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Published on: May 2, 2017
Comparing propofol versus sevoflurane anesthesia for epileptogenic focus detection during positron emission
K J Wagner1, C M Schulz, T Sprenger
1Klinik für Anaesthesiologie, Technische Universität München, Klinikum rechts der Isar, München, Germany - c.m.schulz@lrz.tum.de.
Insights
Propofol and sevoflurane anesthesia are equally suitable for pediatric epilepsy surgery evaluation using Fluorine-18-deoxyglucose-positron emission tomography (FDG-PET) scans. Both anesthetic methods effectively detect hypometabolic lesions for surgical planning.
Area of Science:
- Neurology
- Radiology
- Anesthesiology
Background:
- Fluorine-18-deoxyglucose-positron emission tomography (FDG-PET) is crucial for localizing the epileptogenic zone in epilepsy patients.
- Anesthesia is often necessary for pediatric patients to minimize movement artifacts during FDG-PET imaging.
- This study evaluates the impact of propofol versus sevoflurane anesthesia on FDG-PET image quality for epilepsy surgery planning.
Purpose of the Study:
- To compare the effectiveness of propofol and sevoflurane anesthesia in pediatric focal epilepsy patients undergoing FDG-PET scans.
- To assess the impact of these anesthetics on image quality, hypometabolic lesion detection, and lesion demarcation.
Main Methods:
- Pediatric patients with focal epilepsy received either propofol (N.=37) or sevoflurane (N.=43) anesthesia.
- Two blinded investigators evaluated PET scans using a 3-point Likert scale for image quality, lesion detectability, and demarcation.
- Statistical analysis included Mann-Whitney-U-Test and Cohen's Kappa for inter-rater reliability.
Main Results:
- Anesthesia was uneventful with no peridiagnostic seizures in either group.
- No statistically significant differences were found in image quality ratings or lesion detection/demarcation between propofol and sevoflurane groups.
- Sum scores for image quality were similar (mean 5.8 ± 1.5 for propofol, 5.7 ± 1.5 for sevoflurane).
Conclusions:
- FDG-PET is essential for identifying hypometabolic areas in epilepsy patients for surgical planning.
- Both propofol and sevoflurane based anesthetic regimens are suitable for detecting hypometabolic cerebral lesions during FDG-PET in pediatric epilepsy patients.
- The choice of anesthetic agent does not significantly impact the diagnostic quality of FDG-PET for epilepsy surgery evaluation.
Background:
Fluoro-D-deoxyglucose positron emission tomography (FDG-PET) is a standard procedure for interictal assessment and accurate pre-surgical evaluation of presumed epileptogenic zone localization. Profound sedation or general anesthesia is frequently required to reduce movement artefacts in young or cognitively impaired patients during image acquisition. This study compares the impact of propofol and sevoflurane anesthesia on overall quality of PET images, detectability of a hypometabolic lesion and demarcation of the detected lesion in pediatric patients suffering from focal epilepsia.
Methods:
Pediatric patients with focal epilepsia were anesthesized using propofol (N.=37) or sevoflurane (N.=43). Two independent blinded investigators rated the PET-scans on a 3-point Likert scale with respect to overall quality of PET images, detectability of a hypometabolic lesion and demarcation of the detected lesion. Mann-Whitney-U-Test was conducted to compare the rating results between the two anesthesia regimes. Inter-rater reliability was calculated using Cohen's Kappa.
Results:
Anesthesia was throughout uneventful and there was no clinical evidence for peridiagnostic seizures. Differences in neither single dimension ratings nor in sum scores (mean 5.8 ± SD 1.5 for propofol, and 5.7 ± SD 1.5 for sevoflurane; P=0.567) were statistically significant. Cohen's Kappa was between 0.428 and 0.499.
Conclusion:
For surgical planning in patients with epilepsy, FDG-PET imaging is an indispensable functional imaging technique to detect hypometabolism. We conclude that both, sevoflurane and propofol based anesthetic regimes are suitable to detect hypometabolic cerebral lesions during FDG-PET.
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