.7-3.2; P < .001), and normal groups (2.2%; 95% CI, 1.8-3.0; P < .001). The sevoflurane sensitivities of complex I patients did not reach significance when compared to patients diagnosed with mitochondrial disease but without an identifiable ETC abnormality (P = .172). Correlation of complex I activity with ET sevoflurane % (BIS = 60) gave a Spearman's coefficient of 0.505 (P < .001). The differences in sensitivities between groups were less during the maintenance of the anesthetic than during induction.
Conclusions:
The data indicate that patients with complex I dysfunction are hypersensitive to sevoflurane compared to normal patients. Hypersensitivity was less common in patients presenting with other mitochondrial defects or without a mitochondrial diagnosis.
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